Outcomes of De Novo Allograft Diabetic Nephropathy in Renal Allograft Recipients
| dc.contributor.author | Prasad, Narayan | |
| dc.contributor.author | Gupta, Amit | |
| dc.contributor.author | Kaul, Anupama | |
| dc.contributor.author | Sharma, Raj Kumar | |
| dc.contributor.author | Bhadauria, Dharmendra | |
| dc.contributor.author | Jain, Manoj | |
| dc.contributor.author | Gupta, Pallav | |
| dc.date.accessioned | 2026-05-07T12:37:27Z | |
| dc.date.issued | 2013-06 | |
| dc.description.abstract | Objectives: Despite increased use of diabetogenic immunosuppressive drugs and increased incidence of new-onset diabetes after transplant in renal allograft recipients, there are few case studies on the subject of de novo allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes. We sought to study the outcomes of allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes in patients with new-onset diabetes after transplant. Materials and Methods: We reviewed the case records of all new-onset diabetes after transplant patients who underwent graft biopsy for graft dysfunction from 1992 to 2010. We analyzed the clinical characteristics and outcomes of new-onset diabetes after transplant patients with de novo allograft diabetic nephropathy and interstitial fibrosis/tubular atrophy without specific glomerular changes. Results: Of the 1989 recipients, 421 patients developed new-onset diabetes after transplant and 26 underwent graft biopsy. Of the 26 patients, 9 had histopathologic evidence of de novo allograft diabetic nephropathy, and 17 had interstitial fibrosis/tubular atrophy without specific glomerular changes. The mean duration from transplant to developing novo allograft diabetic nephropathy was 115.2 months (range, 33-192 mo), and from developing new-onset diabetes after transplant to allograft diabetic nephropathy, was 109.66 months (range, 27-188.4 mo). Of the 9 patients with de novo allograft diabetic nephropathy, 3 died (33.3%), 2 reached end-stage renal disease (22.2%), and 4 remained stable (44.4%). Of the 17 with interstitial fibrosis/tubular atrophy, 2 died (11.7%), 5 developed end-stage renal disease (29.4%), and 10 remained stable on triple immunosuppression and insulin therapy during follow-up (58.8%). Conclusions: De novo allograft diabetic nephropathy is a significant cause of graft and patient loss in renal allograft recipients who develop new-onset diabetes after transplant. | |
| dc.identifier.citation | Experimental and Clinical Transplantation, Cilt, 11, Sayı, 3, 2013 ss. 215-221 | en |
| dc.identifier.eissn | 2146-8427 | en |
| dc.identifier.issn | 1304-0855 | |
| dc.identifier.issue | 3 | en |
| dc.identifier.uri | https://hdl.handle.net/11727/15024 | |
| dc.identifier.volume | 11 | en |
| dc.language.iso | en | |
| dc.publisher | Başkent Üniversitesi | |
| dc.source | Experimental and Clinical Transplantation | en |
| dc.subject | New-onset diabetes associated with transplant | |
| dc.subject | Renal allograft | |
| dc.subject | Diabetic nephropathy | |
| dc.subject | Outcomes | |
| dc.title | Outcomes of De Novo Allograft Diabetic Nephropathy in Renal Allograft Recipients | |
| dc.type | Article |