Predictive factors of psychiatric syndrome in patients with systemic lupus erythematosus

医学 自身抗体 内科学 情绪障碍 系统性红斑狼疮 抗磷脂综合征 精神科 疾病 免疫学 抗体 血栓形成 焦虑
作者
Wenqi Geng,Shangzhu Zhang,Jinya Cao,Xia Hong,Yanping Duan,Yinan Jiang,Jing Wei
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:15 被引量:9
标识
DOI:10.3389/fimmu.2024.1323209
摘要

Introduction Early detection of neuropsychiatric systemic lupus erythematosus (NPSLE) remains a challenge in clinical settings. Previous studies have found different autoantibodies as markers for NPSLE. This study aimed to describe the distribution of psychiatric syndromes in a group of patients with systemic lupus erythematosus (SLE) and to investigate the association between psychiatric syndromes and specific autoantibodies. Methods This retrospective study was conducted at a single medical center in China. We reviewed medical records of hospitalized patients with SLE who were consulted by psychiatrists due to potential mental disorders. Results of serum autoantibodies and general laboratory tests were collected. The correlation between clinical variables was examined. Binary logistic regression analyses were used to determine factors related to NPSLE and different psychiatric diagnoses. Results Among the 171 psychiatric manifestations in 160 patients, 141 (82.4%) were attributed to SLE. Acute confusional state (ACS) had the highest prevalence (57.4%). Anti-cardiolipin (ACL) antibody ( X 2 = 142.261, p < 0.001) and anti-β2 glycoprotein I (-β2GP1) antibody ( X 2 = 139.818, p < 0.001) varied significantly between groups, with the highest positive rate found in patients with mood disorders (27.3% and 18.2%). SLE disease activity index – 2000 (SLEDAI-2K) score excluding item ACS and item psychosis was a predictor of NPSLE (OR 1.172 [95% CI 1.105 - 1.243]). Conclusions Disease activity reflected by SLEDAI-2K score is a predictor for NPSLE. Antiphospholipid antibodies are associated with mood disorders in SLE. Further separate investigation of neuropsychiatric disorders is needed in order to better comprehend NPSLE’s pathological mechanism.
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