Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study
NCT06211842 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47
Last updated 2024-01-19
Summary
Many things, like not drinking enough fluids, contribute to making kidney stones and there is also a genetic tendency. We looked into this in 1998-2000 in 14 families with several stone-formers. In four of these the risk for stones was passed down through one line of the family. We have now had a close look at the DNA of 47 members of these four families using a very sensitive technique called exome sequencing. We wanted to see if these individuals had inherited any rare changes (variations) in their DNA which would add to their risk of making stones. We found 11 variations which might be important. Surprisingly, these were not in genes which have been regarded as the main causes of stones. Most of them are unfamiliar to clinicians and scientists world-wide. Experts on the genes gave us helpful advice about the likely significance of the variations. Researchers in Paris, Lille and the UK (Oxford, Cambridge and Sheffield) did analyses to help to decide this. An exciting finding was that one of the variants, not previously identified in stone formers, had just been found in a large Italian family with stones. This small study has shown that: variations in a wide range of genes may contribute to stone formation; these occur in genes that we have not come across before; further laboratory studies are essential to investigate potentially important variants; sharing findings between laboratories doing similar studies world-wide is crucial.
Conditions
- Urolithiasis
Sponsors & Collaborators
-
University of Southampton
collaborator OTHER -
University Hospital Southampton NHS Foundation Trust
lead OTHER
Principal Investigators
-
Paul Cook, MRCPPhDFRCPa · University Hospital Southampton NHS Foundation Trust
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-10-12
- Primary Completion
- 2022-05-25
- Completion
- 2023-11-08
More Related Trials
-
Search for New Genetic Causes of Hypercalcemia by Massively Parallel Sequencing of a Genes Panel
NCT02908542 ·Status: COMPLETED
-
Genetic Variants Associated With the Risk of Gall Stones and Cirrhosis.
NCT06679738 ·Status: NOT_YET_RECRUITING
-
Genetic Causes of FSGS, Nephrotic Syndrome, or Kidney Failure
NCT02194582 ·Status: ACTIVE_NOT_RECRUITING
-
APOL1 Genetic Testing in African Americans
NCT05656261 ·Status: RECRUITING
-
Mapping of End Stage Renal Disease Genetic Susceptibility in African Americans by Admixture Linkage Disequilibrium
NCT00559767 ·Status: COMPLETED
-
Genetics in the Progression of Nephropathies
NCT06416761 ·Status: RECRUITING
-
The Genetics of Kidneys in Diabetes (GoKinD) Study
NCT00024921 ·Status: COMPLETED
-
Genetic Analysis of Familial Brain Aneurysms
NCT00011856 ·Status: COMPLETED
-
Analyzing Genes That May Increase the Risk of Developing High Blood Pressure
NCT00549991 ·Status: COMPLETED
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Hereditary Tubulointerstitial Nephritis
NCT01312727 ·Status: COMPLETED ·Phase: NA
-
Suitability of Some Data Quality Controls Thresholds for Genetic Association Studies of Admixed Population
NCT02770001 ·Status: WITHDRAWN
-
Primary Hyperoxaluria Mutation Genotyping
NCT00589225 ·Status: COMPLETED
-
Uncertain Genetic Test Results for Lynch Syndrome
NCT01646112 ·Status: COMPLETED
-
Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
NCT00359515 ·Status: COMPLETED
-
Genetic Risk: Whether, When, and How to Tell Adolescents
NCT03421327 ·Status: COMPLETED
-
Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm
NCT01801488 ·Status: TERMINATED
-
Nephronophthisis : Clinical and Genetic Study
NCT01022957 ·Status: COMPLETED ·Phase: NA
-
Pain Predict Genetics
NCT02383342 ·Status: RECRUITING
-
Von Hippel-Lindau Disease Genetic Epidemiology Study
NCT00001803 ·Status: TERMINATED
-
Genetic Analysis of Hereditary Disorders of Hearing and Balance
NCT00023049 ·Status: COMPLETED
-
Genetic Markers for Focal Segmental Glomerulosclerosis
NCT00001393 ·Status: COMPLETED
-
Genetic Studies of Non-Alcoholic Fatty Liver Disease
NCT01629095 ·Status: TERMINATED
-
Genetic Analysis of Hereditary Prostate Cancer
NCT00001469 ·Status: COMPLETED
-
Genetic Analysis of Familial Melanoma
NCT00339404 ·Status: COMPLETED