Cytomegalovirus Infection and Risk of Alzheimer Disease in Older Black and White Individuals

Background. Human cytomegalovirus (CMV) is prevalent in older adults and has been implicated in many chronic diseases of aging. This study investigated the relation between CMV and the risk of Alzheimer disease (AD). Methods. Data come from 3 cohort studies that included 849 participants (mean age [...

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Veröffentlicht in:The Journal of infectious diseases 2015-01, Vol.211 (2), p.230-237
Hauptverfasser: Barnes, Lisa L., Capuano, Ana W., Aiello, Alison E., Turner, Arlener D., Yolken, Robert H., Torrey, E. Fuller, Bennett, David A.
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container_end_page 237
container_issue 2
container_start_page 230
container_title The Journal of infectious diseases
container_volume 211
creator Barnes, Lisa L.
Capuano, Ana W.
Aiello, Alison E.
Turner, Arlener D.
Yolken, Robert H.
Torrey, E. Fuller
Bennett, David A.
description Background. Human cytomegalovirus (CMV) is prevalent in older adults and has been implicated in many chronic diseases of aging. This study investigated the relation between CMV and the risk of Alzheimer disease (AD). Methods. Data come from 3 cohort studies that included 849 participants (mean age [± SD], 78.6 ± 7.2 years; mean education duration [± SD], 15.4 ± 3.3 years; 25% black). Results. A solid-phase enzyme-linked immunosorbent assay was used for detecting type-specific immunoglobulin G antibody responses to CMV and herpes simplex virus type 1 (HSV-1) measured in archived serum samples. Of 849 participants, 73.4% had serologie evidence of exposure to CMV (89.0% black and 68.2% white; P< .001). During an average of 5.0 years of follow-up, 93 persons developed AD. CMV seropositivity was associated with an increased risk of AD (relative risk, 2.15; 95% confidence interval, 1.42-3.27) and a faster rate of decline in global cognition (estimate [± standard error], -0.02 ± 0.01; P = .03) in models that controlled for age, sex, education duration, race, vascular risk factors, vascular diseases, and apolipoprotein ε4 level. Results were similar in black and white individuals for both incident AD and change in cognitive function and were independent of HSV-1 status. Conclusions. These results suggest that CMV infection is associated with an increased risk of AD and a faster rate of cognitive decline in older diverse populations.
doi_str_mv 10.1093/infdis/jiu437
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Fuller ; Bennett, David A.</creator><creatorcontrib>Barnes, Lisa L. ; Capuano, Ana W. ; Aiello, Alison E. ; Turner, Arlener D. ; Yolken, Robert H. ; Torrey, E. Fuller ; Bennett, David A.</creatorcontrib><description>Background. Human cytomegalovirus (CMV) is prevalent in older adults and has been implicated in many chronic diseases of aging. This study investigated the relation between CMV and the risk of Alzheimer disease (AD). Methods. Data come from 3 cohort studies that included 849 participants (mean age [± SD], 78.6 ± 7.2 years; mean education duration [± SD], 15.4 ± 3.3 years; 25% black). Results. A solid-phase enzyme-linked immunosorbent assay was used for detecting type-specific immunoglobulin G antibody responses to CMV and herpes simplex virus type 1 (HSV-1) measured in archived serum samples. Of 849 participants, 73.4% had serologie evidence of exposure to CMV (89.0% black and 68.2% white; P&lt; .001). During an average of 5.0 years of follow-up, 93 persons developed AD. CMV seropositivity was associated with an increased risk of AD (relative risk, 2.15; 95% confidence interval, 1.42-3.27) and a faster rate of decline in global cognition (estimate [± standard error], -0.02 ± 0.01; P = .03) in models that controlled for age, sex, education duration, race, vascular risk factors, vascular diseases, and apolipoprotein ε4 level. Results were similar in black and white individuals for both incident AD and change in cognitive function and were independent of HSV-1 status. Conclusions. These results suggest that CMV infection is associated with an increased risk of AD and a faster rate of cognitive decline in older diverse populations.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiu437</identifier><identifier>PMID: 25108028</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>African Continental Ancestry Group ; Age Factors ; Aged ; Aged, 80 and over ; Alzheimer Disease - epidemiology ; Cohort Studies ; Cytomegalovirus Infections - complications ; European Continental Ancestry Group ; Female ; Herpes simplex virus 1 ; Human cytomegalovirus ; Humans ; Longitudinal Studies ; Major and Brief Reports ; Male ; Prevalence ; Risk Assessment ; Time Factors ; VIRUSES</subject><ispartof>The Journal of infectious diseases, 2015-01, Vol.211 (2), p.230-237</ispartof><rights>Copyright © 2015 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-fb3ec4d7eb5f47dbffd26a51d322e07d95e75c33da0b827a05f02732a3fad60d3</citedby><cites>FETCH-LOGICAL-c508t-fb3ec4d7eb5f47dbffd26a51d322e07d95e75c33da0b827a05f02732a3fad60d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43708979$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43708979$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25108028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barnes, Lisa L.</creatorcontrib><creatorcontrib>Capuano, Ana W.</creatorcontrib><creatorcontrib>Aiello, Alison E.</creatorcontrib><creatorcontrib>Turner, Arlener D.</creatorcontrib><creatorcontrib>Yolken, Robert H.</creatorcontrib><creatorcontrib>Torrey, E. Fuller</creatorcontrib><creatorcontrib>Bennett, David A.</creatorcontrib><title>Cytomegalovirus Infection and Risk of Alzheimer Disease in Older Black and White Individuals</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Background. Human cytomegalovirus (CMV) is prevalent in older adults and has been implicated in many chronic diseases of aging. This study investigated the relation between CMV and the risk of Alzheimer disease (AD). Methods. Data come from 3 cohort studies that included 849 participants (mean age [± SD], 78.6 ± 7.2 years; mean education duration [± SD], 15.4 ± 3.3 years; 25% black). Results. A solid-phase enzyme-linked immunosorbent assay was used for detecting type-specific immunoglobulin G antibody responses to CMV and herpes simplex virus type 1 (HSV-1) measured in archived serum samples. Of 849 participants, 73.4% had serologie evidence of exposure to CMV (89.0% black and 68.2% white; P&lt; .001). During an average of 5.0 years of follow-up, 93 persons developed AD. CMV seropositivity was associated with an increased risk of AD (relative risk, 2.15; 95% confidence interval, 1.42-3.27) and a faster rate of decline in global cognition (estimate [± standard error], -0.02 ± 0.01; P = .03) in models that controlled for age, sex, education duration, race, vascular risk factors, vascular diseases, and apolipoprotein ε4 level. Results were similar in black and white individuals for both incident AD and change in cognitive function and were independent of HSV-1 status. Conclusions. These results suggest that CMV infection is associated with an increased risk of AD and a faster rate of cognitive decline in older diverse populations.</description><subject>African Continental Ancestry Group</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - epidemiology</subject><subject>Cohort Studies</subject><subject>Cytomegalovirus Infections - complications</subject><subject>European Continental Ancestry Group</subject><subject>Female</subject><subject>Herpes simplex virus 1</subject><subject>Human cytomegalovirus</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Major and Brief Reports</subject><subject>Male</subject><subject>Prevalence</subject><subject>Risk Assessment</subject><subject>Time Factors</subject><subject>VIRUSES</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFP3DAQhS3UCpYtxx5BOfYSdmwndnKpBFtakJBWqlr1gmQ58Zj1ksRgJyvBrycQuiq3nkaa983TzDxCPlM4pVDyheuscXGxcUPG5R6Z0ZzLVAjKP5AZAGMpLcrygBzGuAGAjAu5Tw5YTqEAVszIzfKx9y3e6sZvXRhictVZrHvnu0R3Jvnp4l3ibXLWPK3RtRiSby6ijpi4Llk1ZmycN7q-e4X_rF2Po4FxW2cG3cRP5KMdCx691Tn5_f3i1_IyvV79uFqeXad1DkWf2opjnRmJVW4zaSprDRM6p4YzhiBNmaPMa86NhqpgUkNugUnONLfaCDB8Tr5OvvdD1aKpseuDbtR9cK0Oj8prp94rnVurW79VGWeCj0-Zky9vBsE_DBh71bpYY9PoDv0QFRWFFJIJCv-BZjRjAl5d0wmtg48xoN1tREG9hKem8NQU3sif_HvGjv6b1ggcT8Am9j7s9HEWilKW_BmfP6L5</recordid><startdate>20150115</startdate><enddate>20150115</enddate><creator>Barnes, Lisa L.</creator><creator>Capuano, Ana W.</creator><creator>Aiello, Alison E.</creator><creator>Turner, Arlener D.</creator><creator>Yolken, Robert H.</creator><creator>Torrey, E. 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Fuller</au><au>Bennett, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytomegalovirus Infection and Risk of Alzheimer Disease in Older Black and White Individuals</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2015-01-15</date><risdate>2015</risdate><volume>211</volume><issue>2</issue><spage>230</spage><epage>237</epage><pages>230-237</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Background. Human cytomegalovirus (CMV) is prevalent in older adults and has been implicated in many chronic diseases of aging. This study investigated the relation between CMV and the risk of Alzheimer disease (AD). Methods. Data come from 3 cohort studies that included 849 participants (mean age [± SD], 78.6 ± 7.2 years; mean education duration [± SD], 15.4 ± 3.3 years; 25% black). Results. A solid-phase enzyme-linked immunosorbent assay was used for detecting type-specific immunoglobulin G antibody responses to CMV and herpes simplex virus type 1 (HSV-1) measured in archived serum samples. Of 849 participants, 73.4% had serologie evidence of exposure to CMV (89.0% black and 68.2% white; P&lt; .001). During an average of 5.0 years of follow-up, 93 persons developed AD. CMV seropositivity was associated with an increased risk of AD (relative risk, 2.15; 95% confidence interval, 1.42-3.27) and a faster rate of decline in global cognition (estimate [± standard error], -0.02 ± 0.01; P = .03) in models that controlled for age, sex, education duration, race, vascular risk factors, vascular diseases, and apolipoprotein ε4 level. Results were similar in black and white individuals for both incident AD and change in cognitive function and were independent of HSV-1 status. Conclusions. 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subjects African Continental Ancestry Group
Age Factors
Aged
Aged, 80 and over
Alzheimer Disease - epidemiology
Cohort Studies
Cytomegalovirus Infections - complications
European Continental Ancestry Group
Female
Herpes simplex virus 1
Human cytomegalovirus
Humans
Longitudinal Studies
Major and Brief Reports
Male
Prevalence
Risk Assessment
Time Factors
VIRUSES
title Cytomegalovirus Infection and Risk of Alzheimer Disease in Older Black and White Individuals
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