Alterations in connectivity of the bed nucleus of the stria terminalis during early abstinence in individuals with alcohol use disorder.

Elizabeth A Flook, Brandee Feola, Margaret M Benningfield, Marisa M Silveri, Danny G Winder, Jennifer Urbano Blackford
Author Information
  1. Elizabeth A Flook: Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA. ORCID
  2. Brandee Feola: Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA. ORCID
  3. Margaret M Benningfield: Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA. ORCID
  4. Marisa M Silveri: Neurodevelopmental Laboratory on Addictions and Mental Health, Brain Imaging Center, McLean Hospital, Belmont, MA, USA. ORCID
  5. Danny G Winder: Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA. ORCID
  6. Jennifer Urbano Blackford: Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA. ORCID

Abstract

BACKGROUND: For individuals with Alcohol Use Disorder (AUD), long-term recovery is difficult in part due to symptoms of anxiety that occur during early abstinence and can trigger relapse. Research in rodent models of AUD has identified the bed nucleus of the stria terminalis (BNST), a small, sexually dimorphic, subcortical region, as critical for regulating anxiety-like behaviors during abstinence, particularly in female mice. Furthermore, prolonged alcohol use and subsequent abstinence alter BNST afferent and efferent connections to other brain regions. To our knowledge, however, no studies of early abstinence have investigated BNST structural connectivity in humans during abstinence; this study addresses that gap.
METHODS: Nineteen participants with AUD currently in early abstinence and 20 healthy controls completed a diffusion tensor imaging (DTI) scan. BNST structural connectivity was evaluated using probabilistic tractography. A linear mixed model was used to test between-groups differences in BNST network connectivity. Exploratory analyses were conducted to test for correlations between BNST connectivity and alcohol use severity and anxiety within the abstinence group. Sex was included as a factor for all analyses.
RESULTS: The BNST showed stronger structural connectivity with the BNST network in early abstinence women than in control women, which was not seen in men. Women also showed region-specific differences, with stronger BNST-hypothalamus structural connectivity but weaker vmPFC-BNST structural connectivity than men. Exploratory analyses also demonstrated a relationship between alcohol use severity and vmPFC-BNST structural connectivity that was moderated by sex.
CONCLUSIONS: This study is the first to demonstrate BNST structural connectivity differences in early abstinence and revealed key sex differences. The sex-specific differences in BNST structural connectivity during early abstinence could underlie known sex differences in abstinence symptoms and relapse risk and help to inform potential sex-specific treatments.

Keywords

References

  1. Alcohol Clin Exp Res. 2019 Oct;43(10):2000-2013 [PMID: 31403699]
  2. J Comp Neurol. 1990 Dec 22;302(4):697-706 [PMID: 1707064]
  3. Alcohol. 2018 Nov;72:33-47 [PMID: 30217435]
  4. Neuropsychopharmacology. 2016 Jan;41(1):126-41 [PMID: 26105138]
  5. J Neurosci. 2019 Jan 16;39(3):472-484 [PMID: 30478032]
  6. Prog Neuropsychopharmacol Biol Psychiatry. 2018 Dec 20;87(Pt A):108-125 [PMID: 29330137]
  7. Psychiatry Res. 2009 Jul 15;173(1):22-30 [PMID: 19442492]
  8. Addict Biol. 2010 Apr;15(2):169-84 [PMID: 20148778]
  9. Cortex. 2015 May;66:60-8 [PMID: 25800506]
  10. Pharmacol Rev. 2016 Apr;68(2):242-63 [PMID: 26772794]
  11. Neuroscience. 1988 Oct;27(1):1-39 [PMID: 3059226]
  12. Hum Brain Mapp. 2015 Oct;36(10):4076-88 [PMID: 26178381]
  13. Neuron. 2004 Mar 4;41(5):825-37 [PMID: 15003180]
  14. Addict Biol. 2017 Mar;22(2):468-478 [PMID: 26537217]
  15. Behav Res Ther. 1990;28(6):487-95 [PMID: 2076086]
  16. Nat Commun. 2019 Mar 18;10(1):1238 [PMID: 30886240]
  17. J Neurosci. 2010 May 19;30(20):7023-7 [PMID: 20484644]
  18. J Neurosci. 1999 Oct 15;19(20):RC35 [PMID: 10516337]
  19. Psychophysiology. 2006 Jul;43(4):344-56 [PMID: 16916430]
  20. Drug Alcohol Depend. 2017 Jun 1;175:42-50 [PMID: 28384535]
  21. Neuroimage. 2002 Mar;15(3):708-18 [PMID: 11848714]
  22. Cortex. 2015 Mar;64:281-8 [PMID: 25569763]
  23. Drug Alcohol Depend. 2015 Nov 1;156:1-13 [PMID: 26371405]
  24. JAMA Psychiatry. 2013 Jul;70(7):727-39 [PMID: 23636842]
  25. Neuroimage. 2014 May 1;91:311-23 [PMID: 24444996]
  26. J Clin Psychiatry. 2006 Feb;67(2):247-57 [PMID: 16566620]
  27. J Stud Alcohol. 1982 Nov;43(11):1157-70 [PMID: 7182675]
  28. Hum Brain Mapp. 2002 Nov;17(3):143-55 [PMID: 12391568]
  29. J Consult Clin Psychol. 1988 Dec;56(6):893-7 [PMID: 3204199]
  30. Alcohol. 2018 Nov;72:75-88 [PMID: 30322482]
  31. eNeuro. 2018 Jul 2;5(3): [PMID: 29971248]
  32. Neuroimage. 2003 Oct;20(2):870-88 [PMID: 14568458]
  33. Am J Psychiatry. 2020 Nov 1;177(11):1048-1059 [PMID: 32854534]
  34. J Psychiatry Neurosci. 2019 Apr 09;44(5):313-323 [PMID: 30964612]
  35. Neuroimage. 2020 Apr 15;210:116555 [PMID: 31954845]
  36. Psychol Med. 2017 Nov;47(15):2675-2688 [PMID: 28485259]
  37. Nat Rev Neurosci. 2017 Feb;18(2):115-126 [PMID: 28053326]
  38. Biol Psychiatry. 2005 Apr 1;57(7):768-76 [PMID: 15820234]
  39. J Anxiety Disord. 2007;21(1):105-17 [PMID: 16647833]
  40. J Neuroendocrinol. 2016 Dec;28(12): [PMID: 27805752]
  41. Neuropsychiatr Dis Treat. 2011;7:65-75 [PMID: 21430796]
  42. Neurosci Lett. 2015 Nov 3;608:45-50 [PMID: 26434353]
  43. Biol Psychiatry. 2018 Apr 15;83(8):638-647 [PMID: 29275839]
  44. Neuropharmacology. 2020 May 15;168:107759 [PMID: 31494142]
  45. Neuroimage. 2018 Mar;168:392-402 [PMID: 28392491]
  46. J Neural Transm (Vienna). 2001;108(7):887-94 [PMID: 11515754]
  47. Proc Natl Acad Sci U S A. 2015 Jul 21;112(29):9118-22 [PMID: 26150480]
  48. Hum Brain Mapp. 2018 Mar;39(3):1291-1312 [PMID: 29235190]
  49. Neuroimage. 2017 Sep;158:242-259 [PMID: 28684331]
  50. Neuroscience. 2004;123(3):793-803 [PMID: 14706792]
  51. Neuropsychopharmacology. 2019 Feb;44(3):526-537 [PMID: 30390064]
  52. Neuropsychopharmacology. 2001 Feb;24(2):97-129 [PMID: 11120394]
  53. Brain Res Brain Res Rev. 2001 Dec;38(1-2):192-246 [PMID: 11750933]
  54. Brain Struct Funct. 2016 Sep;221(7):3561-9 [PMID: 26454651]
  55. Cereb Cortex. 2013 Jan;23(1):114-26 [PMID: 22267308]
  56. Neurobiol Aging. 2006 Jul;27(7):994-1009 [PMID: 15964101]
  57. Mod Probl Pharmacopsychiatry. 1987;22:141-73 [PMID: 2885745]
  58. Neuroimage Clin. 2018 Mar 22;19:98-105 [PMID: 30035007]
  59. Curr Neuropharmacol. 2013 Mar;11(2):141-59 [PMID: 23997750]
  60. Depress Anxiety. 2019 Aug;36(8):666-675 [PMID: 30953446]
  61. Neuropharmacology. 2011 Jun;60(7-8):1318-25 [PMID: 21276806]
  62. Lancet Psychiatry. 2016 Aug;3(8):760-773 [PMID: 27475769]
  63. Psychoneuroendocrinology. 2011 Oct;36(9):1312-26 [PMID: 21481539]
  64. Brain Imaging Behav. 2017 Aug;11(4):1006-1017 [PMID: 27448160]
  65. J Psychiatr Res. 2011 Aug;45(8):1027-35 [PMID: 21439576]
  66. Am J Psychiatry. 2008 Sep;165(9):1179-84 [PMID: 18593776]
  67. PLoS One. 2015 Nov 03;10(11):e0142042 [PMID: 26529515]
  68. Mol Psychiatry. 2012 Feb;17(2):132-41 [PMID: 21788943]
  69. J Neurosci. 2014 Aug 20;34(34):11261-73 [PMID: 25143607]

Grants

  1. R21 AA025385/NIAAA NIH HHS
  2. T32 MH018921/NIMH NIH HHS
  3. T32 GM007347/NIGMS NIH HHS
  4. UL1 TR002243/NCATS NIH HHS
  5. F30 AA027418/NIAAA NIH HHS
  6. T32 GM152284/NIGMS NIH HHS
  7. P50 HD103537/NICHD NIH HHS

MeSH Term

Adult
Alcohol Abstinence
Alcoholism
Anxiety
Case-Control Studies
Diffusion Tensor Imaging
Female
Humans
Male
Neural Pathways
Prefrontal Cortex
Septal Nuclei
Sex Factors
Young Adult

Word Cloud

Created with Highcharts 10.0.0abstinenceconnectivityBNSTstructuralearlydifferencesalcoholuseAUDbednucleusstriaterminalisanalysessexindividualssymptomsanxietyrelapsestudydiffusiontensorimagingtestnetworkExploratoryseverityshowedstrongerwomenmenalsovmPFC-BNSTsex-specificdisorderBACKGROUND:AlcoholUseDisorderlong-termrecoverydifficultpartdueoccurcantriggerResearchrodentmodelsidentifiedsmallsexuallydimorphicsubcorticalregioncriticalregulatinganxiety-likebehaviorsparticularlyfemalemiceFurthermoreprolongedsubsequentalterafferentefferentconnectionsbrainregionsknowledgehoweverstudiesinvestigatedhumansaddressesgapMETHODS:Nineteenparticipantscurrently20healthycontrolscompletedDTIscanevaluatedusingprobabilistictractographylinearmixedmodelusedbetween-groupsconductedcorrelationswithingroupSexincludedfactorRESULTS:controlseenWomenregion-specificBNST-hypothalamusweakerdemonstratedrelationshipmoderatedCONCLUSIONS:firstdemonstraterevealedkeyunderlieknownriskhelpinformpotentialtreatmentsAlterations

Similar Articles

Cited By