Clinicopathologic Significance of Predominant Lambda Light Chain Deposition in IgA Nephropathy.
IgA nephropathy
MEST score
glomerular disease
immunoglobulin light chains
Journal
Kidney international reports
ISSN: 2468-0249
Titre abrégé: Kidney Int Rep
Pays: United States
ID NLM: 101684752
Informations de publication
Date de publication:
Nov 2022
Nov 2022
Historique:
received:
28
03
2022
revised:
02
08
2022
accepted:
08
08
2022
entrez:
19
12
2022
pubmed:
20
12
2022
medline:
20
12
2022
Statut:
epublish
Résumé
IgA nephropathy (IgAN) differs from other glomerular diseases by the frequently predominant lambda over kappa light chain deposition. Using the Cure Glomerulonephropathy (CureGN) IgAN cohort, we aimed to determine whether predominant lambda chain deposition is associated with worse clinical outcomes or histopathologic markers of more active disease. Patients were categorized based on the intensity of light chain staining. The lambda dominant (LD) group was defined by a difference in intensity score of lambda minus kappa ≥ 1+ and the kappa-lambda codominant (KL) group by a difference < 1+. We compared the clinical course of patients in each category from the time of kidney biopsy and time of enrollment into CureGN to the time of remission (proteinuria < 0.3 g/g), 50% reduction in estimated glomerular filtration rate (eGFR), or progression to end-stage kidney disease (ESKD). We also analyzed differences in histopathologic characteristics between the 2 groups. Among 440 patients, we found no significant differences between groups in baseline clinical characteristics nor in rates of remission, 50% reduction in eGFR, or progression to ESKD. Patients in the LD group had a modestly greater frequency of IgG staining ≥ 1+. The biopsy results of 234 patients reviewed by CureGN pathologists revealed a greater frequency of endocapillary hypercellularity (51.1% vs. 36.3%, In IgAN, we found an association between lambda predominance and increased endocapillary hypercellularity, but no association with clinical outcomes.
Identifiants
pubmed: 36531879
doi: 10.1016/j.ekir.2022.08.003
pii: S2468-0249(22)01702-8
pmc: PMC9751582
doi:
Types de publication
Journal Article
Langues
eng
Pagination
2462-2473Subventions
Organisme : NIDDK NIH HHS
ID : U01 DK100846
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK100866
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK100876
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK100845
Pays : United States
Informations de copyright
© 2022 International Society of Nephrology. Published by Elsevier Inc.
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