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1 type, inhalation depth, Fagerstrom-assessed nicotine dependence).
2 s and, instead, may contribute to continuing nicotine dependence.
3 ntrol animals, suggesting a role for NRG3 in nicotine dependence.
4 CI, 52%-89%) and 98% (95% CI, 95%-100%) for nicotine dependence.
5 tress disorder; other anxiety disorders; and nicotine dependence.
6 ing, including use of medicines to help with nicotine dependence.
7 rbB4 signaling may be an important factor in nicotine dependence.
8 nificantly reduced cigarette consumption and nicotine dependence.
9 mokers and for smokers with a high degree of nicotine dependence.
10 ts for the treatment of comorbid alcohol and nicotine dependence.
11 is gene variant modulates various aspects of nicotine dependence.
12 ognitive/affective alterations that underlie nicotine dependence.
13 the pharmacotherapy of Parkinson disease and nicotine dependence.
14 s associated with an elevated risk for later nicotine dependence.
15 e exposure directly increases level of later nicotine dependence.
16 , placebo-controlled trials of naltrexone in nicotine dependence.
17 receptor (nAChR) influence both ethanol and nicotine dependence.
18 s a critical relay circuit in the control of nicotine dependence.
19 onset of regular smoking predicted level of nicotine dependence.
20 appear to be involved in the later stages of nicotine dependence.
21 ning processes contribute to the etiology of nicotine dependence.
22 and is thought to be a critical component of nicotine dependence.
23 tinic receptor variants that affect risk for nicotine dependence.
24 RNA6-CHRNB3 gene clusters that contribute to nicotine dependence.
25 associated with comorbid cocaine, opium, and nicotine dependence.
26 istical Manual (fourth edition) diagnosis of nicotine dependence.
27 associated with a protective effect against nicotine dependence.
28 al molecular component in the development of nicotine dependence.
29 disorders including Parkinson's disease and nicotine dependence.
30 nd loci reported for other smoking traits to nicotine dependence.
31 and controls to test for an association with nicotine dependence.
32 tine dependence with the Fagerstrom Test for Nicotine Dependence.
33 ghlighted in previous studies of smoking and nicotine dependence.
34 be new pharmacotherapeutics for treatment of nicotine dependence.
35 obiology, genetic etiology, and treatment of nicotine dependence.
36 CHRNA3-CHRNB4) and both smoking quantity and nicotine dependence.
37 TA DA neuronal function, DA transmission and nicotine dependence.
38 rug reinforcement and has been implicated in nicotine dependence.
39 nes (i.e., TAS2R16 and TAS2R38) in affecting nicotine dependence.
40 lele association with smoking initiation and nicotine dependence.
41 ntrolled for, with the possible exception of nicotine dependence.
42 o and number of cigarettes smoked per day or nicotine dependence.
43 nabis dependence; the second, on alcohol and nicotine dependence.
44 have been implicated in various measures of nicotine dependence.
45 tanding of the genetic mechanisms underlying nicotine dependence.
46 as measured by using the Fagerstrom Test for Nicotine Dependence.
47 ors (nAChRs) play a role in both alcohol and nicotine dependence.
48 s that can be long lasting and contribute to nicotine dependence.
49 ted in behavioural responses to nicotine and nicotine dependence.
50 ors contribute in part to the development of nicotine dependence.
51 nce to nervous system function, disease, and nicotine dependence.
52 files associated with alcohol, cannabis, and nicotine dependence.
53 m function, some of which must contribute to nicotine dependence.
54 g toward elucidating the basic mechanisms of nicotine dependence.
55 ntake, may be a key trigger of withdrawal in nicotine dependence.
56 nicotine in a key brain circuit involved in nicotine dependence.
57 an hormones on the etiology and treatment of nicotine dependence.
58 riant, but not the N variant associated with nicotine dependence.
59 dly linked to addictive disorders, including nicotine dependence.
60 CHRNA4 and tested them for association with nicotine dependence.
61 HRNB4 gene cluster and smoking heaviness and nicotine dependence.
62 ain dopamine D2-type autoreceptors influence nicotine dependence.
63 le is known about the role of this system in nicotine dependence.
64 ence syndrome they were 1.72 (1.57-1.87) for nicotine dependence, 2.67 (2.38-2.99) for cannabis depen
65 rsion disorder (5.3%; 95% CI, 4.3% to 6.2%), nicotine dependence (4.5%; 95% CI, 3.6% to 5.4%), alcoho
66 , performance in both tasks was modulated by nicotine dependence, abstinence, and pharmacological man
67 s the most significantly associated SNP with nicotine dependence across five independent cohorts (tot
68 significant increases were seen in 12-month nicotine dependence (adjusted risk difference=2.6%) and
70 mia nervosa), and four were "externalizing" (nicotine dependence, alcohol dependence, drug abuse or d
71 anxiety disorder; suicidal ideation/attempt; nicotine dependence; alcohol abuse/dependence; and illic
72 ne self-administration and initial stages of nicotine dependence, alpha7 homomeric nAChRs appear to b
73 the CHRNA5-CHRNA3-CHRNB4 region that predict nicotine dependence also predicted a later age at smokin
75 sion subside, as indicated by high levels of nicotine dependence among individuals with remitted depr
77 pendence (adjusted risk difference=2.6%) and nicotine dependence among users (adjusted risk differenc
78 ncreases in 12-month nicotine dependence and nicotine dependence among users suggests that increases
79 use, DSM-IV nicotine dependence, and DSM-IV nicotine dependence among users were analyzed to test th
80 es in nicotine use, nicotine dependence, and nicotine dependence among users were statistically signi
82 ng reward, E-cigs might maintain a degree of nicotine dependence and also serve as a noncombustible s
83 ard, e-cigarettes might maintain a degree of nicotine dependence and also serve as non-combustible su
84 t increase the risks of both lung cancer and nicotine dependence and associated smoking behavior.
85 is available on the co-occurrence of DSM-IV nicotine dependence and Axis I and II psychiatric disord
87 tify a novel regulatory SNP association with nicotine dependence and connect, for the first time, pre
89 data show an increased risk for the onset of nicotine dependence and drug abuse or dependence in pers
90 nes that were reported to be associated with nicotine dependence and found significant joint action b
91 3239-rs12720071-rs806368 was associated with nicotine dependence and FTND score in the 2 samples (P <
92 -1 gene dysfunctions have been implicated in nicotine dependence and in autism spectrum disorders.
93 erest because of its apparent involvement in nicotine dependence and in the control of dopamine relea
94 thought to influence both susceptibility to nicotine dependence and its comorbid behavioral traits i
97 ith recent reports of NRXN3 association with nicotine dependence and linkage with opiate dependence,
98 low mRNA expression of CHRNA5, the risk for nicotine dependence and lung cancer is significantly low
101 two distinct mechanisms conferring risk for nicotine dependence and lung cancer: altered receptor fu
102 type has recently been genetically linked to nicotine dependence and lung cancer; however, the mode o
103 al clinical applications in the treatment of nicotine dependence and many neuropsychiatric conditions
104 n of the CRF-CRF(1) system may contribute to nicotine dependence and may represent a prominent target
106 rface expression levels are modulated during nicotine dependence and multiple disorders of the nervou
107 use relative to larger increases in 12-month nicotine dependence and nicotine dependence among users
108 disorders, and individuals who have comorbid nicotine dependence and other psychiatric disorders.
109 et for the discovery of novel medication for nicotine dependence and other substance-related disorder
113 -level understanding of the insula's role in nicotine dependence and shows a relationship between inh
115 Combining genetic and mechanistic studies of nicotine dependence and smoking heaviness may reveal nov
119 and in relationships between midbrain BPND, nicotine dependence and striatal dopamine D2-type recept
120 GluR5 is a pathogenetic mechanism underlying nicotine dependence and the high relapse rate in individ
121 In this largest-ever GWAS meta-analysis for nicotine dependence and the largest-ever cross-ancestry
124 ion, echoing the increased susceptibility to nicotine dependence and withdrawal noted for adolescent
125 le provides an overview of recent studies of nicotine dependence and withdrawal that used genetically
127 ing, nicotine dependence (Fagerstrom Test of Nicotine Dependence), and cessation difficulties were ev
128 Weighted estimates of nicotine use, DSM-IV nicotine dependence, and an approximation of the Fagerst
129 ed initiation of all types of substance use, nicotine dependence, and cannabis abuse/dependence (for
132 12-month prevalences of nicotine use, DSM-IV nicotine dependence, and DSM-IV nicotine dependence amon
133 Implications for conceptualizing risk for nicotine dependence, and its treatment, are discussed.
135 h few exceptions, increases in nicotine use, nicotine dependence, and nicotine dependence among users
137 that could be important in the treatment of nicotine dependence, and perhaps other neurological dise
138 ypes in the CNR1 gene may alter the risk for nicotine dependence, and the associations are likely sex
141 ecting risk for vulnerability to cocaine and nicotine dependence as well as bipolar disorder, suggest
143 sk for lung cancer is direct or an effect of nicotine dependence, as evidence for both scenarios exis
144 datasets: the Collaborative Genetic Study of Nicotine Dependence (ascertained for tobacco use disorde
145 2 in lung), and expression of genes spanning nicotine dependence-associated variants is enriched in c
148 4-77%) was associated with increased risk of nicotine dependence at P=3.7 x 10(-8) (odds ratio (OR)=1
149 dence among users suggests that increases in nicotine dependence between the 2001-2002 and 2012-2013
151 pregnancy are at elevated risk of developing nicotine dependence but not marijuana dependence as adul
152 ) have recently been shown to play a role in nicotine dependence, but it is not clear which nAChR sub
153 conduct an empirical study of progression of nicotine dependence by applying the WNA approach to thre
154 s analyzed in several brain areas related to nicotine dependence by immunofluorescence techniques.
156 vances in the understanding and treatment of nicotine dependence, close to 21% of adults in the Unite
157 nterest, and participant-reported ratings of nicotine dependence, craving, and self-efficacy were col
158 rt a genome-wide association study (GWAS) of nicotine dependence defined on the basis of scores on th
159 ndence, as defined by the Fagerstrom Test of Nicotine Dependence, demonstrating that cigarettes smoke
160 he primary eligibility criteria were current nicotine dependence (DSM criteria), smoking 10 or more c
161 daily smoking, progression to heavy smoking, nicotine dependence (Fagerstrom Test of Nicotine Depende
162 1862416 is not associated, likely reflecting nicotine dependence features not captured by the heavine
163 g smokers both with and without a history of nicotine dependence; for other outcomes, increases were
164 garettes smoked per day, Fagerstrom Test for Nicotine Dependence (FTND) and Motivation to Quit (MTQ)
165 ine concentration (COT), Fagerstrom test for nicotine dependence (FTND) and schizophrenia to examine
166 or addiction by both the Fagerstrom Test for Nicotine Dependence (FTND) and the Revised Tolerance Que
167 ddiction assessed by the Fagerstrom test for nicotine dependence (FTND) has received little attention
168 metabolizers) had lower Fagerstrom Test for Nicotine Dependence (FTND) scores, suggesting lower leve
173 analysis of items on the Fagerstrom Test for Nicotine Dependence gave evidence of three classes perti
175 ing that cigarettes smoked per day (CPD) and nicotine dependence have distinct genetic correlates.
176 animal models that replicate key features of nicotine dependence have led to important advancements i
178 fluenced regulation in brain on the risks of nicotine dependence, heavy smoking and consequent lung c
179 derable evidence supports a genetic risk for nicotine dependence; however, less is known about the ph
180 four SNPs in the CHRNB2 gene with respect to nicotine dependence in a collection of 901 subjects (815
181 nd multiple measures of smoking behavior and nicotine dependence in a large, national representative
182 in CHRNB4 are associated with lower risk for nicotine dependence in African Americans and European Am
183 in the development and maintenance of strong nicotine dependence in cigarette smokers posit (i) a rap
184 A5) is the strongest genetic risk factor for nicotine dependence in European Americans and contribute
185 e basis of scores on the Fagerstrom Test for Nicotine Dependence in European-American (EA) and Africa
186 ale smokers but not in male smokers and with nicotine dependence in female but not in male smokers.
187 l signs, and has a protective effect against nicotine dependence in human genetic association studies
190 AChR) family genes that are known to mediate nicotine dependence in mammals, suggesting functional co
194 iants were associated with increased risk of nicotine dependence in the European American primary sam
195 ever, the role of rare variation in risk for nicotine dependence in these nicotinic receptor genes ha
196 or a significantly (P =.004) lower risk (for nicotine dependence, in the prospective data) in persons
197 ransition from smoking to the development of nicotine dependence, including an amino acid change in t
198 s, (1) whether the genetic predisposition of nicotine dependence influence COPD risk and lung functio
199 e identified who would benefit from targeted nicotine dependence intervention programs to help them i
200 ronically exposed to nicotine, implying that nicotine dependence involves the sensitization of nicoti
208 cles of smoking and withdrawal contribute to nicotine dependence, long-term alterations in brain rewa
210 nhanced understanding of these dimensions of nicotine dependence may help to advance progress toward
211 ge was 47.2 years (IQR 36.3-54.5), with high nicotine dependence (mean 24 cigarettes per day [SD 13.2
213 rsisted longer in smoking heavily, developed nicotine dependence more frequently, were more reliant o
214 6969968-A alleles together increased risk of nicotine dependence more than each variant alone: P = 3.
215 iew, we address these issues by developing a nicotine dependence (ND) genetic susceptibility map base
216 didate gene studies for smoking behavior and nicotine dependence (ND) have disclosed too few predispo
217 ne (GABAB2) were tested for association with nicotine dependence (ND) in an extensively phenotyped co
219 ase (DDC) locus with the DSM-IV diagnosis of nicotine dependence (ND) or a quantitative measure for N
220 etic and environmental factors in regulating nicotine dependence (ND) risk, including the effects on
221 is an independent risk factor for offspring nicotine dependence (ND), but mechanisms remain unknown.
222 acetylcholine receptors (nAChR) subunits and nicotine dependence (ND), only few studies were performe
229 study reported that NRXN1 is associated with nicotine dependence (ND); this, together with the intrig
231 ch in the neurobiologic and genetic basis of nicotine dependence offers promise for the development o
232 dissociation between the effects of chronic nicotine dependence on neural representations of reward
233 Furthermore, the effect of prior history of nicotine dependence on subsequent nicotine and alcohol t
234 ving a 2-fold increase in risk of developing nicotine dependence once exposed to cigarette smoking.
235 e to traumatic events increases the risk for nicotine dependence or alcohol or other drug use disorde
237 mprehensive, such as the Fagerstrom Test for Nicotine Dependence or the American Psychiatric Associat
238 to have a diagnosis of drug use disorder or nicotine dependence or to have used tobacco than their n
239 use disorder: OR, 2.6; 95% CI, 1.6-4.4; and nicotine dependence: OR, 1.7; 95% CI, 1.2-2.4), but not
240 applicable), cigarette consumption, level of nicotine dependence, other confounders, definition of qu
241 identifying cellular/receptor mechanisms of nicotine dependence, our results take a step toward impr
244 nterdisciplinary approach to the genetics of nicotine dependence provides a model for testing how fun
245 u-opioid receptor (OPRM1) genotype, or their nicotine dependence questionnaire score (phenotype).
249 ed differences in CHRNA5 mRNA expression and nicotine dependence risk to underlying DNA methylation d
250 her other CHRNA5 coding variation influences nicotine dependence risk, we performed targeted sequenci
253 ation studies, we provide evidence that both nicotine-dependence risk and lung cancer risk are influe
255 d positively with higher Fagerstrom Test for Nicotine Dependence score (r = .58, p = .031) and more c
256 GWAS analysis considered Fagerstrom Test for Nicotine Dependence score as an ordinal trait, separatel
257 dary, quantitative phenotype, the Fagerstrom nicotine dependence score, that is correlated with COPD
258 with ND measured by the Fagerstrom Test for Nicotine Dependence score; of these, 11 SNPs remained si
259 icotine-dependent cases (Fagerstrom Test for Nicotine Dependence score4) and 1238 non-dependent contr
261 elopment of brain-based biomarkers to assess nicotine dependence severity and treatment efficacy are
262 etween cingulate-striatal brain circuits and nicotine dependence severity as indexed by the intensity
263 um that negatively correlated with increased nicotine dependence severity but was unaffected by acute
264 ecies ACC-striatal circuit relationship with nicotine dependence severity is dysregulated following c
269 withdrawal symptoms but not the severity of nicotine dependence, severity of nicotine withdrawal, or
270 in Hb-IP circuits, a key pathway involved in nicotine dependence.SIGNIFICANCE STATEMENT This study un
272 utcomes of smoking, as well as predictors of nicotine dependence, smoking initiation, and smoking ces
275 of Cell, Feng et al. report a worm model of nicotine dependence that shows behavioral adaptations su
276 f the most powerful and extensive studies of nicotine dependence to date and has found novel risk loc
277 de association study (GWAS) meta-analysis of nicotine dependence, totaling 38,602 smokers (28,677 Eur
279 ng rate, number of recent quit attempts, and nicotine dependence; two key mediators of smoking cessat
282 y smoking, number of cigarettes per day, and nicotine dependence was greater in females than in males
285 variation contributes to the development of nicotine dependence, we performed a comprehensive genome
286 nAChRs and/or cell types that play a role in nicotine dependence, we studied these receptors and cell
287 ver genetic variants that influence risk for nicotine dependence, we targeted over 300 candidate gene
288 The odds of progressing from smoking to nicotine dependence were almost twice as great for offsp
290 an approximation of the Fagerstrom Test for Nicotine Dependence were compared for the 2001-2002 NESA
291 or 10 years on average, and met criteria for nicotine dependence were given SPECT scans on two days:
293 spring smoking behavior and lifetime risk of nicotine dependence were obtained by structured intervie
295 as Neurexin 1 (NRXN1), in the development of nicotine dependence while also identifying a known candi
298 and Negative Syndrome Scale (PANSS) and for nicotine dependence with the Fagerstrom Test for Nicotin
299 cingulate cortex (dACC) plays a key role in nicotine dependence, with its functional connections bet
300 variant, Ser9Gly (rs6280) has been linked to nicotine dependence, yet the mechanisms underlying its i