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国家自然科学基金(30925021)

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Leber遗传性视神经病变研究进展和挑战被引量:13
2013年
Leber遗传性视神经病变(Leber hereditary optic neuropathy,LHON;MIM535000)是最典型的线粒体遗传病之一,主要由线粒体DNA(Mitochondrial DNA,mtDNA)3个原发突变(Primary mutation,m.11778G>A、m.3460G>A和m.14484T>C)引起。患者表现为无痛性双侧视力下降或丧失,主要易感人群为青壮年男性。不完全外显(Incomplete penetrance)和性别偏好(Gender bias)是该病亟待解决的两大难题,目前尚无有效的预防及治疗措施。文章对近年来LHON的分子发病机制、临床症状及特点、体外实验和动物模型研究、预防及治疗等方面的研究进展进行综述,并集中介绍了我们近期对于我国LHON患者的研究结果。
张阿梅姚永刚
关键词:LHON线粒体DNA核基因
A Matrilineal Genetic Legacy from the Last Glacial Maximum Confers Susceptibility to Schizophrenia in Han Chinese被引量:2
2014年
Mitochondrial dysfunction has been widely reported in schizophrenia patients. To dissect the matrilineal structure of Han Chinese with or without schizophrenia and to decipher the maternal influence and evolutionary history of schizophrenia, a total of 1212 schizophrenia patients and 1005 matched healthy controls, all of Han Chinese origin, were recruited in Hunan Province, China. We classified haplogroup for each individual based on mitochondrial DNA (mtDNA) sequence variations and compared the haplogroup distribution pattern between cases and controls. Haplogroup B5a presented a higher frequency in cases than in controls (P = 0.02, OR = 1.67, 95% CI = [1.09, 2.56]), and this result could be confirmed by permutation analysis. Age estimation of haplogroup B5a in cases revealed a much younger age than that of controls, which was coincident with the Northern Hemisphere deglaciation at the end of the Last Glacial Maximum. Analysis of complete mtDNA in five patients belonging to haplogroup B5a showed that this background effect might be caused by haplogroup- defining variants m.8584G〉A and m.10398A〉G. Our results showed that matrilineal risk factor for schizophrenia had an ancient origin and might acquire a predisposing effect on schizophrenia due to the environment change and/or orchestration with other nuclear genetic factors appeared recently in human evolutionary history.
Wen ZhangJinsong TangA-Mei ZhangMin-Sheng PengHai-Bing XieLiwen TanLin XuYa-Ping ZhangXiaogang ChenYong-Gang Yao
关键词:SCHIZOPHRENIA
Leber遗传性视神经病变研究进展和挑战
Leber遗传性视神经病变(Leber hereditary optic neuropathy,LHON;MIM535000)是最典型的线粒体遗传病之一,主要由线粒体DNA(Mitochondrial DNA,mtDNA...
张阿梅姚永刚
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