Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Depress Anxiety. 2018 Dec;35(12):1168-1177. doi: 10.1002/da.22827. Epub 2018 Sep 5.
The molecular mechanisms underpinning the progesterone-triggering mood symptoms in women with premenstrual dysphoric disorder (PMDD) are unknown. Cell metabolism is a potential source of variability. Very little is known about the effect of progesterone sensitivity on the metabolome. In this study, we aimed to characterize the effects of progesterone on the global metabolic profile and explore the differences between women with PMDD and controls.
Plasma was obtained from 12 women with prospectively confirmed PMDD and 25 controls under two hormone conditions: (1) gonadal suppression induced by leuprolide acetate (3.75 mg IM monthly) and (2) add-back phase with leuprolide and progesterone (200 mg twice daily by vaginal suppository). The global metabolic profile was obtained using liquid and gas chromatography followed by mass spectrometry. Differences between groups and time points were tested using repeated measures analysis of variance. The false discovery rate was calculated to account for multiple testing.
Amino acids and their derivatives represented 78% (28/36) of the known compounds that were found in significantly lower plasma concentrations after progesterone administration than during gonadal suppression. The concentration of tyrosine was nominally significantly decreased after progesterone add-back in controls, but not in cases (P = 0.02).
Plasma levels of some amino acids are decreased in response to progesterone. Albeit preliminary, evidence further suggests that progesterone has a different effect on the metabolic profiles of women with PMDD compared to controls. Further research is needed to replicate our findings in a larger sample and to identify the unknown compounds, especially those differentially expressed.
经前期烦躁障碍(PMDD)女性中孕酮触发情绪症状的分子机制尚不清楚。细胞代谢是变异性的潜在来源。关于孕酮敏感性对代谢组的影响知之甚少。本研究旨在描述孕酮对整体代谢谱的影响,并探讨 PMDD 患者与对照组之间的差异。
从 12 名经前瞻性确诊的 PMDD 女性和 25 名对照者中获得血浆,在两种激素条件下:(1)醋酸亮丙瑞林(3.75mg IM 每月一次)诱导的性腺抑制;(2)用亮丙瑞林和孕酮(200mg 每日两次阴道栓剂)进行添加-回补阶段。采用液质联用和气质联用技术获得整体代谢谱。使用重复测量方差分析检验组间和时间点的差异。采用错误发现率(FDR)校正多重检验。
在接受孕酮治疗后,与性腺抑制相比,有 78%(28/36)的已知化合物的血浆浓度明显降低,这些化合物包括氨基酸及其衍生物。在对照组中,孕酮添加-回补后酪氨酸浓度名义上显著降低,但在病例组中无变化(P=0.02)。
一些氨基酸的血浆水平对孕酮有反应性降低。尽管是初步的,但证据进一步表明,孕酮对 PMDD 女性的代谢谱有不同于对照组的影响。需要进一步研究在更大样本中复制我们的发现,并识别未知的化合物,尤其是那些差异表达的化合物。