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Plasma insulin-like growth factor I as predictor of progression and all cause mortality in chronic heart failure
Mikkel Andreassen1, Caroline Kistorp, Ilan Raymond
1Department of Endocrinology J, Herlev Hospital, University of Copenhagen, Herlev Ringvej 75, 2730 Herlev, Denmark. andreassenmikkel@hotmail.com
Insights
Insulin-like growth factor I (IGF-I) levels were similar in patients with congestive heart failure (CHF) and healthy individuals. IGF-I did not impact cardiac function or predict mortality risk in CHF patients.
Area of Science:
- Cardiology
- Endocrinology
- Biochemistry
Background:
- Insulin-like growth factor I (IGF-I) is an anabolic hormone with potential roles in cardiac function.
- Reduced IGF-I levels have been hypothesized to contribute to the progression of congestive heart failure (CHF).
Purpose of the Study:
- To compare plasma IGF-I levels between CHF patients and healthy controls.
- To investigate the association between baseline IGF-I levels, cardiac contractility, and prognosis in CHF patients, including all-cause mortality and hospital admissions for worsening CHF.
Main Methods:
- A prospective study involving 194 CHF outpatients and 169 matched controls.
- Echocardiographic examinations were performed at baseline for all participants.
- Patients were followed for a median of 30 months to assess outcomes.
Main Results:
- No significant difference in plasma IGF-I levels was observed between CHF patients and controls.
- IGF-I levels did not correlate with left ventricular ejection fraction (LVEF) or N-terminal B-Type natriuretic peptide (NT-proBNP) levels.
- After adjusting for cardiovascular risk factors, IGF-I levels did not predict overall mortality risk or hospital admission rates for CHF exacerbation.
Conclusions:
- Plasma IGF-I levels are not reduced in patients with CHF compared to healthy individuals.
- Baseline IGF-I levels do not appear to influence cardiac status or long-term prognosis in patients with CHF.
Objectives:
Insulin-like growth factor I (IGF-I) is an anabolic growth factor that seems to increase cardiac contractility. Reduced levels of IGF-I may be implicated in progression of CHF. The objective was to compare plasma IGF-I in CHF patients with healthy controls, and to examine the associations between baseline IGF-I levels, cardiac contractility and the prognosis as judged by all cause mortality and progression of CHF requiring admission to hospital.
Methods:
A prospective study comprising 194 CHF outpatients, and 169 matched controls. All patients and controls underwent echocardiographic examination at baseline. Patients were followed for a median of 30 months.
Results:
There was no difference in IGF-I levels between patients and controls (median and interquartile range), 78 (58-91) vs. 77 (57-94)ng/mL (P=0.92). Age-adjusted IGF-I levels were not related to left ventricular ejection fraction (LVEF) (P=0.58) or levels of N-terminal B-Type natriuretic peptide (NT-proBNP) (P=0.42). During follow-up 44 patients died and 94 were admitted to hospital due to worsening of CHF. Adjusted for cardiovascular risk factors (age, gender, NT-proBNP, lipids, diabetes mellitus, blood pressure, renal function and LVEF) IGF-I levels did not influence the overall mortality risk or the admission rate to hospital, hazard ratio (HR) (95% confidence intervals) 1.05 (0.75-1.47) (P=0.77) and 1.00 (0.80-1.26) (P=0.96), respectively per each SD increase in log IGF-I levels.
Conclusions:
IGF-I levels were not reduced in patients with CHF and did not influence cardiac status at baseline or the prognosis.
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