Quality of Life in Hypoparathyroidism Improves With rhPTH(1-84) Throughout 8 Years of Therapy.


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 07 2019
Historique:
received: 09 11 2018
accepted: 13 02 2019
pubmed: 19 2 2019
medline: 2 6 2020
entrez: 19 2 2019
Statut: ppublish

Résumé

Calcium and vitamin D treatment does not improve reduced quality of life (QOL) in hypoparathyroidism. Recombinant human (rh) PTH(1-84) therapy improves QOL metrics for up to 5 years. Data on QOL beyond this time point are not available. To evaluate the effects of 8 years of rhPTH(1-84) therapy on QOL and factors associated with long-term benefit. Prospective, open-label trial. Referral center. Twenty patients with hypoparathyoidism. RAND 36-Item Short Form Health Survey (SF-36). rhPTH therapy led to substantial improvement in five of the eight SF-36 domains [vitality, social functioning (SF), mental health (MH), bodily pain (BP) and general health] and three of these domains (SF, MH, BP) were no longer lower than the reference population. The improvement in the mental component summary (MCS) score was sustained through 8 years, while the physical component summary (PCS) score improved through 6 years. A lower baseline QOL score was associated with greater improvement. A threshold value <238 (MCS) and <245 (PCS) predicted long-term improvement in 90% and 100% of the cohort, respectively. In patients whose calcium supplementation was reduced, MCS and PCS scores improved more than those whose supplementation did not decline to the same extent. Improvement in PCS was greater in patients whose calcitriol dosage was reduced and duration of disease was shorter. rhPTH(1-84) improves long-term well-being in hypoparathyroidism. The improvements are most prominent in those with impaired SF-36 at baseline and those whose requirements for conventional therapy decreased substantially.

Identifiants

pubmed: 30776291
pii: 5320276
doi: 10.1210/jc.2018-02430
pmc: PMC6530656
doi:

Substances chimiques

Calcium-Regulating Hormones and Agents 0
Ergocalciferols 0
Parathyroid Hormone 0
Recombinant Proteins 0
Vitamin D 1406-16-2
Cholecalciferol 1C6V77QF41
1,25-dihydroxyvitamin D 66772-14-3
25-hydroxyvitamin D A288AR3C9H
Calcitriol FXC9231JVH
Calcium SY7Q814VUP

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

2748-2756

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK032333
Pays : United States

Informations de copyright

Copyright © 2019 Endocrine Society.

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Auteurs

Gaia Tabacco (G)

Division of Endocrinology, Department of Medicine, College of Physicians & Surgeons, Columbia University, New York, New York.
Unit of Endocrinology and Diabetes, Department of Medicine, University Campus Bio-Medico, Rome, Italy.

Yu-Kwang Donovan Tay (YD)

Department of Medicine, Sengkang General Hospital, Singapore.

Natalie E Cusano (NE)

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

John Williams (J)

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

Beatriz Omeragic (B)

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

Rukhana Majeed (R)

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

Maximo Gomez Almonte (MG)

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

Mishaela R Rubin (MR)

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

John P Bilezikian (JP)

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

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