Circadian-related hypothalamic structure differs by chronotype in bipolar disorder

Apr 12, 2026Biological psychiatry. Cognitive neuroscience and neuroimaging

Daily rhythm-related brain area differs by sleep pattern in bipolar disorder

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Abstract

A diagnosis × chronotype interaction revealed significant differences in the volume of the anterior-inferior hypothalamic subunit, with larger volumes observed in bipolar disorder individuals with evening chronotype.

Bipolar disorder individuals with an evening chronotype exhibited greater volume in the anterior-inferior hypothalamic subunit compared to those with a morning chronotype.
The interaction between diagnosis and chronotype was statistically significant (F(6, 586) = 2.84, p = .010).
No similar volume differences were found in other hypothalamic regions or among different psychiatric diagnoses.
These results suggest that hypothalamic structure may vary based on chronotype in bipolar disorder.
Findings provide neuroanatomical evidence linking circadian preference to relevant brain structure in bipolar disorder.

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BACKGROUND: Circadian rhythm disturbances represent a core feature of bipolar disorder (BD), with evening chronotype as a marker for poorer outcomes. We hypothesized that BD psychopathology combined with evening chronotype is associated with structural alterations in circadian-related hypothalamic regions - particularly the suprachiasmatic nucleus (SCN) - specific to BD relative to other psychiatric diagnoses.

METHODS: We investigated structural neuroimaging data from the UK Biobank (113 BD, 205 major depressive disorder, 91 psychotic disorders, 199 healthy controls). The SCN-containing anterior-inferior hypothalamic subunit was segmented, central to circadian functional neuroanatomy. For each group, diagnosis × chronotype interactions on its volume were tested using analysis of variance, with post-hoc estimated marginal means and correction for multiple comparisons. Covariates included age, sex, handedness, and psychiatric medication use. Specificity was examined across four additional hypothalamic subunits.

RESULTS: There was a diagnosis × chronotype interaction in the SCN-containing anterior-inferior hypothalamic subunit volume (F(6, 586) = 2.84, p = .010). This was driven by larger volumes in BD individuals with evening versus morning chronotype (t = 3.24, p= .004). No comparable results were found in other hypothalamic regions or diagnoses. FWER

CONCLUSIONS: Hypothalamic structure differs by chronotype in BD, with chronotype related associations localized to an anterior-inferior hypothalamic region implicated in circadian regulation. These findings support chronotype as a biologically meaningful dimension of variation in BD and provide neuroanatomical evidence linking circadian preference to circadian relevant brain structure. Longitudinal and interventional studies will be important to clarify the temporal dynamics, underlying mechanisms, and potential clinical significance of these associations.

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Circadian-related hypothalamic structure differs by chronotype in bipolar disorder

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