Abstract

Moral behavior has been a key topic of debate for philosophy and psychology for a long time. In recent years, thanks to the development of novel methodologies in cognitive sciences, the question of how we make moral choices has expanded to the study of neurobiological correlates that subtend the mental processes involved in moral behavior. For instance, in vivo brain imaging studies have shown that distinct patterns of brain neural activity, associated with emotional response and cognitive processes, are involved in moral judgment. Moreover, while it is well-known that responses to the same moral dilemmas differ across individuals, to what extent this variability may be rooted in genetics still remains to be understood. As dopamine is a key modulator of neural processes underlying executive functions, we questioned whether genetic polymorphisms associated with decision-making and dopaminergic neurotransmission modulation would contribute to the observed variability in moral judgment. To this aim, we genotyped five genetic variants of the dopaminergic pathway [rs1800955 in the dopamine receptor D4 (DRD4) gene, DRD4 48 bp variable number of tandem repeat (VNTR), solute carrier family 6 member 3 (SLC6A3) 40 bp VNTR, rs4680 in the catechol-O-methyl transferase (COMT) gene, and rs1800497 in the ankyrin repeat and kinase domain containing 1 (ANKK1) gene] in 200 subjects, who were requested to answer 56 moral dilemmas. As these variants are all located in genes belonging to the dopaminergic pathway, they were combined in multilocus genetic profiles for the association analysis. While no individual variant showed any significant effects on moral dilemma responses, the multilocus genetic profile analysis revealed a significant gender-specific influence on human moral acceptability. Specifically, those genotype combinations that improve dopaminergic signaling selectively increased moral acceptability in females, by making their responses to moral dilemmas more similar to those provided by males. As females usually give more emotionally-based answers and engage the “emotional brain” more than males, our results, though preliminary and therefore in need of replication in independent samples, suggest that this increase in dopamine availability enhances the cognitive and reduces the emotional components of moral decision-making in females, thus favoring a more rationally-driven decision process.

Highlights

  • Morality and moral judgments are crucial for human social interactions

  • None of the genotype frequencies deviated from the HardyWeinberg equilibrium and they showed equal distribution in the two genders (Fisher’s exact test: p = 0.87 for rs1800955; p = 0.40 for Dopamine Receptor D4 gene (DRD4) variable number of tandem repeat (VNTR); p = 0.56 for SLC6A3 VNTR; p = 0.64 for rs4680; p = 0.15 for rs1800497)

  • Single variant genotypes were combined in multilocus genetic profiles, which are the representatives of the overall effect of different combinations of these alleles both on dopaminergic neurotransmission and on cognitive processes and behavioral traits associated with moral choices

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Summary

Introduction

Morality and moral judgments are crucial for human social interactions. Since the early days, moral behavior has been a matter of intense philosophical debate. The developments of novel methodologies for the in vivo study of the brain morphological and functional architecture in a non-invasive manner in humans (Pietrini, 2003; Poldrack, 2012; Poldrack and Yarkoni, 2016), along with the enormous acquisitions from molecular biology and genetics that led to the decoding of the human genome (Venter et al, 2001), have prompted cognitive sciences to venture into the study of the neurobiological mechanisms that subtend mental processes involved in moral behavior In this perspective, a few brain-imaging studies have investigated brain neural activity in individuals who were asked to make moral choices in regard to distinct scenarios (Greene et al, 2001, 2004; Hutcherson et al, 2015). Distinct genetic profiles may likely be involved, as different polymorphisms have been associated with definite aspects of behavior including violent and antisocial behaviors (Rigoni et al, 2010; Sartori et al, 2011; Buades-Rotger and Gallardo-Pujol, 2014; Iofrida et al, 2014)

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