Takada Hitomi, Osawa Leona, Komiyama Yasuyuki, Muraoka Masaru, Suzuki Yuichiro, Sato Mitsuaki, Kobayashi Shoji, Yoshida Takashi, Takano Shinichi, Maekawa Shinya, Enomoto Nobuyuki
Gastroenterology and Hepatology Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
PLoS One. 2025 May 15;20(5):e0309852. doi: 10.1371/journal.pone.0309852. eCollection 2025.
Sarcopenia is a prognostic factor in patients with hepatocellular carcinoma (HCC). However, the mechanism underlying sarcopenia development in these patients remains unclear. The chemokine interferon-gamma-induced protein 10/C-X-C motif chemokine ligand 10 (IP-10) has been found to be associated with muscle regeneration or destruction. Thus, we aimed to clarify the role of serum IP-10 levels in predicting sarcopenia development in patients with HCC.
This retrospective study enrolled 120 patients with primary HCC whose serum IP-10 levels were measured both at baseline and 1 year after the confirmed diagnosis of HCC. Patients who had sarcopenia at baseline computed tomography imaging were assigned to the Sarco-base group, whereas those in whom sarcopenia was found for the first time after 3 years were assigned to the Sarco-develop group. Those who never met the criteria during the follow-up period were assigned to the Non-Sarco group.
The baseline IP-10 levels were significantly lower in the Sarco-base group compared to the rest (p = 0.016). Conversely baseline IP-10 levels and IP-10 ratio at 1 year were higher in the Sarco-develop group than in the Non-Sarco group (p = 0.0017, p = 0.025). High IP-10 levels at baseline, and high IP-10 ratios at 1 year were independently related factors for sarcopenia development.
Patients with sarcopenia at baseline more frequently presented with low IP-10 levels than those without. Contrarily, the group without sarcopenia at baseline and with high baseline IP-10 levels and high IP-10 ratios at 1 year were more likely to develop sarcopenia after 3 years. Monitoring of IP-10 levels may enable the identification of groups prone to develop sarcopenia in patients with HCC.
肌肉减少症是肝细胞癌(HCC)患者的一个预后因素。然而,这些患者发生肌肉减少症的潜在机制仍不清楚。已发现趋化因子γ干扰素诱导蛋白10/C-X-C基序趋化因子配体10(IP-10)与肌肉再生或破坏有关。因此,我们旨在阐明血清IP-10水平在预测HCC患者肌肉减少症发生中的作用。
这项回顾性研究纳入了120例原发性HCC患者,在确诊HCC时及确诊后1年测量其血清IP-10水平。基线计算机断层扫描成像显示有肌肉减少症的患者被分配到肌肉减少症基线组,而在3年后首次发现肌肉减少症的患者被分配到肌肉减少症发生组。在随访期间从未符合标准的患者被分配到非肌肉减少症组。
与其他组相比,肌肉减少症基线组的基线IP-10水平显著较低(p = 0.016)。相反,肌肉减少症发生组的基线IP-10水平和1年时的IP-10比值高于非肌肉减少症组(p = 0.0017,p = 0.025)。基线时高IP-10水平和1年时高IP-10比值是肌肉减少症发生的独立相关因素。
与无肌肉减少症的患者相比,基线时有肌肉减少症的患者更常表现为低IP-10水平。相反,基线时无肌肉减少症且基线IP-10水平高和1年时IP-10比值高的组在3年后更有可能发生肌肉减少症。监测IP-10水平可能有助于识别HCC患者中易发生肌肉减少症的群体。