Kim Hyungsuk, Dionne Raymond A
National Institute of Nursing Research, National Institutes of Health, Bethesda, MD, USA.
Mol Pain. 2007 Mar 7;3:6. doi: 10.1186/1744-8069-3-6.
To assess the effect of variations in GTP cyclohydrolase gene (GCH1) on pain sensitivity in humans.
Thermal and cold pain sensitivity were evaluated in a cohort of 735 healthy volunteers. Among this cohort, the clinical pain responses of 221 subjects after the surgical removal of impacted third molars were evaluated. Genotyping was done for 38 single nucleotide polymorphisms (SNPs) whose heterozygosity > 0.2 in GCH1. Influence of the genetic variations including SNPs and haplotypes on pain sensitivity were analyzed.
Minor allele frequencies and linkage disequilibrium show significant differences in European Americans, African Americans, Hispanic Americans and Asian Americans. Association analyses in European Americans do not replicate the previously reported important influence of GCH1 variations on pain sensitivity.
Considering population stratification, previously reported associations between GCH1 genetic variations and pain sensitivity appear weak or negligible in this well characterized model of pain.
评估GTP环化水解酶基因(GCH1)变异对人类疼痛敏感性的影响。
对735名健康志愿者进行热痛和冷痛敏感性评估。在该队列中,评估了221名受试者在拔除阻生第三磨牙手术后的临床疼痛反应。对GCH1中杂合度>0.2的38个单核苷酸多态性(SNP)进行基因分型。分析了包括SNP和单倍型在内的基因变异对疼痛敏感性的影响。
欧洲裔美国人、非裔美国人、西班牙裔美国人和亚裔美国人的次要等位基因频率和连锁不平衡存在显著差异。欧洲裔美国人的关联分析未重复先前报道的GCH1变异对疼痛敏感性的重要影响。
考虑到人群分层,在这个特征明确的疼痛模型中,先前报道的GCH1基因变异与疼痛敏感性之间的关联似乎较弱或可忽略不计。