In
most kinds of dementia,
autopsy reveals widespread degeneration in the cerebral
cortex - such as the plaques and tangles which are the
hallmark of Alzheimer's
disease. Alzheimer's disease and frontotemporal
dementia are therefore sometimes classed as "cortical
dementias." In other kinds of dementia, there is targeted
damage to regions lying under the cortex, giving rise to the
category known as "subcortical dementias". This terminology
is somewhat misleading, because both classes of dementia can
cause damage to both cortical and subcortical areas. However,
it is roughly true that the earliest symptoms in "cortical"
dementia include difficulty with high-level behaviors such
as memory, language, problem-solving and reasoning; these
functions tend to be less impaired in "subcortical" dementia.
Subcortical dementia is more likely to affect attention, motivation
and emotionality. People with subcortical dementia often show
early symptoms of depression, clumsiness, irritability or
apathy. As the disease progresses, though, memory and judgment
problems arise, and the end stages of subcortical dementia
result in the same total breakdown of brain function as in
the cortical dementias.
Parkinson's
Disease is a disease that is usually classed as a motor
disorder; its most obvious symptoms include tremor, muscular
weakness and rigidity. Currently, it is believed that these
symptoms reflect cell loss in a small brain region known as
the substantia nigra which provides a vital neurochemical,
dopamine, to other brain areas. About 30% of patients with
Parkinson's disease also develop subcortical dementia. This
mental deterioration appears to be part of the normal progress
of the disease. In addition, some individuals with Parkinson's
disease appear to develop a kind cortical dementia similar
to Alzheimer's disease. This occurs at a higher rate than
would be expected in the general population. Thus, it may
be that individuals with Parkinson's disease are coincidentally
at higher risk for Alzheimer's disease, for reason or reasons
unknown.
Huntington's
Disease is another "motor" disease, in which patients
develop involuntary dance-like movements. It is an inherited
disease, which means that if a parent passes the appropriate
gene to a child, that child will eventually develop the disease.
Huntington's disease results from degeneration of a brain
area known as the basal ganglia, which is important in generating
voluntary movements. Early in the course of the disease, patients
may also show emotional problems, typically fits of depression
or irritability. Later in the disease, subcortical dementia
occurs. (In some cases, though, memory loss is among the earliest
of symptoms.) There is no cure and no good treatment; tranquilizers
may be used to control the involuntary movements and alleviate
depression, but they cannot reverse the disease nor stop mental
deterioration.
HIV
Dementia is caused by the HIV virus, the virus that causes
AIDS. The HIV virus attacks and progressively destroying the
immune system. The HIV virus can directly infect the brain
and can also weaken the immune system, allowing other infections
to enter the brain and cause encephalitis.
The resulting brain damage may be visible on MRI as generalized
brain atrophy (shrinkage) and also visibly damaged subcortical
areas. The behavioral symptoms parallel dementia - indeed,
the condition is often called the AIDS-dementia complex. Early
symptoms include memory loss, loss of concentration, and personality
changes. In later stages, there can be confusion and sometimes
psychosis.
by Catherine E. Myers. Copyright © 2006 Memory Loss and the Brain |