Is There Really an Association of High Circulating Adiponectin Concentration and Mortality or Morbidity Risk in Stable Coronary Artery Disease?
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
Agency of the Czech Ministry of Health
17-29520A
Charles University Research Fund
PROGRES, project Q39
Academic Research Project of Charles University
SVV-2020-2022
Academic Research Project of Charles University
260 537
PubMed
32746485
DOI
10.1055/a-1212-8759
Knihovny.cz E-resources
- MeSH
- Adiponectin blood MeSH
- Biomarkers blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Survival Rate MeSH
- Morbidity MeSH
- Follow-Up Studies MeSH
- Coronary Artery Disease blood epidemiology genetics mortality MeSH
- Prognosis MeSH
- Prospective Studies MeSH
- Cross-Sectional Studies MeSH
- Risk Factors MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Names of Substances
- Adiponectin MeSH
- ADIPOQ protein, human MeSH Browser
- Biomarkers MeSH
Adiponectin has several beneficial properties, namely, on the level of glucose metabolism, but paradoxically, its high concentrations were associated with increased mortality. We aimed to clarify the impact of high serum adiponectin on mortality and morbidity in patients with stable coronary artery heart disease (CAD). A total of 973 patients after myocardial infarction and/or coronary revascularization were followed in a prospective cohort study. All-cause and cardiovascular (CV) death, non-fatal cardiovascular events, and hospitalizations for heart failure (HF) were registered as outcomes. High serum adiponectin levels (≥8.58 ng/ml, i. e., above median) were independently associated with increased risk of 5-year all-cause, CV mortality or HF [with HRR 1.57 (95% CI: 1.07-2.30), 1.74 (95% CI: 1.08-2.81) or 1.94 (95% CI: 1.20-3.12), respectively] when adjusted just for conventional risk factors. However, its significance disappeared if brain natriuretic peptide (BNP) was included in a regression model. In line with this, we observed strong collinearity of adiponectin and BNP. Additionally, major adverse cardiovascular event (i. e., CV death, non-fatal myocardial infarction or stroke, coronary revascularization) incidence risk was not associated with high adiponectin. In conclusion, the observed inverse association between adiponectin concentrations and mortality risk seems to be attributable to concomitantly increased BNP, rather than high adiponectin being a causal factor.
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