Dept of Clinical Laboratory, Wuhan Univ, Renmin Hospital, Wuhan 430060, Hubei Province, PR China.
Dept of Cardiology, Wuhan Univ, Renmin Hospital, Wuhan 430060, Hubei Province, PR China.
Biomed Pharmacother. 2019 Jun;114:108792. doi: 10.1016/j.biopha.2019.108792. Epub 2019 Mar 22.
This study aimed to explore the association between growth differentiation factor-15 (GDF-15), a stress-induced factor, and sex hormones in male patients with coronary artery disease (CAD). In this study, we recruited 253 male patients with CAD and 205 male controls. Patients were divided into three groups in accordance with GDF-15 tertiles. Serum levels of GDF-15, testosterone, estradiol and other biochemical variables were measured. Serum levels of GDF-15 were significantly increased and serum testosterone and testosterone/estradiol ratio (T/E2 ratio) were significantly decreased in CAD patients compared with controls. Patients with high GDF-15 levels had lower testosterone (203.97, 95% CI 154.67-328.30 vs. 303.98, 95% CI 246.93-345.66; P = 0.001) and T/E2 ratio (8.82, 95% CI 5.77-11.41 vs. 11.07, 95% CI 7.91-14.32; P = 0.013). Correlation analyses showed that serum GDF-15 levels inversely correlated with testosterone levels (r = -0.339) and T/E2 ratio (r = -0.365) (both P < 0.001). In multivariate regression analyses, the association between GDF-15 and T/E2 ratio was maintained (B=-0.442, 95% CI -99.568 to -6.991, P = 0.015). Furthermore, in vitro studies showed a synergistic effect of testosterone and estradiol on GDF-15 secretion, and demonstrated that testosterone association with estradiol decreased GDF-15 secretion through androgen receptor/estrogen receptor-mediated pathways. Together, these results suggest that upregulation of GDF-15 in the presence of low and imbalanced sex hormone levels may contribute to CAD. Thus, restoring the balance of testosterone and estradiol may inhibit the effects of GDF-15 and serve as a promising therapeutic strategy for the treatment of CAD.
本研究旨在探讨生长分化因子 15(GDF-15),一种应激诱导因子,与男性冠心病(CAD)患者性激素之间的关联。在这项研究中,我们招募了 253 名男性 CAD 患者和 205 名男性对照者。患者根据 GDF-15 三分位进行分组。测量血清 GDF-15、睾酮、雌二醇和其他生化变量的水平。与对照组相比,CAD 患者的血清 GDF-15 水平显著升高,而血清睾酮和睾酮/雌二醇比值(T/E2 比值)显著降低。高 GDF-15 水平患者的睾酮水平更低(203.97,95%CI 154.67-328.30 比 303.98,95%CI 246.93-345.66;P=0.001),T/E2 比值更低(8.82,95%CI 5.77-11.41 比 11.07,95%CI 7.91-14.32;P=0.013)。相关性分析显示,血清 GDF-15 水平与睾酮水平(r=-0.339)和 T/E2 比值(r=-0.365)呈负相关(均 P<0.001)。多元回归分析显示,GDF-15 与 T/E2 比值之间的关联仍然存在(B=-0.442,95%CI -99.568 至-6.991,P=0.015)。此外,体外研究显示睾酮和雌二醇对 GDF-15 分泌有协同作用,并表明睾酮与雌二醇通过雄激素受体/雌激素受体介导途径降低 GDF-15 分泌。总之,这些结果表明,在低水平和不平衡性激素水平的情况下 GDF-15 的上调可能导致 CAD。因此,恢复睾酮和雌二醇的平衡可能抑制 GDF-15 的作用,并作为治疗 CAD 的一种有前途的治疗策略。