Division of Clinical Research, Department of Pediatrics, Batchelor Children's Research Institute, University of Miami, Miami, FL, USA.
J Pediatr Gastroenterol Nutr. 2010 Aug;51(2):191-7. doi: 10.1097/MPG.0b013e3181d32756.
Evidence demonstrates that obesity is associated with progression of chronic hepatitis C virus (HCV) infection and poor response to interferon therapy among HCV-infected adults. However, this evidence has been confounded by multiple comorbidities present in adult cohorts and the use of single adult doses.
We performed a retrospective investigation to evaluate the role of body mass index (BMI) in chronic HCV progression and response to therapy in the children. One hundred twenty-three children and teenagers studied at Children's Hospital Boston for HCV infection between 1998 and 2007 were included. Patients' weight and height at the time of liver biopsy or before and after HCV therapy were obtained and BMI was calculated.
The presence of steatosis was statistically associated with higher mean (+/-SE) BMI percentiles (72nd +/- 5.8 vs 58th +/- 3.5) percentile; F(1,101) = 4.2, P = 0.04. Nonresponders to treatment had a higher mean (+/-SE) BMI percentile (70th +/- 7.4) when compared with responders (50th +/- 6.5) in univariate and multivariate analyses (P = 0.04, P = 0.02, respectively). Using a multivariate model, it was calculated that 1 standard deviation (1 z-score unit) increase in baseline BMI z score is associated with a 12% decrease in the probability of sustained virologic response.
Overweight adversely affects the progression of chronic HCV liver disease and is associated with diminished response to antiviral therapy using weight-based dosing in a cohort with minimal comorbidities.
有证据表明,肥胖与慢性丙型肝炎病毒(HCV)感染的进展以及 HCV 感染成年人对干扰素治疗的反应不佳有关。然而,这些证据受到成人队列中存在多种合并症和使用单一成人剂量的影响。
我们进行了一项回顾性研究,以评估体重指数(BMI)在儿童慢性 HCV 进展和治疗反应中的作用。1998 年至 2007 年期间,在波士顿儿童医院接受 HCV 感染治疗的 123 名儿童和青少年被纳入研究。我们获得了患者肝活检时或 HCV 治疗前后的体重和身高,并计算了 BMI。
脂肪变性的存在与较高的平均(+/-SE)BMI 百分位(72 百分位+/-5.8 与 58 百分位+/-3.5)显著相关;F(1,101)=4.2,P=0.04。与应答者相比,治疗无应答者的平均(+/-SE)BMI 百分位(70 百分位+/-7.4)更高,在单变量和多变量分析中(P=0.04,P=0.02)。使用多变量模型,计算得出基线 BMI z 分数增加 1 个标准差(1 z 评分单位),则持续病毒学应答的概率降低 12%。
超重会对慢性 HCV 肝病的进展产生不利影响,并与使用基于体重的剂量治疗最小合并症的患者的抗病毒治疗反应降低相关。