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Regional cortical brain volumes at treatment entry relates to post treatment WHO risk drinking levels in those with alcohol use disorder.
Durazzo, Timothy C; Stephens, Lauren H; Kraybill, Eric P; May, April C; Meyerhoff, Dieter J.
Affiliation
  • Durazzo TC; Sierra-Pacific Mental Illness Research and Education Clinical Centers, VA Palo Alto Health Care System, USA; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, USA. Electronic address: tdurazzo@stanford.edu.
  • Stephens LH; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, USA.
  • Kraybill EP; Sierra-Pacific Mental Illness Research and Education Clinical Centers, VA Palo Alto Health Care System, USA.
  • May AC; Sierra-Pacific Mental Illness Research and Education Clinical Centers, VA Palo Alto Health Care System, USA; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, USA.
  • Meyerhoff DJ; Center for Imaging of Neurodegenerative Diseases (CIND), San Francisco VA Medical Center, San Francisco, CA, USA; Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, USA.
Drug Alcohol Depend ; 255: 111082, 2024 Feb 01.
Article in En | MEDLINE | ID: mdl-38219355
ABSTRACT

BACKGROUND:

Abstinence following treatment for alcohol use disorder (AUD) is associated with significant improvements in psychiatric and physical health, however, recent studies suggest resumption of low risk levels of alcohol use can also be beneficial. The present study assessed whether post-treatment levels of alcohol use were associated with cortical brain volumedifferences at treatment entry.

METHODS:

Individuals seeking treatment for AUD (n=75) and light/non-drinking controls (LN, n=51) underwent 1.5T magnetic resonance imaging. The volumes of 34 bilateral cortical regions of interest (ROIs) were quantitated via FreeSurfer. Individuals with AUD were classified according to post-treatment alcohol consumption using the WHO risk drinking levels (abstainers AB; low risk RL; or higher risk RH). Regional volumes for AB, RL and RH, at treatment entry, were compared to LN.

RESULTS:

Relative to LN, AB demonstrated smaller volumes in 18/68 (26%), RL in 24/68 (35%) and RH in 34/68 (50%) ROIs with the largest magnitude volume differences observed between RH and LN. RH and RL reported a higher frequency of depressive disorders than AB. Among RH and RL, level of depressive and anxiety symptomatology were associated with daily number of drinks consumed after treatment.

CONCLUSIONS:

Volumetric differences, at treatment entry, in brain regions implicated in executive function and salience networks corresponded with post-treatment alcohol consumption levels suggesting that pre-existing differences in neural integrity may contribute to treatment outcomes. Depressive and anxiety symptomatology was also associated with brain morphometrics and alcohol use patterns, highlighting the importance of effectively targeting these conditions during AUD treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcoholism Type of study: Etiology_studies / Risk_factors_studies Limits: Humans Language: En Journal: Drug Alcohol Depend Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcoholism Type of study: Etiology_studies / Risk_factors_studies Limits: Humans Language: En Journal: Drug Alcohol Depend Year: 2024 Document type: Article