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俄罗斯患者中该基因常见的A57F变异源自芬兰-乌戈尔语族的马里人。

The frequent variant A57F in the gene in patients from Russia has Finno-Ugric Mari origin.

作者信息

Subbotin Dmitrii, Ionova Sofya, Marakhonov Andrey, Saifullina Elena, Borovikov Artem, Akhmadeeva Leila, Chausova Polina, Ryzhkova Oksana, Zinchenko Rena, Kutsev Sergey, Murtazina Aysylu

机构信息

Research Centre for Medical Genetics, Moscow, Russia.

Department of Neurology, Bashkir State Medical University, Ufa, Russia.

出版信息

Front Genet. 2024 Dec 11;15:1511304. doi: 10.3389/fgene.2024.1511304. eCollection 2024.

Abstract

INTRODUCTION

GNE-myopathy is a distal myopathy with adult-onset and initial involvement of anterior leg compartment. A founder effect has been demonstrated for some patients from several large cohorts in different countries.

METHODS

In this study, we investigated the allele frequency of the c.169_170delinsTT (p.(Ala57Phe)) variant in the GNE gene (NM_001128227.3) among different ethnic populations (Mari, Tatar, and Bashkir) and estimated the age of the mutation's spread event.

RESULTS

The c.169_170delinsTT variant in the GNE gene was detected in the Mari population with an allele frequency of 0.003788 but was not found in the Tatar or Bashkir populations. The disease incidence is estimated to be 1.43 (95% CI: 0.00092-43.78) per 100,000 in the Mari population. According to our study, the estimated age of the mutation's spread is 160.46 years (95% CI: 45.55-244.14).

DISCUSSION

By comparing the information gathered with historical data on migration patterns in the Middle Volga region and estimating the age of the variant's dissemination, we propose hypotheses regarding its origin and the pathways through which it spread. In the current context of increased rate of interethnic marriages, investigating the spread of common pathogenic variants from historically isolated populations is important for molecular genetic diagnosis. This approach aids in optimizing diagnostic processes and reducing the diagnostic odyssey for patients.

摘要

引言

GNE肌病是一种成人起病的远端肌病,最初累及小腿前侧肌群。在不同国家的几个大型队列研究中,已证实部分患者存在奠基者效应。

方法

在本研究中,我们调查了GNE基因(NM_001128227.3)中c.169_170delinsTT(p.(Ala57Phe))变异在不同种族人群(马里人、鞑靼人、巴什基尔人)中的等位基因频率,并估计了该突变传播事件的发生时间。

结果

在马里人群中检测到GNE基因的c.169_170delinsTT变异,等位基因频率为0.003788,而在鞑靼人群和巴什基尔人群中未检测到。据估计,马里人群中该疾病的发病率为每10万人1.43例(95%置信区间:0.00092 - 43.78)。根据我们的研究,该突变传播的估计时间为160.46年(95%置信区间:45.55 - 244.14)。

讨论

通过将收集到的信息与伏尔加河中游地区历史移民模式的数据进行比较,并估计该变异的传播时间,我们提出了关于其起源和传播途径的假设。在当前族际通婚率上升的背景下,研究常见致病变异在历史上隔离人群中的传播情况,对于分子遗传学诊断具有重要意义。这种方法有助于优化诊断流程,减少患者的诊断探索过程。

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