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本文引用的文献

1
Review article: the endocannabinoid system in liver disease, a potential therapeutic target.综述文章:肝脏疾病中的内源性大麻素系统,一个有潜力的治疗靶点。
Aliment Pharmacol Ther. 2014 Apr;39(8):790-801. doi: 10.1111/apt.12673. Epub 2014 Feb 24.
2
Role of interleukin 28-B in the spontaneous and treatment-related clearance of HCV infection in patients with chronic HBV/HCV dual infection.白细胞介素28-B在慢性HBV/HCV双重感染患者HCV感染的自发清除及治疗相关清除中的作用
Eur J Clin Microbiol Infect Dis. 2014 Apr;33(4):559-67. doi: 10.1007/s10096-013-1985-7. Epub 2013 Oct 1.
3
Hepatitis C virus induces interleukin-1β (IL-1β)/IL-18 in circulatory and resident liver macrophages.丙型肝炎病毒诱导循环和驻留于肝脏的巨噬细胞中白细胞介素-1β(IL-1β)/白细胞介素-18。
J Virol. 2013 Nov;87(22):12284-90. doi: 10.1128/JVI.01962-13. Epub 2013 Sep 4.
4
A Simple Noninvasive Score Based on Routine Parameters can Predict Liver Cirrhosis in Patients With Chronic Hepatitis C.基于常规参数的简单无创评分可预测慢性丙型肝炎患者的肝硬化
Hepat Mon. 2013 May 8;13(5):e8352. doi: 10.5812/hepatmon.8352. eCollection 2013 May.
5
Cannabinoids decrease the th17 inflammatory autoimmune phenotype.大麻素可降低Th17炎症性自身免疫表型。
J Neuroimmune Pharmacol. 2013 Dec;8(5):1265-76. doi: 10.1007/s11481-013-9493-1. Epub 2013 Jul 28.
6
M2 Kupffer cells promote M1 Kupffer cell apoptosis: a protective mechanism against alcoholic and nonalcoholic fatty liver disease.M2 库普弗细胞促进 M1 库普弗细胞凋亡:一种针对酒精性和非酒精性脂肪性肝病的保护机制。
Hepatology. 2014 Jan;59(1):130-42. doi: 10.1002/hep.26607. Epub 2013 Nov 20.
7
Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C.腹部脂肪与 PNPLA3 I148M 相互作用,但与慢性丙型肝炎肝脂肪变性发病机制中的 APOC3 变异体无关。
J Viral Hepat. 2013 Aug;20(8):517-23. doi: 10.1111/jvh.12053. Epub 2013 Jan 7.
8
Kupffer cells in the liver.肝脏中的库普弗细胞。
Compr Physiol. 2013 Apr;3(2):785-97. doi: 10.1002/cphy.c120026.
9
Association between a polymorphism in cannabinoid receptor 2 and severe necroinflammation in patients with chronic hepatitis C.大麻素受体 2 多态性与慢性丙型肝炎患者严重坏死性炎症的关联。
Clin Gastroenterol Hepatol. 2014 Feb;12(2):334-40. doi: 10.1016/j.cgh.2013.05.008. Epub 2013 May 22.
10
Clinical presentation, outcome, and response to therapy among patients with acute exacerbation of chronic hepatitis C.慢性丙型肝炎急性加重患者的临床表现、转归和治疗反应。
Clin Gastroenterol Hepatol. 2013 Sep;11(9):1174-1180.e11. doi: 10.1016/j.cgh.2013.03.025. Epub 2013 Apr 13.

大麻素受体2 - 63 QQ变异体与慢性丙型肝炎患者血清转氨酶水平持续正常有关。

Cannabinoid receptor 2-63 QQ variant is associated with persistently normal aminotransferase serum levels in chronic hepatitis C.

作者信息

Coppola Nicola, Zampino Rosa, Sagnelli Caterina, Bellini Giulia, Marrone Aldo, Stanzione Maria, Capoluongo Nicolina, Boemio Adriana, Minichini Carmine, Adinolfi Luigi Elio, Maione Sabatino, Del Giudice Emanuele Miraglia, Sagnelli Evangelista, Rossi Francesca

机构信息

Department of Mental Health and Public Medicine, Second University of Naples, Naples, Italy.

Internal Medicine and Hepatology, Second University of Naples, Naples, Italy.

出版信息

PLoS One. 2014 Jun 18;9(6):e99450. doi: 10.1371/journal.pone.0099450. eCollection 2014.

DOI:10.1371/journal.pone.0099450
PMID:24940753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4062424/
Abstract

BACKGROUND AND AIM

To evaluate in anti-HCV-positive patients the clinical impact of the rs35761398 variant of the CNR2 gene leading to the substitution of Gln (Q) of codon 63 of the cannabinoid receptor 2 (CB2) with Arg (R).

PATIENTS AND METHODS

253 consecutive anti-HCV-/HCV-RNA-positive patients were enrolled, of whom 53 were HCV carriers with persistently normal ALT (PNALT group) and 200 had a history of steadily abnormal serum ALT values (abnormal ALT group). All patients were naive for antiviral therapy and were screened for the CNR2 rs35761398 polymorphism by a TaqMan assay.

RESULTS

Subjects in the PNALT group, compared with those in the abnormal ALT group were older (58.5±12 vs. 50.7±12.4 years, p = 0.001), more frequently female (66% vs. 42%, p = 0.003), with lower body mass index (BMI) (24.5±3.1 vs. 26.6±4.6, p = 0.003), and more frequently with HCV genotype 2 (43.1% vs 17.7%, p = 0.0002) and CB2-63 QQ variant (34% vs. 11%, p = 0.0001). Considering all 253 patients, no difference in the demographic, biochemical, or virological data was observed between patients in the different CB2-63 variants. The logistic regression analysis identified CB2-63 QQ, HCV genotype 2, older age and lower BMI as independent predictors of PNALT (p<0.00001).

DISCUSSION

The CB2-63 QQ variant in HCV patients was independently associated with the PNALT status.

摘要

背景与目的

评估大麻素受体2(CB2)第63位密码子的谷氨酰胺(Q)被精氨酸(R)取代的CNR2基因rs35761398变体在抗丙型肝炎病毒(HCV)阳性患者中的临床影响。

患者与方法

纳入253例连续的抗HCV/HCV-RNA阳性患者,其中53例为丙氨酸氨基转移酶(ALT)持续正常的HCV携带者(PNALT组),200例有血清ALT值持续异常病史(ALT异常组)。所有患者均未接受过抗病毒治疗,采用TaqMan分析检测CNR2 rs35761398多态性。

结果

与ALT异常组相比,PNALT组患者年龄更大(58.5±12岁对50.7±12.4岁,p = 0.001),女性比例更高(66%对42%,p = 0.003),体重指数(BMI)更低(24.5±3.1对26.6±4.6,p = 0.003),HCV基因2型比例更高(43.1%对17.7%,p = 0.0002),CB2-63 QQ变体比例更高(34%对11%,p = 0.0001)。在所有253例患者中,不同CB2-63变体患者的人口统计学、生化或病毒学数据均无差异。逻辑回归分析确定CB2-63 QQ、HCV基因2型、年龄较大和BMI较低是PNALT的独立预测因素(p<0.00001)。

讨论

HCV患者中的CB2-63 QQ变体与PNALT状态独立相关。