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Vascular stiffness in familial hypercholesterolaemia is associated with C-reactive protein and cholesterol burden

Background  Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims...

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Published in:European journal of clinical investigation 2007-03, Vol.37 (3), p.197-206
Main Authors: Cheng, H. M., Ye, Z. X., Chiou, K. R., Lin, S. J., Charng, M. J.
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description Background  Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims of this study were to quantify atherosclerosis and arterial stiffness and to evaluate their relationship with high sensitive C‐reactive protein (hs‐CRP) and the level of exposure to high serum cholesterol in FH patients. Materials and methods  We measured traditional risk factors, hs‐CRP, intima‐media thickness (IMT) of carotid artery, and brachial‐ankle pulse wave velocity (baPWV) in 35 heterozygous FH subjects and 17 healthy control subjects. Cholesterol‐year score (CYS) was calculated to estimate the lifetime cholesterol burden in FH subjects. Results  FH subjects had significantly elevated total cholesterol, low‐density lipoprotein cholesterol, and carotid IMT compared with those without mutations. Among FH patients, the baPWV and carotid IMT were higher in cases with high cholesterol burden than those without. Similarly, the baPWV and carotid IMT were also higher in cases with elevated hs‐CRP (> 1 mg L−1) than those without. Multiple linear regression analysis demonstrated CYS and hs‐CRP were significant independent predictors of baPWV and IMT in FH patients. Conclusions  Both high cholesterol burden and vascular inflammation are not only associated with atherosclerosis, but also contribute to the development of arterial stiffness in FH patients. Early detection of hypercholesterolaemia in FH patients is warranted to prevent the untoward pathophysiologies.
doi_str_mv 10.1111/j.1365-2362.2007.01772.x
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M. ; Ye, Z. X. ; Chiou, K. R. ; Lin, S. J. ; Charng, M. J.</creator><creatorcontrib>Cheng, H. M. ; Ye, Z. X. ; Chiou, K. R. ; Lin, S. J. ; Charng, M. J.</creatorcontrib><description>Background  Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims of this study were to quantify atherosclerosis and arterial stiffness and to evaluate their relationship with high sensitive C‐reactive protein (hs‐CRP) and the level of exposure to high serum cholesterol in FH patients. Materials and methods  We measured traditional risk factors, hs‐CRP, intima‐media thickness (IMT) of carotid artery, and brachial‐ankle pulse wave velocity (baPWV) in 35 heterozygous FH subjects and 17 healthy control subjects. Cholesterol‐year score (CYS) was calculated to estimate the lifetime cholesterol burden in FH subjects. Results  FH subjects had significantly elevated total cholesterol, low‐density lipoprotein cholesterol, and carotid IMT compared with those without mutations. Among FH patients, the baPWV and carotid IMT were higher in cases with high cholesterol burden than those without. Similarly, the baPWV and carotid IMT were also higher in cases with elevated hs‐CRP (&gt; 1 mg L−1) than those without. Multiple linear regression analysis demonstrated CYS and hs‐CRP were significant independent predictors of baPWV and IMT in FH patients. Conclusions  Both high cholesterol burden and vascular inflammation are not only associated with atherosclerosis, but also contribute to the development of arterial stiffness in FH patients. Early detection of hypercholesterolaemia in FH patients is warranted to prevent the untoward pathophysiologies.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1111/j.1365-2362.2007.01772.x</identifier><identifier>PMID: 17359487</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Arterial stiffness ; atherosclerosis ; Atherosclerosis - genetics ; Atherosclerosis - physiopathology ; Biological and medical sciences ; C-Reactive Protein - physiology ; Case-Control Studies ; Disorders of blood lipids. Hyperlipoproteinemia ; Elasticity ; familial hypercholesterolaemia ; Female ; General aspects ; Humans ; Hypercholesterolemia - genetics ; Hypercholesterolemia - physiopathology ; intima-medial thickness ; Male ; Medical sciences ; Metabolic diseases ; Pedigree ; pulse wave velocity ; Risk Factors ; Tunica Intima - physiopathology ; Vascular Resistance - physiology</subject><ispartof>European journal of clinical investigation, 2007-03, Vol.37 (3), p.197-206</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4352-dd5e026c42e2a720b000fb65b2db7d33e6e45843b70f784a98cf0e33e219041f3</citedby><cites>FETCH-LOGICAL-c4352-dd5e026c42e2a720b000fb65b2db7d33e6e45843b70f784a98cf0e33e219041f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18554531$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17359487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, H. M.</creatorcontrib><creatorcontrib>Ye, Z. X.</creatorcontrib><creatorcontrib>Chiou, K. R.</creatorcontrib><creatorcontrib>Lin, S. J.</creatorcontrib><creatorcontrib>Charng, M. J.</creatorcontrib><title>Vascular stiffness in familial hypercholesterolaemia is associated with C-reactive protein and cholesterol burden</title><title>European journal of clinical investigation</title><addtitle>Eur J Clin Invest</addtitle><description>Background  Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims of this study were to quantify atherosclerosis and arterial stiffness and to evaluate their relationship with high sensitive C‐reactive protein (hs‐CRP) and the level of exposure to high serum cholesterol in FH patients. Materials and methods  We measured traditional risk factors, hs‐CRP, intima‐media thickness (IMT) of carotid artery, and brachial‐ankle pulse wave velocity (baPWV) in 35 heterozygous FH subjects and 17 healthy control subjects. Cholesterol‐year score (CYS) was calculated to estimate the lifetime cholesterol burden in FH subjects. Results  FH subjects had significantly elevated total cholesterol, low‐density lipoprotein cholesterol, and carotid IMT compared with those without mutations. Among FH patients, the baPWV and carotid IMT were higher in cases with high cholesterol burden than those without. Similarly, the baPWV and carotid IMT were also higher in cases with elevated hs‐CRP (&gt; 1 mg L−1) than those without. Multiple linear regression analysis demonstrated CYS and hs‐CRP were significant independent predictors of baPWV and IMT in FH patients. Conclusions  Both high cholesterol burden and vascular inflammation are not only associated with atherosclerosis, but also contribute to the development of arterial stiffness in FH patients. Early detection of hypercholesterolaemia in FH patients is warranted to prevent the untoward pathophysiologies.</description><subject>Adult</subject><subject>Arterial stiffness</subject><subject>atherosclerosis</subject><subject>Atherosclerosis - genetics</subject><subject>Atherosclerosis - physiopathology</subject><subject>Biological and medical sciences</subject><subject>C-Reactive Protein - physiology</subject><subject>Case-Control Studies</subject><subject>Disorders of blood lipids. Hyperlipoproteinemia</subject><subject>Elasticity</subject><subject>familial hypercholesterolaemia</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Hypercholesterolemia - genetics</subject><subject>Hypercholesterolemia - physiopathology</subject><subject>intima-medial thickness</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Pedigree</subject><subject>pulse wave velocity</subject><subject>Risk Factors</subject><subject>Tunica Intima - physiopathology</subject><subject>Vascular Resistance - physiology</subject><issn>0014-2972</issn><issn>1365-2362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNkE9v0zAYxi0EYmXwFZAvcEvw3zg9cEDVGJMq_gm2o-U4r1UXJ-nshLXffs5abRzxxZb9e14_-iGEKSlpXh-2JeWVLBivWMkIUSWhSrFy_wwtHh-eowUhVBRsqdgZepXSlhBSU85eojOquFyKWi3Q7bVJdgom4jR653pICfseO9P54E3Am8MOot0MAdIIcQgGOm-wT9ikNFhvRmjxnR83eFVEMHb0fwHv4jBCHmL6Fv8Txc0UW-hfoxfOhARvTvs5-v354tfqS7H-dnm1-rQurOCSFW0rgbDKCgbMKEaa3N41lWxY26iWc6hAyFrwRhGnamGWtXUE8j2jSyKo4-fo_XFurnM75Q6688lCCKaHYUpa5emcE5rB-gjaOKQUweld9J2JB02JnnXrrZ6t6tmqnnXrB916n6NvT39MTQftU_DkNwPvTkDWbIKLprc-PXG1lELyucPHI3fnAxz-u4C-WF3Np5wvjnmfXe8f8yb-0ZXiSuqbr5daiZ_XN-L7D73m96iirCY</recordid><startdate>200703</startdate><enddate>200703</enddate><creator>Cheng, H. M.</creator><creator>Ye, Z. X.</creator><creator>Chiou, K. R.</creator><creator>Lin, S. J.</creator><creator>Charng, M. J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>200703</creationdate><title>Vascular stiffness in familial hypercholesterolaemia is associated with C-reactive protein and cholesterol burden</title><author>Cheng, H. M. ; Ye, Z. X. ; Chiou, K. R. ; Lin, S. J. ; Charng, M. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4352-dd5e026c42e2a720b000fb65b2db7d33e6e45843b70f784a98cf0e33e219041f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Arterial stiffness</topic><topic>atherosclerosis</topic><topic>Atherosclerosis - genetics</topic><topic>Atherosclerosis - physiopathology</topic><topic>Biological and medical sciences</topic><topic>C-Reactive Protein - physiology</topic><topic>Case-Control Studies</topic><topic>Disorders of blood lipids. Hyperlipoproteinemia</topic><topic>Elasticity</topic><topic>familial hypercholesterolaemia</topic><topic>Female</topic><topic>General aspects</topic><topic>Humans</topic><topic>Hypercholesterolemia - genetics</topic><topic>Hypercholesterolemia - physiopathology</topic><topic>intima-medial thickness</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Pedigree</topic><topic>pulse wave velocity</topic><topic>Risk Factors</topic><topic>Tunica Intima - physiopathology</topic><topic>Vascular Resistance - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, H. M.</creatorcontrib><creatorcontrib>Ye, Z. X.</creatorcontrib><creatorcontrib>Chiou, K. R.</creatorcontrib><creatorcontrib>Lin, S. J.</creatorcontrib><creatorcontrib>Charng, M. J.</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>European journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, H. M.</au><au>Ye, Z. X.</au><au>Chiou, K. R.</au><au>Lin, S. J.</au><au>Charng, M. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular stiffness in familial hypercholesterolaemia is associated with C-reactive protein and cholesterol burden</atitle><jtitle>European journal of clinical investigation</jtitle><addtitle>Eur J Clin Invest</addtitle><date>2007-03</date><risdate>2007</risdate><volume>37</volume><issue>3</issue><spage>197</spage><epage>206</epage><pages>197-206</pages><issn>0014-2972</issn><eissn>1365-2362</eissn><abstract>Background  Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims of this study were to quantify atherosclerosis and arterial stiffness and to evaluate their relationship with high sensitive C‐reactive protein (hs‐CRP) and the level of exposure to high serum cholesterol in FH patients. Materials and methods  We measured traditional risk factors, hs‐CRP, intima‐media thickness (IMT) of carotid artery, and brachial‐ankle pulse wave velocity (baPWV) in 35 heterozygous FH subjects and 17 healthy control subjects. Cholesterol‐year score (CYS) was calculated to estimate the lifetime cholesterol burden in FH subjects. Results  FH subjects had significantly elevated total cholesterol, low‐density lipoprotein cholesterol, and carotid IMT compared with those without mutations. Among FH patients, the baPWV and carotid IMT were higher in cases with high cholesterol burden than those without. Similarly, the baPWV and carotid IMT were also higher in cases with elevated hs‐CRP (&gt; 1 mg L−1) than those without. Multiple linear regression analysis demonstrated CYS and hs‐CRP were significant independent predictors of baPWV and IMT in FH patients. Conclusions  Both high cholesterol burden and vascular inflammation are not only associated with atherosclerosis, but also contribute to the development of arterial stiffness in FH patients. Early detection of hypercholesterolaemia in FH patients is warranted to prevent the untoward pathophysiologies.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17359487</pmid><doi>10.1111/j.1365-2362.2007.01772.x</doi><tpages>10</tpages></addata></record>
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subjects Adult
Arterial stiffness
atherosclerosis
Atherosclerosis - genetics
Atherosclerosis - physiopathology
Biological and medical sciences
C-Reactive Protein - physiology
Case-Control Studies
Disorders of blood lipids. Hyperlipoproteinemia
Elasticity
familial hypercholesterolaemia
Female
General aspects
Humans
Hypercholesterolemia - genetics
Hypercholesterolemia - physiopathology
intima-medial thickness
Male
Medical sciences
Metabolic diseases
Pedigree
pulse wave velocity
Risk Factors
Tunica Intima - physiopathology
Vascular Resistance - physiology
title Vascular stiffness in familial hypercholesterolaemia is associated with C-reactive protein and cholesterol burden
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