Prognostic factors and validation of the histologic chronicity score for C3 glomerulopathy: a registry analysis.

C3 glomerulopathy CKD anemia chronicity prognosis

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 14 10 2023
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 18 10 2024
Statut: epublish

Résumé

Data on the prognostic factors for C3 glomerulopathy (C3G) are limited, and validation of the new C3G histologic index (C3G-HI) in different settings is still needed. We aimed to evaluate the chronicity score of C3G-HI and probable prognostic factors in our population. In this registry study, 74 patients from 20 centers with adequate follow-up data were included. Total chronicity score (TCS) was calculated according to percentages of glomerulosclerosis, interstitial fibrosis, tubular atrophy, and presence of arterio- and arteriolosclerosis. Primary composite outcome was defined as doubling of serum creatinine from baseline, undergoing dialysis or transplantation, development of stage 5 chronic kidney disease, or death. Median age was 34 [interquartile range (IQR) 24-46] years, and 39 patients (52.7%) were male. Median follow-up duration was 36 (IQR 12-60) months, and median TCS was 3 (IQR 1-5). Overall, 19 patients (25.7%) experienced primary composite outcome. Multivariate Cox regression model showed that only hemoglobin [adjusted HR (aHR) 0.67, 95% confidence interval 0.46-0.97, Low hemoglobin levels predicted dismal outcomes in patients with C3G. TCS ≥4 was associated with a worse 3-year kidney survival, which validated the 3-year prognostic value of the TCS of C3G-HI in our population.

Sections du résumé

Background UNASSIGNED
Data on the prognostic factors for C3 glomerulopathy (C3G) are limited, and validation of the new C3G histologic index (C3G-HI) in different settings is still needed. We aimed to evaluate the chronicity score of C3G-HI and probable prognostic factors in our population.
Methods UNASSIGNED
In this registry study, 74 patients from 20 centers with adequate follow-up data were included. Total chronicity score (TCS) was calculated according to percentages of glomerulosclerosis, interstitial fibrosis, tubular atrophy, and presence of arterio- and arteriolosclerosis. Primary composite outcome was defined as doubling of serum creatinine from baseline, undergoing dialysis or transplantation, development of stage 5 chronic kidney disease, or death.
Results UNASSIGNED
Median age was 34 [interquartile range (IQR) 24-46] years, and 39 patients (52.7%) were male. Median follow-up duration was 36 (IQR 12-60) months, and median TCS was 3 (IQR 1-5). Overall, 19 patients (25.7%) experienced primary composite outcome. Multivariate Cox regression model showed that only hemoglobin [adjusted HR (aHR) 0.67, 95% confidence interval 0.46-0.97,
Conclusions UNASSIGNED
Low hemoglobin levels predicted dismal outcomes in patients with C3G. TCS ≥4 was associated with a worse 3-year kidney survival, which validated the 3-year prognostic value of the TCS of C3G-HI in our population.

Identifiants

pubmed: 39421234
doi: 10.1093/ckj/sfae077
pii: sfae077
pmc: PMC11483614
doi:

Types de publication

Journal Article

Langues

eng

Pagination

sfae077

Investigateurs

Yasemin Ozluk (Y)
Ipek Isik Gonul (II)
Gulistan Gumrukcu (G)
Cigdem Vural (C)
Emine Kilinc Gunay (EK)
Aysel Colak (A)
Iclal Gurses (I)
Haci Hasan Esen (HH)
Ayse Aysim Ozagari (AA)
Saba Kiremitci (S)
Handan Kaya (H)
Cigdem Ozdemir (C)
Funda Tasli (F)
Arzu Saglam Ayhan (AS)
Yasemin Yuyucu Karabulut (YY)
Neslihan Guney (N)
Ufuk Usta (U)
Berna Aytac Vuruskan (BA)

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest. Outside the submitted work, S.M. received support for attending meetings and travel from Amgen and Sanofi Genzyme. N.E. received consulting fees from Sanofi and Takeda, payment or honoraria for lectures, presentations, speaker's bureaus, manuscript writing or educational events from Sanofi, Takeda and AstraZeneca, support for attending meetings and travel from Sanofi, Takeda and AstraZeneca, and participated on a data safety monitoring board or advisory board of Takeda. K.T. received payment or honoraria for lectures, presentations, speaker's bureaus, manuscript writing or educational events from Takeda and Sanofi Genzyme. The remaining authors have no disclosures. The results presented in this paper have not been published previously in whole or part, except in abstract format.

Auteurs

Safak Mirioglu (S)

Division of Nephrology, Bezmialem Vakif University Faculty of Medicine, Istanbul, Turkey.

Egemen Cebeci (E)

Division of Nephrology, Istanbul Haseki Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.

Halil Yazici (H)

Division of Nephrology, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey.

Ulver Derici (U)

Division of Nephrology, Gazi University Faculty of Medicine, Ankara, Turkey.

Gulizar Sahin (G)

Division of Nephrology, Sultan 2. Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.

Ganime Coban (G)

Department of Pathology, Bezmialem Vakif University Faculty of Medicine, Istanbul, Turkey.

Necmi Eren (N)

Division of Nephrology, Kocaeli University Faculty of Medicine, Kocaeli, Turkey.

Ozkan Gungor (O)

Division of Nephrology, Kahramanmaras Sutcu Imam University Faculty of Medicine, Kahramanmaras, Turkey.

Fatih Dede (F)

Division of Nephology, Ankara Bilkent City Hospital, University of Health Sciences, Ankara, Turkey.

Tamer Dincer (T)

Division of Nephrology, Istanbul University-Cerrahpasa Cerrahpasa Faculty of Medicine, Istanbul, Turkey.

Kultigin Turkmen (K)

Division of Nephrology, Necmettin Erbakan University Faculty of Medicine, Konya, Turkey.

Taner Basturk (T)

Division of Nephrology, Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.

Murat Duranay (M)

Division of Nephrology, Ankara Training and Research Hospital, University of Health Sciences, Ankara, Turkey.

Hakki Arikan (H)

Division of Nephrology, Marmara University Faculty of Medicine, Istanbul, Turkey.

Onur Tunca (O)

Division of Nephrology, Afyonkarahisar Health Sciences University Faculty of Medicine, Afyonkarahisar, Turkey.

Omer Celal Elcioglu (OC)

Division of Nephrology, Bezmialem Vakif University Faculty of Medicine, Istanbul, Turkey.

Erhan Tatar (E)

Division of Nephrology, Bozyaka Training and Research Hospital, University of Health Sciences, Izmir, Turkey.

Zeki Aydin (Z)

Division of Nephrology, Darica Farabi Training and Research Hospital, University of Health Sciences, Kocaeli, Turkey.

Deren Oygar (D)

Division of Nephrology, Dr Burhan Nalbantoglu State Hospital, Lefkosa, Cyprus.

Serap Demir (S)

Division of Nephrology, Mersin University Faculty of Medicine, Mersin, Turkey.

Mehmet Tanrisev (M)

Division of Nephrology, Tepecik Training and Research Hospital, University of Health Sciences, Izmir, Turkey.

Ilhan Kurultak (I)

Division of Nephrology, Trakya University Faculty of Medicine, Edirne, Turkey.

Aysegul Oruc (A)

Division of Nephrology, Bursa Uludag University Faculty of Medicine, Bursa, Turkey.

Aydin Turkmen (A)

Division of Nephrology, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey.

Omer Faruk Akcay (OF)

Division of Nephrology, Gazi University Faculty of Medicine, Ankara, Turkey.

Hakki Cetinkaya (H)

Division of Nephrology, Sultan 2. Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.

Savas Ozturk (S)

Division of Nephrology, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey.

Classifications MeSH