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脓毒性休克患者中色氨酸途径代谢产物(血清素、5-羟吲哚乙酸、犬尿氨酸)和酶(单胺氧化酶和吲哚胺2,3-双加氧酶):一项针对健康对照的前瞻性观察研究

Tryptophan pathway catabolites (serotonin, 5-hydroxyindolacetic acid, kynurenine) and enzymes (monoamine oxidase and indole amine 2,3 dioxygenase) in patients with septic shock: A prospective observational study versus healthy controls.

作者信息

Troché Gilles, Henry-Lagarrigue Matthieu, Soppelsa Frédérique, Legriel Stephane, Yehia Aihem, Bruneel Fabrice, Bédos Jean-Pierre, Spreux-Varoquaux Odile

机构信息

Service de Réanimation médico-chirurgicale, Centre Hospitalier de Versailles, 78150 Le Chesnay, France.

Service de Réanimation polyvalente, Centre Hospitalier Départemental de Vendée, La Roche sur Yon.

出版信息

Medicine (Baltimore). 2020 May;99(19):e19906. doi: 10.1097/MD.0000000000019906.

Abstract

Septic shock is associated with a strong inflammatory response that induces vasodilation and vascular hyporeactivity. We investigated the role for tryptophan-pathway catabolites of proinflammatory cytokines in septic shock.We prospectively included 30 patients with very recent-onset septic shock and 30 healthy volunteers. The following were assayed once in the controls and on days 1, 2, 3, 7, and 14 in each patient: plasma free and total tryptophan, platelet and plasma serotonin, total blood serotonin, urinary serotonin, plasma and urinary 5-hydroxyindolacetic acid, plasma kynurenine, monoamine oxidase activity, and total indole amine 2,3-dioxygenase activity. Organ-system failure and mortality were recorded.Compared with the healthy controls, the patients with septic shock had 2-fold to 3-fold lower total tryptophan levels throughout the 14-day study period. Platelet serotonin was substantially lower, while monoamine oxidase activity and 5-hydroxyindolacetic acid were markedly higher in the patients than in the controls, consistent with the known conversion of tryptophan to serotonin, which is then promptly and largely degraded to 5-hydroxyindolacetic acid. Plasma kynurenine was moderately increased and indole amine 2,3-dioxygenase activity markedly increased in the patients versus the volunteers, reflecting conversion of tryptophan to kynurenine. Changes over time in tryptophan metabolites were not associated with survival in the patients but were associated with the Sequential Organ Failure Assessment score and hemodynamic variables including hypotension and norepinephrine requirements.Our results demonstrate major tryptophan pathway alterations in septic shock. Marked alterations were found compared with healthy volunteers, and tryptophan metabolite levels were associated with organ failure and hemodynamic alterations. Tryptophan metabolite levels were not associated with surviving septic shock, although this result might be ascribable to the small sample size.Trial registration: ClinicalTrials.gov; No: NCT00684736; URL: www.clinicaltrials.gov.

摘要

脓毒性休克与强烈的炎症反应相关,该反应可导致血管扩张和血管反应性降低。我们研究了促炎细胞因子的色氨酸途径分解代谢产物在脓毒性休克中的作用。我们前瞻性纳入了30例近期发病的脓毒性休克患者和30名健康志愿者。在对照组以及每位患者的第1、2、3、7和14天检测以下指标:血浆游离色氨酸和总色氨酸、血小板和血浆5-羟色胺、全血5-羟色胺、尿5-羟色胺、血浆和尿5-羟吲哚乙酸、血浆犬尿氨酸、单胺氧化酶活性以及总吲哚胺2,3-双加氧酶活性。记录器官系统衰竭情况和死亡率。与健康对照组相比,在为期14天的研究期间,脓毒性休克患者的总色氨酸水平降低了2至3倍。患者的血小板5-羟色胺水平显著降低,而单胺氧化酶活性和5-羟吲哚乙酸水平明显高于对照组,这与已知的色氨酸转化为5-羟色胺,然后迅速大量降解为5-羟吲哚乙酸的过程一致。与志愿者相比,患者的血浆犬尿氨酸适度增加,吲哚胺2,3-双加氧酶活性显著增加,反映了色氨酸向犬尿氨酸的转化。色氨酸代谢产物随时间的变化与患者的生存率无关,但与序贯器官衰竭评估评分以及包括低血压和去甲肾上腺素需求量在内的血流动力学变量相关。我们的结果表明脓毒性休克中色氨酸途径存在重大改变。与健康志愿者相比发现了明显的改变,色氨酸代谢产物水平与器官衰竭和血流动力学改变相关。色氨酸代谢产物水平与脓毒性休克存活无关,尽管这一结果可能归因于样本量较小。试验注册:ClinicalTrials.gov;编号:NCT00684736;网址:www.clinicaltrials.gov。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0e5/7220452/17720e142e00/medi-99-e19906-g001.jpg

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