Therapy of Hypoparathyroidism With rhPTH(1-84): A Prospective, 8-Year Investigation of Efficacy and Safety.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 11 2019
Historique:
received: 15 04 2019
accepted: 10 07 2019
pubmed: 17 7 2019
medline: 4 6 2020
entrez: 17 7 2019
Statut: ppublish

Résumé

Conventional treatment of hypoparathyroidism is associated with decreased renal function and increased bone mineral density (BMD). To evaluate the effects of 8 years of recombinant human parathyroid hormone (1-84) [rhPTH(1-84)] therapy on key biochemical and densitometric indices. Prospective open-label trial. Tertiary medical center. Twenty-four subjects with hypoparathyroidism. Treatment with rhPTH(1-84) for 8 years. Supplemental calcium and vitamin D requirements, serum calcium and phosphorus levels, calcium-phosphate product, urinary calcium excretion, estimated glomerular filtration rate (eGFR) and BMD. PTH therapy was associated with progressive reduction in supplemental calcium (57%; P < 0.01) and active vitamin D (76%; P < 0.001) requirements over 8 years. Serum calcium concentration was stable; urinary calcium excretion declined 38% (P < 0.01). eGFR remained stable and was related to baseline eGFR and serum calcium levels. Calcium-phosphate product was below the recommended limit; serum phosphorus remained within normal range. Lumbar spine and total hip BMD increased, peaking at 4 (mean ± SE, 4.6% ± 1.5%; P = 0.01) and 8 years (2.6% ± 1.1%; P = 0.02), whereas femoral neck BMD did not change and one-third radius BMD decreased (mean ± SE, -3.5% ± 1.1%; P = 0.001). BMD at all sites was higher throughout the 8 years than in the age- and sex-matched reference population. Hypercalcemia and hypocalcemia were uncommon. rhPTH(1-84) is a safe and effective treatment for hypoparathyroidism for 8 years. Long-term reductions in supplemental requirements and biochemical improvements with stable renal function are maintained.

Identifiants

pubmed: 31310310
pii: 5532037
doi: 10.1210/jc.2019-00893
pmc: PMC6977408
doi:

Substances chimiques

Parathyroid Hormone 0
Recombinant Proteins 0
Vitamin D 1406-16-2
Phosphorus 27YLU75U4W
Calcium SY7Q814VUP

Banques de données

ClinicalTrials.gov
['NCT02910466']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5601-5610

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK069350
Pays : United States

Informations de copyright

Copyright © 2019 Endocrine Society.

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Auteurs

Yu-Kwang Donovan Tay (YD)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.
Department of Medicine, Sengkang General Hospital, Singapore.

Gaia Tabacco (G)

Unit of Endocrinology and Diabetes, Department of Medicine, University Campus Bio-Medico, Rome, Italy.

Natalie E Cusano (NE)

Department of Medicine, Division of Endocrinology Lenox Hill Hospital, New York, New York.

John Williams (J)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.

Beatriz Omeragic (B)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.

Rukshana Majeed (R)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.

Maximo Gomez Almonte (M)

Department of Medicine, Division of Cardiology, Wyckoff Heights Medical Center, New York, New York.

John P Bilezikian (JP)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.

Mishaela R Rubin (MR)

Department of Medicine, Division of Endocrinology, College of Physicians and Surgeons, Columbia University, New York, New York.

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Classifications MeSH