AUD
alcohol use disorders
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.
The molecular mechanisms regulating the development and progression of alcohol use disorder (AUD) are largely unknown.
Alcohol use disorder (AUD) affects men more than women globally with significant years of life loss to disability in low, middle and well-developed countries.
Participants were drawn from our ongoing longitudinal studies of people with HIV infection, alcohol use disorder (AUD), HIV + AUD comorbidity, and controls.
Genetic variants were selected on the basis of associations with alcohol consumption (n = 941,280) and alcohol use disorder (AUD) (n = 57,564 cases).
BACKGROUND People with alcohol use disorder (AUD) may be at higher risk for COVID-19.
OBJECTIVE To the authors' knowledge, no data have been reported on dopamine fluctuations on subsecond timescales in humans with alcohol use disorder (AUD).
OBJECTIVES Because alcohol use disorder (AUD) is often accompanied by mood disorder (MD) and both alcoholism and depression result in activation of the immune system, this study compares serum cytokine levels in the presence of co-morbidity with those in either AUD or MD alone.
Observational analysis findings indicated that heavy alcohol drinkers and those with alcohol use disorder (AUD) were significantly more likely to have shorter telomeres — an essential part of our chromosomes linked to aging and the onset of various health concerns.
Genetic variants were selected on the basis of associations with alcohol consumption (n = 941,280) and alcohol use disorder (AUD) (n = 57,564 cases).