4.5 Review

Global prevalence of intellectual developmental disorder in dystrophinopathies: A systematic review and meta-analysis

期刊

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
卷 65, 期 6, 页码 734-744

出版社

WILEY
DOI: 10.1111/dmcn.15481

关键词

-

向作者/读者索取更多资源

The aim of this study was to estimate the global prevalence of intellectual developmental disorder (IDD) and the association between IDD prevalence and genotypes in Becker muscular dystrophy (BMD) or Duchenne muscular dystrophy (DMD). The results showed a high prevalence of IDD in BMD and DMD, and a negative association between the number of affected isoforms and IDD prevalence in DMD. However, no association was found in BMD.
AimTo estimate the global prevalence of intellectual developmental disorder (IDD) and the IDD prevalence-genotype association in Becker muscular dystrophy (BMD) or Duchenne muscular dystrophy (DMD) according to the affected isoforms of the DMD gene: Dp427, Dp140, Dp71. MethodSystematic searches in MEDLINE, Scopus, Web of Science, and the Cochrane Library were conducted from inception of each database to March 2022. Observational studies that determined the prevalence of IDD in the population with BMD or DMD were included. Meta-analyses of IDD prevalence and prevalence ratios of the IDD-genotype association were conducted. ResultsForty-nine studies were included. The prevalence of IDD in BMD was 8.0% (95% confidence interval 5.0-11.0), and in DMD it was 22.0% (18.0-27.0). Meta-analyses of IDD-genotype association showed a deleterious association between IDD and the number of isoforms affected in DMD, with a prevalence ratio = 0.43 (0.28-0.64) and 0.17 (0.09-0.34) for Dp140(+)/Dp71(+) versus Dp140(-)/Dp71(+) and Dp140(+)/Dp71(+) versus Dp140(-)/Dp71(-) comparisons respectively. However, in BMD, there was no association for Dp140(+)/Dp71(+) versus Dp140(-)/Dp71(+). InterpretationThere is a high prevalence of IDD in BMD and DMD. Moreover, the number of isoforms affected is strongly and negatively associated with the prevalence of IDD in DMD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据