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. 2013 Mar 22:11:79.
doi: 10.1186/1741-7015-11-79.

Manipulating the sleep-wake cycle and circadian rhythms to improve clinical management of major depression

Ian B Hickie  1 , Sharon L Naismith, Rébecca Robillard, Elizabeth M Scott, Daniel F Hermens
Affiliations

Manipulating the sleep-wake cycle and circadian rhythms to improve clinical management of major depression

Ian B Hickie et al. BMC Med. .

Abstract

Background: Clinical psychiatry has always been limited by the lack of objective tests to substantiate diagnoses and a lack of specific treatments that target underlying pathophysiology. One area in which these twin failures has been most frustrating is major depression. Due to very considerable progress in the basic and clinical neurosciences of sleep-wake cycles and underlying circadian systems this situation is now rapidly changing.

Discussion: The development of specific behavioral or pharmacological strategies that target these basic regulatory systems is driving renewed clinical interest. Here, we explore the extent to which objective tests of sleep-wake cycles and circadian function - namely, those that measure timing or synchrony of circadian-dependent physiology as well as daytime activity and nighttime sleep patterns - can be used to identify a sub-class of patients with major depression who have disturbed circadian profiles.

Summary: Once this unique pathophysiology is characterized, a highly personalized treatment plan can be proposed and monitored. New treatments will now be designed and old treatments re-evaluated on the basis of their effects on objective measures of sleep-wake cycles, circadian rhythms and related metabolic systems.

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Figures

Figure 1
Figure 1
The master circadian clock in the human brain.
Figure 2
Figure 2
Pathophysiological pathways to early-onset depressive disorders. There are at least three common trajectories that lead to depression in the teenage and early-adult years. These are characterized by (1) ‘anxiety-central nervous system reactivity’, (2) ‘circadian and 24-hour sleep-wake cycle dysfunction’, and (3) ‘developmental brain abnormalities’. The six corresponding phenotypic patterns have distinct ages of onset and characteristics. From age 8 to 10 years onwards these processes are transformed by key neurobiological phenomena: (a) puberty, (b) adolescent brain development, and (c) sleep-wake cycle [see [122].
Figure 3
Figure 3
The normal synchronous relationships between sleep and daytime activity and cortisol, melatonin and body temperature.
Figure 4
Figure 4
Psychoeducation and monitoring worksheet for patients with mood disorders and sleep-wake and circadian disturbance.
See this image and copyright information in PMC

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