Department of Public Health and Clinical Medicine, Medicine, Umeå University, Umeå, Sweden.
Department of Biobank Research, Umeå University, Sweden.
Scand Cardiovasc J. 2023 Dec;57(1):2247193. doi: 10.1080/14017431.2023.2247193.
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).
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.
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).
The adipokine leptin may promote the development of AS.
主动脉瓣狭窄(AS)是成年人中最常见的瓣膜性心脏病。脂肪细胞衍生的激素瘦素和脂联素具有深远的代谢作用。我们研究了这些脂肪因子是否与未来的主动脉瓣置换(AVR)独立相关。
在这项纵向病例对照研究中,我们确定了 336 例因 AS 而接受 AVR 的患者,这些患者之前曾参加过基于人群的健康调查。每个病例都匹配了 2 个对照,从储存的基线调查样本中分析瘦素和脂联素浓度。采用单变量和多变量逻辑回归分析来估计未来 AVR 的风险。还确定了一个额外的队列进行验证,包括 106 例 AVR 患者和 212 例匹配的对照。
在调查时,年龄中位数(四分位距(IQR))为 59.9(10.4)岁,手术时为 68.3(12.7)岁,48%为女性。瘦素浓度升高与未来 AVR 无关(比值比[95%置信区间])(1.10[0.92-1.32]),尽管瘦素与在调查和 AVR 之间有超过 5 年时间的冠心病(CAD)患者的风险增加有关(1.41[1.08-1.84])。脂联素与未来 AVR 风险增加无关(0.95[0.82-1.11]),但在按年龄分层后,对于手术时年龄≥60 岁的人,较高水平与 AVR 风险降低相关(0.79[0.64-0.98])。在验证研究中,瘦素与未来 AVR 相关,而脂联素则不相关。在调整体重指数(BMI)后,这些关联均无统计学意义。
脂肪因子瘦素可能促进 AS 的发展。