MAOA‐VNTR genotype affects structural and functional connectivity in distributed brain networks

• Published in: Human brain mapping Vol. 40; no. 18; pp. 5202 - 5212
• Main Authors: Harneit, Anais, Braun, Urs, Geiger, Lena S., Zang, Zhenxiang, Hakobjan, Marina, Donkelaar, Marjolein M. J., Schweiger, Janina I., Schwarz, Kristina, Gan, Gabriela, Erk, Susanne, Heinz, Andreas, Romanczuk‐Seiferth, Nina, Witt, Stephanie, Rietschel, Marcella, Walter, Henrik, Franke, Barbara, Meyer‐Lindenberg, Andreas, Tost, Heike
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 15-12-2019
• Subjects: Abnormalities; Adult; aggression; Amine oxidase (flavin-containing); Brain; Brain - diagnostic imaging; Brain - physiology; Brain architecture; Brain mapping; Circuits; Cognitive ability; Computer architecture; Computer networks; connectome; Cortex; Female; Frontal Lobe - diagnostic imaging; Frontal Lobe - physiology; Functional magnetic resonance imaging; Gene polymorphism; Genetics; Genotype; Humans; imaging genetics; Impulsive behavior; Links; Magnetic resonance imaging; Magnetic Resonance Imaging - methods; Male; Medical imaging; Minisatellite Repeats - genetics; Monoamine Oxidase - genetics; monoamine oxidase A gene; multimodal imaging; Nerve Net - diagnostic imaging; Nerve Net - physiology; Neural networks; Neuroimaging; Neurology; Phenotypes; Polymorphism; risk factors; Short term memory; Spatial distribution; Spatial memory; Structure-function relationships; Temporal Lobe - diagnostic imaging; Temporal Lobe - physiology; Tensors; Young Adult; monoamine oxidase A gene; risk factors; imaging genetics; impulsive behavior; connectome; aggression; multimodal imaging
• ISSN: 1065-9471; 1097-0193
• DOI: 10.1002/hbm.24766

Previous studies have linked the low expression variant of a variable number of tandem repeat polymorphism in the monoamine oxidase A gene (MAOA‐L) to the risk for impulsivity and aggression, brain developmental abnormalities, altered cortico‐limbic circuit function, and an exaggerated neural serotonergic tone. However, the neurobiological effects of this variant on human brain network architecture are incompletely understood. We studied healthy individuals and used multimodal neuroimaging (sample size range: 219–284 across modalities) and network‐based statistics (NBS) to probe the specificity of MAOA‐L‐related connectomic alterations to cortical‐limbic circuits and the emotion processing domain. We assessed the spatial distribution of affected links across several neuroimaging tasks and data modalities to identify potential alterations in network architecture. Our results revealed a distributed network of node links with a significantly increased connectivity in MAOA‐L carriers compared to the carriers of the high expression (H) variant. The hyperconnectivity phenotype primarily consisted of between‐lobe (“anisocoupled”) network links and showed a pronounced involvement of frontal‐temporal connections. Hyperconnectivity was observed across functional magnetic resonance imaging (fMRI) of implicit emotion processing (pFWE = .037), resting‐state fMRI (pFWE = .022), and diffusion tensor imaging (pFWE = .044) data, while no effects were seen in fMRI data of another cognitive domain, that is, spatial working memory (pFWE = .540). These observations are in line with prior research on the MAOA‐L variant and complement these existing data by novel insights into the specificity and spatial distribution of the neurogenetic effects. Our work highlights the value of multimodal network connectomic approaches for imaging genetics.