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危重症腹腔感染或非感染性腹腔疾病患者血浆三叶因子 3 水平升高。

Elevated trefoil factor 3 plasma levels in critically ill patients with abdominal sepsis or non-infectious abdominal illness.

机构信息

Center for Experimental and Molecular Medicine, Amsterdam University Medical Centers, location Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands; The Amsterdam Institute for Infection and Immunity, Amsterdam University Medical Centers, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.

Center for Experimental and Molecular Medicine, Amsterdam University Medical Centers, location Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands; The Amsterdam Institute for Infection and Immunity, Amsterdam University Medical Centers, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.

出版信息

Cytokine. 2020 Sep;133:155181. doi: 10.1016/j.cyto.2020.155181. Epub 2020 Jun 27.

Abstract

Trefoil factor 3 (TFF3) is a small peptide secreted mainly by goblet cells in the gut, where it plays a key role in gastrointestinal defence and repair. Plasma TFF3 has been reported as a biomarker of intestinal injury and as such it has been evaluated as a marker of disease activity in colitis. Impaired gut barrier function has been postulated as the "motor" of critical illness. We here sought to determine the temporal dynamics of plasma TFF3 in adult patients admitted to intensive care unit with abdominal sepsis or after major abdominal surgery for a non-infectious condition (post-op GI patients). TFF3 was measured in plasma obtained from 143 patients with abdominal sepsis and 98 post-op GI patients on admission to the intensive care (day 0) and at days 2 and 4 thereafter. Abdominal sepsis patients showed sustained elevated plasma TFF3 levels from day 0 to 4 relative to healthy control values, while in post-op GI patients admission TFF3 levels were not increased, only rising at day 2 and 4. In both patient groups, the presence of shock was associated with higher TFF3 levels. Moreover, patients with 3 or more organs failing had higher plasma TFF3 concentrations. While plasma TFF3 was higher in sepsis patients who did not survive until day 30, TFF3 levels were not independently associated with 30-day mortality in a Cox regression analysis. These results could support the theory that intestinal injury contributes to the pathogenesis of critical illness. Future studies are needed to elucidate whether the proposed gut dysfunction precedes or supersedes organ dysfunction in time.

摘要

三叶因子 3(TFF3)主要由肠道中的杯状细胞分泌,在胃肠道防御和修复中发挥关键作用。血浆 TFF3 已被报道为肠道损伤的生物标志物,因此它被评估为结肠炎疾病活动的标志物。受损的肠道屏障功能被认为是危重病的“动力”。我们在这里试图确定成人患者在重症监护病房中因腹部感染或因非感染性疾病(术后胃肠道患者)而接受主要腹部手术后的血浆 TFF3 的时间动态。在重症监护病房入院时(第 0 天)和此后的第 2 天和第 4 天,测量了 143 例腹部感染患者和 98 例术后胃肠道患者的血浆 TFF3。与健康对照组相比,腹部感染患者从第 0 天到第 4 天持续升高的血浆 TFF3 水平,而术后胃肠道患者入院时 TFF3 水平没有升高,仅在第 2 天和第 4 天升高。在这两组患者中,休克的存在与更高的 TFF3 水平相关。此外,有 3 个或更多器官衰竭的患者具有更高的血浆 TFF3 浓度。虽然在没有存活到第 30 天的败血症患者中,TFF3 水平较高,但在 Cox 回归分析中,TFF3 水平与 30 天死亡率无关。这些结果可能支持肠道损伤导致危重病发病机制的理论。未来的研究需要阐明所提出的肠道功能障碍是否先于或取代了器官功能障碍。

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