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Peripheral oxytocin levels are linked to hypothalamic gray matter volume in autistic adults: a cross-sectional secondary data analysis

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Brandi,  Marie-Luise
Independent Max Planck Research Group Social Neuroscience, Max Planck Institute of Psychiatry, Max Planck Society;

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Albantakis,  Laura
Independent Max Planck Research Group Social Neuroscience, Max Planck Institute of Psychiatry, Max Planck Society;

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Lahnakoski,  Juha M.
Independent Max Planck Research Group Social Neuroscience, Max Planck Institute of Psychiatry, Max Planck Society;

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Henco,  Lara
Independent Max Planck Research Group Social Neuroscience, Max Planck Institute of Psychiatry, Max Planck Society;

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Schilbach,  Leonhard
Independent Max Planck Research Group Social Neuroscience, Max Planck Institute of Psychiatry, Max Planck Society;

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Zitation

Haaf Raoul, R., Brandi, M.-L., Albantakis, L., Lahnakoski, J. M., Henco, L., & Schilbach, L. (2024). Peripheral oxytocin levels are linked to hypothalamic gray matter volume in autistic adults: a cross-sectional secondary data analysis. SCIENTIFIC REPORTS, 14(1): 1380. doi:10.1038/s41598-023-50770-5.


Zitierlink: https://hdl.handle.net/21.11116/0000-000F-7C15-F
Zusammenfassung
Oxytocin (OXT) is known to modulate social behavior and cognition and has been discussed as pathophysiological and therapeutic factor for autism spectrum disorder (ASD). An accumulating body of evidence indicates the hypothalamus to be of particular importance with regard to the underlying neurobiology. Here we used a region of interest voxel-based morphometry (VBM) approach to investigate hypothalamic gray matter volume (GMV) in autistic (n = 29, age 36.03 +/- 11.0) and non-autistic adults (n = 27, age 30.96 +/- 11.2). Peripheral plasma OXT levels and the autism spectrum quotient (AQ) were used for correlation analyses. Results showed no differences in hypothalamic GMV in autistic compared to non-autistic adults but suggested a differential association between hypothalamic GMV and OXT levels, such that a positive association was found for the ASD group. In addition, hypothalamic GMV showed a positive association with autistic traits in the ASD group. Bearing in mind the limitations such as a relatively small sample size, a wide age range and a high rate of psychopharmacological treatment in the ASD sample, these results provide new preliminary evidence for a potentially important role of the HTH in ASD and its relationship to the OXT system, but also point towards the importance of interindividual differences.