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
Hauptverfasser: Targher, Giovanni, Bertolini, Lorenzo, Rodella, Stefano, Lippi, Giuseppe, Franchini, Massimo, Zoppini, Giacomo, Muggeo, Michele, Day, Christopher P.
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container_end_page 1399
container_issue 6
container_start_page 1394
container_title Obesity (Silver Spring, Md.)
container_volume 16
creator Targher, Giovanni
Bertolini, Lorenzo
Rodella, Stefano
Lippi, Giuseppe
Franchini, Massimo
Zoppini, Giacomo
Muggeo, Michele
Day, Christopher P.
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.
doi_str_mv 10.1038/oby.2008.64
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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. 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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. 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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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source Wiley Free Content; Wiley Online Library - AutoHoldings Journals; MEDLINE
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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