Slowik Voytek, Borude Prachi, Jaeschke Hartmut, Woolbright Benjamin L, Lee William M, Apte Udayan
Department of Gastroenterology Hepatology and Nutrition, Children's Mercy Kansas City, Kansas City, MO 64108, USA.
Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Transl Gastroenterol Hepatol. 2019 Mar 20;4:17. doi: 10.21037/tgh.2019.03.03. eCollection 2019.
One of the major issues in the field of acute liver failure (ALF) is the lack of reliable biomarkers that predict outcome. Many cases present with very limited treatment options and prognostic indicators are invaluable. We tested whether leukocyte cell derived chemotaxin 2 can be used as a prognostic biomarker to predict patient survival either alone or in combination with other routine clinical parameters.
Serum samples and associated clinical data from came from two independent sources, the Acute Liver Failure Study Group (ALFSG) registry and the University of Kansas Medical Center. We analyzed a total of 61 cases, each with individual time points collected over a period of 0 to 7 days after hospital admission. Analysis was developed to compare responses in survivors non-survivors.
The data indicate that survivors had significantly lower serum levels of leukocyte cell derived chemotaxin 2 compared to non-survivors (P=0.03). Further, it was able to predict patient survival when taken together with either international normalized ratio (INR) alone (71% concordance) or INR and bilirubin (76% concordance) or INR and serum albumin (77% concordance). Furthermore, when we analyzed data for each day, serum Lect2 and INR taken together were able to predict survival at day three after hospital admission with 86.3% concordance.
These studies have revealed test batteries consisting of easily available serum tests that are concordant with survival status of ALF patients early during the clinical course.
急性肝衰竭(ALF)领域的主要问题之一是缺乏可预测预后的可靠生物标志物。许多病例的治疗选择非常有限,预后指标非常重要。我们测试了白细胞衍生趋化因子2是否可以单独或与其他常规临床参数联合用作预测患者生存的预后生物标志物。
血清样本及相关临床数据来自两个独立来源,急性肝衰竭研究组(ALFSG)登记处和堪萨斯大学医学中心。我们共分析了61例病例,每例在入院后0至7天内收集了各个时间点的数据。分析旨在比较幸存者和非幸存者的反应。
数据表明,与非幸存者相比,幸存者的白细胞衍生趋化因子2血清水平显著降低(P = 0.03)。此外,当与单独的国际标准化比值(INR)(一致性为71%)或INR和胆红素(一致性为76%)或INR和血清白蛋白(一致性为77%)一起使用时,它能够预测患者生存。此外,当我们分析每天的数据时,血清Lect2和INR一起能够预测入院后第三天的生存情况,一致性为86.3%。
这些研究揭示了由易于获得的血清检测组成的检测组合,这些检测与ALF患者临床病程早期的生存状态一致。