Tobacco smoking is a complex behaviour determined both by genetic and environmental factors. Classical twin studies demonstrated a strong heritability in the range of 40-70%, supporting a substantial genetic contribution to tobacco use [1, 2]. Allelic association studies conducted from the beginning of the 1990s have indicated that polymorphisms in several candidate genes may predispose to smoking initiation and nicotine dependence [3]. Recent studies on tobacco smoking have focused on polymorphisms of genes involved in the neurotransmission of dopamine in the central nervous system. The rationale for such an approach ensues from the properties of nicotine as the major addictive substance in tobacco smoke [4]. The pleasurable effects arising from nicotine are linked to stimulation of the dopamine reward pathway after binding nicotine with receptors present on the dopaminergic cell bodies, which in turn leads to an increased release of dopamine in the nucleus accumbens of the mesolimbic system [5, 6].

A number of allelic association studies focused on polymorphism of gene for DRD2 dopamine receptor. Several polymorphisms of this gene were identified, including TaqIA polymorphisms [7]. Studies have shown that A1 allele is associated with a reduced dopamine D2 receptor density [8–10]. It has been hypothesised that persons with such a functional deficit in the dopamine reward pathway experience an enhanced reward when exposed to dopaminergic agents, including nicotine, thereby making them more vulnerable to nicotine addiction [11]. Some authors have demonstrated that cigarette smokers more frequently carry A1 allele than never-smokers [11–13]. However, there is some inconsistency in the literature regarding association of TaqI polymorphism of DRD2 and smoking, with some studies indicating the lack of such an association [14–16] and others reporting the association of A2 allele with smoking [17]. More recently, common TaqIA polymorphism, originally thought to be in the DRD2 gene, has been determined to be in a neighbouring gene ANKK1 (ankyrin repeat and kinase domain controlling 1) [18]. However, being in linkage disequilibrium with other variants in the DRD2 gene, but not with variants in the ANKK1 gene, TaqIA polymorphism is considered to have a strong association with DRD2 gene [19].

The dopamine transporter gene (SLC6A3) encodes a protein that regulates synaptic levels of dopamine in the brain and has been studied as another candidate gene for tobacco smoking [20–23]. A 40 base polymorphism of a variable number of tandem repeats (VNTR) has been described in the 3' untranslated region of this gene [24]. Initially, it was suggested that people who carry the less frequent nine-repeat allele (*9R) of the dopamine transporter gene are less likely to be smokers [20, 23]. The 9-repeat allele of SLC6A3 has also been associated with a substantial reduction in dopamine transporter protein, resulting in less clearance and greater bioavailability of dopamine [25]. It was suggested that carriers of the common allele of SLC6A3, the 10-repeat allele, may achieve a greater reward from nicotine's effect on dopamine activity. Thus the 9-repeat allele and eventually the higher level of dopamine in the synaptic cleft appeared to play a protective role from smoking. However, it was subsequently demonstrated that the 9-repeat allele enhances transcription of the dopamine transporter protein, which might result in a greater clearance of synaptic dopamine, and thus lower basal availability [26, 27]. In turn, some reports suggest that there is no functional difference related to particular polymorphism [28]. There are also some allelic association studies which did not replicate the initial positive results [21, 22].

In the light of existing discrepancies and of the lack of surveys on the association between variant alleles of DRD2 and SLC6A3 genes and smoking in Poland, we investigated whether polymorphic variants of these genes and their combinations are associated with the smoking habit in the Polish population.

Out of 310 subjects, two unsuccessfully underwent genotyping, therefore they were excluded from the analyses. Data for the remaining 308 subjects were analysed, including 150 ever-smokers (67 females; mean age 53.1 ± 11.1) and 158 never-smokers (79 females; mean age 45.0 ± 16.2). Distributions of genotypes for TaqIA polymorphism of DRD2 and SLC6A3 VNTR polymorphism did not deviate to any appreciable extent from expectations predicted by the Hardy-Weinberg equilibrium as determined by a chi-square test (p = 0.66 and p = 0.36, respectively).

There were no differences in the distribution of DRD2 and SLC6A3 genotypes or in the frequencies of *9 alleles of SLC6A3 compared to pooled *10 and *11 alleles among ever- and never-smokers. In turn, we found that frequency of A1 alleles was lower in ever-smokers than in never-smokers (p = 0.032). However, the OR for being an ever-smoker for A1 allele carriers did not reach the assumed level of statistical significance, when compared to A2 homozygous subjects and was 0.68 (95% CI: 0.42-1.09); p = 0.108.

Similarly, distribution of genotype combinations did not differ between ever- and never-smokers. Only 41.5% of subjects with a genotype combination A1+/9- were ever-smokers. A relative risk for this genotype combination for ever-smoking as compared to subjects of all other genotype combinations pooled was 0.69 (95% CI: 0.40-1.21); p = 0.192. In turn, the genotype combination A1-/9- was the most strongly associated with ever-smoking status: 52.6% of carriers of this variant combination were ever-smokers. However, OR for smoking for subjects of genotype combination A1-/9- compared to subjects of all other genotype combinations pooled, as well as compared to the genotype combination that had the lowest frequency of smoking (A1+/9-), did not reach statistical significance and were 1.28 (95% CI: 0.81-2.04), p = 0.288, and 1.56 (95% CI: 0.84-2.80), p = 0.152, respectively.

Comparison of mean values of smoking duration, age when starting regular smoking, the number of cigarettes smoked daily and the number of pack-years between ever-smokers with DRD2*A1 or SLC6A3*9, and those homozygous for DRD2*A2 or SLC6A3*10 demonstrated no differences. There were also no differences when FTND scores for current smokers carrying A1 or *9 allele were compared with those for non-carriers. Comparison of mean length of the longest abstinence period on quitting attempts between current smokers with DRD2*A1 or SLC6A3*9 allele and non-carriers for these alleles demonstrated that A1 allelic subjects were more likely to achieve longer abstinence than non-carriers of A1 allele (314 ± 696 days v. 289 ± 925 days, p = 0.049), while no difference was observed between *9 allele carriers and non-carriers. In the smokers group quantitative measures of smoking did not also relate to DRD2xSLC6A3 genotype combinations.

Initial studies suggested that A1 alleles of dopamine receptor D2 gene were associated with susceptibility to smoking [11, 12]. However, several studies failed to replicate this association [14, 15], while other studies on Japanese populations indicated the link of A2 allele with smoking behavior [17, 35].

The results of our study demonstrated no association between DRD2 genotypes and cigarette smoking. However, the frequency of A2 allele was significantly higher in ever-smokers than in never-smokers. These findings might suggest that A2 allele is more important as determinants of smoking status, or that other factors, such as socioeconomic, environmental or cultural ones, might contribute relatively more than DRD2 genotypes in the smoking habit among the Polish population.

In our retrospective analysis of quitting history in ever-smokers we found that A1 allele carriers achieved longer abstinence periods when they had attempted to quit than non-carriers. However, this association was weak and one could not rule out - false positive, considering the limited sample size of the study and used threshold of p = 0.05. Similarly, Spitz et al. [32] in the study conducted in the sample of 283 subjects demonstrated that individuals with A1 genotypes reported a slightly longer mean duration of smoking cessation than subjects with the A2 genotypes. Other studies, however, yielded inconsistent results regarding a possible link of dopaminergic genes polymorphism with smoking cessation [36–38].

The present study also failed to replicate the association between SLC6A3 genotypes and smoking status. Similarly, we found no difference in mean duration of the longest abstinence achieved in the past between allele *9 carriers and non-carriers. Available data on the influence of SLC6A3 gene and smoking cessation are also discordant. Erblich et al. found that non-carriers of nine-repeat allele could abstain from cigarettes for a longer period of time than carriers [13]. In contrast, Lerman et al. reported association between the absence of the nine-repeat allele and shorter quit durations [20].

Reasons for non-replication of allelic association studies in general were previously widely discussed [21, 39]. It was suggested, for instance, that more attention should be focused on refining smoking behaviour phenotypes and exploring genetic influences on them, rather than only on smoking status per se [39]. In fact, only when separating smokers according to their smoking phenotypes related to the number of cigarettes smoked daily and age at starting regular smoking, the possible association between studied polymorphisms and heavier smoking or earlier entering the phase of regular smoking was demonstrated in our investigation. It is likely that other genes than DRD2 and SLC6A3 have a greater impact on ever smoking status (i.e., smoking initiation), and simultaneously many other non-genetic factors, including socio-demographical, pharmacological, psychological, behavioural or cultural ones, independently influence vulnerability to smoking, while these two dopaminergic genes might influence smoking behaviour phenotypes. However, it is possible, that the association between studied polymorphisms and these smoking-related phenotypes was mediated by an unknown confounder, for instance, linkage disequilibrium between a variant under study and true variant related to given smoking-related phenotype. On the other hand, it is likely that ethnical homogeneity of studied population allowed to avoid confounding by ethnicity.

Our survey on association between genotypes and the level of cigarette consumption demonstrated that the risk for smoking a greater number of cigarettes daily was over 2.5 times lower in carriers than in non-carriers of A1 or *9 allele. Moreover, frequency of heavier smoking was the lowest among subjects with A1+/9+ genotype combinations. In turn, possessing even one common allele A2 or *10 in DRD2xSLC6A3 combinations was associated with a higher risk of heavier smoking, with A1-/9- genotypes combination associated with the highest risk of heavier smoking, relatively to the A1+/9+ genotype combination. Previously, Spitz et al. [32] reported that A1 allele carriers were less likely to smoke more cigarettes per day than non-carriers. In turn, Yoshida et al. reported the lack of apparent association between DRD2 genotype and the number of cigarettes smoked daily [17]. Our study indicated that also genotype combination DRD2/SLC6A3 might influence the level of cigarette consumption. Namely, smokers with a relatively regular synaptic cleft dopamine homeostasis might experience a greater reward when stimulated by nicotine and, in consequence, they might be apt to repeat this stimulation more frequently by smoking cigarettes. Assuming the hypothesis that A1 carriers have a lower density of DRD2 receptors [8–10] and 9-repeat allele carriers display decreased expression of dopamine transporter [25], individuals with A1+/9+ genotype combination might have a chronically high level of extra-cellular dopamine protecting them from heavier smoking. In fact, our findings that A1+/9+ genotype combination had the lowest association with heavier smoking might be explained by the higher dopamine availability resulting from lower dopamine receptor density accompanied by decreased activity of dopamine transporter, not sufficient to uptake the whole amount of dopamine from the synaptic cleft. Such subjects might have a lower need to repeat dopaminergic stimuli, because of protracted extracellular dopamine signalling.

Separating smokers by the age when they step onto the stage of regular smoking revealed that carriers of *9 allele of SLC6A3 were less likely to indurate the smoking habit before the age of 20 years than non-carriers, and that this association was modified by gender. In addition, with combined DRD2 and SLC6A3 genotypes, subjects with A1-/9- genotype combination had a higher risk for staring regular smoking before the age of 20 years in comparison to subjects with A1+/9+ genotype combination, with OR reaching in males 7.6. Data from the initial study of Lerman et al. [20] on the association between SLC6A3 VNTR polymorphism and smoking indicated that 9-repeat allele carrier genotypes were significantly less likely to have started smoking before 16 years of age. Our data are consistent with the observation that polymorphism in the SLC6A3 may play an important role in smoking onset and progression to regular smoking, as well as indicate that gender, independently influencing the age of induration of smoking habit, might be a strong effect modifier.

As a limitations of the study the relatively small study sample should be pointed out. It has resulted in quite wide confidence intervals for subgroups referring to particular smoking phenotypes indicating uncertainty in the result. Despite in several studied associations p-values were smaller than used thresholds we are cautious in interpreting arbitrary these findings as significant, keeping in mind the possibility of false positivity due to chance caused by random variation [40]. Thus, we present our results as hypothesis-generating rather than confirmatory and consider that they need validation in studies conducted on larger sample of smokers. However, although a statistical power of the present study seems to be not adequate, our study indicate an importance of extending the allelic association studies by the investigation of the potential link of candidate genes polymorphisms with better defined smoking-related phenotypes rather than only with smoking status per se.

Polymorphic variants of DRD2 and SLC6A3 genes might influence some aspects of the smoking behavior, including age of starting regular smoking, the level of cigarette consumption, and periods of abstinence.

It might help in identifying special subgroups of smokers, which, in turn, could have important clinical implications for more successful interventions. It is likely, however, that due to the great complexity of smoking behaviour, which results from numerous genetic, environmental and psychological influences, the knowledge of genetic risk alone could be insufficient for the development of more effectively targeted cessation therapy.