Fujii Hideki, Fujii Makoto, Iwaki Michihiro, Hayashi Hideki, Toyoda Hidenori, Oeda Satoshi, Hyogo Hideyuki, Kawanaka Miwa, Morishita Asahiro, Munekage Kensuke, Kawata Kazuhito, Tsutsumi Tsubasa, Sawada Koji, Maeshiro Tatsuji, Tobita Hiroshi, Yoshida Yuichi, Naito Masafumi, Araki Asuka, Arakaki Shingo, Kawaguchi Takumi, Noritake Hidenao, Ono Masafumi, Masaki Tsutomu, Yasuda Satoshi, Tomita Eiichi, Yoneda Masato, Kawada Norifumi, Tokushige Akihiro, Kamada Yoshihiro, Takahashi Hirokazu, Ueda Shinichiro, Aishima Shinichi, Sumida Yoshio, Nakajima Atsushi, Okanoue Takeshi
Department of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Division of Health Sciences, Graduate School of Medicine, Osaka University, Suita, Japan.
Hepatol Res. 2023 May;53(5):391-400. doi: 10.1111/hepr.13884. Epub 2023 Feb 17.
Impacts of platelet counts at the time of liver biopsy on hepatocellular carcinoma (HCC) development in patients with nonalcoholic fatty liver disease (NAFLD) remain unknown. The aim of this study was to investigate the prognostic value of platelet counts in patients with biopsy-confirmed NAFLD using data from a multicenter study.
One thousand three hundred ninety-eight patients were included in this subanalysis of the CLIONE (Clinical Outcome Nonalcoholic Fatty Liver Disease) in Asia study. Liver biopsy specimens were pathologically diagnosed, and histologically scored using the NASH Clinical Research Network system. Demographic, clinical, laboratory, and pathological data were collected.
During a median follow-up period of 4.6 years (range, 0.3-21.6 years), which corresponds to 8874 person-years, 37 patients developed HCC. Using a cut-off baseline platelet count of 192 × 109/L, the lower platelet group had a higher HCC rate than the higher platelet group (6.7% vs. 0.4%; p < 0.001). This cut-off value significantly stratified the event-free rate for HCC. Lower platelet counts were associated with an increased risk of HCC development. Relative to patients with platelet counts of 192 × 109/L, patients with platelet counts of 100 × 109/L had an unadjusted hazard ratio (HR) for HCC development of 7.37 (95% confidence interval [CI], 3.81-14.2) and an adjusted HR of 11.2 (95% CI, 3.81-32.7; p < 0.001), adjusting for age, sex, NASH, and diabetes.
Baseline platelet counts of 192 × 109/L and lower are associated with a higher risk of developing HCC in patients with biopsy-confirmed NAFLD and require active surveillance.
肝活检时血小板计数对非酒精性脂肪性肝病(NAFLD)患者肝细胞癌(HCC)发生发展的影响尚不清楚。本研究旨在利用一项多中心研究的数据,探讨活检确诊的NAFLD患者血小板计数的预后价值。
本亚组分析纳入了亚洲CLIONE(非酒精性脂肪性肝病临床结局)研究中的1398例患者。对肝活检标本进行病理诊断,并使用非酒精性脂肪性肝炎临床研究网络系统进行组织学评分。收集人口统计学、临床、实验室和病理数据。
在中位随访期4.6年(范围0.3 - 21.6年),相当于8874人年的时间里,有37例患者发生了HCC。以基线血小板计数192×10⁹/L为界值,血小板计数较低组的HCC发生率高于血小板计数较高组(6.7%对0.4%;p < 0.001)。该界值显著分层了HCC的无事件发生率。较低的血小板计数与HCC发生风险增加相关。与血小板计数为192×10⁹/L的患者相比,血小板计数为100×10⁹/L的患者发生HCC的未调整风险比(HR)为7.37(95%置信区间[CI],3.81 - 14.2),调整年龄、性别、非酒精性脂肪性肝炎和糖尿病后调整HR为11.2(95%CI,3.81 - 32.7;p < 0.001)。
活检确诊的NAFLD患者基线血小板计数低于192×10⁹/L与发生HCC的较高风险相关,需要进行积极监测。