Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Effects of smoking on cognition and BDNF levels in a male Chinese population: relationship with BDNF Val66Met polymorphism


Recent studies demonstrate that brain-derived neurotrophic factor (BDNF) might be associated with nicotine addiction, and circulating BDNF is a biomarker of memory and general cognitive function. Moreover, studies suggest that a functional polymorphism of the BDNF Val66Met may mediate hippocampal-dependent cognitive functions. We aimed to explore the relationships between smoking, cognitive performance and BDNF in a normal Chinese Han population. We recruited 628 male healthy subjects, inducing 322 smokers and 306 nonsmokers, and genotyped them the BDNF Val66Met polymorphism. Of these, we assessed 114 smokers and 98 nonsmokers on the repeatable battery for the assessment of neuropsychological status (RBANS), and 103 smokers and 89 nonsmokers on serum BDNF levels. Smokers scored lower than the nonsmokers on RBANS total score (p = 0.002), immediate memory (p = 0.003) and delayed memory (p = 0.021). BDNF levels among the smokers who were Val allele carriers were correlated with the degree of cognitive impairments, especially attention, as well as with the carbon monoxide concentrations. Our findings suggest that smoking is associated with cognitive impairment in a male Chinese Han population. The association between higher BDNF levels and cognitive impairment, mainly attention in smokers appears to be dependent on the BDNF Val66Met polymorphism.


Despite the significant health risks resulting from tobacco use, the prevalence of smoking worldwide remains high and approximately 20% of the world population still smokes tobacco1,2. In China, over 60% of adult men are current smokers3,4. Substantial evidence demonstrates that nicotine has high addiction liability as well as cognition-enhancing effects5. Individuals may self-medicate with nicotine to enhance cognitive and attentional processes6, which may partially account for the high prevalence of cigarette smoking among individuals with cognitive disorders such as schizophrenia, attention deficit/hyperactivity disorder, Alzheimer’s and Parkinson’s diseases, and age related cognitive decline7,8,9. A recent meta-analysis also showed that nicotine could enhance aspects of cognitive function, including motor abilities, attention and memory9. Moreover, this nicotine-induced enhancement of cognitive function has been observed both in nicotine-deprived smokers, in non-deprived smokers, and in non-smokers5,10. However, several studies suggest that smoking has an adverse effect on cognition11,12,13,14. Some studies show that long-term smokers perform more poorly on tests of cognition later in life than never-smokers, and ex-smokers perform better than those who continue to smoke14. Longitudinal studies have suggested a causal relationship between chronic smoking into late life and an increased risk of cognitive decline and dementia11,12,13. Thus, the smoking-cognition relationship warrants further investigation in a large sample of individuals.

Brain-derived neurotrophic factor (BDNF), a member of the neurotrophin family, is widely expressed in the adult mammalian brain, the highest levels being found in the hippocampus, followed by the cerebral cortex15. BDNF plays an important role in the regulation of neuronal survival, differentiation, growth, and apoptosis16. Studies have shown that BDNF can modulate activity-dependent synaptic plasticity underlying learning and memory in the hippocampus17,18. More specifically, BDNF appears to play an important role in both early long term potentiation (LTP) and late phase LTP in hippocampal neurons19, a cellular model of learning and memory17. Previous studies indicate that circulating BDNF may be a biomarker of memory and general cognitive function in healthy adults20,21. Several studies have shown that BDNF serum levels are significantly decreased in individuals with cognitive decline-related diseases, such as mild cognitive impairment21, Alzheimer’s disease22, and Huntington’s disease23. Interestingly, our own recent study showed that decreased BDNF levels were associated with cognitive impairment, especially immediate memory in schizophrenia24,25.

A single-nucleotide polymorphism (SNP) in the BDNF gene (rs6265) produced a valine (Val)-to-methionine (Met) substitution in the proBDNF protein at codon 66 (Val66Met). This SNP altered the intracellular trafficking and activity dependent secretion of mature BDNF and affected hippocampal function18,26,27,28,29. Consistent with this, both normal controls and schizophrenia patients with Met alleles have significant deficiencies in episodic memory, suggesting that Met carriers show a poorer cognition in both schizophrenia and healthy subjects18,30,31. These findings support a role for the BDNF Val66Met polymorphism in normal hippocampal dependent memory function in healthy controls as well as in individuals with schizophrenia18.

Preclincal data show that acute nicotine administration decreases whereas chronic nicotine, but not cocaine or morphine, increases BDNF mRNA levels in the hippocampus32. Interestingly, genome-wide linkage scans indicate that the region of chromosome 11p13 where the BDNF gene is located likely harbors susceptibility genes for nicotine dependence specifically33. Moreover, Beuten et al. provide evidence of an association between allelic variants of BDNF and nicotine dependence in male European-American smokers34. A recent study demonstrated that the frequencies of both the Met/Met genotype and Met allele were significantly increased in current and in former smokers when compared to never smokers among Germans35, suggesting that carriers of the BDNF Met allele have an increased risk for smoking. While subsequent association studies did not corroborate these findings24,36, recent studies have linked this BDNF polymorphism with smoking initiation37, smoking cessation38 and the age of smoking initiation24. Moreover, a lower plasma concentration of BDNF was reported in the smoking group39. However, a recent study indicated that smoking was associated with increased plasma BDNF levels in depressed patients40. The most recent study by Jamal et al. showed that smokers with and without nicotine dependence had higher levels of serum BDNF than former and never-smokers. Moreover, total number of smoking years was a significant predictor of serum BDNF. However, there was no association of BDNF Val66Met, nor an interaction of this polymorphism and smoking status, with serum BDNF41. Interestingly, they further found that nicotine-dependent smokers had more severe depressive symptoms than non-dependent smokers, former and never-smokers. Moreover, in Val66Val carriers, nicotine-dependent smokers had more severe symptoms of depression and anxiety than the other three groups, suggesting that BDNF Val66Met genetic variants may be crucial for the worse behavioral outcome of nicotine42. Our recent study showed that smoking was associated with cognitive decline, but not with BDNF levels in a normal population. Concomitant alcohol use did not worsen the cognitive decline and had no effect on BDNF levels. However, smoking severity was positively associated with BDNF levels43. Taken together, these findings suggest that smoking may affect the peripheral BDNF levels, and BDNF system may be involved in the etiology of nicotine dependence.

Given the established association between smoking and cognitive performance and the important role of BDNF in cognition and in nicotine dependence, it would be of interest to explore the relationships between smoking, cognitive performance and BDNF in a healthy population. We hypothesized that smoking may enhance some aspects of cognitive function in a Chinese Han population. The underlying mechanisms by which smoking may enhance cognitive performance might be associated with higher BDNF serum levels. Furthermore, Met carriers might show a poorer cognitive performance in smokers or non-smokers, or both. In addition, the relationship between serum BDNF levels and cognitive function may be dependent on the BDNF Val66Met polymorphism in smokers. Because smoking is substantially more common among Chinese men than in women with normal population44, as well as gender differences in smoking behaviors45, we included only male subjects in the present study.


Table 1 shows demographic and clinical characteristics of the smokers and nonsmokers. The mean age, education, marriage, and body mass index (BMI) did not differ between the two groups (all p > 0.05).

Table 1 Characteristics of smokers and non-smokers.

Distributions of the BDNF genotypes were consistent with HWE in both smokers and nonsmokers (both p > 0.05). We found no significant differences in BDNF genotype and allele distributions between smokers and nonsmokers (x2 = 2.26, df = 2, p > 0.05; and x2 = 1.11, df = 1, p > 0.05, respectively) (Table 1).

Genotype effects on cognitive functioning between smokers and nonsmokers

RBANS data were available from 114 smokers and 98 nonsmokers. Table 2 shows RBANS total and index scores, and the effects of the BDNF Val66Met polymorphism on the RBANS total and index scores.

Table 2 Comparisons of RBANS total and index scores by smoking status and BDNF Val66Met genotype.

Smokers performed significantly worse than nonsmokers on the RBANS total score (t = 3.09, df = 210, p = 0.002), immediate memory (t = 3.02, df = 210, p = 0.003) and delayed memory (t = 2.32, df = 210, p = 0.021). After the Bonferroni correction (α = 0.05/6 = 0.0083), only the significant difference in the RBANS total score and immediate memory remained significant. After adjusting for age, education and BMI, these results still remained significant for RBANS total score (F4,204 = 7.95, p = 0.005), and for immediate memory (F4,204 = 9.60, p = 0.002). However, there were no significant differences in other cognitive measures between smokers and nonsmokers (all p > 0.05).

As shown in Table 2, the three genotypes significantly differed on the language index (F = 4.25, p < 0.02), and using the Bonferroni test to control for the two potential comparisons only the Val/Met vs. Met/Met difference was significant (p = 0.027). There were no significant genotype effects for other indices or RBANS total scores.

Genotype effects on serum BDNF levels between smokers and nonsmokers

Serum BDNF levels were available from 103 smokers and 89 nonsmokers. These 192 subjects with BDNF level test overlapped with those subjects who had the RBANS test. Serum BDNF levels were normally distributed in both smokers and nonsmokers (Kolmogorov–Smirnov one-sample test: both p > 0.05). There was not a significant main effect of smoking status on BDNF levels (11.6 ± 2.3 ng/ml for smokers versus 11.5 ± 3.0 ng/ml for nonsmokers, p > 0.05). Furthermore, there was no main effect of genotype on serum BDNF levels (p > 0.05) nor genotype × smoking status effect (p > 0.05).

Differential effects of BDNF genotype on the relationships between BDNF serum levels and cognitive functioning

Since some cognitive domain impairments existed in smokers, we explored whether the cognitive impairments may be related to serum BDNF levels and whether such relationships differed between genotype groupings in smokers. We first tested the overall effect of the BDNF levels on all five cognitive domain scores in a multivariate ANCOVA test. BDNF was the independent variable, and the 5 cognitive domains and RBANS total scores were entered simultaneously as dependent variables. Covariates in the multivariate ANCOVA test were age, education and BMI. A BDNF level-by-genotype interaction term was also entered in the model. The results showed a trend toward significant overall main effect of BDNF on neurocognition (F = 1.96, p = 0.08). The BDNF level-by-genotype interaction term was statistically significant (F = 2.98, p = 0.012), which indicated that the relationships between BDNF levels and cognitive domain scores differed between genotype groupings. Further, post hoc univariate analyses found significant BDNF effects on attention (F = 6.92, p = 0.01), and a trend toward significant effect on RBANS total score (F = 2.89, p = 0.09). Moreover, we also found a significant BDNF level-by genotype interaction effect on language score (F = 3.91, p = 0.024). However, these significances did not pass the Bonferroni corrections (all p > 0.05).

In the smoking group, partial Pearson correlations were significant between BDNF levels and attention (r = −0.28, df = 98, p = 0.014) and non-significant between BDNF and RBANS total score (r = −0.21, df = 98, p = 0.06). Interestingly, BDNF levels were significantly associated with CO levels (r = 0.38, df = 96, p < 0.01), and non-significantly with FTND (r = 0.24, df = 95, p = 0.06). However, only the significant association between BDNF and CO levels passed the Bonferroni corrections (p < 0.05).

Table 3 shows Pearson partial correlation coefficients for the relationships between BDNF levels and cognitive domain scores within each genotype group in the smoking group. Among the Val/Met genotype, BDNF levels were significantly associated with worsening attention performance (r = −0.34, df = 65, p = 0.019). Further, this association was observed especially in Val allele (Val/Met + Val/Val) carriers (r = −0.38, df = 86, p = 0.002). In addition, among the Val/Met genotypes, BDNF was significantly associated with CO concentrations (Val/Met: r = 0.33, df = 65, p = 0.022). Further, this association was observed especially in Val allele carriers (r = 0.38, df = 86, p = 0.006). However, these significant associations did not pass the Bonferroni test (all p > 0.05).

Table 3 Relationships between BDNF levels and cognitive domain scores and carbon monoxide concentration across BDNF Val66Met genotype groupings in smokers.

In nonsmoking groups, no significant correlation was found between BDNF level and any RBANS index or total scores. Moreover, no significant correlation between BDNF level and any RBANS index and total scores was observed when being grouped by BDNF genotype (all p > 0.05), indicating no significant effects of BDNF level, BDNF genotype and their interaction on cognitive performance in the nonsmoking group.


To our best knowledge, this is the first study to investigate the effect of smoking on BDNF and cognition as well as their relationship in a normal Chinese population. The main findings of the present study were that, (1) smokers had significantly lower cognitive scores on the RBANS total score, immediate memory and delayed memory; (2) there was no significant difference in BDNF serum levels and BDNF Val66Met genotype between smokers and nonsmokers; (3) there was a significant negative association between serum BDNF levels and attention only in the smoking group. Moreover, this association was only observed in Val allele carriers; (4) BDNF level was found to be significantly associated with CO levels in the smoking group. Moreover, this association was only observed in Val allele carriers.

The finding of lower cognitive performance in smokers is concordant with numerous studies evaluating cognitive function in smokers among the normal population11,12,13,14, suggesting that chronic smoking may increase the cognitive decline in a normal population. However, some previous studies suggest that nicotine could enhance aspects of cognitive function, including motor abilities, attention and memory9, especially in some diseases that have cognitive deficits, such as schizophrenia, attention deficit/hyperactivity disorder, Alzheimer’s and Parkinson’s diseases, and age related cognitive decline6,7,8. Nicotine’s cognition-enhancing effects have been attributed to enhancing DA signaling in mesolimbic and mesocortical DA pathways5, an up-regulation of nicotinic acetylcholine receptors (nAChRs), or possibly protection from the neurotoxicity induced by free radicals8. However, nicotine also can produce neuronal toxicity, and chronic cigarette smoking potently increases free radical production and antioxidant depletion46. Moreover, the other 4700 components of tobacco smoke include a variety of carcinogens as well as other toxic compounds such as carbon monoxide, heavy metals and cyanide47, and could account for some of the cognitive, intellectual, and behavioral impairments in the non-demented elderly48. Interestingly, a previous study showed that nicotine’s effects may be dose dependent, and low dose nicotine may be an antioxidant and be neuroprotective, whereas high dose nicotine may induce neurotoxicity through oxidative stress and cellular injury49. Taken together, we hypothesize that smoking or nicotine use, especially at low dose and acute administration, may improve cognition in those patients with established cognitive deficits, but long-term use at high doses may damage cognition in healthy controls, suggesting that regular smoking or nicotine use may have a different effect on cognitive function in healthy controls compared to patients with cognitive deficits.

We found no association between the BDNF Val66Met polymorphism and smoking among male Chinese, which is consistent with two recent studies in a healthy Caucasian population36,41,42, but not with two other studies in European-Caucasians34,35. A possible reason for the inconsistencies in genetic association studies is related to ethnic background. For example, the allele frequency distribution of Val66Met has varied significantly between Chinese and Caucasian subjects. The Met allele frequency is around 50% in Chinese consistent with the 48.8% Met allele frequency found in our current study, but it is only around 20% in Caucasian subjects50. Thus, interethnic differences in the genotype frequencies of the BDNF Val66Met polymorphism may play an important role in accounting for the inconsistent results across the different populations. Other factors may include different sample sizes, the methodologies for measuring smoking, and ethnic stratification effects10. Thus, the association of the BDNF gene polymorphism and smoking behavior deservers further investigation.

Interestingly, we found a significant negative association between serum BDNF levels and attention only in the smoking group, and this association was only observed in Val allele carriers. Thus, BDNF was implicated in cognitive function only in smokers. Furthermore, the BDNF Val66Met polymorphism affected the correlation between BDNF and different aspects of cognitive function only in smokers, not in nonsmokers. The BDNF serum level displayed a negative association with attention, but the association was opposite to our expected direction. Studies have shown that BDNF plays a critical role in activity dependent neuroplasticity underlying learning and memory in the hippocampus17,18. Recent studies have shown that BDNF levels are significantly decreased in individuals with cognitive decline-related diseases, such as mild cognitive impairment, Alzheimer disease, and Huntington’s disease20,21,22,23. Moreover, higher BDNF levels are associated with better neuropsychological test performance in these diseases21. However, it is noteworthy that in our present study, smokers had some cognitive deficits, but not lower BDNF levels. Hence, it is possible that smoking-induced cognitive deficits (maybe through free radical mechanisms) lead to an increase in BDNF levels in order to reverse smoking’s harmful effects, and prevent further damage. Hence, increases in BDNF levels may be compensatory processes to attain homeostasis in the cognition-BDNF system, which might lead to higher BDNF levels in smokers. However, in our current study, we found no significant difference in BDNF levels between smokers and nonsmokers, suggesting that smokers had already failed to have sufficient BDNF. Moreover, comparatively high BDNF being associated with more cognitive impairment in smokers needs to be viewed in the context of no overall differences in BDNF in these smokers compared to nonsmokers. In addition, our findings of the significant association between BDNF levels and CO concentrations and the trend toward significant association between BDNF and FTND total score seem to support this hypothesis that greater nicotine dependence or smoking severity elevates BDNF in smokers.

Furthermore, BDNF Val66Met genotype groupings had a significant impact on the relationship between BDNF levels and cognitive impairments in smokers. The correlations between BDNF levels and cognition especially attention was only observed for Val allele carriers, but not for the Met/Met genotype. These divergent serum BDNF- cognitive function relationships across BDNF genotypes in smokers may also provide a clue about the unusual finding of higher BDNF levels with more cognitive impairment. A direct effect of the BDNF Val66Met polymorphism itself may have contributed toward the present findings. This polymorphism has been found to be associated with altered intracellular trafficking of pro-BDNF and secretion of the mature peptide18,27,28, suggesting that the BDNF Val66Met variant is a kind of functional polymorphism. Moreover, the Met66 allele has been associated with impaired depolarization-dependent secretion and intracellular trafficking of BDNF protein in the hippocampus18. Thus, the functional Val66Met polymorphism of the BDNF gene may exert its effect on the cognitive performance of smokers by affecting BDNF expression and protein production. Our failure to observe an association between BDNF levels and cognition in the smoking group with the Met/Met genotype could be due to lack of enough BDNF to counteract the smoking-induced cognitive impairment. However, while the functional effect of the Met66 allele on trafficking of the protein makes this polymorphism a strong candidate for direct involvement in attention function in smokers, we cannot exclude linkage disequilibrium with another polymorphism nearby as an explanation for this association.

Further, it is worthy of mentioning that Met allele carriers have demonstrated poorer episodic memory than their respective Val-homozygous counterparts in healthy controls or in patients with schizophrenia18,31. Moreover, Met allele carriers have lower hippocampal function and have reduced hippocampal and prefrontal gray matter30, brain regions known to participate in memory. However, the current study showed association with other aspect of neuropsychological functioning, such as attention and language, but not in the memory domain. We could not provide the reasonable explanations for the mechanisms by which the BDNF Val66Met variant affects attention, but not memory due to our cross-sectional design in our current study. It is possible that this discrepancy might be related to the study design differences.

Several limitations of this study should be noted. First, this is a cross-sectional study design and cannot show direct causality, although there were many significant associations or correlations in our study. That means, they are not etiology. For example, the BDNF correlation with cognition was only presented in smokers, but not in non-smokers, suggesting that BDNF changes and cognition changes are all downstream effects of smoking, which are pathological changes. Second, both smokers and nonsmokers had a relatively limited sample size, especially when being divided into subgroups by the BDNF genotype. This could lead to false positive or negative results due to the lack of statistical power and selection of samples. Moreover, after the Bonferroni correction, none of the associations remained significant, suggesting a small effect. Hence, a replication study would be needed with a larger sample size. Third, due to the shortcoming of the design for this study and the limits of the experimental and clinical conditions, we only had about 200 subjects who carried out the cognitive test and were on serum BDNF level test, although all the 628 subjects were genotyped with BDNF- Val66Met polymorphism. This might lead to bias in the statistical analysis due to the imbalance in the number of the subjects who took cognitive test, BDNF serum assay and BDNF- Val66Met polymorphism genotyping differentially. Fourth, we only measured the BDNF serum levels following an overnight fast, but not during and after smoking in smokers. Previous studies have shown that smoking influenced the BDNF serum levels39,40. We speculate that BDNF serum levels might change at the different time points of smoking, which warrants further investigation. Besides smoking, exercise level, alcohol and food may affect the BDNF serum levels, which had not been collected in this study and will be remedied in the future investigation. Fifth, our sample was limited to only males and can not be applied to females. It would be interesting to evaluate whether our findings in the present study could generalize to female subjects. Sixth, we focused on the Val66Met polymorphism, because it is functional and previously associated with cognitive performance. However, in our current study, we found that the serum BDNF levels were not related to val66met genotype. We speculated that other genetic variants within BDNF may influence subsequent BDNF expression or activity, suggesting more extensive genotyping to identify haplotype blocks of greater association with cognition. Although we did not find the effects of Val66Met polymorphism on serum BDNF levels, we did find a significant negative association between serum BDNF levels and attention only in Val allele carriers in the smoking group, suggesting the important role of this polymorphism in adjusting the relationship of cognition and serum BDNF levels. Seventh, several cognitive performance tests were used, but there was only a correlation with the attention index and BDNF in the smoker group. We could not give a reasonable explanation why only one domain of cognitive performance was associated with BDNF in the smoker group due to the nature of our cross sectional design. Moreover, the significance is weak, and the positive results were based on a comparatively small sample size. Eighth, we measured BDNF in serum, not in cerebral spinal fluid (CSF). It is still uncertain whether peripheral BDNF levels reflect similar changes in the central nervous system (CNS).

In summary, we have provided new evidence to support that smoking is associated with significant cognitive impairment in a male Han Chinese population, especially on immediate and delayed memory, and total cognitive performance. Although we did not find any associations of BNDF levels or the BDNF Val66Met polymorphism with smoking, we found a significant negative association between serum BDNF levels and attention and a positive association between BDNF levels and CO concentrations in the smoking group. Moreover, these associations in smokers appear to be dependent on the presence of BDNF Val66Met polymorphism, with these associations observed only in Val allele carries. However, these findings still need to be regarded as preliminary because of the relatively small sample size and the cross-sectional design in this study. Future large controlled prospective studies would help clarify the interrelationships between smoking, cognitive functioning and BDNF.



Six hundred and twenty-eight healthy unrelated male volunteers (aged 22–70 years, mean age: 46.3 ± 12.7 years) were recruited from the Haidian district in Beijing. The participants were interviewed by trained investigators, using a detailed questionnaire including general information, socio-demographic characteristics, current and previous smoking behavior, and medical and psychological conditions. All subjects met the following inclusion criteria: 1) age 20–70 years, Han Chinese; 2) no DSM-IV Axis I psychiatric diagnosis by a research psychiatrist using the basis of the Structured Clinical Interview for DSM-IV (SCID); 3) being able to provide the signed informed consent for participating in the study and to complete the cognitive test.

A complete medical history, physical examination and lab test were obtained from all subjects. Those subjects with physical diseases were excluded. All of the subjects were excluded from alcohol or illegal drug abuse/dependence by self-report.

Subjects meeting one or more of the following criteria were excluded: (1) documented disease of the central nervous system that could interfere with the cognitive assessments including, but not limited to epilepsy, stroke, tumor, Parkinson’s disease, Huntington’s disease, seizure disorder, history of brain trauma resulting in significant impairment; (2) acute, unstable and/or significant and untreated medical illness (e.g., infection, diabetes, hypertensions); (3) chronic infection; (5) a clinically significant electrocardiogram (ECG) abnormality in the opinion of the investigator; (6) use of any medication; (7) history of severe allergy or hypersensitivity; (8) dependence on alcohol or illicit drugs.

The Institutional Review Board (IRB) at Beijing HuiLongGuan hospital approved this study and each subject gave written informed consent for participating after the study had been fully explained. In addition, all methods were performed in accordance with Declaration of Helsinki promulgated by the National Institute of Health.

In order to maintain consistency in the use of various terms while gathering data on smoking behavior, the US Centers for Disease Control and Prevention have developed and updated the following definitions2: Never smokers – Adults who have never smoked a cigarette or who have smoked fewer than 100 cigarettes in their entire lifetime. Former Smokers – Adults who have smoked at least 100 cigarettes in their lifetime, but they currently do not smoke. Nonsmokers – Adults who currently do not smoke cigarettes, including both former smokers and never smokers. Current Smokers – Adults who have smoked 100 cigarettes in their lifetime and currently smoke cigarettes every day (daily) or some days (nondaily). Former smokers were excluded from the present study.

In addition, the Chinese translation of the standardized Fagerstrom Test for Nicotine Dependence (FTND) was employed to measure the degree of nicotine dependence (ND)51. Additional visits were requested for subjects with missing or ambiguous data. Exclusion criteria included a history of -Diagnostic and Statistical Manual of Mental Disorders—Fourth Edition | (DSM-IV) psychiatric disorder, alcohol abuse, and other drug abuse. Demographic data are summarized in Table 1.

Cognition Measures

We assessed cognitive functioning using the repeatable battery for the assessment of neuropsychological status (RBANS, Form A)52 from 212 subjects on the same day as the blood samples were taken. The RBANS is comprised of 12 subtests that are used to calculate 5 age-adjusted index scores and a total score. Test indices are Immediate Memory (comprised of List Learning and Story Memory tasks); Visuospatial/Constructional (comprised of Figure Copy and Line Orientation tasks); Language (comprised of Picture Naming and Semantic Fluency tasks); Attention (comprised of Digit Span and Coding tasks); and Delayed Memory (comprised of List Recall, Story Recall, Figure Recall, and List Recognition tasks). The RBANS was previously translated into Chinese by our group and its clinical validity and test–retest reliability were established among controls53.

Measurement of carbon monoxide

Measurement of carbon monoxide (CO) concentrations in exhaled air was performed using BreathICO (Vitalograph Buckingham, UK). Three hundred and thirty-six participants (143 smokers and 193 non-smokers) were instructed to hold their breath for 15 seconds and then exhale into a disposable tube attached to the BreathICO. Breath CO concentrations were expressed in parts per million (ppm).

Serum BDNF measurement

Blood samples were collected between 06:00 and 08:00 following an overnight fast. We measured fasting serum BDNF levels from 192 subjects by sandwich ELISA using a commercially available kit as described in our previous report54. All samples were assayed by a research assistant blind to the clinical situation. Inter- and intra-assay variation coefficients were 7 and 5%, respectively.


The genotypes of the BDNF Val66Met polymorphisms from all subjects (n = 628) were identified as reported in our previous study43. A research assistant who was blinded to the clinical status genotyped every subject twice for accuracy of genotyping55,56,57,58.

Statistical Analysis

Deviation from Hardy–Weinberg equilibrium was calculated by chi-square (χ2) goodness-of-fit test. The BDNF Val66Met allele and genotype frequencies were compared between smokers and nonsmokers using x2 tests. Group differences were compared using Student’s two-sample t-test or one-way analysis of variance (ANOVA) for continuous variables and chi-squared for categorical variables. Correlation between variables was studied using Pearson product moment correlations.

We tested associations between the BDNF Val66Met polymorphism and the cognitive measures or serum BDNF levels using a general factorial design in PASW statistical software version 18.0 (SPSS Inc, Chicago, Illinois). For the main models, the BDNF Val66Met genotype and smoking status (smokers vs nonsmokers) were entered as fixed effects. Scores for each cognitive domain and the total scores of RBANS were entered as the dependent variables, with age, education and body mass index (BMI) included as covariates as appropriate. In each model, the main effect of smoking status group, the main effect of genotype and smoking group × genotype interaction were tested. The smoking group × genotype interaction term in the model detects the differential effects that alleles might have on cognitive scores between smoking status groups. Similarly, the main effect of the BDNF genotype on serum BDNF levels was also analyzed using analyses of covariance (ANCOVA). We applied Bonferroni corrections to adjust for multiple testing. Lastly, we performed exploratory analyses to examine whether the relationships between BDNF serum levels and cognitive function were different across BDNF Val66Met genotype groups. Partial Pearson’s product moment correlation coefficients were used to assess associations of cognitive performance with serum BDNF levels while adjusting for various potentially confounding demographic variables of age, education and BMI. Statistical significance was defined as p < 0.05.


  1. 1.

    Goncalves, R. B. et al. Impact of smoking on inflammation: overview of molecular mechanisms. Inflamm Res 60(5), 409–424 (2011).

    CAS  Article  Google Scholar 

  2. 2.

    Centers for Disease Control and Prevention. Vital signs: Current cigarette smoking among adults aged ≥ 18 years—United States. Morbidity and Mortality Weekly Report 59, 1135–1140 (2010).

  3. 3.

    Au, W. W., Su, D. & Yuan, J. Cigarette smoking in China: public health, science, and policy. Rev Environ Health 27(1), 43–49 (2012).

    Article  Google Scholar 

  4. 4.

    Gruder, C. L. et al. Tobacco smoking, quitting, and relapsing among adult males in Mainland China: the China Seven Cities Study. Nicotine Tob Res 15(1), 223–230 (2013).

    Article  Google Scholar 

  5. 5.

    Jasinska, A. J., Zorick, T., Brody, A. L. & Stein, E. A. Dual role of nicotine in addiction and cognition: A review of neuroimaging studies in humans. Neuropharmacology 84, 111–122 (2014).

    CAS  Article  Google Scholar 

  6. 6.

    Evans, D. E. & Drobes, D. J. Nicotine self-medication of cognitive-attentional processing. Addict Biol 14(1), 32–42 (2009).

    CAS  Article  Google Scholar 

  7. 7.

    Levin, E. D., McClernon, F. J. & Rezvani, A. H. Nicotinic effects on cognitive function: behavioral characterization, pharmacological specification, and anatomic localization. Psychopharmacology 184, 523–539 (2006).

    CAS  Article  Google Scholar 

  8. 8.

    Newhouse, P. A., Potter, A. & Singh, A. Effects of nicotinic stimulation on cognitive performance. Curr Opin Pharmacol 4, 36–46 (2004).

    CAS  Article  Google Scholar 

  9. 9.

    Heishman, S. J., Kleykamp, B. A. & Singleton, E. G. Meta-analysis of the acute effects of nicotine and smoking on human performance. Psychopharmacology 210, 453–469 (2010).

    CAS  Article  Google Scholar 

  10. 10.

    Montag, C. et al. Epistasis of the DRD2/ANKK1 Taq Ia and the BDNF Val66Met polymorphism impacts novelty seeking and harm avoidance. Neuropsychopharmacology 35(9), 1860–1867 (2010).

    Article  Google Scholar 

  11. 11.

    Starr, J. M., Deary, I. J., Fox, H. C. & Whalley, L. J. Smoking and cognitive change from age 11 to 66 years: a confirmatory investigation. Addict Behav 32(1), 63–68 (2007).

    Article  Google Scholar 

  12. 12.

    Nooyens, A. C., van, G. B. M. & Verschuren, W. M. Smoking and cognitive decline among middle-aged men and women: the Doetinchem Cohort Study. Am J Public Health 98(12), 2244–2250 (2008).

    Article  Google Scholar 

  13. 13.

    Sabia, S., Marmot, M., Dufouil, C. & Singh-Manoux, A. Smoking history and cognitive function in middle age from the Whitehall II study. Arch Intern Med 168(11), 1165–1173 (2008).

    Article  Google Scholar 

  14. 14.

    Corley, J., Gow, A. J., Starr, J. M. & Deary, I. J. Smoking, childhood IQ, and cognitive function in old age. Journal of Psychosomatic Research 73, 132–138 (2012).

    Article  Google Scholar 

  15. 15.

    Hofer, M., Pagliusi, S. R., Hohn, A., Leibrock, J. & Barde, Y. A. Regional distribution of brain-derived neurotrophic factor mRNA in the adult mouse brain. EMBO 9(8), 2459–2464 (1990).

    CAS  Article  Google Scholar 

  16. 16.

    Hong, C. J., Liou, Y. J. & Tsai, S. J. Effects of BDNF polymorphisms on brain function and behavior in health and disease. Brain Res Bull 86(5-6), 287–297 (2011).

    CAS  Article  Google Scholar 

  17. 17.

    Poo, M. M. Neurotrophins as synaptic modulators. Nat Rev Neurosci 2(1), 24–32 (2001).

    CAS  Article  Google Scholar 

  18. 18.

    Egan, M. F. et al. The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function. Cell 112, 257–269 (2003).

    CAS  Article  Google Scholar 

  19. 19.

    Lu, B. & Gottschalk, W. Modulation of hippocampal synaptic transmission and plasticity by neurotrophins. Prog Brain Res 128, 231–241 (2000).

    CAS  Article  Google Scholar 

  20. 20.

    Komulainen, P. et al. BDNF is a novel marker of cognitive function in ageing women: the DR’s EXTRA Study. Neurobiol Learn Mem 90(4), 596–603 (2008).

    CAS  Article  Google Scholar 

  21. 21.

    Yu, H. et al. Association study of the decreased serum BDNF concentrations in amnestic mild cognitive impairment and the Val66Met polymorphism in Chinese Han. J Clin Psychiatry 69(7), 1104–1111 (2008).

    CAS  Article  Google Scholar 

  22. 22.

    Gunstad, J. et al. Serum brain-derived neurotrophic factor is associated with cognitive function in healthy older adults. J Geriatr Psychiatry Neurol 21(3), 166–170 (2008).

    Article  Google Scholar 

  23. 23.

    Ciammola, A. et al. Low brain-derived neurotrophic factor (BDNF) levels in serum of Huntington’s disease patients. Am J Med Genet B Neuropsychiatr Genet 144B(4), 574–577 (2007).

    CAS  Article  Google Scholar 

  24. 24.

    Zhang, X. Y. et al. Low BDNF is associated with cognitive impairment in chronic patients with schizophrenia. Psychopharmacology 222(2), 277–284 (2012).

    CAS  Article  Google Scholar 

  25. 25.

    Zhang, X. Y. et al. Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controls. Human Genetics 131, 1187–1195 (2012).

    CAS  Article  Google Scholar 

  26. 26.

    Chiaruttini, C. et al. Dendritic trafficking of BDNF mRNA is mediated by translin and blocked by the G196A (Val66Met) mutation. Proc Natl Acad Sci USA 106(38), 16481–16486 (2009).

    ADS  CAS  Article  Google Scholar 

  27. 27.

    Chen, Z. Y. et al. Variant brain-derived neurotrophic factor (BDNF) (Met66) alters the intracellular trafficking and activity-dependent secretion of wild-type BDNF in neurosecretory cells and cortical neurons. J Neurosci 24(18), 4401–4411 (2004).

    CAS  Article  Google Scholar 

  28. 28.

    Chen, Z. Y. et al. Genetic variant BDNF (Val66Met) polymorphism alters anxiety-related behavior. Science 314(5796), 140–143 (2006).

    ADS  CAS  Article  Google Scholar 

  29. 29.

    Bath, K. G., Akins, M. R. & Lee, F. S. BDNF control of adult SVZ neurogenesis. Dev Psychobiol 54(6), 578–589 (2012).

    CAS  Article  Google Scholar 

  30. 30.

    Hariri, A. R. et al. Brain-derived neurotrophic factor val66met polymorphism affects human memory-related hippocampal activity and predicts memory performance. J Neurosci 23(17), 6690–6694 (2003).

    CAS  Article  Google Scholar 

  31. 31.

    Dempster, E. et al. Association between BDNF val66 met genotype and episodic memory. Am J Med Genet B Neuropsychiatr Genet 134B(1), 73–75 (2005).

    Article  Google Scholar 

  32. 32.

    Kenny, P. J., File, S. E. & Rattray, M. Acute nicotine decreases, and chronic nicotine increases the expression of brain-derived neurotrophic factor mRNA in rat hippocampus. Brain Res Mol Brain Res 85, 234–238 (2000).

    CAS  Article  Google Scholar 

  33. 33.

    Li, M. D. et al. A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population. BMC Genet 4(Suppl 1), S103 (2003).

    Article  Google Scholar 

  34. 34.

    Beuten, J. et al. Significant association of BDNF haplotypes in European-American male smokers but not in European-American female or African-American smokers. Am J Med Genet B Neuropsychiatr Genet 139, 73–80 (2005).

    Article  Google Scholar 

  35. 35.

    Lang, U. E. et al. Association of the met66 allele of brain-derived neurotrophic factor (BDNF) with smoking. Psychopharmacology 190, 433–439 (2007).

    CAS  Article  Google Scholar 

  36. 36.

    Montag, C., Basten, U., Stelzel, C., Fiebach, C. J. & Reuter, M. The BDNF Val66Met polymorphism cand smoking. Neurosci Lett 442, 30–33 (2008).

    CAS  Article  Google Scholar 

  37. 37.

    Tobacco and Genetics Consortium. Genome- wide meta-analyses identify multiple loci associated with smoking behavior. Nat Genet 42(5), 441–447 (2010).

    Article  Google Scholar 

  38. 38.

    Breetvelt, E. J. et al. The association of the alpha-5 subunit of the nicotinic acetylcholine receptor gene and the brain-derived neurotrophic factor gene with different aspects of smoking behavior. Psychiatr Genet 22(2), 96–98 (2012).

    CAS  Article  Google Scholar 

  39. 39.

    Bhang, S. Y., Choi, S. W. & Ahn, J. H. Changes in plasma brain-derived neurotrophic factor levels in smokers after smoking cessation. Neurosci Lett 468, 7–11 (2010).

    CAS  Article  Google Scholar 

  40. 40.

    Colle, R. et al. Tobacco use is associated with increased plasma BDNF levels in depressed patients. Psychiatry Res 246, 370–372 (2016).

    CAS  Article  Google Scholar 

  41. 41.

    Jamal, M., Van der Does, W., Elzinga, B. M., Molendijk, M. L. & Penninx, B. W. Association between smoking, nicotine dependence, and BDNF Val66Met polymorphism with BDNF concentrations in serum. Nicotine Tob Res 17(3), 323–329 (2015).

    CAS  Article  Google Scholar 

  42. 42.

    Jamal, M., Van der Does, W. & Penninx, B. W. Effect of variation in BDNF Val(66)Met polymorphism, smoking, and nicotine dependence on symptom severity of depressive and anxiety disorders. Drug Alcohol Depend 148, 150–157 (2015).

    CAS  Article  Google Scholar 

  43. 43.

    Zhang, X. Y. et al. BDNF levels and genotype are associated with antipsychotic-induced weight gain in patients with chronic schizophrenia. Neuropsychopharmacology 33(9), 2200–2205 (2008).

    CAS  Article  Google Scholar 

  44. 44.

    Zhang, X. Y. et al. Effects of cigarette smoking and alcohol use on neurocognition and BDNF levels in a Chinese population. Psychopharmacology 233(3), 435–445 (2016).

    CAS  Article  Google Scholar 

  45. 45.

    de Leon, J. & Diaz, F. J. A meta-analysis of worldwide studies demonstrates an association between schizophrenia and tobacco smoking behaviors. Schizophr Res 76(2–3), 135–157 (2005).

    Article  Google Scholar 

  46. 46.

    Hritcu, L., Ciobica, A. & Gorgan, L. Nicotine-induced memory impairment by increasing brain oxidative stress. Cent Eur J Biol 4, 335–342 (2009).

    CAS  Google Scholar 

  47. 47.

    Swan, G. E. & Lessov-Schlaggar, C. N. The effects of tobacco smoke and nicotine on cognition and the brain. Neuropsychol Rev 17, 259–273 (2007).

    Article  Google Scholar 

  48. 48.

    Ott, A. et al. Effect of smoking on global cognitive function in nondemented elderly. Neurology 62(6), 920–924 (2004).

    MathSciNet  CAS  Article  Google Scholar 

  49. 49.

    Guan, Z. Z., Yu, W. F. & Nordberg, A. Dual effects of nicotine on oxidative stress and neuroprotection in PC12 cells. Neurochem Int 43, 243–249 (2003).

    CAS  Article  Google Scholar 

  50. 50.

    Varnas, K. et al. Brain-derived neurotrophic factor polymorphisms and frontal cortex morphology in schizophrenia. Psychiatr Genet 18(4), 177–183 (2008).

    Article  Google Scholar 

  51. 51.

    Fagerstrom, K. O. Measuring degree of physical dependence to tobacco smoking with reference to individualization of treatment. Addict Behav 3, 235–241 (1978).

    CAS  Article  Google Scholar 

  52. 52.

    Randolph, C., Tierney, M. C., Mohr, E. & Chase, T. N. The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS): preliminary clinical validity. J Clin Exp Neuropsychol 20, 310–319 (1998).

    CAS  Article  Google Scholar 

  53. 53.

    Zhang, B. H. et al. Repeatable battery for the assessment of neuropsychological status (RBANS) as a screening test in Chinese: reliability and validity. Chin Ment Health J 28, 865–869 (2009).

    Google Scholar 

  54. 54.

    Xiu, M. H. et al. Decreased serum BDNF levels in chronic institutionalized schizophrenia on long-term treatment with typical and atypical antipsychotics. Prog Neuropsychopharmacol Biol Psychiatry 33(8), 1508–1512 (2009).

    CAS  Article  Google Scholar 

  55. 55.

    Di Matteo, V., Pierucci, M., Di Giovanni, G., Benigno, A. & Esposito, E. The neurobiological bases for the pharmacotherapy of nicotine addiction. Curr Pharm Des 13, 1269–1284 (2007).

    Article  Google Scholar 

  56. 56.

    Anstey, K. J., von, S. C., Salim, A. & O’Kearney, R. Smoking as a risk factor for dementia and cognitive decline: a meta-analysis of prospective studies. Am J Epidemiol 1664, 367–378 (2007).

    Article  Google Scholar 

  57. 57.

    Yi, Z. et al. Lack of effect of brain derived neurotrophic factor (BDNF) Val66Met polymorphism on early onset schizophrenia in Chinese Han population. Brain Res 1417, 146–150 (2001).

    Article  Google Scholar 

  58. 58.

    Zhou, D. H. et al. The study of BDNF Val66Met polymorphism in Chinese schizophrenic patients. Progress in Neuropsychopharmacology and Biological Psychiatry 34, 930–933 (2010).

    CAS  Article  Google Scholar 

Download references


Funding for this study was provided by grants from the Science and Technology Program of Guangdong (2016A020216004), Science and Technology Program of Guangzhou (201704020168, 201807010064), Suzhou Key Project (Psychiatry) (Szxk201515), Suzhou Key Medical Center for Psychiatric Diseases (Szzx201509), Suzhou Key Diagnosis and Treatment Program (LCZX201316), Jiangsu Province Natural Science Fund Project (BK20151197), and Suzhou Key Medical Center for Psychiatric Diseases (Szzx201509).

Author information




Haisen Xia, Fengchun Wu and Xiang Yang Zhang were responsible for study design, statistical analysis, and manuscript preparation. Xiaosi Li, Junyi Cai, Xingbing Huang, Yuping Ning, and Fengchun Wu were responsible for recruiting the patients, performing the clinical rating and collecting the clinical data. Xiangdong Du, Guangzhong Yin, Yingyang Zhang, and Jair C. Soares were involved in evolving the ideas and editing the manuscript. Haisen Xia, Fengchun Wu and Xiang Yang Zhang were involved in writing the protocol, and cowrote the paper. Fengchu Wu, Xiangdong Du and Xiang Yang Zhang were responsible for providing the funding for the study. All authors have contributed to and have approved the final manuscript.

Corresponding authors

Correspondence to Fengchun Wu or Xiang Yang Zhang.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Xia, H., Du, X., Yin, G. et al. Effects of smoking on cognition and BDNF levels in a male Chinese population: relationship with BDNF Val66Met polymorphism. Sci Rep 9, 217 (2019).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing