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阻塞性睡眠呼吸暂停的遗传学研究
引用本文:张希龙,殷凯生. 阻塞性睡眠呼吸暂停的遗传学研究[J]. 国际遗传学杂志, 2006, 29(2): 152-154. DOI: 10.3760/cma.j.issn.1673-4386.2008.06.002
作者姓名:张希龙  殷凯生
作者单位:210029,南京医科大学第一附属医院呼吸科;210029,南京医科大学第一附属医院呼吸科
摘    要:阻塞性睡眠呼吸暂停(obstructive sleep apnea, OSA)的遗传学研究尚处在初期,但迄今研究提示OSA有很强的遗传背景,其发病存在着家族聚集性且与相关中间表型有关,如与颅面结构、体内脂肪分布和呼吸调控的异常等有关。目前认为OSA的发病很可能是多基因与环境因素交互作用的结果。对OSA的分子遗传学研究可帮助理解OSA的病因和发病机理,并能促进对OSA的基因诊断和预防。

关 键 词:阻塞性睡眠呼吸暂停  家族聚集性  中间表型  基因
收稿时间:2004-11-26
修稿时间:2004-11-26

Genetic Research of Obstructive Sleep Apnea
ZHANG Xi-long,YIN Kai-sheng. Genetic Research of Obstructive Sleep Apnea[J]. International JOurnal of Genetics, 2006, 29(2): 152-154. DOI: 10.3760/cma.j.issn.1673-4386.2008.06.002
Authors:ZHANG Xi-long  YIN Kai-sheng
Affiliation:Department of Respiratory Medicine, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, P.R. China
Abstract:Genetic studies of obstructive sleep apnea(OSA) are in their infancy.The research so far has indicated a strong genetic background of OSA with an incidence of familial aggregation and OSA-associated intermediate phenotypes,such as abnormalities of craniofacial structure,body fat distribution and respiratory control and so on.It is currently regarded that occurrence of OSA may be a result of interactions between multigene and environmental factors.The molecular genetic research on OSA can assist us in understanding the pathogenesis of OSA and promote genetic diagnosis and prevention of OSA.
Keywords:Obstructive sleep apnea  Familial aggregation  Intermediate phenotype  Gene
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