Literature DB >> 25945865

Effect of Carvedilol on Serum Heart-type Fatty Acid-binding Protein, Brain Natriuretic Peptide, and Cardiac Function in Patients With Chronic Heart Failure.

Yu-Ping Sun1, Chao-Ping Wei, Shao-Chun Ma, Yuan-Feng Zhang, Ling-Yan Qiao, De-Hua Li, Ruo-Bing Shan.   

Abstract

OBJECTIVE: To observe the changes of serum heart-type fatty acid-binding protein (h-FABP) and brain natriuretic peptide (BNP) in children with chronic heart failure (CHF) and evaluate the effects of carvedilol.
METHODS: A total of 36 patients with CHF, including 17 of endocardial fibroelastosis and 19 of dilated cardiomyopathy, were enrolled and were randomly divided into a carvedilol treatment group (group A) and a conventional treatment group (group B). Group A (n = 16) was treated with carvedilol and conventional treatment and group B (n = 20) was managed with conventional treatment only. Thirty healthy children were enrolled as controls. The concentrations of serum h-FABP and BNP were measured by enzyme-linked immunosorbent assay, and the left ventricular end-systolic diameter, left ventricular end-diastolic diameter, left ventricular ejection fraction (LVEF), left ventricular fractional shortening (LVFS), and cardiac index (CI) were measured by echocardiography.
RESULTS: The concentrations of serum h-FABP and BNP in patients with CHF were significantly higher than in the control group (21.7 ± 4.3 ng/mL vs. 6.3 ± 1.7 ng/mL, 582.4 ± 180.6 pg/mL vs.31.2 ± 9.8 pg/mL, all P < 0.01), positively correlated with the degree of heart failure (all P < 0.01), and were both higher in groups endocardial fibroelastosis and dilated cardiomyopathy than in the control group (all P < 0.01), but there was no statistically significant difference between the 2 groups (P > 0.05). h-FABP concentration in patients with CHF was positively correlated with BNP (r = 0.78, P < 0.01) but negatively correlated with LVEF, LVFS, and CI (r = -0.65, -0.64, and -0.71, respectively; all P < 0.01). BNP concentration was also negatively correlated with LVEF, LVFS, and CI (r = -0.75, -0.61, and -0.79, respectively; all P<0.01). After treatment with carvedilol, the serum concentrations of h-FABP and BNP in group A were lower than in group B, and the magnitude of heart rate reduction, improvement of LVEF, LVFS, and CI, and reduction of left ventricular end-systolic diameter and left ventricular end-diastolic diameter in group A were all greater than in group B (all P < 0.01). Treatment with carvedilol had no adverse events.
CONCLUSIONS: Serum concentrations of h-FABP and BNP can be used as biomarkers to evaluate the severity of heart failure, and carvedilol can significantly improve heart function in children with CHF.

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Year:  2015        PMID: 25945865     DOI: 10.1097/FJC.0000000000000217

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  9 in total

1.  Determination and Comparison of the Solubility, Oil-Water Partition Coefficient, Intestinal Absorption, and Biliary Excretion of Carvedilol Enantiomers.

Authors:  Qi Zhang; Xin Wang; Hongjiao Xue; Baolin Huang; Zimin Lin; Zheng Cai
Journal:  AAPS PharmSciTech       Date:  2021-01-10       Impact factor: 3.246

2.  H-FABP: A beacon of hope for prediabetic heart disease.

Authors:  Priyamvadha Ramesh; Ajay Chauhan; Parul Goyal; Akanksha Singh
Journal:  J Family Med Prim Care       Date:  2020-07-30

Review 3.  Cardiovascular Biomarkers: Lessons of the Past and Prospects for the Future.

Authors:  Farah Omran; Ioannis Kyrou; Faizel Osman; Ven Gee Lim; Harpal Singh Randeva; Kamaljit Chatha
Journal:  Int J Mol Sci       Date:  2022-05-19       Impact factor: 6.208

4.  Heart-type fatty acid-binding protein (H-FABP) and coronary heart disease.

Authors:  Undurti N Das
Journal:  Indian Heart J       Date:  2016-01-12

5.  Chronic inflammation and apoptosis propagate in ischemic cerebellum and heart of non-human primates.

Authors:  Sandra A Acosta; Sherwin Mashkouri; Diana Nwokoye; Jea Y Lee; Cesar V Borlongan
Journal:  Oncotarget       Date:  2017-06-01

6.  Uncovering the Molecular Mechanism of the Qiang-Xin 1 Formula on Sepsis-Induced Cardiac Dysfunction Based on Systems Pharmacology.

Authors:  Shasha He; Jingxia Zhao; Xiaolong Xu; Xuran Cui; Ning Wang; Xuyang Han; Yuhong Guo; Qingquan Liu
Journal:  Oxid Med Cell Longev       Date:  2020-08-27       Impact factor: 6.543

Review 7.  Heart-Type Fatty Acid-Binding Protein (H-FABP) and its Role as a Biomarker in Heart Failure: What Do We Know So Far?

Authors:  Richard Rezar; Peter Jirak; Martha Gschwandtner; Rupert Derler; Thomas K Felder; Michael Haslinger; Kristen Kopp; Clemens Seelmaier; Christina Granitz; Uta C Hoppe; Michael Lichtenauer
Journal:  J Clin Med       Date:  2020-01-07       Impact factor: 4.241

8.  Guanxin Danshen Formulation Protects against Myocardial Ischemia Reperfusion Injury-Induced Left Ventricular Remodeling by Upregulating Estrogen Receptor β.

Authors:  Xuehong Deng; Xiaoyan Xing; Guibo Sun; Xudong Xu; Haifeng Wu; Guang Li; Xiaobo Sun
Journal:  Front Pharmacol       Date:  2017-11-01       Impact factor: 5.810

9.  H2O2 Signaling-Triggered PI3K Mediates Mitochondrial Protection to Participate in Early Cardioprotection by Exercise Preconditioning.

Authors:  Yang Yuan; Shan-Shan Pan; Dong-Feng Wan; Jiao Lu; Yue Huang
Journal:  Oxid Med Cell Longev       Date:  2018-07-25       Impact factor: 6.543

  9 in total

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