Prashar Nisha, Tugnet Nicola, Kumar Sunil, Sapsford Mark, Ng Kristine Pek Ling
Rheumatology Department, Health New Zealand Counties Manukau, Auckland, New Zealand.
Rheumatology Department, Health New Zealand, Auckland, New Zealand.
Rheumatol Adv Pract. 2025 Jun 25;9(3):rkaf075. doi: 10.1093/rap/rkaf075. eCollection 2025.
To examine ethnic differences in LLDAS attainment and lupus nephritis (LN) in SLE patients from the Auckland, New Zealand (NZ) cohort of the Asia Pacific Lupus Collaboration (APLC) treat-to-target (T2T) Lupus Low Disease Activity State (LLDAS) study. Secondary outcomes were to explore ethnic differences in medication use, SLE damage and patient-reported health outcomes.
All patients fulfilled either the 1997 American College of Rheumatology classification criteria for SLE or Systemic Lupus International Collaborating Clinics 2012 classification criteria. At each study visit, patients were assessed for LLDAS attainment, flares and medication use and assessed annually for SLE damage and patient-reported health outcomes.
A total of 141 patients from three Auckland tertiary hospitals were analysed during 2018-2020. Seventy-five percent ( = 106) of patients achieved LLDAS on at least one occasion. There was a statistically significant difference in attainment of LLDAS across the three sites in Auckland, where patients from South Auckland exhibited significantly lower LLDAS rates [37% ( = 14)] compared with the other two sites (88-90%; < 0.0001). Forty of 141 (28%) had LN. Non-NZ European patients had proportionally more proliferative (class III/IV) LN compared with NZ European patients [ = 28/34 (82%) and 2/6 (33%), respectively; = 0.01]. A total of 55% ( = 78) of the cohort had ever used prednisone.
This is the first NZ study to provide prospective data on SLE disease outcomes. The majority of patients were able to achieve LLDAS. There were ethnic differences in proliferative LN with overrepresentation in non-NZ European ethnic groups.
在亚太狼疮协作组(APLC)达标治疗(T2T)狼疮低疾病活动状态(LLDAS)研究的新西兰奥克兰队列中,研究系统性红斑狼疮(SLE)患者在实现LLDAS及狼疮性肾炎(LN)方面的种族差异。次要结局是探讨药物使用、SLE损伤及患者报告的健康结局方面的种族差异。
所有患者均符合1997年美国风湿病学会SLE分类标准或2012年系统性红斑狼疮国际协作临床分类标准。在每次研究访视时,评估患者是否实现LLDAS、病情复发及药物使用情况,并每年评估SLE损伤及患者报告的健康结局。
2018年至2020年期间,对奥克兰三家三级医院的141例患者进行了分析。75%(n = 106)的患者至少有一次实现了LLDAS。奥克兰三个研究点在实现LLDAS方面存在统计学显著差异,南奥克兰的患者实现LLDAS的比例显著低于其他两个研究点[37%(n = 14)],其他两个研究点为88% - 90%;P < 0.0001)。141例患者中有40例(28%)患有LN。与新西兰欧洲裔患者相比,非新西兰欧洲裔患者中增殖性(III/IV级)LN的比例更高[分别为28/34(82%)和2/6(33%);P = 0.01]。该队列中共有55%(n = 78)的患者曾使用过泼尼松。
这是新西兰第一项提供SLE疾病结局前瞻性数据的研究。大多数患者能够实现LLDAS。增殖性LN存在种族差异,非新西兰欧洲裔种族群体中比例过高。