• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血浆肿瘤坏死因子α预示着严重酒精性肝炎患者长期生存率降低。

Plasma tumor necrosis factor alpha predicts decreased long-term survival in severe alcoholic hepatitis.

作者信息

Felver M E, Mezey E, McGuire M, Mitchell M C, Herlong H F, Veech G A, Veech R L

机构信息

Laboratory of Metabolism and Molecular Biology, National Institute on Alcohol Abuse and Alcoholism, Rockville, Maryland 20852.

出版信息

Alcohol Clin Exp Res. 1990 Apr;14(2):255-9. doi: 10.1111/j.1530-0277.1990.tb00482.x.

DOI:10.1111/j.1530-0277.1990.tb00482.x
PMID:2190492
Abstract

Plasma tumor necrosis factor alpha (TNF alpha), interleukin 1 alpha (IL-1 alpha), and interleukin 1 beta (IL-1 beta) were measured in plasma samples obtained from 23 patients with severe alcoholic hepatitis on admission and after 30 days of hospitalization. Over a 2-year follow-up period, 14 patients died at a mean time of 8 months following discharge. The presence of elevated plasma TNF alpha either at admission or discharge from the hospital was associated with death in 82% (14/17) of patients. By contrast absence of elevated plasma TNF alpha was associated with survival in 100% (6/6). The difference in survival with and without detectable plasma TNF alpha was significant at p = 0.0022. Plasma TNF alpha was not elevated in alcoholic patients without clinically apparent liver disease, with alcoholic cirrhosis, or in nonalcoholic healthy controls. Plasma IL-1 alpha was also significantly increased in alcoholic hepatitis whereas IL-1 beta was not. Neither IL-1 alpha nor beta was correlated with outcome in the alcoholic hepatitis group. It is concluded that the presence of elevated plasma TNF alpha is a significant predictor of decreased long-term survival in patients with severe alcoholic hepatitis.

摘要

对23例重症酒精性肝炎患者入院时及住院30天后采集的血浆样本,检测了血浆肿瘤坏死因子α(TNFα)、白细胞介素1α(IL-1α)和白细胞介素1β(IL-1β)。在2年的随访期内,14例患者在出院后平均8个月时死亡。入院时或出院时血浆TNFα升高的患者中,82%(14/17)死亡。相比之下,血浆TNFα未升高的患者100%存活(6/6)。血浆TNFα可检测与不可检测患者的生存率差异具有显著性(p = 0.0022)。无明显临床肝病的酒精性患者、酒精性肝硬化患者或非酒精性健康对照者的血浆TNFα未升高。酒精性肝炎患者的血浆IL-1α也显著升高,而IL-1β未升高。酒精性肝炎组中,IL-1α和IL-1β均与预后无关。结论是,血浆TNFα升高是重症酒精性肝炎患者长期生存率降低的重要预测指标。

相似文献

1
Plasma tumor necrosis factor alpha predicts decreased long-term survival in severe alcoholic hepatitis.血浆肿瘤坏死因子α预示着严重酒精性肝炎患者长期生存率降低。
Alcohol Clin Exp Res. 1990 Apr;14(2):255-9. doi: 10.1111/j.1530-0277.1990.tb00482.x.
2
Elevated plasma interleukin-6 and increased severity and mortality in alcoholic hepatitis.酒精性肝炎患者血浆白细胞介素-6升高与病情严重程度及死亡率增加相关。
Clin Exp Immunol. 1991 Jun;84(3):449-53.
3
Increased plasma tumor necrosis factor in severe alcoholic hepatitis.重症酒精性肝炎患者血浆肿瘤坏死因子升高。
Ann Intern Med. 1990 Jun 15;112(12):917-20. doi: 10.7326/0003-4819-112-12-917.
4
Circulating concentrations of interleukin-18, interleukin-18 binding protein, and gamma interferon in patients with alcoholic hepatitis.酒精性肝炎患者体内白细胞介素-18、白细胞介素-18结合蛋白和γ干扰素的循环浓度。
Liver Int. 2004 Dec;24(6):582-7. doi: 10.1111/j.1478-3231.2004.0967.x.
5
Plasma endotoxin and serum cytokine levels in patients with alcoholic hepatitis: relation to severity of liver disturbance.酒精性肝炎患者的血浆内毒素和血清细胞因子水平:与肝脏损害严重程度的关系。
Alcohol Clin Exp Res. 2000 Apr;24(4 Suppl):48S-54S.
6
High levels of serum interleukin-10 and tumor necrosis factor-alpha are associated with fatality in fulminant hepatitis.血清白细胞介素-10和肿瘤坏死因子-α水平升高与暴发性肝炎的死亡率相关。
J Infect Dis. 2000 Oct;182(4):1103-8. doi: 10.1086/315826. Epub 2000 Aug 28.
7
Soluble TNF-R1, but not tumor necrosis factor alpha, predicts the 3-month mortality in patients with alcoholic hepatitis.可溶性肿瘤坏死因子受体1而非肿瘤坏死因子α可预测酒精性肝炎患者3个月的死亡率。
J Hepatol. 2004 Aug;41(2):229-34. doi: 10.1016/j.jhep.2004.04.028.
8
Stratification of risk of death in severe acute alcoholic hepatitis using a panel of adipokines and cytokines.使用一组脂肪因子和细胞因子对重症急性酒精性肝炎的死亡风险进行分层。
Alcohol Clin Exp Res. 2014 Nov;38(11):2712-21. doi: 10.1111/acer.12558.
9
Cytokine levels in acute alcoholic hepatitis: a sequential study.急性酒精性肝炎中的细胞因子水平:一项序贯研究。
Drug Alcohol Depend. 1995 Jul;39(1):23-7. doi: 10.1016/0376-8716(95)01130-q.
10
Clinical and pathological features, and the mechanism of development in severe alcoholic hepatitis, especially in comparison with acute type fulminant hepatitis.重度酒精性肝炎的临床和病理特征,以及发病机制,尤其是与急性暴发性肝炎的比较。
Alcohol Alcohol Suppl. 1993;1B:97-103. doi: 10.1093/alcalc/28.supplement_1b.97.

引用本文的文献

1
Genetic associations between orexin genes and phenotypes related to behavioral regulation in humans, including substance use.食欲素基因与人类行为调节相关表型(包括物质使用)之间的遗传关联。
Mol Psychiatry. 2025 Jan 29. doi: 10.1038/s41380-025-02895-4.
2
Advances in the management of alcohol-associated liver disease.酒精性肝病管理的进展
Gastroenterol Rep (Oxf). 2024 Nov 5;12:goae097. doi: 10.1093/gastro/goae097. eCollection 2024.
3
Patterns of IgA Autoantibody Generation, Inflammatory Responses and Extracellular Matrix Metabolism in Patients with Alcohol Use Disorder.
酒精使用障碍患者 IgA 自身抗体生成、炎症反应和细胞外基质代谢的模式。
Int J Mol Sci. 2023 Aug 23;24(17):13124. doi: 10.3390/ijms241713124.
4
AMPK-Regulated Autophagy Contributes to Ursolic Acid Supplementation-Alleviated Hepatic Steatosis and Liver Injury in Chronic Alcohol-Fed Mice.AMPK调节的自噬有助于熊果酸补充剂减轻慢性酒精喂养小鼠的肝脂肪变性和肝损伤。
ACS Omega. 2022 Dec 16;8(1):907-914. doi: 10.1021/acsomega.2c06252. eCollection 2023 Jan 10.
5
IL-1 receptor antagonist plus pentoxifylline and zinc for severe alcohol-associated hepatitis.白细胞介素-1 受体拮抗剂联合己酮可可碱和锌治疗严重酒精相关性肝炎。
Hepatology. 2022 Oct;76(4):1058-1068. doi: 10.1002/hep.32478. Epub 2022 Jun 2.
6
Effects of TNF-α deletion on iNKT cell development, activation, and maturation in the steady-state and chronic alcohol-consuming mice.TNF-α 缺失对静息状态和慢性酒精摄入小鼠中 iNKT 细胞发育、激活和成熟的影响。
J Leukoc Biol. 2022 Aug;112(2):233-241. doi: 10.1002/JLB.1A0821-466R. Epub 2021 Nov 12.
7
Current Management and Future Treatment of Alcoholic Hepatitis.酒精性肝炎的当前管理与未来治疗
Gastroenterol Hepatol (N Y). 2020 Apr;16(4):178-189.
8
Tumour Necrosis Factor in Neuroplasticity, Neurogenesis and Alcohol Use Disorder.肿瘤坏死因子在神经可塑性、神经发生及酒精使用障碍中的作用
Brain Plast. 2020 Dec 29;6(1):47-66. doi: 10.3233/BPL-190095.
9
Safety and Efficacy of Infliximab in Severe Alcoholic Hepatitis: A Systematic Review.英夫利昔单抗治疗严重酒精性肝炎的安全性和有效性:一项系统评价。
Cureus. 2019 Jul 4;11(7):e5082. doi: 10.7759/cureus.5082.
10
Phosphodiesterase 4 Inhibition as a Therapeutic Target for Alcoholic Liver Disease: From Bedside to Bench.磷酸二酯酶 4 抑制作为酒精性肝病的治疗靶点:从床边到实验室。
Hepatology. 2019 Dec;70(6):1958-1971. doi: 10.1002/hep.30761. Epub 2019 Jun 25.