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[基因名称1]、[基因名称2]和[基因名称3]与龋齿的遗传关联。 (你提供的原文中具体基因名称缺失,我按格式补充了内容以便理解,实际翻译时需根据准确基因名替换)

Genetic Association of , , and with Dental Caries.

作者信息

Lewis D D, Shaffer J R, Feingold E, Cooper M, Vanyukov M M, Maher B S, Slayton R L, Willing M C, Reis S E, McNeil D W, Crout R J, Weyant R J, Levy S M, Vieira A R, Marazita M L

机构信息

Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Int J Dent. 2017;2017:8465125. doi: 10.1155/2017/8465125. Epub 2017 Feb 28.

Abstract

Matrix metalloproteinases (MMPs), which degrade extracellular proteins as part of a variety of physiological processes, and their inhibitors have been implicated in the dental caries process. Here we investigated 28 genetic variants spanning the , , and genes to detect association with dental caries experience in 13 age- and race-stratified ( = 3,587) samples from 6 parent studies. Analyses were performed separately for each sample, and results were combined across samples by meta-analysis. Two SNPs (rs2046315 and rs10429371) upstream of were significantly associated with caries in an individual sample of white adults and via meta-analysis across 8 adult samples after gene-wise adjustment for multiple comparisons. Noteworthy is SNP rs2046315 ( = 8.14 × 10) association with caries in white adults. This SNP was originally nominated in a genome-wide-association study (GWAS) of dental caries in a sample of white adults and yielded associations in a subsequent GWAS of surface level caries in white adults as well. Therefore, in our study, we were able to recapture the association between rs2046315 and dental caries in white adults. Although we did not strengthen evidence that , , and influence caries risk, is still a likely candidate gene to pursue.

摘要

基质金属蛋白酶(MMPs)作为多种生理过程的一部分可降解细胞外蛋白质,其抑制剂与龋齿形成过程有关。在此,我们研究了跨越 、 和 基因的28个基因变异,以检测来自6项亲本研究的13个按年龄和种族分层( = 3587)的样本中与龋齿经历的关联。对每个样本分别进行分析,并通过荟萃分析将各样本的结果合并。 在白人成年人的单个样本中,以及在对多个比较进行基因水平调整后,通过对8个成人样本进行荟萃分析, 上游的两个单核苷酸多态性(SNP,rs2046315和rs10429371)与龋齿显著相关。值得注意的是,SNP rs2046315( = 8.14 × 10)与白人成年人的龋齿有关。该SNP最初是在白人成年人样本的龋齿全基因组关联研究(GWAS)中被提名的,并且在随后的白人成年人表面水平龋齿GWAS中也产生了关联。因此,在我们的研究中,我们能够重现rs2046315与白人成年人龋齿之间的关联。尽管我们没有强化 、 和 影响龋齿风险的证据,但 仍然是一个值得研究的潜在候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d56c/5350286/7f528464ee84/IJD2017-8465125.001.jpg

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