Literature DB >> 3030096

Correction of hypokalemia in Bartter's syndrome by enalapril.

R J Hené, H A Koomans, E J Dorhout Mees, A vd Stolpe, G E Verhoef, P Boer.   

Abstract

Seven patients with Bartter's syndrome were investigated before and after 3 months' treatment by enalapril. Serum potassium rose from 2.4 +/- 0.5 to 3.9 +/- 0.6 mmol/L. In all patients, serum magnesium rose and bicarbonate fell. Hormonal changes were as suspected: a further stimulation of renin and a decline in aldosterone. The BP sensitivity to angiotensin II normalized in the five patients in whom the test was performed. Clearance studies during maximal water diuresis, performed in four patients, were compatible with a high proximal fractional tubular sodium reabsorption and a relatively low distal fractional sodium reabsorption. Fractional free water excretion after furosemide was also low, confirming the concept of a primary sodium reabsorption defect in the furosemide-insensitive part of the nephron in Bartter's syndrome. The only consistent change after enalapril was a further decline in distal fractional sodium reabsorption. Initiation of therapy produced a BP fall in each subject. Clinical important hypotension associated with oliguria was seen twice, but these reactions were short-lasting. The BP rose to pretreatment values within 72 hours, despite continuation of converting-enzyme inhibition. Renal function recovered, though a moderate fall in function persisted. No other side effects were noticed. We conclude that converting-enzyme inhibition improves the potassium metabolism of patients with Bartter's syndrome, without ameliorating the abnormal renal sodium handling.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3030096     DOI: 10.1016/s0272-6386(87)80055-0

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


  9 in total

Review 1.  Anesthetic management of a patient with Bartter's syndrome undergoing orthognathic surgery.

Authors:  J A Roelofse; A J van der Westhuijzen
Journal:  Anesth Prog       Date:  1997

2.  Angiotensin-converting enzyme inhibition as a therapeutic principle in Bartter's syndrome.

Authors:  P Jest; K E Pedersen; N A Klitgaard; N Thomsen; K Kjaer; E Simonsen
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

3.  Bartter syndrome: benefits and side effects of long-term treatment.

Authors:  Maria Helena Vaisbich; Maria Danisi Fujimura; Vera H Koch
Journal:  Pediatr Nephrol       Date:  2004-06-16       Impact factor: 3.714

Review 4.  Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.

Authors:  Hannsjörg W Seyberth; Karl P Schlingmann
Journal:  Pediatr Nephrol       Date:  2011-04-19       Impact factor: 3.714

5.  Primary molecular disorders and secondary biological adaptations in bartter syndrome.

Authors:  Georges Deschênes; Marc Fila
Journal:  Int J Nephrol       Date:  2011-09-20

6.  Bartter syndrome-like phenotype in a patient with diabetes: a case report.

Authors:  Chamara Dalugama; Manoji Pathirage; S A M Kularatne
Journal:  J Med Case Rep       Date:  2018-08-17

Review 7.  Bartter syndrome: causes, diagnosis, and treatment.

Authors:  Tamara da Silva Cunha; Ita Pfeferman Heilberg
Journal:  Int J Nephrol Renovasc Dis       Date:  2018-11-09

8.  A novel compound heterozygous KCNJ1 gene mutation presenting as late-onset Bartter syndrome: Case report.

Authors:  Jingyi Li; Shoulong Hu; Yi Nie; Rongfeng Wang; Ming Tan; Hongmei Li; Shuanli Zhu
Journal:  Medicine (Baltimore)       Date:  2019-08       Impact factor: 1.817

Review 9.  Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians.

Authors:  Laura Nuñez-Gonzalez; Noa Carrera; Miguel A Garcia-Gonzalez
Journal:  Int J Mol Sci       Date:  2021-10-22       Impact factor: 5.923

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.