A global literature review of comorbidities and concomitant supportive medications among individuals with Rett syndrome

Aim: To synthesize evidence on the multisystem clinical burden of Rett syndrome, integrating comorbidity prevalence and concomitant medication use to inform proactive care. Materials & methods: A structured search of PubMed, Embase and Cochrane (January 2000 to July 2024), plus gray literature, identified clinical trials, observational studies, registries, and case series (n >10). Non-English articles, case reports, reviews and commentaries were excluded. Two investigators independently screened studies, extracted data and synthesized the evidence using a descriptive approach with evidence mapping. Results: Of 6253 records screened, 148 studies met inclusion criteria, spanning 24 countries and participants aged 7 months to 37 years. Neurological, musculoskeletal and developmental manifestations predominated (reported in 62.0%, 44.0% and 41.0% of studies, respectively). Epilepsy prevalence ranged from 15.0% to 91.0%, scoliosis 8.9–100% and gastrointestinal dysfunction was common, including constipation (16.4–82.8%) and gastroesophageal reflux (15.8–100.0%). Hand stereotypies were reported in 11.4% of studies, with prevalence of 70.0–100.0%. Among studies reporting developmental burden, inability to walk ranged from 19.0% to 100.0%. Additional comorbidities included sleep, oral, and endocrine disorders, among others. Antiepileptic medications contributed most to treatment burden (14.3–33.0% for monotherapy). Other commonly used medications targeted sleep (melatonin, 7.7–30.0%), gastrointestinal symptoms (proton-pump inhibitors, 37.0–61.0%) and behavioral symptoms (anti-anxiety agents, 10.0–21.4%). Conclusion: Rett syndrome imposes a substantial, lifelong multisystem burden requiring continuous surveillance. Findings highlight the importance of anticipatory, multidisciplinary care rather than symptom-driven management. Patterns of medication use, particularly for epilepsy, reflect reliance on symptom-directed therapies and highlight the need for routine medication review, careful prescribing and longitudinal monitoring to optimize outcomes.

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Journal
Journal of Comparative Effectiveness Research
Published
2026-08-18
DOI
https://doi.org/10.57264/cer-2026-0100
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

A global literature review of comorbidities and concomitant supportive medications among individuals with Rett syndrome

Ismaeel U. Yunusa, Krithika Rajagopalan, Nazia Rashid, Regina Nwamaka Nechi et al.
Journal of Comparative Effectiveness Research
Genetics and Neurodevelopmental Disorders
article

A global literature review of comorbidities and concomitant supportive medications among individuals with Rett syndrome

Ismaeel U. Yunusa, Krithika Rajagopalan, Nazia Rashid, Regina Nwamaka Nechi, S. Syed, Chijioke M Okeke
article en

Abstract

Aim: To synthesize evidence on the multisystem clinical burden of Rett syndrome, integrating comorbidity prevalence and concomitant medication use to inform proactive care. Materials & methods: A structured search of PubMed, Embase and Cochrane (January 2000 to July 2024), plus gray literature, identified clinical trials, observational studies, registries, and case series (n >10). Non-English articles, case reports, reviews and commentaries were excluded. Two investigators independently screened studies, extracted data and synthesized the evidence using a descriptive approach with evidence mapping. Results: Of 6253 records screened, 148 studies met inclusion criteria, spanning 24 countries and participants aged 7 months to 37 years. Neurological, musculoskeletal and developmental manifestations predominated (reported in 62.0%, 44.0% and 41.0% of studies, respectively). Epilepsy prevalence ranged from 15.0% to 91.0%, scoliosis 8.9–100% and gastrointestinal dysfunction was common, including constipation (16.4–82.8%) and gastroesophageal reflux (15.8–100.0%). Hand stereotypies were reported in 11.4% of studies, with prevalence of 70.0–100.0%. Among studies reporting developmental burden, inability to walk ranged from 19.0% to 100.0%. Additional comorbidities included sleep, oral, and endocrine disorders, among others. Antiepileptic medications contributed most to treatment burden (14.3–33.0% for monotherapy). Other commonly used medications targeted sleep (melatonin, 7.7–30.0%), gastrointestinal symptoms (proton-pump inhibitors, 37.0–61.0%) and behavioral symptoms (anti-anxiety agents, 10.0–21.4%). Conclusion: Rett syndrome imposes a substantial, lifelong multisystem burden requiring continuous surveillance. Findings highlight the importance of anticipatory, multidisciplinary care rather than symptom-driven management. Patterns of medication use, particularly for epilepsy, reflect reliance on symptom-directed therapies and highlight the need for routine medication review, careful prescribing and longitudinal monitoring to optimize outcomes.

Journal of Comparative Effectiveness Research
Acadia Pharmaceuticals (United States) (US), University of South Carolina (US), University of Houston (US), The Ohio State University (US)
Reduced inequalities
Openalex Percentile: Top 9%
Genetics and Neurodevelopmental Disorders
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