Winstead Taylor B, Hagwood Spencer, Karlson Cynthia, Dhanrajani Anita
School of Medicine, The University of Mississippi Medical Center, Jackson, MS, USA.
Department of Pediatric Psychology, The University of Mississippi Medical Center, Jackson, MS, USA.
Pediatr Rheumatol Online J. 2025 Apr 7;23(1):38. doi: 10.1186/s12969-025-01085-4.
To characterize the clinical, demographic, and socioeconomic profile of childhood systemic lupus erythematous (cSLE) in the Black Belt of the Southern United States in comparison to the current literature of predominantly Caucasian cohorts.
This is a cross-sectional study characterizing patients with cSLE from two centers in the Southeastern United States- University of Mississippi Medical Center (UMMC) and University of Alabama at Birmingham (UAB). Demographic, social, and clinical data was retrospectively collected by medical chart review for prevalent and incident cSLE patients via electronic medical records for UMMC and the Childhood arthritis and rheumatology research alliance (CARRA) registry database for UAB. The data was combined and analyzed using SPSS statistical software.
Of the 45 patients,82.2%were female, 82.2% were of AA ethnicity, and 66.7% had Medicaid insurance. Mean age at diagnosis was 13.5 years (+/- 2.8). Mean American College of Rheumatology (ACR) score at diagnosis was 5.1 (+/- 1.27), the Systemic Lupus International Collaborating Clinics (SLICC score) was 8.4 (+/- 2.5). Average baseline Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) was 13.06 (+/- 9.3), SLEDAI at 6 months and 1 year respectively was 7.4 and 4.7. Average distance traveled to see a rheumatologist was 74.83 miles compared to a national average of 42.8 miles. 37/45 patients (82%) belonged to medium-high or high Social Vulnerability Index (SVI) group based on zip code.
Compared to previously described multiethnic cohorts of cSLE, this predominantly AA patient population in the Southern United States has significantly higher disease activity and greater damage accrual. Social risk factors for this population include a higher SVI, longer distance from an academic pediatric rheumatology center, and having Medicaid insurance. The effect of these factors on disparity of disease outcomes needs to be further explored with larger cohorts.
与目前主要为白种人队列的文献相比,描述美国南部黑带地区儿童系统性红斑狼疮(cSLE)的临床、人口统计学和社会经济特征。
这是一项横断面研究,对来自美国东南部两个中心——密西西比大学医学中心(UMMC)和阿拉巴马大学伯明翰分校(UAB)的cSLE患者进行特征描述。通过病历回顾,通过UMMC的电子病历以及UAB的儿童关节炎和风湿病研究联盟(CARRA)注册数据库,回顾性收集了cSLE现患和新发病例患者的人口统计学、社会和临床数据。使用SPSS统计软件对数据进行合并和分析。
45例患者中,82.2%为女性,82.2%为非裔美国人,66.7%有医疗补助保险。诊断时的平均年龄为13.5岁(±2.8岁)。诊断时美国风湿病学会(ACR)平均评分为5.1(±1.27),系统性红斑狼疮国际协作临床(SLICC)评分为8.4(±2.5)。系统性红斑狼疮疾病活动指数(SLEDAI)的平均基线值为13.06(±9.3),6个月和1年时的SLEDAI分别为7.4和4.7。与全国平均42.8英里相比,看风湿病医生的平均路程为74.83英里。根据邮政编码,45例患者中有37例(82%)属于中高或高社会脆弱性指数(SVI)组。
与先前描述的多民族cSLE队列相比,美国南部这个主要为非裔美国人的患者群体疾病活动度明显更高,累积损伤更大。该人群的社会风险因素包括较高的SVI、距学术性儿科风湿病中心较远以及拥有医疗补助保险。这些因素对疾病结局差异的影响需要在更大的队列中进一步探讨。