Oxytocin, Orexin-A, and empathy in medication-free major depressive disorder: a neurobiological perspective
Major depressive disorder (MDD) is a common disorder influenced by biopsychosocial factors. There is conflicting and insufficient evidence regarding the role of neuropeptides such as Orexin-A and Oxytocin (OCT) and its association with empathy in MDD. This study aimed to address this question which is not only important for a better neurobiological understanding but could also lead to novel biomarkers. Sixty-nine antidepressant-free patients (48 females, 21 males) diagnosed with MDD according to DSM-5 criteria and 32 healthy controls (19 females, 13 males) were included. Serum Orexin-A and OCT levels were measured, and empathy and depression were assessed using the Basic Empathy Scale and the Hamilton Depression Rating Scale. Patients showed lower cognitive empathy than controls (Z = 4.161, <i>p</i> < 0.001), with significant differences only in females. Emotional and total empathy scores did not differ between groups. Patients had higher serum OCT levels (Z = 1.989, <i>p</i> = 0.047), while Orexin-A levels showed no clear group differences. Longer illness duration and more depressive episodes were modestly associated with higher emotional and total empathy. OCT levels showed a weak positive association with cognitive empathy. Lower cognitive empathy and elevated OCT levels may relate to depressive pathology, but further studies are needed to clarify these relationships.
Authors
- Saliha Özsoy (ORCID: https://orcid.org/0000-0003-2757-9641)
- Ümmühan Abdülrezzak (ORCID: https://orcid.org/0000-0002-7100-1866)
- Didem Şule Erdem (ORCID: https://orcid.org/0000-0001-9035-2947)
Institutions
- Istanbul Metropolitan Municipality (TR)
- İstanbul Başakşehir Çam ve Sakura Şehir Hastanesi
- Erciyes University (TR)
Publication Details
- Journal
- Social Neuroscience
- Published
- 2025-09-03
- DOI
- https://doi.org/10.1080/17470919.2025.2600995
- Primary Topic
- Neuroendocrine regulation and behavior
- Type
- article
- Field-Weighted Citation Impact
- 0.00