Hyperthymic Temperament and Brightness Preference Mayu Makino a, Takeshi Terao a, Koji Hatano a, Kentaro Kohno a, Yasuo Araki a, Yoshinori Mizokami a,

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Hyperthymic Temperament and Brightness Preference Mayu Makino a, Takeshi Terao a, Koji Hatano a, Kentaro Kohno a, Yasuo Araki a, Yoshinori Mizokami a, Kensuke Kodama a, Nobuhiko Hoaki a, Koji Toyokawa a, Toshihiko Izumi a, Miyano Arasaki a, Tsuyoshi Shimomura b, Minoru Fujiki b, Takanori, Kochiyama c a Department of Neuropsychiatry, Oita University Faculty of Medicine, Oita, Japan b Department of Neurosurgery, Oita University Faculty of Medicine, Oita, Japan c ATR Promotions, Brain activity Imaging Center, Kyoto, Japan

Introduction Several reports (Hoaki et al, 2011; Araki et al, 2012) showed that hyperthymic temperament was significantly and positively associated with illuminance. One possibility is that hyperthymic temperament may involve heliotropism and thereby seek brightness as a sunflower. Before examining heliotropism, we hypothesized that more hyperthymic temperament subjects feel darker than less hyperthymic subjects at the same illuminance and thereby seek brightness and investigated this hypothesis (Harada et al, 2013). Consequently, there was no significant difference in the threshold of brightness or darkness judgment between more and less hyperthymic subjects. Nonetheless, there was a significant difference in activations of left inferior orbitofrontal cortex(OFC) during control task, indicating that hyperthymic temperament may be associated with left inferior OFC, which has been reported to be associated with bipolar disorder (Harada et al, 2013). Therefore, in the present study, it can be hypothesized that hyperthymic subjects may prefer brightness (i.e., heliotropism) and thereby seek illuminance, and that percent signal changes of left inferior OFC during the preference task may be associated with hyperthymic temperament scores.

Subjects Thirty-four (16 women and 18 men, 26.1±4.7 of a mean age with range years) healthy subjects. All subjects were right-handed and had normal or corrected to normal vision. None of the subjects had any current or lifetime history of psychiatric disorders, which were determined by Mini-International Neuropsychiatric Interview. They gave informed consent to participate in this study according to procedures approved by the ethical committee at Oita University Faculty of Medicine. Hyperthymic temperament identification The Temperament Scale of Memphis, Pisa, Paris and San Diego-Autoquestionnaire (TEMPS-A) has been developed by Akiskal et al. (2005). Also in Japan, the scale has been validated and widely used to identify affective temperaments (Akiyama et., 2005; Matsumoto et al., 2005), where it was decided that the cut-off point is 6 points. The present subjects were divided into subjects with more hyperthymic temperament (more hyperthymic subjects) and subjects with less hyperthymic temperament (less hyperthymic subjects) using this cut-off point. Methods

All blocks consisted of a sequence of 11 blank screens adjusted by tristimulus value, each blank screen graduating from white to black by 25 tristimulus value. These kinds of blocks graduated blank screens were randomly arranged in each block. Three kinds of blocks were presented to the subjects in randomly allocated pattern of two balanced-order patterns which consisted of 9 blocks (A or B). Prior to each block, an instruction screen was presented for 5 sec with fixation cross for 20 sec. Functional Magnetic Resonance Imaging (fMRI) stimuli

Axial Images of Left Inferior Orbitofrontal Cortex(OFC) Left inferior OFC was depicted in red using automated anatomical labeling, where the region of interest (ROI) was set, and percent signal change (relative to the low- level baseline activity observed during viewing of the fixation cross) in the ROI was measured. Moreover, the association between percent signal changes of the ROI and hyperthymic scores were investigated during brightness preference judgment, darkness preference judgment, and control task by Spearman's rank correlation coefficient.

Results Performance Data The rate of brightness preference judgment at 11 illuminance levels (A) were compared between more hyperthymic subjects and less hyperthymic subjects while the rate of darkness preference judgment at 11 illuminance levels (B) were also compared between more hyperthymic subjects and less hyperthymic subjects. *: p<0.05 The Association Between Hyperthymic Temperament Scores and Percent Signal Changes of Left Inferior OFC during Control Task There was a significantly negative association between percent signal changes of left inferior OFC during control task and hyperthymic temperament scores (ρ=-0.347, p=0.0465), but not during preference judgment or un-preference judgment.

Discussion The results of this study suggest that more hyperthymic subjects may prefer brightness and un-prefer darkness than less hyperthymic subjects (i.e., heliotropism) without the difference in brightness or darkness perception between more and less hyperthymic subjects(Harada et al, 2013). There was a significantly negative association between percent signal changes of left inferior OFC during control task and hyperthymic temperament scores. With regard to left OFC, patients with bipolar disorder have been reported to show different BOLD responses during expectation task, facial emotion processing, reward anticipation, face matching paradigm, emotional face-matching task in comparison to healthy subjects (Bermpohl et al., 2010; Hulvershorn et al., 2012; Nusslock et al., 2012; Altshuler et al., 2008; Vizueta et al., 2012). These findings suggest that left OFC may be associated with bipolar disorder. Taking together with the present findings, hyperthymic temperament may have the neural correlates close to those of bipolar disorder, suggesting hyperthymic temperament as a biologically prodromal trait of bipolar disorder. In conclusion, the present findings suggest that more hyperthymic subjects may prefer brightness and un-prefer darkness than less hyperthymic subjects (i.e., heliotropism), and reconfirm that hyperthymic temperament may be associated with left inferior OFC, which have been reported to be associated with bipolar disorders.

Akiskal HS, Akiskal KK, Haykal RF et al. (2005). TEMPS-A: progress towards validation of a self-rated clinical version of the Temperament Evaluation of the Memphis, Pisa, Paris, and San Diego Autoquestionnaire. J Affect Disord 85:3-16. Akiyama T, Tsuda H, Matsumoto S et al. (2005). The proposed factor structure of temperament and personality in Japan: combining traits from TEMPS-A and MPT. J Affect Disord 85: Altshuler L, Bookheimer S, Townsend J et al. (2008). Regional brain changes in bipolar I depression: a functional magnetic resonance imaging study. Bipolar Disord 10: Bermpohl F, Kahnt T, Dalanay U et al. (2010). Altered representation of expressed value in the orbitofrontal cortex in mania. Hum Brain Mapp 31: Harada M, Hoaki N, Terao T et al.(2013).Hyperthymic Temperament and Brightness Judgment in Healthy Subjects: Involvement of Left Inferior Orbitofrontal Cortex. J Affect Disord 151: Hoaki N, Terao T, Wang Y et al.(2011). Biological aspect of hyperthymic temperament: light, sleep, and serotonin. Psychopharmacology 213: Hulvershorn LA, Karne H, Gunn AD et al.(2012). Neutral activation during facial emotion processing in unmedicated bipolar depression, euthymia, and mania. Biol Psychiatry 71: Kohno K, Hoaki N, Inoue T et al. (2012). Latitude effect on bipolar temperaments. J Affect Disord 142: Matsumoto S, Akiyama T, Tsuda H et al. (2005). Reliability and validity of TEMPS-A in a Japanese non-clinical population: application to unipolar and bipolar depressives. J Affect Disord 85: Nusslock R, Almeida JRC, Forbes EE et al. (2012). Waiting to win: elevated striatal and orbitofrontal cortical activity during reward anticipation in euthymic bipolar disorder adults. Bipolar Disord 14: Vizueta N, Rudie JD, Townsend JD et al.(2012). Regional fMRI hypoactivation and altered functional connectivity during emotion processing in nonmedicated depressed patients with biplar II disorder. Am J Psychiatry 169: References