Budesonide versus systemic corticosteroids in IgA Nephropathy: A retrospective, propensity-matched comparison. Issue 26 (26th June 2020)
- Record Type:
- Journal Article
- Title:
- Budesonide versus systemic corticosteroids in IgA Nephropathy: A retrospective, propensity-matched comparison. Issue 26 (26th June 2020)
- Main Title:
- Budesonide versus systemic corticosteroids in IgA Nephropathy
- Authors:
- Ismail, Gener
Obrişcă, Bogdan
Jurubiţă, Roxana
Andronesi, Andreea
Sorohan, Bogdan
Vornicu, Alexandra
Sinescu, Ioanel
Hârza, Mihai - Other Names:
- Aeddula. Narothama Reddy section editor.
- Abstract:
- Abstract : Abstract: IgA Nephropathy (IgAN) is characterized by mesangial deposition of dominant, polymeric, galactose-deficient IgA1 molecules of gut-associated lymphoid tissue origin. We sought to evaluate the efficacy of targeting the mucosal immune system dysregulation underlying IgAN pathogenesis with a pH-modified formulation of budesonide with a maximum release of active compound in the distal ileum and proximal colon. We did a retrospective study evaluating the efficacy of budesonide (Budenofalk) in the treatment of IgAN. From a retrospective cohort of 143 patients with IgAN followed in our department we identified 21 patients that received treatment with budesonide. These patients received budesonide at a dose of 9 mg/d in the first 12 months, followed by a dose reduction to 3 mg/d for the subsequent period. Only patients that received a 24-month treatment with budesonide were included in the analysis (n = 18). We matched the budesonide-treated cohort to 18 patients with IgAN treated with systemic steroids from the same retrospective cohort. Efficacy was measured as change in proteinuria, hematuria and estimated glomerular filtration rate over a 24-month period. Treatment with budesonide was associated with a 24-month renal function decline of -0.22 (95%CI, -8.2 to 7.8) ml/min/1.73m 2, compared to -5.89 (95%CI, -12.2 to 0.4) ml/min/1.73m 2 in the corticosteroid treatment group (p = 0.44, for between group difference). The median reduction in proteinuria at 24-monthAbstract : Abstract: IgA Nephropathy (IgAN) is characterized by mesangial deposition of dominant, polymeric, galactose-deficient IgA1 molecules of gut-associated lymphoid tissue origin. We sought to evaluate the efficacy of targeting the mucosal immune system dysregulation underlying IgAN pathogenesis with a pH-modified formulation of budesonide with a maximum release of active compound in the distal ileum and proximal colon. We did a retrospective study evaluating the efficacy of budesonide (Budenofalk) in the treatment of IgAN. From a retrospective cohort of 143 patients with IgAN followed in our department we identified 21 patients that received treatment with budesonide. These patients received budesonide at a dose of 9 mg/d in the first 12 months, followed by a dose reduction to 3 mg/d for the subsequent period. Only patients that received a 24-month treatment with budesonide were included in the analysis (n = 18). We matched the budesonide-treated cohort to 18 patients with IgAN treated with systemic steroids from the same retrospective cohort. Efficacy was measured as change in proteinuria, hematuria and estimated glomerular filtration rate over a 24-month period. Treatment with budesonide was associated with a 24-month renal function decline of -0.22 (95%CI, -8.2 to 7.8) ml/min/1.73m 2, compared to -5.89 (95%CI, -12.2 to 0.4) ml/min/1.73m 2 in the corticosteroid treatment group (p = 0.44, for between group difference). The median reduction in proteinuria at 24-month was 45% (interquartile range [IQR]: -79%; -22%) in the budesonide group and 11% (IQR: -39%; 43%) in the corticosteroid group, respectively ( P = .009, for between group difference). The median reduction in hematuria at 24-month was 72% (IQR: -90%; -45%) in the budesonide group and 73% (IQR: -85%; 18%) in the corticosteroid group, respectively ( P = .22, for between group difference). Treatment with budesonide was well tolerated with minimal side effects. Budesonide (Budenofalk) was effective in the treatment of patients with IgAN at high-risk of progression in terms of reducing proteinuria, hematuria and preserving renal function over 24 months of therapy. … (more)
- Is Part Of:
- Medicine. Volume 99:Issue 26(2020)
- Journal:
- Medicine
- Issue:
- Volume 99:Issue 26(2020)
- Issue Display:
- Volume 99, Issue 26 (2020)
- Year:
- 2020
- Volume:
- 99
- Issue:
- 26
- Issue Sort Value:
- 2020-0099-0026-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-06-26
- Subjects:
- budesonide -- corticosteroids -- IgA Nephropathy -- immunosuppression
Medicine -- Periodicals
Medicine -- Periodicals
Médecine -- Périodiques
Geneeskunde
Medicine
Periodicals
Periodicals
610.5 - Journal URLs:
- http://journals.lww.com/md-journal/pages/default.aspx ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&PAGE=toc&D=ovft&MODE=ovid&NEWS=N&AN=00002060-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MD.0000000000021000 ↗
- Languages:
- English
- ISSNs:
- 0025-7974
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5534.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13739.xml