Prevalence of Duchenne and Becker muscular dystrophies in the United States
- PMID: 25687144
- PMCID: PMC4477633
- DOI: 10.1542/peds.2014-2044
Prevalence of Duchenne and Becker muscular dystrophies in the United States
Erratum in
-
Romitti et al. Prevalence of Duchenne and Becker muscular dystrophies in the United States. Pediatrics. 2015;135(3):513-521.Pediatrics. 2015 May;135(5):945. doi: 10.1542/peds.2015-0652. Pediatrics. 2015. PMID: 25934896 No abstract available.
Abstract
Objective: To estimate prevalence of childhood-onset Duchenne and Becker muscular dystrophies (DBMD) in 6 sites in the United States by race/ethnicity and phenotype (Duchenne muscular dystrophy [DMD] or Becker muscular dystrophy [BMD]).
Methods: In 2002, the Centers for Disease Control and Prevention established the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) to conduct longitudinal, population-based surveillance and research of DBMD in the United States. Six sites conducted active, multiple-source case finding and record abstraction to identify MD STARnet cases born January 1982 to December 2011. We used cross-sectional analyses to estimate prevalence of DBMD per 10 000 boys, ages 5 to 9 years, for 4 quinquennia (1991-1995, 1996-2000, 2001-2005, and 2006-2010) and prevalence per 10 000 male individuals, ages 5 to 24 years, in 2010. Prevalence was also estimated by race/ethnicity and phenotype.
Results: Overall, 649 cases resided in an MD STARnet site during ≥1 quinquennia. Prevalence estimates per 10 000 boys, ages 5 to 9 years, were 1.93, 2.05, 2.04, and 1.51, respectively, for 1991-1995, 1996-2000, 2001-2005, and 2006-2010. Prevalence tended to be higher for Hispanic individuals than non-Hispanic white or black individuals, and higher for DMD than BMD. In 2010, prevalence of DBMD was 1.38 per 10 000 male individuals, ages 5 to 24 years.
Conclusions: We present population-based prevalence estimates for DBMD in 6 US sites. Prevalence differed by race/ethnicity, suggesting potential cultural and socioeconomic influences in the diagnosis of DBMD. Prevalence also was higher for DMD than BMD. Continued longitudinal surveillance will permit us to examine racial/ethnic and socioeconomic differences in treatment and outcomes for MD STARnet cases.
Keywords: Becker muscular dystrophy; Duchenne muscular dystrophy; ethnicity; population surveillance; prevalence.
Copyright © 2015 by the American Academy of Pediatrics.
Conflict of interest statement
Figures
Similar articles
-
Duchenne and Becker Muscular Dystrophies' Prevalence in MD STARnet Surveillance Sites: An Examination of Racial and Ethnic Differences.Neuroepidemiology. 2021;55(1):47-55. doi: 10.1159/000512647. Epub 2021 Jan 21. Neuroepidemiology. 2021. PMID: 33477152 Free PMC article.
-
Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - four states, 2007.MMWR Morb Mortal Wkly Rep. 2009 Oct 16;58(40):1119-22. MMWR Morb Mortal Wkly Rep. 2009. PMID: 19834452
-
Muscular Dystrophy Surveillance, Tracking, and Research Network pilot: Population-based surveillance of major muscular dystrophies at four U.S. sites, 2007-2011.Birth Defects Res. 2018 Nov 15;110(19):1404-1411. doi: 10.1002/bdr2.1371. Epub 2018 Aug 2. Birth Defects Res. 2018. PMID: 30070776 Free PMC article.
-
Epileptic disorders in Becker and Duchenne muscular dystrophies: a systematic review and meta-analysis.J Neurol. 2022 Jul;269(7):3461-3469. doi: 10.1007/s00415-022-11040-y. Epub 2022 Mar 1. J Neurol. 2022. PMID: 35229191 Review.
-
Prevalence of Neuropsychiatric Disorders in Duchenne and Becker Muscular Dystrophies: A Systematic Review and Meta-analysis.Arch Phys Med Rehabil. 2022 Dec;103(12):2444-2453. doi: 10.1016/j.apmr.2022.05.015. Epub 2022 Jul 15. Arch Phys Med Rehabil. 2022. PMID: 35839922 Review.
Cited by
-
Development of the Brazilian version of the Performance of Upper Limb scale for children and adolescents with Duchenne muscular dystrophy.Braz J Phys Ther. 2024 Sep-Oct;28(5):101118. doi: 10.1016/j.bjpt.2024.101118. Epub 2024 Sep 12. Braz J Phys Ther. 2024. PMID: 39321683 Free PMC article.
-
Functional cardiac consequences of β-adrenergic stress-induced injury in a model of Duchenne muscular dystrophy.Dis Model Mech. 2024 Oct 1;17(10):dmm050852. doi: 10.1242/dmm.050852. Epub 2024 Oct 9. Dis Model Mech. 2024. PMID: 39268580 Free PMC article.
-
Subspecialty Health Care Utilization in Pediatric Patients With Muscular Dystrophy in the United States.Neurol Clin Pract. 2024 Aug;14(4):e200312. doi: 10.1212/CPJ.0000000000200312. Epub 2024 May 31. Neurol Clin Pract. 2024. PMID: 38855715
-
Casimersen (AMONDYS 45™): An Antisense Oligonucleotide for Duchenne Muscular Dystrophy.Biomedicines. 2024 Apr 20;12(4):912. doi: 10.3390/biomedicines12040912. Biomedicines. 2024. PMID: 38672266 Free PMC article. Review.
-
Functional cardiac consequences of β-adrenergic stress-induced injury in the mdx mouse model of Duchenne muscular dystrophy.bioRxiv [Preprint]. 2024 Apr 20:2024.04.15.589650. doi: 10.1101/2024.04.15.589650. bioRxiv. 2024. Update in: Dis Model Mech. 2024 Oct 1;17(10):dmm050852. doi: 10.1242/dmm.050852 PMID: 38659739 Free PMC article. Updated. Preprint.
References
-
- Ballo R, Viljoen D, Beighton P. Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected. S Afr Med J. 1994;84(8 pt 1):494–497. - PubMed
-
- Chung B, Wong V, Ip P. Prevalence of neuromuscular diseases in Chinese children: a study in southern China. J Child Neurol. 2003;18(3):217–219. - PubMed
-
- Nakagawa M, Nakahara K, Yoshidome H, et al. Epidemiology of progressive muscular dystrophy in Okinawa, Japan. Classification with molecular biological techniques. Neuroepidemiology. 1991;10(4):185–191. - PubMed
-
- Peterlin B, Zidar J, Meznaric-Petrusa M, Zupancic N. Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia. Clin Genet. 1997;51(2):94–97. - PubMed
-
- Monckton G, Hoskin V, Warren S. Prevalence and incidence of muscular dystrophy in Alberta, Canada. Clin Genet. 1982;21(1):19–24. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources

