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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共 34 条
  • [11] A multilocus genotyping assay for candidate markers of cardiovascular disease risk
    Cheng, S
    Grow, MA
    Pallaud, C
    Klitz, W
    Erlich, HA
    Visvikis, S
    Chen, JJ
    Pullinger, CR
    Malloy, MJ
    Siest, G
    Kane, JP
    [J]. GENOME RESEARCH, 1999, 9 (10) : 936 - 949
  • [12] Choi YH, 2003, J GERONTOL A-BIOL, V58, P227
  • [13] A prospective study of HDL-C and cholesteryl ester transfer protein gene mutations and the risk of coronary heart disease in the elderly
    Curb, JD
    Abbott, RD
    Rodriguez, BL
    Masaki, K
    Chen, R
    Sharp, DS
    Tall, AR
    [J]. JOURNAL OF LIPID RESEARCH, 2004, 45 (05) : 948 - 953
  • [14] FOLSTEIN MF, 1975, J PSYCHIATR RES, V12, P198
  • [15] FUNKE H, 1994, CIRCULATION, V90, P241
  • [16] SCREENING FOR DEMENTIA BY MEMORY TESTING
    GROBER, E
    BUSCHKE, H
    CRYSTAL, H
    BANG, S
    DRESNER, R
    [J]. NEUROLOGY, 1988, 38 (06) : 900 - 903
  • [17] SET TEST AS AN AID TO DETECTION OF DEMENTIA IN OLD PEOPLE
    ISAACS, B
    KENNIE, AT
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 1973, 123 (575) : 467 - 470
  • [18] MARKED DECREASE OF PLASMA APOLIPOPROTEIN AI AND AII IN JAPANESE PATIENTS WITH LATE-ONSET NONFAMILIAL ALZHEIMERS-DISEASE
    KAWANO, M
    KAWAKAMI, M
    OTSUKA, M
    YASHIMA, H
    YAGINUMA, T
    UEKI, A
    [J]. CLINICA CHIMICA ACTA, 1995, 239 (02) : 209 - 211
  • [19] KURIYAMA M, 1994, JPN J PSYCHIAT NEUR, V48, P589
  • [20] Lucchi Tiziano, 2005, Ann Ital Med Int, V20, P45