A B S T R A C T We measured plasma calcitonin con- centrations in healthy volunteers (20 men, ages 23-45 yr, mean, 30 yr; 25 women, ages 21-46 yr, mean, 30 yr) with a radioimmunoassay capable of detecting 5 pg of calcitonin/500 ,ul incubation volume, or 25 pg/ml of unextracted plasma. All subjects had 4-h calcium in- fusion (15 mg Ca/kg), and 24 subjects had intravenous pentagastrin injection (0.5,ug/kg) on separate days. Men had higher basal plasma immunoreactive calcitonin concentrations than women (P < 0.001): mean, 49 pg/ ml (range, <25-73) and 31 pg/ml (range, <25-51), re- spectively. 18 of the 20 men (90%) responded to in- duced hypercalcemia with increases in plasma im- munoreactive calcitonin; only 14 of the 25 women (56%) responded. In men, the mean increase of plasma immunoreactive calcitoninSE was 58+9 pg/ml, but for women was only 25+6 pg/ml. 8 of 10 men (80%) responded to pentagastrin with an increase of plasma immunoreactive calcitonin >30 pg/ml, compared with such a response in only 1 of 14 women (7%). These differences of plasma immunoreactive calcitonin re- sponses between the sexes were statistically signif- icant (calcium infusion, P <0.02; pentagastrin, P < 0.001). The physiologic importance of these observa- tions is unknown, but we speculate that a lifelong, relative deficiency of calcitonin in some women could play a role in age-and sex-related bone loss, particu- larly during the estrogen-deficient postmenopausal years.
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Heath et al. (1977) studied this question.
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