Studies on Acid Excretion in Adults with Sickle-Cell Anaemia

Author:

Kong H. HO Ping1,Alleyne G. A. O.1

Affiliation:

1. Medical Research Council, Tropical Metabolism Research Unit, University of the West Indies, Jamaica

Abstract

1. The acid excretion of patients with sickle-cell anaemia has been studied. 2. There is a mild defect in urinary acidification and a decreased H+ excretion in response to ammonium chloride loading. 3. The acidification defect was not corrected by oral administration of a phosphate solution. 4. Infusion of a sodium sulphate solution in subjects who were avidly reabsorbing sodium produced equal degrees of urine acidification in patients and controls. 5. Studies on bicarbonate reabsorption were inconclusive. 6. We conclude that patients with sickle-cell anaemia have a mild form of incomplete distal renal tubular acidosis.

Publisher

Portland Press Ltd.

Subject

General Medicine

Cited by 30 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Sickle Cell Disease;Chronic Renal Disease;2020

2. Jamaica and Research in Sickle Cell Disease;West Indian Medical Journal;2017-08-31

3. Sickle Cell Nephropathy in Children;Pediatric Nephrology;2015-11-12

4. Chronic Kidney Disease and Sickle Cell Disease;Chronic Renal Disease;2015

5. Prevalence and Correlates of Metabolic Acidosis among Patients with Homozygous Sickle Cell Disease;Clinical Journal of the American Society of Nephrology;2014-01-23

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