Pinessi L, Rainero I, Brunetti E, Cerrato P, Cosentino N, Martino C, Vaula G, Bergamini L
Istituto di Clinica delle Malattie del Sistema Nervoso, Università di Torino.
Minerva Psichiatr. 1992 Jul-Sep;33(3):159-64.
This paper examines recent epidemiological and molecular genetic studies on the genetic basis of Alzheimer's disease (AD). Recent epidemiological studies have shown the existence of a genetic etiology in some cases of Alzheimer's disease. Several pedigrees with an increased incidence of AD (familial Alzheimer's disease--FAD) have been described in the literature. Some of these contain sufficient numbers of affected individuals in multiple generations to provide a rigorous argument for an autosomal dominant inheritance of the AD phenotype. FAD pedigrees show several evidences of as phenotypic heterogeneity of the disease. Molecular genetic studies have shown a linkage between several polymorphic DNA markers specific for the pericentromeric region of chromosome 21 and early-onset FAD. In late-onset FAD pedigrees preliminary reports showed evidence for a linkage with chromosome 19 markers. Molecular genetic studies have clearly demonstrated the genetic heterogeneity of familial Alzheimer's disease. The analysis of new, multigenerational pedigrees with FAD and the study of patients with Down's syndrome and Alzheimer's disease should provide useful informations for the characterization of the gene(s) responsible for familial Alzheimer's disease.
本文探讨了近期关于阿尔茨海默病(AD)遗传基础的流行病学和分子遗传学研究。近期的流行病学研究表明,在某些阿尔茨海默病病例中存在遗传病因。文献中描述了几个阿尔茨海默病发病率增加的家系(家族性阿尔茨海默病——FAD)。其中一些家系在多代中有足够数量的患病个体,为AD表型的常染色体显性遗传提供了有力证据。FAD家系显示出该疾病表型异质性的若干证据。分子遗传学研究表明,21号染色体着丝粒周围区域特有的几个多态性DNA标记与早发性FAD之间存在连锁关系。在晚发性FAD家系中,初步报告显示与19号染色体标记存在连锁关系的证据。分子遗传学研究清楚地证明了家族性阿尔茨海默病的遗传异质性。对新的多代FAD家系的分析以及对唐氏综合征和阿尔茨海默病患者的研究,应为确定导致家族性阿尔茨海默病的基因提供有用信息。