Sriprasert Intira, Hilser James R, Kono Naoko, Karim Roksana, Stanczyk Frank Z, Shoupe Donna, Hodis Howard N, Mack Wendy J, Allayee Hooman
Department of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Climacteric. 2025 Jun 13:1-7. doi: 10.1080/13697137.2025.2509838.
This study examined the effect of hormone therapy (HT) on tryptophan-kynurenine pathway metabolites and associations with atherosclerosis among postmenopausal women.
Eighty early postmenopausal participants from the Early versus Late Intervention Trial with Estradiol (40 each from HT vs. placebo) were selected for analysis. Tryptophan, -acetyltryptophan, kynurenine, kynurenic acid and -acetylkynurenine baseline and 36-month levels were measured by mass spectrometry. Mixed models tested HT effects on each metabolite, association of estradiol (E2) level with change in metabolite levels and association between change of metabolite with carotid artery intima-media thickness (CIMT) progression.
Compared with placebo, HT significantly reduced kynurenic acid (mean change HT minus placebo -0.27; 95% confidence interval [CI] - 0.42, -0.12; = 0.0007) and -acetylkynurenine (-0.38; 95% CI -0.68, -0.08; = 0.04) levels. Reduction in kynurenic acid was inversely associated with higher E2 levels. Decreased CIMT progression was associated with lower kynurenic acid (0.0131 µm/year per unit; 95% CI 0.0049, 0.0212; = 0.002) and -acetylkynurenine (0.0061 µm/year per unit; 95% CI 0.0020, 0.0103; = 0.004) levels.
Plasma tryptophan-kynurenine pathway metabolites were reduced by HT and these reduced metabolite levels were associated with decreased atherosclerosis progression. Reduction of kynurenic acid by HT was supported by its association with E2 levels, which may explain, in part, the reduction in atherosclerosis progression with HT in early postmenopausal women.
本研究探讨激素疗法(HT)对绝经后女性色氨酸-犬尿氨酸途径代谢产物的影响及其与动脉粥样硬化的关联。
从雌二醇早期与晚期干预试验中选取80名早期绝经后参与者(激素疗法组和安慰剂组各40名)进行分析。采用质谱法测量色氨酸、N-乙酰色氨酸、犬尿氨酸、犬尿酸和N-乙酰犬尿氨酸的基线水平及36个月时的水平。混合模型用于测试HT对每种代谢产物的影响、雌二醇(E2)水平与代谢产物水平变化的关联以及代谢产物变化与颈动脉内膜中层厚度(CIMT)进展之间的关联。
与安慰剂相比,HT显著降低了犬尿酸(激素疗法组减去安慰剂组的平均变化为-0.27;95%置信区间[CI]为-0.42,-0.12;P = 0.0007)和N-乙酰犬尿氨酸(-0.38;95% CI为-0.68,-0.08;P = 0.04)的水平。犬尿酸的降低与较高的E2水平呈负相关。CIMT进展的减缓与较低的犬尿酸(每单位每年0.0131µm;95% CI为0.0049,0.0212;P = 0.002)和N-乙酰犬尿氨酸(每单位每年0.0061µm;95% CI为0.0020,0.0103;P = 0.004)水平相关。
HT可降低血浆色氨酸-犬尿氨酸途径代谢产物水平,这些降低的代谢产物水平与动脉粥样硬化进展减缓相关。HT降低犬尿酸的作用得到其与E2水平关联的支持,这可能部分解释了早期绝经后女性中HT使动脉粥样硬化进展减缓的原因。