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DOI 10.1038/s41598-025-33114-3

Медицинская библиотека · Scientific reports · 2026

Prognostic value of the ratio of globally sclerotic glomeruli in patients with idiopathic IgA nephropathy.

Kazan Sinan, Öztürk Savaş, Uzerk Kibar Müge, Ozcan Seyda Gul, Alcelik Karacan Raife Dilhan, Eren Necmi, Gok Mahmut, Turkmen Kultigin, Dheir Hamad, Basturk Taner, Tatar Erhan, Akcay Omer Faruk, Gürsu Meltem, Arikan Hakki, Ulu Sena, Ayli Mehmet Deniz, Kurultak Ilhan, Guven Taymez Dilek, Dursun Belda, Ozturk Ramazan, Kutlay Sim, Karakan Sebnem, Yilmaz Murvet, Torun Dilek, Turgutalp Kenan, Azak Alper, Aydin Zeki, Oygar Deren, Yilmaz Nedim Selcuk, Kaya Bulent, Yilmaz Zülfükar, Uzun Ozcan, Sipahioğlu Murat Hayri, Öğütmen Melike Betül, Yadigar Serap, Oruc Aysegul, Islam Mahmud, Doksan Müge, Keles Meryem, Altiparmak Mehmet Riza, Celik Abdulkadir, Dervişoğlu Erkan, Hacer Rabia, Coskun Yenigun Ezgi, Tunca Onur

СтатьяМногоцентровое исследованиеПеревод в очереди

Аннотация

IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. We assessed whether the Ratio of Globally Sclerotic Glomeruli (RoGSG) on diagnostic biopsy predicts subsequent kidney outcomes in a nationwide, multi‑center registry. Among 326 adults with idiopathic IgAN (mean age 39.1 ± 12.8 years; 60.1% male), 43 patients (13.2%) met a 5 year composite outcome defined as any of: doubling of serum creatinine or ≥ 50% decline in eGFR from baseline, eGFR < 15 mL/min/1.73 m2, or initiation of kidney replacement therapy. Receiver operating characteristic analysis identified a RoGSG cutoff of 28.86% for predicting the composite outcome (AUC 0.917, 95% CI 0.885-0.949; sensitivity 93.0%; specificity 84.5%). Using this threshold, 47.6% of patients with RoGSG ≥ 28.86% versus 1.2% with RoGSG < 28.86% reached the composite outcome. In multivariable models adjusted for clinical and pathologic covariates, high RoGSG, grade 2 tubular atrophy/interstitial fibrosis, and non‑response to initial immunosuppression were independent predictors of adverse outcomes. The prognostic association of RoGSG persisted in key subgroups, including those with nephrotic syndrome and those with initial treatment response. These findings support RoGSG as a readily available histopathologic marker that may improve risk stratification in IgAN; however, prospective studies and external validation in independent cohorts are required before any clinical adoption.

Для цитирования: Kazan Sinan, Öztürk Savaş, Uzerk Kibar Müge, Ozcan Seyda Gul, Alcelik Karacan Raife Dilhan, Eren Necmi, Gok Mahmut, Turkmen Kultigin, Dheir Hamad, Basturk Taner, Tatar Erhan, Akcay Omer Faruk, Gürsu Meltem, Arikan Hakki, Ulu Sena, Ayli Mehmet Deniz, Kurultak Ilhan, Guven Taymez Dilek, Dursun Belda, Ozturk Ramazan, Kutlay Sim, Karakan Sebnem, Yilmaz Murvet, Torun Dilek, Turgutalp Kenan, Azak Alper, Aydin Zeki, Oygar Deren, Yilmaz Nedim Selcuk, Kaya Bulent, Yilmaz Zülfükar, Uzun Ozcan, Sipahioğlu Murat Hayri, Öğütmen Melike Betül, Yadigar Serap, Oruc Aysegul, Islam Mahmud, Doksan Müge, Keles Meryem, Altiparmak Mehmet Riza, Celik Abdulkadir, Dervişoğlu Erkan, Hacer Rabia, Coskun Yenigun Ezgi, Tunca Onur. Prognostic value of the ratio of globally sclerotic glomeruli in patients with idiopathic IgA nephropathy.. Scientific reports. 2026. DOI: 10.1038/s41598-025-33114-3.

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