Assessment of Disease Severity in Parkinsonism with Fluorine-18-Fluorodeoxyglucose and PET
Fluorine-18-fluorodeoxyglucose (FDG) and PET have been used to identify an abnormal regional metabolic covariance pattern in Parkinson's disease (PD). To examine the potential use of this covariance pattern as a metabolic imaging marker for PD, we describe the Topographic Profile Rating (TPR),...
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Veröffentlicht in: | The Journal of nuclear medicine (1978) 1995-03, Vol.36 (3), p.378-383 |
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creator | Eidelberg, David Moeller, James R Ishikawa, Tatsuya Dhawan, Vijay Spetsieris, Phoebe Chaly, Thomas Robeson, William Dahl, J. Robert Margouleff, Donald |
description | Fluorine-18-fluorodeoxyglucose (FDG) and PET have been used to identify an abnormal regional metabolic covariance pattern in Parkinson's disease (PD). To examine the potential use of this covariance pattern as a metabolic imaging marker for PD, we describe the Topographic Profile Rating (TPR), which is a method for calculating subject scores for this pattern in individual PD patients. We then assess the relationship between these metabolic measures and objective independent disease severity ratings.
Two independent groups of PD patients were studied with FDG-PET. Group A consisted of 23 patients (mean age 60.2 +/- 12.2; mean Hoehn and Yahr stages 2.4 +/- 1.3) and Group B had 14 patients (mean age 49.0 +/- 12.1; mean Hoehn and Yahr stage 3.2 +/- 1.2). The regional cerebral metabolic rates for glucose (rCMRGlc) in all patients in each group were measured. TPR was used to calculate subject scores for the disease-related covariance pattern on a patient-by-patient basis.
In both PD patient groups, subject scores correlated with Hoehn and Yahr disease severity ratings (Group A: r = 0.59, p < 0.004; Group B: 0.57, p < 0.04), quantitative ratings for bradykinesia (Group A: r = 0.63, p < 0.002; Group B: r = 0.61, p < 0.03), rigidity (Group A: r = 0.59, p < 0.004; Group B: r = 0.59, p < 0.04), but not with tremor.
These findings indicate that regional metabolic covariance patterns are robust imaging markers of disease severity. FDG-PET may be useful clinically in assessing parkinsonian disability and disease progression. |
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Two independent groups of PD patients were studied with FDG-PET. Group A consisted of 23 patients (mean age 60.2 +/- 12.2; mean Hoehn and Yahr stages 2.4 +/- 1.3) and Group B had 14 patients (mean age 49.0 +/- 12.1; mean Hoehn and Yahr stage 3.2 +/- 1.2). The regional cerebral metabolic rates for glucose (rCMRGlc) in all patients in each group were measured. TPR was used to calculate subject scores for the disease-related covariance pattern on a patient-by-patient basis.
In both PD patient groups, subject scores correlated with Hoehn and Yahr disease severity ratings (Group A: r = 0.59, p < 0.004; Group B: 0.57, p < 0.04), quantitative ratings for bradykinesia (Group A: r = 0.63, p < 0.002; Group B: r = 0.61, p < 0.03), rigidity (Group A: r = 0.59, p < 0.004; Group B: r = 0.59, p < 0.04), but not with tremor.
These findings indicate that regional metabolic covariance patterns are robust imaging markers of disease severity. FDG-PET may be useful clinically in assessing parkinsonian disability and disease progression.]]></description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>PMID: 7884498</identifier><language>eng</language><publisher>Reston, VA: Soc Nuclear Med</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Brain - diagnostic imaging ; Deoxyglucose - analogs & derivatives ; Female ; Fluorine Radioisotopes ; Fluorodeoxyglucose F18 ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Nervous system ; Parkinson Disease - diagnostic imaging ; Radionuclide investigations ; Severity of Illness Index ; Tomography, Emission-Computed</subject><ispartof>The Journal of nuclear medicine (1978), 1995-03, Vol.36 (3), p.378-383</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3448542$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7884498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eidelberg, David</creatorcontrib><creatorcontrib>Moeller, James R</creatorcontrib><creatorcontrib>Ishikawa, Tatsuya</creatorcontrib><creatorcontrib>Dhawan, Vijay</creatorcontrib><creatorcontrib>Spetsieris, Phoebe</creatorcontrib><creatorcontrib>Chaly, Thomas</creatorcontrib><creatorcontrib>Robeson, William</creatorcontrib><creatorcontrib>Dahl, J. Robert</creatorcontrib><creatorcontrib>Margouleff, Donald</creatorcontrib><title>Assessment of Disease Severity in Parkinsonism with Fluorine-18-Fluorodeoxyglucose and PET</title><title>The Journal of nuclear medicine (1978)</title><addtitle>J Nucl Med</addtitle><description><![CDATA[Fluorine-18-fluorodeoxyglucose (FDG) and PET have been used to identify an abnormal regional metabolic covariance pattern in Parkinson's disease (PD). To examine the potential use of this covariance pattern as a metabolic imaging marker for PD, we describe the Topographic Profile Rating (TPR), which is a method for calculating subject scores for this pattern in individual PD patients. We then assess the relationship between these metabolic measures and objective independent disease severity ratings.
Two independent groups of PD patients were studied with FDG-PET. Group A consisted of 23 patients (mean age 60.2 +/- 12.2; mean Hoehn and Yahr stages 2.4 +/- 1.3) and Group B had 14 patients (mean age 49.0 +/- 12.1; mean Hoehn and Yahr stage 3.2 +/- 1.2). The regional cerebral metabolic rates for glucose (rCMRGlc) in all patients in each group were measured. TPR was used to calculate subject scores for the disease-related covariance pattern on a patient-by-patient basis.
In both PD patient groups, subject scores correlated with Hoehn and Yahr disease severity ratings (Group A: r = 0.59, p < 0.004; Group B: 0.57, p < 0.04), quantitative ratings for bradykinesia (Group A: r = 0.63, p < 0.002; Group B: r = 0.61, p < 0.03), rigidity (Group A: r = 0.59, p < 0.004; Group B: r = 0.59, p < 0.04), but not with tremor.
These findings indicate that regional metabolic covariance patterns are robust imaging markers of disease severity. FDG-PET may be useful clinically in assessing parkinsonian disability and disease progression.]]></description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Brain - diagnostic imaging</subject><subject>Deoxyglucose - analogs & derivatives</subject><subject>Female</subject><subject>Fluorine Radioisotopes</subject><subject>Fluorodeoxyglucose F18</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system</subject><subject>Parkinson Disease - diagnostic imaging</subject><subject>Radionuclide investigations</subject><subject>Severity of Illness Index</subject><subject>Tomography, Emission-Computed</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLw0AUhQdRaq3-BCELcReYR-aRZamtCgUL1o2bMJ3ctFOTmTqTWPvvrRp0dQ-c75wL5wQNCWc85ULIUzTERJCUc8zP0UWMW4yxUEoN0EAqlWW5GqLXcYwQYwOuTXyV3NkIOkLyDB8QbHtIrEsWOrxZF72zsUn2tt0ks7rzwTpIiUp_tC_Bfx7WdWf8MaxdmSymy0t0Vuk6wlV_R-hlNl1OHtL50_3jZDxPN1SINgVFTcU0VjkxpTRUZlIQSY1UWLKM85U0REuMc2wY05LmgGnJmSgzRnJNKzZCt7-9u-DfO4ht0dhooK61A9_FQkoi8pyKI3jdg92qgbLYBdvocCj6MY7-Te_raHRdBe2MjX8YyzLFM_r_b2PXm70NULjO1KDDd-fWNUwUrGBSsS_NGnV_</recordid><startdate>19950301</startdate><enddate>19950301</enddate><creator>Eidelberg, David</creator><creator>Moeller, James R</creator><creator>Ishikawa, Tatsuya</creator><creator>Dhawan, Vijay</creator><creator>Spetsieris, Phoebe</creator><creator>Chaly, Thomas</creator><creator>Robeson, William</creator><creator>Dahl, J. Robert</creator><creator>Margouleff, Donald</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>7X8</scope></search><sort><creationdate>19950301</creationdate><title>Assessment of Disease Severity in Parkinsonism with Fluorine-18-Fluorodeoxyglucose and PET</title><author>Eidelberg, David ; Moeller, James R ; Ishikawa, Tatsuya ; Dhawan, Vijay ; Spetsieris, Phoebe ; Chaly, Thomas ; Robeson, William ; Dahl, J. Robert ; Margouleff, Donald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h266t-e82cf3a0891cd7c27476172c78073455b7c1a70090c33a729e02d536d4319a2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Brain - diagnostic imaging</topic><topic>Deoxyglucose - analogs & derivatives</topic><topic>Female</topic><topic>Fluorine Radioisotopes</topic><topic>Fluorodeoxyglucose F18</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system</topic><topic>Parkinson Disease - diagnostic imaging</topic><topic>Radionuclide investigations</topic><topic>Severity of Illness Index</topic><topic>Tomography, Emission-Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eidelberg, David</creatorcontrib><creatorcontrib>Moeller, James R</creatorcontrib><creatorcontrib>Ishikawa, Tatsuya</creatorcontrib><creatorcontrib>Dhawan, Vijay</creatorcontrib><creatorcontrib>Spetsieris, Phoebe</creatorcontrib><creatorcontrib>Chaly, Thomas</creatorcontrib><creatorcontrib>Robeson, William</creatorcontrib><creatorcontrib>Dahl, J. Robert</creatorcontrib><creatorcontrib>Margouleff, Donald</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>MEDLINE - Academic</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eidelberg, David</au><au>Moeller, James R</au><au>Ishikawa, Tatsuya</au><au>Dhawan, Vijay</au><au>Spetsieris, Phoebe</au><au>Chaly, Thomas</au><au>Robeson, William</au><au>Dahl, J. Robert</au><au>Margouleff, Donald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of Disease Severity in Parkinsonism with Fluorine-18-Fluorodeoxyglucose and PET</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><addtitle>J Nucl Med</addtitle><date>1995-03-01</date><risdate>1995</risdate><volume>36</volume><issue>3</issue><spage>378</spage><epage>383</epage><pages>378-383</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract><![CDATA[Fluorine-18-fluorodeoxyglucose (FDG) and PET have been used to identify an abnormal regional metabolic covariance pattern in Parkinson's disease (PD). To examine the potential use of this covariance pattern as a metabolic imaging marker for PD, we describe the Topographic Profile Rating (TPR), which is a method for calculating subject scores for this pattern in individual PD patients. We then assess the relationship between these metabolic measures and objective independent disease severity ratings.
Two independent groups of PD patients were studied with FDG-PET. Group A consisted of 23 patients (mean age 60.2 +/- 12.2; mean Hoehn and Yahr stages 2.4 +/- 1.3) and Group B had 14 patients (mean age 49.0 +/- 12.1; mean Hoehn and Yahr stage 3.2 +/- 1.2). The regional cerebral metabolic rates for glucose (rCMRGlc) in all patients in each group were measured. TPR was used to calculate subject scores for the disease-related covariance pattern on a patient-by-patient basis.
In both PD patient groups, subject scores correlated with Hoehn and Yahr disease severity ratings (Group A: r = 0.59, p < 0.004; Group B: 0.57, p < 0.04), quantitative ratings for bradykinesia (Group A: r = 0.63, p < 0.002; Group B: r = 0.61, p < 0.03), rigidity (Group A: r = 0.59, p < 0.004; Group B: r = 0.59, p < 0.04), but not with tremor.
These findings indicate that regional metabolic covariance patterns are robust imaging markers of disease severity. FDG-PET may be useful clinically in assessing parkinsonian disability and disease progression.]]></abstract><cop>Reston, VA</cop><pub>Soc Nuclear Med</pub><pmid>7884498</pmid><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Biological and medical sciences Brain - diagnostic imaging Deoxyglucose - analogs & derivatives Female Fluorine Radioisotopes Fluorodeoxyglucose F18 Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Nervous system Parkinson Disease - diagnostic imaging Radionuclide investigations Severity of Illness Index Tomography, Emission-Computed |
title | Assessment of Disease Severity in Parkinsonism with Fluorine-18-Fluorodeoxyglucose and PET |
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