TY - JOUR
T1 - Assessment of Reward-Related Brain Function After a Single Dose of Oxytocin in Autism
T2 - A Randomized Controlled Trial
AU - Mayer, Annalina V.
AU - Preckel, Katrin
AU - Ihle, Kristin
AU - Piecha, Fabian A.
AU - Junghanns, Klaus
AU - Reiche, Stefan
AU - Rademacher, Lena
AU - Müller-Pinzler, Laura
AU - Stolz, David S.
AU - Kamp-Becker, Inge
AU - Stroth, Sanna
AU - Roepke, Stefan
AU - Küpper, Charlotte
AU - Engert, Veronika
AU - Singer, Tania
AU - Kanske, Philipp
AU - Paulus, Frieder M.
AU - Krach, Sören
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/4
Y1 - 2022/4
N2 - Background: Autism spectrum disorder (ASD) is characterized by difficulties in social communication and interaction, which have been related to atypical neural processing of rewards, especially in the social domain. As intranasal oxytocin has been shown to modulate activation of the brain's reward circuit, oxytocin might ameliorate the processing of social rewards in ASD and thus improve social difficulties. Methods: In this randomized, double-blind, placebo-controlled, crossover functional magnetic resonance imaging study, we examined effects of a 24-IU dose of intranasal oxytocin on reward-related brain function in 37 men with ASD without intellectual impairment and 37 age- and IQ-matched control participants. Participants performed an incentive delay task that allows the investigation of neural activity associated with the anticipation and receipt of monetary and social rewards. Results: Nonsignificant tests suggested that oxytocin did not influence neural processes related to the anticipation of social or monetary rewards in either group. Complementary Bayesian analyses indicated moderate evidence for a null model, relative to an alternative model. Our results were inconclusive regarding possible oxytocin effects on amygdala responsiveness to social rewards during reward consumption. There were no significant differences in reward-related brain function between the two groups under placebo. Conclusions: Our results do not support the hypothesis that intranasal oxytocin generally enhances activation of reward-related neural circuits in men with and without ASD.
AB - Background: Autism spectrum disorder (ASD) is characterized by difficulties in social communication and interaction, which have been related to atypical neural processing of rewards, especially in the social domain. As intranasal oxytocin has been shown to modulate activation of the brain's reward circuit, oxytocin might ameliorate the processing of social rewards in ASD and thus improve social difficulties. Methods: In this randomized, double-blind, placebo-controlled, crossover functional magnetic resonance imaging study, we examined effects of a 24-IU dose of intranasal oxytocin on reward-related brain function in 37 men with ASD without intellectual impairment and 37 age- and IQ-matched control participants. Participants performed an incentive delay task that allows the investigation of neural activity associated with the anticipation and receipt of monetary and social rewards. Results: Nonsignificant tests suggested that oxytocin did not influence neural processes related to the anticipation of social or monetary rewards in either group. Complementary Bayesian analyses indicated moderate evidence for a null model, relative to an alternative model. Our results were inconclusive regarding possible oxytocin effects on amygdala responsiveness to social rewards during reward consumption. There were no significant differences in reward-related brain function between the two groups under placebo. Conclusions: Our results do not support the hypothesis that intranasal oxytocin generally enhances activation of reward-related neural circuits in men with and without ASD.
UR - http://www.scopus.com/inward/record.url?scp=85148560684&partnerID=8YFLogxK
U2 - 10.1016/j.bpsgos.2021.10.004
DO - 10.1016/j.bpsgos.2021.10.004
M3 - Comments/Debates
AN - SCOPUS:85148560684
SN - 2667-1743
VL - 2
SP - 136
EP - 146
JO - Biological Psychiatry Global Open Science
JF - Biological Psychiatry Global Open Science
IS - 2
ER -