Bipolar Disorder is a brain
disorder that produces alterations in mood, energy, activity levels, regular
tasks in life. Even though, it is more prevalent in teenagers and adults,
children as young as 6 can be affected, making this an extremely important disorder
to understand and treat. Currently, there are about 5.7 million adults in
suffering bipolar disorder just in the U.S. A recent study by Psychiatric
Genomic Consortium (PGC), funded by NIMH’s Genomics Research Branch, discovered
that several mental disorders, such as bipolar disorder, depression, and
schizophrenia, all share genetic risk affecting pathways associated for immune
system and neuronal communication. Reducing the potential pathways for these
disorder into a few shared pathways offers hints to shared mechanisms, precise
diagnosis, and more efficient and successful treatments. The researchers
figured the share pathways through finding that disorders that share a
characteristic age-of-onset also share the similar risk gene paths. The study
also narrows the pathways shared to the process of histone methylation, a
mechanism responsible for gene expression and regulation according to the
environment present.
In a
research study conducted by Dr. Weisenbach and team, there showed a strong
correlation between bipolar disorder and aging on the quality of life lead by
the patient. The study found that emotion processing, processing speed, and
functioning skills in all BPD patients are negatively impacted by the disease
and age. Aging and the disease also affect the capacity to execute physical
tasks. The quality of life is extremely deteriorating as age increase. However,
it is proved that the patients will form resilience with the disorder after
experiencing it long term. Through figuring out the share pathways of bipolar
disorder along with depression and schizophrenia, the researchers have opened
up a new door to the potential treatment for all three disorders, which are all
very common among society. Many suffering bipolar disorder also suffer depression
and other brain disorders. These potential treatments can improve the
subjective quality of life of the patient suffering and also form resilience to
the disorder.
Weisenbach, S. L., & Marshall, D.,
& Weldon, A. L., & Ryan, K. A., & Vederman, A. C., & Kamali,
M., & Zubieta, J. (2014). The double burden of age and disease on cognition
and quality of life in bipolar disorder. International
Journal of Geriatric Psychiatry, 29, 952-961. doi: 10.1002/gps.4084
Asher, J. (2015, January 29). Disorders
Share Risk Gene Pathways for Immune, Epigenetic Regulation. National Institute of Mental Health. Retrieved
April 28, 2015, from
http://www.nimh.nih.gov/news/science-news/2015/disorders-share-risk-gene-pathways-for-immune-epigenetic-regulation.shtml
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