Department of Internal Medicine, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung, Taiwan.
J Gastroenterol Hepatol. 2011 Mar;26(3):530-5. doi: 10.1111/j.1440-1746.2010.06438.x.
Cytokines activation is a common feature in chronic hepatitis C (CHC) infection. Visfatin, as a recently-recognized adipocytokine, may correlate with metabolic abnormalities. We aimed to elucidate the characteristics of visfatin in CHC patients.
This retrospective study included 102 treatment-naïve CHC patients and 97 sex-/age-matched healthy adults. Serum visfatin levels were examined by an enzyme linked immunosorbent assay test. The correlation between visfatin and hepatitis C virus (HCV) infection in terms of virological, metabolic, and histopathological profiles was analyzed. The impact of visfatin on the treatment response to pegylated interferon plus ribavirin (PEGIFN/RBV) therapy was also assessed.
The visfatin level was correlated significantly with fibrosis scores (r = 0.23, P = 0.02) in CHC patients. A significant higher visfatin level was observed in CHC patients with histological activity index scores of mild and more (P = 0.01) and advanced fibrosis (P = 0.04). The mean visfatin level (0.81 ± 0.28 log ng/mL) of 26 CHC patients with metabolic syndrome was significantly lower than their counterparts (0.95 ± 0.30 log ng/mL) (P = 0.03). There was no significant correlation between visfatin and HCV genotypes, viral load, and treatment response to PEGIFN/RBV therapy. Multiple logistic regression analyses demonstrated that metabolic syndrome was the leading negative variable (odds ratio = 0.09, 95% confidence interval = 0.02-0.46, P = 0.004) associated with high visfatin level, followed by advanced fibrosis (odds ratio = 2.88, 95% confidence interval = 1.06-6.78, P = 0.03).
Serum visfatin was correlated with disease severity and metabolic syndrome in CHC patients.
细胞因子激活是慢性丙型肝炎(CHC)感染的常见特征。内脏脂肪素(visfatin)作为一种新发现的脂肪细胞因子,可能与代谢异常有关。本研究旨在阐明 CHC 患者内脏脂肪素的特征。
本回顾性研究纳入了 102 例未经治疗的 CHC 患者和 97 名性别和年龄匹配的健康成年人。采用酶联免疫吸附试验检测血清内脏脂肪素水平。分析内脏脂肪素与 HCV 感染的病毒学、代谢和组织病理学特征的相关性。还评估了内脏脂肪素对聚乙二醇干扰素联合利巴韦林(PEGIFN/RBV)治疗反应的影响。
CHC 患者的内脏脂肪素水平与纤维化评分显著相关(r = 0.23,P = 0.02)。CHC 患者组织学活动指数评分轻度及以上(P = 0.01)和进展性纤维化(P = 0.04)者内脏脂肪素水平显著较高。26 例代谢综合征 CHC 患者的平均内脏脂肪素水平(0.81 ± 0.28 log ng/mL)显著低于对照组(0.95 ± 0.30 log ng/mL)(P = 0.03)。内脏脂肪素与 HCV 基因型、病毒载量和 PEGIFN/RBV 治疗反应无显著相关性。多因素 logistic 回归分析显示,代谢综合征是与高内脏脂肪素水平相关的主要负性变量(比值比 = 0.09,95%置信区间 = 0.02-0.46,P = 0.004),其次是进展性纤维化(比值比 = 2.88,95%置信区间 = 1.06-6.78,P = 0.03)。
CHC 患者血清内脏脂肪素与疾病严重程度和代谢综合征相关。