CRP基因变异与幽门螺杆菌相关慢性胃炎风险改变的关系:突尼斯的一项病例对照研究

IF 2.3 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Molecular and Cellular Probes Pub Date : 2022-12-01 DOI:10.1016/j.mcp.2022.101864
Mouna Stayoussef , Sabrina Zidi , Perizat Kanabekova , Leila Mouellhi , Wassim Y. Almawi , Besma Yaacoubi-Loueslati
{"title":"CRP基因变异与幽门螺杆菌相关慢性胃炎风险改变的关系:突尼斯的一项病例对照研究","authors":"Mouna Stayoussef ,&nbsp;Sabrina Zidi ,&nbsp;Perizat Kanabekova ,&nbsp;Leila Mouellhi ,&nbsp;Wassim Y. Almawi ,&nbsp;Besma Yaacoubi-Loueslati","doi":"10.1016/j.mcp.2022.101864","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>We investigated the association between <span><em>CRP</em></span><span> variants and chronic gastritis in </span><span><em>H. </em><em>pylori</em></span>-infected patients at the allele, genotype, and haplotype levels. This was also assessed according to serum hs-CRP levels.</p></div><div><h3>Methods</h3><p>Study subjects consisted of 77 <em>H. pylori</em>-infected patients and 96 <em>H. pylori</em>-negative controls. Genotyping of the <em>CRP</em> rs1572970, rs876537, rs2794520, rs2808630, rs1130864, rs1417938, rs7553007, and rs4285692 variants were analyzed by real-time PCR.</p></div><div><h3>Results</h3><p><span>Significantly higher MAF and increased risk of chronic gastritis were associated with rs1130864, rs1417938, and rs7553007, which persisted after controlling for key covariates. Significant differences in the genotype distribution of rs1130864, rs1417938, and rs7553007 were also seen between </span><em>H</em>. <em>pylori</em>-infected patients and healthy controls. Increased risk of <em>H. pylori</em>-associated chronic gastritis was associated with carriage of rs1130864 C/T, and more with T/T genotype carriers, as well as with rs1417938 T/A and A/A genotype carriers. Functionally, the distribution of rs1130864 and rs1417938 genotypes were significantly different between <em>H</em>. pylori-infected patients and controls in the low hs-CRP (&lt;6 mg/L) group. CRP haplotype analysis identified Block 1 (rs1572970, rs876537, rs2794520), and Block 2 (rs2808630, rs1130864, rs1417938) associated with <em>H. pylori</em> infection. Haplotypes ACC (Block 1) and TTA and TTT (Block 2) were positively associated with <em>H. pylori</em>-associated chronic gastritis with low hs-CRP levels.</p></div><div><h3>Conclusion</h3><p><span>Altered serum levels of hs-CRP, stemming in part from the presence of specific genetic variants in </span><em>CRP</em> gene, modulate the risk of <em>H. pylori</em> infection.</p></div>","PeriodicalId":49799,"journal":{"name":"Molecular and Cellular Probes","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Relation of CRP gene variants to altered risk of Helicobacter pylori - associated chronic gastritis: A case-control study in Tunisia\",\"authors\":\"Mouna Stayoussef ,&nbsp;Sabrina Zidi ,&nbsp;Perizat Kanabekova ,&nbsp;Leila Mouellhi ,&nbsp;Wassim Y. Almawi ,&nbsp;Besma Yaacoubi-Loueslati\",\"doi\":\"10.1016/j.mcp.2022.101864\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>We investigated the association between <span><em>CRP</em></span><span> variants and chronic gastritis in </span><span><em>H. </em><em>pylori</em></span>-infected patients at the allele, genotype, and haplotype levels. This was also assessed according to serum hs-CRP levels.</p></div><div><h3>Methods</h3><p>Study subjects consisted of 77 <em>H. pylori</em>-infected patients and 96 <em>H. pylori</em>-negative controls. Genotyping of the <em>CRP</em> rs1572970, rs876537, rs2794520, rs2808630, rs1130864, rs1417938, rs7553007, and rs4285692 variants were analyzed by real-time PCR.</p></div><div><h3>Results</h3><p><span>Significantly higher MAF and increased risk of chronic gastritis were associated with rs1130864, rs1417938, and rs7553007, which persisted after controlling for key covariates. Significant differences in the genotype distribution of rs1130864, rs1417938, and rs7553007 were also seen between </span><em>H</em>. <em>pylori</em>-infected patients and healthy controls. Increased risk of <em>H. pylori</em>-associated chronic gastritis was associated with carriage of rs1130864 C/T, and more with T/T genotype carriers, as well as with rs1417938 T/A and A/A genotype carriers. Functionally, the distribution of rs1130864 and rs1417938 genotypes were significantly different between <em>H</em>. pylori-infected patients and controls in the low hs-CRP (&lt;6 mg/L) group. CRP haplotype analysis identified Block 1 (rs1572970, rs876537, rs2794520), and Block 2 (rs2808630, rs1130864, rs1417938) associated with <em>H. pylori</em> infection. Haplotypes ACC (Block 1) and TTA and TTT (Block 2) were positively associated with <em>H. pylori</em>-associated chronic gastritis with low hs-CRP levels.</p></div><div><h3>Conclusion</h3><p><span>Altered serum levels of hs-CRP, stemming in part from the presence of specific genetic variants in </span><em>CRP</em> gene, modulate the risk of <em>H. pylori</em> infection.</p></div>\",\"PeriodicalId\":49799,\"journal\":{\"name\":\"Molecular and Cellular Probes\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular and Cellular Probes\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0890850822000755\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and Cellular Probes","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0890850822000755","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

背景:我们从等位基因、基因型和单倍型水平研究了c反应蛋白变异与幽门螺杆菌感染患者慢性胃炎的关系。这也根据血清hs-CRP水平进行评估。方法研究对象为77例幽门螺杆菌感染患者和96例幽门螺杆菌阴性对照。采用实时荧光定量PCR对CRP rs1572970、rs876537、rs2794520、rs2808630、rs1130864、rs1417938、rs7553007和rs4285692变异进行基因分型分析。结果较高的MAF和增加的慢性胃炎风险与rs1130864、rs1417938和rs7553007相关,并在控制关键协变量后持续存在。rs1130864、rs1417938和rs7553007基因型分布在幽门螺杆菌感染患者和健康对照组之间也存在显著差异。幽门螺杆菌相关慢性胃炎的风险增加与携带rs1130864 C/T相关,与T/T基因型携带者、rs1417938 T/A和A/A基因型携带者相关。功能上,低hs-CRP (<6 mg/L)组幽门螺杆菌感染患者与对照组rs1130864和rs1417938基因型分布有显著差异。CRP单倍型分析发现Block 1 (rs1572970、rs876537、rs2794520)和Block 2 (rs2808630、rs1130864、rs1417938)与幽门螺杆菌感染相关。单倍型ACC (Block 1)、TTA和TTT (Block 2)与幽门螺杆菌相关性慢性胃炎伴hs-CRP水平低呈正相关。结论血清hs-CRP水平的改变可调节幽门螺杆菌感染的风险,其部分原因是CRP基因存在特定的遗传变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Relation of CRP gene variants to altered risk of Helicobacter pylori - associated chronic gastritis: A case-control study in Tunisia

Background

We investigated the association between CRP variants and chronic gastritis in H. pylori-infected patients at the allele, genotype, and haplotype levels. This was also assessed according to serum hs-CRP levels.

Methods

Study subjects consisted of 77 H. pylori-infected patients and 96 H. pylori-negative controls. Genotyping of the CRP rs1572970, rs876537, rs2794520, rs2808630, rs1130864, rs1417938, rs7553007, and rs4285692 variants were analyzed by real-time PCR.

Results

Significantly higher MAF and increased risk of chronic gastritis were associated with rs1130864, rs1417938, and rs7553007, which persisted after controlling for key covariates. Significant differences in the genotype distribution of rs1130864, rs1417938, and rs7553007 were also seen between H. pylori-infected patients and healthy controls. Increased risk of H. pylori-associated chronic gastritis was associated with carriage of rs1130864 C/T, and more with T/T genotype carriers, as well as with rs1417938 T/A and A/A genotype carriers. Functionally, the distribution of rs1130864 and rs1417938 genotypes were significantly different between H. pylori-infected patients and controls in the low hs-CRP (<6 mg/L) group. CRP haplotype analysis identified Block 1 (rs1572970, rs876537, rs2794520), and Block 2 (rs2808630, rs1130864, rs1417938) associated with H. pylori infection. Haplotypes ACC (Block 1) and TTA and TTT (Block 2) were positively associated with H. pylori-associated chronic gastritis with low hs-CRP levels.

Conclusion

Altered serum levels of hs-CRP, stemming in part from the presence of specific genetic variants in CRP gene, modulate the risk of H. pylori infection.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular and Cellular Probes
Molecular and Cellular Probes 生物-生化研究方法
CiteScore
6.80
自引率
0.00%
发文量
52
审稿时长
16 days
期刊介绍: MCP - Advancing biology through–omics and bioinformatic technologies wants to capture outcomes from the current revolution in molecular technologies and sciences. The journal has broadened its scope and embraces any high quality research papers, reviews and opinions in areas including, but not limited to, molecular biology, cell biology, biochemistry, immunology, physiology, epidemiology, ecology, virology, microbiology, parasitology, genetics, evolutionary biology, genomics (including metagenomics), bioinformatics, proteomics, metabolomics, glycomics, and lipidomics. Submissions with a technology-driven focus on understanding normal biological or disease processes as well as conceptual advances and paradigm shifts are particularly encouraged. The Editors welcome fundamental or applied research areas; pre-submission enquiries about advanced draft manuscripts are welcomed. Top quality research and manuscripts will be fast-tracked.
期刊最新文献
The activation of SYNJ2/GRB2 axis accelerates the malignant metastasis and angiogenesis of gastric cancer cells. First trimester prediction models for small-for- gestational age and fetal growth restricted fetuses without the presence of preeclampsia Prenatal and postnatal genetic testing toward personalized care: The non-invasive perinatal testing miR-203 suppresses pancreatic cancer cell proliferation and migration by modulating DUSP5 expression Identification of stemness index-related long noncoding RNA SNHG12 in human bladder cancer based on WGCNA
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1