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幼儿期失聪个体的健康状况:对加劳德特大学校友家庭的研究。

Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.

作者信息

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

机构信息

Hussman Institute for Human Genomics, University of Miami, FL 33136, USA.

出版信息

Ann Hum Genet. 2010 Jan;74(1):27-33. doi: 10.1111/j.1469-1809.2009.00553.x. Epub 2009 Nov 20.

DOI:10.1111/j.1469-1809.2009.00553.x
PMID:19930248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2804774/
Abstract

The genetic fitness of an individual is influenced by their phenotype, genotype and family and social structure of the population in which they live. It is likely that the fitness of deaf individuals was quite low in the Western European population during the Middle Ages. The establishment of residential schools for deaf individuals nearly 400 years ago resulted in relaxed genetic selection against deaf individuals which contributed to the improved fitness of deaf individuals in recent times. As part of a study of deaf probands from Gallaudet University, we collected pedigree data, including the mating type and the number and hearing status of the children of 686 deaf adults and 602 of their hearing siblings. Most of these individuals had an onset of severe to profound hearing loss by early childhood. Marital rates of deaf adults were similar to their hearing siblings (0.83 vs. 0.85). Among married individuals, the fertility of deaf individuals is lower than their hearing siblings (2.06 vs. 2.26, p = 0.005). The fitness of deaf individuals was reduced (p = 0.002). Analysis of fertility rates after stratification by mating type reveals that matings between two deaf individuals produced more children (2.11) than matings of a deaf and hearing individual (1.85), suggesting that fertility among deaf individuals is influenced by multiple factors.

摘要

个体的遗传适应性受其表型、基因型以及其所生活群体的家庭和社会结构影响。在中世纪的西欧人群中,聋人的适应性可能相当低。近400年前为聋人设立寄宿学校,导致针对聋人的遗传选择放松,这促使聋人在近代的适应性有所提高。作为对加劳德特大学聋人先证者研究的一部分,我们收集了系谱数据,包括686名成年聋人及其602名听力正常的兄弟姐妹的交配类型、子女数量和听力状况。这些个体中的大多数在幼儿期就开始出现重度至极重度听力损失。成年聋人的结婚率与他们听力正常的兄弟姐妹相似(分别为0.83和0.85)。在已婚个体中,聋人的生育力低于他们听力正常的兄弟姐妹(分别为2.06和2.26,p = 0.005)。聋人的适应性降低了(p = 0.002)。按交配类型分层后对生育率的分析表明,两个聋人之间的交配生育的子女更多(2.11),多于聋人与听力正常个体之间的交配(1.85),这表明聋人的生育力受多种因素影响。

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本文引用的文献

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A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.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。
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2
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.
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
Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family.一个中国大家庭中Y连锁非综合征性听力损失的遗传模式
J Med Genet. 2004 Jun;41(6):e80. doi: 10.1136/jmg.2003.012799.
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
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
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