Nøjgaard C, Johansen J S, Krarup H B, Holten-Andersen M, Møller A, Bendtsen F
Dept. of Gastroenterology, H:S, Hvidovre Hospital, University of Copenhagen, Denmark.
Scand J Gastroenterol. 2003 Jun;38(6):659-65. doi: 10.1080/00365520310002300.
The possible markers of liver fibrosis (plasma YKL-40, PIIINP, MMP-2 and TIMP-1) were measured at the start (t0) and end of treatment (t12) with alpha-interferon and ribavirin and repeated at 6-months follow-up (t18) in 51 patients with chronic hepatitis C.
We evaluated 1) whether treatment response is reflected by a decrease in these markers during antiviral therapy; 2) whether these markers reflect the activity of the disease; and 3) whether these markers could be used as predictors of the treatment response.
Baseline plasma YKL-40, MMP-2, PIIINP and TIMP-1 were significantly increased in patients compared to normal controls. In responders (n = 30), plasma YKL-40 (P < 0.05), MMP-2 (P < 0.05) and TIMP-1 (P < 0.001) decreased significantly at t18, and no changes were observed at t12. Plasma PIIINP was unchanged in responders. In non-responders (n = 19), plasma MMP-2 (P < 0.01) and TIMP-1 (P < 0.01) decreased significantly at t18, whereas plasma YKL-40 and PIIINP were unchanged. The markers were significantly correlated at baseline (P < 0.001). Plasma PIIINP at baseline could predict treatment response (P = 0.01).
Response to antiviral treatment is associated with a decrease in the fibrogenetic markers, but the markers do not reflect the biochemical disease activity during treatment. Baseline plasma PIIINP was the only marker predicting treatment response.
在51例慢性丙型肝炎患者中,于使用α-干扰素和利巴韦林治疗开始时(t0)和结束时(t12)检测了肝纤维化的可能标志物(血浆YKL-40、Ⅲ型前胶原氨基端肽(PIIINP)、基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶组织抑制因子-1(TIMP-1)),并在6个月随访时(t18)重复检测。
我们评估了1)这些标志物在抗病毒治疗期间的降低是否反映治疗反应;2)这些标志物是否反映疾病活动;3)这些标志物是否可作为治疗反应的预测指标。
与正常对照相比,患者的基线血浆YKL-40、MMP-2、PIIINP和TIMP-1显著升高。在治疗有反应者(n = 30)中,血浆YKL-40(P < 0.05)、MMP-2(P < 0.05)和TIMP-1(P < 0.001)在t18时显著降低,而在t12时未观察到变化。治疗有反应者的血浆PIIINP无变化。在无反应者(n = 19)中,血浆MMP-2(P < 0.01)和TIMP-1(P < 0.01)在t18时显著降低,而血浆YKL-40和PIIINP无变化。这些标志物在基线时显著相关(P < 0.001)。基线时的血浆PIIINP可预测治疗反应(P = 0.01)。
对抗病毒治疗的反应与促纤维化标志物的降低相关,但这些标志物不能反映治疗期间的生化疾病活动。基线血浆PIIINP是唯一预测治疗反应的标志物。