Aggression is a prominent feature of many clinical conditions (such as antisocial personality disorder), a common cause of criminal incarceration, and a frequent concomitant of alcohol and other substance abuse. The social costs associated with aggressive behavior also rank among the primary concerns of contemporary society. In addition to environmental determinants, genetic factors contribute to the etiology of aggressive temperament. Reduced central nervous system (CNS) serotonergic activity is also correlated with human aggression, as seen in clinical, forensic and non patient samples. We have previously found that among unrelated individuals in a non patient population, life history of aggression and anger-related personality traits, as well as CNS serotonergic responsivity, are associated with polymorphisms of two genes regulating elements of the serotonergic system: tryptophan hydroxylase and monoamine oxidase A. The purpose of the proposed research is to confirm and extend these observations by more definitive methodology, utilizing family-based controls in conjunction with transmission-disequilibrium (TDT) analysis of adult, community volunteers and their parents. The primary study sample will include 800 individuals comprising relative ends (quartiles) of the population distribution of aggressive phenotype, as assessed by standardized clinical interview. Additional polymorphisms in the serotonergic system will also be evaluated, and if alleles of non-functional polymorphisms are found to differentiate high and low aggressive subjects, detailed molecular analyses will be conducted to identify functional variation that may account for these associations. Psychiatric characterization of study participants will be made by structured diagnostic evaluation and group differences in aggressive behavior will be confirmed by additional interview, questionnaire and observational measures of antagonistic disposition and impulsivity. The findings of this project will advance understanding of the genetic correlates of an important dimension of human temperament germane to antisocial behavior, violence, interpersonal distress, and personality-related psychopathology. This application is the resubmission of a prior proposal of the same title.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL065137-04
Application #
6654890
Study Section
Special Emphasis Panel (ZRG1-BBBP-1 (01))
Program Officer
Jobe, Jared B
Project Start
2000-09-01
Project End
2005-08-31
Budget Start
2003-09-01
Budget End
2005-08-31
Support Year
4
Fiscal Year
2003
Total Cost
$343,983
Indirect Cost
Name
University of Pittsburgh
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Creswell, Kasey G; Wright, Aidan G C; Troxel, Wendy M et al. (2015) OXTR polymorphism predicts social relationships through its effects on social temperament. Soc Cogn Affect Neurosci 10:869-76
Bergman, O; Åhs, F; Furmark, T et al. (2014) Association between amygdala reactivity and a dopamine transporter gene polymorphism. Transl Psychiatry 4:e420
Gujral, Swathi; Manuck, Stephen B; Ferrell, Robert E et al. (2014) The BDNF Val66Met polymorphism does not moderate the effect of self-reported physical activity on depressive symptoms in midlife. Psychiatry Res 218:93-7
Donofry, Shannon D; Roecklein, Kathryn A; Wildes, Jennifer E et al. (2014) COMT met allele differentially predicts risk versus severity of aberrant eating in a large community sample. Psychiatry Res 220:513-8
Sweitzer, Maggie M; Halder, Indrani; Flory, Janine D et al. (2013) Polymorphic variation in the dopamine D4 receptor predicts delay discounting as a function of childhood socioeconomic status: evidence for differential susceptibility. Soc Cogn Affect Neurosci 8:499-508
Erickson, Kirk I; Banducci, Sarah E; Weinstein, Andrea M et al. (2013) The brain-derived neurotrophic factor Val66Met polymorphism moderates an effect of physical activity on working memory performance. Psychol Sci 24:1770-9
Carré, Justin M; Fisher, Patrick M; Manuck, Stephen B et al. (2012) Interaction between trait anxiety and trait anger predict amygdala reactivity to angry facial expressions in men but not women. Soc Cogn Affect Neurosci 7:213-21
Hyde, Luke W; Gorka, Adam; Manuck, Stephen B et al. (2011) Perceived social support moderates the link between threat-related amygdala reactivity and trait anxiety. Neuropsychologia 49:651-6
Gianaros, Peter J; Manuck, Stephen B; Sheu, Lei K et al. (2011) Parental education predicts corticostriatal functionality in adulthood. Cereb Cortex 21:896-910
Manuck, Stephen B; Craig, Anna E; Flory, Janine D et al. (2011) Reported early family environment covaries with menarcheal age as a function of polymorphic variation in estrogen receptor-?. Dev Psychopathol 23:69-83

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