Association of PON2 and PON3 polymorphism with risk of developing cataract

Purpose: Paraoxonases (PON) are calcium bound enzymes offering protection against oxidative stress by working as endogenous free-radical scavenging molecules. Oxidative stress has been implicated in pathophysiology of many diseases including cataract. Lens opacity is an age related disorder which is...

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Main Authors: Amena Baig, Ata-ur-Rehman, Shamshad Zarina
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-04-01
Series:Saudi Journal of Ophthalmology
Online Access:http://www.sciencedirect.com/science/article/pii/S1319453419300232
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spelling doaj-b08e9625b573472cae9ee9c713450c792021-04-02T20:59:47ZengWolters Kluwer Medknow PublicationsSaudi Journal of Ophthalmology1319-45342019-04-01332153158Association of PON2 and PON3 polymorphism with risk of developing cataractAmena Baig0 Ata-ur-Rehman1Shamshad Zarina2National Center for Proteomics, University of Karachi, Karachi, PakistanDepartment of Ophthalmology, Liaquat National Hospital, Karachi, PakistanNational Center for Proteomics, University of Karachi, Karachi, Pakistan; Corresponding author at: National Center for Proteomics, University of Karachi, Karachi 75270, Pakistan. Fax: +92 021 34650726.Purpose: Paraoxonases (PON) are calcium bound enzymes offering protection against oxidative stress by working as endogenous free-radical scavenging molecules. Oxidative stress has been implicated in pathophysiology of many diseases including cataract. Lens opacity is an age related disorder which is a principal cause of blindness in Pakistani population. Relationship of PON2 and PON3 polymorphism with genetic predisposition for incidence of cataract has not been investigated till date. Objective of the current study was to explore possible association between PON2 and PON3 polymorphism with incidence of cataract in local population. Methods: Our study design comprised of fifty-one cataractous and fifty-nine healthy individuals. Identification of single nucleotide polymorphism (SNP) at positions (C311S and G148A) for PON2 and C133A for PON3 was conducted using restriction fragment length polymorphism (RFLP). Results: Statistical analysis revealed significant association of PON2 G148 allele with incidence of cataract. GG allele was found to be higher in cataract patients as compared to control (p < 0.001) suggesting distribution of PON2 G148A genotype and allele frequency is linked with cataractogenesis. There was no noticeable association between PON2 C311S and PON3 C133A. Significant difference was observed in distribution of 311CS/148A combined genotype with highest frequency in control individuals (88.89%), while 311S/148G combined genotypes showed the highest frequencies among the cataract patients (71.42%). Conclusion: Our data suggests mutation at G148A might be related with incidence of cataract in studied population. Keywords: PON2, PON3, Polymorphism, Cataracthttp://www.sciencedirect.com/science/article/pii/S1319453419300232
collection DOAJ
language English
format Article
sources DOAJ
author Amena Baig
Ata-ur-Rehman
Shamshad Zarina
spellingShingle Amena Baig
Ata-ur-Rehman
Shamshad Zarina
Association of PON2 and PON3 polymorphism with risk of developing cataract
Saudi Journal of Ophthalmology
author_facet Amena Baig
Ata-ur-Rehman
Shamshad Zarina
author_sort Amena Baig
title Association of PON2 and PON3 polymorphism with risk of developing cataract
title_short Association of PON2 and PON3 polymorphism with risk of developing cataract
title_full Association of PON2 and PON3 polymorphism with risk of developing cataract
title_fullStr Association of PON2 and PON3 polymorphism with risk of developing cataract
title_full_unstemmed Association of PON2 and PON3 polymorphism with risk of developing cataract
title_sort association of pon2 and pon3 polymorphism with risk of developing cataract
publisher Wolters Kluwer Medknow Publications
series Saudi Journal of Ophthalmology
issn 1319-4534
publishDate 2019-04-01
description Purpose: Paraoxonases (PON) are calcium bound enzymes offering protection against oxidative stress by working as endogenous free-radical scavenging molecules. Oxidative stress has been implicated in pathophysiology of many diseases including cataract. Lens opacity is an age related disorder which is a principal cause of blindness in Pakistani population. Relationship of PON2 and PON3 polymorphism with genetic predisposition for incidence of cataract has not been investigated till date. Objective of the current study was to explore possible association between PON2 and PON3 polymorphism with incidence of cataract in local population. Methods: Our study design comprised of fifty-one cataractous and fifty-nine healthy individuals. Identification of single nucleotide polymorphism (SNP) at positions (C311S and G148A) for PON2 and C133A for PON3 was conducted using restriction fragment length polymorphism (RFLP). Results: Statistical analysis revealed significant association of PON2 G148 allele with incidence of cataract. GG allele was found to be higher in cataract patients as compared to control (p < 0.001) suggesting distribution of PON2 G148A genotype and allele frequency is linked with cataractogenesis. There was no noticeable association between PON2 C311S and PON3 C133A. Significant difference was observed in distribution of 311CS/148A combined genotype with highest frequency in control individuals (88.89%), while 311S/148G combined genotypes showed the highest frequencies among the cataract patients (71.42%). Conclusion: Our data suggests mutation at G148A might be related with incidence of cataract in studied population. Keywords: PON2, PON3, Polymorphism, Cataract
url http://www.sciencedirect.com/science/article/pii/S1319453419300232
work_keys_str_mv AT amenabaig associationofpon2andpon3polymorphismwithriskofdevelopingcataract
AT ataurrehman associationofpon2andpon3polymorphismwithriskofdevelopingcataract
AT shamshadzarina associationofpon2andpon3polymorphismwithriskofdevelopingcataract
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