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Ankylosing spondylitis confers substantially increased risk of clinical spine fractures: a nationwide case-control study

Ankylosing spondylitis confers substantially increased risk of clinical spine fractures: a nationwide case-control study
Ankylosing spondylitis confers substantially increased risk of clinical spine fractures: a nationwide case-control study
Summary
Ankylosing spondylitis (AS) leads to osteopenia/osteoporosis and spine rigidity. We conducted a case-control study and found that AS-affected patients have a 5-fold and 50 % increased risk of clinical spine and all clinical fractures, respectively. Excess risk of both is highest in the first years and warrants an early bone health assessment after diagnosis.

Introduction
Ankylosing spondylitis (AS) is related to spine rigidity and reduced bone mass, but data on its impact on fracture risk are scarce. We aimed to study the association between AS and clinical fractures using a case-control design.

Methods
From the Danish Health Registries, we identified all subjects who sustained a fracture in the year 2000 (cases) and matched up to three controls by year of birth, gender and region. Clinically diagnosed AS was identified using International Classification of Diseases, 8th revision (ICD-8; 71249), and International Classification of Diseases, 10th revision (ICD-10; M45) codes. We also studied the impact of AS duration. Conditional logistic regression was used to estimate crude and adjusted odds ratios (ORs) for non-traumatic fractures (any site, clinical spine and non-vertebral) according to AS status and time since AS diagnosis. Multivariate models were adjusted for fracture history, socio-economic status, previous medical consultations, alcoholism and use of oral glucocorticoids.

Results
We identified 139/124,655 (0.11 %) AS fracture cases, compared to 271/373,962 (0.07 %) AS controls. Unadjusted (age- and gender-matched) odds ratio (OR) were 1.54 [95 % confidence interval (95 %CI) 1.26–1.89] for any fracture, 5.42 [2.50–11.70] for spine and 1.39 [1.12–1.73] for non-vertebral fracture. The risk peaked in the first 2.5 years following AS diagnosis: OR 2.69 [1.84–3.92] for any fracture.

Conclusions
Patients with AS have a 5-fold higher risk of clinical spine fracture and a 35 % increased risk of non-vertebral fracture. This excess risk peaks early, in the first 2.5 years of AS disease. Patients should be assessed for fracture risk early after AS diagnosis.
0937-941X
85-91
Prieto-Alhambra, D.
19a5643f-5969-4c0e-b6a9-863fb9e9d1c7
Munoz-Ortego, J.
a2afad19-77ea-46cf-b2e1-7013df723efc
de Vries, F.
db4c0543-d6e7-476b-a10e-52d9d483f613
Vosse, D.
f0e6946b-baf0-4206-a5f0-a45b6e013be7
Arden, N.K.
23af958d-835c-4d79-be54-4bbe4c68077f
Bowness, P.
2791367b-84e8-4d24-88f2-9f61a8b67556
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Diez-Perez, A.
19f89c53-003a-469c-92ac-69b0b979f3ec
Vestergaard, P.
b00ba0f8-a9b7-45f1-a0c7-579fec88b556
Prieto-Alhambra, D.
19a5643f-5969-4c0e-b6a9-863fb9e9d1c7
Munoz-Ortego, J.
a2afad19-77ea-46cf-b2e1-7013df723efc
de Vries, F.
db4c0543-d6e7-476b-a10e-52d9d483f613
Vosse, D.
f0e6946b-baf0-4206-a5f0-a45b6e013be7
Arden, N.K.
23af958d-835c-4d79-be54-4bbe4c68077f
Bowness, P.
2791367b-84e8-4d24-88f2-9f61a8b67556
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Diez-Perez, A.
19f89c53-003a-469c-92ac-69b0b979f3ec
Vestergaard, P.
b00ba0f8-a9b7-45f1-a0c7-579fec88b556

Prieto-Alhambra, D., Munoz-Ortego, J., de Vries, F., Vosse, D., Arden, N.K., Bowness, P., Cooper, C., Diez-Perez, A. and Vestergaard, P. (2015) Ankylosing spondylitis confers substantially increased risk of clinical spine fractures: a nationwide case-control study. Osteoporosis International, 26 (1), 85-91. (doi:10.1007/s00198-014-2939-3). (PMID:25341971)

Record type: Article

Abstract

Summary
Ankylosing spondylitis (AS) leads to osteopenia/osteoporosis and spine rigidity. We conducted a case-control study and found that AS-affected patients have a 5-fold and 50 % increased risk of clinical spine and all clinical fractures, respectively. Excess risk of both is highest in the first years and warrants an early bone health assessment after diagnosis.

Introduction
Ankylosing spondylitis (AS) is related to spine rigidity and reduced bone mass, but data on its impact on fracture risk are scarce. We aimed to study the association between AS and clinical fractures using a case-control design.

Methods
From the Danish Health Registries, we identified all subjects who sustained a fracture in the year 2000 (cases) and matched up to three controls by year of birth, gender and region. Clinically diagnosed AS was identified using International Classification of Diseases, 8th revision (ICD-8; 71249), and International Classification of Diseases, 10th revision (ICD-10; M45) codes. We also studied the impact of AS duration. Conditional logistic regression was used to estimate crude and adjusted odds ratios (ORs) for non-traumatic fractures (any site, clinical spine and non-vertebral) according to AS status and time since AS diagnosis. Multivariate models were adjusted for fracture history, socio-economic status, previous medical consultations, alcoholism and use of oral glucocorticoids.

Results
We identified 139/124,655 (0.11 %) AS fracture cases, compared to 271/373,962 (0.07 %) AS controls. Unadjusted (age- and gender-matched) odds ratio (OR) were 1.54 [95 % confidence interval (95 %CI) 1.26–1.89] for any fracture, 5.42 [2.50–11.70] for spine and 1.39 [1.12–1.73] for non-vertebral fracture. The risk peaked in the first 2.5 years following AS diagnosis: OR 2.69 [1.84–3.92] for any fracture.

Conclusions
Patients with AS have a 5-fold higher risk of clinical spine fracture and a 35 % increased risk of non-vertebral fracture. This excess risk peaks early, in the first 2.5 years of AS disease. Patients should be assessed for fracture risk early after AS diagnosis.

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More information

Accepted/In Press date: 14 October 2014
e-pub ahead of print date: 24 October 2014
Published date: January 2015
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 374211
URI: http://eprints.soton.ac.uk/id/eprint/374211
ISSN: 0937-941X
PURE UUID: 1a6434c0-f83f-4897-9ac2-65013f394219
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

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Date deposited: 10 Feb 2015 11:53
Last modified: 18 Mar 2024 02:45

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Contributors

Author: D. Prieto-Alhambra
Author: J. Munoz-Ortego
Author: F. de Vries
Author: D. Vosse
Author: N.K. Arden
Author: P. Bowness
Author: C. Cooper ORCID iD
Author: A. Diez-Perez
Author: P. Vestergaard

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