Association between PTCH1 and RAD54B Single-Nucleotide Polymorphisms and Non-syndromic Orofacial Clefts in the Northeast Population of Iran.

Q3 Biochemistry, Genetics and Molecular Biology
Reza Morvaridi Farimani, Mohsen Azimi-Nezhad, Hamid Reza KhorramKhorshid, Asghar Ebadifar, Saba Tohidkhah, Zahra Jafarian, Koorosh Kamali, Zeinab Nazari, Reza Ebrahimzadeh-Vesal
{"title":"Association between <i>PTCH1</i> and <i>RAD54B</i> Single-Nucleotide Polymorphisms and Non-syndromic Orofacial Clefts in the Northeast Population of Iran.","authors":"Reza Morvaridi Farimani,&nbsp;Mohsen Azimi-Nezhad,&nbsp;Hamid Reza KhorramKhorshid,&nbsp;Asghar Ebadifar,&nbsp;Saba Tohidkhah,&nbsp;Zahra Jafarian,&nbsp;Koorosh Kamali,&nbsp;Zeinab Nazari,&nbsp;Reza Ebrahimzadeh-Vesal","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Non-Syndromic Cleft Lip with or without cleft Palate (NSCL/P) is a common developmental disorder of the head and neck with a multifactorial etiology. The current study aimed to evaluate the potential association of <i>PTCH1</i> (rs10512248) and <i>RAD54B</i> (rs12681366) polymorphisms with NSCL/P in the Northeast Iranian population.</p><p><strong>Methods: </strong>In the present study, blood samples were taken from 122 subjects with NSCL/P and 161 healthy controls. Polymerase Chain Reaction (PCR) followed by Restriction Fragment Length Polymorphism (RFLP) were used to conduct genotyping of single-nucleotide polymorphisms.</p><p><strong>Results: </strong>Although differences were observed between cases and controls in rs10512248 and rs12681366, our data did not support a significant association of these polymorphisms with NSCL/P in our population.</p><p><strong>Conclusion: </strong>Our findings suggest that polymorphisms of rs10512248 and rs12681366 may not be potential risk factors for NSCL/P in the Northeast Iranian population due to the multifactorial and multiethnicity characteristics of some genes.</p>","PeriodicalId":8669,"journal":{"name":"Avicenna journal of medical biotechnology","volume":"14 4","pages":"310-316"},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/50/bf/AJMB-14-310.PMC9706251.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Avicenna journal of medical biotechnology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Non-Syndromic Cleft Lip with or without cleft Palate (NSCL/P) is a common developmental disorder of the head and neck with a multifactorial etiology. The current study aimed to evaluate the potential association of PTCH1 (rs10512248) and RAD54B (rs12681366) polymorphisms with NSCL/P in the Northeast Iranian population.

Methods: In the present study, blood samples were taken from 122 subjects with NSCL/P and 161 healthy controls. Polymerase Chain Reaction (PCR) followed by Restriction Fragment Length Polymorphism (RFLP) were used to conduct genotyping of single-nucleotide polymorphisms.

Results: Although differences were observed between cases and controls in rs10512248 and rs12681366, our data did not support a significant association of these polymorphisms with NSCL/P in our population.

Conclusion: Our findings suggest that polymorphisms of rs10512248 and rs12681366 may not be potential risk factors for NSCL/P in the Northeast Iranian population due to the multifactorial and multiethnicity characteristics of some genes.

Abstract Image

Abstract Image

伊朗东北部人群PTCH1和RAD54B单核苷酸多态性与非综合征性口面裂的关系
背景:非综合征性唇裂伴或不伴腭裂(NSCL/P)是一种常见的头颈部发育障碍,具有多因素病因。本研究旨在评估伊朗东北部人群中PTCH1 (rs10512248)和RAD54B (rs12681366)多态性与NSCL/P的潜在关联。方法:本研究采集了122例非急性淋巴细胞白血病患者和161例健康对照者的血液样本。采用聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)对单核苷酸多态性进行基因分型。结果:虽然rs10512248和rs12681366在病例和对照组之间存在差异,但我们的数据并不支持这些多态性与我们人群中NSCL/P的显著关联。结论:rs10512248和rs12681366的多态性可能不是伊朗东北部人群NSCL/P的潜在危险因素,因为一些基因具有多因素和多民族特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Avicenna journal of medical biotechnology
Avicenna journal of medical biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
2.90
自引率
0.00%
发文量
43
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信