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拉米夫定治疗成功可能与慢性乙型肝炎和肝硬化患者血清铁蛋白水平降低相关。

Successful treatment with lamivudine may correlate with reduction of serum ferritin levels in the patients with chronic hepatitis and liver cirrhosis type B.

机构信息

Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences of Niigata University, 1-754, Asahimachi-Dori, Niigata-city, 951-8122, Japan,

出版信息

Hepatol Int. 2008 Sep;2(3):382-7. doi: 10.1007/s12072-008-9084-z. Epub 2008 Jul 25.

DOI:10.1007/s12072-008-9084-z
PMID:19669269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2716891/
Abstract

PURPOSE

To study the changes in serum ferritin levels in lamivudine (LAM)-treated patients with chronic hepatitis and liver cirrhosis type B and determine whether successful treatment with LAM results in a reduction of serum ferritin levels.

METHODS

Thirty patients with chronic hepatitis B virus (HBV) infection were followed prospectively during their treatment with LAM for 12 months. Serum HBV DNA, ferritin levels, and emergence of YMDD mutants were monitored. A case of severe liver cirrhosis with hepatic hemosiderosis that was treated successfully with LAM also is shown as a representative case.

RESULTS

Serum alanine aminotransferase and ferritin levels decreased significantly more in the patients treated with LAM without YMDD mutants (n = 23) than those with mutants (n = 7). Hepatic hemosiderosis along with serum iron markers improved greatly in the representative patient.

CONCLUSION

Successful treatment with LAM may reduce serum ferritin levels and improve hepatic siderosis in a subset of patients with chronic HBV infection.

摘要

目的

研究拉米夫定(LAM)治疗慢性乙型肝炎和肝硬化患者血清铁蛋白水平的变化,确定 LAM 是否能成功降低血清铁蛋白水平。

方法

前瞻性观察 30 例慢性乙型肝炎病毒(HBV)感染者,用 LAM 治疗 12 个月,监测血清 HBV DNA、铁蛋白水平及 YMDD 突变的出现。并以一例成功用 LAM 治疗的严重肝硬化伴肝血色素沉着症患者为例。

结果

在无 YMDD 突变(n=23)的 LAM 治疗患者中,血清丙氨酸氨基转移酶和铁蛋白水平显著降低,而在有突变(n=7)的患者中则无显著变化。该代表患者的肝血色素沉着症和血清铁标志物明显改善。

结论

在慢性 HBV 感染的部分患者中,LAM 的成功治疗可能降低血清铁蛋白水平并改善肝铁沉积。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/fca3ae7f9918/12072_2008_9084_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/a4bc5078ee82/12072_2008_9084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/ef8452a81295/12072_2008_9084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/20fb29d38a6b/12072_2008_9084_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/fca3ae7f9918/12072_2008_9084_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/a4bc5078ee82/12072_2008_9084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/ef8452a81295/12072_2008_9084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/20fb29d38a6b/12072_2008_9084_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81db/2716891/fca3ae7f9918/12072_2008_9084_Fig4_HTML.jpg

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