Weiping Du, Zhixi Hu, Li Wang, Miaomiao Li, Dong Zhao, Hui Li, Junsheng Wei, Rui Zhang
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A genotype model, an allele model, a dominant model, and a recessive model were used to assess susceptibility to T2DM.</p><p><strong>Results: </strong>There were significant associations between rs1800977 and T2DM in different genetic models (TT vs. CC, OR = 0.591 [0.446-0.793], p < 0.001; T vs. C, OR = 0.835 [0.735-0.949], p = 0.006; recessive model, OR = 0.583 [0.449-0.756], p < 0.001). There were also significant associations between rs9282541 and T2DM in different genetic models (CT vs. CC, OR = 1.690 [0.807-1.005], p = 0.048; T vs. C, OR = 1.756 [0.694-1.060], p = 0.029; dominant model, OR = 1.735 [0.715-1.034], p = 0.037).</p><p><strong>Conclusion: </strong>Our case-control study showed that the two SNPs rs1800977 and rs9282541 in the ABCA1 gene are significantly associated with susceptibility to T2DM in our Han Chinese population. Study of further mechanisms should be performed before application to clinical therapy.</p>","PeriodicalId":49650,"journal":{"name":"Public Health Genomics","volume":"23 1-2","pages":"20-25"},"PeriodicalIF":1.3000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000505344","citationCount":"6","resultStr":"{\"title\":\"ABCA1 Variants rs1800977 (C69T) and rs9282541 (R230C) Are Associated with Susceptibility to Type 2 Diabetes.\",\"authors\":\"Weiping Du, Zhixi Hu, Li Wang, Miaomiao Li, Dong Zhao, Hui Li, Junsheng Wei, Rui Zhang\",\"doi\":\"10.1159/000505344\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Accumulated evidence suggests that ATP-binding cassette A1 transporter (ABCA1) contributes to secreting insulin in pancreatic β-cells and amyloid beta formation. This study aimed to investigate the association between three single nucleotide polymorphisms (SNPs) of ABCA1 and susceptibility to type 2 diabetes mellitus (T2DM) in a Han Chinese population.</p><p><strong>Methods: </strong>A total of 996 T2DM patients and 1,002 controls were included in the study. Three SNPs in the ABCA1 gene, i.e., rs2230806 (R219K), rs1800977 (C69T), and rs9282541 (R230C), were genotyped by SNaPshot. A genotype model, an allele model, a dominant model, and a recessive model were used to assess susceptibility to T2DM.</p><p><strong>Results: </strong>There were significant associations between rs1800977 and T2DM in different genetic models (TT vs. CC, OR = 0.591 [0.446-0.793], p < 0.001; T vs. C, OR = 0.835 [0.735-0.949], p = 0.006; recessive model, OR = 0.583 [0.449-0.756], p < 0.001). 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引用次数: 6
摘要
目的:越来越多的证据表明,atp结合盒A1转运蛋白(ABCA1)参与胰腺β细胞分泌胰岛素和β淀粉样蛋白的形成。本研究旨在探讨ABCA1基因的三个单核苷酸多态性(snp)与中国汉族人群2型糖尿病(T2DM)易感性之间的关系。方法:选取T2DM患者996例,对照组1002例。ABCA1基因的3个snp分别为rs2230806 (R219K)、rs1800977 (C69T)和rs9282541 (R230C)。采用基因型模型、等位基因模型、显性模型和隐性模型评估2型糖尿病的易感性。结果:rs1800977与T2DM在不同遗传模型中存在显著相关性(TT vs. CC, OR = 0.591 [0.446 ~ 0.793], p < 0.001;T vs. C, OR = 0.835 [0.735-0.949], p = 0.006;隐性模型,OR = 0.583 [0.449-0.756], p < 0.001)。在不同遗传模型中,rs9282541与T2DM也存在显著相关性(CT vs. CC, OR = 1.690 [0.807-1.005], p = 0.048;T vs. C, OR = 1.756 [0.694-1.060], p = 0.029;优势模型,OR = 1.735 [0.715-1.034], p = 0.037)。结论:我们的病例对照研究表明,ABCA1基因的两个snp rs1800977和rs9282541与我们汉族人群的T2DM易感性显著相关。在应用于临床治疗之前,应进行进一步的机制研究。
ABCA1 Variants rs1800977 (C69T) and rs9282541 (R230C) Are Associated with Susceptibility to Type 2 Diabetes.
Objective: Accumulated evidence suggests that ATP-binding cassette A1 transporter (ABCA1) contributes to secreting insulin in pancreatic β-cells and amyloid beta formation. This study aimed to investigate the association between three single nucleotide polymorphisms (SNPs) of ABCA1 and susceptibility to type 2 diabetes mellitus (T2DM) in a Han Chinese population.
Methods: A total of 996 T2DM patients and 1,002 controls were included in the study. Three SNPs in the ABCA1 gene, i.e., rs2230806 (R219K), rs1800977 (C69T), and rs9282541 (R230C), were genotyped by SNaPshot. A genotype model, an allele model, a dominant model, and a recessive model were used to assess susceptibility to T2DM.
Results: There were significant associations between rs1800977 and T2DM in different genetic models (TT vs. CC, OR = 0.591 [0.446-0.793], p < 0.001; T vs. C, OR = 0.835 [0.735-0.949], p = 0.006; recessive model, OR = 0.583 [0.449-0.756], p < 0.001). There were also significant associations between rs9282541 and T2DM in different genetic models (CT vs. CC, OR = 1.690 [0.807-1.005], p = 0.048; T vs. C, OR = 1.756 [0.694-1.060], p = 0.029; dominant model, OR = 1.735 [0.715-1.034], p = 0.037).
Conclusion: Our case-control study showed that the two SNPs rs1800977 and rs9282541 in the ABCA1 gene are significantly associated with susceptibility to T2DM in our Han Chinese population. Study of further mechanisms should be performed before application to clinical therapy.
期刊介绍:
''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.