The University of Southampton
University of Southampton Institutional Repository

Vitamin D threshold to prevent aromatase inhibitor-related bone loss: the B-ABLE prospective cohort study

Vitamin D threshold to prevent aromatase inhibitor-related bone loss: the B-ABLE prospective cohort study
Vitamin D threshold to prevent aromatase inhibitor-related bone loss: the B-ABLE prospective cohort study
Aromatase inhibitor (AI)-related bone loss is associated with increased fracture rates. Vitamin D might play a role in minimising this effect. We hypothesised that 25-hydroxy-vitamin D concentrations [25(OH)D] after 3 months supplementation might relate to bone loss after 1 year on AItherapy. We conducted a prospective cohort study from January 2006 to December 2011 of a consecutive sample of women initiating AI for early breast cancer who were ineligible for bisphosphonate therapy and stayed on treatment for 1 year (N = 232). Serum 25(OH)D was measured at baseline and 3 months, and lumbar spine (LS) bone mineral density at baseline and 1 year. Subjects were supplemented with daily calcium (1 g) and vitamin D3 (800 IU) and additional oral 16,000 IU every 2 weeks if baseline 25(OH)D was ?30 ng/ml. Linear regression models were fitted to adjust for potential confounders. After 1 year on AI therapy, 232 participants experienced a significant 1.68 % [95 % CI 1.15–2.20 %] bone loss at LS (0.017 g/cm2 [0.012–0.024], P\0.0001). Higher 25(OH)D at 3 months protected against LS bone loss (-0.5 % per 10 ng/ml [95 % CI -0.7 to
-0.3 %], adjusted P = 0.0001), and those who reached levels ?40 ng/ml had reduced bone loss by 1.70 % [95 % CI 0.4–3.0 %; adjusted P = 0.005] compared to those with low 25(OH)D levels (?30 ng/ml). We conclude that improved vitamin D status using supplementation is associated with attenuation of AI-associated bone loss. For this population, the current Institute of Medicine target recommendation of 20 ng/ml might be too low to ensure good bone health.
epidemiology, osteoporosis, vitamin D, aromatase inhibitors, breast neoplasms
0167-6806
1159-1167
Prieto-Alhambra, Daniel
e596722a-2f01-4201-bd9d-be3e180e76a9
Servitja, Sonia
2da093d9-e67f-42c8-84ae-8520c0c6a176
Javaid, M. Kassim
64155236-2ef0-4065-b684-cf723a888117
Garrigós, Laia
7c77fa5d-1ee7-48ca-b85a-35b3b4357456
Arden, Nigel K.
23af958d-835c-4d79-be54-4bbe4c68077f
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Albanell, Joan
9979d4e9-cce5-462b-9b12-b72752cc5484
Tusquets, Ignasi
1fb77bc8-533b-4ac6-9a5b-cad306d0eaa4
Diez-Perez, Adolfo
19f89c53-003a-469c-92ac-69b0b979f3ec
Nogues, Xavier
707bb2b8-3a0f-4a74-a5a0-a47f6739c01e
Prieto-Alhambra, Daniel
e596722a-2f01-4201-bd9d-be3e180e76a9
Servitja, Sonia
2da093d9-e67f-42c8-84ae-8520c0c6a176
Javaid, M. Kassim
64155236-2ef0-4065-b684-cf723a888117
Garrigós, Laia
7c77fa5d-1ee7-48ca-b85a-35b3b4357456
Arden, Nigel K.
23af958d-835c-4d79-be54-4bbe4c68077f
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Albanell, Joan
9979d4e9-cce5-462b-9b12-b72752cc5484
Tusquets, Ignasi
1fb77bc8-533b-4ac6-9a5b-cad306d0eaa4
Diez-Perez, Adolfo
19f89c53-003a-469c-92ac-69b0b979f3ec
Nogues, Xavier
707bb2b8-3a0f-4a74-a5a0-a47f6739c01e

Prieto-Alhambra, Daniel, Servitja, Sonia, Javaid, M. Kassim, Garrigós, Laia, Arden, Nigel K., Cooper, C., Albanell, Joan, Tusquets, Ignasi, Diez-Perez, Adolfo and Nogues, Xavier (2012) Vitamin D threshold to prevent aromatase inhibitor-related bone loss: the B-ABLE prospective cohort study. Breast Cancer Research and Treatment, 133 (3), 1159-1167. (doi:10.1007/s10549-012-2013-9). (PMID:22434523)

Record type: Article

Abstract

Aromatase inhibitor (AI)-related bone loss is associated with increased fracture rates. Vitamin D might play a role in minimising this effect. We hypothesised that 25-hydroxy-vitamin D concentrations [25(OH)D] after 3 months supplementation might relate to bone loss after 1 year on AItherapy. We conducted a prospective cohort study from January 2006 to December 2011 of a consecutive sample of women initiating AI for early breast cancer who were ineligible for bisphosphonate therapy and stayed on treatment for 1 year (N = 232). Serum 25(OH)D was measured at baseline and 3 months, and lumbar spine (LS) bone mineral density at baseline and 1 year. Subjects were supplemented with daily calcium (1 g) and vitamin D3 (800 IU) and additional oral 16,000 IU every 2 weeks if baseline 25(OH)D was ?30 ng/ml. Linear regression models were fitted to adjust for potential confounders. After 1 year on AI therapy, 232 participants experienced a significant 1.68 % [95 % CI 1.15–2.20 %] bone loss at LS (0.017 g/cm2 [0.012–0.024], P\0.0001). Higher 25(OH)D at 3 months protected against LS bone loss (-0.5 % per 10 ng/ml [95 % CI -0.7 to
-0.3 %], adjusted P = 0.0001), and those who reached levels ?40 ng/ml had reduced bone loss by 1.70 % [95 % CI 0.4–3.0 %; adjusted P = 0.005] compared to those with low 25(OH)D levels (?30 ng/ml). We conclude that improved vitamin D status using supplementation is associated with attenuation of AI-associated bone loss. For this population, the current Institute of Medicine target recommendation of 20 ng/ml might be too low to ensure good bone health.

This record has no associated files available for download.

More information

e-pub ahead of print date: 21 March 2012
Published date: June 2012
Keywords: epidemiology, osteoporosis, vitamin D, aromatase inhibitors, breast neoplasms
Organisations: Faculty of Health Sciences

Identifiers

Local EPrints ID: 345399
URI: http://eprints.soton.ac.uk/id/eprint/345399
ISSN: 0167-6806
PURE UUID: c4eb0c18-5256-44a0-8b47-fcf9873166f9
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

Catalogue record

Date deposited: 20 Nov 2012 15:52
Last modified: 18 Mar 2024 02:45

Export record

Altmetrics

Contributors

Author: Daniel Prieto-Alhambra
Author: Sonia Servitja
Author: M. Kassim Javaid
Author: Laia Garrigós
Author: Nigel K. Arden
Author: C. Cooper ORCID iD
Author: Joan Albanell
Author: Ignasi Tusquets
Author: Adolfo Diez-Perez
Author: Xavier Nogues

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×