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Reanalysis of two studies with contrasting results on the association between statin use and fracture risk: the General Practice Research Database

Reanalysis of two studies with contrasting results on the association between statin use and fracture risk: the General Practice Research Database
Reanalysis of two studies with contrasting results on the association between statin use and fracture risk: the General Practice Research Database
BACKGROUND: Two recent case-control studies by Meier et al. and van Staa et al. used the UK General Practice Research Database (GPRD) to examine the association between the use of statins and the risk of fractures, with different results. The objective of the present study was to examine methodological explanations for the discrepant results.
METHODS: We created two datasets, which mimicked the previous study designs: a 'selected population' (SP) case-control dataset, with fracture cases matched to controls nested within a selected cohort (Meier et al.), and an 'entire population' (EP) case-control dataset, with both cases and controls sampled from the total GPRD population (van Staa et al.). Cases and controls were matched by gender, age (year of birth or 5 year age bands), and general practice.
RESULTS: The study included 131 855 fracture cases. The crude odds ratio (OR) for hip fracture in statin users was 0.37 (95% CI 0.27-0.52) in the SP and 0.54 (95% CI 0.39-0.74) in the EP dataset. This difference was reduced when matching by year of birth, rather than by 5 year age bands: crude ORs were 0.58 (95% CI 0.43-0.79) and 0.61 (95% CI 0.44-0.88), respectively. In the SP dataset, 37% of the cases could be matched by year of birth, while this was achieved for 99% in the 'EP' dataset. The exposure time-window, the selection of confounders, and exclusion of high-risk patients also influenced results.
CONCLUSION: Residual confounding by a matching variable and different definitions of the exposure time window explained differences in results. In case-control studies of drug use and fracture risk, broad matching criteria for age should be avoided and the selection of the time-window for exposure should be carefully considered.
case-control studies, cohort, risk, birth, bone, fractures, exposure, hip, methods, research, gender, time, odds ratio
0300-5771
1301-1308
de Vries, F.
db4c0543-d6e7-476b-a10e-52d9d483f613
de Vries, C.
4ce71c39-a454-4762-8fbf-3c06923a0361
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Leufkens, B.
b96fcb5e-2d2b-4703-8d56-506aa1bdbb3c
van Staa, T.P.
31b8bfb4-4e1b-4a48-a5a6-90ca601b94af
de Vries, F.
db4c0543-d6e7-476b-a10e-52d9d483f613
de Vries, C.
4ce71c39-a454-4762-8fbf-3c06923a0361
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Leufkens, B.
b96fcb5e-2d2b-4703-8d56-506aa1bdbb3c
van Staa, T.P.
31b8bfb4-4e1b-4a48-a5a6-90ca601b94af

de Vries, F., de Vries, C., Cooper, C., Leufkens, B. and van Staa, T.P. (2006) Reanalysis of two studies with contrasting results on the association between statin use and fracture risk: the General Practice Research Database. International Journal of Epidemiology, 35 (5), 1301-1308. (doi:10.1093/ije/dyl147).

Record type: Article

Abstract

BACKGROUND: Two recent case-control studies by Meier et al. and van Staa et al. used the UK General Practice Research Database (GPRD) to examine the association between the use of statins and the risk of fractures, with different results. The objective of the present study was to examine methodological explanations for the discrepant results.
METHODS: We created two datasets, which mimicked the previous study designs: a 'selected population' (SP) case-control dataset, with fracture cases matched to controls nested within a selected cohort (Meier et al.), and an 'entire population' (EP) case-control dataset, with both cases and controls sampled from the total GPRD population (van Staa et al.). Cases and controls were matched by gender, age (year of birth or 5 year age bands), and general practice.
RESULTS: The study included 131 855 fracture cases. The crude odds ratio (OR) for hip fracture in statin users was 0.37 (95% CI 0.27-0.52) in the SP and 0.54 (95% CI 0.39-0.74) in the EP dataset. This difference was reduced when matching by year of birth, rather than by 5 year age bands: crude ORs were 0.58 (95% CI 0.43-0.79) and 0.61 (95% CI 0.44-0.88), respectively. In the SP dataset, 37% of the cases could be matched by year of birth, while this was achieved for 99% in the 'EP' dataset. The exposure time-window, the selection of confounders, and exclusion of high-risk patients also influenced results.
CONCLUSION: Residual confounding by a matching variable and different definitions of the exposure time window explained differences in results. In case-control studies of drug use and fracture risk, broad matching criteria for age should be avoided and the selection of the time-window for exposure should be carefully considered.

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More information

Published date: 2006
Keywords: case-control studies, cohort, risk, birth, bone, fractures, exposure, hip, methods, research, gender, time, odds ratio

Identifiers

Local EPrints ID: 61053
URI: http://eprints.soton.ac.uk/id/eprint/61053
ISSN: 0300-5771
PURE UUID: e2f6f663-e60e-40e4-b05f-6462895f680f
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

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Date deposited: 08 Sep 2008
Last modified: 18 Mar 2024 02:44

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Contributors

Author: F. de Vries
Author: C. de Vries
Author: C. Cooper ORCID iD
Author: B. Leufkens
Author: T.P. van Staa

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