Uric Acid Based Renal Stones: Clinical, Metabolic and Genetic Characterization

Sponsor

Mansoura University (Other)

Overall Status

Recruiting

CT.gov ID

NCT05634434

Collaborator

(none)

Enrollment

Location

Anticipated Duration (Months)

2.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Reporting prevalence of uric acid based renal stones among patients with nephrolithiasis admitted to Mansoura Urology and Nephrology center (MUNC).
Furthermore, identification of monogenic and polygenic uric acid stone formers.
Identification of factors associated uric acid stone recurrence as well as determinants of laterality in patients with uric acid based renal stones

Condition or Disease	Intervention/Treatment	Phase
Renal Stone Urinary Stones

Detailed Description

To Report the prevalence of uric acid based renal stones among patients with NL admitted to Mansoura Urology and Nephrology center (MUNC).
To identify monogenic and polygenic uric acid stone formers.
To Identify the factors associated uric acid stone recurrence as well as determinants of their laterality in patients with uric acid based renal stones.
Research Approach and Methodology
Study design: A prospective controlled study
Target population:

Patients admitted in Mansoura urology and nephrology center with unilateral or bilateral renal stones, as proven by imaging techniques (ultrasound and non-contrast spiral CT scan) are targeted in the duration between September 2021 to September 2022.

Healthy stone free individuals proven by imaging are assigned as a control group.

Legible subjects fulfilling inclusion criteria will be included in a prospective study and will be asked to sign an informed consent form according to Good Clinical Practice and the Declaration of Helsinki.

Inclusion criteria should satisfy all the following.
Patients with unilateral or bilateral renal stones (de novo or recurrent) who are candidates for endoscopic treatment (percutaneous nephrolithotomy).
Patients with preoperative NCCT findings of renal stone with stone density equal or less than 600HU.
Patients with dominant uric acid composition will be included as proven by postoperative stone analysis.
Exclusion criteria:
Patients with anatomical abnormalities precipitating stone disease e.g. ureteric stricture, ureteropelvic or ureterovesical junction obstruction, Urinary diversion, History of ureterovesical re-implantation
Patients with non-uric acid stones as proven by post-operative stone analysis.
Study groups
Control group, Healthy stone free individuals proven by imaging will be assigned as a control group.
Study group
Denovo uric acid stone former (DUASF)
Recurrent uric acid stone former (RUASF)
Assessment tools
History includes residence, nutritional history, medical history e.g, DM and its type and history of stone disease +/- previous intervention.
Exam includes BMI, waist and hip circumference, waist-to-hip ratio, and blood pressure reporting.
Preoperative work up includes.
Urine analysis (Dipstick and microscopy)
24-hours urine collection for (Ph, ammonium, citrate, urate, and Tamm-Horsfall Protein (THP))
Blood sample for TLC (neutrophil and lymphocyte count), HgA1c, serum creatinine and uric acid level
Operative procedure and findings After overnight hydration using physiological saline 0.9% at a rate of 1ml/min. PCNL will be carried out in standard approach with bilateral ureteric catheters insertion.
Differential urine sampling from each kidney; Separate renal units' drainage with differential urine sampling will be carried out before creation of the renal puncture. Urine will be tested for Ph, ammonium, citrate, urate, and Tamm-Horsfall Protein (THP).
Stone analysis will be carried out using infrared spectroscopy.
Genetic testing Genomic DNA will be extracted from peripheral blood leukocytes using standard methods. The primer pairs and PCR reaction conditions that will be designed for used SLC22A12 and SLC2A9 to amplify the sequences. For all PCR reactions, we will use 50 to 100 ng of genomic DNA, 5 to 10 pmol of reverse and forward primers Sequencing will be performed in both directions using the ABI PRISM 3700 DNA Analyzer (Applied Biosystems).
Postoperative work up, includes before discharge control NCCT to rule out any residual stones. Patients with any non-targeted lucent residuals will be offered oral dissolution therapy in the form of potassium citrate till deemed stone free by NCCT at 3 months. All stone free patients will be advised for general stone preventive measures e.g, plenty of fluid intake and control of serum uric acid level. Patients will be invited for one year follow up visit for NCCT and any recurrent stone will be depicted, and its characters will be assessed in standard way.
Sample size and data analysis:

All patients with renal stones subjected to PNL will have stone analysis. For genetic, molecular, and metabolic evaluation; control group will be 10 healthy stone free volunteers and study group will include 20 uric acid stone patients.

Data will be collected into IBM SPSS25 program (social package for statistical sciences, IBM Corporation; Armonk, New York, USA). The mean and standard deviation (median and range) of all continuous measures and scores will be reported as indicated. Number (%) for categorical variables if any will be recorded at baseline and all subsequent visits. Proper statistical tests will be utilized accordingly.

Outcomes:
The primary outcome: reporting overall prevalence of uric acid stones among patients with renal stones admitted in Mansoura UNC during study period.
Secondary outcomes, include identification of genetic alterations in patients with uric acid stones and possible correlation with stone recurrence over 1 year following stone clearance. Reporting distinct clinical, metabolic and genetic features among uric acid stone formers with attempt for correlation of these findings to stone laterality.

Study Design

Study Type:

Observational

Anticipated Enrollment :

50 participants

Observational Model:

Cohort

Time Perspective:

Prospective

Official Title:

Uric Acid Based Renal Stones: Clinical, Metabolic and Genetic Characterization Looking for Determinants of Recurrence and Laterality

Actual Study Start Date :

Oct 1, 2021

Anticipated Primary Completion Date :

Dec 30, 2022

Anticipated Study Completion Date :

Oct 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
control group Same patient, stone free kidney
Study group uric acid stone former, diseased kidney (stone harboring)

Outcome Measures

Primary Outcome Measures

reporting overall prevalence of uric acid stones [1 year]
reporting overall prevalence of uric acid stones among patients with renal stones admitted in Mansoura UNC during study period.

Secondary Outcome Measures

identification of genetic alterations in patients with uric acid stones [1year]
identification of genetic alterations in patients with uric acid stones and possible correlation with stone recurrence over 1 year following stone clearance. Reporting distinct clinical, metabolic and genetic features among uric acid stone formers with attempt for correlation of these findings to stone laterality.

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

⦁ Patients with unilateral renal stones (denovo or recurrent) who are candidates for endoscopic treatment (percutaneous nephrolithotomy).
Patients with preoperative NCCT findings of renal stone with stone density equal or less than 600HU.
Patients with dominant uric acid composition will be included as proven by postoperative stone analysis

Exclusion Criteria:

⦁ Patients with anatomical abnormalities precipitating stone disease e.g. ureteric stricture, ureteropelvic or ureterovesical junction obstruction, Urinary diversion, History of ureterovesical re-implantation
Patients with non-uric acid stones as proven by post-operative stone analysis.