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Development and validation of total and regional body composition prediction equations from anthropometry and single frequency segmental bioelectrical impedance with DEXA

Development and validation of total and regional body composition prediction equations from anthropometry and single frequency segmental bioelectrical impedance with DEXA
Development and validation of total and regional body composition prediction equations from anthropometry and single frequency segmental bioelectrical impedance with DEXA
Aims
Single-frequency segmental Bioelectrical Impedance Analysis (BIA) is commonly used to estimate body composition. To enhance the value of information derived from BIA, especially for use in large-scale epidemiological studies, we developed and validated equations to predict total and regional (arms, legs, trunk, android, gynoid, visceral) body composition parameters (lean mass and fat mass) from anthropometry and single-frequency (50 kHz) segmental BIA variables, using Dual Energy X-ray Absorptiometry (DEXA) as the criterion method.

Methods
The 11,559 adults (age 30 to 65) from the UK population-based Fenland Study with data on DEXA, BIA and anthropometry were randomly assigned to a Derivation sample (4,827 men; 5,732 women) or a Validation sample (500 men; 500 women). Prediction equations based on anthropometry and BIA variables were derived using forward stepwise multiple linear regression in the Fenland Derivation sample. These were validated in the Fenland Validation sample and also in the UK Biobank Imaging Study (2,392 men; 2,606 women) using Pearson correlations and Bland–Altman models.

Results and Conclusions
Bland Altman analyses revealed no significant mean bias for any predicted DEXA parameter (all P>0.05) for the fenland population. Bias expressed as % of the mean was between -0.6% and 0.5% for all parameters in both men and women, except for visceral FM and subcutaneous abdominal FM (range -3.6 to 1.1%). However, in UK Biobank most predicted parameters showed significant bias: % mean bias was <2% in both sexes only for total fat mass and total lean mass, and was >10% for leg and visceral fat mass in both sexes. In conclusion, new equations based on anthropometry and BIA variables predicted DEXA parameters with sufficient accuracy to assess relative differences between individuals, and were sufficiently accurate to predict absolute values for total body but not regional fat and lean mass.
medRxiv
Powell, Richard
bc0bad4b-38ce-4431-9f65-6b517cfe0bd0
Rolfe, Emanuella De Lucia
658cc447-bdfc-429f-8cec-cb233a72f84d
Day, Felix R.
f396529a-e582-4980-a445-d77821625464
Perry, John R.B.
e5f5491e-f421-4b29-99e6-195667572a31
Griffin, Simon J.
f12ee1b9-fef5-46ab-b5a4-50b66e6c93c8
Forouhi, Nita G.
39ff4cc0-8d09-442a-826c-114f1282f8dd
Brage, Soren
3705fa6b-2018-4ad6-9143-fa9240ec0fc9
Wareham, Nicholas J.
bbc18cd9-3512-4ca6-806c-75c9a01e5adf
Langenberg, Claudia
d9039854-6499-4391-9e4b-840f6f92d4b5
Ong, Ken K.
11be427c-95c2-4c09-9000-2a915a247885
Powell, Richard
bc0bad4b-38ce-4431-9f65-6b517cfe0bd0
Rolfe, Emanuella De Lucia
658cc447-bdfc-429f-8cec-cb233a72f84d
Day, Felix R.
f396529a-e582-4980-a445-d77821625464
Perry, John R.B.
e5f5491e-f421-4b29-99e6-195667572a31
Griffin, Simon J.
f12ee1b9-fef5-46ab-b5a4-50b66e6c93c8
Forouhi, Nita G.
39ff4cc0-8d09-442a-826c-114f1282f8dd
Brage, Soren
3705fa6b-2018-4ad6-9143-fa9240ec0fc9
Wareham, Nicholas J.
bbc18cd9-3512-4ca6-806c-75c9a01e5adf
Langenberg, Claudia
d9039854-6499-4391-9e4b-840f6f92d4b5
Ong, Ken K.
11be427c-95c2-4c09-9000-2a915a247885

[Unknown type: UNSPECIFIED]

Record type: UNSPECIFIED

Abstract

Aims
Single-frequency segmental Bioelectrical Impedance Analysis (BIA) is commonly used to estimate body composition. To enhance the value of information derived from BIA, especially for use in large-scale epidemiological studies, we developed and validated equations to predict total and regional (arms, legs, trunk, android, gynoid, visceral) body composition parameters (lean mass and fat mass) from anthropometry and single-frequency (50 kHz) segmental BIA variables, using Dual Energy X-ray Absorptiometry (DEXA) as the criterion method.

Methods
The 11,559 adults (age 30 to 65) from the UK population-based Fenland Study with data on DEXA, BIA and anthropometry were randomly assigned to a Derivation sample (4,827 men; 5,732 women) or a Validation sample (500 men; 500 women). Prediction equations based on anthropometry and BIA variables were derived using forward stepwise multiple linear regression in the Fenland Derivation sample. These were validated in the Fenland Validation sample and also in the UK Biobank Imaging Study (2,392 men; 2,606 women) using Pearson correlations and Bland–Altman models.

Results and Conclusions
Bland Altman analyses revealed no significant mean bias for any predicted DEXA parameter (all P>0.05) for the fenland population. Bias expressed as % of the mean was between -0.6% and 0.5% for all parameters in both men and women, except for visceral FM and subcutaneous abdominal FM (range -3.6 to 1.1%). However, in UK Biobank most predicted parameters showed significant bias: % mean bias was <2% in both sexes only for total fat mass and total lean mass, and was >10% for leg and visceral fat mass in both sexes. In conclusion, new equations based on anthropometry and BIA variables predicted DEXA parameters with sufficient accuracy to assess relative differences between individuals, and were sufficiently accurate to predict absolute values for total body but not regional fat and lean mass.

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More information

Published date: 18 December 2020

Identifiers

Local EPrints ID: 504792
URI: http://eprints.soton.ac.uk/id/eprint/504792
PURE UUID: ed4854fc-cb56-445c-a2ee-dfde69e0db20
ORCID for Emanuella De Lucia Rolfe: ORCID iD orcid.org/0000-0003-3542-2767

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Date deposited: 18 Sep 2025 17:09
Last modified: 19 Sep 2025 02:19

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Contributors

Author: Richard Powell
Author: Emanuella De Lucia Rolfe ORCID iD
Author: Felix R. Day
Author: John R.B. Perry
Author: Simon J. Griffin
Author: Nita G. Forouhi
Author: Soren Brage
Author: Nicholas J. Wareham
Author: Claudia Langenberg
Author: Ken K. Ong

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