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論文
タイトル
タイトル(英)
rs12411980 single-nucleotide polymorphism related to <i>PRTFDC1</i> expression is significantly associated with phantom tooth pain
参照URL
https://researchmap.jp/kazutakaikeda/published_papers/47319480
著者
著者(英)
Jun Araida,Seii Ohka,Moe Soeda,Daisuke Nishizawa,Junko Hasegawa,Kyoko Nakayama,Yuko Ebata,Yasukazu Ogai,Ken-ichi Fukuda,Kazutaka Ikeda
担当区分
概要
概要(英)
Phantom tooth pain (PTP) is one type of non-odontogenic neuropathic toothache, which rarely occurs after appropriate pulpectomy or tooth extraction. The cause of PTP is unknown. We investigated pain-related genetic factors that are associated with PTP. Four pain-associated genes, including G protein-coupled receptor 158 ( GPR158) and phosphoribosyl transferase domain containing 1 ( PRTFDC1), are adjacent to each other on the human genome. Some of these four genes or their genomic region may be related to PTP. We statistically analyzed associations between single-nucleotide polymorphisms (SNPs) in the genomic region and PTP in patients with PTP (PTP group), other orofacial pain (OFP group), and healthy control subjects. We then performed a database search of expression quantitative trait loci (eQTLs). For the seven SNPs that were significantly associated with PTP even after Bonferroni correction, we focused on the rs12411980 tag SNP ( P = 9.42 × 10<sup>-4</sup>). Statistical analyses of the PTP group and healthy subject groups (group labels: NOC and TD) revealed that the rate of the GG genotype of the rs12411980 SNP was significantly higher in the PTP group than in the healthy subject groups (PTP group vs. NOC group: P = 2.92 × 10<sup>-4</sup>, PTP group vs. TD group: P = 5.46 × 10<sup>-4</sup>; percentage of GG: 30% in PTP group, 12% in NOC group, 11% in TD group). These results suggest that the GG genotype of the rs12411980 SNP is more susceptible to PTP. The rs2765697 SNP that is in strong linkage disequilibrium with the rs12411980 SNP is an eQTL that is associated with higher PRTFDC1 expression in the minor allele homozygotes in the healthy subject groups of the rs2765697 SNP. Thus, PRTFDC1 expression similarly increases in the minor allele homozygotes (GG genotype) in the healthy subject groups of the rs12411980 SNP, which would lead to greater susceptibility to PTP.
出版者・発行元
出版者・発行元(英)
SAGE Publications
誌名
誌名(英)
Molecular Pain
開始ページ
終了ページ
出版年月
2024年8月2日
査読の有無
招待の有無
掲載種別
研究論文(学術雑誌)
ISSN
1744-8069
DOI URL
https://doi.org/10.1177/17448069241272215
共同研究・競争的資金等の研究課題
研究者
池田 和隆 (イケダ カズタカ) , 西澤 大輔 (ニシザワ ダイスケ) , 大岡 静衣 (オオオカ セイイ)