Division of Hematology, Rheumatology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa, 761-0793, Japan.
Department of Hygiene, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Clin Rheumatol. 2022 Nov;41(11):3345-3353. doi: 10.1007/s10067-022-06282-0. Epub 2022 Jul 18.
In patients with systemic lupus erythematosus (SLE), a higher frequency of atherosclerotic lesions is associated with poor prognosis. Hydroxychloroquine (HCQ) has been reported to improve the lifespan and the prognosis of dyslipidaemia in patients with SLE, but the mechanism is unclear. We investigated the effect of supplemental HCQ treatment on the levels of serum cytokines associated with atherosclerosis in patients with stable SLE.
Patients with SLE who received supplemental HCQ and maintained low disease activity between January 2016 and September 2020 were included in this study. Disease activity was assessed using Safety of Estrogens in Lupus National Assessment-SLE Disease Activity Index, Cutaneous Lupus Erythematous Disease Area and Severity Index, and Lupus Low Disease Activity State. Serum complement titres, anti-dsDNA antibodies, and serum cytokines (adiponectin, resistin, and leptin) were analyzed before and after HCQ treatment.
Forty-one patients (4 males and 37 females, mean age 41.3 ± 13.2 years) were included. Serum adiponectin levels were significantly increased after 3 months of HCQ treatment compared to baseline, and serum resistin levels were significantly reduced. The change in serum resistin level after HCQ administration was correlated with a significant reduction in serum TNF-α, interleukin (IL)-6, IL-8, and IL-1RA levels.
Supplemental HCQ treatment in patients with SLE improved adipokine levels. HCQ may improve prognosis by controlling disease activity in SLE and reducing risk factors for atherosclerosis. Key Points • Hydroxychloroquine has been reported to improve the prognosis of dyslipidaemia in patients with SLE, but the underlying mechanism is unclear. • In this study, hydroxychloroquine improved adipokine levels in patients with SLE, implicating adipokines as a potential mechanism underlying the benefit of hydroxychloroquine on dyslipidaemia. • Supplemental hydroxychloroquine should be considered in patients with SLE harboring lipid abnormalities and risk factors for atherosclerosis.
在系统性红斑狼疮(SLE)患者中,动脉粥样硬化病变的频率较高与预后不良相关。羟氯喹(HCQ)已被报道可改善 SLE 患者的寿命和血脂异常的预后,但机制尚不清楚。我们研究了补充 HCQ 治疗对稳定 SLE 患者与动脉粥样硬化相关的血清细胞因子水平的影响。
本研究纳入了 2016 年 1 月至 2020 年 9 月期间接受补充 HCQ 且疾病活动度保持较低的 SLE 患者。使用安全性评估雌激素在狼疮性肾炎活动指数-系统性红斑狼疮疾病活动指数、皮肤狼疮红斑面积和严重程度指数以及狼疮低疾病活动状态评估疾病活动度。分析了 HCQ 治疗前后的血清补体滴度、抗 dsDNA 抗体和血清细胞因子(脂联素、抵抗素和瘦素)。
共纳入 41 例患者(4 例男性,37 例女性,平均年龄 41.3±13.2 岁)。与基线相比,HCQ 治疗 3 个月后血清脂联素水平显著升高,而血清抵抗素水平显著降低。HCQ 给药后血清抵抗素水平的变化与血清 TNF-α、白细胞介素(IL)-6、IL-8 和 IL-1RA 水平的显著降低相关。
SLE 患者补充 HCQ 治疗可改善脂联素水平。HCQ 可能通过控制 SLE 疾病活动度和降低动脉粥样硬化风险因素来改善预后。
关键点
·羟氯喹已被报道可改善 SLE 患者血脂异常的预后,但潜在机制尚不清楚。
·本研究中,羟氯喹改善了 SLE 患者的脂联素水平,提示脂联素可能是羟氯喹改善血脂异常的潜在机制之一。
·对于存在血脂异常和动脉粥样硬化风险因素的 SLE 患者,应考虑补充羟氯喹。