Back to Search Start Over

A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney disease.

Authors :
Kondo A
Yoshiya K
Sakakibara N
Nagano C
Horinouchi T
Nozu K
Source :
CEN case reports [CEN Case Rep] 2024 Oct; Vol. 13 (5), pp. 326-329. Date of Electronic Publication: 2024 Feb 02.
Publication Year :
2024

Abstract

Pseudo-Bartter/Gitelman syndrome (PBS/PGS) is a disorder that presents with hypokalemia and metabolic alkalosis resembling Gitelman syndrome (GS) due to secondary factors, such as lifestyle and /or medicines. Notably, PBS/PGS is more likely to cause renal dysfunction than GS. We report the first case of PBS/PGS due to long-term laxative abuse leading to end-stage kidney disease (ESKD). The patient was a 49-year-old woman with a history of constipation since school, who had used excessive doses of laxatives on her own judgment for nine years at least from 22 years of age. Two years later, blood tests revealed hypokalemia (serum K 3.1 mEq/L), and nine years later, the patient's renal function began to deteriorate (Cr-eGFR 48.7 mL/min/1.73 m <superscript>2</superscript> ). Since abuse of laxatives was suspected as the cause, it was changed to the proper dosage of laxatives. At 33 years, the patient developed acute kidney injury (AKI), due to a urinary tract infection, and required intensive treatment, including hemodialysis. Although the patient was eventually weaned off dialysis, the renal function did not recover to pre-AKI levels. In suspected GS, comprehensive genetic testing for renal disease-related genes was performed; however, no obvious pathogenic variants were identified. Thereafter, despite decreasing the laxative doses and potassium supplementation, her renal function continued to decline. At 49 years, the patient developed ESKD and was started on maintenance hemodialysis. PBS/PGS is a disease that can lead to ESKD. An early diagnosis of PBS/PGS is crucial to prevent renal function deterioration, and the underlying causes should be removed immediately.<br /> (© 2024. The Author(s), under exclusive licence to Japanese Society of Nephrology.)

Details

Language :
English
ISSN :
2192-4449
Volume :
13
Issue :
5
Database :
MEDLINE
Journal :
CEN case reports
Publication Type :
Academic Journal
Accession number :
38306007
Full Text :
https://doi.org/10.1007/s13730-024-00851-9