Statins, Risk of Dementia, and Cognitive Function: Secondary Analysis of the Ginkgo Evaluation of Memory Study

被引:107
作者
Bettermann, Kerstin [1 ]
Arnold, Alice M. [2 ]
Williamson, Jeff [3 ]
Rapp, Stephen [4 ]
Sink, Kaycee [3 ]
Toole, James F.
Carlson, Michelle C. [6 ]
Yasar, Sevil [7 ]
DeKosky, Steven [8 ]
Burke, Gregory L. [5 ]
机构
[1] Penn State Coll Med, Dept Neurol, Hershey, PA USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[3] Wake Forest Univ, Dept Gerontol & Geriatr Med, Winston Salem, NC 27109 USA
[4] Wake Forest Univ, Dept Psychiat & Biobehav Med, Winston Salem, NC 27109 USA
[5] Wake Forest Univ, Div Publ Hlth Sci, Winston Salem, NC 27109 USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mental Hlth, Baltimore, MD USA
[7] Johns Hopkins Sch Med, Div Geriatr Med & Gerontol, Baltimore, MD USA
[8] Univ Virginia, Dept Neurol, Charlottesville, VA USA
关键词
3HMG-ACoA reductase inhibitors; cognitive function; dementia; mild cognitive impairment; RANDOMIZED CONTROLLED-TRIAL; ALZHEIMER-DISEASE; CARDIOVASCULAR HEALTH; VASCULAR DEMENTIA; INCIDENT DEMENTIA; CHOLESTEROL; PRAVASTATIN; PREVENTION; STROKE; IMPAIRMENT;
D O I
10.1016/j.jstrokecerebrovasdis.2010.11.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Lipid-loweringmedications (LLMs) and especially statin drugs can delay cognitive decline and dementia onset in individuals with and without mild cognitive impairment (MCI) at baseline. Methods: A longitudinal, observational study was conducted of 3069 cognitively healthy elderly patients (>= 75 years of age) who were enrolled in the Ginkgo Evaluation of Memory Study. The primary outcome measure was the time to adjudicated all-cause dementia and Alzheimer dementia (AD). The secondary outcome measure was the change in global cognitive function over time measured by scores from the Modified Mini-Mental State Exam (3MSE) and the cognitive subscale of the ADAssessment Scale (ADAS-Cog). Results: Among participants without MCI at baseline, the current use of statins was consistently associated with a reduced risk of all-cause dementia (hazard ratio [HR], 0.79; 95% confidence interval [95% CI], 0.65-0.96; P = .021) and AD (HR, 0.57; 95% CI, 0.39-0.85; P = .005). In participants who initiated statin therapy, lipophilic statins tended to reduce dementia risk more than nonlipophilic agents. In contrast, there was no significant association between LLM use (including statins), dementia onset, or cognitive decline in individuals with baseline MCI. However, in individuals withoutMCI at baseline, there was a trend for a neuroprotective effect of statins on cognitive decline. Conclusions: Statins may slow the rate of cognitive decline and delay the onset of AD and all-cause dementia in cognitively healthy elderly individuals, whereas individuals with MCI may not have comparable cognitive protection from these agents. However, the results from this observational study need to be interpreted with caution and will require confirmation by randomized clinical trials stratifying treatment groups based on MCI status at baseline.
引用
收藏
页码:436 / 444
页数:9
相关论文
共 40 条
[1]   Using Telephone and Informant Assessments to Estimate Missing Modified Mini-Mental State Exam Scores and Rates of Cognitive Decline The Cardiovascular Health Study [J].
Arnold, Alice M. ;
Newman, Anne B. ;
Dermond, Norma ;
Haan, Mary ;
Fitzpatrick, Annette .
NEUROEPIDEMIOLOGY, 2009, 33 (01) :55-65
[2]   Statins and cognitive function in the elderly - The Cardiovascular Health Study [J].
Bernick, C ;
Katz, R ;
Smith, NL ;
Rapp, S ;
Bhadelia, R ;
Carlson, M ;
Kuller, L .
NEUROLOGY, 2005, 65 (09) :1388-1394
[3]   Membrane dynamics, cholesterol homeostasis, and Alzheimer's disease [J].
Chauhan, NB .
JOURNAL OF LIPID RESEARCH, 2003, 44 (11) :2019-2029
[4]  
Collins R, 2002, LANCET, V360, P7, DOI 10.1016/S0140-6736(02)09327-3
[5]   Mechanisms of statin-mediated inhibition of small G-protein function [J].
Cordle, A ;
Koenigsknecht-Talboo, J ;
Wilkinson, B ;
Limpert, A ;
Landreth, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (40) :34202-34209
[6]   Use of statins and incidence of dementia and cognitive impairment without dementia in a cohort study [J].
Cramer, C. ;
Haan, M. N. ;
Galea, S. ;
Langa, K. M. ;
Kalbfleisch, J. D. .
NEUROLOGY, 2008, 71 (05) :344-350
[7]   Statin therapy in the treatment of Alzheimer disease: what is the rationale? [J].
DeKosky, ST .
AMERICAN JOURNAL OF MEDICINE, 2005, 118 :48S-53S
[8]   Ginkgo biloba for Prevention of Dementia A Randomized Controlled Trial [J].
DeKosky, Steven T. ;
Williamson, Jeff D. ;
Fitzpatrick, Annette L. ;
Kronmal, Richard A. ;
Ives, Diane G. ;
Saxton, Judith A. ;
Lopez, Oscar L. ;
Burke, Gregory ;
Carlson, Michelle C. ;
Fried, Linda P. ;
Kuller, Lewis H. ;
Robbins, John A. ;
Tracy, Russell P. ;
Woolard, Nancy F. ;
Dunn, Leslie ;
Snitz, Beth E. ;
Nahin, Richard L. ;
Furberg, Curt D. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 300 (19) :2253-2262
[9]   The Ginkgo Evaluation of Memory (GEM) study: Design and baseline data of a randomized trial of Ginkgo biloba extract in prevention of dementia [J].
DeKosky, Steven T. ;
Fitzpatrick, Annette ;
Ives, Diane G. ;
Saxton, Judith ;
Williamson, Jeff ;
Lopez, Oscar L. ;
Burke, Gregory ;
Fried, Linda ;
Kuller, Lewis H. ;
Robbins, John ;
Tracy, Russell ;
Woolard, Nancy ;
Dunn, Leslie ;
Kronmal, Richard ;
Nahin, Richard ;
Furberg, Curt .
CONTEMPORARY CLINICAL TRIALS, 2006, 27 (03) :238-253
[10]   Cholesterol and APOE genotype interact to influence Alzheimer disease progression [J].
Evans, RM ;
Hui, S ;
Perkins, A ;
Lahiri, DK ;
Poirier, J ;
Farlow, MR .
NEUROLOGY, 2004, 62 (10) :1869-1871