Bortolato Marco, Walss-Bass Consuelo, Thompson Peter M, Moskovitz Jackob
a Department of Pharmacology and Toxicology, College of Pharmacy , University of Utah , Salt Lake City , UT , USA.
b Department of Psychiatry and Behavioral Science, School of Medicine , University of Texas Health Science Center , Houston , TX , USA.
World J Biol Psychiatry. 2017 Apr;18(3):247-254. doi: 10.1080/15622975.2016.1208844. Epub 2016 Jul 26.
The enzyme catechol-O-methyltransferase (COMT), which catalyses the degradation of dopamine and norepinephrine, is posited to participate in the pathophysiology of bipolar disorder (BD) and schizophrenia. In support of this notion, rich evidence has documented that the severity of various BD and schizophrenia symptoms is moderated by rs4680, a single nucleotide polymorphism of the COMT gene featuring a valine (Val)-to-methionine (Met) substitution that results in lower catalytic activity. Nevertheless, the specific relevance of COMT enzymatic activity in the pathophysiology of BD and schizophrenia dimensions remains elusive.
We measured COMT catalytic activity in post-mortem prefrontal cortices, striata and cerebella of schizophrenia and BD patients, as well as non-affected controls. These values were then correlated with rs4680 genotypes and psychopathology scores in the last week of life.
No direct correlation between COMT activity and rs4680 genotypes was found; however, the severity of manic symptoms was highly correlated with COMT activity in the striatum, irrespective of the diagnostic group.
These results suggest that COMT striatal activity, but not rs4680 genotype, may serve as a biomarker for manic symptoms. Future studies are warranted to confirm these findings and assess the neurobiological links between COMT striatal activity and manic symptoms.
儿茶酚-O-甲基转移酶(COMT)可催化多巴胺和去甲肾上腺素的降解,据推测其参与双相情感障碍(BD)和精神分裂症的病理生理过程。支持这一观点的大量证据表明,COMT基因的单核苷酸多态性rs4680可调节各种BD和精神分裂症症状的严重程度,该多态性表现为缬氨酸(Val)到甲硫氨酸(Met)的替换,导致催化活性降低。然而,COMT酶活性在BD和精神分裂症维度的病理生理过程中的具体相关性仍不清楚。
我们测量了精神分裂症患者、BD患者以及未受影响的对照组死后前额叶皮质、纹状体和小脑的COMT催化活性。然后将这些值与rs4680基因型以及生命最后一周的精神病理学评分进行关联。
未发现COMT活性与rs4680基因型之间存在直接相关性;然而,无论诊断组如何,躁狂症状的严重程度与纹状体中的COMT活性高度相关。
这些结果表明,COMT纹状体活性而非rs4680基因型可能作为躁狂症状的生物标志物。未来的研究有必要证实这些发现,并评估COMT纹状体活性与躁狂症状之间的神经生物学联系。