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Neurobiology of loneliness: a systematic review

Loneliness is associated with increased morbidity and mortality. Deeper understanding of neurobiological mechanisms underlying loneliness is needed to identify potential intervention targets. We did not find any systematic review of neurobiology of loneliness. Using MEDLINE and PsycINFO online datab...

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Autores principales: Lam, Jeffrey A., Murray, Emily R., Yu, Kasey E., Ramsey, Marina, Nguyen, Tanya T., Mishra, Jyoti, Martis, Brian, Thomas, Michael L., Lee, Ellen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258736/
https://www.ncbi.nlm.nih.gov/pubmed/34230607
http://dx.doi.org/10.1038/s41386-021-01058-7
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author Lam, Jeffrey A.
Murray, Emily R.
Yu, Kasey E.
Ramsey, Marina
Nguyen, Tanya T.
Mishra, Jyoti
Martis, Brian
Thomas, Michael L.
Lee, Ellen E.
author_facet Lam, Jeffrey A.
Murray, Emily R.
Yu, Kasey E.
Ramsey, Marina
Nguyen, Tanya T.
Mishra, Jyoti
Martis, Brian
Thomas, Michael L.
Lee, Ellen E.
author_sort Lam, Jeffrey A.
collection PubMed
description Loneliness is associated with increased morbidity and mortality. Deeper understanding of neurobiological mechanisms underlying loneliness is needed to identify potential intervention targets. We did not find any systematic review of neurobiology of loneliness. Using MEDLINE and PsycINFO online databases, we conducted a search for peer-reviewed publications examining loneliness and neurobiology. We identified 41 studies (n = 16,771 participants) that had employed various methods including computer tomography (CT), structural magnetic resonance imaging (MRI), functional MRI (fMRI), electroencephalography (EEG), diffusion tensor imaging (DTI), single-photon emission computed tomography (SPECT), positron emission tomography (PET), and post-mortem brain tissue RNA analysis or pathological analysis. Our synthesis of the published findings shows abnormal structure (gray matter volume or white matter integrity) and/or activity (response to pleasant versus stressful images in social versus nonsocial contexts) in the prefrontal cortex (especially medial and dorsolateral), insula (particularly anterior), amygdala, hippocampus, and posterior superior temporal cortex. The findings related to ventral striatum and cerebellum were mixed. fMRI studies reported links between loneliness and differential activation of attentional networks, visual networks, and default mode network. Loneliness was also related to biological markers associated with Alzheimer’s disease (e.g., amyloid and tau burden). Although the published investigations have limitations, this review suggests relationships of loneliness with altered structure and function in specific brain regions and networks. We found a notable overlap in the regions involved in loneliness and compassion, the two personality traits that are inversely correlated in previous studies. We have offered recommendations for future research studies of neurobiology of loneliness.
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spelling pubmed-82587362021-07-06 Neurobiology of loneliness: a systematic review Lam, Jeffrey A. Murray, Emily R. Yu, Kasey E. Ramsey, Marina Nguyen, Tanya T. Mishra, Jyoti Martis, Brian Thomas, Michael L. Lee, Ellen E. Neuropsychopharmacology Article Loneliness is associated with increased morbidity and mortality. Deeper understanding of neurobiological mechanisms underlying loneliness is needed to identify potential intervention targets. We did not find any systematic review of neurobiology of loneliness. Using MEDLINE and PsycINFO online databases, we conducted a search for peer-reviewed publications examining loneliness and neurobiology. We identified 41 studies (n = 16,771 participants) that had employed various methods including computer tomography (CT), structural magnetic resonance imaging (MRI), functional MRI (fMRI), electroencephalography (EEG), diffusion tensor imaging (DTI), single-photon emission computed tomography (SPECT), positron emission tomography (PET), and post-mortem brain tissue RNA analysis or pathological analysis. Our synthesis of the published findings shows abnormal structure (gray matter volume or white matter integrity) and/or activity (response to pleasant versus stressful images in social versus nonsocial contexts) in the prefrontal cortex (especially medial and dorsolateral), insula (particularly anterior), amygdala, hippocampus, and posterior superior temporal cortex. The findings related to ventral striatum and cerebellum were mixed. fMRI studies reported links between loneliness and differential activation of attentional networks, visual networks, and default mode network. Loneliness was also related to biological markers associated with Alzheimer’s disease (e.g., amyloid and tau burden). Although the published investigations have limitations, this review suggests relationships of loneliness with altered structure and function in specific brain regions and networks. We found a notable overlap in the regions involved in loneliness and compassion, the two personality traits that are inversely correlated in previous studies. We have offered recommendations for future research studies of neurobiology of loneliness. Springer International Publishing 2021-07-06 2021-10 /pmc/articles/PMC8258736/ /pubmed/34230607 http://dx.doi.org/10.1038/s41386-021-01058-7 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021
spellingShingle Article
Lam, Jeffrey A.
Murray, Emily R.
Yu, Kasey E.
Ramsey, Marina
Nguyen, Tanya T.
Mishra, Jyoti
Martis, Brian
Thomas, Michael L.
Lee, Ellen E.
Neurobiology of loneliness: a systematic review
title Neurobiology of loneliness: a systematic review
title_full Neurobiology of loneliness: a systematic review
title_fullStr Neurobiology of loneliness: a systematic review
title_full_unstemmed Neurobiology of loneliness: a systematic review
title_short Neurobiology of loneliness: a systematic review
title_sort neurobiology of loneliness: a systematic review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258736/
https://www.ncbi.nlm.nih.gov/pubmed/34230607
http://dx.doi.org/10.1038/s41386-021-01058-7
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