Chair of Rheumatology and Rheumatology Unit, University Clinic and AOU of Cagliari, SS 554, 09042, Monserrato, Cagliari, Italy.
Arthritis Res Ther. 2017 Nov 10;19(1):247. doi: 10.1186/s13075-017-1451-5.
The aim was to assess the attainability and outcome of the lupus low disease activity state (LLDAS) in the early stages of systemic lupus erythematosus (SLE).
LLDAS prevalence was evaluated at 6 (T1) and 18 (T2) months after diagnosis and treatment initiation (T0) in a monocentric cohort of 107 (median disease duration 9.7 months) prospectively followed Caucasian patients with SLE. Reasons for failure to achieve LLDAS were also investigated. Multivariate models were built to identify factors associated with lack of LLDAS achievement and to investigate the relationship between LLDAS and Systemic Lupus International Collaboration Clinics (SLICC)/Damage Index (SDI) accrual.
There were 47 (43.9%) patients in LLDAS at T1 and 48 (44.9%) at T2. The most frequent unmet LLDAS criterion was prednisolone dose >7.5 mg/day (83% of patients with no LLDAS at T1). Disease manifestations with the lowest remission rate during follow up were increased anti-double-stranded DNA (persistently present in 85.7% and 67.5% of cases at T1 and T2, respectively), low serum complement fractions (73.2% and 66.3%) and renal abnormalities (46.4% and 28.6%). Renal involvement at T0 was significantly associated with failure to achieve LLDAS both at T1 (OR 7.8, 95% CI 1.4-43.4; p = 0.019) and T2 (OR 3.9, 95% CI 1.4-10.6; p = 0.008). Presence of any organ damage (SDI ≥1) at T2 was significantly associated with lack of LLDAS at T1 (OR 5.0, 95% CI 1.5-16.6; p = 0.009) and older age at diagnosis (OR 1.05 per year, 95% CI 1.01-1.09; p = 0.020).
LLDAS is a promising treatment target in the early stages of SLE, being attainable and negatively associated with damage accrual, but it fit poorly to patients with renal involvement.
本研究旨在评估系统性红斑狼疮(SLE)早期狼疮低疾病活动状态(LLDAS)的可达性和结局。
在一项前瞻性单中心队列研究中,对 107 例(中位疾病持续时间 9.7 个月)初诊后接受治疗的白人 SLE 患者,分别在诊断后 6 个月(T1)和 18 个月(T2)评估 LLDAS 的患病率。同时还探讨了无法达到 LLDAS 的原因。建立多变量模型以确定与无法实现 LLDAS 相关的因素,并探讨 LLDAS 与系统性红斑狼疮国际合作临床(SLICC)/损害指数(SDI)累积之间的关系。
T1 时有 47 例(43.9%)患者达到 LLDAS,T2 时有 48 例(44.9%)患者达到 LLDAS。未达到 LLDAS 的最常见标准是泼尼松剂量>7.5mg/天(T1 时无 LLDAS 的患者中 83%存在该情况)。在随访期间缓解率最低的疾病表现是抗双链 DNA 持续升高(分别在 T1 和 T2 时持续存在于 85.7%和 67.5%的病例中)、血清补体成分降低(73.2%和 66.3%)和肾脏异常(46.4%和 28.6%)。T0 时的肾脏受累与 T1 时(OR 7.8,95%CI 1.4-43.4;p=0.019)和 T2 时(OR 3.9,95%CI 1.4-10.6;p=0.008)均无法达到 LLDAS 显著相关。T2 时存在任何器官损害(SDI≥1)与 T1 时无法达到 LLDAS显著相关(OR 5.0,95%CI 1.5-16.6;p=0.009)和诊断时年龄较大(OR 1.05 岁/年,95%CI 1.01-1.09;p=0.020)。
在 SLE 的早期阶段,LLDAS 是一个有前途的治疗目标,其可达到,且与损害累积呈负相关,但对有肾脏受累的患者效果不佳。