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

IMPORTANCE: It is unclear whether female carriers of the apolipoprotein E (APOE) ε4 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 AP...

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Veröffentlicht in:JAMA neurology 2017-10, Vol.74 (10), p.1178-1189
Hauptverfasser: Neu, Scott C, Pa, Judy, Kukull, Walter, Beekly, Duane, Kuzma, Amanda, Gangadharan, Prabhakaran, Wang, Li-San, Romero, Klaus, Arneric, Stephen P, Redolfi, Alberto, Orlandi, Daniele, Frisoni, Giovanni B, Au, Rhoda, Devine, Sherral, Auerbach, Sanford, Espinosa, Ana, Boada, Mercè, Ruiz, Agustín, Johnson, Sterling C, Koscik, Rebecca, Wang, Jiun-Jie, Hsu, Wen-Chuin, Chen, Yao-Liang, Toga, Arthur W
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container_end_page 1189
container_issue 10
container_start_page 1178
container_title JAMA neurology
container_volume 74
creator Neu, Scott C
Pa, Judy
Kukull, Walter
Beekly, Duane
Kuzma, Amanda
Gangadharan, Prabhakaran
Wang, Li-San
Romero, Klaus
Arneric, Stephen P
Redolfi, Alberto
Orlandi, Daniele
Frisoni, Giovanni B
Au, Rhoda
Devine, Sherral
Auerbach, Sanford
Espinosa, Ana
Boada, Mercè
Ruiz, Agustín
Johnson, Sterling C
Koscik, Rebecca
Wang, Jiun-Jie
Hsu, Wen-Chuin
Chen, Yao-Liang
Toga, Arthur W
description IMPORTANCE: It is unclear whether female carriers of the apolipoprotein E (APOE) ε4 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 sets were 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 ε3/ε4 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 ε3/ε4 had an increased risk of AD compared with men with APOE ε3/ε3. The APOE ε2/ε3 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 ε3/ε4 (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 ε4/ε4 showed increased risks vs individuals with ε3/ε4, but no significant differences between men and women with ε4/ε4 were seen. CONCLUSIONS AND RELEVANCE: Contrary to long-standing views, men and women with the APOE ε3/ε4 genotype have nearly the same odds of develo
doi_str_mv 10.1001/jamaneurol.2017.2188
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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 sets were 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 ε3/ε4 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 ε3/ε4 had an increased risk of AD compared with men with APOE ε3/ε3. The APOE ε2/ε3 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 ε3/ε4 (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 ε4/ε4 showed increased risks vs individuals with ε3/ε4, but no significant differences between men and women with ε4/ε4 were seen. CONCLUSIONS AND RELEVANCE: Contrary to long-standing views, men and women with the APOE ε3/ε4 genotype have nearly the same odds of developing AD from age 55 to 85 years, but women have an increased risk at younger ages.</description><identifier>ISSN: 2168-6149</identifier><identifier>EISSN: 2168-6157</identifier><identifier>DOI: 10.1001/jamaneurol.2017.2188</identifier><identifier>PMID: 28846757</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><subject>Aged ; Aged, 80 and over ; Alzheimer Disease - epidemiology ; Alzheimer Disease - genetics ; Apolipoproteins E - genetics ; Case-Control Studies ; Databases, Factual - statistics &amp; numerical data ; Female ; Humans ; Logistic Models ; Male ; Middle Aged ; Risk Factors ; Sex Characteristics</subject><ispartof>JAMA neurology, 2017-10, Vol.74 (10), p.1178-1189</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a326t-37e88a72fe7a403b3595b6509794c8b34b1935b62fb818b72f849edb8ade8c7d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jamaneurology/articlepdf/10.1001/jamaneurol.2017.2188$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jamaneurology/fullarticle/10.1001/jamaneurol.2017.2188$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,315,782,786,3342,27931,27932,76497,76500</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28846757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neu, Scott C</creatorcontrib><creatorcontrib>Pa, Judy</creatorcontrib><creatorcontrib>Kukull, Walter</creatorcontrib><creatorcontrib>Beekly, Duane</creatorcontrib><creatorcontrib>Kuzma, Amanda</creatorcontrib><creatorcontrib>Gangadharan, Prabhakaran</creatorcontrib><creatorcontrib>Wang, Li-San</creatorcontrib><creatorcontrib>Romero, Klaus</creatorcontrib><creatorcontrib>Arneric, Stephen P</creatorcontrib><creatorcontrib>Redolfi, Alberto</creatorcontrib><creatorcontrib>Orlandi, Daniele</creatorcontrib><creatorcontrib>Frisoni, Giovanni B</creatorcontrib><creatorcontrib>Au, Rhoda</creatorcontrib><creatorcontrib>Devine, Sherral</creatorcontrib><creatorcontrib>Auerbach, Sanford</creatorcontrib><creatorcontrib>Espinosa, Ana</creatorcontrib><creatorcontrib>Boada, Mercè</creatorcontrib><creatorcontrib>Ruiz, Agustín</creatorcontrib><creatorcontrib>Johnson, Sterling C</creatorcontrib><creatorcontrib>Koscik, Rebecca</creatorcontrib><creatorcontrib>Wang, Jiun-Jie</creatorcontrib><creatorcontrib>Hsu, Wen-Chuin</creatorcontrib><creatorcontrib>Chen, Yao-Liang</creatorcontrib><creatorcontrib>Toga, Arthur W</creatorcontrib><title>Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease: A Meta-analysis</title><title>JAMA neurology</title><addtitle>JAMA Neurol</addtitle><description>IMPORTANCE: It is unclear whether female carriers of the apolipoprotein E (APOE) ε4 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 sets were 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 ε3/ε4 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 ε3/ε4 had an increased risk of AD compared with men with APOE ε3/ε3. The APOE ε2/ε3 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 ε3/ε4 (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 ε4/ε4 showed increased risks vs individuals with ε3/ε4, but no significant differences between men and women with ε4/ε4 were seen. CONCLUSIONS AND RELEVANCE: Contrary to long-standing views, men and women with the APOE ε3/ε4 genotype have nearly the same odds of developing AD from age 55 to 85 years, but women have an increased risk at younger ages.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - epidemiology</subject><subject>Alzheimer Disease - genetics</subject><subject>Apolipoproteins E - genetics</subject><subject>Case-Control Studies</subject><subject>Databases, Factual - statistics &amp; numerical data</subject><subject>Female</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Risk Factors</subject><subject>Sex Characteristics</subject><issn>2168-6149</issn><issn>2168-6157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1LwzAUhoMobuj-gIjk0pvOfDVJvRvTTWEiqLsuaXuKnW1Tkxacv96M6czNCTnPe054ELqkZEoJoTcb05gWBmfrKSNUTRnV-giNGZU6kjRWx4e7SEZo4v2GhKMJEVycohHTWkgVqzFazzpbV53tnO2havE9XkJr-20H2LQFfoUv_FL5D7wweW-dx6V1eFZ_v0PVgMN3lQfj4RbP8BP0JjKtqbe-8ufopDS1h8lvPUPrxf3b_CFaPS8f57NVZDiTfcQVaG0UK0EZQXjG4yTOZEwSlYhcZ1xkNOHhhZWZpjoLoBYJFJk2BehcFfwMXe_nhu9_DuD7tKl8DnUd5NjBpyHOJZGaJQEVezR31nsHZdq5qjFum1KS7pym_07TndN05zTErn43DFkDxSH0ZzAAF3sgpP-7UiRMEv4Dzap86w</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Neu, Scott C</creator><creator>Pa, Judy</creator><creator>Kukull, Walter</creator><creator>Beekly, Duane</creator><creator>Kuzma, Amanda</creator><creator>Gangadharan, Prabhakaran</creator><creator>Wang, Li-San</creator><creator>Romero, Klaus</creator><creator>Arneric, Stephen P</creator><creator>Redolfi, Alberto</creator><creator>Orlandi, Daniele</creator><creator>Frisoni, Giovanni B</creator><creator>Au, Rhoda</creator><creator>Devine, Sherral</creator><creator>Auerbach, Sanford</creator><creator>Espinosa, Ana</creator><creator>Boada, Mercè</creator><creator>Ruiz, Agustín</creator><creator>Johnson, Sterling C</creator><creator>Koscik, Rebecca</creator><creator>Wang, Jiun-Jie</creator><creator>Hsu, Wen-Chuin</creator><creator>Chen, Yao-Liang</creator><creator>Toga, Arthur W</creator><general>American Medical Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20171001</creationdate><title>Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease: A Meta-analysis</title><author>Neu, Scott C ; Pa, Judy ; Kukull, Walter ; Beekly, Duane ; Kuzma, Amanda ; Gangadharan, Prabhakaran ; Wang, Li-San ; Romero, Klaus ; Arneric, Stephen P ; Redolfi, Alberto ; Orlandi, Daniele ; Frisoni, Giovanni B ; Au, Rhoda ; Devine, Sherral ; Auerbach, Sanford ; Espinosa, Ana ; Boada, Mercè ; Ruiz, Agustín ; Johnson, Sterling C ; Koscik, Rebecca ; Wang, Jiun-Jie ; Hsu, Wen-Chuin ; Chen, Yao-Liang ; Toga, Arthur W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a326t-37e88a72fe7a403b3595b6509794c8b34b1935b62fb818b72f849edb8ade8c7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - epidemiology</topic><topic>Alzheimer Disease - genetics</topic><topic>Apolipoproteins E - genetics</topic><topic>Case-Control Studies</topic><topic>Databases, Factual - statistics &amp; numerical data</topic><topic>Female</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Risk Factors</topic><topic>Sex Characteristics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neu, Scott C</creatorcontrib><creatorcontrib>Pa, Judy</creatorcontrib><creatorcontrib>Kukull, Walter</creatorcontrib><creatorcontrib>Beekly, Duane</creatorcontrib><creatorcontrib>Kuzma, Amanda</creatorcontrib><creatorcontrib>Gangadharan, Prabhakaran</creatorcontrib><creatorcontrib>Wang, Li-San</creatorcontrib><creatorcontrib>Romero, Klaus</creatorcontrib><creatorcontrib>Arneric, Stephen P</creatorcontrib><creatorcontrib>Redolfi, Alberto</creatorcontrib><creatorcontrib>Orlandi, Daniele</creatorcontrib><creatorcontrib>Frisoni, Giovanni B</creatorcontrib><creatorcontrib>Au, Rhoda</creatorcontrib><creatorcontrib>Devine, Sherral</creatorcontrib><creatorcontrib>Auerbach, Sanford</creatorcontrib><creatorcontrib>Espinosa, Ana</creatorcontrib><creatorcontrib>Boada, Mercè</creatorcontrib><creatorcontrib>Ruiz, Agustín</creatorcontrib><creatorcontrib>Johnson, Sterling C</creatorcontrib><creatorcontrib>Koscik, Rebecca</creatorcontrib><creatorcontrib>Wang, Jiun-Jie</creatorcontrib><creatorcontrib>Hsu, Wen-Chuin</creatorcontrib><creatorcontrib>Chen, Yao-Liang</creatorcontrib><creatorcontrib>Toga, Arthur W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>JAMA neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neu, Scott C</au><au>Pa, Judy</au><au>Kukull, Walter</au><au>Beekly, Duane</au><au>Kuzma, Amanda</au><au>Gangadharan, Prabhakaran</au><au>Wang, Li-San</au><au>Romero, Klaus</au><au>Arneric, Stephen P</au><au>Redolfi, Alberto</au><au>Orlandi, Daniele</au><au>Frisoni, Giovanni B</au><au>Au, Rhoda</au><au>Devine, Sherral</au><au>Auerbach, Sanford</au><au>Espinosa, Ana</au><au>Boada, Mercè</au><au>Ruiz, Agustín</au><au>Johnson, Sterling C</au><au>Koscik, Rebecca</au><au>Wang, Jiun-Jie</au><au>Hsu, Wen-Chuin</au><au>Chen, Yao-Liang</au><au>Toga, Arthur W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease: A Meta-analysis</atitle><jtitle>JAMA neurology</jtitle><addtitle>JAMA Neurol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>74</volume><issue>10</issue><spage>1178</spage><epage>1189</epage><pages>1178-1189</pages><issn>2168-6149</issn><eissn>2168-6157</eissn><abstract>IMPORTANCE: It is unclear whether female carriers of the apolipoprotein E (APOE) ε4 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 sets were 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 ε3/ε4 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 ε3/ε4 had an increased risk of AD compared with men with APOE ε3/ε3. The APOE ε2/ε3 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 ε3/ε4 (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 ε4/ε4 showed increased risks vs individuals with ε3/ε4, but no significant differences between men and women with ε4/ε4 were seen. CONCLUSIONS AND RELEVANCE: Contrary to long-standing views, men and women with the APOE ε3/ε4 genotype have nearly the same odds of developing AD from age 55 to 85 years, but women have an increased risk at younger ages.</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>28846757</pmid><doi>10.1001/jamaneurol.2017.2188</doi><tpages>12</tpages></addata></record>
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2168-6157
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source MEDLINE; American Medical Association Journals
subjects Aged
Aged, 80 and over
Alzheimer Disease - epidemiology
Alzheimer Disease - genetics
Apolipoproteins E - genetics
Case-Control Studies
Databases, Factual - statistics & numerical data
Female
Humans
Logistic Models
Male
Middle Aged
Risk Factors
Sex Characteristics
title Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease: A Meta-analysis
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