Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study

Abstract Background Hashimoto's thyroiditis is the most widespread autoimmune illness targeting a specific organ. "Redox homeostasis" is achieved when the production of Reactive Oxygen Species and their elimination are in balance. Advanced glycation end products (AGEs) are formed when...

Full description

Bibliographic Details
Main Authors: Noura Mostafa Mohamed, Azza H. Abd elfatah
Format: Article
Language:English
Published: SpringerOpen 2022-05-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Online Access:https://doi.org/10.1186/s43042-022-00311-y
_version_ 1818532665076219904
author Noura Mostafa Mohamed
Azza H. Abd elfatah
author_facet Noura Mostafa Mohamed
Azza H. Abd elfatah
author_sort Noura Mostafa Mohamed
collection DOAJ
description Abstract Background Hashimoto's thyroiditis is the most widespread autoimmune illness targeting a specific organ. "Redox homeostasis" is achieved when the production of Reactive Oxygen Species and their elimination are in balance. Advanced glycation end products (AGEs) are formed when glucose and/or α-oxaloaldehydes react non-enzymatically with the amino groups of lipids, proteins, and DNA. Nowadays, many studies are concerned with AGEs, the polymorphisms of their receptors, and their association with increased risk of HT. However, few studies investigated the role of receptors of advanced glycation end product (RAGE) SNP in Egyptian females. Objective The goals of this investigation were to ascertain whether oxidative stress plasma malondialdehyde (MDA) and total antioxidant capacity (TAC) were associated with HT, in addition, to assess the association of RAGE polymorphisms (− 374 T > A and the − 429 T > C and Gly82Ser) with HT. Subject and methods. Our case–control study has 80 patients enrolled who have newly been diagnosed with HT and 80 age and sex-matched healthy female controls. Each participant underwent a thorough medical history, physical examination, and laboratory investigations, which included Genotyping of RAGE Gly82Ser, − 374 T > A and − 429 T > C using polymerase chain reaction-restriction fragment length polymorphisms (PCR–RFLP). Results Chi-square revealed a significant association regarding the distribution of RAGE (− 374 T < C) genotypes TT and CC between patients and control (P = 0.04). Non-significant associations regarding the distribution of Gly82Ser genotypes Gly/Gly, Gly/Ser, Ser/Ser were found between patients and control (P = 0.5), and non-significant associations related to − 429 T > C gene polymorphism were revealed. In addition, patients with HT had higher MDA and lower TCA compared with controls. Conclusion The elevated MDA and decreased TAC as an antioxidant may be one of several risk factors associated with the prevalence of HT in individuals with the − 429 T > C RAGE mutation polymorphism that is associated with an increased risk of HT in Egyptian females.
first_indexed 2024-12-11T17:48:29Z
format Article
id doaj.art-ba1d6cbeb19d4f348bd5651f1c3dc3d0
institution Directory Open Access Journal
issn 2090-2441
language English
last_indexed 2024-12-11T17:48:29Z
publishDate 2022-05-01
publisher SpringerOpen
record_format Article
series Egyptian Journal of Medical Human Genetics
spelling doaj.art-ba1d6cbeb19d4f348bd5651f1c3dc3d02022-12-22T00:56:17ZengSpringerOpenEgyptian Journal of Medical Human Genetics2090-24412022-05-012311710.1186/s43042-022-00311-yReceptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control studyNoura Mostafa Mohamed0Azza H. Abd elfatah1Department of Medical Biochemistry, Faculty of Medicine, Zagazig UniversityDepartment of Internal Medicine, Faculty of Medicine, Zagazig UniversityAbstract Background Hashimoto's thyroiditis is the most widespread autoimmune illness targeting a specific organ. "Redox homeostasis" is achieved when the production of Reactive Oxygen Species and their elimination are in balance. Advanced glycation end products (AGEs) are formed when glucose and/or α-oxaloaldehydes react non-enzymatically with the amino groups of lipids, proteins, and DNA. Nowadays, many studies are concerned with AGEs, the polymorphisms of their receptors, and their association with increased risk of HT. However, few studies investigated the role of receptors of advanced glycation end product (RAGE) SNP in Egyptian females. Objective The goals of this investigation were to ascertain whether oxidative stress plasma malondialdehyde (MDA) and total antioxidant capacity (TAC) were associated with HT, in addition, to assess the association of RAGE polymorphisms (− 374 T > A and the − 429 T > C and Gly82Ser) with HT. Subject and methods. Our case–control study has 80 patients enrolled who have newly been diagnosed with HT and 80 age and sex-matched healthy female controls. Each participant underwent a thorough medical history, physical examination, and laboratory investigations, which included Genotyping of RAGE Gly82Ser, − 374 T > A and − 429 T > C using polymerase chain reaction-restriction fragment length polymorphisms (PCR–RFLP). Results Chi-square revealed a significant association regarding the distribution of RAGE (− 374 T < C) genotypes TT and CC between patients and control (P = 0.04). Non-significant associations regarding the distribution of Gly82Ser genotypes Gly/Gly, Gly/Ser, Ser/Ser were found between patients and control (P = 0.5), and non-significant associations related to − 429 T > C gene polymorphism were revealed. In addition, patients with HT had higher MDA and lower TCA compared with controls. Conclusion The elevated MDA and decreased TAC as an antioxidant may be one of several risk factors associated with the prevalence of HT in individuals with the − 429 T > C RAGE mutation polymorphism that is associated with an increased risk of HT in Egyptian females.https://doi.org/10.1186/s43042-022-00311-yHashimoto's thyroiditisAdvanced glycation end product (AGE)Reactive Oxygen Species (ROS)Receptor of Advanced glycation End product (RAGE)
spellingShingle Noura Mostafa Mohamed
Azza H. Abd elfatah
Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
Egyptian Journal of Medical Human Genetics
Hashimoto's thyroiditis
Advanced glycation end product (AGE)
Reactive Oxygen Species (ROS)
Receptor of Advanced glycation End product (RAGE)
title Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
title_full Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
title_fullStr Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
title_full_unstemmed Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
title_short Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto’s thyroiditis in Egyptian female patients: case control study
title_sort receptor of advanced glycation end product rage polymorphism and oxidative status in hashimoto s thyroiditis in egyptian female patients case control study
topic Hashimoto's thyroiditis
Advanced glycation end product (AGE)
Reactive Oxygen Species (ROS)
Receptor of Advanced glycation End product (RAGE)
url https://doi.org/10.1186/s43042-022-00311-y
work_keys_str_mv AT nouramostafamohamed receptorofadvancedglycationendproductragepolymorphismandoxidativestatusinhashimotosthyroiditisinegyptianfemalepatientscasecontrolstudy
AT azzahabdelfatah receptorofadvancedglycationendproductragepolymorphismandoxidativestatusinhashimotosthyroiditisinegyptianfemalepatientscasecontrolstudy