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1 e-time physical activity, smoking, diet, and alcohol consumption.
2 (MC) are the most accepted models of chronic alcohol consumption.
3 ioid receptor antagonist, in the BLA reduced alcohol consumption.
4 s or iMSNs of mice and measured the level of alcohol consumption.
5 aine intake, nor did access to cocaine alter alcohol consumption.
6 3782886 (BRAP) reduced the risk of excessive alcohol consumption.
7 in the BNST in an adaptive response to limit alcohol consumption.
8 abstain from alcohol or continue their usual alcohol consumption.
9 isms were used as instrumental variables for alcohol consumption.
10 luate the effects of this change on RTAs and alcohol consumption.
11 inase (ERK) in an adaptive response to limit alcohol consumption.
12 ic Aldh2 deficiency did not affect voluntary alcohol consumption.
13 r rats and mice, and in turn, FGF2 increases alcohol consumption.
14 e dorsomedial striatum (DMS), which promotes alcohol consumption.
15 ons that occur from suddenly ceasing chronic alcohol consumption.
16 central and unanticipated role in excessive alcohol consumption.
17 position and function of LPLs independent of alcohol consumption.
18 titative phenotype based on maximum habitual alcohol consumption.
19 es may play a causal role on AAF mediated by alcohol consumption.
20 eved hyperalgesia and decreased relapse-like alcohol consumption.
21 ed negative binomial regression analysis for alcohol consumption.
22 ity, education, marital status, smoking, and alcohol consumption.
23 trasound criteria for fatty liver and absent alcohol consumption.
24 er liver function, which is a marker of high alcohol consumption.
25 sed on histologic analysis, compared with no alcohol consumption.
26 isms underlying the development of excessive alcohol consumption.
27 regulatory and tolerance-inducing effect of alcohol consumption.
28 ied by ADH1B*2, even after we controlled for alcohol consumption.
29 icate that ghrelin receptor blockade reduces alcohol consumption.
30 lved in the negative regulation of excessive alcohol consumption.
31 s connecting metabolic shifts with excessive alcohol consumption.
32 categorical variables in the case of sex and alcohol consumption.
33 re associated with heart failure and chronic alcohol consumption.
34 blood could serve as a robust biomarker for alcohol consumption.
35 epigenome-wide significance on self-reported alcohol consumption.
36 3 blocks GalphasDREADD-dependent increase in alcohol consumption.
37 3 (95% CI 0.61-0.88; p < 0.001) for moderate alcohol consumption, 0.66 (95% CI 0.54-0.81; p < 0.001)
39 hol than controls and consistently increased alcohol consumption after repeated alcohol deprivation p
40 y of these thresholds indicate assessment of alcohol consumption alone may be inadequate for identify
43 smoking, body mass index, physical activity, alcohol consumption, Alternative Healthy Eating Index, a
45 Genetic correlation between maximum habitual alcohol consumption and alcohol dependence was 0.87 (p =
46 variants associated with a proxy measure of alcohol consumption and alcohol misuse and to explore th
49 tatistically significant association between alcohol consumption and any other site-specific cancer.
51 ical mechanisms driving associations between alcohol consumption and chronic diseases might include e
52 cate an inverse association between moderate alcohol consumption and chronic inflammatory diseases; h
53 y diseases; however, the association between alcohol consumption and chronic obstructive pulmonary di
55 dual differences, revealing latent traits in alcohol consumption and compulsive drinking despite equa
56 a potentially nonlinear relationship between alcohol consumption and CVD risk, and the generalizabili
58 nalysis showed an association with liters of alcohol consumption and drinkers among population once a
59 ver, the association of age at initiation of alcohol consumption and duration of alcohol drinking wit
60 , sex, study center, education, smoking, and alcohol consumption and for the respective other exposur
62 ys an important role in regulating excessive alcohol consumption and highlight the need for future st
63 the association between ADH1B*2 and moderate alcohol consumption and histologic severity of NAFLD.
64 interventions for those at risk due to high alcohol consumption and increased body mass index (BMI).
66 ence of a causal relationship between higher alcohol consumption and increased risk of stroke and per
67 We investigated the associations of total alcohol consumption and intake of specific alcoholic bev
68 nvestigate if climate has a causal effect on alcohol consumption and its weight on alcoholic cirrhosi
70 rease in burden of liver disease from excess alcohol consumption and obesity, with high levels of hos
71 ffer by socioeconomic status, accounting for alcohol consumption and other health-related factors.
72 nt association between genetically predicted alcohol consumption and overall cancer (n = 75,037 cases
73 o evidence supporting a relationship between alcohol consumption and overall or site-specific cancer
74 its infusion into the DMS of rats, decreased alcohol consumption and preference, with no effects on n
75 in the basolateral amygdala (BLA) decreased alcohol consumption and reduced conditioned place prefer
77 an important role of NBCn1 in regulation of alcohol consumption and sensitivity to alcohol-induced s
83 ultaneously assess the independent impact of alcohol consumption and smoking on a wide range of CVD r
85 We identify genetic pathways associated with alcohol consumption and suggest genetic mechanisms that
86 evidence that an individual's self-reported alcohol consumption and their genotype at rs1229984, a m
87 asal amygdala to CeA projections showed that alcohol consumption and withdrawal were associated with
88 egression, genetic overlap was found between alcohol consumption and years of schooling (rG=0.18, s.e
90 ate hypothetical effects of habits (smoking, alcohol consumption, and fat and carbohydrates consumpti
92 tidylethanol (PEth), an objective measure of alcohol consumption, and for self-reported alcohol consu
93 67:TA was amplified by increasing adiposity, alcohol consumption, and genetic risk of fatty liver dis
95 re education, higher income, moderate vs low alcohol consumption, and low material deprivation were e
96 ce had positive direct effects on income and alcohol consumption, and negative direct effects on mode
98 nd handgrip strength), behavioural (smoking, alcohol consumption, and physical activity), socioeconom
100 luded socioeconomic status, medical history, alcohol consumption, and smoking habits) and had their h
101 enarche, age at first birth, family history, alcohol consumption, and smoking status, which suggests
102 nd social activity, physical activity, diet, alcohol consumption, and smoking-and cognition, adjustin
103 signaling pathway, which promotes excessive alcohol consumption, and that inhibition of FGFR1 may pr
104 receptor, FGF receptor-1 (FGFR1), suppresses alcohol consumption, and that the effects of FGF2-FGFR1
105 oking initiation (ever smoked regularly) and alcohol consumption, and the corresponding associations
106 nment had positive direct effects on income, alcohol consumption, and vigorous physical activity, and
107 4)(3)(beta2)(2) subtype of nAChRs can reduce alcohol consumption, and when administered in combinatio
108 ctors investigated were age, sex, education, alcohol consumption, anxiety, apolipoprotein E epsilon4
111 eta signaling dramatically reduced excessive alcohol consumption, as did selective inhibition of D1-M
113 oid receptor-mediated signaling in escalated alcohol consumption associated with dependence and stres
114 f aging, we sought to identify the amount of alcohol consumption associated with the longest telomere
115 as abstainers showed a greater reduction in alcohol consumption at 12-month follow-up than those cla
118 We assessed the weekly rate of RTAs and alcohol consumption between Jan 1, 2013, and Dec 31, 201
119 tatus, diabetes mellitus, educational level, alcohol consumption, body mass index, physical activity,
120 biologically proximal environmental factors alcohol consumption, body mass index, smoking and matern
121 LDH2 and ADH1B, are strongly associated with alcohol consumption but have limited impact in European
122 Participants in both groups decreased their alcohol consumption, but at week 24 we did not detect a
123 ekly alcohol consumption increases partner's alcohol consumption by 0.26 units (95% C.I. 0.15, 0.38;
124 y the susceptibility gene loci for excessive alcohol consumption by jointly measuring weekly alcohol
126 hysical activity, healthy diet, and moderate alcohol consumption, categorized into favorable, interme
130 se disorder.SIGNIFICANCE STATEMENT Long-term alcohol consumption causes neuroadaptations in the mesos
131 cardiopulmonary fitness, physical activity, alcohol consumption, cigarette smoking, diabetes risk an
132 dy suggests that genetic variants related to alcohol consumption, coffee consumption and obesity were
133 ted loci, 12 have been associated with total alcohol consumption, coffee consumption, plasma caffeine
134 ro, and Dlgap2-deficient mice showed reduced alcohol consumption compared with wild-type controls.
135 mechanisms that prompt or mitigate excessive alcohol consumption could be partly explained by metabol
137 family history of dementia, non-smoking, low alcohol consumption, depression, daytime somnolence, epi
138 for future investigation, in order to reduce alcohol consumption, develop markers for diagnosis and p
140 rom 5 modifiable lifestyle factors: smoking, alcohol consumption, diet, physical activity, and body f
142 independent phenotypes reflecting subjects' alcohol consumption during the past year, based on self-
143 ese data fail to demonstrate any benefits of alcohol consumption, even when consumed in moderation.
144 f-report severe periodontitis was noted when alcohol consumption exceeding > 20 g/day for women and >
151 bsets from EWAS on PEth and on self-reported alcohol consumption from Cohort 1 were separately tested
152 hould continue to be advised to abstain from alcohol consumption from conception throughout pregnancy
155 alysis of genome-wide association studies of alcohol consumption (g d(-1)) from the UK Biobank, the A
158 hort, healthy behaviors-nonsmoking, moderate alcohol consumption, >=2.5 hours per week of moderate to
161 ur previous work in a mouse model of chronic alcohol consumption has detailed that the primary influe
162 th psychiatric disorders, whereas aspects of alcohol consumption have shown stronger links to metabol
163 ociations were independent of age, sex, BMI, alcohol consumption, history of diabetes, left ventricul
164 he patient should be asked about the current alcohol consumption (i.e. active vs. abstinence, determi
165 s included in the models included; age, sex, alcohol consumption, IBS diagnosis, family history of ga
166 Here, we test the hypothesis that chronic alcohol consumption impairs retinoic acid signaling in b
169 signaling in the BNST is linked to excessive alcohol consumption in a manner distinct from behavioral
170 However, prolonged and excessive voluntary alcohol consumption in a two-bottle choice procedure inc
173 ime-series design by use of data on RTAs and alcohol consumption in Scotland (the interventional grou
175 xamine the influence of DYN/KOR signaling on alcohol consumption in the drinking-in-the-dark (DID) mo
176 ed a genome-wide association study (GWAS) of alcohol consumption in the large Genetic Epidemiology Re
177 od pressure, physical activity, smoking, and alcohol consumption) in late adolescence using a cross-c
178 at a unit increase in an individual's weekly alcohol consumption increases partner's alcohol consumpt
181 frequency protein-coding variants in gene by alcohol consumption interactions associated with fasting
185 ts demonstrate that an objective measure for alcohol consumption is a more informative phenotype than
187 GT-catalytic metabolic reaction in excessive alcohol consumption is associated with ALDH2, BRAP and C
195 e association study-defined genomic risk for alcohol consumption is enriched for genes that are prefe
198 al study but provide assurance that moderate alcohol consumption is safe for patients with prostate c
200 and sCD163 were higher among ED with recent alcohol consumption (last drink <10 days before enrollme
204 nsula GMV represent promising biomarkers for alcohol-consumption liability and related psychiatric an
205 nal genome-wide-significant maximum habitual alcohol consumption loci: on chromosome 17, rs77804065 (
207 Low dosages (</=1.37 g of alcohol/day) of alcohol consumption may be beneficial to prevent periodo
209 ypothesised that genetic variants related to alcohol consumption may, via their effect on alcohol beh
210 -1.7 to 1.1; p=0.71), but a 0.7% decrease in alcohol consumption measured by per-capita on-trade sale
211 in Scotland was associated with no change in alcohol consumption, measured by per-capita off-trade sa
212 ng three meals a day, having a regular diet, alcohol consumption, moderate exercise, depression, and
213 rall, these results demonstrate that chronic alcohol consumption negatively affects the resting memor
217 f this study is to investigate the impact of alcohol consumption on clinical attachment loss (AL) pro
219 We evaluated the effects of heavy, chronic alcohol consumption on epigenetic age acceleration (EAA)
220 ittle is known about the impact of excessive alcohol consumption on kidney function in critically ill
222 ut it is difficult to disentangle effects of alcohol consumption on mate-selection from social factor
225 nal hazards models to evaluate the effect of alcohol consumption on survival of patients with NAFLD.
226 demonstrate that the genetic architecture of alcohol consumption only partially overlaps with the gen
232 ange of CVD risk factors and outcomes of any alcohol consumption or smoking MR study to date, we fail
233 after toilet (OR = 1.8, 95% CI; 1.19-2.72), alcohol consumption (OR = 1.34, 95% CI; 1.03-1.74) and g
234 hosis, other chronic liver disease, elevated alcohol consumption, or confounding conditions were pres
236 of negative binomial panel regression and on alcohol consumption outcomes by use of seasonal autoregr
239 of education (P = 0.26), smoking (P = 0.11), alcohol consumption (P = 0.52), history of cardiovascula
241 ngs suggest EA may have important effects on alcohol consumption patterns and may provide potential m
243 annual sunshine hours with liters of annual alcohol consumption per capita (Spearman's rho -0.5 and
244 sly reported SNP rs1229984 in ADH1B and both alcohol consumption phenotypes (OR=0.79, P=2.47 x 10(-20
245 ndex, socioeconomic position, diet, smoking, alcohol consumption, physical activity level, and C-reac
246 associated with colorectal cancer (smoking, alcohol consumption, physical activity, and total meat c
247 e, sex, comorbidity, mood disorder, smoking, alcohol consumption, physical activity, body mass index,
248 omposite score (range, 0-20) involving diet, alcohol consumption, physical activity, body mass index,
249 odium intake, low potassium intake, obesity, alcohol consumption, physical inactivity and unhealthy d
251 IT showed positive genetic correlations with alcohol consumption (r(g)=0.76-0.92) and DSM-IV alcohol
253 by alcohol use disorder (AUD), and excessive alcohol consumption represents the most common cause of
254 s with no or modest, moderate, and increased alcohol consumption, respectively (P(interaction) < .001
257 s preselected from the EWAS on self-reported alcohol consumption showed a poor prediction of HAD with
259 central and unanticipated role in excessive alcohol consumption.SIGNIFICANCE STATEMENT The bed nucle
261 ss index, healthy diet, sedentary lifestyle, alcohol consumption, smoking, and urinary sodium excreti
262 occurrence of four behavioural risk factors (alcohol consumption, smoking, physical inactivity and ob
263 After we adjusted for confounders, including alcohol consumption status, ADH1B*2 was associated with
265 ts enrolled between 2006 and 2010, we tested alcohol consumption (stratified by the Centers of Diseas
266 tinct cohort studies, we found no pattern of alcohol consumption that was associated with longer telo
268 ialty, waist circumference, body mass index, alcohol consumption, tobacco smoking, and physical activ
269 t work aims to evaluate the relation between alcohol consumption trends over a period of 15 y with al
270 oups of smoking intensity, years of smoking, alcohol consumption, trial supplementation, and duration
273 e range (IQR), 40-53 years], age of onset of alcohol consumption was 16 years [IQR, 16-18 years] and
275 ng the Desire for Alcohol Questionnaire, and alcohol consumption was assessed using the timeline foll
278 in this population of younger women, higher alcohol consumption was associated with increased risk o
284 history of heart attack at baseline, and no alcohol consumption were associated with a greater likel
286 moderating effects of physical activity and alcohol consumption were greater in women than men (thre
289 ctivity, healthy diet, and light-to-moderate alcohol consumption were positively associated with cogn
290 ative exposure to estrogen, BMI, and dietary alcohol consumption were the most common influential fac
291 al position, smoking, physical activity, and alcohol consumption were used to estimate total and sex-
292 haviour) and an independent causal effect of alcohol consumption when controlling for smoking (IVW OR
294 in cognitive abilities associated with heavy alcohol consumption, whereas increased cerebellar connec
295 wn of Lmo4 in the nucleus accumbens enhanced alcohol consumption, whereas knockdown in the basolatera
296 seeking/low anxiety associated with enhanced alcohol consumption, which may be related to cortex func
297 s671 (ALDH2) increased the risk of excessive alcohol consumption, while one or two copies of the C al
298 sitive associations of genetically predicted alcohol consumption with coronary artery disease (OR, 1.
299 nce of associations of genetically predicted alcohol consumption with heart failure (OR, 1.00 [95% CI
300 aim to investigate the associations between alcohol consumption with meals, daily frequency of consu