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血清氨是慢性加急性肝衰竭患者的一个强有力的预后因素。

Serum ammonia is a strong prognostic factor for patients with acute-on-chronic liver failure.

机构信息

Collaborative Innovation Center for the Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for the Diagnosis and Treatment of Infectious Diseases, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.

National Clinical Research Center for Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Sci Rep. 2020 Oct 12;10(1):16970. doi: 10.1038/s41598-020-73603-1.

DOI:10.1038/s41598-020-73603-1
PMID:33046732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7550336/
Abstract

Ammonia is thought to be central to the pathogenesis of hepatic encephalopathy (HE), but its prognostic role in acute-on-chronic liver failure (ACLF) is still unknown. We aimed to determine the association between serum ammonia level and short-term prognosis in ACLF. Furthermore, we performed an in-depth evaluation of the independent effect of serum ammonia level on the short-term prognosis of hepatitis B virus (HBV) reactivation-induced ACLF patients. We identified 174 patients as part of prospective observational studies in patients with ACLF. Plasma ammonia levels were measured on admission, and several prognostic scores were used to determine the prognostic effect of ammonia. The 28-day patient survival was determined. Receiver operating characteristic analysis was used to identify the cut-off points for ammonia values, and multivariable analysis was performed using the Cox proportional hazard regression model. Plasma ammonia was significantly higher in nonsurvivors (83.53 ± 43.78 versus 67.13 ± 41.77 µmol/L, P = 0.013), and ACLF patients with hyperammonemia had significantly higher 28-day mortality than those without hyperammonemia. Ammonia was also closely related to ACLF grade (P < 0.001) and organ failure, including liver (P = 0.048), coagulation (P < 0.001) and brain (P < 0.001). HBV reactivation serves as the main precipitating factor in the ACLF population. Subgroup analysis showed that ammonia is also a strong prognostic factor in the HBV reactivation-induced ACLF population. Ammonia level is closely correlated with failure of other organs and is an independent risk factor for mortality in ACLF and the special population defined as HBV reactivation-related ACLF. Based on the results from our study, we measured serum ammonia in the population with ACLF, which strongly indicates their prognosis. It serves as an important biomarker and a therapeutic target.

摘要

氨被认为是肝性脑病(HE)发病机制的核心,但它在急性慢性肝衰竭(ACLF)中的预后作用尚不清楚。我们旨在确定血清氨水平与 ACLF 短期预后之间的关系。此外,我们对乙型肝炎病毒(HBV)再激活诱导的 ACLF 患者血清氨水平对短期预后的独立影响进行了深入评估。我们在 ACLF 患者的前瞻性观察研究中确定了 174 名患者。入院时测量血浆氨水平,并使用几种预后评分来确定氨的预后作用。确定 28 天患者生存率。使用受试者工作特征分析确定氨值的截断点,并使用 Cox 比例风险回归模型进行多变量分析。非幸存者的血浆氨水平明显升高(83.53±43.78 与 67.13±41.77µmol/L,P=0.013),且高氨血症的 ACLF 患者 28 天死亡率明显高于无高氨血症的患者。氨还与 ACLF 分级(P<0.001)和肝(P=0.048)、凝血(P<0.001)和脑(P<0.001)等器官衰竭密切相关。HBV 再激活是 ACLF 人群的主要诱发因素。亚组分析表明,氨也是 HBV 再激活诱导的 ACLF 人群的一个强有力的预后因素。氨水平与其他器官衰竭密切相关,是 ACLF 和定义为 HBV 再激活相关 ACLF 的特殊人群死亡率的独立危险因素。基于我们的研究结果,我们在 ACLF 人群中测量了血清氨,这强烈表明了其预后。它是一个重要的生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/3dd22c16e974/41598_2020_73603_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/e7466185fc57/41598_2020_73603_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/748c808810ef/41598_2020_73603_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/e5461cdda203/41598_2020_73603_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/3dd22c16e974/41598_2020_73603_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/e7466185fc57/41598_2020_73603_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/748c808810ef/41598_2020_73603_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/e5461cdda203/41598_2020_73603_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfc/7550336/3dd22c16e974/41598_2020_73603_Fig4_HTML.jpg

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