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Cross-calibration of dual-energy X-ray densitometers for a large, multi-center genetic study of osteoporosis

Cross-calibration of dual-energy X-ray densitometers for a large, multi-center genetic study of osteoporosis
Cross-calibration of dual-energy X-ray densitometers for a large, multi-center genetic study of osteoporosis
Osteoporosis is a common disease with a strong genetic component characterized by reduced bone mass and an increased risk of fragility fractures. Bone mineral density (BMD) is the most important determinant of osteoporotic fracture risk, but the genes responsible for BMD regulation and fracture are incompletely defined. To enable multi-center studies to examine the genetic influences on BMD there is a requirement to standardize measurements across different manufacturers of bone densitometers, different versions of machines and different normative ranges. This paper describes a method developed to allow near-identical subjects with low age-adjusted BMD (based on Z-scores) to be recruited in 17 centers using 27 different densitometers. Cross-calibration was based on measurements using a European spine phantom circulated to all centers and measured ten times on each individual machine. From theses values an individual exponential curve, based on nominal versus observed BMD, was derived for each machine. As expected, there were large and significant variations in nominal BMD values, not only between scanners from different manufacturers but also between different versions of scanners from the same manufacturer. Hologic scanners tended to underestimate the nominal BMD, while Lunar scanners overestimated the value. Norland scanners gave mixed values over estimating BMD at the lower nominal value (0.5 g/cm(2)) while underestimating the value at the higher value (1.5 g/cm(2)). The validity of the exponential equations was tested using hip and spine measurements on 991 non-proband women from a familial osteoporosis study (FAMOS). After cross-calibration there was a considerable reduction in variation between machines. This observation, coupled with the absence of a similar reduction in variation attributable to a linear regression on age, demonstrated the validity of the cross-calibration approach. Use of the cross-calibration curves along with a standard normative range (in the case of this study, the Hologic normative range) allowed age-specific Z-scores to be used as an inclusion criterion in this genetic study, a method that will be useful for other trials where age-specific BMD inclusion criteria are required.
women, fractures, bone mass, time, gene, bone, osteoporosis, disease, hip, spine, risk, validity, mass
0937-941X
125-132
Reid, D.M.
80c8f859-f13a-4129-b884-c0fbc46d61b8
Mackay, I.
d4f0bd3c-14ae-46e8-bf4b-231ed8346d63
Wilkinson, S.
515fffa9-1b52-4208-9898-563773dda70a
Miller, C.
a7774c5f-bb5e-4ca5-81de-bc5540a36bfd
Schuette, D.G.
9f8ec1be-fac9-459c-98e3-17b85ed07b78
Compston, J.
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Cooper, C.
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Duncan, E.
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Galwey, N.
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Keen, R.
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Langdahl, B.
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McLellan, A.
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Pols, H.
bf755ddd-1f21-462b-a6d5-87c992eacc7a
Uitterlinden, A.
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O'Riordan, J.
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Wass, J.A.
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Ralston, S.H.
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Bennett, S.T.
191ef00c-3991-4687-b2d2-0d10fa0de4d5
Reid, D.M.
80c8f859-f13a-4129-b884-c0fbc46d61b8
Mackay, I.
d4f0bd3c-14ae-46e8-bf4b-231ed8346d63
Wilkinson, S.
515fffa9-1b52-4208-9898-563773dda70a
Miller, C.
a7774c5f-bb5e-4ca5-81de-bc5540a36bfd
Schuette, D.G.
9f8ec1be-fac9-459c-98e3-17b85ed07b78
Compston, J.
b64c0d0e-97dd-44c8-97ba-f756f0bc966d
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Duncan, E.
7888ce84-efa4-4249-bde2-2c95d77211b7
Galwey, N.
5394e616-e491-4e9e-b5fb-b0112302c1ca
Keen, R.
510d049d-5c13-4448-acbd-0f2f3b5f2a64
Langdahl, B.
8a94b2b0-6976-4a0c-ba87-6b95dfbd2961
McLellan, A.
09798b8d-4568-4892-a95a-44c84863e10e
Pols, H.
bf755ddd-1f21-462b-a6d5-87c992eacc7a
Uitterlinden, A.
2d869029-2dce-4cef-a7fc-acef1d246b21
O'Riordan, J.
d458f554-f09f-48b6-83ac-10070e2221c5
Wass, J.A.
b00f401d-5abb-4552-b226-88dea92dfefa
Ralston, S.H.
50a169e7-7b4c-471c-be24-61c8af915f17
Bennett, S.T.
191ef00c-3991-4687-b2d2-0d10fa0de4d5

Reid, D.M., Mackay, I., Wilkinson, S., Miller, C., Schuette, D.G., Compston, J., Cooper, C., Duncan, E., Galwey, N., Keen, R., Langdahl, B., McLellan, A., Pols, H., Uitterlinden, A., O'Riordan, J., Wass, J.A., Ralston, S.H. and Bennett, S.T. (2006) Cross-calibration of dual-energy X-ray densitometers for a large, multi-center genetic study of osteoporosis. Osteoporosis International, 17 (1), 125-132. (doi:10.1007/s00198-005-1936-y).

Record type: Article

Abstract

Osteoporosis is a common disease with a strong genetic component characterized by reduced bone mass and an increased risk of fragility fractures. Bone mineral density (BMD) is the most important determinant of osteoporotic fracture risk, but the genes responsible for BMD regulation and fracture are incompletely defined. To enable multi-center studies to examine the genetic influences on BMD there is a requirement to standardize measurements across different manufacturers of bone densitometers, different versions of machines and different normative ranges. This paper describes a method developed to allow near-identical subjects with low age-adjusted BMD (based on Z-scores) to be recruited in 17 centers using 27 different densitometers. Cross-calibration was based on measurements using a European spine phantom circulated to all centers and measured ten times on each individual machine. From theses values an individual exponential curve, based on nominal versus observed BMD, was derived for each machine. As expected, there were large and significant variations in nominal BMD values, not only between scanners from different manufacturers but also between different versions of scanners from the same manufacturer. Hologic scanners tended to underestimate the nominal BMD, while Lunar scanners overestimated the value. Norland scanners gave mixed values over estimating BMD at the lower nominal value (0.5 g/cm(2)) while underestimating the value at the higher value (1.5 g/cm(2)). The validity of the exponential equations was tested using hip and spine measurements on 991 non-proband women from a familial osteoporosis study (FAMOS). After cross-calibration there was a considerable reduction in variation between machines. This observation, coupled with the absence of a similar reduction in variation attributable to a linear regression on age, demonstrated the validity of the cross-calibration approach. Use of the cross-calibration curves along with a standard normative range (in the case of this study, the Hologic normative range) allowed age-specific Z-scores to be used as an inclusion criterion in this genetic study, a method that will be useful for other trials where age-specific BMD inclusion criteria are required.

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More information

Published date: 2006
Keywords: women, fractures, bone mass, time, gene, bone, osteoporosis, disease, hip, spine, risk, validity, mass

Identifiers

Local EPrints ID: 61461
URI: http://eprints.soton.ac.uk/id/eprint/61461
ISSN: 0937-941X
PURE UUID: e0229911-cabf-4b32-ab5f-9804369b904f
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

Catalogue record

Date deposited: 09 Sep 2008
Last modified: 18 Mar 2024 02:44

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Contributors

Author: D.M. Reid
Author: I. Mackay
Author: S. Wilkinson
Author: C. Miller
Author: D.G. Schuette
Author: J. Compston
Author: C. Cooper ORCID iD
Author: E. Duncan
Author: N. Galwey
Author: R. Keen
Author: B. Langdahl
Author: A. McLellan
Author: H. Pols
Author: A. Uitterlinden
Author: J. O'Riordan
Author: J.A. Wass
Author: S.H. Ralston
Author: S.T. Bennett

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