Incapacity to control emotion in major depression may arise from disrupted white matter integrity and OFC‐amygdala inhibition

Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital...

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Published inCNS neuroscience & therapeutics Vol. 24; no. 11; pp. 1053 - 1062
Main Authors Zheng, Kai‐Zhong, Wang, Hua‐Ning, Liu, Jian, Xi, Yi‐Bin, Li, Liang, Zhang, Xi, Li, Jia‐Ming, Yin, Hong, Tan, Qing‐Rong, Lu, Hong‐Bing, Li, Bao‐Juan
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Published England John Wiley & Sons, Inc 01.11.2018
John Wiley and Sons Inc
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Abstract Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems. Methods This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD. Key Results The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere. Conclusions & Inferences Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity?
AbstractList Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems. Methods This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD. Key Results The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere. Conclusions & Inferences Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity?
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.BACKGROUNDDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.METHODSThis study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere.KEY RESULTSThe results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere.Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity?CONCLUSIONS & INFERENCESOur findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity?
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems. This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD. The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere. Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity?
BackgroundDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.MethodsThis study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.Key ResultsThe results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere.Conclusions & InferencesOur findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity?
Author Wang, Hua‐Ning
Li, Liang
Lu, Hong‐Bing
Liu, Jian
Tan, Qing‐Rong
Li, Bao‐Juan
Xi, Yi‐Bin
Zheng, Kai‐Zhong
Zhang, Xi
Yin, Hong
Li, Jia‐Ming
AuthorAffiliation 1 School of Biomedical Engineering Fourth Military Medical University Xi'an China
2 Xijing Hospital Fourth Military Medical University Xi'an China
3 Network Center Fourth Military Medical University Xi'an China
AuthorAffiliation_xml – name: 2 Xijing Hospital Fourth Military Medical University Xi'an China
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Cites_doi 10.1016/j.jaac.2014.04.021
10.1016/j.pscychresns.2010.06.008
10.1038/tp.2016.81
10.1001/jamapsychiatry.2015.1376
10.1016/S0006-3223(02)01817-6
10.1016/j.biopsych.2009.11.025
10.1007/s00406-015-0614-0
10.1016/j.brat.2016.07.007
10.1016/j.cortex.2008.02.002
10.1001/archpsyc.1965.01730060026004
10.1016/j.jaac.2009.11.005
10.1016/j.cortex.2008.03.005
10.1037/a0019010
10.1159/000165381
10.1001/archpsyc.1965.01720310065008
10.1016/S1053-8119(03)00202-7
10.1038/npp.2011.279
10.1016/j.pscychresns.2016.06.005
10.1016/S0006-3223(03)00168-9
10.1371/journal.pone.0022697
10.1093/brain/awt094
10.1016/j.jpsychires.2016.10.001
10.1002/jmri.21053
10.1136/jnnp.23.1.56
10.1016/j.nicl.2016.09.001
10.1016/j.yebeh.2015.02.022
10.1080/02699930903407948
10.1093/cercor/bht279
10.1001/jamapsychiatry.2015.0161
10.1017/S0033291712000918
10.1016/j.jad.2008.04.027
10.1002/hbm.460020107
10.1016/j.cortex.2008.05.004
10.1016/S0924-9338(13)76335-1
10.1038/mp.2008.82
10.1192/bjp.bp.113.140376
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white matter integrity
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effective connectivity
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References_xml – volume: 6
  start-page: e819
  year: 2016
  article-title: Aberrant emotion networks in early major depressive disorder patients: an eigenvector centrality mapping study[J]
  publication-title: Transl Psychiat
– volume: 112
  start-page: 206
  year: 2009
  article-title: Antidepressant treatment normalizes hypoactivity in dorsolateral prefrontal cortex during emotional interference processing in major depression.[J]
  publication-title: J Affect Disorders
– volume: 13
  start-page: 508
  year: 1965
  article-title: Self‐rating depression scale in an outpatient clinic. Further validation of the SDS[J]
  publication-title: Arch Gen Psychiatry
– volume: 25
  start-page: 895
  year: 2015
  article-title: Disrupted effective connectivity between the amygdala and orbitofrontal cortex in social anxiety disorder during emotion discrimination revealed by dynamic causal modeling for fMRI[J]
  publication-title: Cereb Cortex
– volume: 53
  start-page: 899
  year: 2014
  end-page: 909
  article-title: White matter correlates of adolescent depression: structural evidence for frontolimbic disconnectivity.[J]
  publication-title: J Am Acad Child Adolesc Psychiatry
– volume: 12
  start-page: 1022
  year: 2016
  end-page: 1034
  article-title: Shared white matter alterations across emotional disorders: a voxel‐based meta‐analysis of fractional anisotropy:[J]
  publication-title: Neuroimage Clin
– volume: 45
  start-page: 68
  year: 2015
  end-page: 73
  article-title: Uncinate fasciculus connectivity in patients with psychogenic nonepileptic seizures: a preliminary diffusion tensor tractography study[J]
  publication-title: Epilepsy Behav
– volume: 72
  start-page: 1045
  year: 2015
  article-title: Meta‐analysis of functional neuroimaging of major depressive disorder in youth[J]
  publication-title: Jama Psychiat
– volume: 44
  start-page: 1010
  year: 2008
  end-page: 1022
  article-title: Sensory‐specific amnesia and hypoemotionality in humans and monkeys: gateway for developing a hodology of memory[J]
  publication-title: Cortex
– volume: 72
  start-page: 687
  year: 2015
  article-title: State‐dependent differences in emotion regulation between unmedicated bipolar disorder and major depressive disorder[J]
  publication-title: Jama Psychiat
– volume: 67
  start-page: 422
  year: 2010
  end-page: 431
  article-title: Abnormal left and right amygdala‐orbitofrontal cortical functional connectivity to emotional faces: state versus trait vulnerability markers of depression in bipolar disorder.[J]
  publication-title: Biol Psychiatry
– volume: 205
  start-page: 321
  year: 2014
  article-title: Diffusion tensor imaging predictors of treatment outcomes in major depressive disorder[J]
  publication-title: Br J Psychiatry
– volume: 24
  start-page: 281
  year: 2010
  article-title: Emotion regulation in depression: relation to cognitive inhibition[J]
  publication-title: Cogn Emot
– volume: 26
  start-page: 432
  year: 2008
  end-page: 439
  article-title: The Role of the uncinate fasciculus in memory and emotional recognition in amnestic mild cognitive impairment[J]
  publication-title: Dement Geriatr Cogn Disord
– volume: 86
  start-page: 35
  year: 2016
  end-page: 49
  article-title: Examining emotion regulation in depression: a review and future directions[J]
  publication-title: Behav Res Ther
– year: 2013
  article-title: Resting‐State Functional Connections of the Amygdala in Patients with Major Depressive Disorder[J]
  publication-title: Neuroscience
– volume: 136
  start-page: 1692
  year: 2013
  article-title: Dissecting the uncinate fasciculus: disorders, controversies and a hypothesis.[J]
  publication-title: Brain
– volume: 254
  start-page: 67
  year: 2016
  end-page: 73
  article-title: Amygdala response to explicit sad face stimuli at baseline predicts antidepressant treatment response to scopolamine in major depressive disorder[J]
  publication-title: Psychiat Res
– volume: 13
  start-page: 829
  year: 2008
  article-title: A neural model of voluntary and automatic emotion regulation: implications for understanding the pathophysiology and neurodevelopment of bipolar disorder[J]
  publication-title: Mol Psychiatr
– volume: 10
  start-page: 563
  year: 2010
  end-page: 572
  article-title: Emotion regulation and vulnerability to depression: spontaneous versus instructed use of emotion suppression and reappraisal.[J]
  publication-title: Emotion
– volume: 43
  start-page: 293
  year: 2013
  article-title: Heterogeneity of amygdala response in major depressive disorder: the impact of lifetime subthreshold mania.[J]
  publication-title: Psychol Med
– volume: 54
  start-page: 504
  year: 2003
  article-title: Neurobiology of emotion perception I: the neural basis of normal emotion perception.[J]
  publication-title: Biol Psychiat
– volume: 53
  start-page: 502
  year: 2003
  end-page: 510
  article-title: Neural circuitry underlying voluntary suppression of sadness.[J]
  publication-title: Biol Psychiat
– volume: 44
  start-page: 1105
  year: 2008
  end-page: 1132
  article-title: A diffusion tensor imaging tractography atlas for virtual in vivo dissections[J]
  publication-title: Cortex
– volume: 23
  start-page: 56
  year: 1960
  article-title: A rating scale for depression[J]
  publication-title: J Neurol Neurosurg Psychiatry
– volume: 84
  start-page: 237
  year: 2017
  article-title: Abnormalities in the structural covariance of emotion regulation networks in major depressive disorder.[J]
  publication-title: J Psychiatr Res
– volume: 44
  start-page: 928
  year: 2008
  end-page: 935
  article-title: Medial temporal and prefrontal function: recent behavioural disconnection studies in the macaque monkey.[J]
  publication-title: Cortex
– volume: 2
  start-page: 56
  year: 1993
  end-page: 78
  article-title: Functional and effective connectivity in neuroimaging: a[J]
  publication-title: Hum Brain Mapp
– volume: 19
  start-page: 1273
  year: 2003
  end-page: 1302
  article-title: Dynamic causal modelling[J]
  publication-title: NeuroImage
– volume: 28
  start-page: 1
  year: 2013
  article-title: Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met‐allele of the Val66Met brain‐derived neurotrophic factor genotype[J]
  publication-title: Eur Psychiat
– volume: 49
  start-page: 173
  year: 2010
  end-page: 183
  article-title: Altered white matter microstructure in adolescents with major depression: a preliminary study.[J]
  publication-title: J Am Acad Child Adolesc Psychiatry
– volume: 6
  start-page: e22697
  year: 2011
  article-title: Structural integrity of the uncinate fasciculus and resting state functional connectivity of the ventral prefrontal cortex in late life depression[J]
  publication-title: PLoS ONE
– volume: 266
  start-page: 239
  year: 2016
  article-title: Altered functional connectivity density in major depressive disorder at rest.[J]
  publication-title: Eur Arch Psychiatry Clin Neurosci
– volume: 26
  start-page: 756
  year: 2007
  article-title: Effects of SNR on the accuracy and reproducibility of DTI‐derived fractional anisotropy, mean diffusivity, and principal eigenvector measurements at 1.5T[J]
  publication-title: J Magn Reson Imaging JMRI
– volume: 184
  start-page: 38
  year: 2010
  end-page: 48
  article-title: Depression severity is correlated to the integrity of white matter fiber tracts in late‐onset major depression[J]
  publication-title: Psychiat Res
– volume: 12
  start-page: 63
  year: 1965
  article-title: A self‐rating depression scale.[J]
  publication-title: Arch Gen Psychiatry
– volume: 37
  start-page: 959
  year: 2011
  end-page: 967
  article-title: Quantitative tract‐specific measures of uncinate and cingulum in major depression using diffusion tensor imaging[J]
  publication-title: Neuropsychopharmacology
– year: 2013
  ident: e_1_2_7_9_1
  article-title: Resting‐State Functional Connections of the Amygdala in Patients with Major Depressive Disorder[J]
  publication-title: Neuroscience
– ident: e_1_2_7_26_1
  doi: 10.1016/j.jaac.2014.04.021
– ident: e_1_2_7_29_1
  doi: 10.1016/j.pscychresns.2010.06.008
– ident: e_1_2_7_2_1
  doi: 10.1038/tp.2016.81
– ident: e_1_2_7_11_1
  doi: 10.1001/jamapsychiatry.2015.1376
– ident: e_1_2_7_33_1
  doi: 10.1016/S0006-3223(02)01817-6
– ident: e_1_2_7_14_1
  doi: 10.1016/j.biopsych.2009.11.025
– ident: e_1_2_7_3_1
  doi: 10.1007/s00406-015-0614-0
– ident: e_1_2_7_4_1
  doi: 10.1016/j.brat.2016.07.007
– ident: e_1_2_7_18_1
  doi: 10.1016/j.cortex.2008.02.002
– ident: e_1_2_7_37_1
  doi: 10.1001/archpsyc.1965.01730060026004
– ident: e_1_2_7_19_1
  doi: 10.1016/j.jaac.2009.11.005
– ident: e_1_2_7_17_1
  doi: 10.1016/j.cortex.2008.03.005
– ident: e_1_2_7_6_1
  doi: 10.1037/a0019010
– ident: e_1_2_7_30_1
  doi: 10.1159/000165381
– ident: e_1_2_7_36_1
  doi: 10.1001/archpsyc.1965.01720310065008
– ident: e_1_2_7_22_1
  doi: 10.1016/S1053-8119(03)00202-7
– ident: e_1_2_7_20_1
  doi: 10.1038/npp.2011.279
– ident: e_1_2_7_23_1
  doi: 10.1016/j.pscychresns.2016.06.005
– ident: e_1_2_7_32_1
  doi: 10.1016/S0006-3223(03)00168-9
– ident: e_1_2_7_34_1
  doi: 10.1371/journal.pone.0022697
– ident: e_1_2_7_16_1
  doi: 10.1093/brain/awt094
– ident: e_1_2_7_5_1
  doi: 10.1016/j.jpsychires.2016.10.001
– ident: e_1_2_7_25_1
  doi: 10.1002/jmri.21053
– ident: e_1_2_7_35_1
  doi: 10.1136/jnnp.23.1.56
– ident: e_1_2_7_27_1
  doi: 10.1016/j.nicl.2016.09.001
– ident: e_1_2_7_31_1
  doi: 10.1016/j.yebeh.2015.02.022
– ident: e_1_2_7_7_1
  doi: 10.1080/02699930903407948
– ident: e_1_2_7_13_1
  doi: 10.1093/cercor/bht279
– ident: e_1_2_7_10_1
  doi: 10.1001/jamapsychiatry.2015.0161
– ident: e_1_2_7_8_1
  doi: 10.1017/S0033291712000918
– ident: e_1_2_7_24_1
  doi: 10.1016/j.jad.2008.04.027
– ident: e_1_2_7_21_1
  doi: 10.1002/hbm.460020107
– ident: e_1_2_7_15_1
  doi: 10.1016/j.cortex.2008.05.004
– ident: e_1_2_7_28_1
  doi: 10.1016/S0924-9338(13)76335-1
– ident: e_1_2_7_12_1
  doi: 10.1038/mp.2008.82
– ident: e_1_2_7_38_1
  doi: 10.1192/bjp.bp.113.140376
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Snippet Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in...
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been...
BackgroundDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has...
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StartPage 1053
SubjectTerms Adult
Amygdala
Amygdala - diagnostic imaging
Amygdala - drug effects
Amygdala - physiopathology
Antidepressive Agents - therapeutic use
Brain Mapping
Cortex (frontal)
Depressive Disorder, Major - diagnostic imaging
Depressive Disorder, Major - drug therapy
dynamic causal modeling
effective connectivity
Emotions - drug effects
Emotions - physiology
Female
Frontal Lobe - diagnostic imaging
Frontal Lobe - drug effects
Frontal Lobe - physiopathology
Functional magnetic resonance imaging
Hemispheric laterality
Humans
Image Processing, Computer-Assisted
Limbic system
Magnetic Resonance Imaging
major depressive disorder
Male
Mental depression
Middle Aged
Myelination
Neural Pathways - diagnostic imaging
Neural Pathways - drug effects
Original
Patients
Psychiatric Status Rating Scales
Substantia alba
uncinate fasciculus
White Matter - diagnostic imaging
White Matter - drug effects
white matter integrity
Title Incapacity to control emotion in major depression may arise from disrupted white matter integrity and OFC‐amygdala inhibition
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcns.12800
https://www.ncbi.nlm.nih.gov/pubmed/29368421
https://www.proquest.com/docview/2118680849
https://www.proquest.com/docview/1991182761
https://pubmed.ncbi.nlm.nih.gov/PMC6489955
Volume 24
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