Table 1.
References | N | Renal Histology | Comments |
---|---|---|---|
Ambruzs et al. [12] |
45 CD 38 UC |
24% IgA Nephropathy; 19%Interstitial Nephritis; 12% Nephrosclerosis; 8% Acute Tubular Injury; 7% Proliferative GN; 4% Minimal change disease; |
• Prevalence of IgAN significantly higher in patients with IBD than in healthy population • Association with HLA-DR1described in both IBD and IgAN • All patients with interstitial nephritis were previously exposed to aminosalicylates |
Jang et al. [13] | 7 CD |
5 IgA Nephropathy; 1 Henoch-Schönlein purpura; 1 No alterations; |
|
Archimandritis et al. [14] | 1 CD | Interstitial nephritis with granulomas | • Full recovery after proctocolectomy |
Izzedine et al. [15] | 4 CD | 4 Interstitial Nephritis |
• All diagnosed before administration of mesalazina • Progression to end-stage renal failure in 3 patients • Granulomas were identified in 2 patients |
Hubert et al. [16] |
1 CD 1 UC |
IgA Nephropathy | • Restoration of renal findingsafter treatment for IBD |
Ridder et al. [17] | 1 UC | Membranous Nephropathy |
• Presentation with intestinal manifestation • Improvement after therapy |
Pohjonen et al. [18] |
14 CD 14 UC 7 UND |
7 IgA Nephropathy; 2 Membranous Nephropathy; 2 IgM GN; 4 acute interstitial nephritis; 4 chronic interstitial nephritis; |
• All patients with interstitial nephropathy had an history of mesalazina administration |
Ota et al. [19] | 1 CD | acute tubulointerstitial nephritis | • After the discontinuation of IFX, renal abnormalities resolved |
CD Chron disease, GN glomerulonephrities, IBD inflammatory bowel disease, UC ulcerative colitis, UND undetermined