Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2018 Dec:203:391-399.e1.
doi: 10.1016/j.jpeds.2018.08.010.

Long-Term Parathyroid Hormone 1-34 Replacement Therapy in Children with Hypoparathyroidism

Affiliations
Observational Study

Long-Term Parathyroid Hormone 1-34 Replacement Therapy in Children with Hypoparathyroidism

Karen K Winer et al. J Pediatr. 2018 Dec.

Abstract

Objective: To determine whether multiple daily injections of parathyroid hormone (PTH) 1-34 are safe and effective as long-term therapy for children with hypoparathyroidism.

Study design: Linear growth, bone accrual, renal function, and mineral homeostasis were studied in a long-term observational study of PTH 1-34 injection therapy in 14 children.

Methods: Subjects were 14 children with hypoparathyroidism attributable to autoimmune polyglandular syndrome type 1 (N = 5, ages 7-12 years) or calcium receptor mutation (N = 9, ages 7-16 years). Mean daily PTH 1-34 dose was 0.75 ± 0.15 µg/kg/day. Treatment duration was 6.9 ± 3.1 years (range 1.5-10 years). Patients were evaluated semiannually at the National Institutes of Health Clinical Center.

Results: Mean height velocity and lumbar spine, whole body, and femoral neck bone accretion velocities were normal throughout the study. In the first 2 years, distal one-third radius bone accrual velocity was reduced compared with normal children (P < .003). Serum alkaline phosphatase correlated with PTH 1-34 dose (P < .006) and remained normal (235.3 ± 104.8 [SD] U/L, N: 51-332 U/L). Mean serum and 24-hour urine calcium levels were 2.05 ± 0.11 mmol/L (N: 2.05-2.5 mmol/L) and 6.93 ± 1.3 mmol/24 hour (N: 1.25-7.5 mmol/24 hour), respectively-with fewer high urine calcium levels vs baseline during calcitriol and calcium treatment (P < .001). Nephrocalcinosis progressed in 5 of 12 subjects who had repeated renal imaging although renal function remained normal.

Conclusions: Twice-daily or thrice-daily subcutaneous PTH 1-34 injections provided safe and effective replacement therapy for up to 10 years in children with hypoparathyroidism because of autoimmune polyglandular syndrome type 1 or calcium receptor mutation.

Keywords: ADH; APECED; APS-1; PTH 1-34; Vitamin D; autosomal dominant hypocalcemia; calcium receptor; hypocalcemia; hypomagnesemia; teriparatide.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Boxplots show height velocity and 5 measures of bone accrual velocity, shown as velocity Z scores (VeL-Z) vs study year. Boxplots indicate median, interquartile intervals, and maximum and minimum values for each measure, except where outlier values (> 3 SD from remaining values) have been shown individually as circles. HT (annualized height velocity); WBBMC (whole body bone mineral content); aBMD (areal bone mineral density); LS (lumbar spine); FN (femoral neck); 1/3 radius (distal 1/3 radius).
Figure 2
Figure 2
The distribution of serum calcium (left panel) and 24-h urine calcium (right panel) among low, normal, and high values for each diagnostic group (APS-1 vs. CaR). Figure 2a represents serum and urine calcium distributions measured during baseline evaluation while patients received vitamin D analogs and calcium supplementation. Figure 2b represents serum and urine calcium distributions from 0.5 to 10 years of PTH 1–34 therapy.
Figure 3
Figure 3
The distribution of serum calcium x phosphorus (Ca x P) product for the two diagnostic groups from 0.5 to 10 years of PTH 1–34 therapy.

Similar articles

Cited by

References

    1. Horowitz MJ, Stewart AF. Hypoparathyroidism: Is it time for replacement therapy? J Clin Endocrinol Metab 2008; 93:3307–9 - PMC - PubMed
    1. Bollerslev J, Rejnmark L, Marococci C, Shoback D, Sitges-Serra A, Van Biesen W, et al. European Society of Endocrinology Clinical Guideline: Treatment of Chronic Hypoparathyroidism in adults. European Journal of Endocrinology 2015;173: G1–G20. - PubMed
    1. Winer KK. Perspectives on the Search for a True Physiologic Replacement Therapy for Hypoparathyroidism. European Endocrinology 2016; 12:47–8. - PMC - PubMed
    1. Mancilla EE, De Luca F, Ray K, Winer KK, Fan GF. A Ca (2+) sensing receptor mutation causes hypoparathyroidism by increasing receptor sensitivity to CA2+ and maximal signal transduction. Pediatri Res. 1997; 42:443–7 - PubMed
    1. Winer KK, Yanovski JA, Sarani B, Cutler GB Jr. A randomized, crossover trial of once-daily versus twice-daily human parathyroid hormone 1–34 in the treatment of hypoparathyroidism. J Clin Endocrinol Metab 1998; 83:3480–3486. - PubMed

Publication types

MeSH terms