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Cognitive Function Over Time in the Alzheimer's Disease Anti-inflammatory Prevention Trial (ADAPT): Results of a Randomized, Controlled Trial of Naproxen and Celecoxib.

Author(s): ADAPT Research Group

Affiliation(s): PhD (primary author), and Christine Szekely, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland; Jason Brandt, PhD (writing committee chair), and Steven Piantadosi, PhD, Johns Hopkins School of Medicine, Baltimore; John C. S. Breitner, MD, and Suzanne Craft, PhD, Veterans Affairs Puget Sound Health Care System and University of Washington, Seattle; Denis Evans, MD, Rush University Medical Center, Chicago, Illinois; Robert Green, MD, Boston University School of Medicine, Boston, Massachusetts; and Michael Mullan, MD, The Roskamp Institute Memory Clinic, Tampa, Florida.

Publication date & source: 2008-05-12, Arch Neurol., [Epub ahead of print]

BACKGROUND: Observational studies have shown reduced risk of Alzheimer dementia in users of nonsteroidal anti-inflammatory drugs. OBJECTIVE: To evaluate the effects of naproxen sodium and celecoxib on cognitive function in older adults. DESIGN: Randomized, double-masked chemoprevention trial. SETTING: Six US memory clinics. PARTICIPANTS: Men and women aged 70 years and older with a family history of Alzheimer disease; 2117 of 2528 enrolled had follow-up cognitive assessment. INTERVENTIONS: Celecoxib (200 mg twice daily), naproxen sodium (220 mg twice daily), or placebo, randomly allocated in a ratio of 1:1:1.5, respectively. MAIN OUTCOME MEASURES: Seven tests of cognitive function and a global summary score measured annually. RESULTS: Longitudinal analyses showed lower global summary scores over time for naproxen compared with placebo (- 0.05 SDs; P = .02) and lower scores on the Modified Mini-Mental State Examination over time for both treatment groups compared with placebo (- 0.33 points for celecoxib [P = .04] and - 0.36 points for naproxen [P = .02]). Restriction of analyses to measures collected from persons without dementia attenuated the treatment group differences. Analyses limited to measures obtained while participants were being issued study drugs produced results similar to the intention-to-treat analyses. CONCLUSIONS: Use of naproxen or celecoxib did not improve cognitive function. There was weak evidence for a detrimental effect of naproxen.Trial Registration clinicaltrials.gov identifier: NCT00007189Published online May 12, 2008 (doi:10.1001/archneur.2008.65.7.nct70006).

Page last updated: 2008-06-22

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