Department of Rheumatology, First Faculty of Medicine Charles University, Prague, Czech Republic.
Physiol Res. 2020 Apr 30;69(2):339-346. doi: 10.33549/physiolres.934308. Epub 2020 Mar 23.
The aim of this study was to determine the role of the tumor necrosis factor like weak inducer of apoptosis (TWEAK) as a serum biomarker of neuropsychiatric involvement in systemic lupus erythematosus (NPSLE). Levels of TWEAK levels were measured in sera of 92 patients with systemic lupus erythematosus (SLE), including 28 patients with neuropsychiatric lupus, and in 59 healthy controls using ELISA. All SLE patients underwent rheumatological, neurological and psychiatric assessment. We found no significant differences in TWEAK levels, between SLE patients and the healthy controls (p=0.2411). Similarly, no difference was observed between subgroup of NPSLE and healthy controls (p=0.7658). The mean SLE disease activity (SLEDAI) was 13.25. No correlations between TWEAK levels with disease activity (SLEDAI, r=0.2113, p=0.2805) or the most common NPSLE manifestations such as headache (r=0.2079), seizures (r=0.1101), cerebrovascular disease (r= 0.2347), cognitive dysfunction (r=0.1597) and anxiety (r=0.1397) were observed. Our data do not support the use of serum TWEAK as a discriminating biomarker for NPSLE. The role of the TWEAK in NPSLE remains to be investigated.
本研究旨在确定肿瘤坏死因子样凋亡弱诱导剂(TWEAK)作为系统性红斑狼疮(NPSLE)神经精神受累血清生物标志物的作用。采用 ELISA 法检测 92 例系统性红斑狼疮(SLE)患者(包括 28 例神经精神狼疮患者)和 59 例健康对照者血清中 TWEAK 水平。所有 SLE 患者均接受了风湿病学、神经病学和精神病学评估。我们发现 TWEAK 水平在 SLE 患者与健康对照组之间无显著差异(p=0.2411)。同样,NPSLE 亚组与健康对照组之间也未观察到差异(p=0.7658)。平均 SLE 疾病活动度(SLEDAI)为 13.25。TWEAK 水平与疾病活动度(SLEDAI,r=0.2113,p=0.2805)或最常见的 NPSLE 表现如头痛(r=0.2079)、癫痫发作(r=0.1101)、脑血管病(r=0.2347)、认知功能障碍(r=0.1597)和焦虑(r=0.1397)之间均无相关性。我们的数据不支持使用血清 TWEAK 作为 NPSLE 的鉴别生物标志物。TWEAK 在 NPSLE 中的作用仍有待研究。