Related Experiment Video
Updated: Jun 1, 2026

Mouse Electroacupuncture Fixation Device Fabrication for Electroacupuncture Pretreatment in Diabetic Cardiomyopathy Mouse Model
Published on: April 18, 2025
Adiponectin in chronic heart failure: influence of diabetes and genetic variants
Serge Masson1, Francesca Gori, Roberto Latini
1Department of Cardiovascular Research, Istituto di Ricerche Farmacologiche "Mario Negri", Milan, Italy. serge.masson@marionegri.it
Insights
Higher adiponectin levels in chronic heart failure (CHF) patients predict poor prognosis, independent of type 2 diabetes (T2D) and body mass index (BMI). Genetic variants in the ADIPOQ gene influence adiponectin levels but not its prognostic value.
Area of Science:
- Cardiology
- Genetics
- Metabolic Syndrome
Background:
- Circulating adiponectin levels are influenced by type 2 diabetes (T2D) and body mass index (BMI).
- The prognostic significance of adiponectin in chronic heart failure (CHF) requires further investigation, considering potential confounders.
- The association between ADIPOQ gene variants and adiponectin concentration in CHF patients is not fully understood.
Purpose of the Study:
- To investigate the association between ADIPOQ gene variants and circulating adiponectin levels in patients with CHF.
- To evaluate the influence of T2D, BMI, and ADIPOQ gene variants on the prognostic value of adiponectin in CHF.
- To determine the relationship between adiponectin concentration and mortality in CHF patients.
Main Methods:
- Plasma adiponectin levels and four ADIPOQ gene single-nucleotide polymorphisms (SNPs) were analyzed in approximately 1200 CHF patients from the GISSI-HF trial.
- Associations between adiponectin levels, ADIPOQ SNPs, clinical characteristics, and mortality were assessed.
- The impact of T2D and other confounders on adiponectin's prognostic value was evaluated.
Main Results:
- Adiponectin levels were inversely related to BMI, higher in women and older individuals, and lower in patients with diabetes.
- Specific ADIPOQ gene variants (rs1501299 and rs17300539) were associated with significantly elevated adiponectin concentrations.
- Baseline plasma adiponectin independently predicted mortality in CHF patients, irrespective of diabetes status, and improved risk prediction beyond established factors.
- Increasing adiponectin levels over 3 months were associated with worse outcomes, though this association was attenuated by genetic variants and confounders.
Conclusions:
- Circulating adiponectin levels, but not ADIPOQ genetic variants, are consistently associated with poor prognosis in CHF patients.
- While diabetes and ADIPOQ gene variants affect adiponectin levels, elevated adiponectin is a significant predictor of mortality in CHF.
- Adiponectin's prognostic value in CHF is robust but can be influenced by factors like T2D, BMI, and age.
Background:
We hypothesized that, besides type 2 diabetes (T2D) and body mass index (BMI), circulating adiponectin concentration would be associated with variants of the ADIPOQ gene in patients with chronic heart failure (CHF). We also assessed the influence of these confounders on the prognostic value of adiponectin.
Methods:
Plasma adiponectin was measured at entry and after 3 months in approximately 1200 patients with CHF enrolled in the GISSI-HF trial. Four common single-nucleotide polymorphisms (SNPs) spanning the ADIPOQ gene were studied: rs17300539 (-11391G→A), rs266729 (-11377C→G), rs2241766 (+45T→G) and rs1501299 (+276G→T). Associations with clinical characteristics and mortality were evaluated in patients with or without T2D.
Results:
Adiponectin concentrations were negatively related to BMI, higher in women and older persons, but lower in patients with diabetes. T-allele carriers for rs1501299 and A-allele carriers for rs17300539 had significantly elevated adiponectin concentrations. Irrespective of diabetes, baseline plasma adiponectin was independently associated with mortality (adjusted HR [95%CI] per 1 SD increase in adiponectin concentration = 1·24[1·12-1·37], P < 0·0001) and improved prognostic discrimination beyond clinical risk factors (integrated discrimination improvement, P = 0·005). Patients with increasing adiponectin concentration over 3 months had worse outcome than those with stable levels (unadjusted HR = 1·46[1·09-1·96], P = 0·01); this relation was attenuated by the genetic variants examined and by robust confounders like age, diabetes, BMI or NT-proBNP (adjusted HR = 1·37[0·97-1·94], P = 0·075).
Conclusions:
Although diabetes and genetic variants at the ADIPOQ gene influence the circulating levels of adiponectin in CHF, higher plasma adipokine levels, but not genetic variants, are consistently associated with a poor prognosis.
Related Concept Videos
Heart Failure II: Pathophysiology
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Pathophysiology of Heart Failure
Diabetic Nephropathy
Type II Diabetes II: Pathophysiology
Type I Diabetes II: Pathophysiology

