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已发表论文

IgA 肾病患者蛋白尿的时间加权平均值与肾功能下降:一项回顾性队列研究

 

Authors Xu R , Cao T, Liao Y, Chen Y, Yu Y , Guo J, Zhong A, Chen X, Xu Y, Wan Q

Received 19 January 2025

Accepted for publication 21 March 2025

Published 29 March 2025 Volume 2025:18 Pages 103—110

DOI http://doi.org/10.2147/IJNRD.S517145

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Professor Pravin Singhal

Ricong Xu,* Tao Cao,* Ying Liao, Yuna Chen, Yi Yu, Jianying Guo, Anni Zhong, Xiaojie Chen, Yi Xu, Qijun Wan

Department of Nephrology, Shenzhen Second People’s Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Qijun Wan, Department of Nephrology, The Second People’s Hospital of Shenzhen, 3002 Sungang Road, Shenzhen, 518035, People’s Republic of China, Tel +860755 83366388, Email yiyuan2224@sina.com

Background: IgA nephropathy (IgAN) is the leading primary glomerulonephritis globally, with many patients advancing to end-stage renal disease. Proteinuria is a key predictor of renal function decline in IgAN, yet the best method for long-term assessment is unclear. This study explores the relationship between time-weighted average proteinuria (TWAP), a novel metric of cumulative proteinuria exposure, and renal function decline in IgAN patients.
Methods: This single-center retrospective cohort study encompassed 549 patients with biopsy-confirmed primary IgAN from Shenzhen Second People’s Hospital from 2011 to 2023. TWAP served as the primary exposure variable, calculated using the protein-creatinine ratio values, while changes in estimated glomerular filtration rate (eGFR) constituted the primary outcome. Covariates included age, sex, blood pressure, and mesangial hypercellularity (M), endocapillary hypercellularity (E), segmental glomerulosclerosis (S), tubular atrophy/interstitial fibrosis (T), and crescents (C) (known as the Oxford Classification MEST-C score system). The associations between TWAP and eGFR trajectories were analyzed using Generalized Additive Mixed Models.
Results: In patients with baseline eGFR 15– 60 mL/min/1.73m², higher TWAP levels correlated with accelerated eGFR decline. Compared to TWAP < 0.3 g/g, TWAP 0.3– 0.5 g/g, 0.5– 1 g/g, and ≥ 1 g/g were associated with additional annual eGFR declines of 2.04 (95% CI: − 3.72 to − 0.35), 3.38 (95% CI: − 5.12 to − 1.65), and 4.04 (95% CI: − 6.61 to − 1.47) mL/min/1.73m²/year, respectively. For eGFR ≥ 60 mL/min/1.73m², only TWAP ≥ 1 g/g significantly accelerated eGFR decline 5.70 (95% CI: − 6.84 to − 4.55) mL/min/1.73m²/year.
Conclusion: TWAP significantly predicts renal function decline in IgAN, especially in patients with pre-existing renal dysfunction. Maintaining TWAP below 0.3 g/g may significantly slow disease progression, emphasizing the importance of stringent proteinuria control in IgAN management.

Keywords: IgA nephropathy, mixed methods, renal function, time-weighted average proteinuria, (TWAP)

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