A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy

被引:313
|
作者
Mah, Jean K. [1 ,2 ]
Korngut, Lawrence [1 ,3 ]
Dykeman, Jonathan [1 ,3 ,4 ,5 ,6 ]
Day, Lundy [1 ]
Pringsheim, Tamara [1 ,2 ]
Jette, Nathalie [1 ,3 ,4 ,5 ]
机构
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Alberta Childrens Hosp, Res Inst, Dept Pediat, Calgary, AB T2N 1N4, Canada
[3] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB T2N 1N4, Canada
[4] Univ Calgary, Dept Community Hlth Sci, Calgary, AB T2N 1N4, Canada
[5] Univ Calgary, Inst Publ Hlth, Calgary, AB T2N 1N4, Canada
[6] Univ Calgary, Clin Res Unit, Calgary, AB T2N 1N4, Canada
关键词
Incidence; Prevalence; Epidemiology; Muscular dystrophy; Population-based; PREVALENCE; POPULATION; DISORDERS; CHILDHOOD; DISEASE; GENE;
D O I
10.1016/j.nmd.2014.03.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The muscular dystrophies are a broad group of hereditary muscle diseases with variable severity. Population-based prevalence estimates have been reported but pooled estimates are not available. We performed a systematic review of worldwide population-based studies reporting muscular dystrophies prevalence and/or incidence using MEDLINE and EMBASE databases. The search strategy included key terms related to muscular dystrophies, incidence, prevalence and epidemiology. Two reviewers independently reviewed all abstracts, full text articles and abstracted data using standardized forms. Pooling of prevalence estimates was performed using random effect models. 1104 abstracts and 167 full text articles were reviewed. Thirty-one studies met all eligibility criteria and were included in the final analysis. The studies differed widely in their approaches to case ascertainment, resulting in significant methodological heterogeneity and varied data quality. The pooled prevalence of DMD and BMD was 4.78 (95% CI 1.94-11.81) and 1.53 (95% CI 0.26-8.94) per 100,000 males respectively. The incidence of DMD ranged from 10.71 to 27.78 per 100,000. This is the first meta-analysis of worldwide prevalence estimates for muscular dystrophies. There is a need for more epidemiological studies addressing global estimates on incidence and prevalence of muscular dystrophies, utilizing standardized diagnostic criteria as well as multiple sources of case ascertainment. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:482 / 491
页数:10
相关论文
共 50 条
  • [1] Global prevalence of Duchenne and Becker muscular dystrophy: a systematic review and meta-analysis
    Nader Salari
    Behnaz Fatahi
    Elahe Valipour
    Mohsen Kazeminia
    Reza Fatahian
    Aliakbar Kiaei
    Shamarina Shohaimi
    Masoud Mohammadi
    [J]. Journal of Orthopaedic Surgery and Research, 17
  • [2] Global prevalence of Duchenne and Becker muscular dystrophy: a systematic review and meta-analysis
    Salari, Nader
    Fatahi, Behnaz
    Valipour, Elahe
    Kazeminia, Mohsen
    Fatahian, Reza
    Kiaei, Aliakbar
    Shohaimi, Shamarina
    Mohammadi, Masoud
    [J]. JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH, 2022, 17 (01)
  • [3] Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis
    Crisafulli, Salvatore
    Sultana, Janet
    Fontana, Andrea
    Salvo, Francesco
    Messina, Sonia
    Trifiro, Gianluca
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2020, 15 (01)
  • [4] Global epidemiology of Duchenne muscular dystrophy: An updated systematic review and meta-analysis
    Crisafulli, Salvatore
    Sultana, Janet
    Fontana, Andrea
    Salvo, Francesco
    Messina, Sonia
    Trifiro, Gianluca
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2020, 29 : 565 - 566
  • [5] Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis
    Salvatore Crisafulli
    Janet Sultana
    Andrea Fontana
    Francesco Salvo
    Sonia Messina
    Gianluca Trifirò
    [J]. Orphanet Journal of Rare Diseases, 15
  • [6] Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis
    Shimizu-Motohashi, Yuko
    Murakami, Terumi
    Kimura, En
    Komaki, Hirofumi
    Watanabe, Norio
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2018, 13
  • [7] Antioxidants for Treatment of Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis
    Ren, Shouchen
    Yao, Chunmei
    Liu, Yali
    Feng, Guoshuang
    Dong, Xiaohuan
    Gao, Baoqin
    Qian, Suyun
    [J]. EUROPEAN NEUROLOGY, 2022, 85 (05) : 377 - 388
  • [8] Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis
    Yuko Shimizu-Motohashi
    Terumi Murakami
    En Kimura
    Hirofumi Komaki
    Norio Watanabe
    [J]. Orphanet Journal of Rare Diseases, 13
  • [9] Molecular diagnosis of Duchenne Muscular Dystrophy: Systematic review and meta-analysis
    Alva-Diaz, Carlos
    Julca, Marco Malaga
    Martinez-Esteban, Peggy
    Ballon, Paula Moran
    Ecos, Fabian Chavez
    Pacheco-Barrios, Niels
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 429
  • [10] EXERCISE TRAINING IN DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW AND META-ANALYSIS
    Hammer, Stian
    Toussaint, Michel
    Vollsaeter, Maria
    Tvedt, Marianne Nesbjorg
    Roksund, Ola Drange
    Reychler, Gregory
    Lund, Hans
    Andersen, Tiina
    [J]. JOURNAL OF REHABILITATION MEDICINE, 2022, 54