4.7 Article

Collagen Cross-Linking But Not Collagen Amount Associates With Elevated Filling Pressures in Hypertensive Patients With Stage C Heart Failure Potential Role of Lysyl Oxidase

期刊

HYPERTENSION
卷 60, 期 3, 页码 677-683

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/HYPERTENSIONAHA.112.196113

关键词

collagen; filling pressures; heart failure

资金

  1. Foundation for Applied Medical Research
  2. Union Temporal de Empresas Proyecto Centro de Investigacion Medica Aplicada
  3. Red Tematica de Investigacion Cooperativa en Enfermedades Cardiovasculares from the Instituto de Salud Carlos III, Ministry of Economy and Competitiveness, Spain [RD06/0014/0008]
  4. European Union [HEALTH-2010-261409, HEALTH-2011-278249]
  5. Ministry of Economy and Competitiveness, Spain [RYC-2010-05797]

向作者/读者索取更多资源

We investigated whether the quality of myocardial collagen associates with elevated left-sided filling pressures in 38 hypertensive patients with stage C chronic heart failure. Filling pressures were assessed invasively measuring pulmonary capillary wedge pressure. Left ventricular chamber stiffness constant was calculated from the deceleration time of the early mitral filling wave. The fraction of myocardial volume occupied by total collagen tissue and collagen type I fibers was assessed histomorphologically. The degree of collagen cross-linking (CCL), which determines the formation of insoluble stiff collagen, was assessed by colorimetric and enzymatic procedures. The expression of lysyl oxidase (LOX), which regulates CCL, was assessed by Western blot. Compared with patients with normal pulmonary capillary wedge pressure (<= 12 mm Hg; n = 16), patients with elevated pulmonary capillary wedge pressure (>12 mm Hg; n = 22) exhibited increases of left ventricular chamber stiffness constant, fraction of myocardial volume occupied by total collagen tissue, fraction of myocardial volume occupied by collagen type I fibers, CCL, insoluble stiff collagen, and LOX. Pulmonary capillary wedge pressure was correlated with left ventricular chamber stiffness constant (r = 0.639; P < 0.001), insoluble stiff collagen (r = 0.474; P < 0.005), CCL (r = 0.625; P < 0.001), and LOX (r = 0.410; P < 0.05) in all of the patients but not with fraction of myocardial volume occupied by total collagen tissue or fraction of myocardial volume occupied by collagen type I fibers. In addition, CCL was correlated with insoluble stiff collagen (r = 0.612; P < 0.005), LOX (r = 0.538; P < 0.01), left ventricular chamber stiffness constant (r = 0.535; P < 0.005), peak filling rate (r =- 0.343; P < 0.05), ejection fraction (r =- 0.430; P < 0.01), and amino-terminal propeptide of brain natriuretic peptide (r = 0.421; P < 0.05) in all of the patients. These associations were independent of confounding factors. These findings indicate that, in hypertensive patients with stage C heart failure, it is only the quality of collagen (ie, degree of cross-linking) that associates with elevated filling pressures. It is suggested that LOX-mediated excessive CCL facilitates the increase in left ventricular stiffness with the resulting elevation of filling pressures in these patients. (Hypertension. 2012; 60: 677-683.) . Online Data Supplement

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