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From Rush Alzheimers Disease Center (Z.A., J.A.S., R.S.W., J.F.K., D.A.B.), Department of Neurological Sciences (Z.A., J.A.S., R.S.W., D.A.B.), Rush Institute for Healthy Aging (J.L.B., D.A.E.), Department of Internal Medicine (J.L.B., J.F.K., D.A.E.), Department of Pathology (J.A.S.), and Department of Behavioral Sciences (R.S.W.), Rush University Medical Center, Chicago, IL; and Channing Lab (F.G.), Department of Medicine, Brigham and Womens Hospital, Harvard Medical School, Boston, MA.
Address correspondence and reprint requests to Dr. Zoe Arvanitakis, Rush Alzheimers Disease Center, 600 S. Paulina, Suite 1020, Rush University Medical Center, Chicago, IL 60612
Objective: To examine the relation of nonsteroidal anti-inflammatory drugs (NSAIDs) to incident Alzheimer disease (AD), change in cognition, and AD pathology.
Methods: Participants were 1,019 older Catholic clergy followed up annually for up to 12 years (mean baseline age = 75.0 years, education = 18.1 years, Mini-Mental State Examination score = 28.5), enrolled in the Religious Orders Study, a longitudinal clinical–pathologic study of aging and AD. Clinical evaluations allowed for AD classification and assessment of global cognition and five cognitive domains. NSAIDs were identified by direct medication inspection at baseline and follow-up evaluations. Neuropathologic data were available on 328 deceased participants. AD pathology was summarized as a global measure and as measures of neuritic plaques, diffuse plaques, and neurofibrillary tangles. We used Cox proportional hazards models and mixed models for incident AD and cognitive decline, respectively, and logistic and linear regression for pathologic outcomes, adjusted for age, sex, and education.
Results: Overall, we found no apparent relation of NSAIDs to incident AD (n = 209 cases), change in cognition, or AD pathology. The hazard ratio of incident AD was 1.19 (95% CI 0.87–1.62) comparing those using NSAIDs with those not using NSAIDs at baseline, and 0.84 (95% CI 0.63–1.11) for specific use of aspirin. Findings were similar in analyses in which we considered NSAID use during follow-up. NSAIDs were not related to change in cognition (all p values > 0.14). There was no relation of NSAIDs to global AD pathology or plaques or tangles.
Conclusion: These data do not support a strong relation between nonsteroidal anti-inflammatory drugs and Alzheimer disease or cognition. Consistent findings across clinical and pathologic outcomes provide additional confidence in these results.
Abbreviations: AD = Alzheimer disease; CERAD = Consortium to Establish a Registry for Alzheimers Disease; HR = hazard ratio; MMSE = Mini-Mental State Examination; NSAID = nonsteroidal anti-inflammatory drug.
Supported by National Institute on Aging grants K23 AG23675 (Z.A.), P30 AG10161 (D.A.B.), and R01 AG15819 (D.A.B.).
Disclosure: The authors report no disclosures.
Received December 14, 2007. Accepted in final form February 29, 2008.
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