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

被引:16
作者
Chaba, Anis [1 ]
Devresse, Arnaud [2 ]
Audard, Vincent [3 ,4 ]
Boffa, Jean Jacques [5 ]
Karras, Alexandre [6 ]
Cartery, Claire [7 ]
Deltombe, Clement [8 ]
Chemouny, Jonathan [9 ]
Contamin, Claudine [10 ]
Courivaud, Cecile [11 ]
Duquennoy, Simon [12 ]
Garcia, Hugo [13 ]
Joly, Dominique [14 ]
Goumri, Nabila [15 ]
Hanouna, Guillaume [16 ]
Halimi, Jean Michel [17 ]
Plaisier, Emmanuelle [18 ]
Hamidou, Mohamed [19 ]
Landron, Cedric [20 ]
Launay, David [21 ]
Lebas, Celine [22 ]
Legendre, Mathieu [23 ]
Masseau, Agathe [19 ]
Mathian, Alexis [24 ]
Mercadal, Lucile [13 ]
Morel, Nathalie [24 ]
Mutinelli-Szymanski, Prisca
Palat, Sylvain [25 ]
Pennaforte, Jean-Loup [26 ]
Peraldi, Marie Noelle [27 ]
Pozdzik, Agnieszka [28 ]
Schleinitz, Nicolas [29 ]
Thaunat, Olivier [30 ]
Titeca-Beauport, Dimitri [31 ]
Mussini, Charlotte [32 ]
Touati, Sonia [33 ]
Prinz, Eric [34 ]
Faller, Anne Laure [35 ]
Richter, Sarah [35 ]
Vilaine, Eve [36 ]
Ferlicot, Sophie [32 ]
Von-Kotze, Clarissa [37 ]
Belliere, Julie [38 ]
Olagne, Jerome [39 ]
Mesbah, Rafik [40 ]
Snanoudj, Renaud [1 ]
Nouvier, Mathilde [41 ]
Ebbo, Mikael [29 ]
Zaidan, Mohamad [1 ,42 ,43 ]
机构
[1] Paris Saclay Univ, Bicetre Univ Hosp, Assistance Publ Hop Paris AP HP, Dept Nephrol Dialysis Transplantat, Le Kremlin Bicetre, France
[2] Clin Univ St Luc, Dept Nephrol, Brussels, Belgium
[3] Henri Mondor Hosp Univ, Assistance Publ Hop Paris AP HP, Rare Dis Ctr Idiopath Nephrot syndrome, Nephrol & Renal Transplantat Dept,Federat Hosp Uni, Creteil, France
[4] Univ Paris Est Creteil, Inst Natl Sante & Rech Med INSERM U955, Inst Mondor Rech Biomed IMRB, Creteil, France
[5] CHU Tenon, Dept Nephrol, Paris, France
[6] CHU HEGP, Dept Nephrol, Paris, France
[7] CH Valenciennes, Dept Nephrol, Valenciennes, France
[8] Nantes Univ Hosp, Inst Transplantat Urol & Nephrol ITUN, Nantes, France
[9] CHU Rennes, Dept Nephrol, Rennes, France
[10] GHM Grenoble, Dept Internal Med, Grenoble, France
[11] CHRU Jean Minjoz, Dept Nephrol, Bensancon, France
[12] Fdn AUB Sante Avranches, Dept Nephrol, Avranches, France
[13] Hop Sorbonne Univ, Dept Nephrol, Paris, France
[14] CHU Necker, Dept Nephrol, Paris, France
[15] CH Chartres, Dept Nephrol, Chartres, France
[16] CHU Bichat, Dept Nephrol, Paris, France
[17] CHU Tours, Dept Nephrol, Tours, France
[18] AURA Plaisance, Dept Nephrol, Paris, France
[19] CHU Nantes, Dept Internal Med, Nantes, France
[20] CHU Poitier, Dept Internal Med, Poitier, France
[21] Univ Lille, INFINITE Inst Translat Res Inflammat, Ctr Reference Malad Autoimmunes Syst Rares Nord &, Serv Med Interne & Immunol Clin,Inserm,CHU Lille,U, Lille, France
[22] CHU Valenciennes, Dept Nephrol, Valenciennes, France
[23] CHU Dijon, Dept Nephrol, Dijon, France
[24] Hop Cochin, APHP, Dept Internal Med, Paris, France
[25] CHU Limoges, Dept Internal Med, Limoges, France
[26] CH Epernay, Dept Internal Med, Reims, France
[27] CHU St Louis, Dept Nephrol, Paris, France
[28] CHU Brugmann, Dept Nephrol, Brussels, Belgium
[29] CHU Timone, Dept Internal Med, Marseille, France
[30] CH Edouart Heriot, Dept Nephrol, Lyon, France
[31] CHU Amiens, Dept Nephrol, Amiens, France
[32] Paris Saclay Univ, Bicetre Univ Hosp, Assistance Publ Hop Paris AP HP, Dept Pathol, Le Kremlin Bicetre, France
[33] CH Pontoise, Dept Nephrol, Pontoise, France
[34] NHC Strasbourg, Dept Nephrol, Strasbourg, France
[35] Clin St Anne, Dept Nephrol, Strasbourg, France
[36] CHU Ambroise Pare, Dept Nephrol, Mons, Belgium
[37] ADPC Marseille Michelet, Dept Nephrol, Marseille, France
[38] CHU Toulouse, Dept Nephrol, Toulouse, France
[39] NHC Strasbourg, Dept Pathol, Strasbourg, France
[40] Hop Boulogne Sur Mer, Dept Nephrol, Boulogne Sur Mer, France
[41] CHLS, Dept Nephrol, Lyon, France
[42] Hop Univ Bicetre, Assistance Publ Hop Paris APHP, Serv Nephrol Dialyse & Transplantat, Le Kremlin Bicetre, France
[43] Univ Paris Saclay, 78 Rue Gen Leclerc, F-94270 Le Kremlin Bicetre, France
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2023年 / 18卷 / 08期
关键词
CKD; chronic nephropathy; clinical immunology; clinical nephrology; interstitial fibrosis; RHEUMATOLOGY CLASSIFICATION CRITERIA; 2022; AMERICAN-COLLEGE; AUTOIMMUNE PANCREATITIS; IGG4; ASSOCIATIONS; ALLIANCE; GRANULOMATOSIS; DIAGNOSIS;
D O I
10.2215/CJN.0000000000000193
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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 m(2) 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 m(2) 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 m(2). 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.
引用
收藏
页码:1031 / 1040
页数:10
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