Literature DB >> 8659493

In hereditary nephritis angiotensin-converting enzyme inhibition decreases proteinuria and may slow the rate of progression.

E P Cohen1, J Lemann.   

Abstract

The hereditary nephritides are often progressive, resulting in kidney failure and the need for renal replacement therapy. There is no currently known beneficial treatment for these disorders. We observed three patients with hereditary glomerulonephritis with plasma creatinine concentrations ranging from 1.7 to 2.0 mg/dL who were treated with angiotensin-converting enzyme inhibitors (ACEIs) for 3.5 to 6 years. Angiotensin-converting enzyme inhibitor therapy was accompanied by a decrease in the mean arterial pressure (MAP) from 115 +/- 10 mm Hg to 93 +/- 2 mm Hg (+/- SD), a decrease in the mean urinary protein/creatinine ratio from 2,910 +/- 1,720 mg/g to 391 +/- 355 mg/g, and stabilization of the decline of creatinine clearance with time in two of the three patients. Based on this apparent benefit of ACEIs in hereditary nephritis, we suggest that a prospective controlled trial of ACEIs should be undertaken among a large group of such patients. Pending the results of such a study, ACEIs should be considered for the treatment of patients with proteinuric and progressive hereditary nephritis.

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Year:  1996        PMID: 8659493     DOI: 10.1016/s0272-6386(96)90540-5

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  4 in total

1.  The effect of aldosterone blockade in patients with Alport syndrome.

Authors:  Hiroshi Kaito; Kandai Nozu; Kazumoto Iijima; Koichi Nakanishi; Kunihiko Yoshiya; Kyoko Kanda; Rafal Przybyslaw Krol; Norishige Yoshikawa; Masafumi Matsuo
Journal:  Pediatr Nephrol       Date:  2006-10-13       Impact factor: 3.714

Review 2.  Familial hematurias: what we know and what we don't.

Authors:  Clifford E Kashtan
Journal:  Pediatr Nephrol       Date:  2005-04-27       Impact factor: 3.714

3.  Drugs controlling proteinuria of patients with Alport syndrome.

Authors:  Jian-Guo Li; Jie Ding; Fang Wang; Hong-Wen Zhang
Journal:  World J Pediatr       Date:  2009-11-13       Impact factor: 2.764

4.  Phenotype variability in a large Spanish family with Alport syndrome associated with novel mutations in COL4A3 gene.

Authors:  C Cervera-Acedo; A Coloma; E Huarte-Loza; M Sierra-Carpio; E Domínguez-Garrido
Journal:  BMC Nephrol       Date:  2017-10-31       Impact factor: 2.388

  4 in total

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