Cross-sectional relations of multiple biomarkers from distinct biological pathways to brachial artery endothelial function

被引:74
作者
Kathiresan, S
Gona, P
Larson, MG
Vita, JA
Mitchell, GF
Tofler, GH
Levy, D
Newton-Cheh, C
Wang, TJ
Benjamin, EJ
Vasan, RS
机构
[1] Framingham Heart Dis Epidemiol Study, NHLBI, Framingham, MA 01702 USA
[2] Boston Univ, Dept Math & Stat, Boston, MA 02215 USA
[3] Boston Univ, Evans Dept Med, Boston, MA 02215 USA
[4] Boston Univ, Whitaker Cardiovasc Inst, Boston, MA 02215 USA
[5] Cardiovasc Engn Inc, Holliston, MA USA
[6] Royal N Shore Hosp, Sydney, NSW, Australia
[7] MIT, Broad Inst, Program Med & Populat Genet, Cambridge, MA 02139 USA
[8] Harvard Univ, Cambridge, MA 02138 USA
[9] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Cardiol, Boston, MA USA
关键词
atrial natriuretic factor; endothelium; inflammation; natriuretic peptides; renin;
D O I
10.1161/CIRCULATIONAHA.105.580233
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Endothelial dysfunction is a critical intermediate phenotype in the pathogenesis of cardiovascular disease. We evaluated the relative contributions of distinct biological pathways to interindividual variation in endothelial function by relating prototype biomarkers ( representing these pathways) to brachial artery vasodilator function. Methods and Results - We investigated the cross-sectional relations of a panel of 7 biomarkers measured at a routine examination to brachial artery vasodilator function (flow-mediated dilation [FMD] and reactive hyperemia) assessed at a subsequent examination (mean interval, 2.9 years) in 2113 Framingham Heart Study participants (mean age, 61 years; 54% women). We selected biomarkers from 4 biological domains: neurohormonal (N-terminal pro-atrial natriuretic peptide [N-ANP], B-type natriuretic peptide [BNP], renin, aldosterone), hemostatic factors (plasminogen activator inhibitor-1 [PAI-1]), inflammation (C-reactive protein [CRP]), and target organ damage (urine albumin-creatinine ratio). In age- and sex-adjusted models, several biomarkers were related to baseline brachial artery diameter (PAI-1, CRP, urine albumin-creatinine ratio), baseline mean flow (N-ANP, BNP, PAI-1, CRP, aldosterone), FMD (N-ANP, PAI-1, CRP, renin), and reactive hyperemia (BNP, PAI-1, CRP, renin, urine albumin-creatinine ratio). In multivariable analyses relating the 7 biomarkers conjointly to each vascular function measure (adjusting for known risk factors), N-ANP and renin were positively related to FMD (P = 0.001 and P = 0.04, respectively), and N-ANP was inversely related to baseline mean flow velocity (P = 0.01). None of the other biomarkers was significantly related to the vascular function measures studied. Conclusions - In our large community-based sample, a conservative strategy relating several biomarkers to vascular endothelial function identified plasma N-ANP as a key correlate of mean flow under basal conditions and of FMD in response to forearm cuff occlusion.
引用
收藏
页码:938 / 945
页数:8
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