Evidence map›Paper›PMID 38214752›Full record

ArticleWorld journal of urology2024

Glycolate oxidase-1 gene variants influence the risk of hyperoxaluria and renal stone development.

Yash P Patel, Sandip B Patel, Priyal Patel, Aditya Parikh, Shailesh Soni, Ratika Srivastava, Chintal Raval, Arvind P Ganpule, Mahesh R Desai, Samir G Patel and 1 more

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Article in World journal of urology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Yash P PatelDepartment of Clinical Pharmacy, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Anand, Gujarat, 388421, India.
Sandip B PatelDepartment of Pharmacology, L.M. College of Pharmacy, Ahmedabad, Gujarat, 380009, India.
Priyal PatelDepartment of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Anand, Gujarat, 388421, India.
Aditya ParikhDepartment of Urology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, 387001, India.
Shailesh SoniDepartment of Pathology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, 387001, India.
Ratika SrivastavaSchool of Life Sciences, Department of Biotechnology, Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow, UP, India.
Chintal RavalDepartment of Information Technology Devang Patel Institute of Advance Technology and Research Charotar, University of Science and Technology, Changa, Anand, Gujarat, 388421, India.
Arvind P GanpuleDepartment of Urology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, 387001, India.
Mahesh R DesaiDepartment of Urology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, 387001, India.
Samir G PatelDepartment of Pharmaceutical Chemistry and Analysis, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Anand, Gujarat, 388421, India. samirpatel.ph@charusat.ac.in.
Sachchida Nand PandeyDepartment of Pathology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, 387001, India. sachidanandpandey@gmail.com.
Muljibhai Patel Urological Hospital · INCharotar University of Science and Technology · INB.J. Medical College · INBabasaheb Bhimrao Ambedkar University · IN

Funding

Charotar University of Science and Technology CHARUSATSEEDRESEARCHGRANT/RPCP/SAPAMuljibhai Patel Urological Hospital Urology Research Grant
6 · The paper itself

Abstract

purposeOxalate is an excellent calcium ion attractor with great abundance in the human body, and the liver is the major source of oxalate. The Glycolate oxidase-1 (GOX1) gene is solely responsible for the glycolate and glyoxylate metabolism and produces oxalate. This study has been designed to comprehend the association of genetic variants of the GOX1 gene with the risk of hyperoxaluria and renal stone disease in the Indian population.

methodThe present study is a candidate gene approach prospective case-control study carried out on 300 participants (150 cases and 150 controls) at Muljibhai Patel Urological Hospital, Gujarat, India. Biochemical parameters, including serum levels of calcium, creatinine, parathyroid hormone, and 24-h urine metabolites, were performed. The genotyping of GOX1 gene variants rs6086287, rs2235250, rs2255183, and rs2294303 was performed using a customized TaqMan assay probe by RT-PCR.

resultParathyroid hormone, serum creatinine, and urine metabolites were significantly elevated in nephrolithiasis compared to healthy individuals. All mutated homozygous genotypes GG (rs6086287), TT (rs2235250), GG (rs2255183), and CC (rs2294303) were significantly associated with a high risk of renal stone disease. Individuals diagnosed with hyperoxaluria and carrying TG (rs6086287), AG (rs2255183), and TT (rs2294303) genotypes have a significantly high risk of renal stone disease. Moreover, haplotype analysis and correlation analysis also confirmed the strong association between genetic variants and nephrolithiasis.

conclusionGenetic variants of the GOX1 genes were associated with renal stone disease. In the presence of risk genotype and hyperoxaluria, the susceptibility to develop renal stone disease risk gets modulated.

Indexed as

Alcohol OxidoreductasesHyperoxaluriaKidney CalculiCalciumCase-Control StudiesCreatinineHumansOxalatesParathyroid HormoneAlcohol OxidoreductasesCalciumCreatinineglycollate oxidaseOxalatesParathyroid HormoneGenetic variantsGOX1geneHaplotypeHyperoxaluriaRenal stone disease

Identifiers

PMID38214752
OpenAlexW4390789375

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.