D. Korkus, MD, The Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa.
T. Gazitt, MD, MSc, Amir Haddad, MD, Rheumatology Unit, Carmel Medical Center, Haifa.
J Rheumatol. 2021 Feb;48(2):207-213. doi: 10.3899/jrheum.190940. Epub 2020 May 15.
To assess the prevalence of systemic lupus erythematosus (SLE) in a psoriatic arthritis (PsA) cohort and to compare it to the general population using the database of a large healthcare provider.
We analyzed the database of a PsA cohort (2002-2017), matched for age and sex, with randomly selected controls for demographics, clinical and laboratory manifestations, and dispensed medications. Statistical analysis used test and chi-square test as appropriate. In the PsA group, incidence density sampling was performed matching PsA patients without SLE as controls to each case of PsA with SLE by age and follow-up time. Univariable and multivariable conditional logistic regression analyses were used to assess factors affecting SLE development.
The PsA and control groups consisted of 4836 and 24,180 subjects, respectively, with a median age of 56 ± 15 years, and of whom 53.8% were female. Eighteen patients (0.37%) in the PsA group and 36 patients (0.15%) in the control group were diagnosed with SLE ( = 0.001). SLE patients without PsA had higher anti-dsDNA and anticardiolipin antibodies. The usage of drugs with known potential to induce SLE was higher in the PsA than in the control group. Older age at PsA diagnosis, shorter PsA duration, and statin treatment were associated with SLE in PsA patients.
A 2.3-fold increase in the prevalence of SLE in PsA relative to the control group was found. Risk factors for SLE development included older age at PsA diagnosis, shorter PsA duration, and statin treatment. The association between PsA and SLE may affect treatment choices and medication development.
评估红斑狼疮(SLE)在银屑病关节炎(PsA)患者中的患病率,并使用大型医疗保健机构的数据库将其与普通人群进行比较。
我们分析了 2002 年至 2017 年间的 PsA 队列数据库,该队列按年龄和性别与随机选择的对照组相匹配,以比较人口统计学、临床和实验室表现以及用药情况。统计分析使用 检验和卡方检验。在 PsA 组中,采用发病率密度抽样法,根据年龄和随访时间,将没有 SLE 的 PsA 患者与每个患有 SLE 的 PsA 患者进行匹配。使用单变量和多变量条件逻辑回归分析来评估影响 SLE 发展的因素。
PsA 组和对照组分别包含 4836 例和 24180 例患者,中位年龄为 56 ± 15 岁,其中 53.8%为女性。在 PsA 组中,有 18 例(0.37%)患者被诊断为 SLE,而在对照组中,有 36 例(0.15%)患者被诊断为 SLE( = 0.001)。没有 PsA 的 SLE 患者具有更高的抗 dsDNA 和抗心磷脂抗体。在 PsA 组中,使用已知有潜在诱导 SLE 风险的药物的比例高于对照组。PsA 诊断时年龄较大、PsA 病程较短和他汀类药物治疗与 PsA 患者的 SLE 相关。
与对照组相比,PsA 患者 SLE 的患病率增加了 2.3 倍。SLE 发展的危险因素包括 PsA 诊断时年龄较大、PsA 病程较短和他汀类药物治疗。PsA 与 SLE 之间的关联可能会影响治疗选择和药物开发。