INVERSE ASSOCIATION OF ANTIINFLAMMATORY TREATMENTS AND ALZHEIMERS-DISEASE - INITIAL RESULTS OF A COTWIN CONTROL STUDY

被引:511
作者
BREITNER, JCS
GAU, BA
WELSH, KA
PLASSMAN, BL
MCDONALD, WM
HELMS, MJ
ANTHONY, JC
机构
[1] DUKE UNIV,MED CTR,CTR STUDY AGING & HUMAN DEV,DURHAM,NC
[2] DUKE UNIV,MED CTR,JOSEPH & KATHLEEN BRYAN ALZHEIMERS DIS RES CTR,DURHAM,NC
[3] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,DEPT MENTAL HYG,BALTIMORE,MD
[4] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,DEPT EPIDEMIOL,BALTIMORE,MD 21205
关键词
D O I
10.1212/WNL.44.2.227
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We conducted a co-twin control study among 50 elderly twin pairs with onsets of Alzheimer's disease (AD) separated by 3 or more years. Twenty-three male pairs (46%) were screened from the (U.S.) National Academy of Sciences-National Research Council Registry (NAS-NRC Registry) of World War II veteran twins; others (mostly women) had responded to advertisements or were referred from AD clinics. Twenty-six pairs (52%) were monozygous. The onset of AD was inversely associated with prior use of corticosteroids or ACTH (odds ratio [OR], 0.25; 95% confidence interval [CI], 0.06 to 0.95; p = 0.04). Similar but weaker trends were present among pairs discordant for history of arthritis or for prior daily use of nonsteroidal anti-inflammatory drugs (NSAIDs) or aspirin. The association was strongest when we combined use of steroids/ACTH or NSAIDs post hoc into a single variable of anti-inflammatory drugs (AIs) (OR, 0.24; CI, 0.07 to 0.74; p = 0.01). The inverse relation was strong in female (volunteer) twin pairs but was not present in the younger men from the NAS-NRC Registry. AIs had typically been taken for arthritis or related conditions, but a similar result was apparent after controlling statistically for the arthritis variable (OR, 0.08; CI, 0.01 to 0.69; p = 0.02). AIs have been proposed as a means of retarding the progression of AD symptoms, and these data suggest that AIs may also prevent or delay the initial onset of AD symptoms. Because of limitations in the case-control method, our results require corroboration with hypothesis-driven research designed to control bias and confounding.
引用
收藏
页码:227 / 232
页数:6
相关论文
共 39 条
[1]   AGE-DEPENDENT EXPRESSION OF FAMILIAL RISK IN ALZHEIMERS-DISEASE [J].
BREITNER, JCS ;
MURPHY, EA ;
SILVERMAN, JM ;
MOHS, RC ;
DAVIS, KL .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1988, 128 (03) :536-548
[2]   CRITERIA FOR ONSET CRITICALLY INFLUENCE THE ESTIMATION OF FAMILIAL RISK IN ALZHEIMERS-DISEASE [J].
BREITNER, JCS ;
MAGRUDERHABIB, KM .
GENETIC EPIDEMIOLOGY, 1989, 6 (06) :663-669
[3]   TWIN STUDIES OF ALZHEIMERS-DISEASE - AN APPROACH TO ETIOLOGY AND PREVENTION [J].
BREITNER, JCS ;
MURPHY, EA ;
FOLSTEIN, MF ;
MAGRUDERHABIB, K .
NEUROBIOLOGY OF AGING, 1990, 11 (06) :641-648
[4]   CLINICAL GENETICS AND GENETIC-COUNSELING IN ALZHEIMER-DISEASE [J].
BREITNER, JCS .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (08) :601-606
[5]   USE OF TWIN COHORTS FOR RESEARCH IN ALZHEIMERS-DISEASE [J].
BREITNER, JCS ;
GATZ, M ;
BERGEM, ALM ;
CHRISTIAN, JG ;
MORTIMER, JA ;
MCCLEARN, GE ;
HESTON, LL ;
WELSH, KA ;
ANTHONY, JC ;
FOLSTEIN, MF ;
RADEBAUGH, TS .
NEUROLOGY, 1993, 43 (02) :261-267
[6]   MEDICAL HISTORY AND THE RISK OF ALZHEIMERS-DISEASE - A COLLABORATIVE REANALYSIS OF CASE-CONTROL STUDIES [J].
BRETELER, MMB ;
VANDUIJN, CM ;
CHANDRA, V ;
FRATIGLIONI, L ;
GRAVES, AB ;
HEYMAN, A ;
JORM, AF ;
KOKMEN, E ;
KONDO, K ;
MORTIMER, JA ;
ROCCA, WA ;
SHALAT, SL ;
SOININEN, H ;
HOFMAN, A .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1991, 20 :S36-S42
[7]   EPIDEMIOLOGY OF ALZHEIMERS-DISEASE [J].
BRETELER, MMB ;
CLAUS, JJ ;
VANDUIJN, CM ;
LAUNER, LJ ;
HOFMAN, A .
EPIDEMIOLOGIC REVIEWS, 1992, 14 :59-82
[8]   A CASE-CONTROL STUDY OF ALZHEIMERS-DISEASE IN AUSTRALIA [J].
BROE, GA ;
HENDERSON, AS ;
CREASEY, H ;
MCCUSKER, E ;
KORTEN, AE ;
JORM, AF ;
LONGLEY, W ;
ANTHONY, JC .
NEUROLOGY, 1990, 40 (11) :1698-1707
[9]  
CEDERLOEF R, 1961, ACTA GENET STAT MED, V11, P338
[10]  
CORNFIELD J, 1951, J NATL CANCER I, V11, P1269