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Gut Microbiota in Patients With Urolithiasis

Primary Purpose

Urolithiasis

Status
Recruiting
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Caloric restriction and control oxalate and citrate foods
Caloric restriction
Real-life intervention with control oxalate and citrate foods
Sponsored by
Hospital Regional de Alta Especialidad de la Península de Yucatán
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Urolithiasis

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Subjects living in Merida, Yucatan
  • Female or male
  • Age between 18 and 60 years
  • Confirmed diagnosis of UL confirmed with ultrasound (≥5mm) and/or radiographs or who had expelled a stone in a time no longer than 7 days at the time of selection
  • BMI ≥ 25 and ≤ 39.9 kg/m2; no antibiotic intake (last 30 days)
  • No intake of probiotics, prebiotics or synbiotics (last 15 days)
  • No intake vitamin C supplements (last 15 days)
  • No intake calcium supplements (last 15 days)

Exclusion criteria:

  • Previous medical diagnosis of chronic kidney disease
  • Serum creatinine >1.2 mg/dL
  • Glomerular filtration <60 mL/min or 130 mL/min
  • Type 2 diabetes
  • Renal tubular acidosis
  • Pregnancy

Elimination criteria:

  • Not meeting 80% adherence to treatment
  • Antibiotic consumption during the intervention

Sites / Locations

  • Azalia Avila Nava, PhDRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Experimental

Experimental

Arm Label

Control

Intervention A

Intervention B

Arm Description

Caloric restriction

Caloric restriction and control oxalate and citrate food

Real-life intervention, control of oxalates and citrates without restriction of kilocalories.

Outcomes

Primary Outcome Measures

Relative abundance of gut microbiota
Changes in relative abundance of phylum, gender and species of bacteria in gut microbiota

Secondary Outcome Measures

Concentration of urinary citrate excretion
Changes in concentration of citrate excretion in 24-hour urine
Concentration of urinary oxalate excretion
Changes in concentration of oxalate excretion in 24-hour urine
Concentration of serum creatinine
Changes in concentration of creatinine in serum
Concentration of serum calcium
Changes in concentration of calcium in serum
Concentration of serum uric acid
Changes in concentration of uric acid in serum
Concentration of serum phosphorus
Changes in concentration of phosphorus in serum

Full Information

First Posted
August 19, 2022
Last Updated
March 4, 2023
Sponsor
Hospital Regional de Alta Especialidad de la Península de Yucatán
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1. Study Identification

Unique Protocol Identification Number
NCT05511337
Brief Title
Gut Microbiota in Patients With Urolithiasis
Official Title
Effect of Control in Oxalate and Citrate Intake on Gut Microbiota Composition in Patients With Urolithiasis: Double-blind Randomized Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 15, 2022 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Regional de Alta Especialidad de la Península de Yucatán

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Urolithiasis (UL) is the presence of kidney stones in different compartments such as ureters, bladder and/or urethra. Based on its incidence and prevalence it is considered a public health problem worldwide. In Mexico, especially in Yucatan state, is considered an endemic area of UL with a prevalence of 5.5%. There are several risk factors associated with the development of UL, among which are genetics, age, sex, excess weight, diet, and gut microbiota. In the diet there is promoters and inhibitors of stone formation, such as oxalates and citrates respectively. The gut microbiota is the set of microorganisms that inhabit the gastrointestinal tract, which have been related to the regulation of metabolic processes such as production of short-chain fatty acids (SCFA), vitamin K synthesis, and stimulation of the immune response. However, alterations in the composition of the microbiota have been associated with the development of various pathologies including UL. Recent studies have shown that the intestinal microbiota of people with kidney stones have a lower diversity and a different bacterial composition compared with healthy people, suggesting that interactions in the gut-renal axis could have a direct effect on the development of UL. Furthermore, these modifications could modulate oxalate and citrate transporters. Dietary modifications may decrease the risk of UL formation through increased consumption of citrate-rich foods (>40 mEq per day) and decreased consumption of oxalate-rich foods (< 40mg per day). It is known that dietary modifications can modulate the gut microbiota, however there is no evidence about the effect of a dietary intervention with oxalate and citrate control on the modulation of the microbiota in patients with UL. Thus, it is important to search for strategies to reduce UL, as well as the complications associated with them like chronic kidney disease. The main of the study is evaluate the effect of a dietary intervention with oxalate and citrate control on the composition and diversity of the intestinal microbiota of adults with UL.
Detailed Description
The protocol will be carried out in the Hospital Regional de Alta Especialidad de la Península de Yucatán (HRAEPY). This is double-blind randomized clinical study will be carried out in adults with a diagnosis of UL. Participants with UL are randomized by into three groups for 28 days. Control group: Caloric restriction, restriction of 500 kilocalories from the usual diet, or Intervention A: Restriction of 500 kilocalories from the usual diet plus a decrease in oxalate-rich foods (< 40 mg per day) and an increase in citrate-rich foods (> 40 mEq per day), or Intervention B: Real-life intervention with control oxalate and citrate foods: decrease in oxalate-rich foods (< 40 mg per day) and an increase in citrate-rich foods (> 40 mEq per day) without restriction of kilocalories from the usual diet. Randomization was performed by balanced blocks of three cells, with the research randomizer randomization program, 60 sites were randomized, which 20 participants were divided into three groups. Randomization was carried out by a person outside the study. At the beginning and at the end of the interventions, the following characteristics will be determined anthropometric measurements (weight, height, waist circumference, body mass index (BMI)) and blood pressure. A 24-h urine sample is requested to determine oxalates and citrates. A fasting blood sample of 8-10 hours will be requested for the determination of the concentration of creatinine, uric acid, calcium, phosphorus and sodium. A stool sample will also be requested for DNA extraction, which will be used for analysis of the composition and biodiversity of the intestinal microbiota. The person performing of measurements will be blinded to the group to which each participant belongs. Treatment will be given only through dietary counseling. Follow-up is done by telephone monitoring once a week through logbook and reminders. At the end of the study, the statistical analysis will be performed by a person who is blinded to the group to which the participants belong. The sample size was calculated with the formula for comparison of two proportions, with a one-tailed significance of 0.05 and a power of 80%, with a change in alpha diversity in the intervention group of 57% and in the control group of 18%. The result was 16 patients per group, but a 20% loss was considered. Therefore, a total of 20 participants per group was considered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urolithiasis

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are randomized into three groups for 28 days: Control: caloric restriction or intervention A: Control oxalate and citrate foods or intervention B: Real-life intervention, control of oxalates and citrates without restriction of kilocalories. Randomization was performed by balanced blocks of three cells, with the research randomizer randomization program, 60 sites were randomized, which 20 participants were divided into three groups. Randomization was carried out by a person outside the study. Treatment will be given only through dietary counseling. Treatment adherence will be assessed in all groups through three food diaries (two on weekdays and one on weekends). Adherence will be considered if the participant complies with 80% of the treatment.
Masking
Care ProviderOutcomes Assessor
Masking Description
The person performing the measurements will be blinded to the group to which each participant belongs. The statistical analysis will be performed by a person who is blinded to the group to which the participants belong.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Other
Arm Description
Caloric restriction
Arm Title
Intervention A
Arm Type
Experimental
Arm Description
Caloric restriction and control oxalate and citrate food
Arm Title
Intervention B
Arm Type
Experimental
Arm Description
Real-life intervention, control of oxalates and citrates without restriction of kilocalories.
Intervention Type
Other
Intervention Name(s)
Caloric restriction and control oxalate and citrate foods
Intervention Description
Restriction of 500 kilocalories from the usual diet plus a decrease in oxalate-rich foods (< 40 mg per day) and an increase in citrate-rich foods (> 40 mEq per day) for 28 days. The treatment will be given through an individualized meal plan.
Intervention Type
Other
Intervention Name(s)
Caloric restriction
Intervention Description
Restriction of 500 kilocalories from the usual diet for 28 days. The treatment will be given through an individualized meal plan
Intervention Type
Other
Intervention Name(s)
Real-life intervention with control oxalate and citrate foods
Intervention Description
Decrease in oxalate-rich foods (< 40 mg per day) and an increase in citrate-rich foods (> 40 mEq per day) without restriction in kilocalories from the usual diet for 28 days. Treatment will be given only through dietary counseling.
Primary Outcome Measure Information:
Title
Relative abundance of gut microbiota
Description
Changes in relative abundance of phylum, gender and species of bacteria in gut microbiota
Time Frame
At the beginning of the study and after 28 days of intervention
Secondary Outcome Measure Information:
Title
Concentration of urinary citrate excretion
Description
Changes in concentration of citrate excretion in 24-hour urine
Time Frame
At the beginning of the study and after 28 days of intervention
Title
Concentration of urinary oxalate excretion
Description
Changes in concentration of oxalate excretion in 24-hour urine
Time Frame
At the beginning of the study and after 28 days of intervention
Title
Concentration of serum creatinine
Description
Changes in concentration of creatinine in serum
Time Frame
At the beginning of the study and after 28 days of intervention
Title
Concentration of serum calcium
Description
Changes in concentration of calcium in serum
Time Frame
At the beginning of the study and after 28 days of intervention
Title
Concentration of serum uric acid
Description
Changes in concentration of uric acid in serum
Time Frame
At the beginning of the study and after 28 days of intervention
Title
Concentration of serum phosphorus
Description
Changes in concentration of phosphorus in serum
Time Frame
At the beginning of the study and after 28 days of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Subjects living in Merida, Yucatan Female or male Age between 18 and 60 years Confirmed diagnosis of UL confirmed with ultrasound (≥5mm) and/or radiographs or who had expelled a stone in a time no longer than 7 days at the time of selection BMI ≥ 25 and ≤ 39.9 kg/m2; no antibiotic intake (last 30 days) No intake of probiotics, prebiotics or synbiotics (last 15 days) No intake vitamin C supplements (last 15 days) No intake calcium supplements (last 15 days) Exclusion criteria: Previous medical diagnosis of chronic kidney disease Serum creatinine >1.2 mg/dL Glomerular filtration <60 mL/min or 130 mL/min Type 2 diabetes Renal tubular acidosis Pregnancy Elimination criteria: Not meeting 80% adherence to treatment Antibiotic consumption during the intervention
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Azalia Avila-Nava, PhD
Phone
01 999 94 27600
Ext
54440
Email
azalia.avila@salud.gob.mx
Facility Information:
Facility Name
Azalia Avila Nava, PhD
City
Mérida
State/Province
Yucatán
ZIP/Postal Code
97130
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Azalia A Nava, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15530322
Citation
Areses Trapote R, Urbieta Garagorri MA, Ubetagoyena Arrieta M, Mingo Monge T, Arruebarrena Lizarraga D. [Evaluation of renal stone disease: metabolic study]. An Pediatr (Barc). 2004 Nov;61(5):418-27. doi: 10.1016/s1695-4033(04)78417-9. Spanish.
Results Reference
background
PubMed Identifier
20383456
Citation
Medina-Escobedo M, Zaidi M, Real-de Leon E, Orozco-Rivadeneyra S. [Urolithiasis prevalence and risk factors in Yucatan, Mexico]. Salud Publica Mex. 2002 Nov-Dec;44(6):541-5. Spanish.
Results Reference
background
PubMed Identifier
19918339
Citation
Zuckerman JM, Assimos DG. Hypocitraturia: pathophysiology and medical management. Rev Urol. 2009 Summer;11(3):134-44.
Results Reference
background
PubMed Identifier
29705728
Citation
Ticinesi A, Milani C, Guerra A, Allegri F, Lauretani F, Nouvenne A, Mancabelli L, Lugli GA, Turroni F, Duranti S, Mangifesta M, Viappiani A, Ferrario C, Dodi R, Dall'Asta M, Del Rio D, Ventura M, Meschi T. Understanding the gut-kidney axis in nephrolithiasis: an analysis of the gut microbiota composition and functionality of stone formers. Gut. 2018 Dec;67(12):2097-2106. doi: 10.1136/gutjnl-2017-315734. Epub 2018 Apr 28.
Results Reference
background
PubMed Identifier
24987952
Citation
Del Chierico F, Vernocchi P, Dallapiccola B, Putignani L. Mediterranean diet and health: food effects on gut microbiota and disease control. Int J Mol Sci. 2014 Jul 1;15(7):11678-99. doi: 10.3390/ijms150711678.
Results Reference
background
PubMed Identifier
34579125
Citation
Stanislawski MA, Frank DN, Borengasser SJ, Ostendorf DM, Ir D, Jambal P, Bing K, Wayland L, Siebert JC, Bessesen DH, MacLean PS, Melanson EL, Catenacci VA. The Gut Microbiota during a Behavioral Weight Loss Intervention. Nutrients. 2021 Sep 18;13(9):3248. doi: 10.3390/nu13093248.
Results Reference
background
Links:
URL
https://www.imbiomed.com.mx/articulo.php?id=110852
Description
Manejo nutriológico en el paciente con litiasis renal

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Gut Microbiota in Patients With Urolithiasis

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