{"title":"雄激素受体基因与犯罪:来自国际数据的证据","authors":"Lee Ellis , Anthony Hoskin , Nicholas Hasan Buker","doi":"10.1016/j.earlhumdev.2024.106113","DOIUrl":null,"url":null,"abstract":"<div><p>Beginning early in fetal development, the androgen receptor (AR) gene helps regulate bodily exposure to testosterone. Most studies of individuals have found an inverse correlation between the number of CAG repeats on this gene and serious forms of physical aggression. This two-phased study was primarily undertaken to determine if a link between AR CAGn and physical aggression also exists at an ecological level of analysis. To make this assessment, we first conducted a bivariate analysis of the average number of AR CAG repeats for a large number of countries and the rates of crime victimization in those same countries. Except for motor vehicle theft, as the national average number of CAG repeats increased, crime victimization rates decreased. This inverse relationship was especially strong for violent offenses. In the second phase of this study, we sought to determine if per capita gross domestic product, pathogen prevalence, and average intelligence might be mediating some of the AR CAG repeats-criminality relationship. Mediation analysis analysis indicated that, once gross domestic product and pathogenic prevalence were controlled, average intelligence was able to eliminate most of the links between CAG repeats and crime victimization rates, especially in the case of violent offenses. These findings suggest that the AR gene is not influencing criminality primarily by altering testosterone brain exposure (as we suspected). Instead, it may affect criminality mainly by affecting cognitive ability. In fact, once average national intelligence is included in the mediation analysis model, direct relationships between CAG repeats and measures of homicide, assault, and robbery were no longer statistically significant. Findings from this two-phased study point toward the AR gene as having multiple effects on brain functioning, particularly regarding intellectual development as hypothesized by Manning [62]. Replication is obviously needed.</p></div>","PeriodicalId":11435,"journal":{"name":"Early human development","volume":"198 ","pages":"Article 106113"},"PeriodicalIF":2.2000,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0378378224001828/pdfft?md5=e3d2198d87124c5d0b255a87cb2f2081&pid=1-s2.0-S0378378224001828-main.pdf","citationCount":"0","resultStr":"{\"title\":\"The androgen receptor gene and criminal offending: Evidence derived from international data\",\"authors\":\"Lee Ellis , Anthony Hoskin , Nicholas Hasan Buker\",\"doi\":\"10.1016/j.earlhumdev.2024.106113\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Beginning early in fetal development, the androgen receptor (AR) gene helps regulate bodily exposure to testosterone. Most studies of individuals have found an inverse correlation between the number of CAG repeats on this gene and serious forms of physical aggression. This two-phased study was primarily undertaken to determine if a link between AR CAGn and physical aggression also exists at an ecological level of analysis. To make this assessment, we first conducted a bivariate analysis of the average number of AR CAG repeats for a large number of countries and the rates of crime victimization in those same countries. Except for motor vehicle theft, as the national average number of CAG repeats increased, crime victimization rates decreased. This inverse relationship was especially strong for violent offenses. In the second phase of this study, we sought to determine if per capita gross domestic product, pathogen prevalence, and average intelligence might be mediating some of the AR CAG repeats-criminality relationship. Mediation analysis analysis indicated that, once gross domestic product and pathogenic prevalence were controlled, average intelligence was able to eliminate most of the links between CAG repeats and crime victimization rates, especially in the case of violent offenses. These findings suggest that the AR gene is not influencing criminality primarily by altering testosterone brain exposure (as we suspected). Instead, it may affect criminality mainly by affecting cognitive ability. In fact, once average national intelligence is included in the mediation analysis model, direct relationships between CAG repeats and measures of homicide, assault, and robbery were no longer statistically significant. Findings from this two-phased study point toward the AR gene as having multiple effects on brain functioning, particularly regarding intellectual development as hypothesized by Manning [62]. 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引用次数: 0
摘要
从胎儿发育早期开始,雄激素受体(AR)基因就开始帮助调节身体对睾酮的接触。大多数针对个体的研究发现,该基因上的 CAG 重复序列数与严重的身体攻击行为之间存在反相关关系。本研究分两个阶段进行,主要是为了确定 AR CAGn 与身体攻击性之间是否也存在生态分析层面的联系。为了进行评估,我们首先对许多国家的 AR CAG 重复序列的平均数量和这些国家的犯罪受害率进行了二元分析。除机动车盗窃外,随着全国 CAG 重复平均数的增加,犯罪受害率也随之下降。这种反比关系在暴力犯罪中尤为明显。在本研究的第二阶段,我们试图确定人均国内生产总值、病原体流行率和平均智力是否会在一定程度上调节 AR CAG 重复率与犯罪率之间的关系。中介分析表明,在控制了国内生产总值和病原体流行率之后,平均智力能够消除CAG重复序列与犯罪受害率之间的大部分联系,尤其是在暴力犯罪的情况下。这些研究结果表明,AR 基因并非主要通过改变大脑中的睾酮暴露来影响犯罪率(正如我们所猜测的那样)。相反,它可能主要通过影响认知能力来影响犯罪率。事实上,一旦将国民平均智力纳入中介分析模型,CAG重复序列与杀人、攻击和抢劫行为之间的直接关系就不再具有统计学意义。这项分两个阶段进行的研究结果表明,AR 基因对大脑功能有多重影响,特别是在智力发育方面,正如 Manning 所假设的那样[62]。这显然需要重复研究。
The androgen receptor gene and criminal offending: Evidence derived from international data
Beginning early in fetal development, the androgen receptor (AR) gene helps regulate bodily exposure to testosterone. Most studies of individuals have found an inverse correlation between the number of CAG repeats on this gene and serious forms of physical aggression. This two-phased study was primarily undertaken to determine if a link between AR CAGn and physical aggression also exists at an ecological level of analysis. To make this assessment, we first conducted a bivariate analysis of the average number of AR CAG repeats for a large number of countries and the rates of crime victimization in those same countries. Except for motor vehicle theft, as the national average number of CAG repeats increased, crime victimization rates decreased. This inverse relationship was especially strong for violent offenses. In the second phase of this study, we sought to determine if per capita gross domestic product, pathogen prevalence, and average intelligence might be mediating some of the AR CAG repeats-criminality relationship. Mediation analysis analysis indicated that, once gross domestic product and pathogenic prevalence were controlled, average intelligence was able to eliminate most of the links between CAG repeats and crime victimization rates, especially in the case of violent offenses. These findings suggest that the AR gene is not influencing criminality primarily by altering testosterone brain exposure (as we suspected). Instead, it may affect criminality mainly by affecting cognitive ability. In fact, once average national intelligence is included in the mediation analysis model, direct relationships between CAG repeats and measures of homicide, assault, and robbery were no longer statistically significant. Findings from this two-phased study point toward the AR gene as having multiple effects on brain functioning, particularly regarding intellectual development as hypothesized by Manning [62]. Replication is obviously needed.
期刊介绍:
Established as an authoritative, highly cited voice on early human development, Early Human Development provides a unique opportunity for researchers and clinicians to bridge the communication gap between disciplines. Creating a forum for the productive exchange of ideas concerning early human growth and development, the journal publishes original research and clinical papers with particular emphasis on the continuum between fetal life and the perinatal period; aspects of postnatal growth influenced by early events; and the safeguarding of the quality of human survival.
The first comprehensive and interdisciplinary journal in this area of growing importance, Early Human Development offers pertinent contributions to the following subject areas:
Fetology; perinatology; pediatrics; growth and development; obstetrics; reproduction and fertility; epidemiology; behavioural sciences; nutrition and metabolism; teratology; neurology; brain biology; developmental psychology and screening.