Hobgood Donna K
University of Tennessee, Chattanooga College of Medicine, 1751 Gunbarrel Road, Chattanooga, TN 37421, United States.
Med Hypotheses. 2021 Mar;148:110513. doi: 10.1016/j.mehy.2021.110513. Epub 2021 Jan 26.
Although personality is thought to be 50% heritable, consensus has not been reached about the specific genes involved, interest in genes affecting personality and behavior continues because of the linkage of personality traits with both physical and mental illness. One hundred and twenty years of study of the ABO blood types and the genes causing them has led to more precise assignment of genotype-phenotype linkage. Countries like Japan and Korea with 100 years history of study of ABO blood groups and personality as well as other countries have published research with no consensus. Introversion is a well-studied personality trait with 50% genetic causation. Dopamine system has been linked to the introversion-extroversion spectrum with high dopamine linked to introversion. Dopamine beta hydroxylase determines the ratio of dopamine to norepinephrine. Dopamine beta hydroxylase gene, DBH, is in linkage disequilibrium with ABO gene thus offering insight into the ABO findings related to personality traits. ABO blood groups have been studied with some but not all studies finding type AB associated with introversion. One explanation for the inconsistent replication of findings could be that genotypes would show more differences than phenotypes. ABO A allele, ABO B allele or the synergism of both alleles could be the driver of introversion trait in ABO AB. Patients in an obstetric gynecology practice appeared to demonstrate a tendancy to introversion in phenotype ABO B. Since we had access to ABO blood phenotypes instead of genotypes of our obstetric gynecology office patients, we hypothesized that phenotype ABO AB when compared with ABO O would be associated with higher introversion since these phenotypes were also genotypes and since ABO O unlike ABO AB is not found associated with introversion in extant research. Though ABO B allele was observed to be the likely cause of introversion in patients and since we had available only phenotypes of ABO to use in search of genetic allele that causes introversion trait, ABO AB needs to be dissected to see whether ABO A allele or ABO B allele is the driver of the introspective trait. Based on the literature and on observation, the hypothesis was that ABO B is the driver of introversion trait. A pilot student of 225 obstetric gynecology patients using the online NPA personality test showed higher scores for introversion tendancies in ABO AB compared to ABO O and when ABO AB was compared to ABO A. This supports ABO B as the driver of introversion tendancies in the ABO gene. Studies using ABO genotypes instead of ABO phenotypes should provide further support for this hypothesis. Given the support for introversion tendancies in personality caused by higher dopamine genetically with dopamine beta hydroxylase low activity and this dopamine state being common mechanism for such conditions as schizophrenia and autism, continued discoveries of genes that impact this state will lead to many health implications.
尽管人们认为人格有50%是可遗传的,但对于具体涉及的基因尚未达成共识。由于人格特质与身体和精神疾病都有关联,因此对影响人格和行为的基因的研究兴趣依然存在。对ABO血型及其相关基因长达120年的研究,使得基因型与表型之间的联系得到了更精确的确定。像日本和韩国这样有着100年ABO血型与人格研究历史的国家以及其他国家都发表过相关研究,但并未达成共识。内向是一种经过充分研究的人格特质,有50%由基因决定。多巴胺系统与内向 - 外向谱相关,多巴胺水平高与内向有关。多巴胺β羟化酶决定多巴胺与去甲肾上腺素的比例。多巴胺β羟化酶基因(DBH)与ABO基因处于连锁不平衡状态,从而为与人格特质相关的ABO研究结果提供了深入见解。一些关于ABO血型的研究发现AB型与内向有关,但并非所有研究都如此。研究结果不一致的一个解释可能是,基因型之间的差异可能比表型更多。ABO A等位基因、ABO B等位基因或两者的协同作用可能是AB型人格中内向特质的驱动因素。在妇产科诊所的患者中,ABO B型表型似乎表现出内向倾向。由于我们能够获取妇产科门诊患者的ABO血型表型而非基因型,我们推测,与ABO O型相比,ABO AB型会与更高的内向性相关,因为这些表型也是基因型,而且在现有研究中,ABO O型与内向无关,不像ABO AB型。尽管观察到ABO B等位基因可能是患者内向的原因,并且由于我们只能使用ABO血型表型来寻找导致内向特质的基因等位基因,但需要对ABO AB型进行剖析,以确定是ABO A等位基因还是ABO B等位基因是内向特质的驱动因素。基于文献和观察,假设是ABO B是内向特质的驱动因素。一项对225名妇产科患者进行的初步研究,使用在线NPA人格测试,结果显示ABO AB型患者的内向倾向得分高于ABO O型,且ABO AB型与ABO A型相比也是如此。这支持了ABO B是ABO基因中内向倾向的驱动因素这一观点。使用ABO基因型而非ABO表型的研究应该会为这一假设提供进一步的支持。鉴于基因上多巴胺水平较高且多巴胺β羟化酶活性较低会导致人格内向倾向,而这种多巴胺状态是精神分裂症和自闭症等疾病的常见机制,持续发现影响这种状态的基因将对健康产生诸多影响。