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社会不平等对一家大型三级医疗中心青少年起病的系统性红斑狼疮临床表现的影响。

The Impact of Social Inequities on Presentation of Juvenile-Onset Systemic Lupus Erythematosus at a Large Tertiary Center.

作者信息

Beil Emily F, DeGuzman Marietta, Ramirez Andrea, Yildirim-Toruner Cagri, Oluyomi Abiodun, Rosales Omar, Guffey Danielle, Muscal Eyal, Peckham-Gregory Erin

机构信息

From the Wake Forest School of Medicine, Atrium Health, Levine Children's Hospital, Charlotte, NC.

Texas Children's Hospital.

出版信息

J Clin Rheumatol. 2025 Aug 1;31(5):e84-e90. doi: 10.1097/RHU.0000000000002228. Epub 2025 Mar 19.

Abstract

OBJECTIVE

The prevalence of juvenile-onset systemic lupus erythematosus (JSLE) differs by race/ethnicity with environmental, genetic, and social factors implicated in disease severity and outcomes. Yet, the role of social determinants of health (SDoH) in disease presentation is not well understood. We hypothesized that in an urban center with a large, diverse catchment area, SDoH influence the severity of JSLE at diagnosis.

METHODS

We completed an institutional review board-approved medical record review of children newly diagnosed with JSLE between January 1, 2018, and May 31, 2022, at Texas Children's Hospital in Houston, TX. We collected demographic data, clinical severity measures, and SDoH variables such as Area Deprivation Index (ADI), insurance status, pollution burden, and food accessibility. Statistical analysis to compare SDoH with JSLE severity included Kruskal-Wallis test, Fisher exact test, and univariable and multivariable regression.

RESULTS

Mean diagnosis age for 136 patients was 13.4 years, with 82.4% female, 52.9% Hispanic, and 25.7% non-Hispanic (NH) Black. One-third of patients did not have a documented primary care provider, and one-third preferred non-English language. We found NH Black patients had worse clinical severity measures, with highest Systemic Lupus Erythematosus Disease Activity Index and more central nervous system involvement and cyclophosphamide therapy. Uninsured and publicly insured patients were more likely to use inpatient resources at diagnosis and live in neighborhoods with higher pollution levels and higher ADI. Hispanic patients reside in communities with higher ADI scores and limited access to supermarkets.

CONCLUSION

In children with JSLE from a large urban catchment area, we observed significant association of nonmodifiable (race/ethnicity) and modifiable (insurance status, access to care, food accessibility) factors on disease severity at presentation.

摘要

目的

青少年起病的系统性红斑狼疮(JSLE)的患病率因种族/族裔而异,环境、遗传和社会因素与疾病严重程度及预后相关。然而,健康的社会决定因素(SDoH)在疾病表现中的作用尚未得到充分理解。我们假设,在一个拥有大量多样化服务区域的城市中心,SDoH会影响JSLE诊断时的严重程度。

方法

我们对2018年1月1日至2022年5月31日期间在德克萨斯州休斯顿市德克萨斯儿童医院新诊断为JSLE的儿童进行了一项经机构审查委员会批准的病历审查。我们收集了人口统计学数据、临床严重程度指标以及SDoH变量,如地区贫困指数(ADI)、保险状况、污染负担和食物可及性。比较SDoH与JSLE严重程度的统计分析包括Kruskal-Wallis检验、Fisher精确检验以及单变量和多变量回归。

结果

136例患者的平均诊断年龄为13.4岁,其中82.4%为女性,52.9%为西班牙裔,25.7%为非西班牙裔(NH)黑人。三分之一的患者没有记录在案的初级保健提供者,三分之一的患者更喜欢非英语语言。我们发现NH黑人患者的临床严重程度指标更差,系统性红斑狼疮疾病活动指数最高,中枢神经系统受累更多,且接受环磷酰胺治疗。未参保和参加公共保险的患者在诊断时更有可能使用住院资源,并且居住在污染水平较高和ADI较高的社区。西班牙裔患者居住在ADI得分较高且超市可达性有限的社区。

结论

在来自大型城市服务区域的JSLE儿童中,我们观察到不可改变因素(种族/族裔)和可改变因素(保险状况、医疗服务可及性、食物可及性)与疾病表现时的严重程度之间存在显著关联。

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