{"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 , Sabrina Zidi , Perizat Kanabekova , Leila Mouellhi , Wassim Y. Almawi , 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 (<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 , Sabrina Zidi , Perizat Kanabekova , Leila Mouellhi , Wassim Y. Almawi , 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 (<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}
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.
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.