Insomnia, sleep loss, and circadian sleep disturbances in mood disorders: a pathway toward neurodegeneration and neuroprogression? A theoretical review.
Laura PalaginiPierre-Alexis GeoffroyMario MiniatiGiulio PerugiGiovanni BiggioDonatella MarazzitiDieter RiemannPublished in: CNS spectrums (2021)
The present paper aims at reviewing and commenting on the relationships between sleep and circadian phasing alterations and neurodegenerative/neuroprogressive processes in mood disorder. We carried out a systematic review, according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, in PubMed, PsycINFO, and Embase electronic databases for literature related to mood disorders, sleep disturbances, and neurodegenerative/neuroprogressive processes in relation to (1) neuroinflammation, (2) activation of the stress system, (3) oxidative stress, (4) accumulation of neurotoxic proteins, and (5) neuroprotection deficit. Seventy articles were collectively selected and analyzed. Experimental and clinical studies revealed that insomnia, conditions of sleep loss, and altered circadian sleep may favor neurodegeneration and neuroprogression in mood disorders. These sleep disturbances may induce a state of chronic inflammation by enhancing neuroinflammation, both directly and indirectly, via microglia and astrocytes activation. They may act as neurobiological stressors that by over-activating the stress system may negatively influence neural plasticity causing neuronal damage. In addition, sleep disturbances may favor the accumulation of neurotoxic proteins, favor oxidative stress, and a deficit in neuroprotection hence contributing to neurodegeneration and neuroprogression. Targeting sleep disturbances in the clinical practice may hold a neuroprotective value for mood disorders.
Keyphrases
- sleep quality
- oxidative stress
- physical activity
- depressive symptoms
- bipolar disorder
- systematic review
- cerebral ischemia
- traumatic brain injury
- dna damage
- randomized controlled trial
- meta analyses
- blood brain barrier
- emergency department
- ischemia reperfusion injury
- adverse drug
- artificial intelligence
- big data
- stress induced
- spinal cord
- deep learning
- endoplasmic reticulum stress
- drug induced