Abnormal Cerebral Glucose Metabolism in HIV-1 Seropositive Subjects with and without Dementia
This study was undertaken in order to extend our previous finding of relative basal ganglia hypermetabolism in AIDS dementia complex (ADC) and to develop clinically useful metabolic indices of CNS involvement in HIV-seropositive (HIV+) subjects. Twenty-one HIV+ subjects (11 with AIDS) underwent FDG-...
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Veröffentlicht in: | The Journal of nuclear medicine (1978) 1996-07, Vol.37 (7), p.1133-1141 |
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creator | Rottenberg, David A Sidtis, John J Strother, Stephen C Schaper, Kirt A Anderson, Jon R Nelson, Mary J Price, Richard W |
description | This study was undertaken in order to extend our previous finding of relative basal ganglia hypermetabolism in AIDS dementia complex (ADC) and to develop clinically useful metabolic indices of CNS involvement in HIV-seropositive (HIV+) subjects.
Twenty-one HIV+ subjects (11 with AIDS) underwent FDG-PET scanning; 12 had a follow-up scan at 6 mo and 4 had a third scan at 12 mo. Forty-three age-matched heterosexual volunteers served as controls. FDG-PET scanning was performed with arterial blood sampling, and scan data were analyzed using the Scaled Subprofile Model (SSM) with principal component analysis.
SSM/principal component analysis of the combined (HIV+ and controls) FDG-PET dataset extracted two major disease-related metabolic components: (a) a nonspecific indicator of cerebral dysfunction, which was significantly correlated with age, cerebral atrophy and ADC stage and (b) the striatum, which was heavily weighted (relatively hypermetabolic) and appeared to provide a disease-specific measure of early CNS involvement.
FDG-PET scans provide quantitative measures of abnormal functional connectivity in HIV-seropositives-with or without AIDS or ADC. These measures, which are robust across centers with respect to instrumentation, scanning technique and disease severity, appear to track the progression of CNS involvement in patients with subclinical neurologic or neuropsychologic dysfunction. |
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Twenty-one HIV+ subjects (11 with AIDS) underwent FDG-PET scanning; 12 had a follow-up scan at 6 mo and 4 had a third scan at 12 mo. Forty-three age-matched heterosexual volunteers served as controls. FDG-PET scanning was performed with arterial blood sampling, and scan data were analyzed using the Scaled Subprofile Model (SSM) with principal component analysis.
SSM/principal component analysis of the combined (HIV+ and controls) FDG-PET dataset extracted two major disease-related metabolic components: (a) a nonspecific indicator of cerebral dysfunction, which was significantly correlated with age, cerebral atrophy and ADC stage and (b) the striatum, which was heavily weighted (relatively hypermetabolic) and appeared to provide a disease-specific measure of early CNS involvement.
FDG-PET scans provide quantitative measures of abnormal functional connectivity in HIV-seropositives-with or without AIDS or ADC. These measures, which are robust across centers with respect to instrumentation, scanning technique and disease severity, appear to track the progression of CNS involvement in patients with subclinical neurologic or neuropsychologic dysfunction.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>PMID: 8965184</identifier><identifier>CODEN: JNMEAQ</identifier><language>eng</language><publisher>Reston, VA: Soc Nuclear Med</publisher><subject>Adult ; AIDS Dementia Complex - diagnosis ; AIDS Dementia Complex - diagnostic imaging ; AIDS Dementia Complex - metabolism ; AIDS/HIV ; Biological and medical sciences ; Brain - diagnostic imaging ; Brain - metabolism ; Case-Control Studies ; Dementia ; Deoxyglucose - analogs & derivatives ; Female ; Fluorine Radioisotopes ; Fluorodeoxyglucose F18 ; Follow-Up Studies ; Glucose - metabolism ; HIV Seropositivity - diagnostic imaging ; HIV Seropositivity - metabolism ; HIV-1 ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Neuropsychological Tests ; Time Factors ; Tomography, Emission-Computed</subject><ispartof>The Journal of nuclear medicine (1978), 1996-07, Vol.37 (7), p.1133-1141</ispartof><rights>1996 INIST-CNRS</rights><rights>Copyright Society of Nuclear Medicine Jul 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3159546$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8965184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rottenberg, David A</creatorcontrib><creatorcontrib>Sidtis, John J</creatorcontrib><creatorcontrib>Strother, Stephen C</creatorcontrib><creatorcontrib>Schaper, Kirt A</creatorcontrib><creatorcontrib>Anderson, Jon R</creatorcontrib><creatorcontrib>Nelson, Mary J</creatorcontrib><creatorcontrib>Price, Richard W</creatorcontrib><title>Abnormal Cerebral Glucose Metabolism in HIV-1 Seropositive Subjects with and without Dementia</title><title>The Journal of nuclear medicine (1978)</title><addtitle>J Nucl Med</addtitle><description>This study was undertaken in order to extend our previous finding of relative basal ganglia hypermetabolism in AIDS dementia complex (ADC) and to develop clinically useful metabolic indices of CNS involvement in HIV-seropositive (HIV+) subjects.
Twenty-one HIV+ subjects (11 with AIDS) underwent FDG-PET scanning; 12 had a follow-up scan at 6 mo and 4 had a third scan at 12 mo. Forty-three age-matched heterosexual volunteers served as controls. FDG-PET scanning was performed with arterial blood sampling, and scan data were analyzed using the Scaled Subprofile Model (SSM) with principal component analysis.
SSM/principal component analysis of the combined (HIV+ and controls) FDG-PET dataset extracted two major disease-related metabolic components: (a) a nonspecific indicator of cerebral dysfunction, which was significantly correlated with age, cerebral atrophy and ADC stage and (b) the striatum, which was heavily weighted (relatively hypermetabolic) and appeared to provide a disease-specific measure of early CNS involvement.
FDG-PET scans provide quantitative measures of abnormal functional connectivity in HIV-seropositives-with or without AIDS or ADC. These measures, which are robust across centers with respect to instrumentation, scanning technique and disease severity, appear to track the progression of CNS involvement in patients with subclinical neurologic or neuropsychologic dysfunction.</description><subject>Adult</subject><subject>AIDS Dementia Complex - diagnosis</subject><subject>AIDS Dementia Complex - diagnostic imaging</subject><subject>AIDS Dementia Complex - metabolism</subject><subject>AIDS/HIV</subject><subject>Biological and medical sciences</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Case-Control Studies</subject><subject>Dementia</subject><subject>Deoxyglucose - analogs & derivatives</subject><subject>Female</subject><subject>Fluorine Radioisotopes</subject><subject>Fluorodeoxyglucose F18</subject><subject>Follow-Up Studies</subject><subject>Glucose - metabolism</subject><subject>HIV Seropositivity - diagnostic imaging</subject><subject>HIV Seropositivity - metabolism</subject><subject>HIV-1</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neuropsychological Tests</subject><subject>Time Factors</subject><subject>Tomography, Emission-Computed</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpd0E1LxDAQBuAiyrqu_gQhiOip0Ek6aXtc1k9QPPhxk5KmUzdLm6xJq_jvre7iwdO8MA8vw-xEU0CBMUqZ7UbTBCTEiAnuRwchrJIkkXmeT6JJXkiEPJ1Gr_PKOt-pli3IU-XHcN0O2gVi99SryrUmdMxYdnP7EgN7JO_WLpjefBB7HKoV6T6wT9MvmbL1b3BDzy6oI9sbdRjtNaoNdLSds-j56vJpcRPfPVzfLuZ38ZIXaR9LTRoolUkhSBYIADITnCNghTWqRoGUADVPNa9J58RVgxlS0ug8rSSvxSw62_SuvXsfKPRlZ4KmtlWW3BDKLAcoMs5HePIPrtzg7XhbyaEA5CjSER1v0VB1VJdrbzrlv8rt08b96XavglZt45XVJvwxAVhgKkd2vmFL87b8NJ5KO-iWlP_pXNlOZGVWAgghvgG4vYKh</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>Rottenberg, David A</creator><creator>Sidtis, John J</creator><creator>Strother, Stephen C</creator><creator>Schaper, Kirt A</creator><creator>Anderson, Jon R</creator><creator>Nelson, Mary J</creator><creator>Price, Richard W</creator><general>Soc Nuclear Med</general><general>Society of Nuclear Medicine</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>19960701</creationdate><title>Abnormal Cerebral Glucose Metabolism in HIV-1 Seropositive Subjects with and without Dementia</title><author>Rottenberg, David A ; Sidtis, John J ; Strother, Stephen C ; Schaper, Kirt A ; Anderson, Jon R ; Nelson, Mary J ; Price, Richard W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h294t-6cec1e46093e69511167322515b5d5afa16611d24c2dec8e2af575e0fc84b62d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>AIDS Dementia Complex - diagnosis</topic><topic>AIDS Dementia Complex - diagnostic imaging</topic><topic>AIDS Dementia Complex - metabolism</topic><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Case-Control Studies</topic><topic>Dementia</topic><topic>Deoxyglucose - analogs & derivatives</topic><topic>Female</topic><topic>Fluorine Radioisotopes</topic><topic>Fluorodeoxyglucose F18</topic><topic>Follow-Up Studies</topic><topic>Glucose - metabolism</topic><topic>HIV Seropositivity - diagnostic imaging</topic><topic>HIV Seropositivity - metabolism</topic><topic>HIV-1</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neuropsychological Tests</topic><topic>Time Factors</topic><topic>Tomography, Emission-Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rottenberg, David A</creatorcontrib><creatorcontrib>Sidtis, John J</creatorcontrib><creatorcontrib>Strother, Stephen C</creatorcontrib><creatorcontrib>Schaper, Kirt A</creatorcontrib><creatorcontrib>Anderson, Jon R</creatorcontrib><creatorcontrib>Nelson, Mary J</creatorcontrib><creatorcontrib>Price, Richard W</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rottenberg, David A</au><au>Sidtis, John J</au><au>Strother, Stephen C</au><au>Schaper, Kirt A</au><au>Anderson, Jon R</au><au>Nelson, Mary J</au><au>Price, Richard W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abnormal Cerebral Glucose Metabolism in HIV-1 Seropositive Subjects with and without Dementia</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><addtitle>J Nucl Med</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>37</volume><issue>7</issue><spage>1133</spage><epage>1141</epage><pages>1133-1141</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><coden>JNMEAQ</coden><abstract>This study was undertaken in order to extend our previous finding of relative basal ganglia hypermetabolism in AIDS dementia complex (ADC) and to develop clinically useful metabolic indices of CNS involvement in HIV-seropositive (HIV+) subjects.
Twenty-one HIV+ subjects (11 with AIDS) underwent FDG-PET scanning; 12 had a follow-up scan at 6 mo and 4 had a third scan at 12 mo. Forty-three age-matched heterosexual volunteers served as controls. FDG-PET scanning was performed with arterial blood sampling, and scan data were analyzed using the Scaled Subprofile Model (SSM) with principal component analysis.
SSM/principal component analysis of the combined (HIV+ and controls) FDG-PET dataset extracted two major disease-related metabolic components: (a) a nonspecific indicator of cerebral dysfunction, which was significantly correlated with age, cerebral atrophy and ADC stage and (b) the striatum, which was heavily weighted (relatively hypermetabolic) and appeared to provide a disease-specific measure of early CNS involvement.
FDG-PET scans provide quantitative measures of abnormal functional connectivity in HIV-seropositives-with or without AIDS or ADC. These measures, which are robust across centers with respect to instrumentation, scanning technique and disease severity, appear to track the progression of CNS involvement in patients with subclinical neurologic or neuropsychologic dysfunction.</abstract><cop>Reston, VA</cop><pub>Soc Nuclear Med</pub><pmid>8965184</pmid><tpages>9</tpages></addata></record> |
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subjects | Adult AIDS Dementia Complex - diagnosis AIDS Dementia Complex - diagnostic imaging AIDS Dementia Complex - metabolism AIDS/HIV Biological and medical sciences Brain - diagnostic imaging Brain - metabolism Case-Control Studies Dementia Deoxyglucose - analogs & derivatives Female Fluorine Radioisotopes Fluorodeoxyglucose F18 Follow-Up Studies Glucose - metabolism HIV Seropositivity - diagnostic imaging HIV Seropositivity - metabolism HIV-1 Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Magnetic Resonance Imaging Male Medical sciences Middle Aged Neuropsychological Tests Time Factors Tomography, Emission-Computed |
title | Abnormal Cerebral Glucose Metabolism in HIV-1 Seropositive Subjects with and without Dementia |
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