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Adipokines are possible risk markers for aortic stenosis requiring surgery
- Publication Year :
- 2023
-
Abstract
- Objectives: Aortic stenosis (AS) is the most prevalent valvular heart disease among adults. The adipocyte-derived hormones, leptin and adiponectin, have profound metabolic actions. We examined whether these adipokines are independently associated with future aortic valve replacement (AVR). Design: In this longitudinal case-control study, we identified 336 cases who had undergone AVR due to AS, and who had previously participated in population-based health surveys. Two referents were matched to each case and leptin and adiponectin concentrations were analysed from stored baseline survey samples. Uni- and multivariable logistic regression analyses were used to estimate the risk of future AVR. An additional cohort was identified for validation including 106 cases with AVR and 212 matched referents. Results: Median age (interquartile range (IQR)) in years at survey was 59.9 (10.4) and at surgery 68.3 (12.7), and 48% were women. An elevated concentration of leptin was not associated with future AVR (odds ratio [95% confidence interval]) (1.10 [0.92–1.32]), although leptin was associated with a higher risk in patients with coronary artery disease (CAD) having more than 5 years between survey and AVR (1.41 [1.08–1.84]). Adiponectin was not associated with higher risk for future AVR (0.95 [0.82–1.11]), although after stratification for age, higher levels were associated with reduced risk for AVR in persons aged ≥60 years at surgery (0.79 [0.64–0.98]). In the validation study, leptin was associated with future AVR whereas adiponectin was not. None of the associations remained significant after adjustment for body mass index (BMI). Conclusions: The adipokine leptin may promote the development of AS.
Details
- Database :
- OAIster
- Notes :
- Hansén, Nike, Ljungberg, Johan, Bergdahl, Ingvar, Hultdin, Johan, Näslund, Ulf, Johansson, Bengt, Söderberg, Stefan
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1409350245
- Document Type :
- Electronic Resource
- Full Text :
- https://doi.org/10.1080.14017431.2023.2247193