Suppr超能文献

激素疗法对绝经后女性色氨酸代谢及动脉粥样硬化的影响。

Effect of hormone therapy on tryptophan metabolism and atherosclerosis among postmenopausal women.

作者信息

Sriprasert Intira, Hilser James R, Kono Naoko, Karim Roksana, Stanczyk Frank Z, Shoupe Donna, Hodis Howard N, Mack Wendy J, Allayee Hooman

机构信息

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.

出版信息

Climacteric. 2025 Jun 13:1-7. doi: 10.1080/13697137.2025.2509838.

Abstract

OBJECTIVE

This study examined the effect of hormone therapy (HT) on tryptophan-kynurenine pathway metabolites and associations with atherosclerosis among postmenopausal women.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

相似文献

1
2
Long-term hormone therapy for perimenopausal and postmenopausal women.
Cochrane Database Syst Rev. 2017 Jan 17;1(1):CD004143. doi: 10.1002/14651858.CD004143.pub5.
3
Hormone therapy for sexual function in perimenopausal and postmenopausal women.
Cochrane Database Syst Rev. 2013 Jun 5(6):CD009672. doi: 10.1002/14651858.CD009672.pub2.
4
Short-term and long-term effects of tibolone in postmenopausal women.
Cochrane Database Syst Rev. 2016 Oct 12;10(10):CD008536. doi: 10.1002/14651858.CD008536.pub3.
5
Long term hormone therapy for perimenopausal and postmenopausal women.
Cochrane Database Syst Rev. 2012 Jul 11(7):CD004143. doi: 10.1002/14651858.CD004143.pub4.
9
Plasma kynurenine pathway metabolites in association with diabetes: A cross-sectional study.
Clin Nutr. 2025 Aug;51:342-348. doi: 10.1016/j.clnu.2025.07.003. Epub 2025 Jul 7.
10
Plasma metabolites associated with endometriosis in adolescents and young adults.
Hum Reprod. 2025 May 1;40(5):843-854. doi: 10.1093/humrep/deaf040.

本文引用的文献

1
The Tryptophan and Kynurenine Pathway Involved in the Development of Immune-Related Diseases.
Int J Mol Sci. 2023 Mar 17;24(6):5742. doi: 10.3390/ijms24065742.
2
The Kynurenine Pathway and Polycystic Ovary Syndrome: Inflammation as a Common Denominator.
Int J Tryptophan Res. 2022 May 21;15:11786469221099214. doi: 10.1177/11786469221099214. eCollection 2022.
3
Kynurenine Pathway Metabolites as Potential Clinical Biomarkers in Coronary Artery Disease.
Front Immunol. 2022 Feb 8;12:768560. doi: 10.3389/fimmu.2021.768560. eCollection 2021.
4
Concentrations of endogenous sex steroid hormones and SHBG in healthy postmenopausal women.
J Steroid Biochem Mol Biol. 2022 Oct;223:106080. doi: 10.1016/j.jsbmb.2022.106080. Epub 2022 Feb 16.
5
Associations between estrogen and progesterone, the kynurenine pathway, and inflammation in the post-partum.
J Affect Disord. 2021 Feb 15;281:9-12. doi: 10.1016/j.jad.2020.10.052. Epub 2020 Oct 29.
6
Metabolomic Effects of Hormone Therapy and Associations With Coronary Heart Disease Among Postmenopausal Women.
Circ Genom Precis Med. 2020 Dec;13(6):e002977. doi: 10.1161/CIRCGEN.119.002977. Epub 2020 Nov 3.
7
Tryptophan Metabolism in Inflammaging: From Biomarker to Therapeutic Target.
Front Immunol. 2019 Oct 30;10:2565. doi: 10.3389/fimmu.2019.02565. eCollection 2019.
8
The proatherosclerotic function of indoleamine 2, 3-dioxygenase 1 in the developmental stage of atherosclerosis.
Signal Transduct Target Ther. 2019 Jul 19;4:23. doi: 10.1038/s41392-019-0058-5. eCollection 2019.
9
Serum metabolomic profiles associated with postmenopausal hormone use.
Metabolomics. 2018 Jul 6;14(7):97. doi: 10.1007/s11306-018-1393-1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验