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The NLRP3 Inflammasome in Non-Alcoholic Fatty Liver Disease and Steatohepatitis: Therapeutic Targets and Treatment.非酒精性脂肪性肝病和脂肪性肝炎中的NLRP3炎性小体:治疗靶点与治疗方法
Front Pharmacol. 2022 Mar 8;13:780496. doi: 10.3389/fphar.2022.780496. eCollection 2022.
2
A Bidirectional Relationship Between Hyperuricemia and Metabolic Dysfunction-Associated Fatty Liver Disease.高尿酸血症与代谢相关脂肪性肝病的双向关系。
Front Endocrinol (Lausanne). 2022 Feb 16;13:821689. doi: 10.3389/fendo.2022.821689. eCollection 2022.
3
Association of hyperuricemia and gamma glutamyl transferase as a marker of metabolic risk in alcohol use disorder.高尿酸血症与γ-谷氨酰转移酶作为酒精使用障碍代谢风险标志物的关联。
Sci Rep. 2020 Nov 18;10(1):20060. doi: 10.1038/s41598-020-77013-1.
4
Erratum Regarding "Pathophysiology of AKI to CKD Progression" (Semin Nephrol. 2020;40:206-215).
Semin Nephrol. 2020 May;40(3):328. doi: 10.1016/j.semnephrol.2020.05.001.
5
Higher Serum Uric Acid Level Predicts Non-alcoholic Fatty Liver Disease: A 4-Year Prospective Cohort Study.血清尿酸水平升高预示非酒精性脂肪性肝病:一项为期 4 年的前瞻性队列研究。
Front Endocrinol (Lausanne). 2020 Apr 9;11:179. doi: 10.3389/fendo.2020.00179. eCollection 2020.
6
Uric acid and inflammation in kidney disease.尿酸与肾脏病中的炎症反应。
Am J Physiol Renal Physiol. 2020 Jun 1;318(6):F1327-F1340. doi: 10.1152/ajprenal.00272.2019. Epub 2020 Mar 30.
7
Circulating tumor DNA methylation profiles enable early diagnosis, prognosis prediction, and screening for colorectal cancer.循环肿瘤 DNA 甲基化谱可实现结直肠癌的早期诊断、预后预测和筛查。
Sci Transl Med. 2020 Jan 1;12(524). doi: 10.1126/scitranslmed.aax7533.
8
Hepatic Steatosis in Lean Patients: Risk Factors and Impact on Mortality.瘦型患者的肝脂肪变性:危险因素和对死亡率的影响。
Dig Dis Sci. 2020 Sep;65(9):2712-2718. doi: 10.1007/s10620-019-06000-y. Epub 2019 Dec 24.
9
Higher levels of serum uric acid influences hepatic damage in patients with non-alcoholic fatty liver disease (NAFLD).血清尿酸水平升高影响非酒精性脂肪性肝病(NAFLD)患者的肝损伤。
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肝硬化患者痛风的结局:一项基于全国住院患者样本的研究。

Outcomes of gout in patients with cirrhosis: A national inpatient sample-based study.

作者信息

Khrais Ayham, Kahlam Aaron, Tahir Ali, Shaikh Amjad, Ahlawat Sushil

机构信息

Division of Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, United States.

Division of Medicine, St. Luke's University Health Network, Bethlehem, PA 18015, United States.

出版信息

World J Hepatol. 2023 Feb 27;15(2):303-310. doi: 10.4254/wjh.v15.i2.303.

DOI:10.4254/wjh.v15.i2.303
PMID:36926244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10011910/
Abstract

BACKGROUND

Hyperuricemia is a prerequisite for the development of gout. Elevated serum uric acid (UA) levels result from either overproduction or decreased excretion. A positive correlation between serum UA levels, cirrhosis-related complications and the incidence of nonalcoholic fatty liver disease has been established, but it is unknown whether hyperuricemia results in worsening cirrhosis outcomes. We hypothesize that patients with cirrhosis will have poorer gout outcomes.

AIM

To explore the link between cirrhosis and the incidence of gout-related complications.

METHODS

This was a cross-sectional study. The national inpatient sample was used to identify patients hospitalized with gout, stratified based on a history of cirrhosis, from 2001 to 2013 the International Classification of Diseases, Ninth Revision, Clinical Modification codes. Primary outcomes were mortality, gout complications and joint interventions. The test and independent -test were performed to assess categorical and continuous data, respectively. Multiple logistic regression was used to control for confounding variables.

RESULTS

Patients without cirrhosis were older (70.37 ± 13.53 years 66.21 ± 12.325 years; < 0.05). Most patients were male (74.63% in the cirrhosis group 66.83%; adjusted < 0.05). Patients with cirrhosis had greater rates of mortality (5.49% 2.03%; adjusted < 0.05), gout flare (2.89% 2.77%; adjusted < 0.05) and tophi (0.97% 0.75%; adjusted = 0.677). Patients without cirrhosis had higher rates of arthrocentesis (2.45% 2.21%; adjusted < 0.05) and joint injections (0.72% 0.52%; adjusted < 0.05).

CONCLUSION

Gout complications were more common in cirrhosis. Those without cirrhosis had higher rates of interventions, possibly due to hesitancy with performing these interventions given the higher complication risk in cirrhosis.

摘要

背景

高尿酸血症是痛风发生的前提条件。血清尿酸(UA)水平升高是由尿酸生成过多或排泄减少所致。血清UA水平、肝硬化相关并发症与非酒精性脂肪性肝病的发病率之间已确立存在正相关,但高尿酸血症是否会导致肝硬化结局恶化尚不清楚。我们推测肝硬化患者的痛风结局会更差。

目的

探讨肝硬化与痛风相关并发症发生率之间的联系。

方法

这是一项横断面研究。利用国家住院患者样本,根据肝硬化病史,从2001年至2013年《国际疾病分类,第九版,临床修订本》编码中识别出痛风住院患者。主要结局为死亡率、痛风并发症和关节干预措施。分别采用卡方检验和独立样本t检验来评估分类数据和连续数据。使用多元逻辑回归来控制混杂变量。

结果

无肝硬化患者年龄更大(70.37±13.53岁对66.21±12.325岁;P<0.05)。大多数患者为男性(肝硬化组为74.63%对66.83%;校正后P<0.05)。肝硬化患者的死亡率(5.49%对2.03%;校正后P<0.05)、痛风发作(2.89%对2.77%;校正后P<0.05)和痛风石(0.97%对0.75%;校正后P=0.677)发生率更高。无肝硬化患者的关节穿刺术(2.45%对2.21%;校正后P<0.05)和关节注射(0.72%对0.52%;校正后P<0.05)发生率更高。

结论

痛风并发症在肝硬化患者中更为常见。无肝硬化患者的干预措施发生率更高,这可能是由于考虑到肝硬化患者并发症风险较高而对实施这些干预措施有所顾虑。