Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease A Meta-analysis

被引:411
|
作者
Neu, Scott C. [1 ]
Pa, Judy [1 ]
Kukull, Walter [2 ]
Beekly, Duane [2 ]
Kuzma, Amanda [3 ]
Gangadharan, Prabhakaran [3 ]
Wang, Li-San [3 ]
Romero, Klaus [4 ]
Arneric, Stephen P. [4 ]
Redolfi, Alberto [5 ]
Orlandi, Daniele [5 ]
Frisoni, Giovanni B. [5 ,6 ,7 ]
Au, Rhoda [8 ,9 ,10 ,11 ,12 ,13 ]
Devine, Sherral [14 ]
Auerbach, Sanford [14 ]
Espinosa, Ana [15 ]
Boada, Merce [15 ]
Ruiz, Agustin [15 ]
Johnson, Sterling C. [16 ]
Koscik, Rebecca [16 ]
Wang, Jiun-Jie [17 ,18 ]
Hsu, Wen-Chuin [19 ,20 ]
Chen, Yao-Liang [21 ,22 ]
Toga, Arthur W. [1 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Stevens Inst Neuroimaging & Informat, Lab Neuroimaging, 2025 Zonal Ave, Los Angeles, CA 90033 USA
[2] Univ Washington, Natl Alzheimers Coordinating Ctr, Seattle, WA 98195 USA
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[4] Crit Path Inst, Coalit Major Dis, Tucson, AZ USA
[5] IRCCS Fatebenefratelli, Natl Ctr Alzheimers Dis, Brescia, Italy
[6] Univ Hosp Geneva, Geneva, Switzerland
[7] Univ Geneva, Geneva, Switzerland
[8] Boston Univ, Sch Med, Dept Anat & Neurobiol, Boston, MA 02118 USA
[9] Boston Univ, Sch Publ Hlth, Dept Anat & Neurobiol, Boston, MA USA
[10] Boston Univ, Sch Med, Dept Neurol & Epidemiol, Boston, MA 02118 USA
[11] Boston Univ, Sch Publ Hlth, Dept Neurol & Epidemiol, Boston, MA 02118 USA
[12] Boston Univ, Sch Med, Framingham Heart Study, Boston, MA 02118 USA
[13] Boston Univ, Sch Publ Hlth, Framingham Heart Study, Boston, MA 02118 USA
[14] Boston Univ, Sch Med, Dept Neurol, Framingham Heart Study, Boston, MA 02118 USA
[15] Inst Catala Neurociencies Aplicades, Fundacio ACE, Res Ctr & Memory Clin, Barcelona, Spain
[16] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[17] Chang Gung Univ, Dept Med Imaging & Radiol Sci, Taoyuan, Taiwan
[18] Chang Gung Mem Hosp Linkou, Neurosci Res Ctr, Taoyuan, Taiwan
[19] Chang Gung Mem Hosp Linkou, Dept Neurol, Taoyuan, Taiwan
[20] Chang Gung Mem Hosp Linkou, Dementia Ctr, Taoyuan, Taiwan
[21] Chang Gung Mem Hosp Linkou, Dept Med Imaging & Intervent, Taoyuan, Taiwan
[22] Chang Gung Mem Hosp, Keelung Branch, Dept Med Imaging & Intervent, Keelung, Taiwan
基金
美国国家卫生研究院; 加拿大健康研究院; 英国医学研究理事会;
关键词
MILD COGNITIVE IMPAIRMENT; E EPSILON-4 ALLELE; BASE-LINE CHARACTERISTICS; APOE EPSILON-4; APOE-EPSILON-4; ALLELE; GENDER-DIFFERENCE; DEMENTIA; ASSOCIATION; AGE; COMMUNITY;
D O I
10.1001/jamaneurol.2017.2188
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE It is unclear whether female carriers of the apolipoprotein E (APOE) epsilon 4 allele are at greater risk of developing Alzheimer disease (AD) than men, and the sex-dependent association of mild cognitive impairment (MCI) and APOE has not been established. OBJECTIVE To determine how sex and APOE genotype affect the risks for developing MCI and AD. DATA SOURCES Twenty-seven independent research studies in the Global Alzheimer's Association Interactive Network with data on nearly 58 000 participants. STUDY SELECTION Non-Hispanic white individuals with clinical diagnostic and APOE genotype data. DATA EXTRACTION AND SYNTHESIS Homogeneous data setswere pooled in case-control analyses, and logistic regression models were used to compute risks. MAIN OUTCOMES AND MEASURES Age-adjusted odds ratios (ORs) and 95% confidence intervals for developing MCI and AD were calculated for men and women across APOE genotypes. RESULTS Participants were men and women between ages 55 and 85 years. Across data sets most participants were white, and for many participants, racial/ethnic information was either not collected or not known. Men (OR, 3.09; 95% CI, 2.79-3.42) and women (OR, 3.31; CI, 3.03-3.61) with the APOE epsilon 3/epsilon 4 genotype from ages 55 to 85 years did not show a difference in AD risk; however, women had an increased risk compared with men between the ages of 65 and 75 years (women, OR, 4.37; 95% CI, 3.82-5.00; men, OR, 3.14; 95% CI, 2.68-3.67; P=. 002). Men with APOE epsilon 3/epsilon 4 had an increased risk of AD compared with men with APOE epsilon 3/epsilon 3. The APOE epsilon 2/epsilon 3 genotype conferred a protective effect on women (OR, 0.51; 95% CI, 0.43-0.61) decreasing their risk of AD more (P value =.01) than men (OR, 0.71; 95% CI, 0.60-0.85). There was no difference between men with APOE e3/e4 (OR, 1.55; 95% CI, 1.36-1.76) and women (OR, 1.60; 95% CI, 1.43-1.81) in their risk of developing MCI between the ages of 55 and 85 years, but women had an increased risk between 55 and 70 years (women, OR, 1.43; 95% CI, 1.19-1.73; men, OR, 1.07; 95% CI, 0.87-1.30; P=. 05). There were no significant differences between men and women in their risks for converting from MCI to AD between the ages of 55 and 85 years. Individuals with APOE epsilon 4/epsilon 4 showed increased risks vs individuals with epsilon 3/epsilon 4, but no significant differences between men and women with epsilon 4/epsilon 4 were seen. CONCLUSIONS AND RELEVANCE Contrary to long-standing views, men and women with the APOE epsilon 3/epsilon 4 genotype have nearly the same odds of developing AD from age 55 to 85 years, but women have an increased risk at younger ages. (C) 2017 American Medical Association. All rights reserved.
引用
收藏
页码:1178 / 1189
页数:12
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