Abstract: TH-PO362
Urine Chemistry: A Valuable Link Binding Kidney Physiology to Patient Care
Session Information
- Sodium, Potassium, and Volume Disorders: Clinical
October 24, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Fluid, Electrolytes, and Acid-Base Disorders
- 1102 Fluid, Electrolyte, and Acid-Base Disorders: Clinical
Authors
- Alshwayat, Anas Radi Issa, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
- Karakala, Nithin, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
- Holthoff, Joseph H., University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
Introduction
The intricate dance of electrolytes within the human body orchestrates vital physiological functions, particularly within the renal system. Amidst the myriad diagnostic tools available, the analysis of urine electrolytes emerges as a cornerstone in unraveling the mysteries of renal channel dysfunction. By Analyzing the composition of electrolytes excreted in urine, clinicians gain invaluable insights into the renal handling of these essential ions. We delve into the significance of urine electrolyte analysis as a diagnostic modality for identifying dysfunctional renal channels. We explore the physiological principles underpinning electrolyte handling in the kidneys, elucidate the mechanisms of channel dysfunction, and discuss the clinical implications of aberrant urine electrolyte patterns.
Case Description
A 17-year-old African American pregnant female, G1P0 at 34 weeks gestation, presented to triage three times with muscle weakness. During one episode, she fell because her legs gave out and was unable to stand again due to the leg weakness. Her potassium level in the ED was 2 mEq/L. This was her first experience of such weakness.
We ordered spot urine potassium and creatinine tests, which revealed a K/Cr ratio of 20 mEq/g and a fractional excretion of potassium (FeK) of 4%. This high FeK in the context of hypokalemia prompted us to proceed with a 24-hour urine collection for electrolytes to confirm renal potassium loss.
The 24-hour urine results showed undetectable calcium levels, and elevated levels of sodium, chloride, magnesium, and uric acid in the urine, with normal potassium levels (which are considered high for a patient with hypokalemia). These findings confirmed renal potassium loss and implicated thiazide-sensitive NCC channels as the defective mechanism.
Genetic testing revealed a mutation in the NOTCH2 gene of unknown significance, potentially causing NCC channel dysfunction, as NOTCH genes affect the expression of SLC12A3 (the gene responsible for NCC channel function). Additionally, the patient had a mutation in the SCN4A gene, which can cause periodic hypokalemic paralysis.
Discussion
The urine studies are extremely valuable in assessing perturbations in renal physiology that can help in determining the management of patients with electrolyte abnormalities