No Effect of One-Year Treatment with Indomethacin on Alzheimer's Disease Progression: A Randomized Controlled Trial

被引:116
作者
de Jong, Danielle [1 ,2 ]
Jansen, Rene [2 ,3 ]
Hoefnagels, Willibrord [2 ,3 ]
Jellesma-Eggenkamp, Marja [6 ]
Verbeek, Marcel [1 ,3 ,4 ]
Borm, George [5 ]
Kremer, Berry [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Neurol, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen Med Ctr, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen Med Ctr, Alzheimer Ctr Nijmegen, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen Med Ctr, Lab Pediat & Neurol, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen Med Ctr, Dept Epidemiol & Biostat, Nijmegen, Netherlands
[6] Rijnstate Hosp, Dept Geriat Med, Arnhem, Netherlands
关键词
D O I
10.1371/journal.pone.0001475
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Background. The objective of this study was to determine whether treatment with the nonselective nonsteroidal anti-inflammatory drug (NSAID) indomethacin slows cognitive decline in patients with Alzheimer's disease (AD). Methodology/Principal Findings. This double-blind, randomized, placebo-controlled trial was conducted between May 2000 and September 2005 in two hospitals in the Netherlands. 51 patients with mild to moderate AD were enrolled into the study. Patients received 100 mg indomethacin or placebo daily for 12 months. Additionally, all patients received omeprazole. The primary outcome measure was the change from baseline after one year of treatment on the cognitive subscale of the AD Assessment Scale (ADAS-cog). Secondary outcome measures included the Mini-Mental State Examination, the Clinician's Interview Based Impression of Change with caregiver input, the noncognitive subscale of the ADAS, the Neuropsychiatric Inventory, and the Interview for Deterioration in Daily life in Dementia. Considerable recruitment problems of participants were encountered, leading to an underpowered study. In the placebo group, 19 out of 25 patients completed the study, and 19 out of 26 patients in the indomethacin group. The deterioration on the ADAS-cog was less in the indomethacin group (7.8 +/- 67.6), than in the placebo group (9.3 +/- 10.0). This difference (1.5 points; CI 24.5-7.5) was not statistically significant, and neither were any of the secondary outcome measures. Conclusions/Significance. The results of this study are inconclusive with respect to the hypothesis that indomethacin slows the progression of AD. Trial Registration. ClinicalTrials.gov NCT00432081
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页数:6
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