Evidence map›Paper›PMID 42396145›Full record

ArticleFrontiers in medicine2026

External validation of the international IgA nephropathy prediction tool in a Thai cohort.

Atthaphong Phongphithakchai, Attamon Thongrueang, Thatsaphan Srithongkul, Sukit Raksasuk, Fumitaka Kawakami, Aman Tedasen, Moragot Chatatikun

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Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Atthaphong PhongphithakchaiNephrology Unit, Division of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
Attamon ThongrueangNephrology Unit, Division of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
Thatsaphan SrithongkulDivision of Nephrology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Sukit RaksasukDivision of Nephrology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Fumitaka KawakamiDepartment of Regulatory Biochemistry, Graduate School of Medical Sciences, Kitasato University, Sagamihara, Japan.
Aman TedasenDepartment of Medical Technology, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand.
Moragot ChatatikunDepartment of Medical Technology, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To externally validate the performance of the International IgA Nephropathy Prediction Tool (IIgANPT) in a Thai cohort with biopsy-proven IgA nephropathy and to compare the predictive accuracy of model versions with and without the race variable. Methods: We conducted a retrospective cohort study to externally validate the IIgANPT in Thai adults with biopsy-proven IgAN at a tertiary-care center. Both model versions (with and without race) were evaluated. The primary outcome was a composite of a sustained 50% decline in estimated glomerular filtration rate (eGFR) or progression to end-stage renal disease (ESKD). Model performance was assessed using discrimination (C-statistic, AUC), calibration (slope and plots), and risk stratification with Kaplan-Meier analysis. Results: A total of 133 patients were included, with a median follow-up of 3.4 years. During follow-up, 45 patients (33.8%) reached the renal endpoint. The model demonstrated good discrimination, with C-statistics of 0.753 (95% CI 0.68-0.82) and 0.754 (95% CI 0.69-0.82) for models with and without race, respectively. Five-year AUC values were similar (0.790 vs. 0.787). Calibration was broadly preserved, although confidence intervals around calibration slopes were wide. Risk stratification showed clear separation of kidney survival across predefined risk groups (log-rank Conclusion: The IIgANPT demonstrated good discrimination and effective risk stratification in this Thai cohort of patients with biopsy-proven IgAN. Calibration point estimates were close to the ideal range, although precision was limited by wide confidence intervals. Both model versions performed similarly, suggesting that exclusion of the race variable may have limited impact on prognostic performance in this relatively homogeneous population.

Indexed as

external validationIgA nephropathyprognostic modelrisk stratificationSoutheast Asia

Identifiers

PMID42396145
PMCPMC13322946

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.