Prophylaxis With Valganciclovir in Anti–Melanoma Differentiation Associated 5 Gene Antibody Dermatomyositis: A Cohort Study in China

医学 皮肌炎 队列 伐更昔洛韦 抗体 内科学 队列研究 肿瘤科 皮肤病科 免疫学 病毒 人巨细胞病毒 巨细胞病毒感染
作者
Li Shanshan,Xiaoxing Wang,Ling Zhang,Duan Jianghui,Xia Liu,Lu Zhang
出处
期刊:Jcr-journal of Clinical Rheumatology [Ovid Technologies (Wolters Kluwer)]
标识
DOI:10.1097/rhu.0000000000002274
摘要

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. 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. 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). 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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