首页> 外文期刊>JAMA: the Journal of the American Medical Association >A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families.
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A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families.

机译:早老素1的创始人突变在无关的加勒比海西班牙裔家庭中引起早发型阿尔茨海默氏病。

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CONTEXT: Genetic determinants of Alzheimer disease (AD) have not been comprehensively examined in Caribbean Hispanics, a population in the United States in whom the frequency of AD is higher compared with non-Hispanic whites. OBJECTIVE: To identify variant alleles in genes related to familial early-onset AD among Caribbean Hispanics. DESIGN AND SETTING: Family-based case series conducted in 1998-2001 at an AD research center in New York, NY, and clinics in the Dominican Republic. PATIENTS: Among 206 Caribbean Hispanic families with 2 or more living members with AD who were identified, 19 (9.2%) had at least 1 individual with onset of AD before the age of 55 years. MAIN OUTCOME MEASURE: The entire coding region of the presenilin 1 gene and exons 16 and 17 of the amyloid precursor protein gene were sequenced in probands from the 19 families and their living relatives. RESULTS: A G-to-C nucleotide change resulting in a glycine-alanine amino acid substitution at codon 206 (Gly206Ala) in exon 7 of presenilin 1 was observed in 23 individuals from 8 (42%) of the 19 families. A Caribbean Hispanic individual with the Gly206Ala mutation and early-onset familial disease was also found by sequencing the corresponding genes of 319 unrelated individuals in New York City. The Gly206Ala mutation was not found in public genetic databases but was reported in 5 individuals from 4 Hispanic families with AD referred for genetic testing. None of the members of these families were related to one another, yet all carriers of the Gly206Ala mutation tested shared a variant allele at 2 nearby microsatellite polymorphisms, indicating a common ancestor. No mutations were found in the amyloid precursor protein gene. CONCLUSIONS: The Gly206Ala mutation was found in 8 of 19 unrelated Caribbean Hispanic families with early-onset familial AD. This genetic change may be a prevalent cause of early-onset familial AD in the Caribbean Hispanic population.
机译:语境:尚未在加勒比西班牙裔中对阿尔茨海默氏病(AD)的遗传决定因素进行全面检查。加勒比裔美国人的AD发病率高于非西班牙裔白人。目的:鉴定加勒比西班牙裔与家族性早发AD相关的基因中的变异等位基因。设计与地点:基于家庭的病例系列于1998-2001年在纽约州纽约的AD研究中心和多米尼加共和国的诊所中进行。患者:在206个加勒比西班牙裔家庭中,有2个或更多AD活体成员被确定,其中19个(9.2%)在55岁之前至少有1个人患有AD。主要观察指标:早老素1基因的整个编码区以及淀粉样蛋白前体蛋白基因的外显子16和17在来自19个家庭及其活近亲属的先证者中进行了测序。结果:在19个家族的8个(42%)的23个个体中观察到早老素1外显子7的G到C核苷酸变化,导致在206位密码子(Gly206Ala)处有甘氨酸-丙氨酸取代。通过对纽约市319名无关亲戚的相应基因进行测序,还发现了一名患有Gly206Ala突变和早发家族病的加勒比海西班牙裔个体。在公共遗传数据库中未发现Gly206Ala突变,但在来自4个西班牙裔家庭的5个个体中报告了Gly206Ala突变,并进行了基因检测。这些家族的成员之间没有任何亲缘关系,但是所有测试的Gly206Ala突变携带者在附近的2个微卫星多态性处共享一个变异等位基因,表明其共同祖先。在淀粉样前体蛋白基因中未发现突变。结论:Gly206Ala突变发现于19个不相关的加勒比西班牙裔家庭中,其中8个患有早发性家族性AD。这种遗传变化可能是加勒比西班牙裔人群中早发性家族性AD的普遍原因。

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