Gray and white matter differences in adolescents and young adults with prior suicide attempts across bipolar and major depressive disorders.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
15 02 2019
Historique:
received: 02 07 2018
revised: 24 09 2018
accepted: 17 11 2018
entrez: 1 2 2019
pubmed: 1 2 2019
medline: 4 4 2019
Statut: ppublish

Résumé

Findings regarding brain circuitry abnormalities in suicide attempters (SAs) converge across bipolar disorder (BD) and major depressive disorder (MDD), the most common disorders observed in suicides. These abnormalities appear to be present during adolescence/young adulthood when suicide rates increase steeply, and suicide is a leading cause of death in this age group. Identification of brain circuitry common to adolescent/young adult SAs with BD and MDD is important for generating widely effective early prevention strategies. We examined brain circuitry in SAs in adolescents/young adults across these two disorders. Eighty-three participants (ages 14-25 years), 46 with BD (21 SAs) and 37 with MDD (19 SAs), underwent structural and diffusion-weighted magnetic resonance scanning. Whole-brain analyses compared gray matter (GM) volume and white matter (WM) fractional anisotropy (FA) between SAs and non-suicide attempters (NSAs) across and within BD and MDD (p < 0.005). Across and within BD and MDD, SAs showed differences compared to NSAs in ventral prefrontal cortex (PFC) GM volume and fronto-limbic (including uncinate fasciculus (UF)) WM FA. Exploratory analyses showed additional within-disorder differences for BD SAs in dorsolateral PFC (dlPFC) and hippocampus GM volume and UF FA, and for MDD SAs dorsomedial and dlPFC GM and dorsal frontal WM. However, there was no significant interaction between suicide attempt status and diagnosis. Modest sample size. Common fronto-limbic gray and white matter alterations in adolescent/young adult SAs are potential targets for suicide prevention strategies across mood disorders. Preliminary findings of disorder-specific regional findings could suggest diagnostic-specific optimal targets may exist.

Sections du résumé

BACKGROUND
Findings regarding brain circuitry abnormalities in suicide attempters (SAs) converge across bipolar disorder (BD) and major depressive disorder (MDD), the most common disorders observed in suicides. These abnormalities appear to be present during adolescence/young adulthood when suicide rates increase steeply, and suicide is a leading cause of death in this age group. Identification of brain circuitry common to adolescent/young adult SAs with BD and MDD is important for generating widely effective early prevention strategies. We examined brain circuitry in SAs in adolescents/young adults across these two disorders.
METHODS
Eighty-three participants (ages 14-25 years), 46 with BD (21 SAs) and 37 with MDD (19 SAs), underwent structural and diffusion-weighted magnetic resonance scanning. Whole-brain analyses compared gray matter (GM) volume and white matter (WM) fractional anisotropy (FA) between SAs and non-suicide attempters (NSAs) across and within BD and MDD (p < 0.005).
RESULTS
Across and within BD and MDD, SAs showed differences compared to NSAs in ventral prefrontal cortex (PFC) GM volume and fronto-limbic (including uncinate fasciculus (UF)) WM FA. Exploratory analyses showed additional within-disorder differences for BD SAs in dorsolateral PFC (dlPFC) and hippocampus GM volume and UF FA, and for MDD SAs dorsomedial and dlPFC GM and dorsal frontal WM. However, there was no significant interaction between suicide attempt status and diagnosis.
LIMITATIONS
Modest sample size.
CONCLUSIONS
Common fronto-limbic gray and white matter alterations in adolescent/young adult SAs are potential targets for suicide prevention strategies across mood disorders. Preliminary findings of disorder-specific regional findings could suggest diagnostic-specific optimal targets may exist.

Identifiants

pubmed: 30699851
pii: S0165-0327(17)32639-3
doi: 10.1016/j.jad.2018.11.095
pmc: PMC6903411
mid: NIHMS1543562
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1089-1097

Subventions

Organisme : NIDA NIH HHS
ID : T32 DA022975
Pays : United States
Organisme : NIMH NIH HHS
ID : RC1 MH088366
Pays : United States
Organisme : NIMH NIH HHS
ID : T32 MH014276
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000142
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH069747
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH070902
Pays : United States

Informations de copyright

Copyright © 2018. Published by Elsevier B.V.

Références

Neuroimage. 2008 Apr 1;40(2):570-582
pubmed: 18255316
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1501-7
pubmed: 18572296
Curr Opin Neurol. 2005 Dec;18(6):734-9
pubmed: 16280687
Eur Child Adolesc Psychiatry. 2012 Jul;21(7):369-77
pubmed: 22447195
J Am Acad Child Adolesc Psychiatry. 1997 Jul;36(7):980-8
pubmed: 9204677
Transl Psychiatry. 2015 Feb 24;5:e516
pubmed: 25710122
J Consult Clin Psychol. 1974 Dec;42(6):861-5
pubmed: 4436473
J Affect Disord. 2011 Mar;129(1-3):47-55
pubmed: 20708276
World J Biol Psychiatry. 2015;16(8):544-66
pubmed: 25112792
Am J Prev Med. 2014 Sep;47(3 Suppl 2):S152-62
pubmed: 25145733
Brain Res. 1995 Aug 7;688(1-2):121-33
pubmed: 8542298
Brain. 2011 Jul;134(Pt 7):2005-12
pubmed: 21666263
Am J Psychiatry. 2017 Jul 1;174(7):667-675
pubmed: 28135845
Bipolar Disord. 2016 Jun;18(4):363-72
pubmed: 27233466
J Affect Disord. 2017 Jun;215:213-217
pubmed: 28340447
Trends Cogn Sci. 2004 Apr;8(4):170-7
pubmed: 15050513
Bipolar Disord. 2018 Jun;20(4):334-348
pubmed: 29457330
Cortex. 2012 Jan;48(1):82-96
pubmed: 22088488
Anat Rec A Discov Mol Cell Evol Biol. 2004 Nov;281(1):1212-25
pubmed: 15470678
J Psychiatr Res. 2014 Apr;51:60-67
pubmed: 24462041
Psychiatry Res. 2012 Apr 30;202(1):30-7
pubmed: 22595508
J Affect Disord. 2015 Jan 1;170:237-54
pubmed: 25261630
Prog Neurobiol. 2004 Apr;72(5):341-72
pubmed: 15157726
Arch Gen Psychiatry. 2003 Jan;60(1):14-22
pubmed: 12511168
Am J Med Genet B Neuropsychiatr Genet. 2012 Jul;159B(5):537-48
pubmed: 22585743
Braz J Psychiatry. 2009 Sep;31(3):271-80
pubmed: 19787156
Neurosci Biobehav Rev. 2011 Jan;35(3):688-98
pubmed: 20826179
J Psychiatry Neurosci. 2014 May;39(3):170-7
pubmed: 24119793
Hum Brain Mapp. 2009 Jan;30(1):312-26
pubmed: 18072281
Dev Cogn Neurosci. 2015 Aug;14:50-61
pubmed: 26143154
JAMA. 2001 Dec 26;286(24):3120-5
pubmed: 11754678
Arch Gen Psychiatry. 2003 Jun;60(6):601-9
pubmed: 12796223
Annu Rev Public Health. 2013;34:119-38
pubmed: 23514317
Neurosci Lett. 1993 Nov 26;163(1):109-13
pubmed: 8295722
Am J Psychiatry. 1975 Mar;132(3):285-7
pubmed: 1115273
J Psychiatr Res. 2012 Nov;46(11):1449-55
pubmed: 22868048
J Clin Psychiatry. 1999;60 Suppl 2:57-62; discussion 75-6, 113-6
pubmed: 10073389
Neuroimage. 2011 Jan 15;54(2):1607-14
pubmed: 20832482
Biol Psychiatry. 2009 Sep 1;66(5):516-21
pubmed: 19427632
Arch Gen Psychiatry. 2011 Mar;68(3):241-51
pubmed: 21383262
Mol Psychiatry. 2007 Apr;12(4):360-6
pubmed: 17389903
Bipolar Disord. 2012 Feb;14(1):80-9
pubmed: 22329475
Arch Gen Psychiatry. 2005 Oct;62(10):1097-106
pubmed: 16203955
Annu Rev Neurosci. 2001;24:167-202
pubmed: 11283309
J Consult Clin Psychol. 1979 Apr;47(2):343-52
pubmed: 469082
J Clin Psychol. 1995 Nov;51(6):768-74
pubmed: 8778124
J Clin Psychiatry. 2015 Mar;76(3):293-4
pubmed: 25830448
Psychiatry Res. 1995 Jul 28;57(2):169-80
pubmed: 7480383
Curr Top Behav Neurosci. 2011;5:227-45
pubmed: 25236558
J Geriatr Psychiatry Neurol. 2010 Sep;23(3):171-84
pubmed: 20430976
Biol Psychiatry. 2011 Jun 15;69(12):1140-6
pubmed: 20728878
J Affect Disord. 2005 Jun;86(2-3):281-7
pubmed: 15935248
Acta Psychiatr Scand. 2004 Dec;110(6):446-51
pubmed: 15521829
Bipolar Disord. 2013 Jun;15(4):365-76
pubmed: 23621705
Brain Imaging Behav. 2017 Oct;11(5):1515-1525
pubmed: 27738995
Crisis. 2010;31(6):311-6
pubmed: 21190929
J Affect Disord. 2011 Dec;135(1-3):139-47
pubmed: 21807414
Am J Psychiatry. 2010 Nov;167(11):1381-90
pubmed: 20843871

Auteurs

Siyan Fan (S)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA. Electronic address: siyan.fan@yale.edu.

Elizabeth T C Lippard (ETC)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA; Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA; Department of Psychiatry, Dell Medical School, University of Texas at Austin, Austin, TX, USA.

Anjali Sankar (A)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Amanda Wallace (A)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Jennifer A Y Johnston (JAY)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Fei Wang (F)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Brian Pittman (B)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Linda Spencer (L)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA.

Maria A Oquendo (MA)

Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Hilary P Blumberg (HP)

Departments of Psychiatry, Yale School of Medicine, New Haven, CT, USA; Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA; Child Study Center, Yale School of Medicine, New Haven, CT, USA.

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Classifications MeSH