Rosen Ami R, Steenland N Kyle, Hanfelt John, Factor Stewart A, Lah James J, Levey Allan I
Department of Neurology, Emory University, 1841 Clifton Rd, Atlanta, GA 30329, USA.
Neurogenetics. 2007 Nov;8(4):263-70. doi: 10.1007/s10048-007-0100-6. Epub 2007 Sep 6.
This case-control study examined the potential for a common etiology of Parkinson's disease (PD) and Alzheimer's disease (AD) using reported family history. Structured interviews were used to collect AD and PD family history from subjects (n = 1,531) with AD, PD, AD/PD, or controls. Intergroup analysis compared reported AD and PD family histories in the three case groups to the histories reported in the control group. Intragroup analysis stratified each diagnostic group based on positive family history of AD, then compared the subgroups for a family history of PD. Subjects with AD had a higher risk of having a family history of AD [odds ratio (OR) 2.3; 1.5-3.4] and subjects with PD had a higher risk of having a family history of PD (OR 2.2; 1.2-4.0) as compared to control subjects. Intergroup analyses revealed no significant crossed risk, increased risk of subjects with AD having a family history of PD vs controls and vice versa. Intragroup analysis found that subjects with PD and a family history of AD were more likely to have a family history of PD (OR 1.7; 1.1-2.6) when compared to subjects with PD and no family history of AD. A similar trend was found for subjects with AD (OR 1.7; 0.9-3.1). AD and PD cases each have an increased familial risk of their respective disease. Probands with AD or PD and a family history of either disease have a higher crossed risk of a family history of the other disease. These findings suggest the existence of common genetic and/or environmental factors that predispose to both AD and PD in the subset of cases with positive family history of both neurodegenerative diseases.
这项病例对照研究利用所报告的家族病史,探讨了帕金森病(PD)和阿尔茨海默病(AD)存在共同病因的可能性。采用结构化访谈从患有AD、PD、AD/PD或作为对照的受试者(n = 1531)中收集AD和PD家族病史。组间分析将三个病例组所报告的AD和PD家族病史与对照组所报告的病史进行比较。组内分析根据AD家族病史阳性对每个诊断组进行分层,然后比较各亚组的PD家族病史情况。与对照受试者相比,患有AD的受试者有家族性AD病史的风险更高[比值比(OR)2.3;1.5 - 3.4],患有PD的受试者有家族性PD病史的风险更高(OR 2.2;1.2 - 4.0)。组间分析未发现显著的交叉风险,即患有AD的受试者有家族性PD病史的风险相较于对照组并未增加,反之亦然。组内分析发现,与无AD家族病史的PD受试者相比,有AD家族病史的PD受试者更有可能有家族性PD病史(OR 1.7;1.1 - 2.6)。在患有AD的受试者中也发现了类似趋势(OR 1.7;0.9 - 3.1)。AD和PD病例各自患其相应疾病的家族风险均增加。患有AD或PD且有其中一种疾病家族病史的先证者,患另一种疾病家族病史的交叉风险更高。这些发现表明,在两种神经退行性疾病家族病史均为阳性的病例子集中,存在易导致AD和PD的共同遗传和/或环境因素。