PATHOGENETIC ASPECTS OF RESPONSIVENESS TO ONDANSETRON (5-HYDROXYTRYPTAMINE TYPE-3 RECEPTOR ANTAGONIST) IN PATIENTS WITH PRIMARY FIBROMYALGIA SYNDROME - A PRELIMINARY-STUDY
P. Hrycaj et al., PATHOGENETIC ASPECTS OF RESPONSIVENESS TO ONDANSETRON (5-HYDROXYTRYPTAMINE TYPE-3 RECEPTOR ANTAGONIST) IN PATIENTS WITH PRIMARY FIBROMYALGIA SYNDROME - A PRELIMINARY-STUDY, Journal of rheumatology, 23(8), 1996, pp. 1418-1423
Objective. To study the efficacy of 5-hydroxytryptamine type 3 recepto
r (5-HT-3R) antagonist (ondansetron) vs paracetamol in primary fibromy
algia (FM) syndrome. Methods, A double blind, crossover, latin square
study of 31 patients with FM. Visual analog scale (VAS) and body drawi
ngs were used to record pain intensity. Functional symptoms were deter
mined for using a Likert-type self-developed protocol. Quantitative do
lorimetry was applied to assess the number of painful tender points an
d the average pain threshold. Serum serotonin levels were measured by
a commercial ELISA. Results. A marked improvement in pain intensity me
asured by VAS (p < 0.005), pain score (p < 0.05), tender points (p < 0
.05), and average pain threshold (p < 0.01) was obtained with ondanset
ron, whereas no improvement was seen with paracetamol. After ondansetr
on treatment, there was also significant reduction in both functional
symptoms (p < 0.01) and headache intensity (p < 0.05). In patients who
did not respond to ondansetron there was higher baseline pain intensi
ty measured by VAS (p < 0.05) and pain score (p < 0.01), and a lower p
ain threshold (p < 0.05) compared to those who did respond well. In th
e responsive group, no significant differences were seen in the seroto
nin level before and after therapy, whereas a significant increase in
serum serotonin concentration (p < 0.01) was observed in nonresponders
after ondansetron treatment. Conclusion. Ondansetron appears to be an
effective drug in about 50% of patients with FM. Then may be 2 subset
s of patients with FM that differ clinically and pathogenetically with
regard to the disturbance in the 5-HT-3R system.