AI Article Synopsis

  • Previous research indicates that sex hormones play a role in alcohol use disorder (AUD), but studies focusing on the sulphated form of dehydroepiandrosterone (DHEA-S) are limited, especially in relation to its neuromodulatory effects in the brain.
  • A study compared DHEA-S levels between 200 AUD inpatients and 240 healthy controls, finding lower levels in female AUD patients and a decrease in both genders from initial assessment to follow-up, along with correlations between DHEA-S concentrations and alcohol cravings and liver enzyme activity in patients.
  • The findings suggest that DHEA-S may be linked to AUD and its related characteristics, leading to the need for more research on its potential influence on alcohol cravings and

Article Abstract

Previous studies have established a role of sex hormones in alcohol use disorder (AUD).Only few clinical investigations with low numbers of patients with AUD have focused on the sulphated form of dehydroepiandrosterone (DHEA-S), despite its function as a neuromodulating sex steroid on receptors in the central nervous system (γ-aminobutyric acid type A, N-methyl-D-aspartate, sigma-1 receptors). DHEA-S serum levels were compared between 200 inpatients with AUD (44% women) admitted for withdrawal treatment and 240 healthy controls (45% women) and analysed longitudinally in patients from early abstinence (baseline) to a median of 5 days later. We also correlated DHEA-S levels with craving, liver enzyme activities, and prospective alcohol-related readmissions during a 24-month follow-up. DHEA-S concentrations were lower in female patients than in female healthy controls during baseline (70%) and decreased from baseline to follow-up in the female and male patients groups (down to: women, 92%; men, 76%). Baseline DHEA-S concentrations correlated with the total and obsessive subscales of the Obsessive-Compulsive Drinking Scale and with maximum visual analogue scale craving scores in female patients (Rho ≤ -0.240) and gamma-glutamyl transferase activity in female (Rho = -0.292) and male (Rho = -0.391) patients. DHEA-S did not significantly predict outcome. We found interactions with smoking behaviour and age. This is the first study based on large cohorts of inpatients with AUD undergoing a qualified detoxification treatment to provide sex-separated evidence for associations of DHEA-S serum concentrations with AUD and related phenotypes. The results stimulate further investigations whether DHEA-S directly influences alcohol craving building a basis to develop sex-sensitive prevention and treatment strategies.

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Source
http://dx.doi.org/10.1111/adb.13135DOI Listing

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