Ran Y, Wang X Y, Yang Z, Li J W, Zhang X, Shen M, Wang X Y, Jia H, Han Z Z, Yang H, Zhou L
Department of Gastroenterology and Hepatology, General Hospital, Tianjin Medical University, Tianjin 300052, China.
Zhonghua Gan Zang Bing Za Zhi. 2025 Jul 20;33(7):637-644. doi: 10.3760/cma.j.cn501113-20250504-00170.
To explore the clinical characteristics and identification of the independent risk factors for disease progression in patients with anti-gp210 antibody-positive primary biliary cholangitis (PBC). A retrospective cohort study was performed. A total of 323 cases with PBC diagnosed in Tianjin Medical University General Hospital from January 2013 to June 2023 (125 patients with anti-gp210 antibody-positive and 198 patients with anti-gp210 antibody-negative) were included. Baseline and follow-up data were collected. The independent sample t-test and Mann-Whitney rank sum test were used for comparison between groups of continuous data. The test was used to compare the data between groups for the count data. The Pearson test was used for correlation analysis between continuous variables. The Kaplan-Meier method was used to analyze the disease progression-free survival rate. The Cox regression model was used to analyze the risk factors for disease progression. The male proportion (11.2% . 5.1%, =0.040) and IgM level [3.29(1.88, 4.80) g/L . 2.56(1.44, 3.87) g/L, =0.019] were significantly higher in patients with PBC with positive anti-gp210 antibodies than those of the negative group. Histopathological analysis showed that the Scheuer score [1(0,3) . 0(0,2)], bile duct inflammation [(2(1,3) . 1(1,2)] and bile duct reaction score [(2(1,3) . 1(1,2)] were higher in the positive group than those of the negative group (<0.05), and the maturity of the tertiary lymphoid structure was higher (=0.011). Kaplan-Meier analysis showed that the 5-year disease-free survival rate was significantly lower in patients with positive anti-gp210 antibodies than that of the negative group (55.8% . 79.7%, =0.006) at a median follow-up of 3(2,6) years. Multivariate Cox regression analysis showed that γ-glutamyl transferase [=1.002 (95%: 1.000~1.003)] and platelet count [=0.993 (95%: 0.988~0.999)] were the independent influencing factors for disease progression in patients with anti-gp210 antibody-positive PBC (=0.002, 0.017). Patients with anti-gp210 antibody-positive PBC have more severe clinical pathological manifestations and a higher risk of disease progression. Higher levels of γ-glutamyl transferase and lower platelet counts during the first visit are independent risk factors for disease progression in patients with anti-gp210 antibody-positive PBC, which can be used as dynamic monitoring indicators for this population, suggesting the need for early intensive intervention.
探讨抗糖蛋白210(gp210)抗体阳性原发性胆汁性胆管炎(PBC)患者的临床特征及疾病进展独立危险因素的识别。进行了一项回顾性队列研究。纳入2013年1月至2023年6月在天津医科大学总医院诊断的323例PBC患者(125例抗gp210抗体阳性患者和198例抗gp210抗体阴性患者)。收集基线和随访数据。连续数据组间比较采用独立样本t检验和曼-惠特尼秩和检验。计数资料组间数据比较采用检验。连续变量间采用Pearson检验进行相关性分析。采用Kaplan-Meier法分析无疾病进展生存率。采用Cox回归模型分析疾病进展的危险因素。抗gp210抗体阳性的PBC患者男性比例(11.2%对5.1%,P = 0.040)和IgM水平[3.29(1.88,4.80)g/L对2.56(1.44,3.87)g/L,P = 0.019]显著高于阴性组。组织病理学分析显示,阳性组的Scheuer评分[1(0,3)对0(0,2)]、胆管炎症[(2(1,3)对1(1,2)]和胆管反应评分[(2(1,3)对1(1,2)]高于阴性组(P < 0.05),三级淋巴结构成熟度更高(P = 0.011)。Kaplan-Meier分析显示,抗gp210抗体阳性患者的5年无病生存率明显低于阴性组(55.8%对79.7%,P = 0.006),中位随访时间为3(2,6)年。多因素Cox回归分析显示,γ-谷氨酰转移酶[HR = 1.002(95%CI:1.000~1.003)]和血小板计数[HR = 0.993(95%CI:0.988~0.999)]是抗gp210抗体阳性PBC患者疾病进展的独立影响因素(P = 0.002,0.017)。抗gp210抗体阳性的PBC患者临床病理表现更严重,疾病进展风险更高。首次就诊时较高的γ-谷氨酰转移酶水平和较低的血小板计数是抗gp210抗体阳性PBC患者疾病进展的独立危险因素,可作为该人群的动态监测指标,提示需要早期强化干预。