Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2024 Jun 13;16(12):1852.
doi: 10.3390/nu16121852.

A Symbiotic Meal Containing Extruded Sorghum and Probiotic (Bifidobacterium longum) Ameliorated Intestinal Health Markers in Individuals with Chronic Kidney Disease: A Secondary Analysis of a Subsample from a Previous Randomized and Controlled Clinical Trial

Affiliations
Randomized Controlled Trial

A Symbiotic Meal Containing Extruded Sorghum and Probiotic (Bifidobacterium longum) Ameliorated Intestinal Health Markers in Individuals with Chronic Kidney Disease: A Secondary Analysis of a Subsample from a Previous Randomized and Controlled Clinical Trial

Haira Guedes Lúcio et al. Nutrients. .

Abstract

Background: Chronic kidney disease increases uremic toxins concentrations, which have been associated with intestinal dysbiosis. Sorghum bicolor L. Moench has dietary fiber and bioactive compounds, while Bifidobacterium longum can promote beneficial health effects.

Methods: It is a controlled, randomized, and single-blind clinical trial. Thirty-nine subjects were randomly separated into two groups: symbiotic group (SG), which received 100 mL of unfermented probiotic milk with Bifidobacterium longum strain and 40 g of extruded sorghum flakes; and the control group (CG), which received 100 mL of pasteurized milk and 40 g of extruded corn flakes for seven weeks.

Results: The uremic toxins decreased, and gastrointestinal symptoms improved intragroup in the SG group. The acetic, propionic, and butyric acid production increased intragroup in the SG group. Regarding α-diversity, the Chao1 index was enhanced in the SG intragroup. The KEGG analysis revealed that symbiotic meal increased the intragroup energy and amino sugar metabolism, in addition to enabling essential amino acid production and metabolism, sucrose degradation, and the biosynthesis of ribonucleotide metabolic pathways.

Conclusions: The consumption of symbiotic meal reduced BMI, improved short-chain fatty acid (SCFA) synthesis and gastrointestinal symptoms, increased diversity according to the Chao1 index, and reduced uremic toxins in chronic kidney disease patients.

Keywords: SCFAs; Sorghum bicolor L. Moench; gut microbiota; symbiotic meal; uremic toxins.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Study design of research.
Figure 2
Figure 2
Consort flow diagram of study design of intervention protocol.
Figure 3
Figure 3
Effect of extruded sorghum BRS 305 plus Bifidobacterium longum on α-diversity index. (A) Chao1 index at baseline and endpoint, (B) Shannon–Weiner index at baseline and endpoint, (C) Simpson index at baseline and endpoint. CG: control group; SG: symbiotic group. The data were subjected to a paired t-test or unpaired t-test (α = 0.05) in GraphPad version 9.0.
Figure 4
Figure 4
Effect of extruded sorghum BRS 305 plus Bifidobacterium longum on the β-diversity estimated by principal coordinate analysis (PcoA), based on the Jaccard similarity distance of gut microbial communities in chronic kidney disease patients. (A) PCoA of the symbiotic group at baseline and endpoint; (B) PCoA of the control group at baseline and endpoint; (C) PCoA of the control and symbiotic groups at baseline; (D) PCoA of the control and symbiotic groups at endpoint. Permutational multivariate analysis of variance (PERMANOVA) was conducted using the STAMP software system version 2.0.2 considering α = 5%.

Similar articles

References

    1. Charles C., Ferris A.H. Chronic Kidney Disease. Prim. Care Clin. Off. Pract. 2020;47:585–595. doi: 10.1016/j.pop.2020.08.001. - DOI - PubMed
    1. Bikbov B., Purcell C.A., Levey A.S., Smith M., Abdoli A., Abebe M., Adebayo O.M., Afarideh M., Agarwal S.K., Agudelo-Botero M., et al. Global, regional, and national burden of chronic kidney disease, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2020;395:709–733. doi: 10.1016/S0140-6736(20)30045-3. - DOI - PMC - PubMed
    1. Poesen R., Viaene L., Verbeke K., Augustijns P., Bammens B., Claes K., Kuypers D., Evenepoel P., Meijers B. Cardiovascular disease relates to intestinal uptake of p-cresol in patients with chronic kidney disease. BMC Nephrol. 2014;15:87. doi: 10.1186/1471-2369-15-87. - DOI - PMC - PubMed
    1. Wong J., Piceno Y.M., DeSantis T.Z., Pahl M., Andersen G.L., Vaziri N.D. Expansion of Urease- and Uricase-Containing, Indole- and p-Cresol-Forming and Contraction of Short-Chain Fatty Acid-Producing Intestinal Microbiota in ESRD. Am. J. Nephrol. 2014;39:230–237. doi: 10.1159/000360010. - DOI - PMC - PubMed
    1. Chen Y.-Y., Chen D.-Q., Chen L., Liu J.-R., Vaziri N.D., Guo Y., Zhao Y.-Y. Microbiome–metabolome reveals the contribution of gut–kidney axis on kidney disease 11 Medical and Health Sciences 1103 Clinical Sciences. J. Transl. Med. 2019;17:5. doi: 10.1186/s12967-018-1756-4. - DOI - PMC - PubMed

Publication types