缬更昔洛韦预防抗黑色素瘤分化相关5基因抗体皮肌炎:中国的一项队列研究

IF 1.8
Li Shanshan, Wang Xiaoxing, Zhang Ling, Duan Jianghui, Liu Xia, Zhang Lu
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引用次数: 0

摘要

背景:巨细胞病毒(CMV)感染在抗黑色素瘤分化相关5基因抗体阳性皮肌炎(MDA5+DM)患者中普遍存在,并影响预后。本研究旨在评价缬更昔洛韦预防治疗MDA5+DM的疗效。方法:于2023年5月1日至2023年12月31日,连续招募成年活动性MDA5+DM患者,随访6个月。参与者根据是否服用缬更昔洛韦分为两组。分析巨细胞病毒感染的发生率和疾病活动性的变化。结果:本研究纳入49例活动性MDA5+DM患者。对18例患者给予缬更昔洛韦预防,其中包括9例快速进展性间质性肺病(RP-ILD)患者。在其余31例患者中,15例为RP-ILD。在随访期间,未观察到巨细胞病毒感染、不适或与缬更昔洛韦相关的异常实验室结果。对照组感染CMV 9例(p = 0.032)。在生存分析中,缬更昔洛韦组和对照组分别有2例和9例RP-ILD患者死亡(p = 0.084)。3个月和6个月时,两组患者的疾病活动度和糖皮质激素剂量无显著差异。此外,在治疗开始时使用生物和靶向合成抗风湿药物被确定为对照组活动性MDA5+DM患者CMV感染的危险因素(p = 0.007)。结论:缬更昔洛韦预防治疗可降低MDA5+DM患者CMV感染的发生率。对MDA5+DM治疗有潜在的辅助作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prophylaxis With Valganciclovir in Anti-Melanoma Differentiation Associated 5 Gene Antibody Dermatomyositis: A Cohort Study in China.

Background: Cytomegalovirus (CMV) infection is prevalent in patients with anti-melanoma differentiation-associated 5 gene antibody-positive dermatomyositis (MDA5+DM) and affects the prognosis. This study aimed to evaluate the efficacy of valganciclovir prophylaxis during MDA5+DM treatment.

Methods: Adult patients with active MDA5+DM were consecutively recruited from May 1, 2023 to December 31, 2023, and followed up for 6 months. Participants were categorized into 2 groups based on whether they received valganciclovir or not. The incidence of CMV infection and changes in disease activity were analyzed.

Results: This study included 49 patients with active MDA5+DM. Prophylaxis with valganciclovir was administered to 18 patients, including 9 patients with rapidly progressive interstitial lung disease (RP-ILD). Of the remaining 31 patients, 15 had RP-ILD. During the follow-up, no CMV infection, discomfort, or abnormal laboratory findings associated with valganciclovir were observed during the prophylaxis period. Nine patients in the control group were infected with CMV (p = 0.032). In the survival analysis, 2 and 9 patients with RP-ILD died in the valganciclovir and control groups, respectively (p = 0.084). No significant difference in disease activity and glucocorticoid dosage was observed between two groups at 3 and 6 months. Furthermore, the use of biological and targeted synthetic disease-modifying antirheumatic drugs at the initiation of treatment was identified as a risk factor for CMV infection in active MDA5+DM patients in the control group (p = 0.007).

Conclusion: Prophylaxis with valganciclovir can reduce the incidence of CMV infection during MDA5+DM treatment. It exerts a potential auxiliary effect on MDA5+DM treatment.

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