Klotho mediates the association between serum testosterone and severe abdominal aortic calcification: a cross-sectional study from the NHANES database.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-09-01 Epub Date: 2025-03-21 DOI:10.1007/s00210-025-04048-4
Shengwei Lai, Handai Qin, Xinhao Wang, Guanchao Sun, Long Cao, Zheqi Fan, Hongpeng Zhang, Wei Guo
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Abstract

Severe abdominal aortic calcification (SAAC) is acknowledged as a significant contributor to cardiovascular morbidity and mortality, yet its relationship with sex steroid hormones remains unclear. Here, the unexplored link between serum sex steroid hormone levels and SAAC was investigated within the National Health and Nutrition Examination Survey (NHANES) cohort. This study utilized data from NHANES 2013-2014. SAAC was determined using the abdominal aortic calcification 24-point scale. Serum sex steroid hormones were categorized into quintiles 1-5 for analysis. Multivariable logistic regression and subgroup analyses were employed to investigate the potential relationship between serum sex steroid hormones and SAAC risk. Moreover, the Johnson-Neyman plot was applied to identify the presence of any threshold effects. Finally, to reveal the potential pathophysiological mechanism, mediation analyses were performed. A total of 1852 enrolled individuals were included, and the prevalence of SAAC stood at 8.00%. After adjusting for potential confounding factors, multivariate analysis suggested the association of higher level of serum testosterone with a reduced incidence of SAAC (AOR = 0.33, 95%CI:0.13-0.87, P = 0.0247 for quintile 5, P for trend = 0.025). Subgroup analyses demonstrated the negative associations were more significant in participants aged ≥ 60 (AOR = 0.20, 95%CI:0.07-0.56, P = 0.0023 for quintile 5) and non-hypertensive population (AOR = 0.29, 95%CI:0.09-0.96, P = 0.0436 for quintile 5). The restricted cubic spline curve indicated that among the non-hypertensive male population aged ≥ 60, there was a dose-response relationship between serum testosterone and SAAC risk. Furthermore, Johnson-Neyman plot showed that sex hormone binding globulin exhibited a threshold effect on the modulation of the association between serum testosterone and SAAC. Finally, mediation analysis identified the role of Klotho in mediating high levels of serum testosterone's association with SAAC. This study reported that serum testosterone was inversely associated with SAAC, and further highlighted the mediation effect of anti-ageing protein Klotho on that association. Our findings have positive implications for the prevention and treatment of SAAC.

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Klotho介导血清睾酮与腹主动脉严重钙化之间的关系:一项来自NHANES数据库的横断面研究。
严重腹主动脉钙化(SAAC)被认为是心血管疾病发病率和死亡率的重要因素,但其与性类固醇激素的关系尚不清楚。在这里,在国家健康和营养检查调查(NHANES)队列中调查了血清性类固醇激素水平和SAAC之间未被探索的联系。本研究使用的数据来自NHANES 2013-2014。采用腹主动脉钙化24分制测定SAAC。血清性类固醇激素分为1-5分位数进行分析。采用多变量logistic回归和亚组分析探讨血清性类固醇激素与SAAC风险的潜在关系。此外,应用Johnson-Neyman图来识别任何阈值效应的存在。最后,为了揭示潜在的病理生理机制,进行了中介分析。共纳入1852人,SAAC患病率为8.00%。在校正了潜在的混杂因素后,多因素分析显示血清睾酮水平升高与SAAC发生率降低相关(AOR = 0.33, 95%CI:0.13-0.87,第五分位数P = 0.0247,趋势P = 0.025)。亚组分析显示,年龄≥60岁(AOR = 0.20, 95%CI:0.07-0.56, P = 0.0023,第五分位数)和非高血压人群(AOR = 0.29, 95%CI:0.09-0.96, P = 0.0436,第五分位数)之间的负相关更为显著。限制三次样条曲线显示,在年龄≥60岁的非高血压男性人群中,血清睾酮与SAAC风险之间存在剂量-反应关系。此外,Johnson-Neyman图显示性激素结合球蛋白在调节血清睾酮和SAAC之间的关系中表现出阈值效应。最后,中介分析确定了Klotho在介导高水平血清睾酮与SAAC的关联中的作用。本研究报道血清睾酮与SAAC呈负相关,并进一步强调抗衰老蛋白Klotho在这一关联中的中介作用。我们的研究结果对SAAC的预防和治疗具有积极的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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