Loading…

Accelerated and accentuated neurocognitive aging in HIV infection

There is debate as to whether the neurocognitive changes associated with HIV infection represent an acceleration of the typical aging process or more simply reflect a greater accentuated risk for age-related declines. We aimed to determine whether accelerated neurocognitive aging is observable in a...

Full description

Saved in:
Bibliographic Details
Published in:Journal of neurovirology 2017-06, Vol.23 (3), p.492-500
Main Authors: Sheppard, David P., Iudicello, Jennifer E., Morgan, Erin E., Kamat, Rujvi, Clark, Lindsay R., Avci, Gunes, Bondi, Mark W., Woods, Steven Paul
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653
cites cdi_FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653
container_end_page 500
container_issue 3
container_start_page 492
container_title Journal of neurovirology
container_volume 23
creator Sheppard, David P.
Iudicello, Jennifer E.
Morgan, Erin E.
Kamat, Rujvi
Clark, Lindsay R.
Avci, Gunes
Bondi, Mark W.
Woods, Steven Paul
description There is debate as to whether the neurocognitive changes associated with HIV infection represent an acceleration of the typical aging process or more simply reflect a greater accentuated risk for age-related declines. We aimed to determine whether accelerated neurocognitive aging is observable in a sample of older HIV-infected individuals compared to age-matched seronegatives and older old (i.e., aged ≥65) seronegative adults. Participants in a cross-sectional design included 48 HIV-seronegative (O−) and 40 HIV-positive (O+) participants between the ages of 50–65 (mean ages = 55 and 56, respectively) and 40 HIV-seronegative participants aged ≥65 (OO−; mean age = 74) who were comparable for other demographics. All participants were administered a brief neurocognitive battery of attention, episodic memory, speeded executive functions, and confrontation naming (i.e., Boston Naming Test). The O+ group performed more poorly than the O− group (i.e., accentuated aging), but not differently from the OO− on digit span and initial recall of a supraspan word list, consistent with an accelerating aging profile. However, the O+ group’s performance was comparable to the O− group on all other neurocognitive tests ( p s > 0.05). These data partially support a model of accelerated neurocognitive aging in HIV infection, which was observed in the domain of auditory verbal attention, but not in the areas of memory, language, or speeded executive functions. Future studies should examine whether HIV-infected adults over 65 evidence accelerated aging in downstream neurocognitive domains and subsequent everyday functioning outcomes.
doi_str_mv 10.1007/s13365-017-0523-2
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5441968</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1879667784</sourcerecordid><originalsourceid>FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653</originalsourceid><addsrcrecordid>eNp9kEtLAzEUhYMoPqo_wI106WY0r0kyG6GI2kLBjboNmcydMaVNNJkp-O9NbRXduAg3l3Puyc2H0DnBVwRjeZ0IY6IsMJEFLikr6B46JiVTBeWc7ec7K7NKFT9CJyktMCZMUHWIjqhilIhKHKPJxFpYQjQ9NGPj88m974ev3sMQgw2dd71bw9h0zndj58fT2UsuLdjeBX-KDlqzTHC2qyP0fH_3dDst5o8Ps9vJvLCc074gjTIgbSVaUtfA25q0rKor0wCVosWYN3XdUMBK1IRXpiRZERI3rVUWpCjZCN1sc9-GegXNZstolvotupWJHzoYp_8q3r3qLqx1yTmphMoBl7uAGN4HSL1euZQ_vzQewpA0UbISQkrFs5VsrTaGlCK0P88QrDfo9Ra9zuj1Br2meebi934_E9-ss4FuDSlLvoOoF2GIPjP7J_UTnoOQ2Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1879667784</pqid></control><display><type>article</type><title>Accelerated and accentuated neurocognitive aging in HIV infection</title><source>Springer Link</source><creator>Sheppard, David P. ; Iudicello, Jennifer E. ; Morgan, Erin E. ; Kamat, Rujvi ; Clark, Lindsay R. ; Avci, Gunes ; Bondi, Mark W. ; Woods, Steven Paul</creator><creatorcontrib>Sheppard, David P. ; Iudicello, Jennifer E. ; Morgan, Erin E. ; Kamat, Rujvi ; Clark, Lindsay R. ; Avci, Gunes ; Bondi, Mark W. ; Woods, Steven Paul ; HIV Neurobehavioral Research Program (HNRP) Group ; The HIV Neurobehavioral Research Program (HNRP) Group</creatorcontrib><description>There is debate as to whether the neurocognitive changes associated with HIV infection represent an acceleration of the typical aging process or more simply reflect a greater accentuated risk for age-related declines. We aimed to determine whether accelerated neurocognitive aging is observable in a sample of older HIV-infected individuals compared to age-matched seronegatives and older old (i.e., aged ≥65) seronegative adults. Participants in a cross-sectional design included 48 HIV-seronegative (O−) and 40 HIV-positive (O+) participants between the ages of 50–65 (mean ages = 55 and 56, respectively) and 40 HIV-seronegative participants aged ≥65 (OO−; mean age = 74) who were comparable for other demographics. All participants were administered a brief neurocognitive battery of attention, episodic memory, speeded executive functions, and confrontation naming (i.e., Boston Naming Test). The O+ group performed more poorly than the O− group (i.e., accentuated aging), but not differently from the OO− on digit span and initial recall of a supraspan word list, consistent with an accelerating aging profile. However, the O+ group’s performance was comparable to the O− group on all other neurocognitive tests ( p s &gt; 0.05). These data partially support a model of accelerated neurocognitive aging in HIV infection, which was observed in the domain of auditory verbal attention, but not in the areas of memory, language, or speeded executive functions. Future studies should examine whether HIV-infected adults over 65 evidence accelerated aging in downstream neurocognitive domains and subsequent everyday functioning outcomes.</description><identifier>ISSN: 1355-0284</identifier><identifier>EISSN: 1538-2443</identifier><identifier>DOI: 10.1007/s13365-017-0523-2</identifier><identifier>PMID: 28321696</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Aged ; Aging ; Attention - physiology ; Biomedical and Life Sciences ; Biomedicine ; Cognitive Dysfunction - diagnosis ; Cognitive Dysfunction - physiopathology ; Cognitive Dysfunction - virology ; Cross-Sectional Studies ; Executive Function - physiology ; Female ; HIV Infections - diagnosis ; HIV Infections - physiopathology ; HIV Infections - virology ; Humans ; Immunology ; Infectious Diseases ; Male ; Memory - physiology ; Middle Aged ; Neurology ; Neuropsychological Tests ; Neurosciences ; Time Factors ; Virology</subject><ispartof>Journal of neurovirology, 2017-06, Vol.23 (3), p.492-500</ispartof><rights>Journal of NeuroVirology, Inc. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653</citedby><cites>FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28321696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sheppard, David P.</creatorcontrib><creatorcontrib>Iudicello, Jennifer E.</creatorcontrib><creatorcontrib>Morgan, Erin E.</creatorcontrib><creatorcontrib>Kamat, Rujvi</creatorcontrib><creatorcontrib>Clark, Lindsay R.</creatorcontrib><creatorcontrib>Avci, Gunes</creatorcontrib><creatorcontrib>Bondi, Mark W.</creatorcontrib><creatorcontrib>Woods, Steven Paul</creatorcontrib><creatorcontrib>HIV Neurobehavioral Research Program (HNRP) Group</creatorcontrib><creatorcontrib>The HIV Neurobehavioral Research Program (HNRP) Group</creatorcontrib><title>Accelerated and accentuated neurocognitive aging in HIV infection</title><title>Journal of neurovirology</title><addtitle>J. Neurovirol</addtitle><addtitle>J Neurovirol</addtitle><description>There is debate as to whether the neurocognitive changes associated with HIV infection represent an acceleration of the typical aging process or more simply reflect a greater accentuated risk for age-related declines. We aimed to determine whether accelerated neurocognitive aging is observable in a sample of older HIV-infected individuals compared to age-matched seronegatives and older old (i.e., aged ≥65) seronegative adults. Participants in a cross-sectional design included 48 HIV-seronegative (O−) and 40 HIV-positive (O+) participants between the ages of 50–65 (mean ages = 55 and 56, respectively) and 40 HIV-seronegative participants aged ≥65 (OO−; mean age = 74) who were comparable for other demographics. All participants were administered a brief neurocognitive battery of attention, episodic memory, speeded executive functions, and confrontation naming (i.e., Boston Naming Test). The O+ group performed more poorly than the O− group (i.e., accentuated aging), but not differently from the OO− on digit span and initial recall of a supraspan word list, consistent with an accelerating aging profile. However, the O+ group’s performance was comparable to the O− group on all other neurocognitive tests ( p s &gt; 0.05). These data partially support a model of accelerated neurocognitive aging in HIV infection, which was observed in the domain of auditory verbal attention, but not in the areas of memory, language, or speeded executive functions. Future studies should examine whether HIV-infected adults over 65 evidence accelerated aging in downstream neurocognitive domains and subsequent everyday functioning outcomes.</description><subject>Aged</subject><subject>Aging</subject><subject>Attention - physiology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Cognitive Dysfunction - physiopathology</subject><subject>Cognitive Dysfunction - virology</subject><subject>Cross-Sectional Studies</subject><subject>Executive Function - physiology</subject><subject>Female</subject><subject>HIV Infections - diagnosis</subject><subject>HIV Infections - physiopathology</subject><subject>HIV Infections - virology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Male</subject><subject>Memory - physiology</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Neurosciences</subject><subject>Time Factors</subject><subject>Virology</subject><issn>1355-0284</issn><issn>1538-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLAzEUhYMoPqo_wI106WY0r0kyG6GI2kLBjboNmcydMaVNNJkp-O9NbRXduAg3l3Puyc2H0DnBVwRjeZ0IY6IsMJEFLikr6B46JiVTBeWc7ec7K7NKFT9CJyktMCZMUHWIjqhilIhKHKPJxFpYQjQ9NGPj88m974ev3sMQgw2dd71bw9h0zndj58fT2UsuLdjeBX-KDlqzTHC2qyP0fH_3dDst5o8Ps9vJvLCc074gjTIgbSVaUtfA25q0rKor0wCVosWYN3XdUMBK1IRXpiRZERI3rVUWpCjZCN1sc9-GegXNZstolvotupWJHzoYp_8q3r3qLqx1yTmphMoBl7uAGN4HSL1euZQ_vzQewpA0UbISQkrFs5VsrTaGlCK0P88QrDfo9Ra9zuj1Br2meebi934_E9-ss4FuDSlLvoOoF2GIPjP7J_UTnoOQ2Q</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Sheppard, David P.</creator><creator>Iudicello, Jennifer E.</creator><creator>Morgan, Erin E.</creator><creator>Kamat, Rujvi</creator><creator>Clark, Lindsay R.</creator><creator>Avci, Gunes</creator><creator>Bondi, Mark W.</creator><creator>Woods, Steven Paul</creator><general>Springer International Publishing</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><scope>5PM</scope></search><sort><creationdate>20170601</creationdate><title>Accelerated and accentuated neurocognitive aging in HIV infection</title><author>Sheppard, David P. ; Iudicello, Jennifer E. ; Morgan, Erin E. ; Kamat, Rujvi ; Clark, Lindsay R. ; Avci, Gunes ; Bondi, Mark W. ; Woods, Steven Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Aging</topic><topic>Attention - physiology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Cognitive Dysfunction - physiopathology</topic><topic>Cognitive Dysfunction - virology</topic><topic>Cross-Sectional Studies</topic><topic>Executive Function - physiology</topic><topic>Female</topic><topic>HIV Infections - diagnosis</topic><topic>HIV Infections - physiopathology</topic><topic>HIV Infections - virology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Male</topic><topic>Memory - physiology</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Neurosciences</topic><topic>Time Factors</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheppard, David P.</creatorcontrib><creatorcontrib>Iudicello, Jennifer E.</creatorcontrib><creatorcontrib>Morgan, Erin E.</creatorcontrib><creatorcontrib>Kamat, Rujvi</creatorcontrib><creatorcontrib>Clark, Lindsay R.</creatorcontrib><creatorcontrib>Avci, Gunes</creatorcontrib><creatorcontrib>Bondi, Mark W.</creatorcontrib><creatorcontrib>Woods, Steven Paul</creatorcontrib><creatorcontrib>HIV Neurobehavioral Research Program (HNRP) Group</creatorcontrib><creatorcontrib>The HIV Neurobehavioral Research Program (HNRP) Group</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurovirology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheppard, David P.</au><au>Iudicello, Jennifer E.</au><au>Morgan, Erin E.</au><au>Kamat, Rujvi</au><au>Clark, Lindsay R.</au><au>Avci, Gunes</au><au>Bondi, Mark W.</au><au>Woods, Steven Paul</au><aucorp>HIV Neurobehavioral Research Program (HNRP) Group</aucorp><aucorp>The HIV Neurobehavioral Research Program (HNRP) Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accelerated and accentuated neurocognitive aging in HIV infection</atitle><jtitle>Journal of neurovirology</jtitle><stitle>J. Neurovirol</stitle><addtitle>J Neurovirol</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>23</volume><issue>3</issue><spage>492</spage><epage>500</epage><pages>492-500</pages><issn>1355-0284</issn><eissn>1538-2443</eissn><abstract>There is debate as to whether the neurocognitive changes associated with HIV infection represent an acceleration of the typical aging process or more simply reflect a greater accentuated risk for age-related declines. We aimed to determine whether accelerated neurocognitive aging is observable in a sample of older HIV-infected individuals compared to age-matched seronegatives and older old (i.e., aged ≥65) seronegative adults. Participants in a cross-sectional design included 48 HIV-seronegative (O−) and 40 HIV-positive (O+) participants between the ages of 50–65 (mean ages = 55 and 56, respectively) and 40 HIV-seronegative participants aged ≥65 (OO−; mean age = 74) who were comparable for other demographics. All participants were administered a brief neurocognitive battery of attention, episodic memory, speeded executive functions, and confrontation naming (i.e., Boston Naming Test). The O+ group performed more poorly than the O− group (i.e., accentuated aging), but not differently from the OO− on digit span and initial recall of a supraspan word list, consistent with an accelerating aging profile. However, the O+ group’s performance was comparable to the O− group on all other neurocognitive tests ( p s &gt; 0.05). These data partially support a model of accelerated neurocognitive aging in HIV infection, which was observed in the domain of auditory verbal attention, but not in the areas of memory, language, or speeded executive functions. Future studies should examine whether HIV-infected adults over 65 evidence accelerated aging in downstream neurocognitive domains and subsequent everyday functioning outcomes.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>28321696</pmid><doi>10.1007/s13365-017-0523-2</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1355-0284
ispartof Journal of neurovirology, 2017-06, Vol.23 (3), p.492-500
issn 1355-0284
1538-2443
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5441968
source Springer Link
subjects Aged
Aging
Attention - physiology
Biomedical and Life Sciences
Biomedicine
Cognitive Dysfunction - diagnosis
Cognitive Dysfunction - physiopathology
Cognitive Dysfunction - virology
Cross-Sectional Studies
Executive Function - physiology
Female
HIV Infections - diagnosis
HIV Infections - physiopathology
HIV Infections - virology
Humans
Immunology
Infectious Diseases
Male
Memory - physiology
Middle Aged
Neurology
Neuropsychological Tests
Neurosciences
Time Factors
Virology
title Accelerated and accentuated neurocognitive aging in HIV infection
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T18%3A15%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Accelerated%20and%20accentuated%20neurocognitive%20aging%20in%20HIV%20infection&rft.jtitle=Journal%20of%20neurovirology&rft.au=Sheppard,%20David%20P.&rft.aucorp=HIV%20Neurobehavioral%20Research%20Program%20(HNRP)%20Group&rft.date=2017-06-01&rft.volume=23&rft.issue=3&rft.spage=492&rft.epage=500&rft.pages=492-500&rft.issn=1355-0284&rft.eissn=1538-2443&rft_id=info:doi/10.1007/s13365-017-0523-2&rft_dat=%3Cproquest_pubme%3E1879667784%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c442t-1d8ae7c96f1bbe4fb1f39b9ade276f004dbbd2e086b149a51ade670dfc8ce7653%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1879667784&rft_id=info:pmid/28321696&rfr_iscdi=true