Yoon S K, Kim S S, Park Y M, Shim K S, Lee C D, Sun H S, Park D H, Kim B S, Ryu W S, Cho J M
Department of Internal Medicine, Catholic University Medical College, Seoul, Korea.
Korean J Intern Med. 1995 Jul;10(2):94-102. doi: 10.3904/kjim.1995.10.2.94.
Interferon is the only established treatment for chronic hepatitis C but the host-dependent or virus-related factors affecting the response rate to interferon therapy are not yet clear. The purpose of this study was to investigate the factors predictive of response to interferon-alfa therapy in chronic hepatitis C.
Twenty-five consecutive patients with chronic hepatitis C were randomized to three regimens of interferon-alfa: group A (n = 7, 3 MU every day for 3 months), group B (n = 8, 3 MU every other day for 3 months) and group C (n = 10, 3 MU every other day for 6 months). We quantified serum HC RNA levels by competitive reverse transcription-polymerase chain reaction (RT-PCR) and performed HCV genotyping using type-specific primers deduced form the NS5 region of the HCV genome. We also attempted to identify which demographic, biochemical and histologic factors in addition to virus-related factors would significantly predict beneficial response to interferon by multivariate analysis.
Sustained responders were 8 (36.4%), nonsustained responders were 2 (9.1%) and nonresponders were 12 (54.5%) of 22 patients who had received complete therapy. The initial HCV RNA level (logarithmic transformed copy numbers per ml of serum) in sustained responders (5.75 +/- 0.39) was significantly lower than that of nonsustained responders (6.80 +/- 0.71) and nonresponders (6.70 +/- 0.52) (p < 0.05). In multivariate multiple logistic regression analysis, the serum HCV RNA level before therapy was only the independent predictor of a sustained response to interferon-alfa therapy (p = 0.001).
Serum HCV RNA level before therapy was the most useful predictor of a sustained response to interferon-alfa therapy for chronic hepatitis C.
干扰素是目前治疗慢性丙型肝炎的唯一已确立的疗法,但影响干扰素治疗反应率的宿主依赖性或病毒相关因素尚不清楚。本研究的目的是调查预测慢性丙型肝炎患者对α干扰素治疗反应的因素。
25例连续的慢性丙型肝炎患者被随机分为三种α干扰素治疗方案:A组(n = 7,每天3MU,共3个月),B组(n = 8,隔日3MU,共3个月)和C组(n = 10,隔日3MU,共6个月)。我们通过竞争性逆转录-聚合酶链反应(RT-PCR)定量血清HC RNA水平,并使用从HCV基因组NS5区域推导的型特异性引物进行HCV基因分型。我们还试图通过多变量分析确定除病毒相关因素外,哪些人口统计学、生化和组织学因素能显著预测对干扰素的有益反应。
在接受完整治疗的22例患者中,持续应答者为8例(36.4%),非持续应答者为2例(9.1%),无应答者为12例(54.5%)。持续应答者的初始HCV RNA水平(每毫升血清的对数转换拷贝数)(5.75±0.39)显著低于非持续应答者(6.80±0.71)和无应答者(6.70±0.52)(p<0.05)。在多变量多元逻辑回归分析中,治疗前血清HCV RNA水平是对α干扰素治疗持续应答的唯一独立预测因素(p = 0.001)。
治疗前血清HCV RNA水平是慢性丙型肝炎患者对α干扰素治疗持续应答的最有用预测指标。