genetic underpinnings of neuroticism a replication study 2155 6105.1000119

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Volume 3 • Issue 1 • 1000119 J Addict Res Ther ISSN:2155-6105 JART an open access journal Research Article Open Access Addiction Research & Therapy Aleksandrova et al., J Addict Res Ther 2012, 3:1 http://dx.doi.org/10.4172/2155-6105.1000119 Genetic Underpinnings of Neuroticism: A Replication Study Lily R Aleksandrova 1,2 , Renan P. Souza 1,3 , Michael R. Bagby 4 , David M. Casey 5 , David C. Hodgins 5 , Garry J. Smith 6 , Rob J. Williams 7 , Don P. Schopflocher 8 , Rob T. Wood 9 , Nady el-Guebaly 10 , James L. Kennedy 1,3# and Daniela S. S. Lobo 1,3,11# * 1 Neurogenetics Section, Neuroscience Department, Centre for Addiction and Mental Health, Toronto, ON, Canada 2 Department of Pharmacology, University of Toronto, Toronto, ON, Canada 3 Department of Psychiatry, University of Toronto, Toronto, ON, Canada 4 Clinical Research Department, Centre for Addiction and Mental Health, Toronto, ON, Canada 5 Department of Psychology, University of Calgary, Calgary, AB, Canada 6 Faculty of Extension, University of Alberta, Edmonton, AB, Canada 7 School of Health Sciences, University of Lethbridge, Lethbridge, AB, Canada 8 Faculty of Nursing, University of Alberta, Edmonton, AB, Canada 9 Department of Sociology, University of Lethbridge Lethbridge, AB, Canada 10 Division of Addiction, Department of Psychiatry, University of Calgary, Calgary, AB, Canada 11 Problem Gambling Service, Addictions Program, Centre for Addiction and Mental Health, Toronto, ON, Canada # contributed equally as senior authors Keywords: NEO; Neuroticism; Genetics Introduction Neuroticism is a core personality trait that reflects an individual’s emotional reactivity, with an estimated heritability of 40 to 60% [1- 3]. Individuals who score high on measures of neuroticism tend to be more sensitive to negative mood states and to have excessive responses to environmental stresses. Maladaptive efforts to regulate affect and cope with negative emotional life events can result in the development of an addiction or a psychiatric disorder [4-7]. In fact, high levels of neuroticism have been extensively linked to psychiatric disorders, such as depression [8-10], anxiety [7,11] and substance use disorders [12,13]. Neuroticism, as assessed by the NEO Personality Inventory (Neuroticism Extraversion and Openness Personality Inventory), is therefore considered an important vulnerability factor for psychopathology [14,15], and a strong positive correlation exists between NEO neuroticism scores and the risk of relapse in several psychiatric conditions, including psychosis, depression and substance abuse [12,16,17]. Furthermore, neuroticism scores and negative life events were found to be the two strongest predictors of onset of psychotic and depressive symptoms during remission and relapse from both alcoholism and opioid addiction [12,17,18]. Taken together, these results suggest that neuroticism may be an underlying vulnerability factor for mental illness and addiction. Recent findings support the hypothesis that genetic factors underlying individual differences in neuroticism could increase the susceptibility to both addiction and mental illness [19,20]. Twin studies have suggested a heritability coefficient in the range of 0.4- 0.6 for this personality trait, which has spurred attempts to map the genetic basis of neuroticism. e current study aimed to verify if previously reported associations of genetic variants with NEO neuroticism [3,21-26] scores would be replicated in a sample of healthy subjects of European Caucasian descent. Subjects and Methods Our sample of 215 unrelated healthy European Caucasian subjects (35% male, age 48.9±16.1) was collected as part of the “Leisure, Lifestyle, and Lifecycle” Project in the province of Alberta, Canada [27]. Presence of a lifetime psychiatric disorders was an exclusion criteria and was assessed through the Composite International Diagnostic Interview (CIDI) [28]. Personality traits were assessed using the NEO-FFI, which is a 60-item short version of the NEO-PI-R (Revised NEO Personality Inventory). is personality assessment measures Abstract Background: Neuroticism, as defined and measured by the NEO Personality Inventory (Neuroticism Extraversion and Openness Personality Inventory), is a core personality trait reflecting an individual’s emotional reactivity. High neuroticism is thought to be an important vulnerability factor for various psychiatric disorders in the general population, including substance abuse, depression, anxiety, and psychosis. Recent findings support the hypothesis that genetic factors underlying the neuroticism trait could increase the susceptibility to psychiatric disorders. The current study aimed to replicate genetic associations with high neuroticism previously reported in the literature. Methods: We genotyped four polymorphisms: CNR1 (rs7766029), GABRA2 (rs9291283), GABRA6 (rs3219151) and MAMDC1 (rs7151262) in 215 healthy Caucasian subjects, who completed a short version of the NEO-PI. NEO neuroticism scores of the three genotype groups were compared using ANCOVA, with age as a covariate. Results: All four genetic polymorphisms were found to be significantly associated with NEO neuroticism scores (p < 0.0025), but not with any other NEO personality domain. Conclusion: Our results corroborate other studies proposing a role for the GABAergic and cannabinoid systems in the modulation of affective states and stress responses, as measured through neuroticism scores. It is important to replicate the genetic findings of neuroticism, in order to gain a better understanding of this personality domain that has been reported as an important risk factor for mood and anxiety disorders and substance addiction. *Corresponding author: Daniela S. S. Lobo, M.D, Ph.D, Centre for Addiction and Mental Health, 33 Russell St, RS 3039 Toronto, ON - M5S 2S1, Canada, Tel: 1-416-535-8501 Ext 6568; Fax: 1-416-979-4666; E-mail: [email protected] Received November 12, 2011; Accepted January 12, 2012; Published January 16, 2012 Citation: Aleksandrova LR, Souza RP, Bagby MR, Casey DM, Hodgins DC, et al. (2012) Genetic Underpinnings of Neuroticism: A Replication Study. J Addict Res Ther 3:119. doi:10.4172/2155-6105.1000119 Copyright: © 2012 Aleksandrova LR, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Page 1: Genetic Underpinnings of Neuroticism a Replication Study 2155 6105.1000119

Volume 3 • Issue 1 • 1000119J Addict Res TherISSN:2155-6105 JART an open access journal

Research Article Open Access

Addiction Research & Therapy

Aleksandrova et al., J Addict Res Ther 2012, 3:1http://dx.doi.org/10.4172/2155-6105.1000119

Genetic Underpinnings of Neuroticism: A Replication StudyLily R Aleksandrova1,2, Renan P. Souza1,3, Michael R. Bagby4, David M. Casey5, David C. Hodgins5, Garry J. Smith6, Rob J. Williams7, Don P. Schopflocher8, Rob T. Wood9, Nady el-Guebaly10, James L. Kennedy1,3# and Daniela S. S. Lobo1,3,11#*1Neurogenetics Section, Neuroscience Department, Centre for Addiction and Mental Health, Toronto, ON, Canada2Department of Pharmacology, University of Toronto, Toronto, ON, Canada3Department of Psychiatry, University of Toronto, Toronto, ON, Canada4Clinical Research Department, Centre for Addiction and Mental Health, Toronto, ON, Canada5Department of Psychology, University of Calgary, Calgary, AB, Canada6Faculty of Extension, University of Alberta, Edmonton, AB, Canada7School of Health Sciences, University of Lethbridge, Lethbridge, AB, Canada8Faculty of Nursing, University of Alberta, Edmonton, AB, Canada 9Department of Sociology, University of Lethbridge Lethbridge, AB, Canada10Division of Addiction, Department of Psychiatry, University of Calgary, Calgary, AB, Canada 11Problem Gambling Service, Addictions Program, Centre for Addiction and Mental Health, Toronto, ON, Canada #contributed equally as senior authors

Keywords: NEO; Neuroticism; Genetics

IntroductionNeuroticism is a core personality trait that reflects an individual’s

emotional reactivity, with an estimated heritability of 40 to 60% [1-3]. Individuals who score high on measures of neuroticism tend to be more sensitive to negative mood states and to have excessive responses to environmental stresses. Maladaptive efforts to regulate affect and cope with negative emotional life events can result in the development of an addiction or a psychiatric disorder [4-7]. In fact, high levels of neuroticism have been extensively linked to psychiatric disorders, such as depression [8-10], anxiety [7,11] and substance use disorders [12,13]. Neuroticism, as assessed by the NEO Personality Inventory (Neuroticism Extraversion and Openness Personality Inventory), is therefore considered an important vulnerability factor for psychopathology [14,15], and a strong positive correlation exists between NEO neuroticism scores and the risk of relapse in several psychiatric conditions, including psychosis, depression and substance abuse [12,16,17]. Furthermore, neuroticism scores and negative life events were found to be the two strongest predictors of onset of psychotic and depressive symptoms during remission and relapse from both alcoholism and opioid addiction [12,17,18]. Taken together, these results suggest that neuroticism may be an underlying vulnerability factor for mental illness and addiction.

Recent findings support the hypothesis that genetic factors underlying individual differences in neuroticism could increase the susceptibility to both addiction and mental illness [19,20]. Twin studies have suggested a heritability coefficient in the range of 0.4-

0.6 for this personality trait, which has spurred attempts to map the genetic basis of neuroticism. The current study aimed to verify if previously reported associations of genetic variants with NEO neuroticism [3,21-26] scores would be replicated in a sample of healthy subjects of European Caucasian descent.

Subjects and MethodsOur sample of 215 unrelated healthy European Caucasian subjects

(35% male, age 48.9±16.1) was collected as part of the “Leisure, Lifestyle, and Lifecycle” Project in the province of Alberta, Canada [27]. Presence of a lifetime psychiatric disorders was an exclusion criteria and was assessed through the Composite International Diagnostic Interview (CIDI) [28]. Personality traits were assessed using the NEO-FFI, which is a 60-item short version of the NEO-PI-R (Revised NEO Personality Inventory). This personality assessment measures

AbstractBackground: Neuroticism, as defined and measured by the NEO Personality Inventory (Neuroticism Extraversion

and Openness Personality Inventory), is a core personality trait reflecting an individual’s emotional reactivity. High neuroticism is thought to be an important vulnerability factor for various psychiatric disorders in the general population, including substance abuse, depression, anxiety, and psychosis. Recent findings support the hypothesis that genetic factors underlying the neuroticism trait could increase the susceptibility to psychiatric disorders. The current study aimed to replicate genetic associations with high neuroticism previously reported in the literature. Methods: We genotyped four polymorphisms: CNR1 (rs7766029), GABRA2 (rs9291283), GABRA6 (rs3219151) and MAMDC1 (rs7151262) in 215 healthy Caucasian subjects, who completed a short version of the NEO-PI. NEO neuroticism scores of the three genotype groups were compared using ANCOVA, with age as a covariate.

Results: All four genetic polymorphisms were found to be significantly associated with NEO neuroticism scores (p < 0.0025), but not with any other NEO personality domain.

Conclusion: Our results corroborate other studies proposing a role for the GABAergic and cannabinoid systems in the modulation of affective states and stress responses, as measured through neuroticism scores. It is important to replicate the genetic findings of neuroticism, in order to gain a better understanding of this personality domain that has been reported as an important risk factor for mood and anxiety disorders and substance addiction.

*Corresponding author: Daniela S. S. Lobo, M.D, Ph.D, Centre for Addiction and Mental Health, 33 Russell St, RS 3039 Toronto, ON - M5S 2S1, Canada, Tel: 1-416-535-8501 Ext 6568; Fax: 1-416-979-4666; E-mail: [email protected]

Received November 12, 2011; Accepted January 12, 2012; Published January 16, 2012

Citation: Aleksandrova LR, Souza RP, Bagby MR, Casey DM, Hodgins DC, et al. (2012) Genetic Underpinnings of Neuroticism: A Replication Study. J Addict Res Ther 3:119. doi:10.4172/2155-6105.1000119

Copyright: © 2012 Aleksandrova LR, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Page 2: Genetic Underpinnings of Neuroticism a Replication Study 2155 6105.1000119

Citation: Aleksandrova LR, Souza RP, Bagby MR, Casey DM, Hodgins DC, et al. (2012) Genetic Underpinnings of Neuroticism: A Replication Study. J Addict Res Ther 3:119. doi:10.4172/2155-6105.1000119

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Volume 3 • Issue 1 • 1000119J Addict Res TherISSN:2155-6105 JART an open access journal

the following five personality dimensions: Neuroticism, Extraversion, Openness to Experience, Agreeableness and Conscientiousness [14].

DNA extraction was performed on blood samples using a standard high-salt method. We genotyped four polymorphisms previously associated with neuroticism in the literature: rs7766029 in the CNR1 [24], rs9291283 in GABRA2 [26,29], rs3219151 in GABRA6 [21,25] and rs7151262 in MAMDC1 [3,23,30]. Genotyping was performed using TaqMan allele-specific assays (ABI Prism 7000/7500, Applied Biosystems, Foster City, CA). According to published guidelines, we have included four negative controls in each 96-well genotyping plate and 10% of the total sample was re-genotyped to ensure sufficient accuracy.

NEO domain scores of the three genotype groups were compared using ANCOVA with age as a covariate, implemented on the Statistical Package for the Social Sciences (SPSS), version 15.0. Age was incorporated in our model because it is a key factor influencing personality; including neuroticism scores [3,31]. The significance level was set to p=0.0025 after a Bonferroni correction for multiple testing (0.05/ 20 tests).

ResultsWe obtained 100% genotyping accuracy and all polymorphisms

were in Hardy-Weinberg equilibrium (p > 0.05). Our sample had over 80% statistical power to detect association of the GABRA2 polymorphism (lowest allele frequency among the evaluated polymorphisms) with a minimum r2 of 2.5% [32]. All four variants were found to be significantly associated with neuroticism scores in our sample (p < 0.0025). We have not observed significant association of these polymorphisms with any of the other four NEO personality dimensions analyzed. The common allelic variants of CNR1 rs7766029 and GABRA2 rs9291283 were associated with higher neuroticism scores than the rare alleles; while the common alleles of

GABRA6 rs3219151 and MAMDC1 rs7151262 were associated with lower neuroticism scores (Table 1).

DiscussionWe replicated previously reported associations of polymorphisms

in GABRA2 and 6, CNR1, and MAMDC1 with the personality trait of neuroticism. Taken together with previous results, the current study supports the roles of the endocannabinoid and GABAergic neurotransmitter systems in the regulation of emotionality and responsiveness to stress. Limitations to this study would include a moderate sample size, but our power calculations showed we would have 80% power to detect medium genetic effects [33]. Also, the functional role of the polymorphisms investigated here is yet to be determined.

The first genome-wide association study (GWAS) for neuroticism highlighted the significance of a common polymorphism in the mam domain-containing glycosylphosphatidyl-inositol anchor 2 gene (MAMDC1) [3], which was recently confirmed in a second GWAS [23]. Although no functional studies of rs7151262 have been published, the MAMDC1 gene is predominantly expressed in areas associated with memory and emotional regulation (hippocampus and amygdala), and is thought to be involved in regulating neuronal migration and axonal guidance [34].

Cannabinoids are known to have both anxiolytic and anxiogenic properties, implicating the endocannabinoid system in mood and stress response regulation. It has been hypothesized that temporal changes in the endocannabinoid system during development can affect a person s emotional stability and stress responsiveness later in life [35-37]. For example, cannabis use during adolescence has been recently highlighted as a significant risk factor for the development of psychotic symptoms in adulthood [37]. Moreover, adolescent exposure to cannabinoids is associated with an earlier onset of schizophrenia [35]. Not surprisingly, genetic variants in the cannabinoid receptor

Genetic Variant Personality Domain

Genotype ANCOVA (covariate: age)1 1 1 2 2 2

mean n SD mean n SD mean n SD F p*

CNR1 rs7766029 1 = T 2 = C

Neuroticism 14.5 51 7.4 15.9 86 7.8 14.8 74 7.0 6.6 <0.001Extraversion 28.5 51 6.7 29.3 86 6.4 28.5 74 6.2 1.4 0.25Openness 29.8 51 5.8 29.5 86 6.2 30.3 74 6.2 2.1 0.09Agreeableness 35.5 51 6.0 34.4 86 5.6 34.5 74 4.2 3.0 0.03Conscientiousness 34.8 51 6.0 34.7 86 6.0 34.8 74 5.6 1.8 0.14

GABRA2 rs9291283 1 = C 2 = T

Neuroticism 15.3 122 8.1 14.9 80 6.6 13.6 11 5.3 6.1 <0.001Extraversion 28.5 122 6.4 29.2 80 6.6 29.2 11 4.1 1.1 0.34Openness 29.9 122 6.3 29.7 80 5.7 32.7 11 6.9 3.0 0.03Agreeableness 34.8 122 5.2 34.6 80 5.6 35.6 11 4.4 2.6 0.06Conscientiousness 35.1 122 5.7 34.6 80 6.0 33.8 11 7.0 2.2 0.09

GABRA6 rs3219151 1 = T 2 = C

Neuroticism 13.7 75 6.1 15.2 95 7.5 17.2 43 9.0 7.9 <0.0001Extraversion 28.8 75 6.3 29.1 95 6.2 28.2 43 7.0 1.2 0.31Openness 28.6 75 6.0 31.0 95 5.7 30.1 43 6.7 4.3 0.01Agreeableness 34.9 75 5.0 34.2 95 5.0 35.7 43 6.1 3.6 0.02Conscientiousness 35.5 75 5.2 34.1 95 5.6 35.3 43 7.5 3.0 0.03

MAMDC1 rs7151262 1 = G 2 = C

Neuroticism 15.1 87 7.9 14.6 85 7.2 16.1 41 7.0 6.0 <0.001Extraversion 28.9 87 6.4 28.3 85 6.0 29.5 41 7.1 1.2 0.30Openness 30.1 87 5.7 29.5 85 6.0 30.6 41 7.1 2.1 0.10Agreeableness 35.4 87 5.4 34.5 85 5.3 34.0 41 5.0 3.3 0.02Conscientiousness 35.4 87 6.3 35.0 85 5.5 33.4 41 5.7 3.0 0.03

*The significance level was set to p=0.0025 after a Bonferroni correction for multiple testing (0.05/ 20 tests)

Table 1: Association analysis between CNR1, GABRA2, GABRA6 and MAMDC1 polymorphisms with the five personality domains assessed by the NEO-FFI scale, using age as covariate (ANCOVA).

Page 3: Genetic Underpinnings of Neuroticism a Replication Study 2155 6105.1000119

Citation: Aleksandrova LR, Souza RP, Bagby MR, Casey DM, Hodgins DC, et al. (2012) Genetic Underpinnings of Neuroticism: A Replication Study. J Addict Res Ther 3:119. doi:10.4172/2155-6105.1000119

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Volume 3 • Issue 1 • 1000119J Addict Res TherISSN:2155-6105 JART an open access journal

1 gene (CNR1) have been reported to be significantly associated with high neuroticism scores [24].

Similarly, the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) has long been implicated in modulating anxiety, and may therefore partially underlie the personality dimension of neuroticism [38,39]. Post-mortem studies have found that the prefrontal cortex of patients who suffered from depression or an anxiety disorder contained less GABAergic neurons [38]. Furthermore, prior genetic studies have shown associations of neuroticism with polymorphisms located in the GABAergic system genes. Common polymorphisms within the glutamic acid decarboxylase 1 (GAD1) gene, which encodes the enzyme responsible for GABA synthesis, have been significantly associated with high neuroticism scores [11]. Moreover, variants in the GABA receptor subunit alpha (GABRA) have been previously found to be associated with neuroticism and other emotional reactivity-associated traits (e.g. attenuated stress response and harm avoidance), and could confer a genetic susceptibility to major depression and anxiety disorders [25,26,29,40].

The current study investigated the association of four previously reported polymorphisms with neuroticism and these associations were replicated. Neuroticism is thought to have a moderate genetic component and may be important in the acquisition, development, and maintenance of psychiatric disorders, including substance addiction. Thus, together with previous research, our results may help clarify the genetic underpinnings of neuroticism and its role as a vulnerability factor for both mood and anxiety disorders and substance addiction.

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Citation: Aleksandrova LR, Souza RP, Bagby MR, Casey DM, Hodgins DC, et al. (2012) Genetic Underpinnings of Neuroticism: A Replication Study. J Addict Res Ther 3:119. doi:10.4172/2155-6105.1000119

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