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PRDM16 驱动的信号调节经睾酮治疗的性腺功能减退男性的身体成分。

A PRDM16-driven signal regulates body composition in testosterone-treated hypogonadal men.

机构信息

Division of Endocrinology Diabetes and Metabolism at Baylor College of Medicine, Houston, TX, United States.

Department of Medicine, Michael E. DeBakey Veterans Affairs (VA) Medical Center, Houston, TX, United States.

出版信息

Front Endocrinol (Lausanne). 2024 Sep 2;15:1426175. doi: 10.3389/fendo.2024.1426175. eCollection 2024.

Abstract

BACKGROUND

Testosterone (T) therapy increases lean mass and reduces total body and truncal fat mass in hypogonadal men. However, the underlying molecular mechanisms for the reciprocal changes in fat and lean mass in humans are not entirely clear.

METHODS

Secondary analysis of specimens obtained from a single-arm, open-label clinical trial on pharmacogenetics of response to T therapy in men with late-onset hypogonadism, conducted between 2011 and 2016 involving 105 men (40-74 years old), who were given intramuscular T cypionate 200 mg every 2 weeks for 18 months. Subcutaneous fat (SCF), peripheral blood mononuclear cells (PBMC) and serum were obtained from the participants at different time points of the study. We measured transcription factors for adipogenesis and myogenesis in the SCF, and PBMC, respectively, by real-time quantitative PCR at baseline and 6 months. Serum levels of FOLLISTATIN, PAX7, MYOSTATIN, ADIPSIN, and PRDM16 were measured by ELISA.

RESULTS

As expected, there was a significant increase in T and estradiol levels after 6 months of T therapy. There was also a reduction in fat mass and an increase in lean mass after 6 months of T therapy. Gene-protein studies showed a significant reduction in the expression of the adipogenic markers in SCF and ADIPSIN levels in the serum, together with a concomitant significant increase in the expression of myogenic markers, in PBMC and PAX7 and FOLLISTATIN levels in the serum after 6 months of T therapy compared to baseline. Interestingly, there was a significant increase in the adipo-myogenic switch, , expression in SCF and PBMC, and in circulating protein levels in the serum after 6 months of T therapy, which is likely from increased estradiol.

CONCLUSION

Our study supports that molecular shift from the adipogenic to the myogenic pathway in men with hypogonadism treated with T could be mediated directly or indirectly by enhanced PRDM16 activity, in turn a result from increased estradiol level. This might have led to the reduction in body fat and increase in lean mass commonly seen in hypogonadal men treated with T.

摘要

背景

睾酮(T)治疗可增加去势男性的瘦体重,并减少全身和躯干脂肪量。然而,人类脂肪和瘦体重的这种相反变化的潜在分子机制尚不完全清楚。

方法

对 2011 年至 2016 年间进行的一项关于迟发性性腺功能减退症男性 T 治疗反应的药物遗传学的单臂、开放标签临床试验的标本进行二次分析,该试验共纳入 105 名(40-74 岁)男性,他们每 2 周接受肌内注射 200mg 十一酸睾酮,共 18 个月。从研究的不同时间点采集参与者的皮下脂肪(SCF)、外周血单核细胞(PBMC)和血清。我们分别通过实时定量 PCR 测量 SCF 和 PBMC 中的脂肪生成和肌肉生成转录因子,在基线和 6 个月时进行测量。通过 ELISA 测量血清中 FOLLISTATIN、PAX7、MYOSTATIN、ADIPSIN 和 PRDM16 的水平。

结果

正如预期的那样,T 治疗 6 个月后 T 和雌二醇水平显著升高。T 治疗 6 个月后,脂肪量减少,瘦体重增加。基因-蛋白研究表明,SCF 中脂肪生成标记物的表达显著降低,血清中 ADIPSIN 水平降低,同时 PBMC 中肌肉生成标记物的表达显著增加,6 个月后血清中 PAX7 和 FOLLISTATIN 水平升高与基线相比。有趣的是,T 治疗 6 个月后,SCF 和 PBMC 中的脂肪-肌肉转化表达以及循环蛋白水平均显著增加,这可能是由于雌二醇水平升高所致。

结论

我们的研究支持这样一种观点,即去势男性接受 T 治疗后,从脂肪生成途径向肌肉生成途径的分子转变可能是直接或间接通过增强 PRDM16 活性介导的,而这种活性又可能是由于雌二醇水平升高所致。这可能导致接受 T 治疗的去势男性体脂减少和瘦体重增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e3/11402695/6317c5a5cff5/fendo-15-1426175-g001.jpg

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