Population-Level Risk Factors for Kidney Outcomes in IgA Nephropathy: The CURE-CKD Registry

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Katherine R. Tuttle , Lindsey M. Kornowske , Cami R. Jones , Kenn B. Daratha , Radica Z. Alicic , Christina L. Reynolds , Joshua J. Neumiller , Mark E. Bensink , Wu Gong , Keith C. Norris , Susanne B. Nicholas , CURE-CKD Consortium
{"title":"Population-Level Risk Factors for Kidney Outcomes in IgA Nephropathy: The CURE-CKD Registry","authors":"Katherine R. Tuttle ,&nbsp;Lindsey M. Kornowske ,&nbsp;Cami R. Jones ,&nbsp;Kenn B. Daratha ,&nbsp;Radica Z. Alicic ,&nbsp;Christina L. Reynolds ,&nbsp;Joshua J. Neumiller ,&nbsp;Mark E. Bensink ,&nbsp;Wu Gong ,&nbsp;Keith C. Norris ,&nbsp;Susanne B. Nicholas ,&nbsp;CURE-CKD Consortium","doi":"10.1016/j.xkme.2025.100981","DOIUrl":null,"url":null,"abstract":"<div><h3>Rationale &amp; Objective</h3><div>Although IgA nephropathy (IgAN) therapies are advancing quickly, therapeutic interventions are hampered by a lack of kidney disease identification and risk assessment. The study aim was to use population-level data from health systems to identify IgAN and assess risks.</div></div><div><h3>Study Design</h3><div>A longitudinal and real-world cohort study.</div></div><div><h3>Setting &amp; Participants</h3><div>Electronic health record data for patients ≥18 years old with IgAN at Providence and University of California Los Angeles health systems during 2016-2022.</div></div><div><h3>Predictors</h3><div>Health insurance and care utilization along with age, gender, race, ethnicity, estimated glomerular filtration rate (eGFR), urine albumin/creatinine ratio (UACR) or urine protein/creatinine ratio (UPCR), diabetes, hypertension, and medications.</div></div><div><h3>Outcomes</h3><div>Time to first major adverse kidney event (MAKE): ≥40% eGFR decline; eGFR &lt;15 mL/min/1.73 m2; administrative codes for kidney failure, dialysis, or transplant; and death.</div></div><div><h3>Analytical Approach</h3><div>Kaplan-Meier survival curves and Cox proportional hazards models.</div></div><div><h3>Results</h3><div>Patients with IgAN (n = 2,571) were 50% (n = 1,277) women and 58 ± 18 (mean ± SD) years old. At baseline, eGFR was 78 ± 27 mL/min/1.73 m<sup>2</sup> (chronic kidney disease epidemiologic 2021 equation); median UACR and UPCR were 166 (interquartile range 25-795) mg/g and 0.7 (0.2-1.8) g/g, respectively, among those with baseline measurements (n = 669). MAKE occurred in 22% of the cohort by 3 years. In Cox proportional hazards models, MAKE was predicted by noncommercial (Medicare or Medicaid) health insurance, hospitalization, more frequent outpatient encounters, lower eGFR, and a higher UACR or UPCR.</div></div><div><h3>Limitations</h3><div>Missingness, miscoding, and retrospective data.</div></div><div><h3>Conclusions</h3><div>Substantial loss of kidney function, kidney failure, and death were common events over a short period of time in patients with IgAN. Within health system populations, noncommercial health insurance and greater care utilization augmented risk prediction and could help to identify those who may benefit from closer monitoring and implementation of therapeutic interventions.</div></div><div><h3>Plain Language Summary</h3><div>IgA nephropathy therapies have advanced quickly. However, therapeutic interventions are hampered by lack of disease identification and risk assessment. We identified patients with IgA nephropathy at 2 United States health systems and assessed predictors of risk for major adverse kidney events (major adverse kidney event [MAKE]—substantial loss of kidney function, kidney failure, or death). More than one in 5 patients experienced MAKE by 3 years. In addition to demographic and clinical predictors, MAKE was predicted by noncommercial health insurance, hospitalization, and more frequent outpatient encounters. A population health approach within health systems could improve outcomes by identification of IgA nephropathy and assessment of health insurance status and care utilization to help risk stratify patients for closer monitoring and implementation of therapeutic interventions.</div></div>","PeriodicalId":17885,"journal":{"name":"Kidney Medicine","volume":"7 4","pages":"Article 100981"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590059525000172","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Rationale & Objective

Although IgA nephropathy (IgAN) therapies are advancing quickly, therapeutic interventions are hampered by a lack of kidney disease identification and risk assessment. The study aim was to use population-level data from health systems to identify IgAN and assess risks.

Study Design

A longitudinal and real-world cohort study.

Setting & Participants

Electronic health record data for patients ≥18 years old with IgAN at Providence and University of California Los Angeles health systems during 2016-2022.

Predictors

Health insurance and care utilization along with age, gender, race, ethnicity, estimated glomerular filtration rate (eGFR), urine albumin/creatinine ratio (UACR) or urine protein/creatinine ratio (UPCR), diabetes, hypertension, and medications.

Outcomes

Time to first major adverse kidney event (MAKE): ≥40% eGFR decline; eGFR <15 mL/min/1.73 m2; administrative codes for kidney failure, dialysis, or transplant; and death.

Analytical Approach

Kaplan-Meier survival curves and Cox proportional hazards models.

Results

Patients with IgAN (n = 2,571) were 50% (n = 1,277) women and 58 ± 18 (mean ± SD) years old. At baseline, eGFR was 78 ± 27 mL/min/1.73 m2 (chronic kidney disease epidemiologic 2021 equation); median UACR and UPCR were 166 (interquartile range 25-795) mg/g and 0.7 (0.2-1.8) g/g, respectively, among those with baseline measurements (n = 669). MAKE occurred in 22% of the cohort by 3 years. In Cox proportional hazards models, MAKE was predicted by noncommercial (Medicare or Medicaid) health insurance, hospitalization, more frequent outpatient encounters, lower eGFR, and a higher UACR or UPCR.

Limitations

Missingness, miscoding, and retrospective data.

Conclusions

Substantial loss of kidney function, kidney failure, and death were common events over a short period of time in patients with IgAN. Within health system populations, noncommercial health insurance and greater care utilization augmented risk prediction and could help to identify those who may benefit from closer monitoring and implementation of therapeutic interventions.

Plain Language Summary

IgA nephropathy therapies have advanced quickly. However, therapeutic interventions are hampered by lack of disease identification and risk assessment. We identified patients with IgA nephropathy at 2 United States health systems and assessed predictors of risk for major adverse kidney events (major adverse kidney event [MAKE]—substantial loss of kidney function, kidney failure, or death). More than one in 5 patients experienced MAKE by 3 years. In addition to demographic and clinical predictors, MAKE was predicted by noncommercial health insurance, hospitalization, and more frequent outpatient encounters. A population health approach within health systems could improve outcomes by identification of IgA nephropathy and assessment of health insurance status and care utilization to help risk stratify patients for closer monitoring and implementation of therapeutic interventions.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Kidney Medicine
Kidney Medicine Medicine-Internal Medicine
CiteScore
4.80
自引率
5.10%
发文量
176
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信