Alendronate after denosumab discontinuation in women previously exposed to bisphosphonates was not effective in preventing the risk of spontaneous multiple vertebral fractures: two case reports.


Journal

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
ISSN: 1433-2965
Titre abrégé: Osteoporos Int
Pays: England
ID NLM: 9100105

Informations de publication

Date de publication:
May 2019
Historique:
received: 21 08 2018
accepted: 18 12 2018
pubmed: 8 1 2019
medline: 18 12 2019
entrez: 8 1 2019
Statut: ppublish

Résumé

At denosumab discontinuation, an antiresorptive agent is indicated to reduce the high bone turnover, the rapid bone loss, and the risk of spontaneous vertebral fractures. We report two cases of postmenopausal women, previously exposed to bisphosphonates, treated with alendronate at denosumab discontinuation. Alendronate was ineffective to avoid spontaneous clinical vertebral fractures. They presented three and nine spontaneous vertebral fractures 8 and 12 months after denosumab discontinuation, respectively. Ineffectiveness of alendronate was attributed to insufficient control of the rebound as assessed by B-crosslaps measures in the first case, and partially to the high risk of fractures in the later. In both situations, the increased fracture risk may have favoured these new fractures. It is urgent to define effective therapeutic strategies to avoid spontaneous vertebral fractures after denosumab discontinuation.

Identifiants

pubmed: 30613866
doi: 10.1007/s00198-018-04820-8
pii: 10.1007/s00198-018-04820-8
doi:

Substances chimiques

Bone Density Conservation Agents 0
Denosumab 4EQZ6YO2HI
Alendronate X1J18R4W8P

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1111-1115

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Auteurs

O Lamy (O)

Center of Bone Diseases, Bone and Joint Department, Lausanne University Hospital, Lausanne, Switzerland. olivier.lamy@chuv.ch.
Service of Internal Medicine, CHUV, Lausanne University Hospital, Rue du Bugnon 46, CH-1011, Lausanne, Switzerland. olivier.lamy@chuv.ch.

E Fernández-Fernández (E)

Service of Rheumatology, La Paz University Hospital, Madrid, Spain.

I Monjo-Henry (I)

Service of Rheumatology, La Paz University Hospital, Madrid, Spain.

D Stoll (D)

Center of Bone Diseases, Bone and Joint Department, Lausanne University Hospital, Lausanne, Switzerland.

B Aubry-Rozier (B)

Center of Bone Diseases, Bone and Joint Department, Lausanne University Hospital, Lausanne, Switzerland.

D Benavent-Núñez (D)

Service of Rheumatology, La Paz University Hospital, Madrid, Spain.

P Aguado (P)

Service of Rheumatology, La Paz University Hospital, Madrid, Spain.

E Gonzalez-Rodriguez (E)

Center of Bone Diseases, Bone and Joint Department, Lausanne University Hospital, Lausanne, Switzerland.
Service of Endocrinology, Diabetes and Metabolism, Lausanne University Hospital, Lausanne, Switzerland.

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Classifications MeSH