Literature DB >> 31477459

Disruption of Neural Homeostasis as a Model of Relapse and Recurrence in Late-Life Depression.

Carmen Andreescu1, Olusola Ajilore2, Howard J Aizenstein3, Kimberly Albert4, Meryl A Butters1, Bennett A Landman5, Helmet T Karim1, Robert Krafty6, Warren D Taylor7.   

Abstract

The significant public health burden associated with late-life depression (LLD) is magnified by the high rates of recurrence. In this manuscript, we review what is known about recurrence risk factors, conceptualize recurrence within a model of homeostatic disequilibrium, and discuss the potential significance and challenges of new research into LLD recurrence. The proposed model is anchored in the allostatic load theory of stress. We review the allostatic response characterized by neural changes in network function and connectivity and physiologic changes in the hypothalamic-pituitary-adrenal axis, autonomic nervous system, immune system, and circadian rhythm. We discuss the role of neural networks' instability following treatment response as a source of downstream disequilibrium, triggering and/or amplifying abnormal stress response, cognitive dysfunction and behavioral changes, ultimately precipitating a full-blown recurrent episode of depression. We propose strategies to identify and capture early change points that signal recurrence risk through mobile technology to collect ecologically measured symptoms, accompanied by automated algorithms that monitor for state shifts (persistent worsening) and variance shifts (increased variability) relative to a patient's baseline. Identifying such change points in relevant sensor data could potentially provide an automated tool that could alert clinicians to at-risk individuals or relevant symptom changes even in a large practice. Published by Elsevier Inc.

Entities:  

Keywords:  Depression; aging; allostatic load; cognition; default mode network; depressive disorder; executive control network; geriatric; homeostasis; recurrence; relapse; remission; remitted; review; risk factors; stress

Year:  2019        PMID: 31477459      PMCID: PMC6842700          DOI: 10.1016/j.jagp.2019.07.016

Source DB:  PubMed          Journal:  Am J Geriatr Psychiatry        ISSN: 1064-7481            Impact factor:   4.105


  146 in total

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2.  Efficacy of antidepressants for late-life depression: a meta-analysis and meta-regression of placebo-controlled randomized trials.

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Authors:  Amy L Byers; Kristine Yaffe
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Authors:  Bruce S McEwen; Peter J Gianaros
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8.  The natural history of late-life depression: a 6-year prospective study in the community.

Authors:  Aartjan T F Beekman; Sandra W Geerlings; Dorly J H Deeg; Jan H Smit; Robert S Schoevers; Edwin de Beurs; Arjan W Braam; Brenda W J H Penninx; Willem van Tilburg
Journal:  Arch Gen Psychiatry       Date:  2002-07

9.  The nature and determinants of neuropsychological functioning in late-life depression.

Authors:  Meryl A Butters; Ellen M Whyte; Robert D Nebes; Amy E Begley; Mary Amanda Dew; Benoit H Mulsant; Michelle D Zmuda; Rishi Bhalla; Carolyn Cidis Meltzer; Bruce G Pollock; Charles F Reynolds; James T Becker
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10.  Vascular depression consensus report - a critical update.

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2.  The Role of Exercise in Management of Mental Health Disorders: An Integrative Review.

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Review 3.  The enigma of vascular depression in old age: a critical update.

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4.  White Matter Integrity Underlying Depressive Symptoms in Dementia Caregivers.

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5.  Preliminary Evidence That Cortical Amyloid Burden Predicts Poor Response to Antidepressant Medication Treatment in Cognitively Intact Individuals With Late-Life Depression.

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6.  The Effects of Gait Speed and Psychomotor Speed on Risk for Depression and Anxiety in Older Adults with Medical Comorbidities.

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Review 7.  Brain-based mechanisms of late-life depression: Implications for novel interventions.

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8.  Structural MRI-Based Measures of Accelerated Brain Aging do not Moderate the Acute Antidepressant Response in Late-Life Depression.

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9.  Accelerated brain aging predicts impaired cognitive performance and greater disability in geriatric but not midlife adult depression.

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10.  Mild cognitive impairment and major depressive disorder are associated with molecular senescence abnormalities in older adults.

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Journal:  Alzheimers Dement (N Y)       Date:  2021-03-31
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