epidermal-growth-factor has been researched along with Heart-Failure* in 4 studies
1 review(s) available for epidermal-growth-factor and Heart-Failure
Article | Year |
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[HB-EGF therapy for chronic heart failure].
Topics: Animals; Cardiotonic Agents; Chronic Disease; Epidermal Growth Factor; Heart Failure; Heparin-binding EGF-like Growth Factor; Humans; Intercellular Signaling Peptides and Proteins; Myocytes, Cardiac; Signal Transduction | 2007 |
3 other study(ies) available for epidermal-growth-factor and Heart-Failure
Article | Year |
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Effects of endogenous serum neuregulin-1β on morbidity and mortality in patients with heart failure and left ventricular systolic dysfunction.
Improved left ventricular ejection fraction (LVEF) following administration of recombinant human Neuregulin-1β (NRG), epidermal growth factor (EGF) involved in cardiomyocyte repair/survival, has been observed in patients with systolic heart failure (HF).. Serum NRG was measured by ELISA in 248 patients with NYHA class I-IV HF.. NRG exhibited a marginally significant effect on LVEF trajectory over 11 months (p = 0.07). There is no apparent level of NRG that predicts improved survival.. There is a potential relationship between serum NRG and improved LVEF, indicating the need to investigate the utility of NRG in predicting HF outcomes, including LVEF maintenance. Topics: Epidermal Growth Factor; Female; Heart Failure; Humans; Male; Middle Aged; Neuregulin-1; Neuregulins; Predictive Value of Tests; Prognosis; Stroke Volume; Ventricular Dysfunction, Left | 2018 |
Genetic expression profiles during physiological and pathological cardiac hypertrophy and heart failure in rats.
Cardiac hypertrophy is a complex and nonhomogenous response to various stimuli. In this study, we used high-density oligonucleotide microarray to examine gene expression profiles during physiological hypertrophy, pathological hypertrophy, and heart failure in Dahl salt-sensitive rats. There were changes in 404/3,160 and 874/3,160 genes between physiological and pathological hypertrophy and the transition from hypertrophy to heart failure, respectively. There were increases in stress response genes (e.g., heat shock proteins) and inflammation-related genes (e.g., pancreatitis-associated protein and arachidonate 12-lipoxygenase) in pathological processes but not in physiological hypertrophy. Furthermore, atrial natriuretic factor and brain natriuretic protein showed distinctive changes that are very specific to different conditions. In addition, we used a resampling-based gene score-calculating method to define significantly altered gene clusters, based on Gene Ontology classification. It revealed significant alterations in genes involved in the apoptosis pathway during pathological hypertrophy, suggesting that the apoptosis pathway may play a role during the transition to heart failure. In addition, there were significant changes in glucose/insulin signaling, protein biosynthesis, and epidermal growth factor signaling during physiological hypertrophy but not during pathological hypertrophy. Topics: Animals; Apoptosis; Atrial Natriuretic Factor; Blotting, Northern; Cardiomegaly; Echocardiography; Epidermal Growth Factor; Gene Expression Profiling; Gene Expression Regulation; Heart Failure; Hypertrophy; Inflammation; Insulin; Natriuretic Peptide, Brain; Oligonucleotide Array Sequence Analysis; Pancreatitis-Associated Proteins; Physical Conditioning, Animal; Rats; Rats, Inbred Dahl; RNA; Signal Transduction | 2005 |
Bibliography. Current world literature. Cardiac failure.
Topics: Epidermal Growth Factor; Heart Failure; Humans; Hypertension, Pulmonary; Tumor Necrosis Factor-alpha | 2004 |