Author/Editor | Szabó, Tibor; Lainščak, Mitja | |
Title | Plasma adiponectin in heart failure with and without cachexia | |
Type | članek | |
Publication year | 2013 | |
Volume | str. 1-7 | |
ISSN | 0939-4753 - Nutrition, metabolism, and cardiovascular diseases : NMCD | |
Language | eng | |
Abstract | Background and aims: Adiponectin (ADPN) as an adipose tissue hormone contributes to regulation of energy metabolism and body composition and is associated with cardiovascular risk profile parameters. Cardiac cachexia may develop as a result of severe catabolic derangement in chronic heart failure (CHF). We aimed to determinate an abnormal ADPN regulation as a link between catabolic signalling, symptomatic deterioration and poor prognosis. Methods and results: We measured plasma ADPN in 111 CHF patients (age 65 +- 11,90% male, left ventricular ejection fraction (LVEF) 36 +- 11%, peak oxygen consumption (peakVO2) 18.1 +- 5.7 l/kg*min, body mass index (BMI) 27 +- 4 kg/m2, all mean +- standard deviation) and 36 healthy controls of similar age and BMI. Body composition was assessed by dual energy X-ray absorptiometry, insulin sensitivity was evaluated by homoeostasis model assessment, exercise capacity by spiroergometry. Plasma ADPN did not differ between CHF vs. controls (13.5 +- 11.0 vs. 10.5 +- 5.3 mg/l, p > 0.4), but increased stepwise with NZHA functional class (I/II/III: 5.7 +- 1.4/10.7 +- 8.3/19.2 +- 14.0 mg/l, ANOVA p < 0.01). Furthermore, ADPN correlated with VO2 at anaerobic threshold (r = -0.34, p < 0.05). ADPN was highest in cachectic patients (cCHF, 16%) vs. non-cachectic (ncCHF) (18.7 +- 15.0 vs. 12.5 +- 9.9 mg/l; p < 0.05). ADPN indicated mortality risk independently of established prognosticators (HR: 1.04 95% CI: 1.02-1.07; p < 0.0001). ADPN above the mean (13.5 mg/l) was associated with a 3.4 times higher mortality risk in CHF vs. patients with ADPN levels below the mean. Conclusion: Circulating ADPN is abnormally regulated in CHF. ADPN may be involved in impaired metabolic signalling linking disease progression, tissue wasting, and poor outcome in CHF. | |
Keywords | chronic heart failure cachexia metabolism adiponectin |