The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults
Proton magnetic resonance spectroscopy (1H-MRS) is a noninvasive imaging technique that measures the concentration of metabolites in defined areas of the human brain in vivo. The underlying structure of natural metabolism-emotion relationships is unknown. Further, there is a wide range of between-pe...
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Elsevier
2021-01-01
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Series: | NeuroImage |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1053811920309940 |
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doaj-03618fcf563b4829880411147a1f2020 |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tara L. White Meghan A. Gonsalves Ronald A. Cohen Ashley D. Harris Mollie A. Monnig Edward G. Walsh Adam Z. Nitenson Eric C. Porges Damon G. Lamb Adam J. Woods Cara B. Borja |
spellingShingle |
Tara L. White Meghan A. Gonsalves Ronald A. Cohen Ashley D. Harris Mollie A. Monnig Edward G. Walsh Adam Z. Nitenson Eric C. Porges Damon G. Lamb Adam J. Woods Cara B. Borja The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults NeuroImage Trait emotion Personality Single voxel proton magnetic spectroscopy Dorsal anterior cingulate tNAA Neurotypical adult volunteers |
author_facet |
Tara L. White Meghan A. Gonsalves Ronald A. Cohen Ashley D. Harris Mollie A. Monnig Edward G. Walsh Adam Z. Nitenson Eric C. Porges Damon G. Lamb Adam J. Woods Cara B. Borja |
author_sort |
Tara L. White |
title |
The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
title_short |
The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
title_full |
The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
title_fullStr |
The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
title_full_unstemmed |
The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
title_sort |
neurobiology of wellness: 1h-mrs correlates of agency, flexibility and neuroaffective reserves in healthy young adults |
publisher |
Elsevier |
series |
NeuroImage |
issn |
1095-9572 |
publishDate |
2021-01-01 |
description |
Proton magnetic resonance spectroscopy (1H-MRS) is a noninvasive imaging technique that measures the concentration of metabolites in defined areas of the human brain in vivo. The underlying structure of natural metabolism-emotion relationships is unknown. Further, there is a wide range of between-person differences in metabolite concentration in healthy individuals, but the significance of this variation for understanding emotion in healthy humans is unclear. Here we investigated the relationship of two emotional constructs, agency and flexibility, with the metabolites glutamate and glutamine (Glx), N-acetylaspartate (tNAA), choline (Cho), creatine (tCr), and myo-inositol (Ins) in the right dorsal anterior cingulate cortex (dACC) in medically and psychiatrically healthy volunteers (N = 20, 9 female; mean age = 22.8 years, SD = 3.40). The dACC was selected because this region is an integrative hub involved in multiple brain networks of emotion, cognition and behavior. Emotional traits were assessed using the Multidimensional Personality Questionnaire Brief Form (MPQ-BF), an empirically derived self-report instrument with an orthogonal factor structure. Phenotypes evaluated were positive and negative agency (MPQ-BF Social Potency, Aggression), emotional and behavioral flexibility (MPQ-BF Absorption, Control-reversed), and positive and negative affect (MPQ-BF Social Closeness; Stress Reaction, Alienation). The resting concentration of tNAA in the dACC was robustly positively correlated with Absorption (r = +0.56, unadjusted p = .005), moderately positively correlated with Social Potency (r = +0.42, unadjusted p = .03), and robustly negatively correlated with Aggression (r = -0.59, unadjusted p = .003). Absorption and Aggression accounted for substantial variance in tNAA (R2 = 0.31, 0.35; combined R2 = 0.50), and survived correction for multiple comparisons (Holm-Bonferroni adjusted p = .032, 0.021, respectively). dACC Glx and Cho had modest relationships with behavioral flexibility and social affiliation that did not survive this multiple correction, providing effect sizes for future work. Principal Component Analysis (PCA) revealed a three-factor orthogonal solution indicating specific relationships between: 1) Glx and behavioral engagement; 2) Cho and affiliative bonding; and 3) tNAA and a novel dimension that we term neuroaffective reserves. Our results inform the neurobiology of agency and flexibility and lay the groundwork for understanding mechanisms of natural emotion using 1H-MRS. |
topic |
Trait emotion Personality Single voxel proton magnetic spectroscopy Dorsal anterior cingulate tNAA Neurotypical adult volunteers |
url |
http://www.sciencedirect.com/science/article/pii/S1053811920309940 |
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doaj-03618fcf563b4829880411147a1f20202020-12-17T04:47:21ZengElsevierNeuroImage1095-95722021-01-01225117509The neurobiology of wellness: 1H-MRS correlates of agency, flexibility and neuroaffective reserves in healthy young adultsTara L. White0Meghan A. Gonsalves1Ronald A. Cohen2Ashley D. Harris3Mollie A. Monnig4Edward G. Walsh5Adam Z. Nitenson6Eric C. Porges7Damon G. Lamb8Adam J. Woods9Cara B. Borja10Center for Alcohol and Addiction Studies, Brown University, Box G-S121-4, 121 South Main St., Providence, RI 02912, USA; Department of Behavioral and Social Sciences, School of Public Health, Brown University, Providence, RI, USA; Carney Institute for Brain Science, Brown University, Providence, RI, USA; Corresponding author at: Center for Alcohol and Addiction Studies, Brown University, Box G-S121-5, 121 South Main St., Providence, RI 02912, USA.Neuroscience Graduate Program, Brown University, Providence, RI, USADepartment of Clinical and Health Psychology, Center for Cognitive Aging and Memory, and McKnight Brain Research Foundation, University of Florida, Gainesville, FL, USADepartment of Radiology, CAIR Program, Alberta Children's Hospital Research Institute, and Hotchkiss Brain Institute, University of Calgary, Calgary, AB, CanadaCenter for Alcohol and Addiction Studies, Brown University, Box G-S121-4, 121 South Main St., Providence, RI 02912, USADepartment of Neuroscience, Brown University, Providence, RI, USANeuroscience Graduate Program, Brown University, Providence, RI, USADepartment of Clinical and Health Psychology, Center for Cognitive Aging and Memory, and McKnight Brain Research Foundation, University of Florida, Gainesville, FL, USADepartment of Psychiatry, and Center for Cognitive Aging and Memory, McKnight Brain Research Foundation, University of Florida, Gainesville, FL, USA; Center for Neuropsychological Studies, Department of Neurology, University of Florida College of Medicine, Gainesville, FL, USA; Brain Rehabilitation Research Center, Malcom Randall Veterans Affairs Medical Center, Gainesville, FL, USADepartment of Clinical and Health Psychology, Center for Cognitive Aging and Memory, and McKnight Brain Research Foundation, University of Florida, Gainesville, FL, USANeuroscience Graduate Program, Brown University, Providence, RI, USAProton magnetic resonance spectroscopy (1H-MRS) is a noninvasive imaging technique that measures the concentration of metabolites in defined areas of the human brain in vivo. The underlying structure of natural metabolism-emotion relationships is unknown. Further, there is a wide range of between-person differences in metabolite concentration in healthy individuals, but the significance of this variation for understanding emotion in healthy humans is unclear. Here we investigated the relationship of two emotional constructs, agency and flexibility, with the metabolites glutamate and glutamine (Glx), N-acetylaspartate (tNAA), choline (Cho), creatine (tCr), and myo-inositol (Ins) in the right dorsal anterior cingulate cortex (dACC) in medically and psychiatrically healthy volunteers (N = 20, 9 female; mean age = 22.8 years, SD = 3.40). The dACC was selected because this region is an integrative hub involved in multiple brain networks of emotion, cognition and behavior. Emotional traits were assessed using the Multidimensional Personality Questionnaire Brief Form (MPQ-BF), an empirically derived self-report instrument with an orthogonal factor structure. Phenotypes evaluated were positive and negative agency (MPQ-BF Social Potency, Aggression), emotional and behavioral flexibility (MPQ-BF Absorption, Control-reversed), and positive and negative affect (MPQ-BF Social Closeness; Stress Reaction, Alienation). The resting concentration of tNAA in the dACC was robustly positively correlated with Absorption (r = +0.56, unadjusted p = .005), moderately positively correlated with Social Potency (r = +0.42, unadjusted p = .03), and robustly negatively correlated with Aggression (r = -0.59, unadjusted p = .003). Absorption and Aggression accounted for substantial variance in tNAA (R2 = 0.31, 0.35; combined R2 = 0.50), and survived correction for multiple comparisons (Holm-Bonferroni adjusted p = .032, 0.021, respectively). dACC Glx and Cho had modest relationships with behavioral flexibility and social affiliation that did not survive this multiple correction, providing effect sizes for future work. Principal Component Analysis (PCA) revealed a three-factor orthogonal solution indicating specific relationships between: 1) Glx and behavioral engagement; 2) Cho and affiliative bonding; and 3) tNAA and a novel dimension that we term neuroaffective reserves. Our results inform the neurobiology of agency and flexibility and lay the groundwork for understanding mechanisms of natural emotion using 1H-MRS.http://www.sciencedirect.com/science/article/pii/S1053811920309940Trait emotionPersonalitySingle voxel proton magnetic spectroscopyDorsal anterior cingulatetNAANeurotypical adult volunteers |