Epidemiology of Huntington's Disease in Latin America: A Systematic Review and Meta‐Analysis

Author:

Medina Escobar Alex1ORCID,Pringsheim Tamara2345ORCID,Gautreau Sylvia1,Rivera‐Duarte Jose D.6,Amorelli Gabriel7,Cornejo‐Olivas Mario89ORCID,Rossi Malco10ORCID

Affiliation:

1. Moncton Interdisciplinary Neurodegenerative Diseases Clinic, Horizon Health Network Moncton New Brunswick Canada

2. Department of Clinical Neurosciences Psychiatry, Pediatrics and Community Health Sciences, University of Calgary Calgary Alberta Canada

3. Department of Clinical Neurosciences University of Calgary Calgary Alberta Canada

4. Hotchkiss Brain Institute, University of Calgary Calgary Alberta Canada

5. Mathison Centre for Mental Health Research and Education Calgary Alberta Canada

6. Laboratorio de Hidrobiología, Departamento de Ecología y Recursos Naturales, Escuela de Biología, Facultad de Ciencias, Universidad Nacional Autónoma de Honduras, Ciudad Universitaria Tegucigalpa Honduras

7. The Ottawa Health Research Institute, Ottawa University Ottawa Ontario Canada

8. Neurogenetics Working Group, Universidad Cientifica del Sur Lima Peru

9. Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas Lima Peru

10. Servicio de Movimientos Anormales, Departamento de Neurología, FLENI, Ciudad Autónoma de Buenos Aires Buenos Aires Argentina

Abstract

AbstractBackgroundLatin America has played a crucial role in advancing our understanding of Huntington's disease (HD). However, previous global reviews include limited data from Latin America. It is possible that English‐based medical search engines may not capture all the relevant studies.MethodsWe searched databases in Spanish, Portuguese, and English. The names of every country in Latin America in English‐based search engines were used to ensure we found any study that had molecular ascertainment and provided general epidemiological information or subpopulation data. Additionally, we contacted experts across the region.ResultsThe search strategy yielded 791 citations; 24 studies met inclusion criteria, representing 12 of 36 countries. The overall pooled prevalence was 0.64 per 100,000 (prediction interval, 0.06–7.22); for cluster regions, it was 54 per 100,000 (95% CI, 34.79–84.92); for juvenile HD, it was 8.7% (prediction interval, 5.12–14.35), and 5.9% (prediction interval, 2.72–13.42) for late‐onset HD. The prevalence was higher for Mexico, Peru, and Brazil. However, there were no significant differences between Central America and the Caribbean versus South America.ConclusionThe prevalence of HD appears to be similar across Latin America. However, we infer that our findings are underestimates, in part because of limited research and underdiagnosis of HD because of limited access to molecular testing and the availability of neurologists and movement disorders specialists. Future research should focus on identifying pathways to improve access to molecular testing and education and understanding differences among different ancestral groups in Latin America. © 2024 International Parkinson and Movement Disorder Society.

Publisher

Wiley

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