Abstract
Calcitonin pharmacokinetics and pharmacodynamics were studied in two groups of patients
with postmenopausal osteoporosis, who, treated for one year with intranasal Asu1,7-eel calcitonin (eCT), had (Ab+) and had not (Ab-) developed a specific immune response
to the drug. The treatment consisted of daily intranasal administrations of eCT (80
IU/die) with 1 g supplemental calcium. Eight women who had developed specific antibodies
and 5 who had not, were given 50 IU of CT i.m., in order to assess the pharmacokinetics
and pharmacodynamics of the drug. The rise of serum levels of the hormone was significantly
greater in Ab+ than in Ab- patients. At the end of the study, no significant differences
in mineral bone loss between the two groups were found. In conclusion, the presence
of antibodies to eCT does not represent a negative event in the therapy of osteoporosis,
but significantly affects the pharmacokinetics of the drug.
Key words
Asu1,7-eel Calcitonin - Antibodies - Calcitonins - Osteoporosis - Intranasal Therapy