Fluorodeoxyglucose positron emission tomography scans in patients with alcohol use disorder DOI
Marie‐Cécile Bralet, Serge A. Mitelman, Chelain R. Goodman

и другие.

Alcoholism Clinical and Experimental Research, Год журнала: 2022, Номер 46(6), С. 994 - 1010

Опубликована: Апрель 22, 2022

Diminished uptake of fluorodeoxyglucose (FDG) has been observed in patients with alcohol use disorder (AUD) but little statistical contrast the regional brain deficits undertaken. This study examined prefrontal cortex inter-regional Brodmann area differences to delineate patterns associated behavioral, neurotransmitter, and general toxicity hypotheses cerebral involvement AUD.We obtained data from FDG positron emission tomography (PET) anatomical magnetic resonance imaging (MRI) for 87 AUD 41 age- sex-matched healthy volunteers. Patients were dependent had negative breathalyzer tests at time imaging. They assessed Beck Depression Inventory, Alcohol Urge Questionnaire, Obsessive Compulsive Drinking Scale, Spielberger State/Trait Anxiety Buss-Durkee Hostility Drinker Inventory Consequences (DrInC). PET images co-registered MRI both voxel × mapping stereotaxic regions interest obtained.Compared volunteers, lower relative metabolic rates frontal, temporal, parietal lobes, localizable most prominently dorsolateral nearly all orbital cortex, superior temporal gyrus, inferior lobule. In contrast, medial orbitofrontal anterior cingulate subcortical structures (thalamus, cerebellum, ventral striatum, dorsal raphe nucleus) significantly greater. The severity alcohol-related consequences as by DrInC scale was highly metabolism caudate, prefrontal, frontopolar, anteroposterior cortex.Despite widespread abnormalities, decreases marked frontal executive areas, consistent diminished impulse control, increases prominent striatum a suppressed reward system.

Язык: Английский

Associations between alcohol consumption and gray and white matter volumes in the UK Biobank DOI Creative Commons
Remi Daviet, Gökhan Aydogan, Kanchana Jagannathan

и другие.

Nature Communications, Год журнала: 2022, Номер 13(1)

Опубликована: Март 4, 2022

Abstract Heavy alcohol consumption has been associated with brain atrophy, neuronal loss, and poorer white matter fiber integrity. However, there is conflicting evidence on whether light-to-moderate shows similar negative associations structure. To address this, we examine the between intake structure using multimodal imaging data from 36,678 generally healthy middle-aged older adults UK Biobank, controlling for numerous potential confounds. Consistent prior literature, find macrostructure microstructure. Specifically, negatively global volume measures, regional gray volumes, Here, show that microstructure are already apparent in individuals consuming an average of only one to two daily units, become stronger as increases.

Язык: Английский

Процитировано

137

Hazardous drinking and alcohol use disorders DOI
James MacKillop, Roberta Agabio, Sarah W. Feldstein Ewing

и другие.

Nature Reviews Disease Primers, Год журнала: 2022, Номер 8(1)

Опубликована: Дек. 22, 2022

Язык: Английский

Процитировано

93

Alcohol-Induced Oxidative Stress and the Role of Antioxidants in Alcohol Use Disorder: A Systematic Review DOI Creative Commons
Evangelia Eirini Tsermpini, Anja Plemenitaš Ilješ, Vita Dolžan

и другие.

Antioxidants, Год журнала: 2022, Номер 11(7), С. 1374 - 1374

Опубликована: Июль 15, 2022

Alcohol use disorder (AUD) is a highly prevalent, comorbid, and disabling disorder. The underlying mechanism of ethanol neurotoxicity the involvement oxidative stress still not fully elucidated. However, metabolism has been associated with increased through alcohol dehydrogenase, microsomal oxidation system, catalase metabolic pathways. We searched PubMed genome-wide association studies (GWAS) catalog databases to review literature systematically summarized findings focusing on AUD abstinence in relation stress. In addition, we reviewed ClinicalTrials.gov resource US National Library Medicine identify all ongoing completed clinical trials that include therapeutic interventions based antioxidants. retrieved preclinical show impacts genetics, metabolism, inflammation, neurodegeneration.

Язык: Английский

Процитировано

89

Blood-based epigenome-wide association study and prediction of alcohol consumption DOI Creative Commons
Elena Bernabeu, Aleksandra D. Chybowska, Jacob K. Kresovich

и другие.

Clinical Epigenetics, Год журнала: 2025, Номер 17(1)

Опубликована: Янв. 25, 2025

Abstract Alcohol consumption is an important risk factor for multiple diseases. It typically assessed via self-report, which open to measurement error through recall bias. Instead, molecular data such as blood-based DNA methylation (DNAm) could be used derive a more objective measure of alcohol by incorporating information from cytosine-phosphate-guanine (CpG) sites known linked the trait. Here, we explore epigenetic architecture self-reported weekly units in Generation Scotland study. We first create score (EpiScore) using elastic net penalized linear regression. effect pre-filtering CpG features ahead net, well differential patterns sex and consumed last week relative average week. The final EpiScore was trained on 16,717 individuals tested four external cohorts: Lothian Birth Cohorts (LBC) 1921 1936, Sister Study, Avon Longitudinal Study Parents Children (total N across studies > 10,000). maximum Pearson correlation between within cohort ranged 0.41 0.53. In LBC1936, higher levels had significant associations with poorer global brain imaging metrics, whereas did not. Finally, identified two novel loci Bayesian regression epigenome-wide association study consumption. Together, these findings show how DNAm can objectively characterize that associate health, unlike estimates.

Язык: Английский

Процитировано

0

Structural brain changes associated with risky drinking in late-life depression DOI Creative Commons
David C. Steffens, Lihong Wang, Kevin J. Manning

и другие.

Deleted Journal, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Factors influencing aging in high-income countries DOI
Jin Hui Joo, Daniel E. Jimenez,

Omar Muñoz Abraham

и другие.

Oxford University Press eBooks, Год журнала: 2025, Номер unknown, С. 23 - 34

Опубликована: Фев. 1, 2025

Abstract Aging is a critical issue for families, policymakers, healthcare providers, and society at large. This chapter explores the biological, environmental, behavioural, psychosocial factors that influence experience of aging in high-income countries. Age-related decline, emergence chronic disease, social isolation, functional changes occur context urbanization, population shifts, limitations workforce among other factors. Responses to include programmes support informal carers, implementation integrated models healthcare, mitigation impact health well-being. In parallel ideas age-related concepts positive emphasize independence minimize disability also countries, although these benefits security are unequally experienced due differential exposure environments promote well-being or illness. Therapies disease policies bolster poorly resourced decrease harmful exposures need be implemented within framework equity.

Язык: Английский

Процитировано

0

Alcohol and aging: Next‐generation epigenetic clocks predict biological age acceleration in individuals with alcohol use disorder DOI Creative Commons

Theodore Perlstein,

Jeesun Jung,

A Wagner

и другие.

Alcohol Clinical and Experimental Research, Год журнала: 2025, Номер unknown

Опубликована: Март 28, 2025

Abstract Background Chronic heavy alcohol use is a major risk factor for premature aging and age‐related diseases. DNA methylation (DNAm)‐based epigenetic clocks are novel tools predicting biological age. However, the newest configurations, causality‐enriched clocks, have not been assessed in context of consumption disorder (AUD). Methods Epigenetic was evaluated sample 615 individuals (372 AUD patients 243 healthy controls) by applying GrimAge Version 1 (V1) 2 (V2) alongside three (CausAge, DamAge, AdaptAge). A linear model controlling diagnosis, sex, race, BMI, smoking status, five blood cell types leveraged to test associations between alcohol‐related metrics age‐adjusted clocks. Results V1 V2 maintained significant with drinking behavior measures within total both young (<40 years old) old (≥40 subgroups. Generally, slightly outperformed V1, while none demonstrated AUD. subgroup, DamAge had association number drinks. Across age subgroups, liver function enzymes, consistently sustained stronger compared V1. Among fourth‐generation exhibited gamma‐glutamyl transferase (GGT) aspartate aminotransferase subgroup; CausAge displayed GGT sample. Examining clinical biomarkers, showed improved C‐reactive protein Conclusions Overall, we observed moderately performance majority parameters tested. The lacked but demonstrate complexities inspire further research dynamics.

Язык: Английский

Процитировано

0

Reactive Oxygen Species as a Common Pathological Link Between Alcohol Use Disorder and Alzheimer’s Disease with Therapeutic Implications DOI Open Access
Ho-Young Song, Jiyong Lee, Yeeun Lee

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(7), С. 3272 - 3272

Опубликована: Апрель 1, 2025

Chronic alcohol consumption leads to excessive production of reactive oxygen species (ROS), driving oxidative stress that contributes both use disorder (AUD) and Alzheimer's disease (AD). This review explores how ROS-mediated mitochondrial dysfunction neuroinflammation serve as shared pathological mechanisms linking these conditions. We highlight the role alcohol-induced damage in exacerbating neurodegeneration compare ROS-related pathways AUD AD. Finally, we discuss emerging therapeutic strategies, including antioxidants inflammasome inhibitors, target mitigate neurodegeneration. Understanding overlapping may provide new insights for preventing treating ROS-driven neurodegenerative disorders.

Язык: Английский

Процитировано

0

Accelerated Aging of the Amygdala in Alcohol Use Disorders: Relevance to the Dark Side of Addiction DOI Creative Commons
Dardo Tomasi, Corinde E. Wiers, Peter Manza

и другие.

Cerebral Cortex, Год журнала: 2021, Номер 31(7), С. 3254 - 3265

Опубликована: Янв. 19, 2021

Abstract Here we assessed changes in subcortical volumes alcohol use disorder (AUD). A simple morphometry-based classifier (MC) was developed to identify that distinguished 32 healthy controls (HCs) from 33 AUD patients, who were scanned twice, during early and later withdrawal, assess the effect of abstinence on MC-features (Discovery cohort). We validated novel an independent Validation cohort (19 patients 20 HCs). MC-accuracy reached 80% (Discovery) 72% (Validation). MC features included hippocampus, amygdala, cerebellum, putamen, corpus callosum, brain stem, which smaller showed stronger age-related decreases than HCs, ventricles cerebrospinal fluid, larger older participants. The volume amygdala a positive association with anxiety negative urgency AUD. Repeated imaging third week detoxification revealed slightly consistent partial recovery abstinence. steeper age-associated volumetric reductions stress- reward-related regions are accelerated aging, whereas amygdalar associations support its involvement “dark side addiction”.

Язык: Английский

Процитировано

25

The Relaxin-3 Receptor, RXFP3, Is a Modulator of Aging-Related Disease DOI Open Access
Hanne Leysen, Deborah Walter,

Lore Clauwaert

и другие.

International Journal of Molecular Sciences, Год журнала: 2022, Номер 23(8), С. 4387 - 4387

Опубликована: Апрель 15, 2022

During the aging process our body becomes less well equipped to deal with cellular stress, resulting in an increase unrepaired damage. This causes varying degrees of impaired functionality and increased risk mortality. One most effective anti-aging strategies involves interventions that combine simultaneous glucometabolic support augmented DNA damage protection/repair. Thus, it seems prudent develop therapeutic target this combinatorial approach. Studies have shown ADP-ribosylation factor (ARF) GTPase activating protein GIT2 (GIT2) acts as a keystone process. can control both repair glucose metabolism. Through vivo co-regulation analyses was found forms close coexpression-based relationship relaxin-3 receptor (RXFP3). Cellular RXFP3 expression is directly affected by oxidative stress. Overexpression or stimulation receptor, its endogenous ligand relaxin 3 (RLN3), regulate response processes. Interestingly, RLN3 insulin-like peptide has been multiple disease processes linked mechanisms, e.g., anxiety, depression, memory dysfunction, appetite, anti-apoptotic mechanisms. Here we discuss molecular mechanisms underlying various roles RXFP3/RLN3 signaling age-related disorders.

Язык: Английский

Процитировано

15