Rice J, McGuffin P, Shaskan E G
Psychiatry Res. 1982 Dec;7(3):325-35. doi: 10.1016/0165-1781(82)90069-5.
The distribution of platelet monoamine oxidase (MAO) activity is examined in a large cohort of 18-year-olds from a college setting. A mixture of three distributions is needed to describe the data, even when a power transformation is used to remove skewness in the distribution. This is compatible with MAO activity being controlled by a single major locus with a gene frequency of 0.02 for high-MAO activity. Accordingly, it is unlikely that such a locus could serve as a genetic marker for a disorder which is associated with low activity. However, this finding does not rule out the possibility that MAO activity is an associated risk factor in disease.
在一大群来自大学环境的18岁人群中,对血小板单胺氧化酶(MAO)活性的分布进行了检测。即便使用幂变换来消除分布中的偏态,仍需要三种分布的混合来描述数据。这与MAO活性由一个主要位点控制相一致,该位点高MAO活性的基因频率为0.02。因此,这样一个位点不太可能作为与低活性相关疾病的遗传标记。然而,这一发现并不排除MAO活性是疾病相关风险因素的可能性。