Aoki Yoshinori, Nishizawa Daisuke, Yoshida Kaori, Hasegawa Junko, Kasai Shinya, Takahashi Kaori, Koukita Yoshihiko, Ichinohe Tatsuya, Hayashida Masakazu, Fukuda Ken-Ichi, Ikeda Kazutaka
Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Department of Dental Anesthesiology, Tokyo Dental College, Tokyo, Japan.
Neuropsychopharmacol Rep. 2018 Jun;38(2):86-91. doi: 10.1002/npr2.12012. Epub 2018 Mar 22.
Activating transcription factor 2 (ATF2) is a member of the leucine zipper family of DNA binding proteins and is widely distributed in tissues. Several recent studies have demonstrated that this protein is involved in mechanisms that are related to pain and inflammation. However, unclear is whether polymorphisms of the ATF2 gene, which encodes the human ATF2 protein, influence pain or analgesic sensitivity. This study examined associations between the analgesic effect of fentanyl in the cold pressor-induced pain test and polymorphisms in the ATF2 gene in 355 Japanese subjects.
In this study, 33 single nucleotide polymorphisms (SNPs) were selected, and a total of 2 linkage disequilibrium blocks with 6 Tag SNPs (rs1153702, rs7583431, rs2302663, rs3845744, rs268214, and rs1982235) were observed in the region within and around the ATF2 gene. We further analyzed associations between these Tag SNPs and clinical data. Even after multiple testing with Bonferroni adjustments, an increase in the analgesic effect of fentanyl in the cold pressor-induced pain test was significantly associated with a greater number of the A allele of the rs7583431 SNP (linear regression, P = .001).
The present findings may contribute to adequate pain relief in individual patients. Although more research on the genetic factors that influence opioid sensitivity is needed, analgesic requirements may be predicted by analyzing ATF2SNPs, together with other polymorphisms of genes that are reportedly associated with opioid sensitivity, such as CREB1, OPRM1, and GIRK2.
活化转录因子2(ATF2)是DNA结合蛋白亮氨酸拉链家族的成员,广泛分布于组织中。最近的几项研究表明,该蛋白参与了与疼痛和炎症相关的机制。然而,编码人类ATF2蛋白的ATF2基因多态性是否会影响疼痛或镇痛敏感性尚不清楚。本研究在355名日本受试者中检测了芬太尼在冷加压诱导疼痛试验中的镇痛效果与ATF2基因多态性之间的关联。
在本研究中,选择了33个单核苷酸多态性(SNP),在ATF2基因内部及周围区域共观察到2个连锁不平衡块,包含6个标签SNP(rs1153702、rs7583431、rs2302663、rs3845744、rs268214和rs1982235)。我们进一步分析了这些标签SNP与临床数据之间的关联。即使经过Bonferroni校正的多重检验后,在冷加压诱导疼痛试验中芬太尼镇痛效果的增加仍与rs7583431 SNP的A等位基因数量增加显著相关(线性回归,P = 0.001)。
本研究结果可能有助于实现个体患者的充分疼痛缓解。尽管需要对影响阿片类药物敏感性的遗传因素进行更多研究,但通过分析ATF2 SNP以及其他据报道与阿片类药物敏感性相关的基因多态性(如CREB1、OPRM1和GIRK2),可能预测镇痛需求。