Abstract
A positive effect of fluoxetine has been shown in some children with autism. The present
study was undertaken to correlate striatal dopamine transporter (DAT) binding and
cerebrospinal fluid insulin-like growth factor-1 (CSF-IGF-1) with clinical response
in autistic children (n=13, age 5–16 years) after a 6-month fluoxetine treatment.
Good clinical responders (n=6) had a decrease (p=0.031) in DAT binding as assessed
using single-photon emission computed tomography with [123I]-nor-β-CIT, whereas poor responders had a trend to an increase. An increase in CSF-IGF-1
(p=0.003) was detected after the treatment period, but no correlation between the
clinical response and CSF-IGF-1 was found. In conclusion, fluoxetine decreases DAT
binding indicating alleviation of the hyperdopaminergic state and increases CSF-IGF-1
concentration, which may also have a neuroprotective effect against dopamine-induced
neurotoxicity in autistic children.
Key words
autism - dopamine transporter - fluoxetine - insulin-like growth factor-1