Kosarek Noelle N, Romano Megan E, Moen Erika L, Simms Robert W, Erickson Ashleigh, Khanna Dinesh, Pioli Patricia A, Whitfield Michael L
Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire.
Geisel School of Medicine at Dartmouth and Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Arthritis Care Res (Hoboken). 2025 Jul;77(7):855-866. doi: 10.1002/acr.25504. Epub 2025 Feb 28.
Systemic sclerosis (SSc) is a rare autoimmune disease characterized by fibrosis of the skin and other organs. SSc is thought to arise in genetically predisposed individuals with occupational triggers, although further environmental etiologies still need to be identified. Limited research exists detailing which environmental factors lead to the downstream inflammatory and fibrotic symptoms experienced by patients with SSc across the United States. This study describes a retrospective cohort of 179,188 individuals with an SSc or SSc-related diagnosis code enrolled in the Medicare beneficiary program between the years 2014 and 2018.
The incidence of SSc and SSc-related diagnosis codes in all US zip codes with beneficiary counts greater than 11 was calculated. We conducted global and local Moran's Index (Moran's I) as well as a hot spot analysis with the Getis Ord Gi statistic to determine whether SSc and SSc-related diagnosis codes exhibited clustered or dispersed patterns across the United States. We identified clusters of SSc and SSc-related diagnosis code with high incidences in or around Superfund sites, which are federally identified areas of environmental contamination.
SSc exhibited clustered patterns in two analyzed cohorts based on global Moran's I statistics of 0.588 and 0.521. Results of local Moran's I indicated clusters of disease in Mississippi, New York, Wisconsin, and Michigan, among others. Some zip codes with high disease incidences were home to at least one Superfund site.
SSc exhibits nonrandom, clustered distributions in a US Medicare beneficiary cohort composed of 179,188 individuals from 2014 to 2018.
系统性硬化症(SSc)是一种罕见的自身免疫性疾病,其特征为皮肤和其他器官的纤维化。尽管仍需确定更多环境病因,但SSc被认为在具有遗传易感性的个体中因职业触发因素而发病。关于哪些环境因素导致美国各地SSc患者出现下游炎症和纤维化症状的研究有限。本研究描述了一个回顾性队列,该队列由2014年至2018年参加医疗保险受益计划的179,188名患有SSc或与SSc相关诊断代码的个体组成。
计算了所有受益人数超过11人的美国邮政编码地区中SSc及与SSc相关诊断代码的发病率。我们进行了全局和局部莫兰指数(Moran's I)以及使用Getis Ord Gi统计量的热点分析,以确定SSc及与SSc相关诊断代码在美国各地是呈现聚集还是分散模式。我们在超级基金场地(联邦认定的环境污染区域)内或周边识别出了SSc及与SSc相关诊断代码发病率高的聚集区。
基于全局莫兰指数统计量0.588和0.521,SSc在两个分析队列中呈现聚集模式。局部莫兰指数结果表明,密西西比州、纽约州、威斯康星州和密歇根州等地存在疾病聚集区。一些疾病发病率高的邮政编码地区至少有一个超级基金场地。
在一个由2014年至2018年的179,188名个体组成的美国医疗保险受益队列中,SSc呈现非随机的聚集分布。