Urolithiasis Clinical Trial
Official title:
Understanding the Urine Electrolyte Profile of the Individual Renal Unit
The investigators objective is to determine if urinary electrolyte abnormalities exist in only one or both kidneys in participants with and without a history of kidney stones. To meet this objective, the investigators are going to take urine samples from each kidney at the time of kidney stone surgery. The samples will then be analyzed for absolute and relative differences in the concentrations of urine electrolytes, such as calcium.
Nephrolithiasis is common within the general population. Although the majority of patients
with a symptomatic stone event will not require surgical intervention, the rate of recurrence
is high. Therefore, reducing this rate of recurrence is important.
Traditionally, this has been achieved with a combination of serum and urine metabolic
evaluation followed by targeted medication and dietary interventions. Specifically, it is
recommended that a single 24-hour urine collection for analysis of urine electrolytes be
performed. A 24-hour urine collection is bladder urine, which is pooled urine from both
kidneys. The urine is then analyzed for the relative and absolute concentrations of
electrolytes and small molecules known to be associated with stone formation. These include
creatinine, calcium, citrate, oxalate, potassium, magnesium, phosphate, uric acid, and urate.
When an abnormality is detected on a 24-hour urine collection the assumption is that this is
due to a global metabolic defect present in both kidneys. However, this may not be the case.
It is possible there could be a relative imbalance with both kidneys having a defect, but to
different degrees (or different defects in one or multiple electrolytes). It is also possible
that one kidney has a dominant defect, but the contralateral kidney is normal, and therefore
the 24-hour urine collection would only represent the dominant kidney with the defect.
Finally, it is possible that the converse is true. One kidney has no defect, but the
contralateral kidney has a minor defect. In this example, the 24-hour urine collection would
appear normal as the dominant normal kidney masks the minor defect. This concept of
differential kidney electrolyte handling was previously described in children. Therefore,
understanding individual kidney metabolic profiles is important.
The purpose of the investigators' study will be to (1) characterize the urine electrolyte
profile of each individual renal unit; (2) identify participants who have differences between
their renal unit urine electrolyte profiles, and their renal units and bladder urine
electrolyte profiles; and (3) correlate differences in renal unit urine electrolyte profiles
with clinical manifestations of kidney stones, such as stone formation or growth. By
characterizing individual renal unit urine electrolyte profiles, the investigators' may be
able to isolate a phenotype of stone formers who would not otherwise be identified with
traditional 24-hour urine collection. The investigators' can then target this phenotype in
future investigations with dietary and medication interventions to hopefully prevent future
stone events.
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