White matter microstructural correlates of relapse in alcohol dependence. (30th November 2018)

• Record Type: Journal Article
• Authors: Zou, Yukai; Murray, Donna E.; Durazzo, Timothy C.; Schmidt, Thomas P.; Murray, Troy A.; Meyerhoff, Dieter J.
• Is Part Of: Psychiatry research. Volume 281(2018)
• Page Start: 92
• Page End: 100
• Publication Date: 2018-11-30
• Subjects: Diffusion tensor imaging -- White matter -- Alcohol use disorder -- Relapse risk -- Abstinence -- Smoking; Psychiatry -- Periodicals; Brain -- Imaging -- Periodicals; Psychiatry -- Periodicals; Diagnostic Imaging -- Periodicals; Psychiatrie -- Périodiques; Cerveau -- Imagerie pour le diagnostic -- Périodiques; 616.890754
• DOI: 10.1016/j.pscychresns.2018.09.004
• Languages: English
• ISSNs: 0925-4927

Abstract

Abstract: Identification of neural correlates of relapse to alcohol after treatment is clinically important as it may inform better substance abuse treatment. Few studies have specifically analyzed the white matter microstructure in treatment seekers as it might relate to relapse risk versus long-term abstinence. Using 4 Tesla diffusion tensor imaging, we compared two groups of one-month-abstinent treatment-seekers, who were classified based on their drinking status between six and nine months after treatment initiation. We hypothesized that subsequent relapsers had greater white matter microstructural deficits in specific brain regions than long-term abstainers. At one month of abstinence, 37 future relapsers versus 25 future abstainers had lower fractional anisotropy (a measure of axonal organization and membrane integrity) in the corpus callosum and right stria terminalis/fornix, higher diffusivity in the genu of the corpus callosum, left and right stria terminalis/fornix, and lower diffusivity in left anterior corona radiata. These differences existed despite similar lifetime and recent drinking and smoking histories in the groups. Longer smoking duration in relapsers was associated with lower fractional anisotropy in right stria terminalis/fornix. The study identified specific microstructural biomarkers of alcohol relapse risk in adults, contributing to the definition of a neurobiological relapse risk profile in alcohol use disorder.