评估美国少数民族类风湿关节炎疾病活动度:来自少数民族类风湿关节炎联盟注册的真实世界数据

IF 1.8
Mercedes Quiñones, Sharon Dowell, Rodolfo Perez Alamino, Christopher J Swearingen, Edward Treadwell, Ignacio Garcia-Valladares, Theresa Lawrence-Ford, Cynthia Lawrence-Elliott, Akgun Ince, Yvonne Sherrer, Angelia Mosley-Williams, Yusuf Yazici, Gail S Kerr
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引用次数: 0

摘要

目的:确定影响少数民族(EM)类风湿性关节炎(RA)患者评估、管理和预后的疾病活动参数的差异。方法:研究2010年至2018年在少数民族类风湿性关节炎协会登记的RA患者。使用单变量分析方法估计自我识别的种族和民族亚群之间的比较以及与随机对照试验(RCT)纳入标准的RA疾病活动性测量和阈值的关联。结果:对1315例平均病程10.3年的RA患者进行了观察性队列研究,其中包括380例黑人(28.9%)、178例西班牙裔(13.5%)和126例亚洲人(9.6%)。与白人参与者相比,黑人参与者的社会经济地位较低,并且与西班牙裔参与者一样,报告的受教育年限和烟草使用年限较短,但疾病活动和合并症较多。所有3个种族亚群都有更普遍的血清阳性类风湿关节炎,黑人和西班牙裔参与者使用类风湿关节炎治疗较少,而亚洲参与者使用最高的疾病改善抗风湿药物。包括实验室参数的综合疾病活动度测量发现,在整个队列中,与单独的患者报告测量相比,缓解的人数更多。然而,黑人参与者在所有测量中缓解的频率较低(带有c反应蛋白的疾病活动评分-28关节与带有红细胞沉降率的疾病活动评分-28关节的缓解率约为2倍),并且更频繁地符合RCT纳入标准。结论:在真实世界的EM RA队列中,主观疾病活动性测量与客观参数不一致。此外,在黑人参与者中,达到缓解标准取决于所选择的实验室检测,但经常满足rct的活动性疾病阈值资格。需要对EM患者的RA疾病措施进行标准化,以达到当前最佳RA护理的阈值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing Rheumatoid Arthritis Disease Activity Measures in Ethnic Minority Patients in the United States: Real-World Data From the Ethnic Minority Rheumatoid Arthritis Consortium Registry.

Objective: To identify differences in disease activity parameters that influence assessment, management, and outcomes of ethnic minority (EM) rheumatoid arthritis (RA) patients.

Methods: RA patients enrolled in the Ethnic Minority Rheumatoid Arthritis Consortium registry between 2010 and 2018 were studied. Comparisons among self-identified racial and ethnic subsets and associations with RA disease activity measures and thresholds for randomized controlled trial (RCT) inclusion criteria were estimated using univariable analytical methods.

Results: An observational cohort of 1315 RA patients of mean disease duration of 10.3 years was studied and comprised 380 (28.9%) Black, 178 (13.5%) Hispanic, and 126 (9.6%) Asian individuals. Compared with White participants, Black participants had lower socioeconomic status and, along with Hispanic participants, reported less years of education and tobacco use but greater disease activity and comorbidity. All 3 ethnic subsets had more prevalent seropositive RA with Black and Hispanic participants having less use of RA therapies compared with Asian participants who had the highest disease-modifying antirheumatic drug use. Composite disease activity measures that included a laboratory parameter found greater numbers to be in remission compared with patient-reported measures alone in the entire cohort. However, Black participants were less frequently in remission across all measures (approximately 2-fold for Disease Activity Score-28 joints with C-reactive protein vs. Disease Activity Score-28 joints with erythrocyte sedimentation rate) and more frequently met the RCT inclusion criteria.

Conclusion: In a real-world EM RA cohort, subjective disease activity measures were discordant with objective parameters. Further, in Black participants, achieving remission criteria was dependent on laboratory assay chosen but frequently met active disease threshold eligibility for RCTs. Standardization of RA disease measures in EM patients is needed to achieve parity with current thresholds of optimum RA care.

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