Serum 25-hydroxyvitamin D3 levels affect treatment outcome in pegylated interferon/ribavirin combination therapy for compensated cirrhotic patients with hepatitis C virus genotype 1b and high viral load

被引:10
作者
Atsukawa, Masanori [1 ]
Tsubota, Akihito [2 ]
Shimada, Noritomo [3 ]
Kondo, Chisa [1 ]
Itokawa, Norio [1 ]
Nakagawa, Ai [1 ]
Hashimoto, Satomi [4 ]
Fukuda, Takeshi [4 ]
Matsushita, Yoko [4 ]
Narahara, Yoshiyuki [4 ]
Iwakiri, Katsuhiko [1 ]
Nakatsuka, Katsuhisa [4 ]
Kawamoto, Chiaki [4 ]
Sakamoto, Choitsu [4 ]
机构
[1] Chiba Hokusoh Hosp, Nippon Med Sch, Dept Internal Med, Div Gastroenterol, Inzai, Japan
[2] Jikei Univ, Sch Med, ICMR, Kashiwa, Chiba, Japan
[3] Shinmatsudo Cent Gen Hosp, Div Gastroenterol & Hepatol, Matsudo, Chiba, Japan
[4] Nippon Med Sch, Dept Internal Med, Div Gastroenterol & Hepatol, Tokyo 113, Japan
关键词
cirrhosis; hepatitis C virus; 25-hydroxyvitamin D-3; pegylated interferon; ribavirin; sustained virological response; SUSTAINED VIROLOGICAL RESPONSE; COMMON GENETIC-DETERMINANTS; GENOME-WIDE ASSOCIATION; VITAMIN-D; HEPATOCELLULAR-CARCINOMA; PLUS RIBAVIRIN; PEGINTERFERON ALPHA-2B; NATURAL-HISTORY; SEVERE FIBROSIS; PEG-INTERFERON;
D O I
10.1111/hepr.12298
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimMuch is unknown about the effect of 25-hydroxyvitamin D-3 levels on the outcome of pegylated interferon/ribavirin (PEG IFN/RBV) therapy for hepatitis C virus-related cirrhosis. The purpose of the present study was to analyze and elucidate factors, including 25-hydroxyvitamin D-3, that contribute to a sustained virological response (SVR) in patients with cirrhosis. MethodsWe analyzed whether 25-hydroxyvitamin D-3 contributes to the response to PEG IFN/RBV therapy among 134 cirrhotic patients. ResultsSVR was achieved in 43 patients. The median 25-hydroxyvitamin D-3 level was 20ng/mL. Univariate analysis showed that the following factors contributed to SVR: low-density lipoprotein cholesterol, albumin, 25-hydroxyvitamin D-3, core a.a.70 (a.a.70) substitutions, the number of mutations at the interferon sensitivity-determining region and IL28B genotype. Multivariate analysis identified IL28B genotype and 25-hydroxyvitamin D-3 as independent factors contributing to SVR. Subsequently, SVR rate was examined by using 25-hydroxyvitamin D-3 and other important factors. The SVR rate was 51.8% in patients with core a.a.70 wild and 15ng/mL of 25-hydroxyvitamin D-3, whereas the SVR rate was 7.1% in patients with core a.a.70 wild and <15ng/mL of 25-hydroxyvitamin D-3. The SVR rate was 56.9% in patients with IL28B major genotype and 15ng/mL of 25-hydroxyvitamin D-3. Surprisingly, the SVR rate was 0% in patients with IL28B minor genotype and <15ng/mL of 25-hydroxyvitamin D-3. ConclusionIL28B genotype and 25-hydroxyvitamin D-3 were identified as independent factors contributing to SVR. Stratified analyses according to core a.a.70 substitution and IL28B genotype suggested that 25-hydroxyvitamin D-3 influences the outcome of PEG IFN/RBV therapy for cirrhosis.
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收藏
页码:1277 / 1285
页数:9
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