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SUMMARY
In
the D.S.M. IV, classification system of the American Psychiatric
Association (1), which is the most used document in investigation
and communication in psychiatry, it is stated that the Depressive
Disorder affects between 5 and 9% in women and 2 3% of men,
while border line personality disorder, correspond to 2% of the
general population. Both pathological disorders share dimensions
of regulation of affection and control of impulses (2).
In
these pathologies there are important impaired functions in at least
three common systems of neurotransmission with behavioral features
such as the cholinergic system, noradrenergic system and serotoninergic
systems (3).
In
this paper an intracomparisson of brain blood flow is reported of
a group of patients with Mayor Depression and Borderline Personality,
in basal conditions versus activation conditions with the Wisconsin
Test, as well an intercomparisson between the results of both pathologies
are reported.
In
this work brain blood flow is quantified by SPECT Tc99m HMPAO evaluating
the compromise in areas of the brain cortex, which are part of the
three brain separate circuits (4) such as the frontal orbit circuit,
the anterior cyngulate and the dorsolateral prefrontal circuit,
with its afferences and efferences (5).
In
the analysis of results we can see a compromise shared in structures
linked to motivation, where the anterior cyngulate stands out, while
the hipofuncionality induced by the Wisconsin test in borderline
patients (P< 0.00005 to the right and< 0.0003 to the left)
is more marked than in depressive patients ( P< 0.002 to the
right and < 0.003 to the left).
The
same happens in the area 32 of Brodmann (part of the limbic system),
and the area 25 mentioned by Damasio (6) as the area of the "anhedonia"
where the compromise exists in both pathologies.
There
is only in borderline patients a significative compromise of the
dorsolateral prefrontal area or executive area induced by the stress
of the Wisconsin test. In the other hand in the depressive patients
it was detected a more than 50%, more extensive hypoperfusion in
the frontal orbit area related to emotions and this is evident (7)
in basal conditions as well as with stimulation.
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