Glomerulonephritis with non-Randall-type, non-cryoglobulinaemic monoclonal immunoglobulin G deposits (PGNMID and ITG).

DNAJB9 PGNMID electron microscopy monoclonal gammopathy of renal significance monoclonal immunoglobulin G

Journal

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

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 04 11 2021
entrez: 25 8 2022
pubmed: 26 8 2022
medline: 26 8 2022
Statut: epublish

Résumé

Glomerulonephritis (GN) with non-Randall-type, non-cryoglobulinaemic monoclonal immunoglobulin G deposits encompasses rare diseases [proliferative GN with non-organized deposits (PGNMID) and immunotactoid GN] that cannot be distinguished without ultrastructural analysis by electron microscopy (EM). Here, we report and analyse the prognosis of 41 EM-proven (PGNMID for 39/41) and 22 non-EM-proven/DNAJB9-negative cases, diagnosed between 2001 and 2019 in 12 French nephrology centres. Median (interquartile range) serum creatinine (SCr) at presentation was 150 (92-256) µmol/L. The predominant histological pattern was membranoproliferative GN (79%), with IgG3 (74%) kappa (78%) deposits the most frequently observed. Disease presentation and patient management were similar between EM-proven and non-EM-proven cases. A serum monoclonal spike was detected for 21 patients and 10 had an underlying haematological malignancy. First-line therapy was mixed between clone-targeted therapy ( Our results confirm that non-cryoglobulinaemic and non-Randall GN with monoclonal IgG deposits are rarely associated with haematological malignancy. The prognosis is uncertain but may be improved by early introduction of a specific therapy.

Sections du résumé

Background UNASSIGNED
Glomerulonephritis (GN) with non-Randall-type, non-cryoglobulinaemic monoclonal immunoglobulin G deposits encompasses rare diseases [proliferative GN with non-organized deposits (PGNMID) and immunotactoid GN] that cannot be distinguished without ultrastructural analysis by electron microscopy (EM).
Methods UNASSIGNED
Here, we report and analyse the prognosis of 41 EM-proven (PGNMID for 39/41) and 22 non-EM-proven/DNAJB9-negative cases, diagnosed between 2001 and 2019 in 12 French nephrology centres.
Results UNASSIGNED
Median (interquartile range) serum creatinine (SCr) at presentation was 150 (92-256) µmol/L. The predominant histological pattern was membranoproliferative GN (79%), with IgG3 (74%) kappa (78%) deposits the most frequently observed. Disease presentation and patient management were similar between EM-proven and non-EM-proven cases. A serum monoclonal spike was detected for 21 patients and 10 had an underlying haematological malignancy. First-line therapy was mixed between clone-targeted therapy (
Conclusions UNASSIGNED
Our results confirm that non-cryoglobulinaemic and non-Randall GN with monoclonal IgG deposits are rarely associated with haematological malignancy. The prognosis is uncertain but may be improved by early introduction of a specific therapy.

Identifiants

pubmed: 36003672
doi: 10.1093/ckj/sfac085
pii: sfac085
pmc: PMC9394706
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1727-1736

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.

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Auteurs

Ophélie Fourdinier (O)

Department of Nephrology, Dialysis and Transplantation, University Hospital, and MP3CV Research Laboratory, Jules Verne Picardie University, Amiens, France.

Marc Ulrich (M)

Department of Nephrology, Hôpital Jean Bernard, Valenciennes, France.

Alexandre Karras (A)

Department of Nephrology, Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris (APHP), Paris, France.

Jérôme Olagne (J)

Department of Nephrology and Transplantation, Department of Pathology, University Hospital, Strasbourg, France.

David Buob (D)

Department of Pathology, Hôpital Tenon, APHP, Paris, France.

Vincent Audard (V)

Department of Nephrology and Transplantation, Henri Mondor University Hospital, APHP, and Univ Paris Est Créteil, Institut National de la Santé et de la Recherche Médicale (INSERM) U 955, Institut Mondor de Recherche Biomédicale (IMRB), Créteil, France.

Cécile Vigneau (C)

Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France.

Jean-Baptiste Gibier (JB)

Institute of Pathology, University Hospital, Lille, France.

Dominique Guerrot (D)

Department of Nephrology, University Hospital, Rouen, France.

Ziad Massy (Z)

Department of Nephrology, Ambroise Paré Hospital, APHP, Boulogne Billancourt, Paris, and Inserm Unit 1018, Team 5, CESP, Versailles Saint-Quentin-en-Yvelines University, Paris Saclay University, Villejuif, France.

Vincent Vuiblet (V)

Department of Nephrology and Transplantation, University Hospital, Reims, France.

Nolwenn Rabot (N)

Department of Nephrology, University Hospital, Tours, France.

Jean-Michel Goujon (JM)

Department of Nephrology, and Department of Pathology and Ultrastructural Pathology, University Hospital, Poitiers, France.

Carole Cordonnier (C)

Department of Pathology, University Hospital, Amiens, France.

Gabriel Choukroun (G)

Department of Nephrology, Dialysis and Transplantation, University Hospital, and MP3CV Research Laboratory, Jules Verne Picardie University, Amiens, France.

Dimitri Titeca-Beauport (D)

Department of Nephrology, Dialysis and Transplantation, University Hospital, and MP3CV Research Laboratory, Jules Verne Picardie University, Amiens, France.

Classifications MeSH