小儿登革热休克综合征中心血管和炎症生物标记物的动力学研究

Chanh Ho Quang, Trieu Huynh Trung, Tam Dong Thi Hoai, Tran Kim Hung, Huynh Ngoc Thien Vuong, Phan Tu Qui, Huyen Vu Ngo Thanh, Alexandra Moncada, Thanh Kieu Nguyen Thi, Duyen Huynh Thi Le, Ngan Nguyen-Lyle, Vuong Nguyen Lam, Lam Phung Khanh, Angela McBride, Bridget Wills, Sophie Yacoub
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引用次数: 0

摘要

糖萼破坏和高炎症反应与登革热相关血管渗漏的发病机制有关,但它们与登革热休克综合征(DSS)患者临床预后的关系却鲜为人知。我们研究了血管和炎症生物标志物与临床预后的关系及其与血管渗漏临床标志物的相关性。 我们在越南进行了一项前瞻性队列研究。临床诊断为DSS的≥5岁儿童被纳入本研究。在重症监护室住院期间和出院后 7-10 天每天采集血样,测量血浆中的辛迪加-1、透明质酸、抑制肿瘤生成 2 (ST-2)、铁蛋白、N 端脑钠肽(NT-proBNP)和心房钠肽(ANP)水平。主要结果是复发性休克。 共纳入 90 名 DSS 患者。16 名患者出现了复发性休克。除 NT-proBNP 外,所有生物标志物在休克发生时均升高。代偿期和失代偿期 DSS 患者之间没有差异。糖萼标记物与炎症生物标记物、血细胞比容、血液浓缩百分比呈正相关,与卒中容量指数呈负相关。随着时间的推移,Syndecan-1、透明质酸、铁蛋白和 ST-2 均有所改善,而 ANP 在随访时继续升高。据观察,入院时的 Syndecan-1 水平与发生复发性休克有关,但在 P < 0.01 时,该关联未达到统计学意义(OR = 1.82,95% CI 1.07-3.35,P = 0.038)。 心血管和炎症生物标志物在 DSS 中升高,与临床血管渗漏参数相关,并随着时间的推移呈不同的动力学变化。Syndecan-1可能有助于对ICU中的DSS患者进行风险分层。
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Kinetics of cardiovascular and inflammatory biomarkers in paediatric dengue shock syndrome
Glycocalyx disruption and hyperinflammatory responses are implicated in the pathogenesis of dengue-associated vascular leak, however little is known about their association with clinical outcomes of patients with dengue shock syndrome (DSS). We investigated the association of vascular and inflammatory biomarkers with clinical outcomes and their correlations with clinical markers of vascular leakage. We performed a prospective cohort study in Viet Nam. Children ≥ 5 years of age with a clinical diagnosis of DSS were enrolled into this study. Blood samples were taken daily during ICU stay and 7–10 days after hospital discharge for measurements of plasma levels of Syndecan-1, Hyaluronan, Suppression of tumorigenicity 2 (ST-2), Ferritin, N-terminal pro Brain Natriuretic Peptide (NT-proBNP), and Atrial Natriuretic Peptide (ANP). The primary outcome was recurrent shock. 90 DSS patients were enrolled. Recurrent shock occurred in 16 patients. All biomarkers, except NT-proBNP, were elevated at presentation with shock. There were no differences between compensated and decompensated DSS patients. Glycocalyx markers were positively correlated with inflammatory biomarkers, haematocrit, percentage hemoconcentration, and negatively correlated with stroke volume index. While Syndecan-1, Hyaluronan, Ferritin, and ST-2 improved with time, ANP continued to be raised at follow-up. Enrolment Syndecan-1 levels were observed to be associated with developing recurrent shock although the association did not reach the statistical significance at the P < 0.01 (OR = 1.82, 95% CI 1.07–3.35, P = 0.038). Cardiovascular and inflammatory biomarkers are elevated in DSS, correlate with clinical vascular leakage parameters and follow different kinetics over time. Syndecan-1 may have potential utility in risk stratifying DSS patients in ICU.
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