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抗病毒治疗可降低 HBeAg 阴性慢性乙型肝炎和显著门静脉高压所致肝硬化患者的门静脉压力。

Antiviral therapy reduces portal pressure in patients with cirrhosis due to HBeAg-negative chronic hepatitis B and significant portal hypertension.

机构信息

Department of Gastroenterology, Polyclinic General Hospital, Athens, Greece.

出版信息

J Hepatol. 2009 Sep;51(3):468-74. doi: 10.1016/j.jhep.2009.05.031. Epub 2009 Jul 3.

Abstract

BACKGROUND/AIMS: Lamivudine improves liver histology in patients with chronic hepatitis B (CHB), but its effects on portal pressure remain unknown. We evaluated the effect of lamivudine monotherapy on hepatic venous pressure gradient (HVPG) in CHB-related cirrhosis with significant portal hypertension.

METHODS

We studied 19 patients with cirrhosis due to HBeAg-negative CHB and HVPG >or=10 mm Hg treated with oral lamivudine (100mg daily). Liver biochemistry, Child-Pugh and MELD score were determined every 3 months, alpha-fetoprotein and HBV DNA every 6 months and HVPG at baseline and at 12 months after lamivudine initiation. Diuretics, beta-blockers, antibiotics and/or endoscopic therapy were used for routine indications.

RESULTS

At 12 months, a significant reduction was observed in ALT (p=0.001), HBV DNA (p=0.002), Child-Pugh (p=0.012) and MELD score (p=0.006). Four patients developed virological breakthrough during treatment. At 12 months, HVPG decreased in all but one patient [baseline: 14.4+/-3.9 and 12 months: 12.4+/-3.3 mm Hg (p=0.007)]. HVPG decreased >20% or below the 12 mm Hg threshold in 10 of 13 patients with baseline HVPG >or=12 mm Hg. HVPG increased in a patient with hepatic flare after virological breakthrough.

CONCLUSION

In conclusion, in patients with cirrhosis due to HBeAg-negative CHB, lamivudine monotherapy reduces HVPG, especially when virological suppression and biochemical remission is achieved.

摘要

背景/目的:拉米夫定可改善慢性乙型肝炎(CHB)患者的肝脏组织学,但对门脉压的影响尚不清楚。我们评估了拉米夫定单药治疗 HBeAg 阴性 CHB 相关肝硬化伴显著门脉高压患者的肝静脉压力梯度(HVPG)的效果。

方法

我们研究了 19 例 HBV DNA 阳性、HBeAg 阴性 CHB 相关肝硬化且 HVPG≥10mmHg 的患者,这些患者接受口服拉米夫定(100mg 每天)治疗。每 3 个月检测一次肝功能、Child-Pugh 和 MELD 评分,每 6 个月检测一次甲胎蛋白和 HBV DNA,在基线和拉米夫定治疗 12 个月后检测 HVPG。利尿剂、β受体阻滞剂、抗生素和/或内镜治疗根据常规适应证使用。

结果

12 个月时,ALT(p=0.001)、HBV DNA(p=0.002)、Child-Pugh(p=0.012)和 MELD 评分(p=0.006)显著降低。4 例患者在治疗期间发生病毒学突破。12 个月时,除 1 例患者外,所有患者的 HVPG 均下降[基线:14.4±3.9mmHg 和 12 个月:12.4±3.3mmHg(p=0.007)]。在基线 HVPG≥12mmHg 的 13 例患者中,有 10 例 HVPG 下降超过 20%或降至 12mmHg 以下。1 例发生病毒学突破后肝脏炎症加重的患者 HVPG 增加。

结论

总之,在 HBeAg 阴性 CHB 相关肝硬化患者中,拉米夫定单药治疗可降低 HVPG,尤其是在实现病毒学抑制和生化缓解时。

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