Effect of Weight Loss on Urinary Oxalate Excretion in Obese Calcium Oxalate Kidney Stone Formers

The University of Alabama at Birmingham

Status

Active, not recruiting

Conditions

Kidney Stone

Treatments

Dietary Supplement: Low Oxalate Diet after Weight Loss

Dietary Supplement: Oral load of oxalate and sucralose after Weight Loss

Dietary Supplement: Optifast VLCD Program

Dietary Supplement: Oral load of oxalate and sucralose before Weight Loss

Dietary Supplement: Optifast VLCD Transition Phase

Dietary Supplement: Low Oxalate Diet before Weight Loss

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT04633811

IRB-300006133

R01DK128160 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This protocol seeks to determine if weight reduction with the Optifast VLCD program leads to reduced contribution of endogenous oxalate synthesis and dietary oxalate absorption to the urinary oxalate pool in obese calcium oxalate stone formers.

Full description

Obese adults (≥19 and ≤ 65 years) with a history of calcium oxalate kidney stone disease will be recruited at both University of Alabama at Birmingham (UAB) and University of Texas South Western (UTSW). Following consent, subjects will complete a screening phase, which includes (1) a meeting with a dietitian to ensure willingness to consume controlled ultra-low oxalate diets and determine anthropometric measurements and blood pressure, (2) collection of fasted blood and 2 x 24-hour urine specimens on self-choice diets to determine general health status and urinary chemistries, respectively, (3) completion of a 7-day run-in diet that includes the use of one serving of an Optifast meal daily to assess tolerance to Optifast VLCD® products. Participants will then consume an eucaloric, ultra-low oxalate controlled diet for 6 days. The controlled dietary phase involves 2 days of dietary equilibration, followed by 2 x 24-hour urine collections, and on the 5th day a dietary oxalate/sucralose oral load. Following the dietary oxalate/sucralose oral load, subjects will have blood collected every 30 minutes and collect 1-hour urines. Participants will then go on an intensive 14-week Optifast VLCD® Program to induce weight loss. At the end of this Optifast VLCD® Program participants will again perform the low oxalate controlled diet and dietary/sucralose oral load study. A total of 40 adult obese calcium oxalate kidney stone formers (20 male and 20 female) will be enrolled (20 at UAB and 20 at UTSW).

Enrollment

14 patients

Sex

All

Ages

19 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

First time or recurrent calcium oxalate stone formers defined as composition of most recent stone >50% calcium oxalate without uric acid component
Last stone passage or removal greater than 3 months prior to screening
Body Mass Index (BMI) >35 kg/m2
Able to provide consent
Hemoglobin A1C <6.5%
Normal fasting blood CMP: Normal serum Na, K, Cl, CO2, Calcium, Albumin, AST, ALT <2 times upper limit of normal, Glucose <126 mg/dl, eGFR >60 ml/min/1.73 m2.
24-hour urine collection with creatinine within 20% of gender appropriate (mg creat/kg body weight) and consistent between collections (within 20% of each other)
Willing to ingest menus prepared at the University of Alabama and University of Texas Southwestern Clinical Research Units
Willing to consume the Optifast VLCD diet
Willing to ingest menus prepared in Metabolic kitchen. No food allergies or intolerance to any of the foods in study menus. Substitutions for lactose intolerance will be made.
Willing to avoid vigorous exercise during eucaloric, low-oxalate dietary phase
Willing to stop use of weight-loss medications
Willing to stop for 14 days before and during study: medications for stone prevention including diuretics, potassium citrate, allopurinol, febuxostat, and calcium, nutritional, or herbal supplements
Those with controlled hypertension (systolic blood pressure <160 mmHg, diastolic <90 mmHg) will be included.
Those without severe dyslipidemia (LDL <200 mg/dL, HDL >30 mg/dL, and triglycerides <250 mg/dL) will be included. Treated and controlled dyslipidemia is accepted
Smoking/chewing tobacco/vaping will be allowed

Exclusion criteria

Renal colic or past stone surgery in the past 3 months
Estimated Glomerular Filtration Rate (eGFR) less than 60 ml/min/1.73m2
History of type 2 diabetes or screening hgb A1c greater than or equal to 6.5%
Alcohol or drug abuse. Alcohol consumption >12 units per week and/or unwillingness to abstain from alcohol consumption 2 days before and during the study.
Mental/medical condition likely to impede study completion
Current/planned pregnancy or breastfeeding in coming 6 months, unwillingness to use effective method of birth control during the study for individuals of childbearing potential.
Planned vacation in coming 4 months
Febrile illness including flu/common cold/COVID-19 within 21 days of study start
Primary or enteric hyperoxaluria
Gastrointestinal disorder or surgery that impacts oxalate transport
Cirrhosis, pancreatic or biliary disorder, porphyria, gout
Malignancy treated within the past 12 months
Nephrotic syndrome, neurogenic bladder, urinary diversion
History of primary hyperparathyroidism, cystinuria, renal tubular acidosis, sarcoidosis, cystic fibrosis
Uncontrolled hypertension, myocardial infarction in past 6 months, unstable angina, congestive heart failure
Medications: Topiramate, acetazolamide, zonisamide, diuretics, SGLT2-inhibitors, immunosuppressants

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

14 participants in 1 patient group

Controlled Diet and Weight Loss Program

Experimental group

Description: