Background: Substantial evidence now shows that the genetic vulnerability t
o schizophrenia can be manifested clinically in first-degree relatives of p
eople with schizophrenia, even without the full manifestations of the disor
der. One pattern of problems observed involves the combination of negative
symptoms and neuropsychological deficits. We have investigated whether a lo
w dose of a novel antipsychotic medication, risperidone, could attenuate th
ese clinical problems in non-psychotic, first-degree relatives, and report
here findings from our first 4 cases.
Methods: Twelve adults who were first-degree relatives of patients with sch
izophrenia were evaluated for the presence of negative symptoms and neurops
ychological deficits:(in attention and working memory, long-term verbal mem
ory and executive functions). Four subjects who met our predetermined crite
ria, and who did not demonstrate medical contraindications, were enrolled i
n a 6-week trial of risperidone. Clinical and medical measures were assesse
d before, during and after treatment Doses of risperidone started at 0.25 m
g and were increased to 1.0-2.0 mg/day.
Results: Three subjects showed substantial reductions in negative symptoms,
and one subject showed modest reductions. All four subjects showed substan
tial improvements on some tests of attention and working memory. Side effec
ts of risperidone were temporary and mainly mild
Conclusions: These initial findings support two conclusions, First, clinica
l deficits in non-psychotic first-degree relatives of people with schizophr
enia are identifiable, and to a significant extent, reversible. Second, ris
peridone may eventually serve as an effective treatment for people whose li
ves are impaired by similar or related problems. (C) 1999 Society of Biolog
ical Psychiatry.