ECTS2014 Poster Presentations Bone development/growth and fracture repair (55 abstracts)
Department of Endocrinology and Internal Medicine, Aarhus, Denmark.
PTH replacement therapy in hypoparathyroidism (hypoPT) has become more accepted after proving successful in several clinical studies. Intact PTH (PTH184) was in 2012 withdrawn, leaving teriparatide (PTH134) the only therapeutic option available.
All patients with postoperative HypoPT who changed medication from PTH184 (100 μg) to PTH134 (20 μg), after at least 12 months of conventional therapy and a minimum of 6 months of PTH184 were included. The following treatment with PTH134 was for at least 3 months. Plasma ionized calcium, daily dose of 1α-hydroxylated-vitamin D metabolites (Etalpha), calcium and PTH was collected.
Eight patients (women=88%) with a mean age of 54±12 years and a duration of hypoPT of 13±6 years were included. Before initiation of PTH1-84 the mean daily dose of Etalpha was 1.9±1.1 μg and calcium supplements were 1550±705 mg. Etalpha dose was reduced with 86±35% (P=0.01) after 6 months of PTH184 treatment and terminated in seven patients. Calcium were reduced with 78±36% (P=0.02) to 273±353 mg and stopped in four patients. Six patients received 100 μg PTH184 a day, the seventh received PTH 2 out of 3 days and the last one received PTH184 every other day.
When changing from PTH184 to PTH134, plasma ionized calcium initially dropped and the demand for supplements increased. Etalpha was resumed in four patients; mean daily dose increased to 0.99±1.26 μg (P=0.04) and calcium increased to 329±368 mg (P=0.72). Five patients received 20 μg PTH1-34 a day; two patients twice a day and one 20/40 μg alternately.
Compared with PTH134, PTH184 has a longer plasma half-life and a higher calcemic response. We have shown a need for higher doses of Etalpha and calcium supplements to maintain normal serum calcium when treated with PTH134 compared to PTH184 and in some a need for more than one daily dose.