THE CONSORTIUM TO ESTABLISH A REGISTRY FOR ALZHEIMERS-DISEASE (CERAD) .6. FAMILY HISTORY ASSESSMENT - A MULTICENTER STUDY OF FIRST-DEGREE RELATIVES OF ALZHEIMERS-DISEASE PROBANDS AND NONDEMENTED SPOUSE CONTROLS

被引:63
作者
SILVERMAN, JM
RAIFORD, K
EDLAND, S
FILLENBAUM, G
MORRIS, JC
CLARK, CM
KUKULL, W
HEYMAN, A
机构
[1] CUNY MT SINAI SCH MED,NEW YORK,NY 10029
[2] DUKE UNIV,MED CTR,DURHAM,NC
[3] UNIV WASHINGTON,SEATTLE,WA 98195
[4] WASHINGTON UNIV,ST LOUIS,MO
[5] UNIV PENN,PHILADELPHIA,PA 19104
关键词
D O I
10.1212/WNL.44.7.1253
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Although familial factors in Alzheimer's disease (AD) are well established, uniform family-history assessment in genetic and epidemiologic studies of AD is needed to reconcile the divergent estimates of the cumulative risk of this illness among relatives of AD probands. To answer the need, the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) has developed a standardized Family History Assessment of AD to identify the presence of AD, Parkinson's disease (PD), and Down's syndrome (DS) in family members. This paper describes the use of this new assessment instrument in 118 patients with AD (estimated mean age at onset [+/-SD] = 64.5 +/- 7.7 years) and their nondemented spouses who were enrolled in 11 different CERAD sites in the U.S. The first-degree relatives of the probands with AD had a significantly greater cumulative risk (p < 0.005) of AD or primary progressive dementia (24.8%) than did the relatives of spouse controls (15.2%). Furthermore, the cumulative risk for this disorder among female relatives of probands was significantly greater than that among male relatives. There were no differences between the families of probands and controls for the numbers of affected first-degree relatives with PD or DS. This is the first reported multicenter family-history study of AD, and it supports earlier reports of familial factors in AD and indicates a higher risk to female relatives of AD probands. The CERAD Family History Assessment instrument may be useful for further multicenter and epidemiologic studies designed to delineate familial factors associated with AD.
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页码:1253 / 1259
页数:7
相关论文
共 31 条
[1]  
BREITNER JCS, 1988, NEUROLOGY, V38, P207
[2]   FAMILIAL ALZHEIMER DEMENTIA - A PREVALENT DISORDER WITH SPECIFIC CLINICAL-FEATURES [J].
BREITNER, JCS ;
FOLSTEIN, MF .
PSYCHOLOGICAL MEDICINE, 1984, 14 (01) :63-80
[3]   ASSESSMENT OF GENETIC RISK FOR ALZHEIMERS-DISEASE AMONG 1ST-DEGREE RELATIVES [J].
FARRER, LA ;
OSULLIVAN, DM ;
CUPPLES, LA ;
GROWDON, JH ;
MYERS, RH .
ANNALS OF NEUROLOGY, 1989, 25 (05) :485-493
[4]  
Fisher LD, 1993, BIOSTATISTICS METHOD
[5]  
HESTON LL, 1977, ARCH GEN PSYCHIAT, V34, P976
[6]  
HESTON LL, 1981, ARCH GEN PSYCHIAT, V38, P976
[7]   ALZHEIMERS-DISEASE - GENETIC-ASPECTS AND ASSOCIATED CLINICAL DISORDERS [J].
HEYMAN, A ;
WILKINSON, WE ;
HURWITZ, BJ ;
SCHMECHEL, D ;
SIGMON, AH ;
WEINBERG, T ;
HELMS, MJ ;
SWIFT, M .
ANNALS OF NEUROLOGY, 1983, 14 (05) :507-515
[8]   HISTORY OF DEMENTIA AND PARKINSONS-DISEASE IN 1ST-DEGREE RELATIVES OF PATIENTS WITH ALZHEIMERS-DISEASE [J].
HOFMAN, A ;
SCHULTE, W ;
TANJA, TA ;
VANDUIJN, CM ;
HAAXMA, R ;
LAMERIS, AJ ;
OTTEN, VM ;
SAAN, RJ .
NEUROLOGY, 1989, 39 (12) :1589-1592
[9]   RISK OF DEMENTIA IN RELATIVES OF PATIENTS WITH ALZHEIMERS-DISEASE [J].
HUFF, FJ ;
AUERBACH, J ;
CHAKRAVARTI, A ;
BOLLER, F .
NEUROLOGY, 1988, 38 (05) :786-790
[10]   DEVELOPMENT OF DEMENTING ILLNESSES IN AN 80-YEAR-OLD VOLUNTEER COHORT [J].
KATZMAN, R ;
ARONSON, M ;
FULD, P ;
KAWAS, C ;
BROWN, T ;
MORGENSTERN, H ;
FRISHMAN, W ;
GIDEZ, L ;
EDER, H ;
OOI, WL .
ANNALS OF NEUROLOGY, 1989, 25 (04) :317-324