【风湿病伴肝功能异常患者的临床特点】。

C Y Wu, M C Li, X W Duan, H B Li, Y H Wang, Q Li, H Luo, J Xu, L J Wu, Y F Wang, C Zhao, Y F Fang, S D Lin, D Xu, X P Tian, M T Li, X F Zeng
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引用次数: 0

摘要

目的:探讨风湿性疾病合并肝功能异常患者的临床特点,确定肝功能异常的比例及严重程度。方法:横断面研究。数据收集自2011年至2021年在中国风湿病数据中心登记的患者。本研究分析的风湿性疾病包括类风湿关节炎(RA)、系统性红斑狼疮(SLE)、干燥综合征(SS)、强直性脊柱炎(AS)和痛风。收集患者资料,包括人口统计学特征[年龄、性别、体重指数(BMI)、吸烟史等]、肝功能检查结果[谷丙转氨酶(ALT)、天冬氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、总胆红素等]、抗风湿免疫药物和保肝药物的使用情况,比较肝功能正常组和肝功能异常组之间的差异。此外,还比较了不同性别和年龄组的肝功能异常比例。结果:本研究共纳入116 308例患者,其中RA 49 659例,SLE 17 597例,SS 9 039例,AS 11 321例,痛风28 692例。RA患者肝功能异常比例最低[11.02%(5 470/49 659)],其次是SS[17.97%(1 624/9 039)]和AS [18.22% (2 063/11 321)], SLE[21.14%(3 720/17 597)]和痛风[28.73%(8 242/28 692)]患者肝功能异常比例最高。ALT升高,通常被归类为1级,是最常见的肝功能异常,而ALP升高是最不常见的。部分服用保肝药物的患者肝功能正常,其中痛风患者的比例最低[7.45% (36/483)],RA、SLE、SS、AS患者的比例为21.7% ~ 30.34%。在所有疾病类型中,男性肝功能异常的比例均高于女性[RA: 13.8%(1 368/9 906)比10.3%(4 102/39 753);SLE: 33.6% (479/1 424) vs. 20.0% (3 241/16 173);SS: 25.4%(111/437) vs. 17.6%(1 513/8 602);AS: 20.1%(1 629/8 119) vs. 13.6% (434/3 202);痛风:29.3% (8 033/27 394)vs. 16.1%(209/1 298)。在RA、SLE和AS中,所有年龄组的肝功能异常比例相似。SS患者肝功能异常比例随年龄增长而增加[结论:风湿病患者合并肝功能异常比例高,保肝药物使用率低。]在风湿病治疗过程中,应重视患者肝功能的监测,及时使用保肝药物,优化保肝方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical characteristics of patients with rheumatic diseases and abnormal liver function].

Objective: To investigate the clinical characteristics of patients with rheumatic diseases and abnormal liver function, as well as determine the proportion and severity of liver function abnormalities. Methods: Cross-sectional study. Data were collected from patients registered in the Chinese Rheumatism Date Center from 2011 to 2021. The rheumatic diseases analyzed in this study were rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), Sjogren syndrome (SS), ankylosing spondylitis (AS), and gout. Patient data, including demographic characteristics [ such as age, sex, body mass index,(BMI), and smoking history], liver function test results [including alanine aminotransferase (ALT), aspartate aminotransferase, alkaline phosphatase(ALP), and total bilirubin], and use of anti-rheumatic immune drugs and liver-protective drugs, were collected and compared between groups with normal and abnormal liver functions. In addition, the proportions of abnormal liver function were compared between sex and age groups. Results: A total of 116 308 patients were included in this study, including 49 659 with RA, 17 597 with SLE, 9 039 with SS, 11 321 with AS, and 28 692 with gout. The lowest proportion of liver function abnormalities was observed in patients with RA[11.02% (5 470/49 659)], followed by those with SS[17.97% (1 624/9 039)] and AS [18.22% (2 063/11 321) ], whereas patients with SLE [21.14% (3 720/17 597) ] and gout [28.73% (8 242/28 692)] exhibited the highest proportion of these abnormalities. Elevated ALT, mostly classified as grade 1, was the most commonly noted liver function abnormality, whereas elevated ALP was the least common. Some patients who took liver-protective drugs had normal liver function, with the lowest percentage observed in patients with gout [7.45% (36/483) ] and ranging from 21.7% to 30.34% in patients with RA, SLE, SS, and AS. The proportion of liver function abnormalities was higher in males than in females for all disease types [RA: 13.8%(1 368/9 906) vs. 10.3%(4 102/39 753); SLE: 33.6% (479/1 424) vs. 20.0% (3 241/16 173); SS: 25.4%(111/437) vs. 17.6%(1 513/8 602); AS: 20.1%(1 629/8 119) vs. 13.6% (434/3 202); and gout: 29.3% (8 033/27 394) vs. 16.1% (209/1 298)]. In RA, SLE, and AS, the proportions of liver function abnormalities were similar across all age groups. In SS, the proportion of liver function abnormalities increased with age [<40 years: 14.9%(294/1 979); 40-59 years: 18.1%(858/4 741); ≥60 years: 20.4%(472/2 319)], whereas a reversal of this trend was observed in gout [<40 years: 34.9%(4 294/12 320); 40-59 years: 25.5%(2 905/11 398);≥60 years: 21.0%(1 042/4 971)]. Conclusions: The proportions of combined liver function abnormalities in patients with rheumatologic diseases were high, and the utilization rates of liver-protective drugs were low. It is necessary to pay more attention to monitoring patients' liver function, timely administer liver-protective drugs, and optimize liver-protective regimens during the treatment of rheumatic diseases.

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