摘要 8 - 银屑病和类风湿关节炎的肝损伤风险与代谢风险因素而非甲氨蝶呤和来氟米特有关

Ho Yin Chung, S. C. Chan, Christina Sze Man Wong
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引用次数: 0

摘要

目的 评估银屑病(PsO)和类风湿性关节炎(RA)患者肝损伤和肝纤维化的相关性。方法 在 2020 年 7 月至 2022 年 8 月期间,连续招募了 318 名在玛丽医院皮肤科和/或风湿病门诊就诊、临床诊断为银屑病、银屑病关节炎(PsA)或类风湿性关节炎(RA)的患者。研究人员记录了人口统计学数据、合并症和用药情况。测量了体重指数(BMI)。测定了肝损伤的血清生物标志物,包括自体免疫球蛋白、基质金属蛋白酶(MMP)3、MMP 8 和 MMP 9。通过瞬态弹性成像(TE)测定肝脏硬度(LSM)和受控衰减参数(CAP)。建立回归模型以确定甲氨蝶呤和来氟米特累积剂量、血清生物标记物和 TE 评分之间的关联。结果 共有 67 例(20.4%)患者的 LSM>7.1 kPa。多变量线性回归显示,甲氨蝶呤累积用量与自体表皮生长因子水平相关(B=4.77,95% CI 1.39; 8.15,P=0.001)。甲氨蝶呤累积剂量与 MMP 3、MMP 8、MMP 9、LSM 和 CAP 之间没有关联。来氟米特(leflunomide)的累积剂量与自旋霉素、MMP 3、MMP 8、MMP 9、LSM、CAP之间也没有关联。BMI(B=6.18,95% CI 4.95;7.41,p<0.001)、高血压(B=18.98,95% CI 4.15;31.82,p=0.01)、高脂血症(B=20.21,95% CI 3.50;36.92,p=0.02)与 CAP 相关。结论 甲氨蝶呤和来氟米特对PsO和RA患者的肝脏风险极小。代谢风险因素与肝损伤密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 8 — Risk of Liver Injury in Psoriasis and Rheumatoid Arthritis is Associated with Metabolic Risk Factors Rather than Methotrexate and Leflunomide
Objectives To assess the associations of hepatic injury and fibrosis in patients with psoriasis (PsO) and rheumatoid arthritis (RA). Methods A total of 318 patients attending dermatology and/or rheumatology out-patient clinics in Queen Mary Hospital, with clinical diagnosis of PsO, psoriatic arthritis (PsA) or RA were consecutively recruited from July 2020 to August 2022. Demographic data, comorbidities, and medications were recorded. Body mass index (BMI) was measured. Serum biomarkers for hepatic injury including autotaxin, matrix metalloproteinase (MMP) 3, MMP 8, and MMP 9 were determined. Transient elastography (TE) was performed to determine liver stiffness measure (LSM) and controlled attenuation parameter (CAP). Regression models were built to determine the association between methotrexate and leflunomide cumulative dosage, serum biomarkers and TE scores. Results A total of 67 (20.4%) patients had LSM>7.1 kPa. Multivariate linear regression showed methotrexate cumulative dosage was associated with autotaxin level (B=4.77, 95% CI 1.39; 8.15, p=0.001). There was no association between methotrexate cumulative dosage and MMP 3, MMP 8, MMP 9, LSM, CAP. There was also no association between leflunomide cumulative dosage and autotaxin, MMP 3, MMP 8, MMP 9, LSM, CAP. BMI (B=6.18, 95% CI 4.95; 7.41, p<0.001), hypertension (B=18.98, 95% CI 4.15; 31.82, p=0.01), hyperlipidaemia (B=20.21, 95% CI 3.50; 36.92, p=0.02) were associated with CAP. Conclusion Methotrexate and leflunomide have minimal hepatic risk in patient with PsO and RA. Metabolic risk factors had strong associations with hepatic injury.
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