Markers of inflammation, metabolic risk factors, and incident heart failure in American Indians: the Strong Heart Study.

MedStar author(s):
Citation: Journal of Clinical Hypertension. 14(1):13-9, 2012 Jan.PMID: 22235819Institution: MedStar Health Research Institute | MedStar Heart & Vascular InstituteForm of publication: Journal ArticleMedline article type(s): Journal Article | Research Support, N.I.H., ExtramuralSubject headings: *C-Reactive Protein/me [Metabolism] | *Fibrinogen/me [Metabolism] | *Heart Failure | *Inflammation | Aged | Biological Markers | Diabetes Mellitus/ep [Epidemiology] | Female | Health Surveys | Heart Failure/ep [Epidemiology] | Heart Failure/et [Etiology] | Heart Failure/me [Metabolism] | Humans | Indians, North American | Inflammation/co [Complications] | Inflammation/me [Metabolism] | Male | Metabolic Syndrome X/ep [Epidemiology] | Middle Aged | Obesity/ep [Epidemiology] | Prevalence | Proportional Hazards Models | Risk Factors | United States/eh [Ethnology] | United States/ep [Epidemiology]Year: 2012Local holdings: Available online from MWHC library: 2001 - presentISSN:
  • 1524-6175
Name of journal: Journal of clinical hypertension (Greenwich, Conn.) Abstract: Inflammation may play a role in increased risk of heart failure (HF) that is associated with obesity, metabolic syndrome (MS), and diabetes. This study investigated associations between inflammatory markers, MS, and incident HF in a population with a high prevalence of diabetes, obesity, and MS. The cohort consisted of 3098 American Indians without prevalent cardiovascular disease who had C-reactive protein (CRP) and fibrinogen measured at the Strong Heart Study phase II examination. Independent associations between inflammatory markers, MS, and HF were analyzed by Cox hazard models. During a mean follow-up of 11 years, 218 participants developed HF. After the adjustment for cardiovascular risk factors, fibrinogen, (hazard ratio [HR], 1.36; 95% confidence interval [CI], 1.15-1.59) but not CRP (HR, 1.25; 95% CI, 0.97-1.32) remained a significant HF predictor. In individuals without diabetes, concomitant presence of MS and elevated CRP or fibrinogen increased HF risk (for MS and CRP: HR, 2.02; 95% CI, 0.95-4.31; for CRP and fibrinogen: HR, 1.75; 95% CI, 0.83-3.72). In a population with a high prevalence of obesity, MS, and diabetes, elevated CRP and fibrinogen increased HF risk. These associations are attenuated by the adjustments for conventional risk factors suggesting that inflammation acts in concert with metabolic and clinical risk factors in increasing HF risk. 2011 Wiley Periodicals, Inc.All authors: Barac A, Best LG, Carter EA, de Simone G, Devereux RB, Dixon DB, Howard BV, Panza JA, Shara NM, Umans JG, Wang H, Yeh JFiscal year: FY2012Digital Object Identifier: Date added to catalog: 2013-09-17
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Item type Current library Collection Call number Status Date due Barcode
Journal Article MedStar Authors Catalog Article 22235819 Available 22235819

Available online from MWHC library: 2001 - present

Inflammation may play a role in increased risk of heart failure (HF) that is associated with obesity, metabolic syndrome (MS), and diabetes. This study investigated associations between inflammatory markers, MS, and incident HF in a population with a high prevalence of diabetes, obesity, and MS. The cohort consisted of 3098 American Indians without prevalent cardiovascular disease who had C-reactive protein (CRP) and fibrinogen measured at the Strong Heart Study phase II examination. Independent associations between inflammatory markers, MS, and HF were analyzed by Cox hazard models. During a mean follow-up of 11 years, 218 participants developed HF. After the adjustment for cardiovascular risk factors, fibrinogen, (hazard ratio [HR], 1.36; 95% confidence interval [CI], 1.15-1.59) but not CRP (HR, 1.25; 95% CI, 0.97-1.32) remained a significant HF predictor. In individuals without diabetes, concomitant presence of MS and elevated CRP or fibrinogen increased HF risk (for MS and CRP: HR, 2.02; 95% CI, 0.95-4.31; for CRP and fibrinogen: HR, 1.75; 95% CI, 0.83-3.72). In a population with a high prevalence of obesity, MS, and diabetes, elevated CRP and fibrinogen increased HF risk. These associations are attenuated by the adjustments for conventional risk factors suggesting that inflammation acts in concert with metabolic and clinical risk factors in increasing HF risk. 2011 Wiley Periodicals, Inc.

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