Variable Ethnic Frequency and Risk Ratio of DMPK Gene: A Meta-Analysis Survey

Ashok Kumar, S. Agarwal, S. Pradhan
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引用次数: 2

Abstract

Aim: Myotonic dystrophy type 1 (DM1) is due to CTG repeats in the 3’UTR region of DMPK gene. It has an incidence of 1 in 8000 in the Western European and North American populations and a lower incidence of 1 in 20,000 in Japan. However, prevalence of the disease in diverse Indian populations is still unknown. Materials and Methods: The intention of the present study was to perform the meta-analysis to investigate the different ethnic frequency and risk ratio of DM1 in different populations of the world including India. Total twelve populations belong from Europeans, Asians and American were included in the present study. Meta-analyst was used for the analysis. Results: The meta-analysis of the seven European populations demonstrated that Italian population had higher risk ratio in comparison to other studied population. Similarly, the three Asian populations demonstrated that South Indian population had higher risk ratio in comparison of North India and Korean population. In addition, the meta-analysis of two American population postulated that Canada had higher risk ratio in comparison of Brazil. Conclusion: A vast ethnic variation in frequency of DMPK gene of different population of DM1, and expanded CTG repeat alleles as well as associated risk.
DMPK基因变异的民族频率和风险比:一项荟萃分析调查
目的:肌强直性营养不良1型(DM1)是由DMPK基因3'UTR区CTG重复引起的。它在西欧和北美人口中的发病率为1 / 8000,在日本的发病率较低,为1 / 20000。然而,这种疾病在不同的印度人口中的流行程度仍然未知。材料和方法:本研究的目的是进行荟萃分析,以调查包括印度在内的世界不同人群DM1的不同种族频率和风险比。本研究共包括来自欧洲、亚洲和美洲的12个种群。Meta-analyst用于分析。结果:对七个欧洲人群的荟萃分析表明,意大利人群与其他研究人群相比具有更高的风险比。同样,三个亚洲人群也表明,南印度人群的风险比高于北印度人群和朝鲜人群。此外,对两个美国人群的荟萃分析认为,与巴西相比,加拿大的风险比更高。结论:不同人群DM1的DMPK基因频率、扩增的CTG重复等位基因及其相关风险存在较大的民族差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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