Next Article in Journal
Development, Optimization and Evaluation of a Sensitive Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detection of Chicken-Based IgY Polyclonal Antibodies against Toxins of D. polylepis Venom
Previous Article in Journal
Adoptive Cell Therapy in Mice Sensitized to a Grass Pollen Allergen
 
 
Journals
Antibodies
Volume 13
Issue 2
10.3390/antib13020049
antibodies-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Screening for TORCH Antibodies in Croatian Childbearing-Aged Women, 2014–2023

by
Tatjana Vilibic-Cavlek
1,2,*,†,
Branko Kolaric
3,4,*,†,
Marko Belamaric
5,
Mario Sviben
2,6,
Thomas Ferenc
7,
Dan Navolan
8,
Viktor Bekic
1,
Ljiljana Milasincic
1,
Ljiljana Antolasic
1,
Maja Vilibic
9,10,
Mateja Vujica Ferenc
11,
Ema Reicher
2,
Tadej Jezek
2,
Ioana Ciohat
12,
Raluca Catalina Parvanescu
12,
Matea Kos
13 and
Maja Bogdanic
1,2
1
Department of Virology, Croatian Institute of Public Health, 10000 Zagreb, Croatia
2
School of Medicine, University of Zagreb, 10000 Zagreb, Croatia
3
Andrija Stampar Teaching Institute of Public Health, 10000 Zagreb, Croatia
4
Department of Social Medicine and Epidemiology, Medical Faculty, University of Rijeka, 51000 Rijeka, Croatia
5
Teaching Institute for Emergency Medicine, 10000 Zagreb, Croatia
6
Department of Parasitology, Croatian Institute of Public Health, 10000 Zagreb, Croatia
7
Department of Diagnostic and Interventional Radiology, University Hospital Merkur, 10000 Zagreb, Croatia
8
Department of Obstetrics and Gynecology, ‘Victor Babes’ University of Medicine and Pharmacy, 300041 Timisoara, Romania
9
Department of Psychiatry, Sestre Milosrdnice University Hospital Center, 10000 Zagreb, Croatia
10
School of Medicine, Catholic University of Croatia, 10000 Zagreb, Croatia
11
Department of Obstetrics and Gynecology, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
12
Antenatal Medicine Laboratory, Timisoara City Emergency Hospital, 300202 Timisoara, Romania
13
Synlab Polyclinic for Medicine Laboratory Diagnostics, 10000 Zagreb, Croatia
 
add Show full affiliation list
 
remove Hide full affiliation list
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Antibodies 2024, 13(2), 49; https://doi.org/10.3390/antib13020049
Submission received: 26 April 2024 / Revised: 28 May 2024 / Accepted: 11 June 2024 / Published: 18 June 2024
Browse Figure
Versions Notes

Abstract

:
TORCH infections usually result in mild maternal morbidity, but may cause severe congenital abnormalities. Therefore, it is important to detect maternal infections, monitor the fetus after the disease has been recognized, and define the seronegative women who are at risk of primary infection during pregnancy. From 2014 to 2023, serum samples from 1032 childbearing-aged and pregnant women (16–45 years) were tested for IgM/IgG antibodies to the most common TORCH pathogens: Toxoplasma gondii, rubella virus (RUBV), cytomegalovirus (CMV), and herpes simplex viruses (HSV-1 and HSV-2). The overall IgG seroprevalence rates were 20.1% for T. gondii, 91.3% for RUBV, 70.5% for CMV, 66.8% for HSV-1, and 3.5% for HSV-2. Only HSV-2 seroprevalence was age-related, with a significant progressive increase in seropositivity from 0% in those aged less than 26 years to 9.3% in those older than 40 years. The seroprevalence of T. gondii was higher in residents of suburban/rural areas than in residents of urban areas (27.4% vs. 17.1%). In addition, participants from continental regions were more often toxoplasma-seropositive than those from coastal regions (22.2% vs. 15.3%). HSV-1 seroprevalence was also higher in suburban/rural areas (71.7% vs. 64.7%). Obstetric history was not associated with TORCH seropositivity. Univariate and multivariate risk analysis showed that suburban/rural areas of residence and continental geographic regions were significant risk factors for T. gondii seroprevalence. Furthermore, suburban/rural area of residence was a significant risk factor for HSV-1 seroprevalence, while older age was a significant risk factor for HSV-2 seroprevalence. A declining trend in the seroprevalence of all TORCH pathogens was observed compared to previous Croatian studies (2005–2011). Similarly, the proportion of women simultaneously IgG-seropositive to two or three pathogens decreased over time. The maternal serology before pregnancy could potentially reduce the burden of congenital TORCH infections.

1. Introduction

TORCH—Toxoplasma gondii, others (Treponema pallidum, varicella-zoster virus, parvovirus B19, etc.), rubella virus (RUBV), cytomegalovirus (CMV), and herpes simplex viruses type 1 and 2 (HSV-1, HSV-2)—encompasses some of the most prevalent pathogens associated with congenital abnormalities. The majority of TORCH infections result in mild maternal morbidity, but have severe fetal consequences, and treatment of the mother’s illness often does not affect the fetal outcome. Therefore, it is important for clinicians to identify maternal infections and monitor the fetus once the disease has been identified [1]. In addition, it is important to define the seronegative women who are at risk of primary infection during pregnancy [2].
Toxoplasmosis is a parasitic infection caused by the protozoon T. gondii. The majority of immunocompetent individuals do not develop symptoms or might have nonspecific flu-like symptoms and lymphadenopathy [3]. Congenital toxoplasmosis is a complication of a primary maternal T. gondii infection during pregnancy. The mother’s immune system, the virulence of the strain, the parasite load, and the gestational age at which the mother was infected all affect the severity of a newborn or fetal disease [4]. The risk of T. gondii transmission increases with increasing gestational age, but the disease severity decreases [5]. The spectrum of clinical manifestations of congenital toxoplasmosis varies from mild symptoms to severe consequences, such as chorioretinitis, hydrocephalus, microcephaly, mental retardation, and even death [6].
Rubella is a viral disease caused by RUBV. It is a highly contagious but generally mild and in most cases self-limiting disease. However, maternal RUBV infection during the first trimester of pregnancy can cause congenital rubella syndrome (CRS). CRS represents a global public health concern, with more than 100,000 estimated annual reported cases worldwide. The risk of transplacental transmission depends on the time of infection. If a maternal infection occurs within the first 12 weeks of gestation, up to 85% of newborns will have congenital defects compared to 50% in maternal infections within 13 to 16 weeks of gestation and 25% in maternal infections during the second part of the second trimester [7]. Congenital heart diseases, cataracts, hearing impairment, and developmental delay are common congenital abnormalities associated with CRS [8].
CMV is a widely distributed human beta-herpesvirus. CMV commonly causes asymptomatic or mild mononucleosis-like disease in immunocompetent children and adults; however, congenital CMV infection is a public health problem, affecting 0.67% of live births [9,10]. Congenital infection may occur in primary or recurrent CMV infection (reactivation or reinfection with a different viral strain). Although mostly asymptomatic, primary maternal CMV infection in pregnancy poses the highest risk of transplacental transmission (30–35%) compared to 1.1–1.7% for non-primary infections. Fetal abnormalities include intrauterine growth restriction, intracranial calcifications, microcephaly, ventriculomegaly, chorioretinitis, and hepatomegaly [11].
HSV-1 and HSV-2 are among the most widely distributed viruses worldwide. HSV-1 predominates in orofacial lesions, while HSV-2 mainly causes genital herpes. Nevertheless, both these viruses can infect orofacial areas and the genital tract. For HSV infections that occur in the last trimester of pregnancy, the risk of neonatal infection ranges from 30% to 50%, while the risk for early pregnancy infections is only 1% [12]. Several forms of neonatal infections can be identified based on the time of maternal infection: intrauterine infections (5% of cases), postnatal infections (10% of cases), and perinatal infections (85% of cases) [13]. Spontaneous abortion, intrauterine growth retardation, preterm birth, and congenital and neonatal HSV infections are all linked to genital herpes infections during pregnancy. HSV infections in neonates infected intrapartum or postnatally can manifest as disease localized to the skin, eye, and/or mouth, HSV encephalitis, or disseminated HSV infection, with mortality rates of more than 80% in untreated patients [12].
Only a few studies have analyzed the prevalence of TORCH infections in Croatia. Toxoplasma seropositivity was analyzed in the childbearing-aged female population in Split-Dalmatia County (1994–1995), showing a seropositivity ranging from 28.1% to 42.6% [14]. A subsequent study conducted from 2005 to 2009 tested childbearing-aged women for T. gondii, RUBV, CMV, and HSV-1/2 [15]. Three other studies analyzed seroprevalence in pregnant women: HSV-1/2 (2008–2010 and 2011–2023) [2,16] and CMV (2013–2015) [17]. Since recent data are lacking, this study aimed to analyze the seroprevalence of and risk factors for TORCH infections in childbearing-aged women over a 10-year period (2014–2023).

2. Materials and Methods

2.1. Study Participants

The study included 1032 childbearing-aged women (16–45 years; Figure 1) tested at the Croatian Institute of Public Health, the largest public health institute in the country. All women tested for TORCH pathogens consecutively from January 2014 to December 2023 were included. All of the participants were of Croatian nationality and there were no migrants tested. For this study, participants were classified according to age (a five-year age group), area of residence (urban or suburban/rural), geographic region (continental or coastal), and obstetric history (non-pregnant, normal pregnancy, unfavorable obstetric history: previous spontaneous abortions, children with congenital malformations, infertility).

2.2. Methods

Initial serological screening (IgM and IgG antibodies) was performed using commercial enzyme-linked immunoassay (ELISA) for RUBV (Novatec Immunodiagnostica, Dietzenbach, Germany), CMV (Vircell Microbiologists, Granada, Spain), and HSV-1/2 (Virotech Diagnostics, Dietzenbach, Germany) and enzyme-linked fluorescence assay (ELFA) for T. gondii (Vidas, Marcy-l’Étoile, France). IgM/IgG-positive samples were further tested for IgG avidity for T. gondii (Vidas, Marcy-l’Étoile, France), RUBV (Euroimmun, Lübeck, Germany), and CMV (Euroimmun, Lübeck, Germany), and Western blot (WB) was used for HSV-1/2 (Euroimmun, Lübeck, Germany) (Table 1).

2.3. Statistical Analysis

Differences between groups of categorical variables were assessed using chi-squared and Fisher’s exact tests. Odds ratios (ORs) and adjusted odds ratios (AORs) ± 95% confidence intervals (CIs) were used to assess the univariate and multivariate association of positive serological tests and explanatory variables (age, area of residence, geographic region, and obstetric history). Statistical analysis was performed using STATA/MP 17.0 for Windows (StataCorp LLC, Lakeway Drive, College Station, TX, USA). The level of statistical significance was set at p < 0.05.

3. Results

3.1. Characteristics of Study Participants

Mean participant age was 31.9 ± 5.1 years. The area of residence was urban for 725 (70.3%) of participants and suburban/rural for 307 (29.7%) of participants. The geographic region of residence was continental for 724 (70.2%) and coastal for 308 (29.8%) participants. Regarding obstetric history, 271 (26.3%) of women were not pregnant, 608 (58.9%) had a normal pregnancy and 153 (14.8%) reported an unfavorable obstetric history.

3.2. TORCH Seroprevalence

Toxoplasma gondii IgG antibodies were detected in 208 (20.2%; 95% CI = 17.8–22.7%) participants. Toxoplasma gondii IgM antibodies were found in four (0.4%; 95% CI = 0.1–1.0%) IgG-seropositive participants; however, all showed high IgG avidity, which ruled out acute toxoplasmosis. There was no significant difference in IgG seroprevalence according to age (18.8–25.6%). Significant differences were observed according to area of residence and geographic region. Participants from suburban/rural areas were more often seropositive compared to those from urban areas (27.4% vs. 17.1%; p < 0.001). In addition, higher seropositivity was observed in continental areas than in coastal areas (22.2% vs. 15.3%; p = 0.011). IgG seropositivity was not associated with obstetric history (non-pregnant women 23.6%, normal pregnancy 19.4%, unfavorable obstetric history 17.0%) (Table 2).
RUBV IgG antibodies were detected in 942 (91.3%; 95% CI = 89.6–93.0%) participants. RUBV IgM antibodies were found in two (0.2%; 95% CI = <0.1–0.7%) IgG-seropositive participants. Both participants showed high AI (77% and 83%, respectively). There was no significant difference in IgG seroprevalence according to age (81.3–95.4%), urban and suburban/rural area of residence (91.3% and 91.2%), continental and coastal geographic region (91.7% and 90.3%), or obstetric history (90.5–91.5%) (Table 3).
CMV IgG antibodies were detected in 728 (70.5%, 95% CI = 67.7–73.3%) participants. Sixty-five of the IgG-seropositive women were IgM-positive (8.9%, 95% CI = 6.9–11.2%); however, based on IgG avidity, only two showed low/borderline AI (35% and 51%, respectively), suggesting recent primary CMV infection. No significant differences in IgG seroprevalence were observed among age groups (62.5–72.4%), urban and suburban/rural areas of residence (69.1% vs. 73.9%), or continental and coastal regions (70.1% vs. 71.8%). Higher CMV IgG seropositivity was found in women with an unfavorable obstetric history (75.2%) compared to non-pregnant women (69.4%) and women with normal pregnancy (69.9%); however, these differences were not significant (Table 4).
HSV-1 IgG antibodies were found in 689 (66.8%, 95% CI = 63.8–69.6%) women. Using ELISA, ten (0.9%, 95% CI = 0.5–1.8%) of the participants were IgM-seropositive, but only one (0.1%, 95% CI = <0.1–0.5%) was confirmed IgM-positive by WB. There was no significant difference in seroprevalence between age groups (63.7–75.0%). The seroprevalence rates were similar in residents of continental (66.9%) and coastal areas (66.6%); however, significant differences were observed among residents of urban and suburban/rural areas (64.7% vs. 71.7%, p = 0.030). Obstetric history was not associated with HSV-1 seropositivity (64.8–70.8%) (Table 5).
HSV-2 IgG antibodies were detected in 36 (3.5%, 95% CI = 2.4–4.8%) participants. HSV-2 IgG seropositivity increased significantly with age. None of the participants aged less than 26 years was IgG-seropositive. A progressive increase with age was observed from 1.7% in the 26- to 30-year age group to 9.3% in participants older than 40 years (p = 0.005). Area of residence, geographic region, and obstetric history were not associated with HSV-2 IgG seropositivity (Table 6).

3.3. Simultaneous TORCH Seroprevalence

Analyzing the simultaneous IgG seroprevalence of two TORCH pathogens, seropositivity to T. gondii–RUBV was found in 190 (18.4%; 95% CI = 16.1–20.9%) participants, T. gondii–CMV in 146 (14.1%, 95% CI = 12.1–16.4%), and RUBV–CMV in 663 (64.2%; 95% CI = 61.2–67.2%) participants. Only area of residence and geographic region were associated with seropositivity. Residents of suburban/rural areas and those from continental geographic regions were more often seropositive to T. gondii–RUBV and T. gondii–CMV IgG antibodies, while these differences were not observed for RUBV–CMV seroprevalence (Table 7).
Simultaneous seropositivity to three TORCH pathogens (T. gondii–RUBV–CMV) was found in 137 (13.1%; 95% CI = 11.3–15.5%) participants. Suburban/rural area of residence and continental region were also found to be significant risk factors for the simultaneous seropositivity (Table 8).

3.4. Risk Analysis for TORCH Seropositivity

Both univariate and multivariate risk analysis showed that area of residence (OR = 1.826, 95% CI = 1.330–2.511, p < 0.001; AOR = 1.981, 95% CI = 1.334–2.931, p = 0.001) and geographic region (OR = 1.587, 95% CI = 1.120–2.268, p = 0.011; AOR = 1.912, 95% CI = 1.217–3.012, p = 0.005) were associated with T. gondii IgG seropositivity (Table 9). There was no association of age, area of residence, or geographic region with RUBV or CMV IgG seropositivity (Table 10 and Table 11). Suburban/rural area of residence was associated with HSV-1 IgG seropositivity (OR = 1.380, 95% CI = 1.032–1.847, p = 0.030; AOR = 1.421, 95% CI = 1.007–2.001, p = 0.045) (Table 12). Age was a significant risk factor for HSV-2 IgG seropositivity. The ORs and AORs for a one-year increase in age were 1.164 (95% CI = 1.082–1.251, p < 0.001) and 1.130 (95% CI = 1.030–1.240, p = 0.010) (Table 13).

4. Discussion

The overall TORCH seropositivity in this study (2014–2023) was found to be 20.2% for T. gondii, 91.3% for RUBV, 70.5% for CMV, 66.8% for HSV-1, and 3.5% for HSV-2. All detected seroprevalence rates were lower compared to a previous Croatian study (2005–2009) conducted in the same population group (T. gondii 29.1%, RUBV 94.6%, CMV 75.3%, HSV-1 78.7% and HSV-2 6.8%) [15]. Better living standards, improved hygiene standards, and safer sexual contact are the possible reasons for declining trends in overall TORCH seroprevalence.
Comparing the overall T. gondii seropositivity, the detected seroprevalence rate in Croatia (20.2%) was similar to the seroprevalence in Italy (20.9%, Palermo, 2012–2022) [18], Spain (21%, Albacete, 2006) [19], Poland (22.3%, 2018–2019) [20] and northern Kosovo and Metohija (24.1%, 2011–2012) [21]. Lower seropositivity was found in Serbia (12.7%, Belgrade, 2018–2019) [22], the United Kingdom (9.1%, Kent, 1999–2001; 17.32%, London, 2006–2008) [23,24] and in Turkey (14%, Karabük, 2008) [25], while higher seropositivity was found in France (31.3%, 2016) [26], Germany (39.5%, 2006–2018) [20], and the Netherlands (40.5%, 1995–1996) [27].
Seroepidemiologic studies in Romania showed regional differences in the prevalence of T. gondii IgG antibodies, ranging from 38.24% in Bucharest to 55.8% in western Romania [28,29,30,31,32,33,34]. In addition, significant regional differences in seropositivity within France were observed, from 19.1% in Grand Est to 35.1% in Occitanie, while the highest seroprevalence of 50.7% was detected in overseas departments (Guadeloupe, French Guyana, La Réunion, Martinique and Mayotte combined) [26]. Studies from Italy showed similar results. From 2013 to 2017, a seroprevalence study on toxoplasmosis was conducted in childbearing-aged women from Siena (Tuscany, central Italy) and Bari (Apulia, southern Italy) and pregnant women in Bari (2016–2017). The prevalence of seropositive childbearing-aged women in Bari was significantly higher than in Siena (22.4% vs. 12.4%), while a low prevalence (13.8%) was observed among the pregnant women tested [35].
The toxoplasma IgG seroprevalence rates differed regionally in Croatia as well, with significantly higher seropositivity in continental (22.2%) than in coastal regions (15.3%). Eating undercooked pork is one of the main sources of toxoplasmosis [36]. The production and consumption of numerous traditional pork dishes in continental regions may be the explanation for a higher toxoplasma seroprevalence than in coastal regions.
As with the decreasing seroprevalence in Croatia (29.1% seropositive women in 2005–2009 and 20.2% seropositive women in 2014–2023), toxoplasma seropositivity shows declining trends in several countries [32,35,37]. A decreasing trend in the overall seroprevalence of toxoplasmosis from 25–43% to 10–20% was observed in Sweden between 1969 and 1998 in pregnant women born in the Nordic countries who resided in Stockholm [37]. In Romania, seropositivity declined in 10 years from 43.79% (2008–2010) to 38.81% (2015–2018) in pregnant women residing in Timisoara [32].
Numerous studies have shown that toxoplasma seropositivity is age-related, with higher seropositivity as age increases [19,26,38]. In contrast, no significant differences in IgG prevalence between age groups were observed in our study, ranging from 18.8% to 25.6% with a reverse U-shaped seroprevalence curve. Seroprevalence was lowest in the age group of 31 to 35 years. In a 2005–2009 Croatian study, these differences were significant and showed a similar seroprevalence curve with the lowest seroprevalence in the 26- to 35-year group [15].
Our study found significantly higher toxoplasma seropositivity among residents of suburban and rural areas (27.4%) compared to urban areas (17.1%). Significantly higher seroprevalence in rural areas was also observed in a Romanian study (46 vs. 36%) [31], while it was of borderline significance in a Serbian study (22.5 vs. 11.5%) [22]. In Slovakia, women who lived in Bratislava’s surroundings had a considerably higher seropositivity rate (63.5%) than those who lived in Bratislava (36.6%) [39]. In addition to the consumption of pork, more frequent contact with cats, a definite host of T. gondii, in rural areas is the probable reason for the differences in the seroprevalence rates, since cat ownership was confirmed to be associated with toxoplasma seroprevalence [25].
A meta-analysis of RUBV prevalence in childbearing-aged and pregnant women that included the period between 2000 and 2016 found a pooled global RUBV seropositivity of 90.7%. When considering subpopulation groups, a seropositivity pooled estimate was 90.6% in pregnant women and 90.5% in childbearing-aged women, with no mention of ongoing pregnancy [40]. In the Croatian childbearing-aged and pregnant women tested in this study, the seroprevalence of RUBV was 91.3%, which is lower than the 94.6% in 2005–2009 [15]. Other European countries showed a seropositivity rate of 93.6% in Ireland [41], 94.4% in Norway [42], 93.4–97.7% in Spain [43,44,45], and 95.8% in Sweden [46]. In the United Kingdom, seroprevalence in Liverpool was lower (93.7%) than average for the northwestern region (96.3%) [47]. Italian studies showed lower seropositivity rates of 85.8% in Messina (2006–2007) [48], 88.6% in Tuscany and 84.3% in Apulia (2014–2016) [49] and 81.2% in Palermo (2012–2022) [18]. Similar seroprevalence of 83.5% was also found in Portugal [50]. Although data on the rubella vaccination status of the participants included in this study were not available, data on measles–mumps–rubella (MMR) vaccine coverage in Croatia from the Reference Center for Epidemiology, Croatian Institute of Public Health showed a decline in the past decade. MMR primo vaccination and revaccination rates in 2013 and 2023 were 93.9/97.1% and 90.1/90.1%, respectively, which impacted the lower seroprevalence rate detected in childbearing-aged women tested in this study.
In Romania, 94.1% of fertile women tested from 2008 to 2010 were rubella IgG-seropositive, while seropositivity was lower (91.5%) in those tested from 2015 to 2018 [51]. A decline in RUBV seropositivity in Croatia is a result of a decrease in immunization coverage, which was also observed in Serbia (92.9% seropositive) [52].
In our study, no significant differences were observed in RUBV seropositivity between age groups (81.3–95.4%), area of residence, geographic region, or obstetric history. Similarly, seroprevalence was stable in different age groups in Romania. In addition, there was no significant difference in seroprevalence among urban and rural populations [51]. In contrast, the highest proportion of seronegative women was found in the youngest age group (15–20 years, 18.7%) compared to 1.9% in the 30- to 35-year age group in northwest England [47]. Similarly, the proportion of RUBV-seronegative women declined with increasing maternal age in Spain [53].
The European studies showed widely differing levels of immunity to CMV in childbearing-aged women. Compared to the seroprevalence of 70.5% observed in our study, very high CMV seropositivity was found in Bosnia and Herzegovina (93%) [54], moderate seropositivity in Italy (70.8%) [55] and Western Europe (73.2%) [56], and lower seroprevalence in the United Kingdom (49%) [57], France (45.6%) [58], Germany (42.3–45.2%) [59,60], and Norway (62.8%) [42]. Studies from Poland showed CMV seroprevalence rates of 76.7% [61] and 62.4%, respectively [62]. Very low seropositivity of 30.4% was found in pregnant Irish women [63].
Similar to decreasing trends in other TORCH pathogens, CMV seroprevalence has also decreased in many European countries. A cross-sectional study conducted in Finland at three time points (1992, 2002, and 2012) showed that seroprevalence decreased significantly from 84.5% to 71.5% over 20 years [64]. Our results also showed a decline in CMV IgG seropositivity. In a previous Croatian study (2005–2009), 78.7% of childbearing-aged women were CMV-seropositive [15] compared to 70.5% in this study. Romania found stable seropositivity rates of 93.68% and 94.96% in 2013–2016 and 2019–2022, respectively, in southwestern regions [65] and a decrease from 94.6% (2008–2010) to 91.80% (2015–2018) in the western region [66].
In our study, no significant differences in CMV IgG seropositivity were observed among age groups, although seroprevalence rates were lower in groups aged up to 25 years (62.5% and 66.7%, respectively) compared to groups aged above 26 years (69.7–72.4%). Stable but higher seroprevalence rates were also found in Croatia in 2005–2009 [15]. Similarly, no significant differences in seropositivity by age group were found in Italy [55]. In addition, no correlation between seroprevalence and maternal age was observed in one Polish study [61]. However, in another study from Poland, seroprevalence differed significantly between age-stratified groups, with the highest IgG prevalence in women above 36 years of age (76.2%) compared to 58.5–66.0% in younger women [62]. Moreover, in the United Kingdom, a significant increase in CMV seroprevalence was observed with maternal age from 50.9% to 75.5% [57].
In contrast to Romanian studies, which found higher CMV seropositivity in pregnant women residing in rural areas [65,66], our study found no difference in seroprevalence between residents of suburban/rural and urban areas (73.9% vs. 69.1%).
Like other TORCH pathogens, the reported HSV seroprevalence rates were heterogeneous within Europe. In our study, HSV-1 and HSV-2 seroprevalence was 66.8% and 3.5%, respectively. HSV-1 seropositivity was found to be 79.4% in Switzerland [67], 88% in Estonia [68], 88.2% in France [69], 91.2% in Italy [70], and 94.7% in Turkey [71]. In Finland, HSV-1 seropositivity varied in different studies, ranging from 46.8% [72] to 69.5% [64]. HSV-2 seroprevalence was high in Estonia (24%) [68], Switzerland (21.2%) [67], and lower in Italy (9.9%) [70] and Turkey (8.2%) [71]. Both HSV-1 and HSV-2 seroprevalence differed between regions in the Netherlands due to the multiethnic composition of the population. Seroprevalence rates were 61% and 11% in Nijmegen, 73% and 35% in Amsterdam, and 75% and 27% in Rotterdam [73].
Our study found no difference in either HSV-1 or HSV-2 IgG seroprevalence among residents of continental and coastal regions. However, higher HSV-1 seropositivity was observed in women from suburban/rural areas (71.7%) than women from urban areas (64.7%). The higher HSV-1 seroprevalence in rural areas could be attributed to the lifestyle of the rural population, typically living in large households with many children and relatives. Since primary infections mainly occur in preschool- and school-aged children, close contact with these cohorts is associated with an increased risk of HSV-1 transmission [2].
Our study showed a significant increase in HSV-2 seropositivity with age. All women aged less than 25 years were HSV-2 IgG-seronegative, while a progressive increase in seroprevalence was observed starting with the 26- to 30-year age group, from 1.7 to 9.3%. Higher seropositivity in older groups reflects longer and cumulative exposure to the virus. Similar to our results, an increase in HSV-2 seropositivity with age was observed in many studies [67,72,74]. No association of HSV-2 seroprevalence with age was found in Romania, with peak seroprevalence (18.3%) between 30 and 34 years of age and a slight decrease thereafter [75].
While obstetric history was not associated with HSV-1 or HSV-2 seroprevalence in Croatian childbearing-aged or pregnant women, a history of abortion was associated with HSV-2 seropositivity in German and Hungarian studies [76,77].
A Romanian study analyzed the simultaneous seroprevalence of TORCH pathogens in childbearing-aged women. Similar to each TORCH pathogen, the proportion of women simultaneously IgG-seropositive decreased over time: T. gondii–CMV 41.4% vs. 36.1%, T. gondii–RUBV 41.8% vs. 35.7%, CMV–RUBV 88.9% vs. 83.6%, and T. gondii–CMV–RUBV 39.6% vs. 33.2% [78]. Simultaneous seropositivity to two or three TORCH pathogens in participants included in our study was generally low (T. gondii–RUBV 18.4%, T. gondii–CMV 14.1%, T. gondii–RUBV–CMV 13.1%) and moderate for RUBV–CMV (64.2%). In a previous Croatian study, simultaneous seropositivity was not analyzed; therefore, it was not possible to compare seroprevalence trends over time. When comparing women from urban and suburban–rural areas, simultaneous seroprevalence was higher in suburban and rural regions, which is in line with the results from Romania [78].
One recently published study analyzed the impact of latent CMV infections on spontaneous abortion history and pregnancy outcomes. In healthy women, latent CMV infection does not affect the risk of complications, while borderline-significant higher prevalence of miscarriage history was observed in women with latent CMV infection [79]. Furthermore, the observed differences between the rate of pregnancy complications in groups of pregnant women with and without latent T. gondii infection were not significant [30]. In our study, data on pregnancy complications and outcomes were not available, which is one of the limitations of the study.
In addition, a limitation of this study that needs to be addressed is the small number of participants in the youngest (≤25 years) and oldest (>40 years) age groups, which should be considered when interpreting the results.

5. Conclusions

Based on the decline in seroprevalence rates observed in many European countries, a similar trend was expected in Croatia. The results of this study confirmed this hypothesis, showing a decrease in TORCH-seroprevalence rates in Croatian childbearing-aged women in 2014–2023 compared to 2005–2009.
Information on TORCH serostatus in childbearing-aged women is important to define seronegative women who are at risk of primary infections during pregnancy. Although cases of rubella reinfections in previously vaccinated seropositive women during pregnancy are reported in the literature, CRS is rarely recorded [80,81]. In addition, CMV reactivation or reinfection during pregnancy can lead to transient viremia and fetal infection, but such infections tend to be less severe and newborns are usually asymptomatic [82,83]. Congenital toxoplasmosis as a result of reinfection in immunocompetent pregnant women or reactivation in pregnant women with altered immune status is exceptional [84]. Since rubella is a vaccine-preventable disease, serological testing of childbearing-aged women is encouraged with the aim of vaccinating seronegative individuals before pregnancy.
The results of our study also impact other population groups, especially the immunocompromised, who are at risk of toxoplasmosis, HSV, and CMV infection. Similarly to the observed declining seroprevalence in childbearing-aged women, decreasing seroprevalence and increased susceptibility to infections probably occur in this population, which should be kept in mind. Therefore, the present results also highlight the need to monitor these pathogens in other high-risk population groups as well.

Author Contributions

T.V.-C., B.K. and M.B. (Maja Bogdanic); methodology, T.V.-C., B.K., M.S., L.M. and L.A.; validation, T.V.-C. and M.B.; investigation, M.B. (Marko Belamaric), M.S., T.F., V.B., L.M., L.A., M.V., M.V.F., E.R., T.J., I.C., R.C.P. and M.K.; data curation, T.V.-C. and M.B. (Maja Bogdanic); writing—original draft preparation, T.V.-C., B.K. and M.B. (Maja Bogdanic); writing—review and editing, T.V.-C., B.K. and D.N.; supervision, T.V.-C., B.K. and D.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Ethics Committee of the Croatian Institute of Public Health (protocol code 030-02/17-10/0, approved on 2 January 2017).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data are contained within the article.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Stegmann, B.J.; Carey, J.C. TORCH Infections. Toxoplasmosis, Other (syphilis, varicella-zoster, parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes infections. Curr. Women’s Health Rep. 2002, 2, 253–258. [Google Scholar]
  2. Vilibic-Cavlek, T.; Belamaric, M.; Ferenc, T.; Navolan, D.; Kolaric, B.; Milasincic, L.; Antolasic, L.; Vujica Ferenc, M.; Vilibic, M.; Lukunic, A.; et al. Seroepidemiology of Herpes Simplex Viruses Type 1 and 2 in Pregnant Women in Croatia. Medicina 2024, 60, 284. [Google Scholar] [CrossRef] [PubMed]
  3. Layton, J.; Theiopoulou, D.-C.; Rutenberg, D.; Elshereye, A.; Zhang, Y.; Sinnott, J.; Kim, K.; Montoya, J.G.; Contopoulos-Ioannidis, D.G. Clinical Spectrum, Radiological Findings, and Outcomes of Severe Toxoplasmosis in Immunocompetent Hosts: A Systematic Review. Pathogens 2023, 12, 543. [Google Scholar] [CrossRef] [PubMed]
  4. Damar Çakırca, T.; Can, İ.N.; Deniz, M.; Torun, A.; Akçabay, Ç.; Güzelçiçek, A. Toxoplasmosis: A Timeless Challenge for Pregnancy. Trop. Med. Infect. Dis. 2023, 8, 63. [Google Scholar] [CrossRef] [PubMed]
  5. Deganich, M.; Boudreaux, C.; Benmerzouga, I. Toxoplasmosis Infection during Pregnancy. Trop. Med. Infect. Dis. 2022, 8, 3. [Google Scholar] [CrossRef]
  6. Khan, K.; Khan, W. Congenital toxoplasmosis: An overview of the neurological and ocular manifestations. Parasitol. Int. 2018, 67, 715–721. [Google Scholar] [CrossRef] [PubMed]
  7. Shukla, S.; Maraqa, N.F. Congenital Rubella. In StatPearls [Internet]; StatPearls Publishing: Treasure Island, FL, USA, 2024. [Google Scholar]
  8. Lanzeri, T.; Redd, S.; Abernathy, E.; Icenogle, J. Congenital Rubella Syndrome. In Manual for the Surveillance of Vaccine-Preventable Diseases. Available online: https://www.cdc.gov/vaccines/pubs/surv-manual/chpt15-crs.html (accessed on 15 March 2024).
  9. Ssentongo, P.; Hehnly, C.; Birungi, P.; Roach, M.A.; Spady, J.; Fronterre, C.; Wang, M.; Murray-Kolb, L.E.; Al-Shaar, L.; Chinchilli, V.M.; et al. Congenital Cytomegalovirus Infection Burden and Epidemiologic Risk Factors in Countries With Universal Screening: A Systematic Review and Meta-analysis. JAMA Netw. Open 2021, 4, e2120736. [Google Scholar] [CrossRef]
  10. Korndewal, M.J.; Oudesluys-Murphy, A.M.; Kroes, A.C.M.; van der Sande, M.A.B.; de Melker, H.E.; Vossen, A.C.T.M. Longterm impairment attributable to congenital cytomegalovirus infection: A retrospective cohort study. Dev. Med. Child Neurol. 2017, 59, 1261–1268. [Google Scholar] [CrossRef]
  11. Akpan, U.S.; Pillarisetty, L.S. Congenital Cytomegalovirus Infection. In StatPearls [Internet]; StatPearls Publishing: Treasure Island, FL, USA, 2024. [Google Scholar]
  12. Straface, G.; Selmin, A.; Zanardo, V.; De Santis, M.; Ercoli, A.; Scambia, G. Herpes simplex virus infection in pregnancy. Infect. Dis. Obstet. Gynecol. 2012, 2012, 385697. [Google Scholar] [CrossRef]
  13. De Rose, D.U.; Bompard, S.; Maddaloni, C.; Bersani, I.; Martini, L.; Santisi, A.; Longo, D.; Ronchetti, M.P.; Dotta, A.; Auriti, C. Neonatal herpes simplex virus infection: From the maternal infection to the child outcome. J. Med. Virol. 2023, 95, e29024. [Google Scholar] [CrossRef]
  14. Punda-Polić, V.; Tonkić., M.; Capkun, V. Prevalence of antibodies to Toxoplasma gondii in the female population of the County of Split Dalmatia, Croatia. Eur. J. Epidemiol. 2000, 16, 875–877. [Google Scholar] [CrossRef]
  15. Vilibic-Cavlek, T.; Ljubin-Sternak, S.; Ban, M.; Kolaric, B.; Sviben, M.; Mlinaric-Galinovic, G. Seroprevalence of TORCH infections in women of childbearing age in Croatia. J. Matern. Fetal Neonatal Med. 2011, 24, 280–283. [Google Scholar] [CrossRef]
  16. Vilibic-Cavlek, T.; Kolaric, B.; Ljubin-Sternak, S.; Mlinaric-Galinovic, G. Herpes simplex virus infection in the Croatian population. Scand. J. Infect. Dis. 2011, 43, 918–922. [Google Scholar] [CrossRef]
  17. Vilibic-Cavlek, T.; Kolaric, B.; Beader, N.; Vrtar, I.; Tabain, I.; Mlinaric-Galinovic, G. Seroepidemiology of cytomegalovirus infections in Croatia. Wien. Klin. Wochenschr. 2017, 129, 129–135. [Google Scholar] [CrossRef]
  18. Palazzotto, E.; Bonura, F.; Calà, C.; Capra, G.; Pistoia, D.; Mangione, D.; Mascarella, C.; Minì, G.; Enea, M.; Giammanco, G.M.; et al. Serological status for TORCH in women of childbearing age: A decade-long surveillance (2012–2022) in Italy. J. Med. Microbiol. 2023, 72, 7. [Google Scholar] [CrossRef]
  19. Bartolomé Alvarez, J.; Martínez Serrano, M.; Moreno Parrado, L.; Lorente Ortuño, S.; Crespo Sánchez, M.D. Prevalencia e incidencia de la infección por Toxoplasma gondii en mujeres en edad fértil en Albacete (2001–2007) [Prevalence and incidence in Albacete, Spain, of Toxoplasma gondii infection in women of childbearing age: Differences between immigrant and non-immigrant (2001–2007)]. Rev. Esp. Salud. Publica 2008, 82, 333–342. (In Spanish) [Google Scholar] [CrossRef]
  20. Warnecke, J.; Pollmann, M.; Borchardt-Lohölter, V.; Moreira-Soto, A.; Kaya, S.; Sener, A.G.; Gómez-Guzmán, E.; Figueroa-Hernández, L.; Li, W.; Li, F. Seroprevalences of antibodies against ToRCH infectious pathogens in women of childbearing age residing in Brazil, Mexico, Germany, Poland, Turkey and China. Epidemiol. Infect. 2020, 148, E271. [Google Scholar] [CrossRef]
  21. Pribakovic, J.A.; Katanic, N.; Radevic, T.; Tasic, M.S.; Kostic, M.; Stolic, B.; Radulovic, A.; Minic, V.; Bojovic, K.; Katanic, R. Serological status of childbearing-aged women for Toxoplasma gondii and cytomegalovirus in northern Kosovo and Metohija. Rev. Soc. Bras. Med. Trop. 2019, 52, e20170313. [Google Scholar] [CrossRef]
  22. Marković-Denić, L.; Stopić, M.; Bobić, B.; Nikolić, V.; Djilas, I.; Srzentić, S.J.; Štajner, T. Factors Associated with Toxoplasma gondii Seroprevalence in Pregnant Women: A Cross-Sectional Study in Belgrade, Serbia. Pathogens 2023, 12, 1240. [Google Scholar] [CrossRef]
  23. Nash, J.Q.; Chissel, S.; Jones, J.; Warburton, F.; Verlander, N.Q. Risk factors for toxoplasmosis in pregnant women in Kent, United Kingdom. Epidemiol. Infect. 2005, 133, 475–483. [Google Scholar] [CrossRef]
  24. Flatt, A.; Shetty, N. Seroprevalence and risk factors for toxoplasmosis among antenatal women in London: A re-examination of risk in an ethnically diverse population. Eur. J. Public Health 2013, 23, 648–652. [Google Scholar] [CrossRef]
  25. Eroglu, S.; Asgin, N. Awareness, knowledge and risk factors of Toxoplasma gondii infection among pregnant women in the Western Black Sea region of Turkey. J. Obstet. Gynaecol. 2021, 41, 714–720. [Google Scholar] [CrossRef]
  26. Robinson, E.; de Valk, H.; Villena, I.; Le Strat, Y.; Tourdjman, M. National perinatal survey demonstrates a decreasing seroprevalence of Toxoplasma gondii infection among pregnant women in France, 1995 to 2016: Impact for screening policy. Euro Surveill. 2021, 26, 1900710. [Google Scholar] [CrossRef]
  27. Kortbeek, L.M.; De Melker, H.E.; Veldhuijzen, I.K.; Conyn-Van Spaendonck, M.A. Population-based Toxoplasma seroprevalence study in The Netherlands. Epidemiol. Infect. 2004, 132, 839–845. [Google Scholar] [CrossRef]
  28. Neagoe, I.M.; Cretu, C.M.; Lazar, L.E. Serological and Molecular Diagnosis of Toxoplasma gondii Infection in Pregnant Women in Romania. Rom. Arch. Microbiol. Immunol. 2018, 77, 58–66. [Google Scholar]
  29. Costache, C.A.; Ţigan, Ş.I.; Colosi, I.; Coroiu, Z. Toxoplasmic Infection in Pregnant Women from Cluj County and Neighbouring Area. Appl. Med. Inform. 2008, 23, 31–36. [Google Scholar]
  30. Mocanu, A.G.; Stoian, D.L.; Craciunescu, E.L.; Ciohat, I.M.; Motofelea, A.C.; Navolan, D.B.; Vilibic-Cavlek, T.; Stevanovic, V.; Nemescu, D.; Forga, M.; et al. The Impact of Latent Toxoplasma gondii Infection on Spontaneous Abortion History and Pregnancy Outcomes: A Large-Scale Study. Microorganisms 2022, 10, 1944. [Google Scholar] [CrossRef]
  31. Mihu, A.G.; Balta, C.; Marti, D.T.; Paduraru, A.A.; Lupu, M.A.; Olariu, T.R. Seroprevalence of Toxoplasma gondii infection among women of childbearing age in an endemic region of Romania, 2016–2018. Parasite 2020, 27, 59. [Google Scholar] [CrossRef]
  32. Motoi, S.; Navolan, D.B.; Malita, D.; Ciohat, I.; Nemescu, D.; Manciuc, C.; Gorun, F.; Vilibic-Cavlek, T.; Boda, D.; Craina, M.; et al. A decreasing trend in Toxoplasma gondii seroprevalence among pregnant women in Romania—Results of a large scale study. Exp. Ther. Med. 2020, 20, 3536–3540. [Google Scholar] [CrossRef]
  33. Csep, A.; Vaida, L.L.; Negruțiu, B.M.; Todor, B.I.; Judea-Pusta, C.T.; Buhaș, C.; Sava, C. Research on demographic, clinical and paraclinical aspects in pregnant women infected with Toxoplasma gondii. Exp. Ther. Med. 2022, 23, 123. [Google Scholar] [CrossRef]
  34. Olariu, T.R.; Ursoniu, S.; Hotea, I.; Dumitrascu, V.; Anastasiu, D.; Lupu, M.A. Seroprevalence and Risk Factors of Toxoplasma gondii Infection in Pregnant Women from Western Romania. Vector Borne Zoonotic Dis. 2020, 20, 763–767. [Google Scholar] [CrossRef]
  35. Fanigliulo, D.; Marchi, S.; Montomoli, E.; Trombetta, C.M. Toxoplasma gondii in women of childbearing age and during pregnancy: Seroprevalence study in Central and Southern Italy from 2013 to 2017. Parasite 2020, 27, 2. [Google Scholar] [CrossRef]
  36. Guo, M.; Dubey, J.P.; Hill, D.; Buchanan, R.L.; Gamble, H.R.; Jones, J.L.; Pradhan, A.K. Prevalence and risk factors for Toxoplasma gondii infection in meat animals and meat products destined for human consumption. J. Food Prot. 2015, 78, 457–476. [Google Scholar] [CrossRef]
  37. Petersson, K.; Stray-Pedersen, B.; Malm, G.; Forsgren, M.; Evengård, B. Seroprevalence of Toxoplasma gondii among pregnant women in Sweden. Acta Obstet. Gynecol. Scand. 2000, 79, 824–829. [Google Scholar] [CrossRef]
  38. Nowakowska, D.; Stray-Pedersen, B.; Spiewak, E.; Sobala, W.; Małafiej, E.; Wilczyński, J. Prevalence and estimated incidence of Toxoplasma infection among pregnant women in Poland: A decreasing trend in the younger population. Clin. Microbiol. Infect. 2006, 12, 913–917. [Google Scholar] [CrossRef]
  39. Studenicová, C.; Ondriska, F.; Holková, R. Séroprevalencia Toxoplasma gondii u gravidných zien na Slovensku [Seroprevalence of Toxoplasma gondii among pregnant women in Slovakia]. Epidemiol. Mikrobiol. Imunol. 2008, 57, 8–13. (In Slovak) [Google Scholar]
  40. Pandolfi, E.; Gesualdo, F.; Rizzo, C.; Bella, A.; Agricola, E.; Mastroiacovo, P.; Tozzi, A.E. Global seroprevalence of rubella among pregnant and childbearing age women: A meta-analysis. Eur. J. Public Health 2017, 27, 530–537. [Google Scholar] [CrossRef]
  41. O’Dwyer, V.; Bonham, S.; Mulligan, A.; O’Connor, C.; Farah, N.; Kennelly, M.M.; Turner, M.J. Antenatal rubella immunity in Ireland. Ir. Med. J. 2013, 106, 232–235. [Google Scholar]
  42. Barlinn, R.; Vainio, K.; Samdal, H.H.; Nordbø, S.A.; Nøkleby, H.; Dudman, S.G. Susceptibility to cytomegalovirus, parvovirus B19 and age-dependent differences in levels of rubella antibodies among pregnant women. J. Med. Virol. 2014, 86, 820–826. [Google Scholar] [CrossRef]
  43. Dominguez, A.; Plans, P.; Espuñes, J.; Costa, J.; Torner, N.; Cardeñosa, N.; Plasencia, A.; Salleras, L. Rubella immune status of indigenous and immigrant pregnant women in Catalonia, Spain. Eur. J. Public Health 2007, 17, 560–564. [Google Scholar] [CrossRef]
  44. Plans, P.; de Ory, F.; Campins, M.; Álvarez, E.; Payà, T.; Guisasola, E.; Compte, C.; Vellbé, K.; Sánchez, C.; Lozano, M.J.; et al. Prevalence of anti-rubella, anti-measles and anti-mumps IgG antibodies in neonates and pregnant women in Catalonia (Spain) in 2013: Susceptibility to measles increased from 2003 to 2013. Eur. J. Clin. Microbiol. Infect. Dis. 2015, 34, 1161–1171. [Google Scholar] [CrossRef]
  45. Ramos, J.M.; Milla, A.; Rodríguez, J.C.; Gutiérrez, F. Rubella immune status among immigrant and nonimmigrant women in Spain. J. Med. Virol. 2012, 84, 548–550. [Google Scholar] [CrossRef]
  46. Kakoulidou, M.; Forsgren, M.; Lewensohn-Fuchs, I.; Johansen, K. Serum levels of rubella-specific antibodies in Swedish women following three decades of vaccination programmes. Vaccine 2010, 28, 1002–1007. [Google Scholar] [CrossRef]
  47. Ogundele, M.; Ghebrehewet, S.; Chawla, A. Some factors affecting rubella seronegative prevalence among pregnant women in a North West England region between April 2011 and March 2013. J. Public Health 2016, 38, 243–249. [Google Scholar] [CrossRef]
  48. Calimeri, S.; Capua, A.; La Fauci, V.; Squeri, R.; Grillo, O.C.; Lo Giudice, D. Prevalence of serum anti-rubella virus antibodies among pregnant women in southern Italy. Int. J. Gynaecol. Obstet. 2012, 116, 211–213. [Google Scholar] [CrossRef]
  49. Marchi, S.; Viviani, S.; Montomoli, E.; Trombetta, C.M. Elimination of congenital rubella: A seroprevalence study of pregnant women and women of childbearing age in Italy. Hum. Vaccin. Immunother. 2020, 16, 895–898. [Google Scholar] [CrossRef]
  50. Gonçalves, G.; Nascimento, M.S.; Réu, C.; Cutts, F.T. Levels of rubella antibody among vaccinated and unvaccinated Portuguese mothers and their newborns. Vaccine 2006, 24, 7142–7147. [Google Scholar] [CrossRef]
  51. Gorun, F.; Malita, D.; Ciohat, I.; Vilibic-Cavlek, T.; Feier, H.; Tabain, I.; Crainam, M.; Cretu, O.; Navolan, D. Prevalence of Rubella Antibodies among Fertile Women in the West of Romania, 18 Years after the Implementation of Immunization. Vaccines 2021, 9, 104. [Google Scholar] [CrossRef]
  52. Patić, A.; Štrbac, M.; Petrović, V.; Milošević, V.; Ristić, M.; Hrnjaković Cvjetković, I.; Medić, S. Seroepidemiological study of rubella in Vojvodina, Serbia: 24 years after the introduction of the MMR vaccine in the national immunization programme. PLoS ONE 2020, 15, e0227413. [Google Scholar] [CrossRef]
  53. Vilajeliu, A.; García-Basteiro, A.L.; Valencia, S.; Barreales, S.; Oliveras, L.; Calvente, V.; Goncé, A.; Bayas, J.M. Rubella susceptibility in pregnant women and results of a postpartum immunization strategy in Catalonia, Spain. Vaccine 2015, 33, 1767–1772. [Google Scholar] [CrossRef]
  54. Porobic-Jahic, H.; Skokic, F.; Ahmetagic, S.; Piljic, D.; Jahic, R.; Petrovic, J. Cytomegalovirus Infection in Pregnancy—Our Experiences. Med. Arch. 2019, 73, 149–153. [Google Scholar] [CrossRef] [PubMed]
  55. Trombetta, C.M.; Viviani, S.; Montomoli, E.; Marchi, S. Seroprevalence of antibodies to cytomegalovirus in pregnant women in the Apulia region (Italy). J. Prev. Med. Hyg. 2021, 62, E372–E376. [Google Scholar] [CrossRef] [PubMed]
  56. Kuessel, L.; Husslein, H.; Marschalek, J.; Brunner, J.; Ristl, R.; Popow-Kraupp, T.; Kiss, H. Prediction of Maternal Cytomegalovirus Serostatus in Early Pregnancy: A Retrospective Analysis in Western Europe. PLoS ONE 2015, 10, e0145470. [Google Scholar] [CrossRef] [PubMed]
  57. Pembrey, L.; Raynor, P.; Griffiths, P.; Chaytor, S.; Wright, J.; Hall, A.J. Seroprevalence of cytomegalovirus, Epstein Barr virus and varicella zoster virus among pregnant women in Bradford: A cohort study. PLoS ONE 2013, 8, e81881. [Google Scholar] [CrossRef] [PubMed]
  58. Antona, D.; Lepoutre, A.; Fonteneau, L.; Baudon, C.; Halftermeyer-Zhou, F.; LE Strat, Y.; Lévy-Bruhl, D. Seroprevalence of cytomegalovirus infection in France in 2010. Epidemiol. Infect. 2017, 145, 1471–1478. [Google Scholar] [CrossRef] [PubMed]
  59. Enders, G.; Daiminger, A.; Lindemann, L.; Knotek, F.; Bäder, U.; Exler, S.; Enders, M. Cytomegalovirus (CMV) seroprevalence in pregnant women, bone marrow donors and adolescents in Germany, 1996–2010. Med. Microbiol. Immunol. 2012, 201, 303–309. [Google Scholar] [CrossRef] [PubMed]
  60. Greye, H.; Wex, T.; Taneva, E.; Redlich, A.; Costa, S.D.; Rissmann, A. Cytomegalovirus seronegativity rate in pregnant women and primary cytomegalovirus infection during pregnancy in rural Germany. BMC Pregnancy Childbirth 2023, 23, 299. [Google Scholar] [CrossRef] [PubMed]
  61. Gaj, Z.; Rycel, M.; Wilczyński, J.; Nowakowska, D. Seroprewalencja zakazeń cytomegalowirusem w populacji polskich kobiet ciezarnych [Seroprevalence of cytomegalovirus infection in the population of Polish pregnant women]. Ginekol. Pol. 2012, 83, 337–341. [Google Scholar] [PubMed]
  62. Wujcicka, W.; Gaj, Z.; Wilczyński, J.; Sobala, W.; Spiewak, E.; Nowakowska, D. Impact of socioeconomic risk factors on the seroprevalence of cytomegalovirus infections in a cohort of pregnant Polish women between 2010 and 2011. Eur. J. Clin. Microbiol. Infect. Dis. 2014, 33, 1951–1958. [Google Scholar] [CrossRef]
  63. Knowles, S.J.; Grundy, K.; Cahill, I.; Cafferkey, M.T.; Geary, M. Low cytomegalovirus sero-prevalence in Irish pregnant women. Ir. Med. J. 2005, 98, 210–212. [Google Scholar]
  64. Puhakka, L.; Sarvikivi, E.; Lappalainen, M.; Surcel, H.M.; Saxen, H. Decrease in seroprevalence for herpesviruses among pregnant women in Finland: Cross-sectional study of three time points 1992, 2002 and 2012. Infect. Dis. 2016, 48, 406–410. [Google Scholar] [CrossRef] [PubMed]
  65. Radoi, C.L.; Zlatian, O.; Balasoiu, M.; Dragomir, T.-L.; Sorop, M.I.; Bagiu, I.C.; Boeriu, E.; Susan, M.; Sorop, B.; Oprisoni, L.A.; et al. Seroprevalence of Anti-Cytomegalovirus Antibodies in Pregnant Women from South-West Romania. Microorganisms 2024, 12, 268. [Google Scholar] [CrossRef] [PubMed]
  66. Gorun, F.; Motoi, S.; Malita, D.; Navolan, D.B.; Nemescu, D.; Olariu, T.R.; Craina, M.; Vilibic-Cavlek, T.; Ciohat, I.; Boda, D.; et al. Cytomegalovirus seroprevalence in pregnant women in the western region of Romania: A large-scale study. Exp. Ther. Med. 2020, 20, 2439–2443. [Google Scholar] [CrossRef] [PubMed]
  67. Kucera, P.; Gerber, S.; Marques-Vidal, P.; Meylan, P.R. Seroepidemiology of herpes simplex virus type 1 and 2 in pregnant women in Switzerland: An obstetric clinic based study. Eur. J. Obstet. Gynecol. Reprod. Biol. 2012, 160, 13–17. [Google Scholar] [CrossRef] [PubMed]
  68. Uusküla, A.; Nygard-Kibur, M.; Cowan, F.M.; Mayaud, P.; French, R.S.; Robinson, J.N.; Brown, D.W. The burden of infection with herpes simplex virus type 1 and type 2: Seroprevalence study in Estonia. Scand. J. Infect. Dis. 2004, 36, 727–732. [Google Scholar] [CrossRef] [PubMed]
  69. LeGoff, J.; Saussereau, E.; Boulanger, M.C.; Chemin, C.; Si-Mohamed, A.; Bélec, L.; Maisonneuve, L. Unexpected high prevalence of herpes simplex virus (HSV) type 2 seropositivity and HSV genital shedding in pregnant women living in an East Parissuburban area. Int. J. STD AIDS 2007, 18, 593–595. [Google Scholar] [CrossRef]
  70. Marchi, S.; Trombetta, C.M.; Gasparini, R.; Temperton, N.; Montomoli, E. Epidemiology of herpes simplex virus type 1 and 2 in Italy: A seroprevalence study from 2000 to 2014. J. Prev. Med. Hyg. 2017, 58, E27–E33. [Google Scholar] [PubMed]
  71. Ozdemir, R.; Er, H.; Baran, N.; Vural, A.; Demirci, M. HSV-1 and HSV-2 seropositivity rates in pregnant women admitted to Izmir Ataturk Research and Training Hospital, Turkey. Mikrobiyol. Bul. 2009, 43, 709–711. [Google Scholar] [PubMed]
  72. Alanen, A.; Kahala, K.; Vahlberg, T.; Koskela, P.; Vainionpää, R. Seroprevalence, incidence of prenatal infections and reliability of maternal history of varicella zoster virus, cytomegalovirus, herpes simplex virus and parvovirus B19 infection in South West-ern Finland. BJOG 2005, 112, 50–56. [Google Scholar] [CrossRef]
  73. Gaytant, M.A.; Steegers, E.A.; van Laere, M.; Semmekrot, B.A.; Groen, J.; Weel, J.F.; van der Meijden, W.I.; Boer, K.; Galama, J.M. Seroprevalences of herpes simplex virus type 1 and type 2 among pregnant women in the Netherlands. Sex Transm. Dis. 2002, 29, 710–714. [Google Scholar] [CrossRef]
  74. Patton, M.E.; Bernstein, K.; Liu, G.; Zaidi, A.; Markowitz, L.E. Seroprevalence of Herpes Simplex Virus Types 1 and 2 Among Pregnant Women and Sexually Active, Nonpregnant Women in the United States. Clin. Infect. Dis. 2018, 67, 1535–1542. [Google Scholar] [CrossRef] [PubMed]
  75. Arama, V.; Vladareanu, R.; Mihailescu, R.; Streinu Cercel, A.; Mihai, C.; Hristea, A.; Iosipenco, M.; Stefan Arama, S.; Rabilloud, M. Seroprevalence and Risk Factors Associated with Herpes Simplex Virus Infection among Pregnant Women. J. Perinat. Med. 2008, 36, 206–212. [Google Scholar] [CrossRef] [PubMed]
  76. Korr, G.; Thamm, M.; Czogiel, I.; Poethko-Mueller, C.; Bremer, V.; Jansen, K. Decreasing seroprevalence of herpes simplex virus type 1 and type 2 in Germany leaves many people susceptible to genital infection: Time to raise awareness and enhance control. BMC Infect. Dis. 2017, 17, 471. [Google Scholar] [CrossRef]
  77. Hettmann, A.; Gerle, B.; Barcsay, E.; Csiszár, C.; Takács, M. Seroprevalence of HSV-2 in Hungary and comparison of the HSV-2 prevalence of pregnant and infertile women. Acta Microbiol. Immunol. Hung. 2008, 55, 429–436. [Google Scholar] [CrossRef] [PubMed]
  78. Mocanu, A.G.; Gorun, F.; Ciohat, I.; Navolan, D.; Malita, D.; Vilibic-Cavlek, T.; Dahma, G.; Neamtu, R.; Popescu, D.; Cioca, A.; et al. Simultaneous Seroprevalence to Toxoplasma gondii, Cytomegalovirus and Rubella Virus in Childbearing Women from Western Romania. Medicina 2021, 57, 927. [Google Scholar] [CrossRef] [PubMed]
  79. Mocanu, A.G.; Stoian, D.L.; Daescu, A.M.; Motofelea, A.C.; Ciohat, I.M.; Navolan, D.B.; Vilibic-Cavlek, T.; Bogdanic, M.; Nemescu, D.; Tomescu, L.; et al. The Impact of Latent Cytomegalovirus Infection on Spontaneous Abortion History and Pregnancy Outcomes in Romanian Pregnant Women. Microorganisms 2024, 12, 731. [Google Scholar] [CrossRef] [PubMed]
  80. Aboudy, Y.; Fogel, A.; Barnea, B.; Mendelson, E.; Yosef, L.; Frank, T.; Shalev, E. Subclinical rubella reinfection during pregnancy followed by transmission of virus to the fetus. J. Infect 1997, 34, 273–276. [Google Scholar] [CrossRef]
  81. Bullens, D.; Smets, K.; Vanhaesebrouck, P. Congenital rubella syndrome after maternal reinfection. Clin. Pediatr. 2000, 39, 113–116. [Google Scholar] [CrossRef] [PubMed]
  82. Carlson, A.; Norwitz, E.R.; Stiller, R.J. Cytomegalovirus infection in pregnancy: Should all women be screened? Rev. Obstet. Gynecol. 2010, 3, 172–179. [Google Scholar]
  83. Ciobanu, A.M.; Gica, N.; Gica, C.; Botezatu, R.; Furtuna, M.; Peltecu, G.; Panaitescu, A.M. Cytomegalovirus Infection in Pregnancy—Counselling Challenges in the Setting of Generalised Testing. Maedica 2020, 15, 253–257. [Google Scholar] [CrossRef]
  84. Elbez-Rubinstein, A.; Ajzenberg, D.; Dardé, M.L.; Cohen, R.; Dumètre, A.; Year, H.; Gondon, E.; Janaud, J.C.; Thulliez, P. Congenital toxoplasmosis and reinfection during pregnancy: Case report, strain characterization, experimental model of reinfection, and review. J. Infect. Dis. 2009, 199, 280–285. [Google Scholar] [CrossRef]
Antibodies 13 00049 g001
Figure 1. Distribution of study participants by age.
Figure 1. Distribution of study participants by age.
Antibodies 13 00049 g001
Table 1. Serology methods used for detection of TORCH antibodies.
Table 1. Serology methods used for detection of TORCH antibodies.
TORCH PathogenMethod (Reference Values)
IgM AntibodiesIgG AntibodiesIgG AvidityWestern Blot
T. gondiiELFA
(Index < 0.55 negative, 0.55–0.65 borderline, >0.65 positive)		ELFA
(IU/mL < 4 negative, 4–8 borderline, >8 positive)		ELFA
(Index < 0.3 low, 0.3–0.5
borderline, >0.5 high)
RUBVELISA
(NTU < 9 negative, 9–11
borderline, >11 positive)		ELISA
(IU/mL < 10 negative, 10–15 borderline, 15 positive)		ELISA
(AI % < 40 low, 40–60
borderline, >60% high)
CMVELISA
(AI < 9 negative, 9–11
borderline, >11 positive)		ELISA
(AI < 9 negative, 9–11
borderline, >11 positive)		ELISA
(AI % < 40 low, 40–60
borderline, >60% high)
HSV-1ELISA
(VE < 9 negative, 9–11
borderline, >11 positive)		ELISA
(VE < 9 negative, 9–11
borderline, >11 positive)		 Positive, borderline, negative
HSV-2ELISA
(VE < 9 negative, 9–11
borderline, >11 positive)		ELISA
(VE < 9 negative, 9–11
borderline, >11 positive)		 Positive, borderline, negative
ELFA = enzyme-linked fluorescence assay, ELISA = enzyme-linked immunosorbent assay; NTU = Novatec units, AI = avidity index, IU/mL = international units/mL, VE = Virotech units.
Table 2. Prevalence of Toxoplasma gondii antibodies.
Table 2. Prevalence of Toxoplasma gondii antibodies.
CharacteristicTested
N (%)		Toxoplasma gondii IgMToxoplasma gondii IgG
N (%)95% CIpN (%)95% CIp
Age group≤20 years16 (1.6)1 (6.3)0.1–30.20.0074 (25.0)7.3–52.40.896
21–25 years87 (8.4)0 (0)NA18 (20.7)12.7–30.7
26–30 years300 (29.1)1 (0.3)<0.1–1.263 (21.0)16.5–26.1
31–35 years373 (36.1)2 (0.5)0.1–1.970 (18.8)14.9–23.1
36–40 years213 (20.6)0 (0)NA42 (19.7)14.6–25.7
>40 years43 (4.2)0 (0)NA11 (25.6)13.5–41.2
Area of residenceUrban725 (70.3)2 (0.3)<0.1–1.00.375124 (17.1)14.4–20<0.001
Suburban/rural307 (29.7)2 (0.7)0.1–2.384 (27.4)22.5–32.7
Geographic regionContinental724 (70.2)3 (0.4)<0.1–1.20.832161 (22.2)19.3–25.40.011
Coastal308 (29.8)1 (0.3)<0.1–1.847 (15.3)11.4–19.8
Obstetric historyNon-pregnant271 (26.3)0 (0)NA0.24764 (23.6)18.7–29.10.204
Normal pregnancy608 (58.9)4 0.7)0.2–1.7118 (19.4)16.3–22.8
Unfavorable obstetric history153 (14.8)0 (0)NA26 (17.0)11.4–23.9
NA = not applicable, CI = confidence interval.
Table 3. Prevalence of rubella virus antibodies.
Table 3. Prevalence of rubella virus antibodies.
CharacteristicTested
N (%)		Rubella Virus IgMRubella Virus IgG
N (%)95% CIpN (%)95% CIp
Age group≤20 years16 (1.6)0 (0)NA0.37813 (81.3)54.4–96.00.319
21–25 years87 (8.4)1 (1.1)<0.1–6.283 (95.4)88.6–98.7
26–30 years300 (29.1)0 (0)NA268 (89.3)85.3–92.4
31–35 years373 (36.1)1 (0.3)<0.1–1.5341 (91.4)88.1–94.1
36–40 years213 (20.6)0 (0)NA197 (92.5)88.1–95.6
>40 years43 (4.2)0 (0)NA40 (93.0)80.9–98.5
Area of residenceUrban725 (70.3)2 (0.3)<0.1–10.357662 (91.3)89–93.30.956
Suburban/rural307 (29.7)0 (0)NA280 (91.2)87.5–94.1
Geographic regionContinental724 (70.2)2 (0.3)<0.1–10.356664 (91.7)89.5–93.60.449
Coastal308 (29.8)0 (0)NA278 (90.3)86.4–93.3
Obstetric historyNon-pregnant271 (26.3)0 (0)NA0.498248 (91.5)87.5–94.50.976
Normal pregnancy608 (58.9)2 (0.3)<0.1–1.2554 (91.1)88.6–93.3
Unfavorable obstetric history153 (14.8)0 (0)NA140 (90.5)85.9–95.4
NA = not applicable, CI = confidence interval.
Table 4. Prevalence of cytomegalovirus antibodies.
Table 4. Prevalence of cytomegalovirus antibodies.
CharacteristicTested
N (%)		Cytomegalovirus IgMCytomegalovirus IgG
N (%)95% CIpN (%)95% CIp
Age group≤20 years16 (1.6)1 (6.3)0.2–39.20.24810 (62.5)35.4–84.80.863
21–25 years87 (8.4)10 (11.5)5.7–20.158 (66.7)55.7–76.4
26–30 years300 (29.1)22 (7.3)4.7–10.9206 (69.7)63.1–73.9
31–35 years373 (36.1)17 (4.6)2.7–7.2270 (72.4)67.5–76.9
36–40 years213 (20.6)13 (6.1)3.3–10.2150 (70.4)63.8–76.5
>40 years43 (4.2)2 (4.7)0.6–15.831 (72.1)56.3–84.7
Area of residenceUrban725 (70.3)47 (6.5)4.8–8.50.708501 (69.1)65.6–72.50.119
Suburban/rural307 (29.7)18 (5.9)3.5–9.1227 (73.9)68.7–78.8
Geographic regionContinental724 (70.241 (5.7)4.1–7.60.198507 (70.0)66.5–73.30.587
Coastal308 (29.824 (7.8)5.1–11.4221 (71.8)66.4–76.7
Obstetric historyNon-pregnant271 (26.3)21 (7.7)4.9–11.60.495188 (69.4)63.5–74.80.393
Normal pregnancy608 (58.9)36 (5.9)4.2–8.1425 (69.9)66.1–73.5
Unfavorable obstetric history153 (14.8)8 (5.2)2.3–10115 (75.2)67.5–81.8
CI = confidence interval.
Table 5. Prevalence of herpes simplex virus type 1 antibodies.
Table 5. Prevalence of herpes simplex virus type 1 antibodies.
CharacteristicTested
N (%)		Herpes Simplex Type 1 IgMHerpes Simplex Type 1 IgG
N (%)95% CIpN (%)95% CIp
Age group≤20 years16 (1.6)0 (0)NA0.53812 (75.0)47.6–92.70.598
21–25 years87 (8.4)0 (0)NA57 (65.5)54.6–75.4
26–30 years300 (29.1)5 (1.7)0.5–3.8191 (63.7)57.9–69.1
31–35 years373 (36.1)2 (0.5)<0.1–1.9249 (66.8)61.7–71.5
36–40 years213 (20.6)2 (0.9)0.1–3.4148 (69.5)62.8–75.6
>40 years43 (4.2)1 (2.3)<0.1–12.332 (74.4)58.8–86.5
Area of residenceUrban725 (70.3)9 (1.2)0.6–2.30.170469 (64.7)61.1–68.20.030
Suburban/rural307 (29.7)1 (0.3)<0.1–1.8220 (71.7)66.3–76.6
Geographic regionContinental724 (70.2)7 (1.0)0.4–20.991484 (66.9)63.3–70.30.927
Coastal308 (29.8)3 (1.0)0.2–2.8205 (66.6)61–71.8
Obstetric historyNon-pregnant271 (26.3)2 (0.7)<0.1–2.60.300192 (70.8)65–76.20.211
Normal pregnancy608 (58.9)8 (1.3)0.6–2.6394 (64.8)60.9–68.6
Unfavorable obstetric history153 (14.8)0 (0)NA103 (67.3)59.3–74.7
NA = not applicable, CI = confidence interval.
Table 6. Prevalence of herpes simplex virus type 2 antibodies.
Table 6. Prevalence of herpes simplex virus type 2 antibodies.
CharacteristicTested
N (%)		Herpes Simplex Type 2 IgMHerpes Simplex Type 2 IgG
N (%)95% CIpN (%)95% CIp
Age group≤20 years16 (1.6)0 (0)NA0.8800 (0)NA0.005
21–25 years87 (8.4)0 (0)NA0 (0)NA
26–30 years300 (29.1)0 (0)NA5 (1.7)0.5–3.8
31–35 years373 (36.1)1 (0.3)<0.1–1.513 (3.5)1.9–5.9
36–40 years213 (20.6)0 (0)NA14 (6.6)3.6–10.8
>40 years43 (4.2)0 (0)NA4 (9.3)2.6–22.1
Area of residenceUrban725 (70.3)0 (0)NA0.12427 (3.7)2.5–5.40.526
Suburban/rural307 (29.7)1 (0.3)<0.1–1.89 (2.9)1.3–5.5
Geographic regionContinental724 (70.2)1 (0.1)<0.1–0.80.51427 (3.7)2.5–5.40.518
Coastal308 (29.8)0 (0)NA9 (2.9)1.3–5.5
Obstetric historyNon-pregnant271 (26.3)0 (0)NA0.70614 (5.2)2.9–8.50.106
Normal pregnancy608 (58.9)1 (0.2)<0.1–120 (3.3)2–5
Unfavorable obstetric history153 (14.8)0 (0)NA 2 (1.3)0.2–4.6
NA = not applicable, CI = confidence interval.
Table 7. Simultaneous IgG seroprevalence of two TORCH pathogens.
Table 7. Simultaneous IgG seroprevalence of two TORCH pathogens.
CharacteristicTested
N (%)		Toxoplasma gondii–
Rubella Virus IgG		Toxoplasma gondii–
Cytomegalovirus IgG		Rubella Virus–
Cytomegalovirus IgG
N (%)95% CIpN (%)95% CIpN (%)95% CIp
Age group
≤20 years16 (1.6)4 (25.0)7.0–52.40.7542 (12.5)1.5–38.30.9627 (43.8)19.8–79.10.408
21–25 years87 (8.4)18 (20.7)12.7–30.712 (13.8)7.3–22.956 (64.4)53.4–74.4
26–30 years300 (29.1)59 (19.7)15.3–24.644 (14.7)10.9–19.2185 (61.7)55.9–67.2
31–35 years373 (36.1)63 (16.9)13.2–21.152 (13.9)10.6–17.9250 (67.0)62.0–71.8
36–40 years213 (20.6)36 (16.9)12.1–22.628 (13.1)8.9–18.4137 (64.3)57.5–70.7
>40 years43 (4.2)10 (23.3)11.8–38.68 (18.6)8.4–33.428 (65.1)49.1–79.0
Area of residence
Urban725 (70.3) 112 (15.4)12.9–18.3<0.00185 (11.7)9.5–14.3<0.001458 (63.2)59.5–66.70.270
Suburban/rural307 (29.7) 78 (25.4)20.6–30.761 (19.9)15.6–24.5205 (66.8)61.2–72.0
Geographic region
Continental724 (70.2) 145 (20.0)17.2–23.10.04115 (15.9)13.3–18.80.014465 (64.2)60.6–67.70.986
Coastal308 (29.8) 45 (14.0)10.9–19.131 (10.1)6.9–14198 (63.3)58.7–69.6
Obstetric history
Non-pregnant271 (26.3)57 (21.0)16.3–26.40.35144 (16.2)12.1–21.2 172 (63.5)57.4–69.20.281
Normal pregnancy608 (58.9)109 (17.9)15–21.283 (13.7)11.0–16.6384 (63.2)59.2–67.0
Unfavorable obstetric history153 (14.8)24 (15.7)10.3–22.419 (12.4)7.6–18.7107 (69.4)62.0–77.1
CI = confidence interval.
Table 8. Simultaneous IgG seroprevalence of three TORCH pathogens.
Table 8. Simultaneous IgG seroprevalence of three TORCH pathogens.
CharacteristicTested
N (%)		Toxoplasma gondii–Rubella Virus–Cytomegalovirus IgG
N (%)95% CIp
Age group≤20 years16 (1.6)2 (12.5)1.6–38.30.946
21–25 years87 (8.4)12 (13.8)7.3–22.9
26–30 years300 (29.1)42 (14.0)10.3–18.4
31–35 years373 (36.1)49 (13.1)9.9–17.0
36–40 years213 (20.6)25 (11.7)7.7–16.8
>40 years43 (4.2)7 (16.3)6.8–30.7
Area of residenceUrban725 (70.3)80 (11.0)8.8–13.50.002
Suburban/rural307 (29.7)57 (18.6)14.4–23.4
Geographic regionContinental724 (70.2)107 (14.8)12.3–17.60.029
Coastal308 (29.8)30 (9.7)6.7–13.6
Non-pregnant271 (26.3)40 (14.8)10.8–19.60.697
Obstetric historyNormal pregnancy608 (58.9)78 (12.8)10.3–15.8
Unfavorable obstetric history153 (14.8)19 (12.4)7.6–18.7
CI = confidence interval.
Table 9. Univariate and multivariate risk for Toxoplasma gondii IgG seropositivity.
Table 9. Univariate and multivariate risk for Toxoplasma gondii IgG seropositivity.
CharacteristicOR95% CIpAOR95% CIp
Age (one-year increase) 0.990 0.960–1.030 0.614 1.000 0.961–1.040 0.854
Suburban/rural (Ref.) vs. urban area of residence1.8261.330–2.511<0.0011.9811.334–2.9310.001
Continental (Ref.) vs. coastal geographic region1.5871.120–2.2680.0111.9121.217–3.0120.005
Unfavorable obstetric history (Ref.) vs. normal pregnancy0.8500.533–1.3570.4960.8820.547–1.4210.605
OR = odds ratio, AOR = adjusted odds ratio, CI = confidence interval.
Table 10. Univariate and multivariate risk for rubella virus IgG seropositivity.
Table 10. Univariate and multivariate risk for rubella virus IgG seropositivity.
CharacteristicOR95% CIpAOR95% CIp
Age (one-year increase) 1.016 0.975–1.059 0.473 1.014 0.964–1.068 0.585
Suburban/rural (Ref.) vs. urban area of residence0.9860.616–1.5820.9581.0230.585–1.7880.937
Continental (Ref.) vs. coastal geographic region1.1950.754–1.9120.4501.4580.855–2.4880.167
Unfavorable obstetric history (Ref.) vs. normal pregnancy1.0500.557–1.9770.8811.0970.579–2.0790.772
OR = odds ratio, AOR = adjusted odds ratio, CI = confidence interval.
Table 11. Univariate and multivariate risk for cytomegalovirus IgG seropositivity.
Table 11. Univariate and multivariate risk for cytomegalovirus IgG seropositivity.
CharacteristicOR95% CIpAOR95% CIp
Age (one-year increase) 1.001 0.982–1.035 0.558 1.002 0.970–1.034 0.912
Suburban/rural (Ref.) vs. urban area of residence1.2690.940–1.7120.1201.2890.899–1.8490.168
Continental (Ref.) vs. coastal geographic region0.9200.684–1.2350.5780.9830.690–1.4030.927
Unfavorable obstetric history (Ref.) vs. normal pregnancy1.3030.869–1.9550.2011.2880.855–1.9390.226
OR = odds ratio, AOR = adjusted odds ratio, CI = confidence interval.
Table 12. Univariate and multivariate risk for herpes simplex virus type 1 IgG seropositivity.
Table 12. Univariate and multivariate risk for herpes simplex virus type 1 IgG seropositivity.
CharacteristicOR95% CIpAOR95% CIp
Age (one-year increase) 1.016 0.990–1.042 0.231 1.009 0.978–1.040 0.588
Suburban/rural (Ref.) vs. urban area of residence1.3801.032–1.8470.0301.4211.007–2.0010.045
Continental (Ref.) vs. coastal geographic region1.0130.764–1.3440.9271.0350.740–1.4490.841
Unfavorable obstetric history (Ref.) vs. normal pregnancy1.1190.768–1.6310.5591.1060.756–1.6190.604
OR = odds ratio, AOR = adjusted odds ratio, CI = confidence interval.
Table 13. Univariate and multivariate risk for herpes simplex virus type 2 IgG seropositivity.
Table 13. Univariate and multivariate risk for herpes simplex virus type 2 IgG seropositivity.
CharacteristicOR95% CIpAOR95% CIp
Age (one-year increase) 1.164 1.082–1.251 <0.001 1.130 1.030–1.240 0.010
Suburban/rural (Ref.) vs. urban area of residence0.7810.363–1.6800.5270.9390.333–1.6510.906
Continental (Ref.) vs. coastal geographic region1.2870.598–2.7710.5191.6950.553–5.1810.356
Unfavorable obstetric history (Ref.) vs. normal pregnancy0.3890.900–1.6840.2070.3940.900–1.7240.216
OR = odds ratio, AOR = adjusted odds ratio, CI = confidence interval.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Vilibic-Cavlek, T.; Kolaric, B.; Belamaric, M.; Sviben, M.; Ferenc, T.; Navolan, D.; Bekic, V.; Milasincic, L.; Antolasic, L.; Vilibic, M.; et al. Screening for TORCH Antibodies in Croatian Childbearing-Aged Women, 2014–2023. Antibodies 2024, 13, 49. https://doi.org/10.3390/antib13020049

AMA Style

Vilibic-Cavlek T, Kolaric B, Belamaric M, Sviben M, Ferenc T, Navolan D, Bekic V, Milasincic L, Antolasic L, Vilibic M, et al. Screening for TORCH Antibodies in Croatian Childbearing-Aged Women, 2014–2023. Antibodies. 2024; 13(2):49. https://doi.org/10.3390/antib13020049

Chicago/Turabian Style

Vilibic-Cavlek, Tatjana, Branko Kolaric, Marko Belamaric, Mario Sviben, Thomas Ferenc, Dan Navolan, Viktor Bekic, Ljiljana Milasincic, Ljiljana Antolasic, Maja Vilibic, and et al. 2024. "Screening for TORCH Antibodies in Croatian Childbearing-Aged Women, 2014–2023" Antibodies 13, no. 2: 49. https://doi.org/10.3390/antib13020049

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop