UCLA scientists have made a major development in
understanding the biology of schizophrenia. While analyzing DNA, the scientists
found tons of genes and two major biological pathways that are most likely
involved in the development of schizophrenia. Schizophrenia is
a chronic, disabling mental illness whose symptoms can include hallucinations,
delusions and cognitive problems. The illness affects about one percent of
Americans. The cause of schizophrenia is not fully understood. Current
medications can help reduce the symptoms, but they do not cure the disorder. The
study is expected to have an impact beyond schizophrenia research because it shows
a general and powerful new strategy for revealing the mechanisms of human
disease.
Schizophrenia has been known to be very genetic; it
often runs in families. A large genome-wide association study of individuals
with schizophrenia, linked the disorder to small DNA
variations at more than one hundred different locations on the human genome. Most
of those locations lie outside of the actual genes, so their roles in schizophrenia
have been unclear. Schizophrenia is a disorder that is known to be abnormal in
the cerebral cortex. In the study, the genes linked to schizophrenia include some
for brain cell receptors that are activated by the neurotransmitter
acetylcholine. Variations in the functions of these receptors can help create schizophrenia.
As more studies explain the roles of these genes in
schizophrenia, scientists will get a greater understanding of how the disorder
develops. I am glad scientists are trying to understand the causes of
schizophrenia. Through this, they should eventually be able to develop more
effective treatments and be able to alleviate the symptoms from people who are suffering
from it.
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