Answer 1:
Thank you for the fascinating question – it’s
one that many scientists spend their entire
careers exploring. When studying the etiology,
or cause, of brain diseases, scientists must
consider both nature and nurture. While
these are often talked about as being separate
(like the common saying “nature versus nurture”),
it is the case that every brain disease is the
result of an interaction between genes and the
environment.
As you point out, brain diseases exhibit a high
degree of heritability, meaning that the children
of parents that have a brain disease are much more
likely to have it as well. However, it often
takes certain environmental factors to trigger the
development of a brain disease.
Let’s consider an example. Imagine identical
twins, which share 100% of the same genes, who
have parents that have both suffered Major
Depression. Because the disease runs in this
family, it is likely the twins have the genes that
predispose them to it as well. However this alone
does not mean that both of the kids will develop
depression – it still takes certain environmental
factors to trigger the development of the
disorder. For instance, suppose one of the twins
consumes psychoactive drugs, which alter the
chemistry of the brain. This makes it possible for
one twin to develop depression and the other to
not, even though they share the same exact genes
that make it possible.
This example is greatly simplified. For any
given brain disease, scientists have not
determined all of the very subtle and massively
complicated interactions between genes and the
many environmental factors that exist. Because of
this, scientists cannot often say who will get a
particular brain disease and who will not. They
advise, however, that we look into our family
histories to get a sense of the potential
genetic predispositions and then adjust the
environmental factors under our control (like
avoiding drug use) to try to prevent their
development.
Thank you for the very interesting question!
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