Evidence map›Paper›PMID 42832476›Full record

ArticlePloS one2026

Impact of GST and TP53 gene polymorphisms on susceptibility to end stage renal disease: A case-control analysis.

Rashid Mehmood, Pei-Chun Chiang, Madiha Rasool, Muhammad Asif, Abdul Ghafar, Mustansar Khalid, Saba Razaq, Muhammad Khaleeq Alam, Iram Fatima, Iqra Jabeen and 3 more

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Rashid MehmoodInstitute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Pei-Chun ChiangDivision of Nephrology, Department of Internal Medicine, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan.
Madiha RasoolInstitute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Muhammad AsifDepartment of Nephrology, Allama Iqbal Teaching Hospital, Dera Ghazi Khan, Pakistan.
Abdul GhafarInstitute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Mustansar KhalidInstitute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.
Saba RazaqDepartment of Zoology, Ghazi University, Dera Ghazi Khan, Pakistan.
Muhammad Khaleeq AlamDepartment of Zoology, Emerson University Multan, Multan, Pakistan.
Iram FatimaDepartment of Zoology, Emerson University Multan, Multan, Pakistan.
Iqra JabeenDepartment of Zoology, Emerson University Multan, Multan, Pakistan.
Sehrish AshrafDepartment of Zoology, Ghazi University, Dera Ghazi Khan, Pakistan.
Furhan IqbalInstitute of Zoology, Bahauddin Zakariya University, Multan, Pakistan.ORCID https://orcid.org/0000-0003-4996-0152
Chien-Chin ChenDepartment of Pathology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan.ORCID https://orcid.org/0000-0001-9599-0884

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEnd-stage renal disease (ESRD) is a major global non-communicable condition associated with substantial morbidity and mortality. The current investigation aimed to report the association of GSTM1, GSTT1 genotypes and single nucleotide polymorphisms (SNPs) in GSTP1 (rs1695) and TP53 (rs1042522) genes with ESRD.

methodsClinically confirmed ESRD patients (n = 305) and healthy controls (n = 305) were enrolled from District Multan in Punjab, Pakistan, during 30-10-2023 till 28-02-2024, following their informed verbal consent. Multiplex and T-ARMS PCR based approaches were used to document the genotype at GSTs and SNPs of targeted genes and their associations with ESRD were analyzed individually as well as in combination.

resultsA significant association of absence of GSTM1, presence of GSTT1, presence of "G" polymorphic allele at rs1695 in GSTP1, and the presence of "C" polymorphic allele at rs1042522 in TP53 gene was observed with ESRD during the present study. Participants having age ranging between 26-40 years, males and smokers suffered more from ESRD.

conclusionGenetic variations in the studied GSTs, along with rs1695 in GSTP1 and rs1042522 in the TP53 gene, may influence the progression of ESRD.

Indexed as

Genetic Predisposition to DiseaseGlutathione S-Transferase piGlutathione TransferaseKidney Failure, ChronicPolymorphism, Single NucleotideTumor Suppressor Protein p53AdultAllelesCase-Control StudiesFemaleGenotypeHumansMaleMiddle AgedPakistanGlutathione S-Transferase piglutathione S-transferase T1Glutathione TransferaseGSTP1 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID42832476
PMCPMC13637908

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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.