肝脏 ›› 2024, Vol. 29 ›› Issue (7): 852-856.

• 其他肝病 • 上一篇    下一篇

学龄前儿童传染性单核细胞增多症合并肝功能异常的临床特征及影响因素

岳贇, 马丽, 王卫国   

  1. 236000 安徽 阜阳市人民医院检验科
  • 收稿日期:2024-03-01 出版日期:2024-07-31 发布日期:2024-08-27
  • 基金资助:
    2022年度安徽省高校科研项目(2022AH040107)

Clinical characteristics and influencing factors of liver function abnormalities in preschool children with infectious mononucleosis

YUE Yun, MA Li, WANG Wei-guo   

  1. Fuyang People's Hostital, Anhui 236000, China
  • Received:2024-03-01 Online:2024-07-31 Published:2024-08-27

摘要: 目的 分析传染性单核细胞增多症(IM)合并肝功能异常患儿的临床特征及影响因素。方法 回顾性分析阜阳市人民医院2020年1月至2023年7月IM并接受治疗的140例学龄前儿童的临床资料。将患儿分为肝功能正常组和肝功能异常组,比较两组患儿的基本情况、临床症状、住院时间及实验室指标。logistic二元回归分析IM合并肝功能异常的影响因素。受试者工作特征曲线(ROC)分析相关指标的临床价值。结果 IM合并肝功能异常的患儿61例,肝功能正常79例。两组患儿年龄、性别、发病季节,临床症状及EBV阳性病毒载量比较,差异无统计学意义(P>0.05)。肝功能异常组患儿住院天数为7(6,9)d、淋巴细胞计数为10.10(8.65,14.82)×109/L,CD8+T淋巴细胞为7690.00(4585.37,11164.50)/μL,高于肝功能正常组的6(5,7)d、9.33(6.79,12.11)×109/L、5900.66(3637.12, 8746.00)/μL,差异有统计学意义(P<0.05);而CD4+/CD8+比值为0.21(0.17,0.29)、中性粒细胞为2.7(2.06,4.12)×109/L、血小板计数为199(148,228.5)×109/L、系统炎症免疫指数(SII)为46.34(26.63,93.78),明显低于肝功能正常组患儿,差异均有统计学意义(P<0.05)。低SII与IM合并肝功能异常密切相关。SII诊断并发肝功能异常临界值为59.13,曲线下面积为0.758,诊断价值较高,且优于CD8+T淋巴细胞及CD4+/CD8+比值。结论 IM合并肝功能异常患儿存在明显的细胞免疫功能紊乱。当患儿存在高CD8+T淋巴细胞,低SII和低CD4+/CD8+比值时合并肝功能异常的风险较高。

关键词: 传染性单核细胞增多症, EB病毒, 肝功能异常, 系统炎症免疫指数

Abstract: Objective To analyze the clinical characteristics and factors influencing liver function abnormalities in preschool children with infectious mononucleosis (IM). Methods A retrospective analysis was conduced on the clinical and laboratory data of 140 preschool children diagnosed with IM and treated at Fuyang People's Hospital from January 2020 to July 2023. Based on alanine aminotransferase (ALT) levels, the children were categorized into a normal liver function group(ALT <50 U/L) and an abnormal liver function group(ALT ≥50 U/L). Basic conditions, clinical symptoms, hospitalization duration, and laboratory indices were compared between the two groups. Statistically significant indices were further analyzed using covariance adjustment and binary regression analysis. Additionally, the clinical value of relevant indices was assessed using receiver operating characteristic (ROC) analysis, with pairwise comparisons of the area under the curve (AUC) to determine statistical significance. Results The incidence of liver function abnormalities in preschool children with IMwas 43.6%. There were no statistically significant differences in age, gender, season of onset, clinical symptoms, and viral load of EBV-positive children between the two groups (P>0.05). Compared to the group with normal liver function, the group with abnormal liver function had significantly higher hospitalization days[7(6,9)d], lymphocyte count[10.10(8.65,14.82)×109/L] and CD8+ T lymphocytes[7690.00(4585.37,11164.50)/uL] (P<0.05), Conversely, the CD4+/CD8+ ratio[0.21(0.17,0.29)], neutrophil count[2.7(2.06,4.12)×109/L], platelet count[199(148,228.5)×109/L], and systemic immune-inflammation index (SII) [46.34(26.63, 93.78)]were significantly lower in the abnormal liver gunction group (P<0.05). Low SII was closely associated with liver function abnormalities in IM preschoolers. The diagnostic efficacy of SII for liver function abnormalities was assessed using ROC curve analysis, with a critical value of 59.13 and an AUC of 0.758, indicating high diagnostic value, superior to CD8+T lymphocytes and CD4+/CD8+ ratio. Conclusion Preschool children with IM and concurrent liver function abnormalities exhibit significant cellular immune dysfunction. Elevated CD8+ T-lymphocytes, low SII and low CD4+/ CD8+ ratio are associated with a high risk of liver abnormalities. These findings suggest that clinical attention should be focused on these immunological markers to better manage and monitor the risk of liver function abnormalitis in IM preschool children.

Key words: infectious mononucleosis, EBV, hepatic dysfunction, systemic immune-inflammation index