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The Brain Derived Neurotrophic Factor and Personality

DOI: 10.1155/2014/719723

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Abstract:

The study of the biological basis of personality is a timely research endeavor, with the aim of deepening our understanding of human nature. In recent years, a growing body of research has investigated the role of the brain derived neurotrophic factor (BDNF) in the context of individual differences across human beings, with a focus on personality traits. A large number of different approaches have been chosen to illuminate the role of BDNF for personality, ranging from the measurement of BDNF in the serum/plasma to molecular genetics to (genetic) brain imaging. The present review provides the reader with an overview of the current state of affairs in the context of BDNF and personality. 1. What Is Personality? 1.1. Why Study Human Personality? The study of the individual differences of humans is as old as mankind. The first Greek philosophers, such as Hippocrates, were interested in finding an answer to the question of why humans differ. According to Hippocrates, the essence of individuality was found in four bodily fluids; for example, black bile was associated with a melancholic personality structure [1, 2]. Since then, generations of scientists have strived to shed light on human personality. Beyond the scientist’s pure curiosity in this topic, the study of personality yields important insights into the nature of humans. Here, it has been put forward that an understanding of the healthy aspects of personality must inform the understanding of psychopathological conditions, because the latter are much harder to study given imbalances, for example, in the neurotransmitter systems of humans (e.g., [3, 4]). Many personality traits, such as neuroticism, are known to be of large importance for public health outcomes [5]. Therefore, an understanding of personality is also a key to disentangling the complex nature of psychopathology. 1.2. A Short Definition of Personality Definitions of personality are numerous in the literature (e.g., [6–8]). In my opinion, the most common denominator among these definitions represents the concept of “traits,” referring to the stability of personality dimensions, such as being cooperative or curious over long time periods across the lifespan. These personality characteristics influence the way a person thinks, behaves, and reacts emotionally towards a large number of environmental stimuli [6]. Of note, and for a better understanding of the above introduced term “traits,” it needs to be mentioned that in some situations a person will always show a particular emotional reaction such as being sad, for example, when a beloved

References

[1]  M. Bujalkova, S. Straka, and A. Jureckova, “Hippocrates' humoral pathology in nowaday's reflections,” Bratislavske Lekarske Listy, vol. 102, no. 10, pp. 489–492, 2001.
[2]  A. Katsambas and S. G. Marketos, “Hippocratic messages for modern medicine (the vindication of Hippocrates),” Journal of the European Academy of Dermatology and Venereology, vol. 21, no. 6, pp. 859–861, 2007.
[3]  M. Bateson, B. Brilot, and D. Nettle, “Anxiety: an evolutionary approach,” Canadian Journal of Psychiatry, vol. 56, no. 12, pp. 707–715, 2011.
[4]  C. Montag, M. Eichner, S. Markett, C. M. Quesada, J. C. Schoene-Bake, and M. Melchers, “An interaction of a NR3C1 polymorphism and antenatal solar activity impacts both hippocampus volume and neuroticism in adulthood,” Frontiers in Human Neuroscience, vol. 7, article 243, 2013.
[5]  B. B. Lahey, “Public health significance of neuroticism,” American Psychologist, vol. 64, no. 4, pp. 241–256, 2009.
[6]  G. W. Allport, Pattern and Growth in Personality, Holt, Rinehart and Winston, New York, NY, USA, 1961.
[7]  C. R. Cloninger, D. M. Svrakic, and T. R. Przybeck, “A psychobiological model of temperament and character,” Archives of General Psychiatry, vol. 50, no. 12, pp. 975–990, 1993.
[8]  R. R. McCrae and O. P. John, “An introduction to the five-factor model and its applications,” Journal of personality, vol. 60, no. 2, pp. 175–215, 1992.
[9]  T. Robinson and S. Marwit, “An investigation of the relationship of personality, coping, and grief intensity among bereaved mothers,” Death Studies, vol. 30, no. 7, pp. 677–696, 2006.
[10]  A. A. Augustine and R. J. Larsen, “Is a trait really the mean of states? Similarities and differences between traditional and aggregate assessments of personality,” Journal of Individual Differences, vol. 33, no. 3, p. 131, 2012.
[11]  K. Martinowich, H. Manji, and B. Lu, “New insights into BDNF function in depression and anxiety,” Nature Neuroscience, vol. 10, no. 9, pp. 1089–1093, 2007.
[12]  J. Panksepp, Affective Neuroscience: the Foundations of Human and Animal Emotions, Oxford University Press, 1998.
[13]  J. Panksepp, “Affective neuroscience of the emotional Brain Mind: evolutionary perspectives and implications for understanding depression,” Dialogues in Clinical Neuroscience, vol. 12, no. 4, pp. 533–545, 2010.
[14]  J. Panksepp, “Affective consciousness: core emotional feelings in animals and humans,” Consciousness and Cognition, vol. 14, no. 1, pp. 30–80, 2005.
[15]  K. L. Davis and J. Panksepp, “The brain's emotional foundations of human personality and the Affective Neuroscience Personality Scales,” Neuroscience and Biobehavioral Reviews, vol. 35, no. 9, pp. 1946–1958, 2011.
[16]  J. Panksepp, “Cross-Species affective neuroscience decoding of the primal affective experiences of humans and related animals,” PLoS ONE, vol. 6, no. 9, Article ID e21236, 2011.
[17]  C. Darwin, The Expression of the Emotions in Man and Animals, Oxford University Press, 1998.
[18]  C. Holden, “Paul MacLean and the triune brain,” Science, vol. 204, no. 4397, pp. 1066–1068, 1979.
[19]  C. Montag, M. Jurkiewicz, and M. Reuter, “The role of the catechol-O-methyltransferase (COMT) gene in personality and related psychopathological disorders,” CNS & Neurological Disorders-Drug Targets, vol. 11, no. 3, pp. 236–250, 2012.
[20]  C. Montag, M. Reuter, M. Jurkiewicz, S. Markett, and J. Panksepp, “Imaging the structure of the human anxious brain: a review of findings from neuroscientific personality psychology,” Reviews in the Neurosciences, vol. 24, no. 2, pp. 167–190, 2013.
[21]  P. T. Costa and R. R. McCrae, Neo PI-R Professional Manual, vol. 396, Psychological Assessment Resources, Odessa, Ukraine, 1992.
[22]  C. R. Cloninger, “A systematic method for clinical description and classification of personality variants: a proposal,” Archives of General Psychiatry, vol. 44, no. 6, pp. 573–588, 1987.
[23]  R. J. Larsen and T. Ketelaar, “Extraversion, neuroticism and susceptibility to positive and negative mood induction procedures,” Personality and Individual Differences, vol. 10, no. 12, pp. 1221–1228, 1989.
[24]  C. L. Rusting and R. J. Larsen, “Extraversion, neuroticism, and susceptibility to positive and negative affect: a test of two theoretical models,” Personality and Individual Differences, vol. 22, no. 5, pp. 607–612, 1997.
[25]  D. Watson, R. O. M. A. N. Kotov, and W. Gamez, “Basic dimensions of temperament in relation to personality and psychopathology,” Personality and Psychopathology, pp. 7–38, 2006.
[26]  H. J. Eysenck, Eysenck Personality Inventory, Educational and Industrial Testing Service, San Diego, Calif, USA, 1968.
[27]  P. Seeman, “Dopamine receptors and the dopamine hypothesis of schizophrenia,” Synapse, vol. 1, no. 2, pp. 133–152, 1987.
[28]  A. Soliman, G. A. O'Driscoll, J. Pruessner et al., “Stress-induced dopamine release in humans at risk of psychosis: a [11C] raclopride PET study,” Neuropsychopharmacology, vol. 33, no. 8, pp. 2033–2041, 2008.
[29]  R. A. Wise and P. P. Rompre, “Brain dopamine and reward,” Annual Review of Psychology, vol. 40, pp. 191–225, 1989.
[30]  R. A. Wise, “Dopamine, learning and motivation,” Nature Reviews Neuroscience, vol. 5, no. 6, pp. 483–494, 2004.
[31]  R. A. Depue and P. F. Collins, “Neurobiology of the structure of personality: dopamine, facilitation of incentive motivation, and extraversion,” Behavioral and Brain Sciences, vol. 22, no. 3, pp. 491–517, 1999.
[32]  R. A. Bevins, “Novelty seeking and reward: implications for the study of high-risk behaviors,” Current Directions in Psychological Science, vol. 10, no. 6, pp. 189–193, 2001.
[33]  M. X. Cohen, J. Young, J.-M. Baek, C. Kessler, and C. Ranganath, “Individual differences in extraversion and dopamine genetics predict neural reward responses,” Cognitive Brain Research, vol. 25, no. 3, pp. 851–861, 2005.
[34]  J. J. Simon, S. Walther, C. J. Fiebach et al., “Neural reward processing is modulated by approach- and avoidance-related personality traits,” NeuroImage, vol. 49, no. 2, pp. 1868–1874, 2010.
[35]  C. Tsigos and G. P. Chrousos, “Hypothalamic-pituitary-adrenal axis, neuroendocrine factors and stress,” Journal of Psychosomatic Research, vol. 53, no. 4, pp. 865–871, 2002.
[36]  M. A. Schlesser, G. Winokur, and B. M. Sherman, “Hypothalamic-pituitary-adrenal axis activity in depressive illness. Its relationship to classification,” Archives of General Psychiatry, vol. 37, no. 7, pp. 737–743, 1980.
[37]  C. Kirschbaum, D. Bartussek, and C. J. Strasburger, “Cortisol responses to psychological stress and correlations with personality traits,” Personality and Individual Differences, vol. 13, no. 12, pp. 1353–1357, 1992.
[38]  L. M. Oswald, P. Zandi, G. Nestadt, J. B. Potash, A. E. Kalaydjian, and G. S. Wand, “Relationship between cortisol responses to stress and personality,” Neuropsychopharmacology, vol. 31, no. 7, pp. 1583–1591, 2006.
[39]  C. Montag, C. J. Fiebach, P. Kirsch, and M. Reuter, “Interaction of 5-HTTLPR and a variation on the oxytocin receptor gene influences negative emotionality,” Biological Psychiatry, vol. 69, no. 6, pp. 601–603, 2011.
[40]  H. Tost, B. Kolachana, S. Hakimi et al., “A common allele in the oxytocin receptor gene (OXTR) impacts prosocial temperament and human hypothalamic-limbic structure and function,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 31, pp. 13936–13941, 2010.
[41]  C. R. Bramham and E. Messaoudi, “BDNF function in adult synaptic plasticity: the synaptic consolidation hypothesis,” Progress in Neurobiology, vol. 76, no. 2, pp. 99–125, 2005.
[42]  M. E. Greenberg, B. Xu, B. Lu, and B. L. Hempstead, “New insights in the biology of BDNF synthesis and release: implications in CNS function,” Journal of Neuroscience, vol. 29, no. 41, pp. 12764–12767, 2009.
[43]  H. W. Horch and L. C. Katz, “BDNF release from single cells elicits local dendritic growth in nearby neurons,” Nature Neuroscience, vol. 5, no. 11, pp. 1177–1184, 2002.
[44]  Y. Ji, P. T. Pang, L. Feng, and B. Lu, “Cyclic AMP controls BDNF-induced TrkB phosphorylation and dendritic spine formation in mature hippocampal neurons,” Nature Neuroscience, vol. 8, no. 2, pp. 164–172, 2005.
[45]  B. Lu, P. T. Pang, and N. H. Woo, “The yin and yang of neurotrophin action,” Nature Reviews Neuroscience, vol. 6, no. 8, pp. 603–614, 2005.
[46]  L. Zhou, J. Xiong, Y. Lim, et al., “Upregulation of blood proBDNF and its receptors in major depression,” Journal of Affective Disorders, vol. 150, no. 3, pp. 776–784.
[47]  H. K. Teng, K. K. Teng, R. Lee, et al., “ProBDNF induces neuronal apoptosis via activation of a receptor complex of p75NTR and sortilin,” The Journal of Neuroscience, vol. 25, no. 22, pp. 5455–5463, 2005.
[48]  R. Lee, P. Kermani, K. K. Teng, and B. L. Hempstead, “Regulation of cell survival by secreted proneurotrophins,” Science, vol. 294, no. 5548, pp. 1945–1948, 2001.
[49]  F. Karege, G. Perret, G. Bondolfi, M. Schwald, G. Bertschy, and J.-M. Aubry, “Decreased serum brain-derived neurotrophic factor levels in major depressed patients,” Psychiatry Research, vol. 109, no. 2, pp. 143–148, 2002.
[50]  A. Deveci, O. Aydemir, O. Taskin, F. Taneli, and A. Esen-Danaci, “Serum BDNF levels in suicide attempters related to psychosocial stressors: a comparative study with depression,” Neuropsychobiology, vol. 56, no. 2-3, pp. 93–97, 2008.
[51]  B. Chen, D. Dowlatshahi, G. M. MacQueen, J.-F. Wang, and L. T. Young, “Increased hippocampal BDNF immunoreactivity in subjects treated with antidepressant medication,” Biological Psychiatry, vol. 50, no. 4, pp. 260–265, 2001.
[52]  E. Shimizu, K. Hashimoto, N. Okamura et al., “Alterations of serum levels of brain-derived neurotrophic factor (BDNF) in depressed patients with or without antidepressants,” Biological Psychiatry, vol. 54, no. 1, pp. 70–75, 2003.
[53]  R. S. Duman and L. M. Monteggia, “A neurotrophic model for stress-related mood disorders,” Biological Psychiatry, vol. 59, no. 12, pp. 1116–1127, 2006.
[54]  J. O. Groves, “Is it time to reassess the BDNF hypothesis of depression?” Molecular Psychiatry, vol. 12, no. 12, pp. 1079–1088, 2007.
[55]  Y. I. Sheline, M. H. Gado, and H. C. Kraemer, “Untreated depression and hippocampal volume loss,” American Journal of Psychiatry, vol. 160, no. 8, pp. 1516–1518, 2003.
[56]  P. Videbech and B. Ravnkilde, “Hippocampal volume and depression: a meta-analysis of MRI studies,” American Journal of Psychiatry, vol. 161, no. 11, pp. 1957–1966, 2004.
[57]  H. Yamasue, O. Abe, M. Suga et al., “Gender-common and -specific neuroanatomical basis of human anxiety-related personality traits,” Cerebral Cortex, vol. 18, no. 1, pp. 46–52, 2008.
[58]  H. D. Schmidt and R. S. Duman, “Peripheral BDNF produces antidepressant-like effects in cellular and behavioral models,” Neuropsychopharmacology, vol. 35, no. 12, pp. 2378–2391, 2010.
[59]  W. Pan, W. A. Banks, M. B. Fasold, J. Bluth, and A. J. Kastin, “Transport of brain-derived neurotrophic factor across the blood-brain barrier,” Neuropharmacology, vol. 37, no. 12, pp. 1553–1561, 1998.
[60]  F. Karege, M. Schwald, and M. Cisse, “Postnatal developmental profile of brain-derived neurotrophic factor in rat brain and platelets,” Neuroscience Letters, vol. 328, no. 3, pp. 261–264, 2002.
[61]  B. Martin, M. Pearson, L. Kebejian et al., “Sex-dependent metabolic, neuroendocrine, and cognitive responses to dietary energy restriction and excess,” Endocrinology, vol. 148, no. 9, pp. 4318–4333, 2007.
[62]  U. E. Lang, R. Hellweg, and J. Gallinat, “BDNF serum concentrations in healthy volunteers are associated with depression-related personality traits,” Neuropsychopharmacology, vol. 29, no. 4, pp. 795–798, 2004.
[63]  A. Terracciano, M. Lobina, M. G. Piras et al., “Neuroticism, depressive symptoms, and serum BDNF,” Psychosomatic Medicine, vol. 73, no. 8, pp. 638–642, 2011.
[64]  S. Tsuchimine, N. Yasui-Furukori, A. Kaneda et al., “No association between polymorphism in tyrosine hydroxylase and personality traits in healthy Japanese subjects,” Psychiatry and Clinical Neurosciences, vol. 64, no. 2, pp. 196–198, 2010.
[65]  K. Okuno, R. Yoshimura, N. Ueda et al., “Relationships between stress, social adaptation, personality traits, brain-derived neurotrophic factor and 3-methoxy-4-hydroxyphenylglycol plasma concentrations in employees at a publishing company in Japan,” Psychiatry Research, vol. 186, no. 2-3, pp. 326–332, 2011.
[66]  V. Trajkovska, M. Vinberg, S. Aznar, G. M. Knudsen, and L. V. Kessing, “Whole blood BDNF levels in healthy twins discordant for affective disorder: association to life events and neuroticism,” Journal of Affective Disorders, vol. 108, no. 1-2, pp. 165–169, 2008.
[67]  A. Terracciano, B. Martin, D. Ansari et al., “Plasma BDNF concentration, Val66Met genetic variant and depression-related personality traits,” Genes, Brain and Behavior, vol. 9, no. 5, pp. 512–518, 2010.
[68]  A. Minelli, R. Zanardini, C. Bonvicini et al., “BDNF serum levels, but not BDNF Val66Met genotype, are correlated with personality traits in healthy subjects,” European Archives of Psychiatry and Clinical Neuroscience, vol. 261, no. 5, pp. 323–329, 2011.
[69]  B. Arias, M. Aguilera, J. Moya et al., “The role of genetic variability in the SLC6A4, BDNF and GABRA6 genes in anxiety-related traits,” Acta Psychiatrica Scandinavica, vol. 125, no. 3, pp. 194–202, 2012.
[70]  L. De Beaumont, A. J. Fiocco, G. Quesnel, S. Lupien, and J. Poirier, “Altered declarative memory in introverted middle-aged adults carrying the BDNF val66met allele,” Behavioural Brain Research, vol. 253, pp. 152–156, 2013.
[71]  P. Gong, S. Xi, S. Li, et al., “Effect of Val66Met polymorphism in BDNF on attentional bias in an extroverted Chinese Han population,” Acta Neurobiologiae Experimentalis, vol. 73, pp. 280–288, 2013.
[72]  B. J. Ham, H. B. An, S. M. Cho et al., “An association study of the brain-derived neurotrophic factor genes polymorphisms and personality traits,” Korean Journal of Biological Psychiatry, vol. 12, no. 2, pp. 216–220, 2005.
[73]  K. Hiio, L. Meren?kk, N. Nordquist et al., “Effects of serotonin transporter promoter and BDNF Val66Met genotype on personality traits in a population representative sample of adolescents,” Psychiatric Genetics, vol. 21, no. 5, pp. 261–264, 2011.
[74]  R. Hünnerkopf, A. Strobel, L. Gutknecht, B. Brocke, and K. P. Lesch, “Interaction between BDNF Val66Met and dopamine transporter gene variation influences anxiety-related traits,” Neuropsychopharmacology, vol. 32, no. 12, pp. 2552–2560, 2007.
[75]  K. Itoh, K. Hashimoto, C. Kumakiri, E. Shimizu, and M. Iyo, “Association between brain-derived neurotrophic factor 196 G/A polymorphism and personality traits in healthy subjects,” American Journal of Medical Genetics: Neuropsychiatric Genetics, vol. 124, no. 1, pp. 61–63, 2004.
[76]  S. J. Kim, S.-J. Cho, H. M. Jang et al., “Interaction between brain-derived neurotrophic factor Val66Met polymorphism and recent negative stressor in harm avoidance,” Neuropsychobiology, vol. 61, no. 1, pp. 19–26, 2009.
[77]  X. Jiang, K. Xu, J. Hoberman et al., “BDNF variation and mood disorders: a novel functional promoter polymorphism and Val66Met are associated with anxiety but have opposing effects,” Neuropsychopharmacology, vol. 30, no. 7, pp. 1353–1361, 2005.
[78]  R. T. Joffe, J. M. Gatt, A. H. Kemp et al., “Brain derived neurotrophic factor Val66Met polymorphism, the five factor model of personality and hippocampal volume: Implications for depressive illness,” Human Brain Mapping, vol. 30, no. 4, pp. 1246–1256, 2009.
[79]  U. E. Lang, R. Hellweg, P. Kalus et al., “Association of a functional BDNF polymorphism and anxiety-related personality traits,” Psychopharmacology, vol. 180, no. 1, pp. 95–99, 2005.
[80]  C. Montag, U. Basten, C. Stelzel, C. J. Fiebach, and M. Reuter, “The BDNF Val66Met polymorphism and anxiety: support for animal knock-in studies from a genetic association study in humans,” Psychiatry Research, vol. 179, no. 1, pp. 86–90, 2010.
[81]  C. Montag, S. Markett, U. Basten et al., “Epistasis of the DRD2/ANKK1 Taq Ia and the BDNF Val66Met polymorphism impacts novelty seeking and harm avoidance,” Neuropsychopharmacology, vol. 35, no. 9, pp. 1860–1867, 2010.
[82]  J. Savitz, L. Van Der Merwe, and R. Ramesar, “Personality endophenotypes for bipolar affective disorder: a family-based genetic association analysis,” Genes, Brain and Behavior, vol. 7, no. 8, pp. 869–876, 2008.
[83]  S. Sen, R. M. Nesse, S. F. Stoltenberg et al., “A BDNF coding variant is associated with the NEO personality inventory domain neuroticism, a risk factor for depression,” Neuropsychopharmacology, vol. 28, no. 2, pp. 397–401, 2003.
[84]  A. Suzuki, Y. Matsumoto, N. Shibuya et al., “The brain-derived neurotrophic factor Val66Met polymorphism modulates the effects of parental rearing on personality traits in healthy subjects,” Genes, Brain and Behavior, vol. 10, no. 4, pp. 385–391, 2011.
[85]  A. Terracciano, T. Tanaka, A. R. Sutin et al., “BDNF Val66Met is associated with introversion and interacts with 5-HTTLPR to influence neuroticism,” Neuropsychopharmacology, vol. 35, no. 5, pp. 1083–1089, 2010.
[86]  M. Tochigi, T. Otowa, M. Suga et al., “No evidence for an association between the BDNF Val66Met polymorphism and schizophrenia or personality traits,” Schizophrenia Research, vol. 87, no. 1-3, pp. 45–47, 2006.
[87]  S.-J. Tsai, C.-J. Hong, Y. W.-Y. Yu, and T.-J. Chen, “Association study of a brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and personality trait and intelligence in healthy young females,” Neuropsychobiology, vol. 49, no. 1, pp. 13–16, 2004.
[88]  N. T. Walter, C. Montag, S. A. Markett, and M. Reuter, “Interaction effect of functional variants of the BDNF and DRD2/ANKK1 gene is associated with alexithymia in healthy human subjects,” Psychosomatic Medicine, vol. 73, no. 1, pp. 23–28, 2011.
[89]  S. A. G. Willis-Owen, J. Fullerton, P. G. Surtees, N. W. J. Wainwright, S. Miller, and J. Flint, “The Val66Met coding variant of the brain-derived neurotrophic factor (BDNF) gene does not contribute toward variation in the personality trait neuroticism,” Biological Psychiatry, vol. 58, no. 9, pp. 738–742, 2005.
[90]  H. Fujimura, C. A. Altar, R. Chen et al., “Brain-derived neurotrophic factor is stored in human platelets and released by agonist stimulation,” Thrombosis and Haemostasis, vol. 87, no. 4, pp. 728–734, 2002.
[91]  A. Piccinni, D. Marazziti, A. Del Debbio et al., “Diurnal variation of plasma brain-derived neurotrophic factor (BDNF) in humans: an analysis of sex differences,” Chronobiology International, vol. 25, no. 5, pp. 819–826, 2008.
[92]  S.-W. Choi, S. Bhang, and J.-H. Ahn, “Diurnal variation and gender differences of plasma brain-derived neurotrophic factor in healthy human subjects,” Psychiatry Research, vol. 186, no. 2-3, pp. 427–430, 2011.
[93]  R. Katoh-Semba, R. Wakako, T. Komori et al., “Age-related changes in BDNF protein levels in human serum: differences between autism cases and normal controls,” International Journal of Developmental Neuroscience, vol. 25, no. 6, pp. 367–372, 2007.
[94]  M. L. Molendijk, B. A. A. Bus, P. Spinhoven et al., “Serum levels of brain-derived neurotrophic factor in major depressive disorder: State-trait issues, clinical features and pharmacological treatment,” Molecular Psychiatry, vol. 16, no. 11, pp. 1088–1095, 2011.
[95]  P. Jylh?, M. Ketokivi, O. Mantere et al., “Do antidepressants change personality?—a five-year observational study,” Journal of Affective Disorders, vol. 142, no. 1, pp. 200–207, 2012.
[96]  M. F. Egan, M. Kojima, J. H. Callicott et al., “The BDNF Val66Met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function,” Cell, vol. 112, no. 2, pp. 257–269, 2003.
[97]  L. Pezawas, B. A. Verchinski, V. S. Mattay et al., “The brain-derived neurotrophic factor Val66Met polymorphism and variation in human cortical morphology,” Journal of Neuroscience, vol. 24, no. 45, pp. 10099–10102, 2004.
[98]  J. A. Bueller, M. Aftab, S. Sen, D. Gomez-Hassan, M. Burmeister, and J.-K. Zubieta, “BDNF Val66Met Allele is associated with reduced hippocampal volume in healthy subjects,” Biological Psychiatry, vol. 59, no. 9, pp. 812–815, 2006.
[99]  C. Montag, B. Weber, K. Fliessbach, C. Elger, and M. Reuter, “The BDNF Val66Met polymorphism impacts parahippocampal and amygdala volume in healthy humans: incremental support for a genetic risk factor for depression,” Psychological Medicine, vol. 39, no. 11, pp. 1831–1839, 2009.
[100]  M. E. Sublette, E. Baca-Garcia, R. V. Parsey et al., “Effect of BDNF Val66Met polymorphism on age-related amygdala volume changes in healthy subjects,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 32, no. 7, pp. 1652–1655, 2008.
[101]  J. Cole, D. R. Weinberger, V. S. Mattay et al., “No effect of 5HTTLPR or BDNF Val66Met polymorphism on hippocampal morphology in major depression,” Genes, Brain and Behavior, vol. 10, no. 7, pp. 756–764, 2011.
[102]  J. P. Kambeitz, S. Bhattacharyya, L. M. Ilankovic, I. Valli, and D. A. Collier, “Effect of BDNF Met66Val-Polymorphism on declarative memory and its neural substrate: a meta-analysis,” Neuroscience & Biobehavioral Reviews, vol. 36, no. 9, pp. 2165–2177, 2012.
[103]  C. Montag, M. Reuter, B. Newport, C. Elger, and B. Weber, “The BDNF Val66Met polymorphism affects amygdala activity in response to emotional stimuli: Evidence from a genetic imaging study,” NeuroImage, vol. 42, no. 4, pp. 1554–1559, 2008.
[104]  P. Mukherjee, H. C. Whalley, J. W. McKirdy et al., “Effects of the BDNF Val66Met polymorphism on neural responses to facial emotion,” Psychiatry Research: Neuroimaging, vol. 191, no. 3, pp. 182–188, 2011.
[105]  J. Y. F. Lau, D. Goldman, B. Buzas et al., “BDNF gene polymorphism (Val66Met) predicts amygdala and anterior hippocampus responses to emotional faces in anxious and depressed adolescents,” NeuroImage, vol. 53, no. 3, pp. 952–961, 2010.
[106]  A. Terracciano, M. G. Piras, M. Lobina, A. Mulas, O. Meirelles, and A. R. Sutin, “Genetics of serum BDNF: meta-analysis of the Val66Met and genome-wide association study,” World Journal of Biological Psychiatry, vol. 14, no. 8, pp. 583–589, 2011.
[107]  Z.-Y. Chen, D. Jing, K. G. Bath et al., “Genetic variant BDNF (Val66Met) polymorphism alters anxiety-related behavior,” Science, vol. 314, no. 5796, pp. 140–143, 2006.
[108]  P. G. Surtees, N. W. J. Wainwright, S. A. G. Willis-Owen et al., “No association between the BDNF Val66Met polymorphism and mood status in a non-clinical community sample of 7389 older adults,” Journal of Psychiatric Research, vol. 41, no. 5, pp. 404–409, 2007.
[109]  A. Frustaci, G. Pozzi, F. Gianfagna, L. Manzoli, and S. Boccia, “Meta-analysis of the brain-derived neurotrophic factor gene (BDNF) Val66Met polymorphism in anxiety disorders and anxiety-related personality traits,” Neuropsychobiology, vol. 58, no. 3-4, pp. 163–170, 2008.
[110]  W. D. Taylor, S. Züchner, D. R. McQuoid, D. C. Steffens, D. G. Blazer, and K. R. R. Krishnan, “Social support in older individuals: the role of the BDNF Val66Met polymorphism,” American Journal of Medical Genetics, B: Neuropsychiatric Genetics, vol. 147, no. 7, pp. 1205–1212, 2008.
[111]  X. Ma, J. Sun, J. Yao et al., “A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population,” Psychiatry Research, vol. 153, no. 1, pp. 7–15, 2007.
[112]  K.-P. Lesch, D. Bengel, A. Heils et al., “Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region,” Science, vol. 274, no. 5292, pp. 1527–1531, 1996.
[113]  T. Canli and K.-P. Lesch, “Long story short: the serotonin transporter in emotion regulation and social cognition,” Nature Neuroscience, vol. 10, no. 9, pp. 1103–1109, 2007.
[114]  L. Pezawas, A. Meyer-Lindenberg, A. L. Goldman et al., “Evidence of biologic epistasis between BDNF and SLC6A4 and implications for depression,” Molecular Psychiatry, vol. 13, no. 7, pp. 709–716, 2008.
[115]  O. Berton, C. A. McClung, R. J. DiLeone et al., “Essential role of BDNF in the mesolimbic dopamine pathway in social defeat stress,” Science, vol. 311, no. 5762, pp. 864–868, 2006.
[116]  C. Hyman, M. Hofer, Y.-A. Barde et al., “BDNF is a neurotrophic factor for dopaminergic neurons of the substantia nigra,” Nature, vol. 350, no. 6315, pp. 230–232, 1991.
[117]  E. G. J?nsson, M. M. N?then, F. Grünhage et al., “Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers,” Molecular Psychiatry, vol. 4, no. 3, pp. 290–296, 1999.
[118]  J. I. Kang, D.-H. Song, K. Namkoong, and S. J. Kim, “Interaction effects between COMT and BDNF polymorphisms on boredom susceptibility of sensation seeking traits,” Psychiatry Research, vol. 178, no. 1, pp. 132–136, 2010.
[119]  S. Fuke, “The VNTR polymorphism of the human dopamine transporter (DAT!) gene affects gene expression,” Pharmacogenomics Journal, vol. 1, no. 2, pp. 152–156, 2001.
[120]  G. M. Miller and B. K. Madras, “Polymorphisms in the 3′-untranslated region of human and monkey dopamine transporter genes affect reporter gene expression,” Molecular Psychiatry, vol. 7, no. 1, pp. 44–55, 2002.
[121]  H. M. Lachman, D. F. Papolos, T. Saito, Y.-M. Yu, C. L. Szumlanski, and R. M. Weinshilboum, “Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders,” Pharmacogenetics, vol. 6, no. 3, pp. 243–250, 1996.
[122]  R. M. Bilder, J. Volavka, H. M. Lachman, and A. A. Grace, “The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes,” Neuropsychopharmacology, vol. 29, no. 11, pp. 1943–1961, 2004.
[123]  M. Zuckerman, “The psychophysiology of sensation seeking,” Journal of personality, vol. 58, no. 1, pp. 313–345, 1990.
[124]  A. Caspi, K. Sugden, T. E. Moffitt et al., “Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene,” Science, vol. 301, no. 5631, pp. 386–389, 2003.
[125]  L. Mandelli, N. Antypa, F. A. Nearchou et al., “The role of serotonergic genes and environmental stress on the development of depressive symptoms and neuroticism,” Journal of Affective Disorders, vol. 142, no. 1–3, pp. 82–89, 2012.
[126]  M. Pluess, J. Belsky, B. M. Way, and S. E. Taylor, “5-HTTLPR moderates effects of current life events on neuroticism: differential susceptibility to environmental influences,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 34, no. 6, pp. 1070–1074, 2010.
[127]  S. Wagner, ?. Baskaya, K. Lieb, N. Dahmen, and A. Tadi?, “The 5-HTTLPR Polymorphism modulates the association of serious life events (SLE) and impulsivity in patients with Borderline Personality Disorder,” Journal of Psychiatric Research, vol. 43, no. 13, pp. 1067–1072, 2009.
[128]  J. M. Gatt, C. B. Nemeroff, C. Dobson-Stone et al., “Interactions between BDNF Val66Met polymorphism and early life stress predict brain and arousal pathways to syndromal depression and anxiety,” Molecular Psychiatry, vol. 14, no. 7, pp. 681–695, 2009.
[129]  M. Aguilera, B. Arias, M. Wichers et al., “Early adversity and 5-HTT/BDNF genes: new evidence of gene-environment interactions on depressive symptoms in a general population,” Psychological Medicine, vol. 39, no. 9, pp. 1425–1432, 2009.
[130]  M. Wichers, G. Kenis, N. Jacobs et al., “The BDNF Val66Met x 5-HTTLPR x child adversity interaction and depressive symptoms: an attempt at replication,” American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 147, no. 1, pp. 120–123, 2008.
[131]  A. Terracciano, S. Sanna, M. Uda et al., “Genome-wide association scan for five major dimensions of personality,” Molecular Psychiatry, vol. 15, no. 6, pp. 647–656, 2010.
[132]  T.-Y. Zhang and M. J. Meaney, “Epigenetics and the environmental regulation of the genome and its function,” Annual Review of Psychology, vol. 61, pp. 439–466, 2010.
[133]  T. L. Roth and J. D. Sweatt, “Epigenetic marking of the BDNF gene by early-life adverse experiences,” Hormones and Behavior, vol. 59, no. 3, pp. 315–320, 2011.
[134]  E. Dempster, T. Toulopoulou, C. McDonald et al., “Association between BDNF val66 met genotype and episodic memory,” American Journal of Medical Genetics: Neuropsychiatric Genetics, vol. 134, no. 1, pp. 73–75, 2005.
[135]  T. E. Goldberg and D. R. Weinberger, “Genes and the parsing of cognitive processes,” Trends in Cognitive Sciences, vol. 8, no. 7, pp. 325–335, 2004.
[136]  Y. Kovas and R. Plomin, “Generalist genes: implications for the cognitive sciences,” Trends in Cognitive Sciences, vol. 10, no. 5, pp. 198–203, 2006.

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