Pericak-Vance M A, Yamaoka L H, Haynes C S, Speer M C, Haines J L, Gaskell P C, Hung W Y, Clark C M, Heyman A L, Trofatter J A
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Exp Neurol. 1988 Dec;102(3):271-9. doi: 10.1016/0014-4886(88)90220-8.
Alzheimer's disease is a devastating neurological disorder and the leading cause of dementia among the elderly. Recent studies have localized the gene for familial Alzheimer's disease to chromosome 21 in a series of early onset AD families (mean age of onset less than 60). Familial late onset AD (mean age of onset greater than 60) is a more common clinical form of the disorder. Thirteen families with multiply affected Alzheimer's disease family members were identified and sampled. Ten of these families were of the late onset Alzheimer's disease type. Simulation studies were used to evaluate the usefulness of these pedigrees in linkage studies in familial Alzheimer's disease. Linkage studies undertaken to test the localization of both early onset and late onset Alzheimer's disease families to chromosome 21 failed to establish linkage and excluded linkage from a large portion of the region where the early onset Alzheimer's disease gene was localized. These findings suggest that more than one etiology may exist for familial Alzheimer's disease and indicate the need for continued screening of the genome in familial Alzheimer's disease families.
阿尔茨海默病是一种具有毁灭性的神经疾病,也是老年人痴呆症的主要病因。最近的研究已将家族性阿尔茨海默病的基因定位到21号染色体上,涉及一系列早发性阿尔茨海默病家族(发病平均年龄小于60岁)。家族性晚发性阿尔茨海默病(发病平均年龄大于60岁)是该疾病更常见的临床形式。确定并采集了13个有多名阿尔茨海默病家族成员的家庭样本。其中10个家庭属于晚发性阿尔茨海默病类型。采用模拟研究来评估这些家系在家族性阿尔茨海默病连锁研究中的效用。为检测早发性和晚发性阿尔茨海默病家族与21号染色体的定位关系而进行的连锁研究未能确立连锁关系,并排除了早发性阿尔茨海默病基因所在大部分区域的连锁关系。这些发现表明,家族性阿尔茨海默病可能存在不止一种病因,并表明有必要继续对家族性阿尔茨海默病家族的基因组进行筛查。