A genotype of exceptional longevity is associated with preservation of cognitive function

被引:79
作者
Barzilai, N.
Atzmon, G.
Derby, CA.
Bauman, J. M.
Lipton, R. B.
机构
[1] Albert Einstein Coll Med, Inst Aging Res, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Inst Diabet Res, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Training Ctr, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Dept Neurol, Bronx, NY 10461 USA
[5] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
关键词
D O I
10.1212/01.wnl.0000249116.50854.65
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To test whether cholesterol ester transfer protein (CETP) genotype (VV homozygosity for I405V) is associated with preservation of cognitive function in addition to its association with exceptional longevity. Methods: We studied Ashkenazi Jews with exceptional longevity (n = 158; age 99.2 +/- 0.3 years) for the associations of CETP VV genotype and lipoprotein phenotype, using the Mini- Mental State Examination (MMSE). To confirm the role of CETP in a younger cohort, we studied subjects from the Einstein Aging Study (EAS) for associations between CETP VV and cognitive impairment. Results: Subjects with MMSE > 25 were twice as likely to have the CETP VV genotype (29% vs 14%, p = 0.02), and those with the VV genotype were more likely (61% vs 30%, p = 0.02) to have MMSE > 25. Subjects with the VV genotype had lower levels of CETP (1.73 +/- 0.11 vs 2.12 +/- 0.10 mu g/ mL, p = 0.01), higher high- density lipoprotein (HDL) levels (p = 0.02), and larger lipoprotein particles (p = 0.03). In the EAS cohort, an approximately fivefold increase in the VV genotype (21% vs 4%, p = 0.02), higher HDL levels, and larger lipoprotein particle sizes were associated with less dementia and improved memory. Conclusions: Using two independent cohorts, we implicate the longevity CETP gene as a modulator of age- related cognitive function. A specific CETP genotype is associated with lower CETP levels and a favorable lipoprotein profile. It has not been determined whether modulation of this gene prevents age- related decline or AD.
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页码:2170 / 2175
页数:6
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