Cholesterol as a risk factor for dementia and cognitive decline: A systematic review of prospective studies with meta-analysis

被引:331
|
作者
Anstey, Kaarin J. [1 ]
Lipnicki, Darren M. [1 ]
Low, Lee-Fay [2 ]
机构
[1] Australian Natl Univ, Ageing Res Unit, Mental Hlth Res Ctr, Canberra, ACT 0200, Australia
[2] Univ New S Wales, Primary Dementia Collaborat Res Ctr, Sydney, NSW, Australia
来源
关键词
Alzheimer disease; vascular dementia; mild cognitive impairment; lipoprotein; APOE; systematic review;
D O I
10.1097/JGP.0b013e31816b72d4
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The relationships between total serum cholesterol ( TC) and dementia and between TC and cognitive decline were investigated in a systematic review of 18 prospective studies. Follow-ups ranged from 3 to 29 years, and included a total of 14,331 participants evaluated for Alzheimer disease ( AD), 9,458 participants evaluated for Vascular dementia ( VaD), 1,893 participants evaluated for cognitive decline, and 4,793 participants evaluated for cognitive impairment. Compatible results were pooled using meta-analysis. Consistent associations between high midlife TC and increased risk of AD, and high midlife TC and increased risk of any dementia were found. There was no evidence supporting an association between late-life TC and AD, or between late-life TC and any dementia. No study reported a significant association between TC ( measured in midlife or late-life) and VaD. An association between high midlife TC and cognitive impairment was found but there was only weak evidence for an association between TC and cognitive decline. Two of seven studies reporting data on the interaction between TC and apolipoprotein e4-allele had significant effects. Results suggest the effect of TC on dementia risk occurs in midlife but not late-life, and that there may be different cardiovascular risk factor profiles for AD and VaD. Results from additional studies involving long-term follow-up of midlife samples will allow for clarification of the association between age, TC and risk of specific types of dementia. These data are required to inform recommendations of modulation of cholesterol to reduce or delay dementia risk.
引用
收藏
页码:343 / 354
页数:12
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