Active Mental Health Brain & Nervous System

Validation of a translatable chronobiological signature of early relapse in bipolar disorder

In plain English

AI plain-English summary

A wrist-worn actigraph, tracking movement and rest around the clock, could reveal when someone with bipolar disorder is about to relapse. People with bipolar disorder often experience disrupted sleep and daily rhythms, but it is unclear whether these disruptions are a cause or a consequence of mood episodes. This project aims to parse the 24-hour rest-activity signal—using machine learning to separate sleep patterns from circadian rhythm features—and test which specific signatures predict early relapse. The researchers will validate this across three countries: Australia (predicting relapse in stable patients), New Zealand (tracking recovery from mania and depression), and India (linking rhythms to underlying circadian biology). If successful, the work will produce a validated, translatable chronobiological signature of early relapse. This could form the basis for an automated early-warning system—a wearable or app-based tool that alerts patients or clinicians days before a mood episode begins. The project will also generate a shared multinational dataset and analysis pipelines, enabling other researchers to build on the findings. This is applied clinical science with a clear path to a practical diagnostic tool.

View original technical description
The aim of this multi-national project is to provide a quantum advance in understanding the mechanisms of sleep and circadian rhythm disruption amongst people with established bipolar disorder (BD). Our methodological focus is a high-resolution signal of specific relevance to BD – the 24-hour rest-activity rhythm as measured by actigraphy. Across four work packages, distinct sleep and circadian features from this signal will be parsed through a machine learning approach called network analysis, and validated as a predictor of early relapse amongst inter-episode patients (Study 1 Australia), as a covariate of recovery from acute manic and depressive illness (Study 2 New Zealand), and as a proxy of endogenous circadian pathogenesis of BD (Study 3 India). In the integrative Work Package 4, findings from these complementary investigations will be cross-validated and synthesised into a theoretically and empirically grounded chronobiological signature of early relapse in BD. This biosignature could be the basis for a future automated early warning technology for BD (our long-term goal). Work Package 4 will also generate a new multi-national dataset and data processing pipelines to be shared with future researchers. Our multi-disciplinary team is uniquely qualified to undertake this project in collaboration with our long-standing lived experience collaborators.

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Researchers

Denny Meyer (EPMC Awardee)Fatemeh Hadaeghi (EPMC Awardee)Greg Murray (EPMC Awardee)Jan Scott (EPMC Awardee)Richard Porter (EPMC Awardee)Sandipan Ray (EPMC Awardee)

Related Research

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