Sagnelli Caterina, Uberti-Foppa Caterina, Hasson Hamid, Bellini Giulia, Minichini Carmine, Salpietro Stefania, Messina Emanuela, Barbanotti Diletta, Merli Marco, Punzo Francesca, Coppola Nicola, Lazzarin Adriano, Sagnelli Evangelista, Rossi Francesca
Department of Mental Health and Public Medicine, Section of Infectious Diseases, University of Campania Luigi Vanvitelli, Naples, Italy.
Department of Infectious Diseases, Vita-Salute University, San Raffaele Scientific Institute, Milan, Italy.
PLoS One. 2017 Jul 31;12(7):e0181890. doi: 10.1371/journal.pone.0181890. eCollection 2017.
This is the first study to analyze the 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) on the clinical presentation of chronic hepatitis in HIV/HCV coinfected patients.
Enrolled in this study were 166 consecutive HIV/HCV coinfected patients, naïve for HCV treatment. A pathologist unaware of the patients' condition graded liver fibrosis, necroinflammation (Ishak) and steatosis. All patients were screened for the CB2 rs35761398 polymorphism.
Of the 166 HIV/HCV coinfected patients, 72.9% were males, 42.5% were infected with HCV-genotype-3 and 60.2% had been intravenous drug users. The median age was 40.6 years and the immunological condition good (median CD4+ cells/mm3 = 507, IQR: 398.0-669.5). Thirty-five (21.1%) patients were naive for ART and 131(78.9%) were on ART. The CB2-RR variant was detected in 45.8% of patients, QR in 38.6% and QQ in 15.7%. Patients with CB2-RR showed a necroinflammation score (HAI) ≥9 more frequently than those with CB2-QQ or CB2-QR (32.9% vs. 11.5% and 14.1%, respectively, p≤0.001). In the multivariate analysis, the CB2-RR variant (p = 0.03) and liver fibrosis were both identified as independent predictors of the entity of liver necroinflammation (p = 0.0001).
This study shows interesting interplay between the CB2-RR variant and liver necroinflammation in chronic hepatitis patients with HIV/HCV coinfection, an observation of clinical value that coincides with the interest in the use of the CB2 agonists and antagonists in clinical practice emerging from the literature.
本研究首次分析大麻素受体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变异对HIV/HCV合并感染患者慢性肝炎临床表现的影响。
本研究纳入166例连续的未接受过HCV治疗的HIV/HCV合并感染患者。一名不了解患者病情的病理学家对肝纤维化、坏死性炎症(Ishak评分)和脂肪变性进行分级。所有患者均接受CB2 rs35761398多态性筛查。
166例HIV/HCV合并感染患者中,72.9%为男性,42.5%感染HCV-3型,60.2%曾是静脉吸毒者。中位年龄为40.6岁,免疫状况良好(中位CD4+细胞/mm³ = 507,四分位间距:398.0 - 669.5)。35例(21.1%)患者未接受抗逆转录病毒治疗(ART),131例(78.9%)正在接受ART治疗。45.8%的患者检测到CB2-RR变异,38.6%为QR,15.7%为QQ。与CB2-QQ或CB2-QR患者相比,CB2-RR患者坏死性炎症评分(HAI)≥9更为常见(分别为32.9%、11.5%和14.1%,p≤0.001)。在多变量分析中,CB2-RR变异(p = 0.03)和肝纤维化均被确定为肝脏坏死性炎症程度的独立预测因素(p = 0.0001)。
本研究显示了HIV/HCV合并感染的慢性肝炎患者中CB2-RR变异与肝脏坏死性炎症之间存在有趣的相互作用,这一具有临床价值的观察结果与文献中对CB2激动剂和拮抗剂在临床实践中应用的关注相契合。