Shigefuku Ryuta, Iwasa Motoh, Katayama Kazuhiro, Eguchi Akiko, Kawaguchi Takumi, Shiraishi Koichi, Ito Toshifumi, Suzuki Kazutomo, Koreeda Chizu, Ohtake Takaaki, Tokumoto Yoshio, Endo Ryujin, Kawamura Naohiro, Shiraki Makoto, Habu Daiki, Sakai Hironori, Kato Akinobu, Nishiguchi Shuhei, Moriwaki Hisataka, Suzuki Kazuyuki, Takei Yoshiyuki
Department of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Japan.
Department of Hepato-Biliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Hepatol Res. 2019 Oct;49(10):1127-1135. doi: 10.1111/hepr.13388. Epub 2019 Jul 16.
Hypozincemia is associated with the progression of chronic liver diseases, but it is unknown whether hypozincemia promotes human hepatocarcinogenesis. Our aim is to evaluate the serum zinc levels in liver cirrhosis (LC) patients and clarify the relationship between the serum zinc levels and the development of hepatocellular carcinoma (HCC).
Cirrhotic patients without HCC (n = 299) were enrolled from 14 medical institutes in Japan as a multicenter prospective study (No. 2028). Of the 299 patients, 157 were included in the present study based on reliable and consistent serum zinc levels and no history of oral zinc supplementation. Clinical parameters associated with the development of HCC were determined. Furthermore, the cumulative incidence of HCC was analyzed using Kaplan-Meier methods and was calculated using the log-rank test. A Cox regression analysis was utilized for the multivariate analysis to evaluate the predictors of hepatocarcinogenesis.
Thirty of 157 patients (19.1%) developed HCC during an observation period of 3 years. Serum zinc levels were significantly decreased in hepatitis C virus-related LC (C-LC) patients with HCC (0.0180). The risk factors for incidence of HCC were hypozincemia (0.0014), high α-fetoprotein (0.0080), low branched chain amino acids-to-tyrosine ratio (0.0128), or female sex (0.0228). Hypozincemia (hazard ratio 1.61, 0.0324) was the only significant predictor of hepatocarcinogenesis by multivariate Cox regression analysis.
Hypozincemia is associated with hepatocarcinogenesis in C-LC patients.
低锌血症与慢性肝病的进展相关,但低锌血症是否促进人类肝癌发生尚不清楚。我们的目的是评估肝硬化(LC)患者的血清锌水平,并阐明血清锌水平与肝细胞癌(HCC)发生之间的关系。
作为一项多中心前瞻性研究(第2028号),从日本14家医疗机构招募了无HCC的肝硬化患者(n = 299)。在这299例患者中,基于可靠且一致的血清锌水平以及无口服补锌史,157例被纳入本研究。确定了与HCC发生相关的临床参数。此外,使用Kaplan-Meier方法分析HCC的累积发病率,并使用对数秩检验进行计算。采用Cox回归分析进行多变量分析,以评估肝癌发生的预测因素。
在3年的观察期内,157例患者中有30例(19.1%)发生了HCC。HCC的丙型肝炎病毒相关LC(C-LC)患者血清锌水平显著降低(0.0180)。HCC发生的危险因素为低锌血症(0.0014)、高甲胎蛋白(0.0080)、低支链氨基酸与酪氨酸比值(0.0128)或女性(0.0228)。通过多变量Cox回归分析,低锌血症(风险比1.61,0.0324)是肝癌发生的唯一显著预测因素。
低锌血症与C-LC患者的肝癌发生相关。