Literature DB >> 21398601

Circulating inflammatory and endothelial markers and risk of hypertension in white and black postmenopausal women.

Lu Wang1, Joann E Manson, J Michael Gaziano, Simin Liu, Barbara Cochrane, Nancy R Cook, Paul M Ridker, Nader Rifai, Howard D Sesso.   

Abstract

BACKGROUND: Systemic inflammation and endothelial activation are implicated in the development of hypertension. However, epidemiologic studies have yet to compare multiple corresponding biomarkers in relation to risk of hypertension, particularly in multiethnic populations.
METHODS: We identified 800 individuals with incident hypertension and 800 matched controls, each group with equal numbers of white and black women, in a nested case-control study within the Women's Health Initiative Observational Study. We measured markers of inflammation [high-sensitivity C-reactive protein (hsCRP), interleukin (IL)-6, IL-1β, tumor necrosis factor receptor 2 (TNF-r2)] and endothelial activation [soluble intercellular adhesion molecule-1 (sICAM-1)] in baseline blood samples.
RESULTS: Before adjustment for measures of adiposity, higher hsCRP and IL-6 concentrations were associated with increased risk of hypertension in both white and black women, higher TNF-r2 was associated with increased risk of hypertension in black women only, and IL-1β and sICAM-1 were not associated with risk of hypertension. All the positive associations were attenuated after adjustment for body mass index. The resulting multivariable-adjusted relative risks (95% CI) of hypertension comparing the highest vs lowest quartile were 1.52 (0.94-2.48) and 1.23 (0.76-1.97) for hsCRP and IL-6 in white women and 1.30 (0.81-2.07), 1.58 (0.96-2.59), and 1.49 (0.94-2.36) for hsCRP, IL-6, and TNF-r2 in black women. The results after adjustment for waist circumference were similar.
CONCLUSIONS: After adjustment for measures of adiposity, there was no significant association of hsCRP, IL-6, IL-1β, TNF-r2, or sICAM-1 with incident hypertension in either white or black women. The interrelationships between inflammation and adiposity in development of hypertension need further investigation.

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Year:  2011        PMID: 21398601      PMCID: PMC3084895          DOI: 10.1373/clinchem.2010.156794

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  39 in total

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2.  Multiple biomarkers and the risk of incident hypertension.

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4.  Interrelationships among circulating interleukin-6, C-reactive protein, and traditional cardiovascular risk factors in women.

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6.  Comparison of interleukin-6 and C-reactive protein for the risk of developing hypertension in women.

Authors:  Howard D Sesso; Lu Wang; Julie E Buring; Paul M Ridker; J Michael Gaziano
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7.  High sensitivity C-reactive protein as an independent risk factor for essential hypertension.

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10.  Cellular adhesion molecules and blood pressure: interaction with sex in a multi-ethnic population.

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1.  Association of Periodontal Disease and Edentulism With Hypertension Risk in Postmenopausal Women.

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4.  Inflammation markers and risk of developing hypertension: a meta-analysis of cohort studies.

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5.  Association of clinical measures of periodontal disease with blood pressure and hypertension among postmenopausal women.

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6.  Plasma Inflammatory Markers and the Risk of Developing Hypertension in Men.

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7.  Evaluation of Toll-Like receptor 2 and 4 RNA expression and the cytokine profile in postmenopausal women with metabolic syndrome.

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8.  Sex-Specific Associations Between Alcohol Consumption and Incidence of Hypertension: A Systematic Review and Meta-Analysis of Cohort Studies.

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Journal:  J Am Heart Assoc       Date:  2018-06-27       Impact factor: 5.501

9.  The association between high-sensitivity C-reactive protein and hypertension in women of the CARDIA study.

Authors:  Imo A Ebong; Pamela Schreiner; Cora E Lewis; Duke Appiah; Azmina Ghelani; Mellissa Wellons
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10.  The association of glycemic index and glycemic load with elevated blood pressure in Iranian women.

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Journal:  J Cardiovasc Thorac Res       Date:  2019-10-24
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