Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1

Parathyroid-independent hypercalcaemia of pregnancy, due to biallelic loss of function of the P450 enzyme CYP24A1, the principal inactivator of 1,25(OH)2D results in hypervitaminosis D, hypercalcaemia and hypercalciuria. We report two cases of this disorder, with intractable hypercalcaemia, one occu...

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Main Authors: Nirusha Arnold, Victor O’Toole, Tien Huynh, Howard C Smith, Catherine Luxford, Roderick Clifton-Bligh, Creswell J Eastman
Format: Article
Language:English
Published: Bioscientifica 2019-11-01
Series:Endocrinology, Diabetes & Metabolism Case Reports
Online Access:https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0114.xml
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spelling doaj-499fa2f358bf4986bfc6fc4625fd35e72020-11-25T01:34:39ZengBioscientificaEndocrinology, Diabetes & Metabolism Case Reports2052-05732052-05732019-11-01111610.1530/EDM-19-0114Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1Nirusha Arnold0Victor O’Toole1Tien Huynh2Howard C Smith3Catherine Luxford4Roderick Clifton-Bligh5Creswell J Eastman6Westmead Private Hospital, Westmead, Sydney, New South Wales, AustraliaWestmead Private Hospital, Westmead, Sydney, New South Wales, AustraliaWestmead Private Hospital, Westmead, Sydney, New South Wales, AustraliaWestmead Teaching HospitalKolling Institute of Medical Research, Royal North Shore Teaching Hospital, The University of Sydney, Sydney, New South Wales, AustraliaKolling Institute of Medical Research, Royal North Shore Teaching Hospital, The University of Sydney, Sydney, New South Wales, AustraliaWestmead Private Hospital, Westmead, Sydney, New South Wales, Australia; Westmead Teaching HospitalParathyroid-independent hypercalcaemia of pregnancy, due to biallelic loss of function of the P450 enzyme CYP24A1, the principal inactivator of 1,25(OH)2D results in hypervitaminosis D, hypercalcaemia and hypercalciuria. We report two cases of this disorder, with intractable hypercalcaemia, one occurring during gestation and into the postpartum, and the other in the postpartum period. Case 1, a 47-year-old woman with a twin pregnancy conceived by embryo transfer, presented with hypercalcaemia at 23 weeks gestation with subnormal serum parathyroid hormone (PTH) and normal serum 25-OH D levels. She was admitted to hospital at 31 weeks gestation with pregnancy-induced hypertension, gestational diabetes and increasing hypercalcaemia. Caesarean section at 34 weeks gestation delivered two healthy females weighing 2.13 kg and 2.51 kg. At delivery, the patient’s serum calcium level was 2.90 mmol/L. Postpartum severe hypercalcaemia was treated successfully with Denosumab 60 mg SCI, given on two occasions. CYP24A1 testing revealed she was compound heterozygous for pathogenic variants c.427_429delGAA, (p.Glu143del) and c.1186C>T, (p.Arg396Trp). Case 2, a 36-year-old woman presented 4 days after the delivery of healthy twins with dyspnoea, bradycardia, severe headaches, hypertension and generalized tonic-clonic seizures after an uneventful pregnancy. She was hypercalcaemic with a suppressed PTH, normal 25(OH)D, and elevated 1,25(OH)2D levels. Her symptoms partially responded to i.v. saline and corticosteroids in the short term but bisphosphonates such as Pamidronate and Zoledronic acid did not result in sustained improvement. Denosumab 120 mg SCI successfully treated the hypercalcaemia which resolved completely 2 months post-partum. CYP24A1 testing revealed she was homozygous for the pathogenic variant c.427_429delGAA, (p.Glu143del).https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0114.xml
collection DOAJ
language English
format Article
sources DOAJ
author Nirusha Arnold
Victor O’Toole
Tien Huynh
Howard C Smith
Catherine Luxford
Roderick Clifton-Bligh
Creswell J Eastman
spellingShingle Nirusha Arnold
Victor O’Toole
Tien Huynh
Howard C Smith
Catherine Luxford
Roderick Clifton-Bligh
Creswell J Eastman
Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
Endocrinology, Diabetes & Metabolism Case Reports
author_facet Nirusha Arnold
Victor O’Toole
Tien Huynh
Howard C Smith
Catherine Luxford
Roderick Clifton-Bligh
Creswell J Eastman
author_sort Nirusha Arnold
title Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
title_short Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
title_full Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
title_fullStr Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
title_full_unstemmed Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1
title_sort intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in cyp24a1
publisher Bioscientifica
series Endocrinology, Diabetes & Metabolism Case Reports
issn 2052-0573
2052-0573
publishDate 2019-11-01
description Parathyroid-independent hypercalcaemia of pregnancy, due to biallelic loss of function of the P450 enzyme CYP24A1, the principal inactivator of 1,25(OH)2D results in hypervitaminosis D, hypercalcaemia and hypercalciuria. We report two cases of this disorder, with intractable hypercalcaemia, one occurring during gestation and into the postpartum, and the other in the postpartum period. Case 1, a 47-year-old woman with a twin pregnancy conceived by embryo transfer, presented with hypercalcaemia at 23 weeks gestation with subnormal serum parathyroid hormone (PTH) and normal serum 25-OH D levels. She was admitted to hospital at 31 weeks gestation with pregnancy-induced hypertension, gestational diabetes and increasing hypercalcaemia. Caesarean section at 34 weeks gestation delivered two healthy females weighing 2.13 kg and 2.51 kg. At delivery, the patient’s serum calcium level was 2.90 mmol/L. Postpartum severe hypercalcaemia was treated successfully with Denosumab 60 mg SCI, given on two occasions. CYP24A1 testing revealed she was compound heterozygous for pathogenic variants c.427_429delGAA, (p.Glu143del) and c.1186C>T, (p.Arg396Trp). Case 2, a 36-year-old woman presented 4 days after the delivery of healthy twins with dyspnoea, bradycardia, severe headaches, hypertension and generalized tonic-clonic seizures after an uneventful pregnancy. She was hypercalcaemic with a suppressed PTH, normal 25(OH)D, and elevated 1,25(OH)2D levels. Her symptoms partially responded to i.v. saline and corticosteroids in the short term but bisphosphonates such as Pamidronate and Zoledronic acid did not result in sustained improvement. Denosumab 120 mg SCI successfully treated the hypercalcaemia which resolved completely 2 months post-partum. CYP24A1 testing revealed she was homozygous for the pathogenic variant c.427_429delGAA, (p.Glu143del).
url https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0114.xml
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