Decreased prevalence of Alzheimer disease associated with 3-hydroxy-3-methyglutaryl coenzyme A reductase inhibitors

Citation
B. Wolozin et al., Decreased prevalence of Alzheimer disease associated with 3-hydroxy-3-methyglutaryl coenzyme A reductase inhibitors, ARCH NEUROL, 57(10), 2000, pp. 1439-1443
Citations number
17
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ARCHIVES OF NEUROLOGY
ISSN journal
00039942 → ACNP
Volume
57
Issue
10
Year of publication
2000
Pages
1439 - 1443
Database
ISI
SICI code
0003-9942(200010)57:10<1439:DPOADA>2.0.ZU;2-R
Abstract
Context: Increasing evidence suggests that cholesterol plays a role in the pathophysiology of Alzheimer disease (AD). For instance, an elevated serum cholesterol level has been shown to be a risk factor for AD. Objective: To determine whether patients taking 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins), which are a group of medicines t hat inhibit the synthesis of cholesterol, have a lower prevalence of probab le AD. Design: The experiment uses a cross-sectional analysis comparing the preval ence of probable AD in 3 groups of patients from hospital records: the enti re population, patients receiving 3-hydroxy-3-methylglutaryl coenzyme A red uctase inhibitors (hereafter referred to as the statins), and patients rece iving medications used to treat hypertension or cardiovascular disease. Patients: The subjects studied were those included in the computer database s of 3 different hospitals for the years October 1, 1996, through August 31 , 1998. Main Outcome Measures: Diagnosis of probable AD. Results: We find that the prevalence of probable AD in the cohort taking st atins during the study interval is 60% to 73% (P<.001) lower than the total patient population or compared with patients taking other medications typi cally used in the treatment of hypertension or cardiovascular disease. Conclusions: There is a lower prevalence of diagnosed probable AD in patien ts taking 2 different 3-hydroxy-3-methylglutaryl coenzyme A reductase inhib itors-lovastatin and pravastatin. While one cannot infer causative mechanis ms based on these data, this study reveals an interesting association in th e data, which warrants further study.