MicroRNAs as Critical Biomarkers of Major Depressive Disorder: A Comprehensive Perspective.
Miguel Ángel OrtegaMiguel Angel Alvarez-MonCielo Garcia-MonteroOscar Fraile-MartínezGuillermo LaheraJorge Monserrat SanzLuis Muñoz-MeridaFernando MoraRoberto Rodríguez-JiménezSonia Fernandez-RojoJavier QuinteroMelchor Álvarez-MonPublished in: Biomedicines (2021)
Major Depressive Disorder (MDD) represents a major global health concern, a body-mind malady of rising prevalence worldwide nowadays. The complex network of mechanisms involved in MDD pathophysiology is subjected to epigenetic changes modulated by microRNAs (miRNAs). Serum free or vesicles loaded miRNAs have starred numerous publications, denoting a key role in cell-cell communication, systematically and in brain structure and neuronal morphogenesis, activity and plasticity. Upregulated or downregulated expression of these signaling molecules may imply the impairment of genes implicated in pathways of MDD etiopathogenesis (neuroinflammation, brain-derived neurotrophic factor (BDNF), neurotransmitters, hypothalamic-pituitary-adrenal (HPA) axis, oxidative stress, circadian rhythms...). In addition, these miRNAs could serve as potential biomarkers with diagnostic, prognostic and predictive value, allowing to classify severity of the disease or to make decisions in clinical management. They have been considered as promising therapy targets as well and may interfere with available antidepressant treatments. As epigenetic malleable regulators, we also conclude emphasizing lifestyle interventions with physical activity, mindfulness and diet, opening the door to new clinical management considerations.
Keyphrases
- major depressive disorder
- physical activity
- bipolar disorder
- global health
- oxidative stress
- single cell
- cell therapy
- gene expression
- dna methylation
- public health
- cerebral ischemia
- weight loss
- poor prognosis
- dna damage
- chronic pain
- body mass index
- cardiovascular disease
- metabolic syndrome
- cognitive impairment
- traumatic brain injury
- type diabetes
- multiple sclerosis
- brain injury
- binding protein
- lps induced
- mesenchymal stem cells
- subarachnoid hemorrhage
- endoplasmic reticulum stress
- genome wide identification
- stress induced