Intira Sriprasert, James R Hilser, Naoko Kono, Roksana Karim, Frank Z Stanczyk, Donna Shoupe, Howard N Hodis, Wendy J Mack, Hooman Allayee
{"title":"激素治疗对绝经后妇女色氨酸代谢和动脉粥样硬化的影响。","authors":"Intira Sriprasert, James R Hilser, Naoko Kono, Roksana Karim, Frank Z Stanczyk, Donna Shoupe, Howard N Hodis, Wendy J Mack, Hooman Allayee","doi":"10.1080/13697137.2025.2509838","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study examined the effect of hormone therapy (HT) on tryptophan-kynurenine pathway metabolites and associations with atherosclerosis among postmenopausal women.</p><p><strong>Methods: </strong>Eighty early postmenopausal participants from the Early versus Late Intervention Trial with Estradiol (40 each from HT vs. placebo) were selected for analysis. Tryptophan, <i>N</i>-acetyltryptophan, kynurenine, kynurenic acid and <i>N</i>-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.</p><p><strong>Results: </strong>Compared with placebo, HT significantly reduced kynurenic acid (mean change HT minus placebo -0.27; 95% confidence interval [CI] - 0.42, -0.12; <i>p</i> = 0.0007) and <i>N</i>-acetylkynurenine (-0.38; 95% CI -0.68, -0.08; <i>p</i> = 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; <i>p</i> = 0.002) and <i>N</i>-acetylkynurenine (0.0061 µm/year per unit; 95% CI 0.0020, 0.0103; <i>p</i> = 0.004) levels.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":10213,"journal":{"name":"Climacteric","volume":" ","pages":"1-7"},"PeriodicalIF":3.2000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of hormone therapy on tryptophan metabolism and atherosclerosis among postmenopausal women.\",\"authors\":\"Intira Sriprasert, James R Hilser, Naoko Kono, Roksana Karim, Frank Z Stanczyk, Donna Shoupe, Howard N Hodis, Wendy J Mack, Hooman Allayee\",\"doi\":\"10.1080/13697137.2025.2509838\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>This study examined the effect of hormone therapy (HT) on tryptophan-kynurenine pathway metabolites and associations with atherosclerosis among postmenopausal women.</p><p><strong>Methods: </strong>Eighty early postmenopausal participants from the Early versus Late Intervention Trial with Estradiol (40 each from HT vs. placebo) were selected for analysis. Tryptophan, <i>N</i>-acetyltryptophan, kynurenine, kynurenic acid and <i>N</i>-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.</p><p><strong>Results: </strong>Compared with placebo, HT significantly reduced kynurenic acid (mean change HT minus placebo -0.27; 95% confidence interval [CI] - 0.42, -0.12; <i>p</i> = 0.0007) and <i>N</i>-acetylkynurenine (-0.38; 95% CI -0.68, -0.08; <i>p</i> = 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; <i>p</i> = 0.002) and <i>N</i>-acetylkynurenine (0.0061 µm/year per unit; 95% CI 0.0020, 0.0103; <i>p</i> = 0.004) levels.</p><p><strong>Conclusions: </strong>Plasma tryptophan-kynurenine pathway metabolites were reduced by HT and these reduced metabolite levels were associated with decreased atherosclerosis progression. 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引用次数: 0
摘要
目的:本研究探讨激素治疗(HT)对绝经后妇女色氨酸-犬尿氨酸途径代谢产物的影响及其与动脉粥样硬化的关系。方法:从雌二醇早期与晚期干预试验中选择80名早期绝经后参与者(HT与安慰剂各40名)进行分析。色氨酸、n -乙酰色氨酸、犬尿氨酸、犬尿氨酸酸和n -乙酰犬尿氨酸基线和36个月水平采用质谱法测定。混合模型测试了HT对每种代谢物的影响,雌二醇(E2)水平与代谢物水平变化的关系,以及代谢物变化与颈动脉内膜-中膜厚度(CIMT)进展的关系。结果:与安慰剂相比,HT显著降低了犬尿酸(HT减去安慰剂的平均变化-0.27;95%置信区间[CI] - 0.42, -0.12;p = 0.0007)和n -乙酰尿氨酸(-0.38;95% ci -0.68, -0.08;P = 0.04)水平。肌尿酸的减少与E2水平升高呈负相关。减少CIMT进展与较低的尿酸相关(0.0131µm/年/单位;95% ci 0.0049, 0.0212;p = 0.002)和n -乙酰基尿氨酸(0.0061 μ m/年/单位;95% ci 0.0020, 0.0103;P = 0.004)水平。结论:HT降低了血浆色氨酸-犬尿氨酸途径代谢物水平,这些代谢物水平的降低与动脉粥样硬化进展的减缓有关。羟色胺与E2水平的相关性支持了羟色胺对犬尿酸的降低作用,这可能部分解释了羟色胺在早期绝经后妇女中减少动脉粥样硬化进展的原因。
Effect of hormone therapy on tryptophan metabolism and atherosclerosis among postmenopausal women.
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, N-acetyltryptophan, kynurenine, kynurenic acid and N-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; p = 0.0007) and N-acetylkynurenine (-0.38; 95% CI -0.68, -0.08; p = 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; p = 0.002) and N-acetylkynurenine (0.0061 µm/year per unit; 95% CI 0.0020, 0.0103; p = 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.
期刊介绍:
Climacteric is the official journal of the International Menopause Society (IMS). As an international peer-reviewed journal it publishes original research and reviews of all aspects of aging in women.
Climacteric was founded by the IMS in 1998 and today has become a leading journal in the publication of peer-reviewed papers on the menopause, climacteric and mid-life health. Topics covered include endocrine changes, symptoms attributed to the menopause and their treatment, hormone replacement and alternative therapies, lifestyles, and the counselling and education of peri- and postmenopausal women. Climacteric, published bimonthly, also features regular invited reviews, editorials and commentaries on recent developments.
The editorial review board of Climacteric includes leading scientific and clinical experts in the field of midlife medicine and research and is headed by its Editor-in-Chief, Professor Rod Baber of Australia. He and his team of Associate Editors act independently to set a clear editorial policy, co-ordinate peer review, and ensure a rapid response to submitted papers.