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本文引用的文献

1
Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification.土耳其先天性/语前聋的遗传流行病学研究:群体结构和交配类型是突变识别的主要决定因素。
Am J Med Genet A. 2007 Jul 15;143A(14):1583-91. doi: 10.1002/ajmg.a.31702.
2
Expression of GJB2 and GJB6 is reduced in a novel DFNB1 allele.在一个新的DFNB1等位基因中,GJB2和GJB6的表达降低。
Am J Hum Genet. 2006 Jul;79(1):174-9. doi: 10.1086/505333. Epub 2006 May 17.
3
Newborn hearing screening--a silent revolution.新生儿听力筛查——一场无声的革命。
N Engl J Med. 2006 May 18;354(20):2151-64. doi: 10.1056/NEJMra050700.
4
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.在患有DFNB1非综合征性听力障碍的受试者中发现一种涉及连接蛋白30基因的新型缺失,即del(GJB6-d13s1854),它与GJB2基因(连接蛋白26)的突变呈反式排列。
J Med Genet. 2005 Jul;42(7):588-94. doi: 10.1136/jmg.2004.028324.
5
Relevance of connexin deafness (DFNB1) to human evolution.连接蛋白性耳聋(DFNB1)与人类进化的相关性。
Am J Hum Genet. 2004 Jun;74(6):1081-7. doi: 10.1086/420979. Epub 2004 Apr 9.
6
Genetics of hereditary disorders of magnesium homeostasis.镁稳态遗传性疾病的遗传学
Pediatr Nephrol. 2004 Jan;19(1):13-25. doi: 10.1007/s00467-003-1293-z. Epub 2003 Nov 22.
7
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.听力受损受试者中DFNB1位点del(GJB6-D13S1830)突变的患病率及进化起源:一项多中心研究
Am J Hum Genet. 2003 Dec;73(6):1452-8. doi: 10.1086/380205. Epub 2003 Oct 21.
8
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.北美一个大型先天性耳聋先证者数据库中GJB2(连接蛋白26)和GJB6(连接蛋白30)突变的频率及分布情况
Genet Med. 2003 Jul-Aug;5(4):295-303. doi: 10.1097/01.GIM.0000078026.01140.68.
9
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.连接蛋白26(GJB2)突变及奠基者效应在印度非综合征性听力损失中的作用
J Med Genet. 2003 May;40(5):e68. doi: 10.1136/jmg.40.5.e68.
10
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.连接蛋白26听力障碍中35delG GJB2基因突变的共同起源。
J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515.

对美国耳聋遗传流行病学的比较分析,基于两组相隔一个多世纪收集的家系。

A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.

作者信息

Arnos Kathleen S, Welch Katherine O, Tekin Mustafa, Norris Virginia W, Blanton Susan H, Pandya Arti, Nance Walter E

机构信息

Department of Biology, Gallaudet University, Washington, DC 20002, USA.

出版信息

Am J Hum Genet. 2008 Aug;83(2):200-7. doi: 10.1016/j.ajhg.2008.07.001. Epub 2008 Jul 24.

DOI:10.1016/j.ajhg.2008.07.001
PMID:18656178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2495057/
Abstract

In 1898, E.A. Fay published an analysis of nearly 5000 marriages among deaf individuals in America collected during the 19(th) century. Each pedigree included three-generation data on marriage partners that included at least one deaf proband, who were ascertained by complete selection. We recently proposed that the intense phenotypic assortative mating among the deaf might have greatly accelerated the normally slow response to relaxed genetic selection against deafness that began in many Western countries with the introduction of sign language and the establishment of residential schools. Simulation studies suggest that this mechanism might have doubled the frequency of the commonest forms of recessive deafness (DFNB1) in this country during the past 200 years. To test this prediction, we collected pedigree data on 311 contemporary marriages among deaf individuals that were comparable to those collected by Fay. Segregation analysis of the resulting data revealed that the estimated proportion of noncomplementary matings that can produce only deaf children has increased by a factor of more than five in the past 100 years. Additional analysis within our sample of contemporary pedigrees showed that there was a statistically significant linear increase in the prevalence of pathologic GJB2 mutations when the data on 441 probands were partitioned into three 20-year birth cohorts (1920 through 1980). These data are consistent with the increase in the frequency of DFNB1 predicted by our previous simulation studies and provide convincing evidence for the important influence that assortative mating can have on the frequency of common genes for deafness.

摘要

1898年,E.A.费伊发表了一项对19世纪美国近5000例聋人婚姻的分析。每个家系都包含了婚姻伴侣的三代数据,其中至少有一名聋人先证者,这些先证者是通过完全筛选确定的。我们最近提出,聋人之间强烈的表型选型交配可能极大地加速了对耳聋的放松遗传选择的正常缓慢反应,这种反应在许多西方国家随着手语的引入和寄宿学校的建立而开始。模拟研究表明,在过去200年里,这种机制可能使该国最常见的隐性耳聋(DFNB1)形式的频率增加了一倍。为了验证这一预测,我们收集了311例当代聋人婚姻的家系数据,这些数据与费伊收集的数据相当。对所得数据的分离分析表明,在过去100年里,只能生育聋儿的非互补交配的估计比例增加了五倍多。在我们当代家系样本中的进一步分析表明,当将441名先证者的数据分为三个20年出生队列(1920年至1980年)时,病理性GJB2突变的患病率有统计学意义的线性增加。这些数据与我们之前模拟研究预测的DFNB1频率增加一致,并为选型交配对常见耳聋基因频率可能产生的重要影响提供了令人信服的证据。