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High-sensitivity C-reactive protein at different stages of atherosclerosis: results of the INVADE study
Evidence on the role of high-sensitivity C-reactive protein (hsCRP) at different stages of atherosclerosis is limited. We therefore analyzed the relationship between hsCRP and measures of subclinical and advanced atherosclerosis in a population-based sample of the INVADE study ( n = 3,092, >55 y...
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Published in: | Journal of neurology 2009-05, Vol.256 (5), p.783-791 |
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description | Evidence on the role of high-sensitivity C-reactive protein (hsCRP) at different stages of atherosclerosis is limited. We therefore analyzed the relationship between hsCRP and measures of subclinical and advanced atherosclerosis in a population-based sample of the INVADE study (
n
= 3,092, >55 years). The parameters of interest were IMT, ABI, and the stage of atherosclerosis. Differences between participants with normal and pathological hsCRP were analyzed by
t
test for independent samples or Fishers’ exact test. Differences of hsCRP between IMT quartiles, ABI quartiles, and different stages of atherosclerosis were analyzed by one-way ANOVA. Adjusted stepwise multiple linear regression analysis (IMT and ABI) and adjusted analysis of variance (stage of atherosclerosis) were performed, including significant baseline parameters as covariates. ANOVA showed significant differences of hsCRP among IMT quartiles, ABI quartiles, and patients with and without atherosclerosis. The adjusted analyses confirmed that the effects of IMT, ABI, and atherosclerosis on hsCRP were independent from other significant baseline parameters, but did not yield a significant difference between subclinical and advanced stages of atherosclerosis. The present analysis indicates an independent relationship between hsCRP and both IMT and ABI as measures of subclinical atherosclerosis. The comparison of subclinical and advanced stages of atherosclerosis yielded no significant difference, indicating that hsCRP is sensitive to identify vascular risk patients, but not suited to monitor progression of the disease. |
doi_str_mv | 10.1007/s00415-009-5017-6 |
format | article |
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n
= 3,092, >55 years). The parameters of interest were IMT, ABI, and the stage of atherosclerosis. Differences between participants with normal and pathological hsCRP were analyzed by
t
test for independent samples or Fishers’ exact test. Differences of hsCRP between IMT quartiles, ABI quartiles, and different stages of atherosclerosis were analyzed by one-way ANOVA. Adjusted stepwise multiple linear regression analysis (IMT and ABI) and adjusted analysis of variance (stage of atherosclerosis) were performed, including significant baseline parameters as covariates. ANOVA showed significant differences of hsCRP among IMT quartiles, ABI quartiles, and patients with and without atherosclerosis. The adjusted analyses confirmed that the effects of IMT, ABI, and atherosclerosis on hsCRP were independent from other significant baseline parameters, but did not yield a significant difference between subclinical and advanced stages of atherosclerosis. The present analysis indicates an independent relationship between hsCRP and both IMT and ABI as measures of subclinical atherosclerosis. The comparison of subclinical and advanced stages of atherosclerosis yielded no significant difference, indicating that hsCRP is sensitive to identify vascular risk patients, but not suited to monitor progression of the disease.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-009-5017-6</identifier><identifier>PMID: 19240956</identifier><identifier>CODEN: JNRYA9</identifier><language>eng</language><publisher>Heidelberg: D. Steinkopff-Verlag</publisher><subject>Aged ; Angina pectoris ; Atherosclerosis ; Atherosclerosis - blood ; Atherosclerosis - diagnostic imaging ; Atherosclerosis - physiopathology ; Biological and medical sciences ; Biomarkers - analysis ; Biomarkers - blood ; Blood Pressure - physiology ; C-Reactive Protein - analysis ; C-Reactive Protein - metabolism ; Cardiovascular disease ; Carotid Stenosis - blood ; Carotid Stenosis - diagnostic imaging ; Carotid Stenosis - physiopathology ; Cohort Studies ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Disease Progression ; Female ; Germany ; Heart attacks ; High density lipoprotein ; Humans ; Inflammation - blood ; Inflammation - complications ; Inflammation - physiopathology ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Middle Aged ; Neurology ; Neuroradiology ; Neurosciences ; Older people ; Original Communication ; Predictive Value of Tests ; Prognosis ; Proteins ; Sensitivity and Specificity ; Severity of Illness Index ; Stroke ; Tibial Arteries - physiopathology ; Triglycerides ; Ultrasonography - methods ; Up-Regulation - physiology ; Variance analysis ; Veins & arteries</subject><ispartof>Journal of neurology, 2009-05, Vol.256 (5), p.783-791</ispartof><rights>Springer-Verlag 2009</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-3764882f7c2bd9da3cbc6117dd7e8879f18f02bb79c74dcd8bdb55614f844a723</citedby><cites>FETCH-LOGICAL-c496t-3764882f7c2bd9da3cbc6117dd7e8879f18f02bb79c74dcd8bdb55614f844a723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21517097$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19240956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schulze Horn, Carla</creatorcontrib><creatorcontrib>Ilg, Ruediger</creatorcontrib><creatorcontrib>Sander, Kerstin</creatorcontrib><creatorcontrib>Bickel, Horst</creatorcontrib><creatorcontrib>Briesenick, Claus</creatorcontrib><creatorcontrib>Hemmer, Bernhard</creatorcontrib><creatorcontrib>Poppert, Holger</creatorcontrib><creatorcontrib>Sander, Dirk</creatorcontrib><title>High-sensitivity C-reactive protein at different stages of atherosclerosis: results of the INVADE study</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Evidence on the role of high-sensitivity C-reactive protein (hsCRP) at different stages of atherosclerosis is limited. We therefore analyzed the relationship between hsCRP and measures of subclinical and advanced atherosclerosis in a population-based sample of the INVADE study (
n
= 3,092, >55 years). The parameters of interest were IMT, ABI, and the stage of atherosclerosis. Differences between participants with normal and pathological hsCRP were analyzed by
t
test for independent samples or Fishers’ exact test. Differences of hsCRP between IMT quartiles, ABI quartiles, and different stages of atherosclerosis were analyzed by one-way ANOVA. Adjusted stepwise multiple linear regression analysis (IMT and ABI) and adjusted analysis of variance (stage of atherosclerosis) were performed, including significant baseline parameters as covariates. ANOVA showed significant differences of hsCRP among IMT quartiles, ABI quartiles, and patients with and without atherosclerosis. The adjusted analyses confirmed that the effects of IMT, ABI, and atherosclerosis on hsCRP were independent from other significant baseline parameters, but did not yield a significant difference between subclinical and advanced stages of atherosclerosis. The present analysis indicates an independent relationship between hsCRP and both IMT and ABI as measures of subclinical atherosclerosis. The comparison of subclinical and advanced stages of atherosclerosis yielded no significant difference, indicating that hsCRP is sensitive to identify vascular risk patients, but not suited to monitor progression of the disease.</description><subject>Aged</subject><subject>Angina pectoris</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - blood</subject><subject>Atherosclerosis - diagnostic imaging</subject><subject>Atherosclerosis - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Biomarkers - blood</subject><subject>Blood Pressure - physiology</subject><subject>C-Reactive Protein - analysis</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cardiovascular disease</subject><subject>Carotid Stenosis - blood</subject><subject>Carotid Stenosis - diagnostic imaging</subject><subject>Carotid Stenosis - physiopathology</subject><subject>Cohort Studies</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Germany</subject><subject>Heart attacks</subject><subject>High density lipoprotein</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Inflammation - complications</subject><subject>Inflammation - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Older people</subject><subject>Original Communication</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><subject>Stroke</subject><subject>Tibial Arteries - physiopathology</subject><subject>Triglycerides</subject><subject>Ultrasonography - methods</subject><subject>Up-Regulation - physiology</subject><subject>Variance analysis</subject><subject>Veins & arteries</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkV1rFDEUhoModq3-AG9kEPQumpPv8a6srS0UvVFvQyYf25TZmZpkCvvvzbpLC4J4k5C8z3tyTl6EXgP5AISoj4UQDgIT0mNBQGH5BK2AM4qBi_4pWhHGCRZM8BP0opRbQohuwnN0Aj3lpBdyhTaXaXODS5hKquk-1V23xjlY1w6hu8tzDWnqbO18ijHkMNWuVLsJpZtju74JeS5u3K-pfOpyKMtY_2hN6q6-_jz7fN4Mi9-9RM-iHUt4ddxP0Y-L8-_rS3z97cvV-uwaO97LipmSXGsalaOD771lbnASQHmvgtaqj6AjocOgeqe4d14PfhBCAo-ac6soO0XvD3Vb77-WUKrZpuLCONopzEsxUlGhGFP_BSmRgjGABr79C7ydlzy1IQwFDYIDFQ2CA-TaV5QcornLaWvzzgAx-6zMISvTsjL7rIxsnjfHwsuwDf7RcQynAe-OgC3OjjHbyaXywFEQoEi_H4UeuNKkaRPyY4f_fv03hj-rnQ</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Schulze Horn, Carla</creator><creator>Ilg, Ruediger</creator><creator>Sander, Kerstin</creator><creator>Bickel, Horst</creator><creator>Briesenick, Claus</creator><creator>Hemmer, Bernhard</creator><creator>Poppert, Holger</creator><creator>Sander, Dirk</creator><general>D. Steinkopff-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20090501</creationdate><title>High-sensitivity C-reactive protein at different stages of atherosclerosis: results of the INVADE study</title><author>Schulze Horn, Carla ; Ilg, Ruediger ; Sander, Kerstin ; Bickel, Horst ; Briesenick, Claus ; Hemmer, Bernhard ; Poppert, Holger ; Sander, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-3764882f7c2bd9da3cbc6117dd7e8879f18f02bb79c74dcd8bdb55614f844a723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Angina pectoris</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - blood</topic><topic>Atherosclerosis - diagnostic imaging</topic><topic>Atherosclerosis - physiopathology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Biomarkers - blood</topic><topic>Blood Pressure - physiology</topic><topic>C-Reactive Protein - analysis</topic><topic>C-Reactive Protein - metabolism</topic><topic>Cardiovascular disease</topic><topic>Carotid Stenosis - blood</topic><topic>Carotid Stenosis - diagnostic imaging</topic><topic>Carotid Stenosis - physiopathology</topic><topic>Cohort Studies</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Germany</topic><topic>Heart attacks</topic><topic>High density lipoprotein</topic><topic>Humans</topic><topic>Inflammation - blood</topic><topic>Inflammation - complications</topic><topic>Inflammation - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Older people</topic><topic>Original Communication</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proteins</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><topic>Stroke</topic><topic>Tibial Arteries - physiopathology</topic><topic>Triglycerides</topic><topic>Ultrasonography - methods</topic><topic>Up-Regulation - physiology</topic><topic>Variance analysis</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schulze Horn, Carla</creatorcontrib><creatorcontrib>Ilg, Ruediger</creatorcontrib><creatorcontrib>Sander, Kerstin</creatorcontrib><creatorcontrib>Bickel, Horst</creatorcontrib><creatorcontrib>Briesenick, Claus</creatorcontrib><creatorcontrib>Hemmer, Bernhard</creatorcontrib><creatorcontrib>Poppert, Holger</creatorcontrib><creatorcontrib>Sander, Dirk</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>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma 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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schulze Horn, Carla</au><au>Ilg, Ruediger</au><au>Sander, Kerstin</au><au>Bickel, Horst</au><au>Briesenick, Claus</au><au>Hemmer, Bernhard</au><au>Poppert, Holger</au><au>Sander, Dirk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-sensitivity C-reactive protein at different stages of atherosclerosis: results of the INVADE study</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>256</volume><issue>5</issue><spage>783</spage><epage>791</epage><pages>783-791</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><coden>JNRYA9</coden><abstract>Evidence on the role of high-sensitivity C-reactive protein (hsCRP) at different stages of atherosclerosis is limited. We therefore analyzed the relationship between hsCRP and measures of subclinical and advanced atherosclerosis in a population-based sample of the INVADE study (
n
= 3,092, >55 years). The parameters of interest were IMT, ABI, and the stage of atherosclerosis. Differences between participants with normal and pathological hsCRP were analyzed by
t
test for independent samples or Fishers’ exact test. Differences of hsCRP between IMT quartiles, ABI quartiles, and different stages of atherosclerosis were analyzed by one-way ANOVA. Adjusted stepwise multiple linear regression analysis (IMT and ABI) and adjusted analysis of variance (stage of atherosclerosis) were performed, including significant baseline parameters as covariates. ANOVA showed significant differences of hsCRP among IMT quartiles, ABI quartiles, and patients with and without atherosclerosis. The adjusted analyses confirmed that the effects of IMT, ABI, and atherosclerosis on hsCRP were independent from other significant baseline parameters, but did not yield a significant difference between subclinical and advanced stages of atherosclerosis. The present analysis indicates an independent relationship between hsCRP and both IMT and ABI as measures of subclinical atherosclerosis. The comparison of subclinical and advanced stages of atherosclerosis yielded no significant difference, indicating that hsCRP is sensitive to identify vascular risk patients, but not suited to monitor progression of the disease.</abstract><cop>Heidelberg</cop><pub>D. Steinkopff-Verlag</pub><pmid>19240956</pmid><doi>10.1007/s00415-009-5017-6</doi><tpages>9</tpages></addata></record> |
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subjects | Aged Angina pectoris Atherosclerosis Atherosclerosis - blood Atherosclerosis - diagnostic imaging Atherosclerosis - physiopathology Biological and medical sciences Biomarkers - analysis Biomarkers - blood Blood Pressure - physiology C-Reactive Protein - analysis C-Reactive Protein - metabolism Cardiovascular disease Carotid Stenosis - blood Carotid Stenosis - diagnostic imaging Carotid Stenosis - physiopathology Cohort Studies Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Disease Progression Female Germany Heart attacks High density lipoprotein Humans Inflammation - blood Inflammation - complications Inflammation - physiopathology Male Medical sciences Medicine Medicine & Public Health Middle Aged Neurology Neuroradiology Neurosciences Older people Original Communication Predictive Value of Tests Prognosis Proteins Sensitivity and Specificity Severity of Illness Index Stroke Tibial Arteries - physiopathology Triglycerides Ultrasonography - methods Up-Regulation - physiology Variance analysis Veins & arteries |
title | High-sensitivity C-reactive protein at different stages of atherosclerosis: results of the INVADE study |
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