Department of Psychiatry, University of Naples SUN, Largo Madonna delle Grazie, 80138 Naples, Italy.
Pharmacol Res. 2010 May;61(5):400-4. doi: 10.1016/j.phrs.2010.01.002. Epub 2010 Jan 18.
Experimental data suggest that the endogenous cannabinoid system is involved in mood regulation, but no study has been performed so far to investigate the role of endocannabinoid genes in the susceptibility to major depression (MD) and/or bipolar disorder (BD). We assessed the CB1 receptor gene (CNR1) single nucleotide polymorphism (SNP) rs1049353 (1359 G/A) and the fatty acid amide hydrolase (FAAH) gene rs324420 SNP (cDNA 385C to A) for their associations with MD and/or BD in 83 Caucasian patients with recurrent MD, 134 Caucasian individuals with BD, and 117 Caucasian healthy subjects. The distribution of the CNR1 1359 G/A genotypes and alleles significantly differed among the groups (chi(2)=12.595; df=4, P=0.01 for genotypes; chi(2)=13.773; df=2, P=0.001 for alleles) with MD patients showing a higher frequency of both AG, GG genotypes and A allele as compared to healthy controls. The distribution of the FAAH cDNA 385C to A genotypes, according to the CC dominant model (AA+AC vs. CC), significantly differed among the groups (chi(2)=6.626; df=2, P=0.04), with both BD patients and MD patients showing a non-significant slightly higher frequency of the AC genotype. These findings, although preliminary, suggest that the CNR1 1359 G/A and the FAAH cDNA 385C to A gene variants may contribute to the susceptibility to mood disorders.
实验数据表明,内源性大麻素系统参与了情绪调节,但迄今为止,尚无研究调查内源性大麻素基因在易患重度抑郁症(MD)和/或双相情感障碍(BD)中的作用。我们评估了 CB1 受体基因(CNR1)单核苷酸多态性(SNP)rs1049353(1359 G/A)和脂肪酸酰胺水解酶(FAAH)基因 rs324420 SNP(cDNA 385C 到 A)与 MD 和/或 BD 的相关性,共纳入 83 例反复发作 MD 的高加索患者、134 例 BD 高加索患者和 117 例高加索健康对照者。CNR1 1359 G/A 基因型和等位基因的分布在各组之间存在显著差异(卡方检验=12.595;df=4,P=0.01 用于基因型;卡方检验=13.773;df=2,P=0.001 用于等位基因),MD 患者的 AG 和 GG 基因型以及 A 等位基因频率均高于健康对照组。根据 CC 显性模型(AA+AC 与 CC),FAAH cDNA 385C 到 A 基因型的分布在各组之间存在显著差异(卡方检验=6.626;df=2,P=0.04),BD 患者和 MD 患者的 AC 基因型频率略高,但无统计学意义。这些发现虽然初步,但表明 CNR1 1359 G/A 和 FAAH cDNA 385C 到 A 基因变异可能与情绪障碍的易感性有关。