The Interaction Between Brain-Derived Neurotrophic Factor Levels and Alcohol Consumption, Sleep Disturbance and Sex-Hormones in Alcohol Use Disorders

Abstract Aims Brain-derived neurotrophic factor (BDNF) levels may be associated with alcohol use disorders (AUD) and alcohol consumption, correlate with sleep disturbance and be influenced by sex differences and sex hormones. These associations have not been examined in a single sample accounting fo...

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Veröffentlicht in:Alcohol and alcoholism (Oxford) 2023-03, Vol.58 (2), p.209-215
Hauptverfasser: Kolla, Bhanu Prakash, Winham, Stacey J, Ho, Ada Man-Choi, Mansukhani, Meghna P, Loukianova, Larissa L, Pazdernik, Vanessa, Karpyak, Victor M
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Sprache:eng
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Zusammenfassung:Abstract Aims Brain-derived neurotrophic factor (BDNF) levels may be associated with alcohol use disorders (AUD) and alcohol consumption, correlate with sleep disturbance and be influenced by sex differences and sex hormones. These associations have not been examined in a single sample accounting for all these factors. Methods Data from 190 participants (29.4% female) with AUD were utilized. Sleep quality, craving intensity, depression, anxiety and alcohol consumption were assessed using the Pittsburgh Sleep Quality Index (PSQI), Penn Alcohol Craving Scale (PACS), Patient Health Questionnaire-9 (PHQ-9), Generalized Anxiety Disorder-7 (GAD-7) and Timeline Follow Back for 90 days(TLFB 90). Inventory of Drug Taking Situations (IDTS) assessed the tendency to drink in positive/negative emotional states. Serum BDNF (sBDNF) and plasma sex hormones (estrogen, progesterone, testosterone, FSH and SHBG) were measured. Pearson correlation analyses were used to examine the association between sBDNF and these measures in the entire sample and in men and women separately. Higher order interaction effects between these factors were evaluated for their association with sBDNF using a backward selection model. Results No significant correlations between sBDNF levels and sex hormones, PSQI, PHQ-9, PACS, IDTS scores and alcohol consumption were found (all P-values > 0.05). sBDNF levels were negatively correlated with GAD-7 scores in men (r = −0.1841; P = 0.03). When considering all quadratic and two-way interactions among PSQI, PHQ-9, GAD-7, mean and max drinks/day, number of drinking days, heavy drinking days, and sex no higher order moderating effects of sBDNF levels were found. Conclusion Our study revealed no significant associations between sBDNF and alcohol measures, sleep, depression and sex hormones suggesting limited utility as a biomarker. Short Summary: This was the first study to examine the association between sBDNF and alcohol consumption, severity of depression, and sleep disturbance and examine whether there were higher-order interaction effects between these factors. There were no significant associations between sBDNF and alcohol measures, sleep, depression and sex-hormones suggesting that sBDNF has limited utility as a biomarker.
ISSN:0735-0414
1464-3502
1464-3502
DOI:10.1093/alcalc/agad001