TY - JOUR
T1 - Genetic and neurocognitive foundations of emotion abnormalities in bipolar disorder
AU - Van Rheenen, Tamsyn
AU - Rossell, Susan Lee
PY - 2013
Y1 - 2013
N2 - Bipolar Disorder (BD) is a serious mood disorder, the aetiology of
which is still unclear. The disorder is characterised by extreme mood variability in
which patients fluctuate between markedly euphoric, irritable, and elevated states to
periods of severe depression. The current research literature shows that BD patients
demonstrate compromised neurocognitive ability in addition to these mood
symptoms. Viable candidate genes implicated in neurocognitive and socioemotional
processes may explain the development of these core emotion abnormalities.
Additionally, links between faulty neurocognition and impaired socioemotional
ability complement genetic explanations of BD pathogenesis. This review examines
associations between cognition indexing prefrontal neural regions and socioemotional
impairments including emotion processing and regulation. A review of
the effect of COMT and TPH2 on these functions is also explored.
Methods. Major computer databases including PsycINFO, Google Scholar, and
Medline were consulted in order to conduct a comprehensive review of the genetic
and cognitive literature in BD.
Results. This review determines that COMT and TPH2 genetic variants contribute
susceptibility to abnormal prefrontal neurocognitive function which oversees the
processing and regulation of emotion. This provides for greater understanding of
some of the emotional and cognitive symptoms in BD.
Conclusions. Current findings in this direction show promise, although the
literature is still in its infancy and further empirical research is required to
investigate these links explicitly.
AB - Bipolar Disorder (BD) is a serious mood disorder, the aetiology of
which is still unclear. The disorder is characterised by extreme mood variability in
which patients fluctuate between markedly euphoric, irritable, and elevated states to
periods of severe depression. The current research literature shows that BD patients
demonstrate compromised neurocognitive ability in addition to these mood
symptoms. Viable candidate genes implicated in neurocognitive and socioemotional
processes may explain the development of these core emotion abnormalities.
Additionally, links between faulty neurocognition and impaired socioemotional
ability complement genetic explanations of BD pathogenesis. This review examines
associations between cognition indexing prefrontal neural regions and socioemotional
impairments including emotion processing and regulation. A review of
the effect of COMT and TPH2 on these functions is also explored.
Methods. Major computer databases including PsycINFO, Google Scholar, and
Medline were consulted in order to conduct a comprehensive review of the genetic
and cognitive literature in BD.
Results. This review determines that COMT and TPH2 genetic variants contribute
susceptibility to abnormal prefrontal neurocognitive function which oversees the
processing and regulation of emotion. This provides for greater understanding of
some of the emotional and cognitive symptoms in BD.
Conclusions. Current findings in this direction show promise, although the
literature is still in its infancy and further empirical research is required to
investigate these links explicitly.
UR - http://www.tandfonline.com/doi/pdf/10.1080/13546805.2012.690938
U2 - 10.1080/13546805.2012.690938
DO - 10.1080/13546805.2012.690938
M3 - Article
SN - 1354-6805
VL - 18
SP - 168
EP - 207
JO - Cognitive Neuropsychiatry
JF - Cognitive Neuropsychiatry
IS - 3
ER -