Risk of Vertebral Fracture in Individuals with End-Stage Renal Disease Secondary to Vasculitis.

IF 3.2 Q1 UROLOGY & NEPHROLOGY Kidney360 Pub Date : 2025-01-15 DOI:10.34067/KID.0000000696
Yagni Patel, Jennifer L Waller, Joanna El Hajj, Wendy B Bollag, Stephanie Baer, Jackson C Elam, Rachel E Elam
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Abstract

Background: Glucocorticoids are central to vasculitis treatment but increase vertebral fracture risk. This study assessed whether vasculitis as the cause of ESRD is associated with incident vertebral fracture, controlling for corticosteroid use.

Methods: A retrospective cohort study was conducted from 2006-2019 on adults in the U.S. Renal Data System initiating dialysis between 2006 and 2017, surviving ≥1 year, with continuous Medicare Part D coverage during the first year of dialysis. Primary exposure was vasculitis as the cause of ESRD determined from form Centers for Medicare & Medicaid Services (CMS)-2728, completed by a physician at dialysis initiation. A granulomatosis with polyangiitis (GPA) subgroup had ≥1 International Classification of Diseases (ICD)-9/10 code for GPA in the first dialysis year. One inpatient or two outpatient ICD-9/10 codes within 90 days defined incident vertebral fracture. Clinical covariates were ascertained from form CMS-2728 and ICD-9/10 codes and pharmacy claims over the first dialysis year. Multivariable logistic regression examined the association of ESRD secondary to vasculitis with incident vertebral fracture, and in GPA in a secondary analysis.

Results: Among 633,543 individuals with ESRD, vertebral fracture occurred in 6.18% with and 3.23% without ESRD from vasculitis. After multivariable adjustment including corticosteroid daily dose in the first dialysis year, ESRD secondary to vasculitis was associated with vertebral fracture (relative risk (RR):1.33, 95% confidence interval (CI):1.17-1.52), and similarly in those with GPA (RR:1.47, 95% CI:1.23-1.75).

Conclusions: ESRD from vasculitis, and from GPA specifically, increases vertebral fracture risk among individuals with ESRD after accounting for first dialysis year corticosteroid dose.

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继发于血管炎的终末期肾病患者椎体骨折的风险
背景:糖皮质激素是血管炎治疗的核心,但会增加椎体骨折的风险。本研究评估了血管炎作为ESRD的病因是否与椎体骨折事件相关,并控制了皮质类固醇的使用。方法:2006年至2019年,对2006年至2017年在美国肾脏数据系统中开始透析的成年人进行了一项回顾性队列研究,存活≥1年,在透析的第一年连续享受医疗保险D部分覆盖。从医疗保险和医疗补助服务中心(CMS)-2728中确定的ESRD的主要原因是血管炎,由医生在透析开始时完成。血透第一年肉芽肿合并多血管炎(GPA)亚组GPA的国际疾病分类(ICD)-9/10编码≥1。一个住院患者或两个门诊患者在90天内的ICD-9/10代码定义了偶发性椎体骨折。临床协变量从CMS-2728和ICD-9/10代码和第一个透析年的药房索赔中确定。多变量logistic回归检验了继发于血管炎的ESRD与椎体骨折的关系,并在二次分析中与GPA的关系。结果:在633,543例ESRD患者中,血管炎导致ESRD的椎体骨折发生率分别为6.18%和3.23%。在多变量调整后,包括第一个透析年度皮质类固醇日剂量,继发于血管炎的ESRD与椎体骨折相关(相对危险度(RR):1.33, 95%可信区间(CI):1.17-1.52),与GPA患者相似(RR:1.47, 95% CI:1.23-1.75)。结论:血管炎引起的ESRD,特别是GPA引起的ESRD,在考虑了第一个透析年皮质类固醇剂量后,增加了ESRD患者椎体骨折的风险。
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Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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0.00%
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