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雄激素活性的新型蛋白质标志物:来自年轻化学去势男性血浆的蛋白质组学研究。

Novel protein markers of androgen activity in humans: proteomic study of plasma from young chemically castrated men.

机构信息

Molecular Reproductive Medicine, Department of Translational Medicine, Lund University, Malmo, Sweden.

Section for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Lund, Sweden.

出版信息

Elife. 2022 Mar 1;11:e74638. doi: 10.7554/eLife.74638.

Abstract

BACKGROUND

Reliable biomarkers of androgen activity in humans are lacking. The aim of this study was, therefore, to identify new protein markers of biological androgen activity and test their predictive value in relation to low vs normal testosterone values and some androgen deficiency linked pathologies.

METHODS

Blood samples from 30 healthy GnRH antagonist treated males were collected at three time points: (1) before GnRH antagonist administration; (2) 3 weeks later, just before testosterone undecanoate injection, and (3) after additional 2 weeks. Subsequently, they were analyzed by mass spectrometry to identify potential protein biomarkers of testosterone activity. Levels of proteins most significantly associated with testosterone fluctuations were further tested in a cohort of 75 hypo- and eugonadal males suffering from infertility. Associations between levels of those markers and cardiometabolic parameters, bone mineral density as well as androgen receptor (AR) CAG repeat lengths, were explored.

RESULTS

Using receiver operating characteristic analysis, 4-hydroxyphenylpyruvate dioxygenase (4HPPD), insulin-like growth factor-binding protein 6 (IGFBP6), and fructose-bisphosphate aldolase (ALDOB), as well as a Multi Marker Algorithm, based on levels of 4HPPD and IGFBP6, were shown to be best predictors of low (<8 nmol/l) vs normal (>12 nmol/l) testosterone. They were also more strongly associated with metabolic syndrome and diabetes than testosterone levels. Levels of ALDOB and 4HPPD also showed association with AR CAG repeat lengths.

CONCLUSIONS

We identified potential new protein biomarkers of testosterone action. Further investigations to elucidate their clinical potential are warranted.

FUNDING

The work was supported by ReproUnion2.0 (grant no. 20201846), which is funded by the Interreg V EU program.

摘要

背景

目前缺乏可靠的人类雄激素活性生物标志物。因此,本研究旨在鉴定新的雄激素生物活性蛋白标志物,并测试其与低睾酮值和一些雄激素缺乏相关疾病的预测价值。

方法

30 名接受 GnRH 拮抗剂治疗的健康男性在三个时间点采集血样:(1)在 GnRH 拮抗剂给药前;(2)3 周后,在注射十一酸睾酮前;(3)在额外的 2 周后。随后,通过质谱分析鉴定潜在的与睾酮活性相关的蛋白生物标志物。进一步在患有不育症的 75 名低促性腺激素和正常促性腺激素男性的队列中测试与睾酮波动最显著相关的蛋白质水平。探讨这些标志物的水平与心血管代谢参数、骨密度以及雄激素受体(AR)CAG 重复长度之间的关系。

结果

使用受试者工作特征分析,4-羟苯丙酮酸双加氧酶(4HPPD)、胰岛素样生长因子结合蛋白 6(IGFBP6)和果糖二磷酸醛缩酶(ALDOB)以及基于 4HPPD 和 IGFBP6 水平的多标志物算法,被证明是低(<8nmol/l)与正常(>12nmol/l)睾酮的最佳预测指标。它们与代谢综合征和糖尿病的相关性也强于睾酮水平。ALDOB 和 4HPPD 的水平也与 AR CAG 重复长度有关。

结论

我们鉴定了潜在的新的雄激素作用的蛋白生物标志物。进一步的研究阐明其临床潜力是必要的。

基金

这项工作得到了 ReproUnion2.0(第 20201846 号)的支持,该项目由欧盟 Interreg V 计划资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dec3/8993215/2828cf132705/elife-74638-fig1.jpg

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