NASH Predicts Plasma Inflammatory Biomarkers Independently of Visceral Fat in Men
We assessed the differential contribution of nonalcoholic steatohepatitis (NASH) and visceral adiposity to nontraditional cardiovascular risk biomarkers in adult men. We enrolled 45 consecutive, overweight, male patients with biopsy‐proven NASH, 45 overweight male patients without ultrasound‐diagnos...
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Veröffentlicht in: | Obesity (Silver Spring, Md.) Md.), 2008-06, Vol.16 (6), p.1394-1399 |
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description | We assessed the differential contribution of nonalcoholic steatohepatitis (NASH) and visceral adiposity to nontraditional cardiovascular risk biomarkers in adult men. We enrolled 45 consecutive, overweight, male patients with biopsy‐proven NASH, 45 overweight male patients without ultrasound‐diagnosed hepatic steatosis, and 45 healthy male volunteers. All participants were matched for age; NASH and overweight patients were also matched for BMI and visceral adiposity (as estimated by abdominal ultrasonography). Nontraditional cardiovascular risk biomarkers were measured in all participants. Plasma concentrations of high‐sensitivity C‐reactive protein (hs‐CRP), fibrinogen, plasminogen activator inhibitor‐1 (PAI‐1) activity, and adiponectin were markedly different among the groups; the lowest values (the highest for adiponectin) were in nonobese healthy subjects, intermediate in overweight nonsteatotic patients, and the highest (the lowest for adiponectin) in those with biopsy‐proven NASH. The marked differences in these cardiovascular risk biomarkers that were observed between overweight and NASH patients were only slightly weakened after adjustment for age, BMI, smoking, plasma triglycerides, and insulin resistance (IR) as assessed by homeostasis model assessment (HOMA). In multivariate regression analysis, NASH and visceral adiposity predicted cardiovascular risk biomarkers independently of potential confounders. In conclusion, our results suggest that NASH can predict a more atherogenic risk profile in a manner that is partly independent from the contribution of visceral adiposity in adult men. |
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We enrolled 45 consecutive, overweight, male patients with biopsy‐proven NASH, 45 overweight male patients without ultrasound‐diagnosed hepatic steatosis, and 45 healthy male volunteers. All participants were matched for age; NASH and overweight patients were also matched for BMI and visceral adiposity (as estimated by abdominal ultrasonography). Nontraditional cardiovascular risk biomarkers were measured in all participants. Plasma concentrations of high‐sensitivity C‐reactive protein (hs‐CRP), fibrinogen, plasminogen activator inhibitor‐1 (PAI‐1) activity, and adiponectin were markedly different among the groups; the lowest values (the highest for adiponectin) were in nonobese healthy subjects, intermediate in overweight nonsteatotic patients, and the highest (the lowest for adiponectin) in those with biopsy‐proven NASH. The marked differences in these cardiovascular risk biomarkers that were observed between overweight and NASH patients were only slightly weakened after adjustment for age, BMI, smoking, plasma triglycerides, and insulin resistance (IR) as assessed by homeostasis model assessment (HOMA). In multivariate regression analysis, NASH and visceral adiposity predicted cardiovascular risk biomarkers independently of potential confounders. In conclusion, our results suggest that NASH can predict a more atherogenic risk profile in a manner that is partly independent from the contribution of visceral adiposity in adult men.</description><identifier>ISSN: 1930-7381</identifier><identifier>EISSN: 1930-739X</identifier><identifier>DOI: 10.1038/oby.2008.64</identifier><identifier>PMID: 18369343</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adiponectin - blood ; Biomarkers ; Biomarkers - blood ; Biopsy ; Body fat ; C-Reactive Protein - metabolism ; Cardiovascular Diseases - epidemiology ; Case-Control Studies ; Enzymes ; Epidemiology ; Fatty Liver - blood ; Fibrinogen - metabolism ; Hepatitis ; Homeostasis ; Hospitals ; Humans ; Inflammation - blood ; Inflammation - physiopathology ; Insulin resistance ; Insulin Resistance - physiology ; Intra-Abdominal Fat - metabolism ; Linear Models ; Liver diseases ; Male ; Metabolic syndrome ; Middle Aged ; Obesity ; Obesity - blood ; Overweight ; Plasma ; Plasminogen Activator Inhibitor 1 - blood ; Predictive Value of Tests ; Risk Factors ; Triglycerides - blood ; Ultrasonic imaging</subject><ispartof>Obesity (Silver Spring, Md.), 2008-06, Vol.16 (6), p.1394-1399</ispartof><rights>2008 North American Association for the Study of Obesity (NAASO)</rights><rights>Copyright Nature Publishing Group Jun 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4596-b178e75ec3af537fb1a8e04a97ee74730c7d62ba186ca6fd3eb64acd49c108983</citedby><cites>FETCH-LOGICAL-c4596-b178e75ec3af537fb1a8e04a97ee74730c7d62ba186ca6fd3eb64acd49c108983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1038%2Foby.2008.64$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1038%2Foby.2008.64$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18369343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Targher, Giovanni</creatorcontrib><creatorcontrib>Bertolini, Lorenzo</creatorcontrib><creatorcontrib>Rodella, Stefano</creatorcontrib><creatorcontrib>Lippi, Giuseppe</creatorcontrib><creatorcontrib>Franchini, Massimo</creatorcontrib><creatorcontrib>Zoppini, Giacomo</creatorcontrib><creatorcontrib>Muggeo, Michele</creatorcontrib><creatorcontrib>Day, Christopher P.</creatorcontrib><title>NASH Predicts Plasma Inflammatory Biomarkers Independently of Visceral Fat in Men</title><title>Obesity (Silver Spring, Md.)</title><addtitle>Obesity (Silver Spring)</addtitle><description>We assessed the differential contribution of nonalcoholic steatohepatitis (NASH) and visceral adiposity to nontraditional cardiovascular risk biomarkers in adult men. We enrolled 45 consecutive, overweight, male patients with biopsy‐proven NASH, 45 overweight male patients without ultrasound‐diagnosed hepatic steatosis, and 45 healthy male volunteers. All participants were matched for age; NASH and overweight patients were also matched for BMI and visceral adiposity (as estimated by abdominal ultrasonography). Nontraditional cardiovascular risk biomarkers were measured in all participants. Plasma concentrations of high‐sensitivity C‐reactive protein (hs‐CRP), fibrinogen, plasminogen activator inhibitor‐1 (PAI‐1) activity, and adiponectin were markedly different among the groups; the lowest values (the highest for adiponectin) were in nonobese healthy subjects, intermediate in overweight nonsteatotic patients, and the highest (the lowest for adiponectin) in those with biopsy‐proven NASH. The marked differences in these cardiovascular risk biomarkers that were observed between overweight and NASH patients were only slightly weakened after adjustment for age, BMI, smoking, plasma triglycerides, and insulin resistance (IR) as assessed by homeostasis model assessment (HOMA). In multivariate regression analysis, NASH and visceral adiposity predicted cardiovascular risk biomarkers independently of potential confounders. In conclusion, our results suggest that NASH can predict a more atherogenic risk profile in a manner that is partly independent from the contribution of visceral adiposity in adult men.</description><subject>Adiponectin - blood</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biopsy</subject><subject>Body fat</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Case-Control Studies</subject><subject>Enzymes</subject><subject>Epidemiology</subject><subject>Fatty Liver - blood</subject><subject>Fibrinogen - metabolism</subject><subject>Hepatitis</subject><subject>Homeostasis</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Inflammation - physiopathology</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - physiology</subject><subject>Intra-Abdominal Fat - metabolism</subject><subject>Linear Models</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Metabolic syndrome</subject><subject>Middle Aged</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Overweight</subject><subject>Plasma</subject><subject>Plasminogen Activator Inhibitor 1 - blood</subject><subject>Predictive Value of Tests</subject><subject>Risk Factors</subject><subject>Triglycerides - blood</subject><subject>Ultrasonic imaging</subject><issn>1930-7381</issn><issn>1930-739X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90M1LwzAYBvAgipvTk3cJCF5kM2myJD1uw7nBdBM_0FNJ07fQ2Y-ZtEj_ezM2FDx4SUL48fC-D0LnlAwoYeqmittBQIgaCH6AujRkpC9Z-Hb481a0g06cWxPCBRnSY9ShiomQcdZFjw-jpxleWUgyUzu8yrUrNJ6Xaa6LQteVbfE4qwptP8A6_5_ABvxR1nmLqxS_Zs6A1Tme6hpnJb6H8hQdpTp3cLa_e-hlevs8mfUXy7v5ZLToGz4MRT-mUoEcgmE6HTKZxlQrIFyHEkByyYiRiQhiTZUwWqQJg1hwbRIeGkpUqFgPXe1yN7b6bMDVUbEdJs91CVXjIklFEDBOPbz8A9dVY0s_W-T7IzzwedKr650ytnLOQhptbOb3bj3aOhX5nqNtz5HgXl_sM5u4gOTX7ov1gOzAV5ZD-19WtBy_U0IF-wZC44bs</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Targher, Giovanni</creator><creator>Bertolini, Lorenzo</creator><creator>Rodella, Stefano</creator><creator>Lippi, Giuseppe</creator><creator>Franchini, Massimo</creator><creator>Zoppini, Giacomo</creator><creator>Muggeo, Michele</creator><creator>Day, Christopher P.</creator><general>Blackwell Publishing Ltd</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>K9.</scope><scope>7X8</scope></search><sort><creationdate>200806</creationdate><title>NASH Predicts Plasma Inflammatory Biomarkers Independently of Visceral Fat in Men</title><author>Targher, Giovanni ; Bertolini, Lorenzo ; Rodella, Stefano ; Lippi, Giuseppe ; Franchini, Massimo ; Zoppini, Giacomo ; Muggeo, Michele ; Day, Christopher P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4596-b178e75ec3af537fb1a8e04a97ee74730c7d62ba186ca6fd3eb64acd49c108983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adiponectin - blood</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Biopsy</topic><topic>Body fat</topic><topic>C-Reactive Protein - metabolism</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>Case-Control Studies</topic><topic>Enzymes</topic><topic>Epidemiology</topic><topic>Fatty Liver - blood</topic><topic>Fibrinogen - metabolism</topic><topic>Hepatitis</topic><topic>Homeostasis</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Inflammation - blood</topic><topic>Inflammation - physiopathology</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - physiology</topic><topic>Intra-Abdominal Fat - metabolism</topic><topic>Linear Models</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Metabolic syndrome</topic><topic>Middle Aged</topic><topic>Obesity</topic><topic>Obesity - blood</topic><topic>Overweight</topic><topic>Plasma</topic><topic>Plasminogen Activator Inhibitor 1 - blood</topic><topic>Predictive Value of Tests</topic><topic>Risk Factors</topic><topic>Triglycerides - blood</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Targher, Giovanni</creatorcontrib><creatorcontrib>Bertolini, Lorenzo</creatorcontrib><creatorcontrib>Rodella, Stefano</creatorcontrib><creatorcontrib>Lippi, Giuseppe</creatorcontrib><creatorcontrib>Franchini, Massimo</creatorcontrib><creatorcontrib>Zoppini, Giacomo</creatorcontrib><creatorcontrib>Muggeo, Michele</creatorcontrib><creatorcontrib>Day, Christopher P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Obesity (Silver Spring, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Targher, Giovanni</au><au>Bertolini, Lorenzo</au><au>Rodella, Stefano</au><au>Lippi, Giuseppe</au><au>Franchini, Massimo</au><au>Zoppini, Giacomo</au><au>Muggeo, Michele</au><au>Day, Christopher P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NASH Predicts Plasma Inflammatory Biomarkers Independently of Visceral Fat in Men</atitle><jtitle>Obesity (Silver Spring, Md.)</jtitle><addtitle>Obesity (Silver Spring)</addtitle><date>2008-06</date><risdate>2008</risdate><volume>16</volume><issue>6</issue><spage>1394</spage><epage>1399</epage><pages>1394-1399</pages><issn>1930-7381</issn><eissn>1930-739X</eissn><abstract>We assessed the differential contribution of nonalcoholic steatohepatitis (NASH) and visceral adiposity to nontraditional cardiovascular risk biomarkers in adult men. We enrolled 45 consecutive, overweight, male patients with biopsy‐proven NASH, 45 overweight male patients without ultrasound‐diagnosed hepatic steatosis, and 45 healthy male volunteers. All participants were matched for age; NASH and overweight patients were also matched for BMI and visceral adiposity (as estimated by abdominal ultrasonography). Nontraditional cardiovascular risk biomarkers were measured in all participants. Plasma concentrations of high‐sensitivity C‐reactive protein (hs‐CRP), fibrinogen, plasminogen activator inhibitor‐1 (PAI‐1) activity, and adiponectin were markedly different among the groups; the lowest values (the highest for adiponectin) were in nonobese healthy subjects, intermediate in overweight nonsteatotic patients, and the highest (the lowest for adiponectin) in those with biopsy‐proven NASH. The marked differences in these cardiovascular risk biomarkers that were observed between overweight and NASH patients were only slightly weakened after adjustment for age, BMI, smoking, plasma triglycerides, and insulin resistance (IR) as assessed by homeostasis model assessment (HOMA). In multivariate regression analysis, NASH and visceral adiposity predicted cardiovascular risk biomarkers independently of potential confounders. In conclusion, our results suggest that NASH can predict a more atherogenic risk profile in a manner that is partly independent from the contribution of visceral adiposity in adult men.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18369343</pmid><doi>10.1038/oby.2008.64</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adiponectin - blood Biomarkers Biomarkers - blood Biopsy Body fat C-Reactive Protein - metabolism Cardiovascular Diseases - epidemiology Case-Control Studies Enzymes Epidemiology Fatty Liver - blood Fibrinogen - metabolism Hepatitis Homeostasis Hospitals Humans Inflammation - blood Inflammation - physiopathology Insulin resistance Insulin Resistance - physiology Intra-Abdominal Fat - metabolism Linear Models Liver diseases Male Metabolic syndrome Middle Aged Obesity Obesity - blood Overweight Plasma Plasminogen Activator Inhibitor 1 - blood Predictive Value of Tests Risk Factors Triglycerides - blood Ultrasonic imaging |
title | NASH Predicts Plasma Inflammatory Biomarkers Independently of Visceral Fat in Men |
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