Life-threatening metabolic alkalosis in Pendred syndrome

Narayanan Kandasamy, Laura Fugazzola, Mark Evans, Krishna Chatterjee, Fiona Karet

Research output: Contribution to journalArticle

Abstract

Introduction: Pendred syndrome, a combination of sensorineural deafness, impaired organification of iodide in the thyroid and goitre, results from biallelic defects in pendrin (encoded by SLC26A4), which transports chloride and iodide in the inner ear and thyroid respectively. Recently, pendrin has also been identified in the kidneys, where it is found in the apical plasma membrane of non-α-type intercalated cells of the cortical collecting duct. Here, it functions as a chloride-bicarbonate exchanger, capable of secreting bicarbonate into the urine. Despite this function, patients with Pendred syndrome have not been reported to develop any significant acid-base disturbances, except a single previous reported case of metabolic alkalosis in the context of Pendred syndrome in a child started on a diuretic. Case report: We describe a 46-year-old female with sensorineural deafness and hypothyroidism, who presented with severe hypokalaemic metabolic alkalosis during inter-current illnesses on two occasions, and who was found to be homozygous for a loss-of-function mutation (V138F) in SLC26A4. Her acid-base status and electrolytes were unremarkable when she was well. Conclusion: This case illustrates that, although pendrin is not usually required to maintain acid-base homeostasis under ambient condition, loss of renal bicarbonate excretion by pendrin during a metabolic alkalotic challenge may contribute to life-threatening acid-base disturbances in patients with Pendred syndrome.

Original languageEnglish
Pages (from-to)167-170
Number of pages4
JournalEuropean Journal of Endocrinology
Volume165
Issue number1
DOIs
Publication statusPublished - Jul 2011

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Alkalosis
Acids
Iodides
Deafness
Bicarbonates
Thyroid Gland
Chloride-Bicarbonate Antiporters
Goiter
Inner Ear
Hypothyroidism
Diuretics
Electrolytes
Chlorides
Homeostasis
Cell Membrane
Urine
Kidney
Mutation
Pendred syndrome

ASJC Scopus subject areas

  • Endocrinology
  • Medicine(all)
  • Endocrinology, Diabetes and Metabolism

Cite this

Kandasamy, N., Fugazzola, L., Evans, M., Chatterjee, K., & Karet, F. (2011). Life-threatening metabolic alkalosis in Pendred syndrome. European Journal of Endocrinology, 165(1), 167-170. https://doi.org/10.1530/EJE-11-0101

Life-threatening metabolic alkalosis in Pendred syndrome. / Kandasamy, Narayanan; Fugazzola, Laura; Evans, Mark; Chatterjee, Krishna; Karet, Fiona.

In: European Journal of Endocrinology, Vol. 165, No. 1, 07.2011, p. 167-170.

Research output: Contribution to journalArticle

Kandasamy, N, Fugazzola, L, Evans, M, Chatterjee, K & Karet, F 2011, 'Life-threatening metabolic alkalosis in Pendred syndrome', European Journal of Endocrinology, vol. 165, no. 1, pp. 167-170. https://doi.org/10.1530/EJE-11-0101
Kandasamy N, Fugazzola L, Evans M, Chatterjee K, Karet F. Life-threatening metabolic alkalosis in Pendred syndrome. European Journal of Endocrinology. 2011 Jul;165(1):167-170. https://doi.org/10.1530/EJE-11-0101
Kandasamy, Narayanan ; Fugazzola, Laura ; Evans, Mark ; Chatterjee, Krishna ; Karet, Fiona. / Life-threatening metabolic alkalosis in Pendred syndrome. In: European Journal of Endocrinology. 2011 ; Vol. 165, No. 1. pp. 167-170.
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