Associations of age, sex, sexual abuse, and genotype with monoamine oxidase a gene methylation

被引:10
作者
Checknita, David [1 ,2 ,3 ]
Tiihonen, Jari [4 ,5 ,6 ]
Hodgins, Sheilagh [2 ,6 ]
Nilsson, Kent W. [1 ,3 ]
机构
[1] Uppsala Univ, Dept Neurosci, Uppsala, Sweden
[2] Karolinska Inst, Dept Clin Neurosci, Psychiat Bldg R5 00 Jari Tiihonen,Karolinska Univ, S-17176 Stockholm, Sweden
[3] Uppsala Univ, Ctr Clin Res, Vastmanland Cty Council, Uppsala, Sweden
[4] Stockholm City Council, Ctr Psychiat Res, Stockholm, Sweden
[5] Univ Eastern Finland, Niuvanniemi Hosp, Dept Forens Psychiat, Kuopio, Finland
[6] Univ Montreal, Inst Univ Sante Mentale Montreal, Dept Psychiat & Addictol, Ctr Rech, Montreal, PQ, Canada
关键词
Epigenetics; Methylation; Age; Sex differences; Child abuse; Gene-environment interaction; DNA METHYLATION; AGGRESSIVE-BEHAVIOR; ENVIRONMENTAL-INFLUENCES; CHILDHOOD MALTREATMENT; PROMOTER METHYLATION; MAOA METHYLATION; DEPRESSION; EXPRESSION; SEROTONIN; MECHANISMS;
D O I
10.1007/s00702-021-02403-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Epigenome-wide studies report higher methylation among women than men with decreasing levels with age. Little is known about associations of sex and age with methylation of monoamine oxidase A (MAOA). Methylation of the first exonic and partial first intronic region of MAOA has been shown to strengthen associations of interactions of MAOA-uVNTR genotypes and adversity with aggression and substance misuse. Our study examined associations of sex and age with MAOA first exon and intron methylation levels in 252 women and 157 men aged 14-73 years. Participants included adolescents recruited at a substance misuse clinic, their siblings and parents, and healthy women. Women showed similar to 50% higher levels of exonic, and similar to 15% higher intronic, methylation than men. Methylation levels were similar between younger (M = 22.7 years) and older (M = 46.1 years) participants, and stable across age. Age modified few associations of methylation levels with sex. MAOA genotypes modified few associations of methylation with sex and age. Higher methylation levels among women were not explained by genotype, nor interaction of genotype and sexual abuse. Findings were similar after adjusting for lifetime diagnoses of substance dependence (women = 24.3%; men = 34.2%). Methylation levels were higher among women who experienced sexual abuse than women who did not. Results extend on prior studies by showing that women display higher levels of methylation than men within first intronic/exonic regions of MAOA, which did not decrease with age in either sex. Findings were not conditioned by genotype nor interactions of genotype and trauma, and indicate X-chromosome inactivation.
引用
收藏
页码:1721 / 1739
页数:19
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