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波多黎各杜氏和贝克型肌营养不良症的患病率和遗传特征。

Prevalence and Genetic Profile of Duchene and Becker Muscular Dystrophy in Puerto Rico.

机构信息

Department of Physical Medicine, Rehabilitation & Sport Medicine, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.

Biomedical Sciences Graduate Program, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.

出版信息

J Neuromuscul Dis. 2016 May 27;3(2):261-266. doi: 10.3233/JND-160147.

Abstract

BACKGROUND

Duchenne and Becker Muscular Dystrophy (DMD and BMD, respectively), are common forms of inherited muscle disease. Information regarding the epidemiology of these conditions, including genotype, is still sparse.

OBJECTIVE

To establish the prevalence and genetic profile of DMD and BMD in Puerto Rico.

METHODS

We collected data from medical records in all Muscular Dystrophy Association (MDA) clinics in Puerto Rico in order to estimate the prevalence of DMD and BMD and to describe the genotypic profile of these patients. Patients selected for data analysis matched "definite", "probable" and "possible" case definitions as established by MD STARnet.

RESULTS

A total of 141 patients matched the inclusion criteria, with 64.5% and 35.5% being categorized into DMD and BMD, respectively. DMD and BMD prevalence in Puerto Rico was estimated at 5.18 and 2.84 per 100,000 males, respectively. Deletion was the most common form of mutation (66.7%) in the dystrophin gene, with exons in segment 45 to 47 being the most frequently affected.

CONCLUSIONS

This is the first report of the prevalence and genetic profile characteristics of DMD and BMD in Puerto Rico. Prevalence of DMD was similar to that reported worldwide, while prevalence of BMD was higher. Genetic profile was consistent with that reported in the literature.

摘要

背景

杜氏肌营养不良症(DMD)和贝克肌营养不良症(BMD)分别是常见的遗传性肌肉疾病。关于这些疾病的流行病学信息,包括基因型,仍然很少。

目的

确定波多黎各杜氏肌营养不良症和贝克肌营养不良症的患病率和遗传特征。

方法

我们从波多黎各所有肌肉萎缩症协会(MDA)诊所的病历中收集数据,以估计 DMD 和 BMD 的患病率,并描述这些患者的基因谱。选择用于数据分析的患者符合 MD STARnet 确定的“明确”、“可能”和“可能”病例定义。

结果

共有 141 名患者符合纳入标准,其中 64.5%和 35.5%分别归类为 DMD 和 BMD。波多黎各的 DMD 和 BMD 患病率估计分别为每 10 万男性 5.18 和 2.84。缺失是肌营养不良蛋白基因突变最常见的形式(66.7%),受影响最频繁的外显子在 45 到 47 段。

结论

这是波多黎各首次报道 DMD 和 BMD 的患病率和遗传特征。DMD 的患病率与世界范围内报道的相似,而 BMD 的患病率较高。基因谱与文献报道一致。

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