Clinical and Prognostic Factors in Patients with IgG4-Related Kidney Disease

Author:

Chaba Anis1ORCID,Devresse Arnaud2ORCID,Audard Vincent34ORCID,Boffa Jean Jacques5,Karras Alexandre6,Cartery Claire7ORCID,Deltombe Clément8ORCID,Chemouny Jonathan9ORCID,Contamin Claudine10,Courivaud Cecile11,Duquennoy Simon12ORCID,Garcia Hugo13ORCID,Joly Dominique14,Goumri Nabila15,Hanouna Guillaume16ORCID,Halimi Jean Michel17ORCID,Plaisier Emmanuelle18,Hamidou Mohamed19,Landron Cédric20,Launay David21ORCID,Lebas Celine22,Legendre Mathieu23,Masseau Agathe19,Mathian Alexis24ORCID,Mercadal Lucile13ORCID,Morel Nathalie24,Mutinelli-Szymanski Prisca17,Palat Sylvain25ORCID,Pennaforte Jean-Loup26,Peraldi Marie Noelle27ORCID,Pozdzik Agnieszka28,Schleinitz Nicolas29ORCID,Thaunat Olivier30ORCID,Titeca-Beauport Dimitri31ORCID,Mussini Charlotte32,Touati Sonia33ORCID,Prinz Eric34,Faller Anne Laure35,Richter Sarah35,Vilaine Eve36,Ferlicot Sophie32,Von-Kotze Clarissa37,Belliere Julie38ORCID,Olagne Jerome39ORCID,Mesbah Rafik40ORCID,Snanoudj Renaud1ORCID,Nouvier Mathilde41,Ebbo Mikael29,Zaidan Mohamad1ORCID

Affiliation:

1. Departement of Nephrology-Dialysis-Transplantation, Assistance Publique des Hôpitaux de Paris (AP-HP), Bicêtre University Hospital, Paris-Saclay University, Le Kremlin Bicêtre, France

2. Department of Nephrology, Cliniques universitaires Saint-Luc, Bruxelles, Belgium

3. Nephrology and Renal Transplantation Department, Assistance Publique des Hôpitaux de Paris (AP-HP), Henri Mondor Hospital University, Rare Disease Center « Idiopathic Nephrotic syndrome », Fédération Hospitalo-Universitaire « Innovative therapy for immune disorders, Créteil, France

4. Univ Paris Est Créteil, Institut National de la Santé et de la Recherche Médicale (INSERM) U955, Institut Mondor de Recherche Biomédicale (IMRB), Créteil, France

5. Department of Nephrology, CHU Tenon, Paris, France

6. Department of Nephrology, CHU HEGP, Paris, France

7. Department of Nephrology, CH Valenciennes, Valenciennes, France

8. Institute for Transplantation, Urology and Nephrology (ITUN) Nantes University Hospital, Nantes, France

9. Department of Nephrology, CHU Rennes, Rennes, France

10. Department of Internal Medicine, GHM Grenoble, France

11. Department of Nephrology, CHRU Jean Minjoz, Bensançon, France

12. Department of Nephrology, Fondation AUB Santé Avranches, France

13. Department of Nephrology, Hôpitaux Sorbonne Université, Paris, France

14. Department of Nephrology, CHU Necker, Paris, France

15. Department of Nephrology, CH Chartres, Chartres, France

16. Department of Nephrology, CHU Bichat, Paris, France

17. Department of Nephrology, CHU Tours, Tours, France

18. Department of Nephrology, AURA Plaisance, Paris, France

19. Department of Internal Medicine, CHU Nantes, Nantes, France

20. Department of Internal Medicine, CHU Poitier, Poitier, France

21. Univ. Lille, Inserm, CHU Lille, Service de Médecine Interne et Immunologie Clinique, Centre de référence des maladies autoimmunes systémiques rares du Nord et Nord-Ouest de France (CeRAINO), U1286—INFINITE—Institute for Translational Research in Inflammation, Lille, France

22. Department of Nephrology, CHU Valenciennes, Valenciennes, France

23. Department of Nephrology, CHU Dijon, Dijon, France

24. Department of Internal Medicine, Hôpital Cochin, APHP, Paris, France

25. Department of Internal Medicine, CHU Limoges, Limoges, France

26. Department of Internal Medicine, CH Epernay, Reims, France

27. Department of Nephrology, CHU Saint Louis, Paris, France

28. Department of Nephrology, CHU Brugmann, Bruxelles, Belgium

29. Department of Internal Medicine, CHU Timone, Marseille, France

30. Department of Nephrology, CH Edouart Heriot, Lyon, France

31. Department of Nephrology, CHU Amiens, Amiens, France

32. Departement of Pathology, Assistance Publique des Hôpitaux de Paris (AP-HP), Bicêtre University Hospital, Paris-Saclay University, Le Kremlin Bicêtre, France

33. Department of Nephrology, CH Pontoise, Pontoise, France

34. Department of Nephrology, NHC Strasbourg, France

35. Department of Nephrology, Clinique Sainte Anne, Strasbourg, France

36. Department of Nephrology, CHU Ambroise Paré, France

37. Department of Nephrology, ADPC Marseille Michelet, Marseille, France

38. Departement of Nephrology, CHU Toulouse, Toulouse, France

39. Department of Pathology, NHC Strasbourg, France

40. Department of Nephrology, Hopital Boulogne-sur-mer, Boulogne-sur-mer, France

41. Department of Nephrology, CHLS, Lyon, France

Abstract

Background IgG4-related kidney disease is a major manifestation of IgG4-related disease, a systemic fibroinflammatory disorder. However, the clinical and prognostic kidney-related factors in patients with IgG4-related kidney disease are insufficiently defined. Methods We conducted an observational cohort study using data from 35 sites in two European countries. Clinical, biologic, imaging, and histopathologic data; treatment modalities; and outcomes were collected from medical records. Logistic regression was performed to identify the possible factors related to an eGFR ≤30 ml/min per 1.73 m2 at the last follow-up. Cox proportional hazards model was performed to assess the factors associated with the risk of relapse. Results We studied 101 adult patients with IgG4-related disease with a median follow-up of 24 (11–58) months. Of these, 87 (86%) patients were male, and the median age was 68 (57–76) years. Eighty-three (82%) patients had IgG4-related kidney disease confirmed by kidney biopsy, with all biopsies showing tubulointerstitial involvement and 16 showing glomerular lesions. Ninety (89%) patients were treated with corticosteroids, and 18 (18%) patients received rituximab as first-line therapy. At the last follow-up, the eGFR was below 30 ml/min per 1.73 m2 in 32% of patients; 34 (34%) patients experienced a relapse, while 12 (13%) patients had died. By Cox survival analysis, the number of organs involved (hazard ratio [HR], 1.26; 95% confidence interval [CI], 1.01 to 1.55) and low C3 and C4 concentrations (HR, 2.31; 95% CI, 1.10 to 4.85) were independently associated with a higher risk of relapse, whereas first-line therapy with rituximab was protective (HR, 0.22; 95% CI, 0.06 to 0.78). At their last follow-up, 19 (19%) patients had an eGFR ≤30 ml/min per 1.73 m2. Age (odd ratio [OR], 1.11; 95% CI, 1.03 to 1.20), peak serum creatinine (OR, 2.74; 95% CI, 1.71 to 5.47), and serum IgG4 level ≥5 g/L (OR, 4.46; 95% CI, 1.23 to 19.40) were independently predictive for severe CKD. Conclusions IgG4-related kidney disease predominantly affected middle-aged men and manifested as tubulointerstitial nephritis with potential glomerular involvement. Complement consumption and the number of organs involved were associated with a higher relapse rate, whereas first-line therapy with rituximab was associated with lower relapse rate. Patients with high serum IgG4 concentrations (≥5 g/L) had more severe kidney disease.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

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