*Department of Emergency Medicine, University of Florida College of Medicine, Jacksonville, Florida †Department of Family and Community Medicine, College of Medicine, Mayo Clinic, Jacksonville, Florida ‡Department of Surgery, University of Florida College of Medicine, Gainesville, Florida §Department of Aging and Geriatrics, University of Florida College of Medicine, Gainesville, Florida ||Department of Emergency Medicine, University of Mississippi College of Medicine, Jackson, Mississippi ¶Department of Medicine, Molecular, and Medical Pharmacology, UCLA School of Medicine, Los Angeles, California.
Shock. 2017 Nov;48(5):539-544. doi: 10.1097/SHK.0000000000000887.
High density lipoprotein (HDL) can be readily oxidized in inflammatory conditions and exhibit pro-inflammatory and dysfunctional (Dys-HDL) characteristics. We hypothesize that Dys-HDL may predict adverse outcomes and correlate with inflammatory cytokines in sepsis.
Emergency department (ED) patients with sepsis were enrolled. Blood was drawn at enrollment and after 48 h. Dys-HDL, expressed as HDL inflammatory index (HII), and cytokines were measured. Multivariable logistic regression was used to determine the predictive ability of Dys-HDL for adverse outcomes (death, discharge to hospice, or nursing home).
Thirty-five patients were included in the study. HII was not significantly different at baseline or 48 h between patients with adverse outcomes versus those without. However, there was a significant difference in change in HII over the first 48 h between those with adverse outcomes (+0.21, 95% CI -0.13 to 0.31) versus those without (-0.11, 95% CI -1 to 0.11) (P = 0.025). Logistic regression revealed increasing HII to be an independent predictor of adverse outcomes (OR 5.2, 95% CI 1.1-25.1 P = 0.040). Of the 24 patents with cytokine measurements at both time points, significant inverse correlations between change in HII and change in GRO (rs = -0.52, P = 0.0088) and monocyte chemotactic protein-1 (rs = -0.61, P = 0.0014) concentrations over 48 h were observed.
Increasing Dys-HDL concentrations in the first 48 h of sepsis are associated with an ongoing inflammatory response and adverse clinical outcomes. Early changes in HII may be a potential biomarker in ED patients admitted with sepsis.
高密度脂蛋白(HDL)在炎症条件下容易氧化,并表现出促炎和功能失调(Dys-HDL)的特征。我们假设 Dys-HDL 可能预测败血症的不良结局,并与炎症细胞因子相关。
纳入急诊科(ED)败血症患者。在入组时和 48 小时后采集血液。测量 Dys-HDL,以 HDL 炎症指数(HII)表示,并测量细胞因子。多变量逻辑回归用于确定 Dys-HDL 对不良结局(死亡、临终关怀或疗养院出院)的预测能力。
研究纳入了 35 名患者。在不良结局患者和无不良结局患者之间,基线或 48 小时时 HII 没有显著差异。然而,在 48 小时内,不良结局患者的 HII 变化(+0.21,95%CI -0.13 至 0.31)与无不良结局患者(-0.11,95%CI -1 至 0.11)之间存在显著差异(P=0.025)。逻辑回归显示,HII 的增加是不良结局的独立预测因子(OR 5.2,95%CI 1.1-25.1,P=0.040)。在 24 名具有两个时间点细胞因子测量值的患者中,HII 的变化与 GRO(rs=-0.52,P=0.0088)和单核细胞趋化蛋白-1(rs=-0.61,P=0.0014)浓度的变化之间存在显著的负相关。
败血症的前 48 小时内,Dys-HDL 浓度的增加与持续的炎症反应和不良临床结局相关。HII 的早期变化可能是 ED 患者因败血症入院的潜在生物标志物。