期刊
EUROPEAN JOURNAL OF NEUROLOGY
卷 22, 期 11, 页码 1421-1428出版社
WILEY
DOI: 10.1111/ene.12774
关键词
Alzheimer disease; case-control; electronic medical records; glucocorticoids; Lewy body dementia; non-steroidal anti-inflammatories; vascular dementia
资金
- NIHR Biomedical Research Centre at Guy's and St Thomas' National Health Service Foundation Trust
- King's College London
Background and purposeThere is limited primary-care-based evidence about a potential association between anti-inflammatory therapy and dementia subtypes. The present study addressed this limitation by using electronic health records from a large primary care database. MethodA case-control study was implemented using electronic medical records. Cases had a diagnosis of dementia between 1992 and 2014. Up to four controls matched on age, gender, family practice and index date were selected for each case. Use of non-steroidal anti-inflammatory drugs (NSAIDs) and glucocorticoid drugs represented the exposure variables. Primary outcome measures included all-cause dementia and main dementia subtypes, including Alzheimer disease (AD), vascular dementia (VaD) and Lewy body dementia (LBD). Data were analysed using conditional logistic regression. ResultsThe study identified 31083 patients with AD, 23465 with VaD and 1694 with LBD. Ever-used NSAIDs were associated with a modest increase in the risk of all-cause dementia (odds ratio 1.04, 95% confidence interval 1.02-1.05, P<0.006), whilst no association was apparent for ever-used glucocorticoids (0.98, 0.96-1.01, P=0.152). There was no evidence for an association between NSAIDs and AD (1.03, 0.99-1.06, P=0.07) or LBD (1.13, 0.99-1.29, P=0.08). However, a significant increase in the risk for VaD (1.33, 1.29-1.38, P<0.001) was observed. Similar patterns emerged for glucocorticoid therapy. ConclusionIn a large primary care population, there was no robust evidence for a potential association between anti-inflammatory drugs and risk of AD or LBD. NSAIDs and glucocorticoid drugs were associated with higher risk of VaD. Click for the corresponding questions to this CME article.
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