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Index serum hyaluronic acid independently and accurately predicts mortality in patients with liver disease

机译:指数血清透明质酸独立地,准确地预测肝病患者的死亡率

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Summary Background Hyaluronic acid is a recognised noninvasive marker of liver fibrosis. However, its prognostic ability has not been extensively studied. Aims To investigate the ability of an index serum hyaluronic acid measurement to independently predict transplant‐free survival in patients with liver disease of varying aetiology and severity. Methods This was a retrospective single‐centre cohort study. Serum hyaluronic acid was measured at the discretion of the attending clinicians, in patients attending the liver clinic, to assess disease severity. Patients with a hyaluronic acid measurement between 1995 and 2010 were identified. Patient characteristics at the point of hyaluronic acid measurement were recorded from medical records. Follow‐up was from date of index hyaluronic acid measurement to date of death, date of transplant or censor date (July 01, 2015). Primary outcomes were all‐cause and liver‐related mortality. Kaplan–Meier analysis was used to compare survival in 3 patient groups with hyaluronic acid levels of 100?μg/L, 100‐300?μg/L and 300?μg/L. Survival models were constructed using Cox proportional hazard and prediction accuracy was assessed by Harrell's C‐statistic. Results Five hundred and eighty nine patients fulfilled inclusion criteria. Median follow‐up was 5.6?years (range 0.1‐19.7). Transplant‐free survival was significantly different between patients with hyaluronic acid 100?μg/L, 100‐300?μg/L and 300?μg/L for liver‐related as well as all‐cause mortality ( P ??0.001). Hyaluronic acid level was an independent predictor of survival (liver‐related: HR 1.39, 95% CI 1.20‐1.60, P ??0.001; all‐cause: HR 1.04, 95% CI 1.02‐1.06, P ?=?0.001). The liver‐related prediction accuracy of hyaluronic acid was 0.74 (Standard error 0.03). Conclusion Index hyaluronic acid measurement can accurately and independently predict liver‐related and all‐cause mortality in patients with liver disease.
机译:发明内容背景透明质酸是肝纤维化的公认的非侵入性标记。然而,其预后能力尚未得到广泛研究。旨在探讨指数血清透明质酸测量的能力,以独立地预测肝脏疾病患者的自然和严重程度的肝病的移植生存。方法这是一个回顾性单中心队列研究。血清透明质酸由参加临床医生的判断,参加肝脏诊所的患者,以评估疾病严重程度。鉴定了1995年至2010年间透明质酸测量的患者。从病历中记录了透明质酸测量点处的患者特征。随访是从指数透明质酸测量的日期到死亡日期,移植日期或审查日期(2015年7月1日)。主要结果是全因和肝脏相关的死亡率。 Kaplan-Meier分析用于将3例患者组的存活率与透明质酸水平进行比较,其含透明质酸水平为100-300μg/ l和&300Ω·μg/升。使用Cox比例危险构建生存模型,并通过Harrell的C统计评估预测准确性。结果五百八十八名患者满足纳入标准。中位后续时间为5.6?年(范围0.1-19.7)。无透明质酸患者之间的移植存活率显着差异,肝脏患者与肝脏相关的肝硬化以及肝脏相关以及全导致死亡率(P?&lt ;?0.001)。透明质酸水平是生存期的独立预测因子(肝脏相关的:HR 1.39,95%CI 1.20-1.60,P = 0.001; 0.001;全原因:HR 1.04,95%CI 1.02-1.06,P?= 0.001 )。透明质酸的肝相关预测精度为0.74(标准误差0.03)。结论指数透明质酸测量可以准确且独立地预测肝病患者的肝病相关和全导致的死亡率。

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    Department of GastroenterologyWestern General HospitalEdinburgh UK;

    Centre for Liver and Digestive DisordersEdinburgh UK;

    Critical CareRoyal Infirmary of EdinburghEdinburgh UK;

    Department of MedicineRoyal Alexandra Hospital PaisleyUK;

    Centre for Liver and Digestive DisordersEdinburgh UK;

    Department of HepatologyRoyal Infirmary of EdinburghEdinburgh UK;

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  • 正文语种 eng
  • 中图分类 药理学;
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