Cardiac dysautonomia in depression - heart rate variability biofeedback as a potential add-on therapy
- PMID: 31190834
- PMCID: PMC6529729
- DOI: 10.2147/NDT.S200360
Cardiac dysautonomia in depression - heart rate variability biofeedback as a potential add-on therapy
Abstract
Depressive disorders are among the most important health problems and are predicted to constitute the leading cause of disease burden by the year 2030. Aside significant impact on quality of life, psychosocial well-being and socioeconomic status of affected patients, depression is associated with impaired cardiovascular health and increased mortality. The link between affective and cardiovascular disease has largely been attributed to dysregulation of the autonomic nervous system resulting in a chronic shift toward increased sympathetic and decreased parasympathetic activity and, consecutively, cardiac dysautonomia. Among proposed surrogate parameters to capture and quantitatively analyze this shift, heart rate variability (HRV) and baroreflex sensitivity have emerged as reliable tools. Attenuation of these parameters is frequently seen in patients suffering from depression and is closely linked to cardiovascular morbidity and mortality. Therefore, diagnostic and therapeutic strategies were designed to assess and counteract cardiac dysautonomia. While psychopharmacological treatment can effectively improve affective symptoms of depression, its effect on cardiac dysautonomia is limited. HRV biofeedback is a non-invasive technique which is based on a metronomic breathing technique to increase parasympathetic tone. While some small studies observed beneficial effects of HRV biofeedback on dysautonomia in patients with depressive disorders, larger confirmatory trials are lacking. We reviewed the current literature on cardiac dysautonomia in patients suffering from depression with a focus on the underlying pathophysiology as well as diagnostic workup and treatment.
Keywords: autonomic dysfunction; biofeedback; brain-heart axis; cardiovascular disease; mood disorder.
Conflict of interest statement
TS and KB are editorial board members of Neuropsychiatric Disease and Treatment. TH was sponsored by the National Research, Development and Innovation Office (NKFIH) postdoctoral program, grant number: PD 121186. SS Jr reports grants from New National Excellence Program (UNKP-17-3) of the Ministry of Human Resources of the Government of Hungary, grants from Society of Transylvanian Museum – Section of Medicine and Pharmacy, outside the submitted work. The authors report no other conflicts of interest in this work.
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