[HTML][HTML] Characterization, treatment patterns, and patient-related outcomes of patients with Fragile X syndrome in Germany: final results of the observational EXPLAIN�…
F Haessler, F Gaese, M Huss, C Kretschmar…�- BMC psychiatry, 2016 - Springer
F Haessler, F Gaese, M Huss, C Kretschmar, M Brinkman, H Peters, S Elstner, M Colla…
BMC psychiatry, 2016•SpringerBackground As data on the phenotype, characteristics and management of patients with
Fragile X Syndrome (FXS) are limited, we aimed to collect such data in Germany in
experienced centres involved in the treatment of such patients. Methods EXPLAIN-FXS is a
prospective observational (non-interventional) study (registry) performed between April
2013 and January 2016 at 18 sites in Germany. Requirements for patient participation
included confirmed diagnosis of FXS by genetic testing (> 200 CGG repeats) and written�…
Fragile X Syndrome (FXS) are limited, we aimed to collect such data in Germany in
experienced centres involved in the treatment of such patients. Methods EXPLAIN-FXS is a
prospective observational (non-interventional) study (registry) performed between April
2013 and January 2016 at 18 sites in Germany. Requirements for patient participation
included confirmed diagnosis of FXS by genetic testing (> 200 CGG repeats) and written�…
Background
As data on the phenotype, characteristics and management of patients with Fragile X Syndrome (FXS) are limited, we aimed to collect such data in Germany in experienced centres involved in the treatment of such patients.
Methods
EXPLAIN-FXS is a prospective observational (non-interventional) study (registry) performed between April 2013 and January 2016 at 18 sites in Germany. Requirements for patient participation included confirmed diagnosis of FXS by genetic testing (>200 CGG repeats) and written informed consent. Patients were followed for up to 2�years.
Results
Seventy-five patients (84.0�% males, mean age 16.7 � 14.5�years, ranging from 2 - 82�years) were analysed. The mean 6-item score, determined according to Giangreco (J Pediatr 129:611-614, 1996), was 6.9 � 2.5 points. At least one neurological finding each was noted in 53 patients (69.7�%). Specifically, ataxia was noted in 5 patients (6.6�%), lack of fine motor skills in 40 patients, (52.6�%), muscle tonus disorder in 4 patients (5.3�%), and other neurological disorders in 39 patients (51.3�%). Spasticity was not noted in any patient.
Seizures were reported in 6 patients (8.1�%), anxiety disorders in 22 patients (30.1�%), depression in 7 patients (9.6�%), ADHD/ADD in 36 patients (49.3�%), impairment of social behavior in 39 patients (53.4�%), and other comorbidities in 23 patients (31.5�%). The mean Aberrant Behaviour Checklist Community Edition (ABC-C) score on behavioral symptoms, obtained in 71 patients at first documentation, was 48.4 � 27.8 (median 45.0, range 5-115). The mean visual analogue scale (VAS) score, obtained in 59 patients at first documentation, was 84.9 � 14.6 points (median 90; range 50 – 100).
Conclusions
This report describes the largest cohort of patients with FXS in Europe. The reported observations indicate a substantial burden of disease for patients and their caregivers. Based on these observations, an early expert psychiatric diagnosis is recommended for suspected FXS patients. Further recommendations include multimodal and multi-professional management that is tailored to the individual patient’s needs.
Trial registration
The ClinTrials.gov identifier is NCT01711606 . Registered on 18 October 2012.
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