Pregnancy-associated polyuria in familial renal glycosuria

Am J Kidney Dis. 2013 Dec;62(6):1160-4. doi: 10.1053/j.ajkd.2013.05.018. Epub 2013 Jul 18.

Abstract

A pregnant woman presented at gestational week 28 with loss of consciousness and profound polyuria. Further characterization revealed osmotic diuresis due to massive glycosuria without hyperglycemia. Glycosuria reduced substantially postpartum, from approximately 100 to approximately 30 g/1.73 m2 per day. DNA sequencing analysis of the SLC5A2 gene encoding the renal glucose transporter SGLT2 showed a homozygous frame-shift mutation (occurring after the glutamine at amino acid 168 and leading to premature termination of the protein at amino acid 186) diagnostic of familial renal glycosuria. Pregnant women with familial renal glycosuria can be at risk of profound polyuria during pregnancy due to the associated increase in glycosuria. These findings also have implications for the use of SGLT2 inhibitors in clinical practice.

Keywords: Familial renal glycosuria; SGLT2, SCL5A2; natriuresis; polyuria; vasopressin.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Female
  • Frameshift Mutation / genetics
  • Glucose Intolerance / diagnosis
  • Glucose Intolerance / genetics
  • Glycosuria, Renal / diagnosis
  • Glycosuria, Renal / genetics*
  • Homozygote
  • Humans
  • Kidney Function Tests
  • Polyuria / genetics*
  • Pregnancy
  • Pregnancy Complications / diagnosis
  • Pregnancy Complications / genetics*
  • Pregnancy Trimester, Second
  • Sequence Analysis, DNA
  • Sodium-Glucose Transporter 2 / genetics

Substances

  • SLC5A2 protein, human
  • Sodium-Glucose Transporter 2