Diagnosis of sarcopenia by evaluating skeletal muscle mass by adjusted bioimpedance analysis validated with dual-energy X-ray absorptiometry

Keith Yu-Kin Cheng, Simon Kwoon-Ho Chow, Vivian Wing-Yin Hung, Carissa Hing-Wai Wong, Ronald Man-Yeung Wong, Charlotte Sau-Lan Tsang, Timothy Kwok, Wing-Hoi Cheung, Keith Yu-Kin Cheng, Simon Kwoon-Ho Chow, Vivian Wing-Yin Hung, Carissa Hing-Wai Wong, Ronald Man-Yeung Wong, Charlotte Sau-Lan Tsang, Timothy Kwok, Wing-Hoi Cheung

Abstract

Background: This study aimed to adjust and cross-validate skeletal muscle mass measurements between bioimpedance analysis (BIA) and dual-energy X-ray absorptiometry (DXA) for the screening of sarcopenia in the community and to estimate the prevalence of sarcopenia in Hong Kong.

Methods: Screening of sarcopenia was provided to community-dwelling older adults. Appendicular skeletal muscle mass (ASM) was evaluated by BIA (InBody 120 or 720) and/or DXA. Handgrip strength and/or gait speed were assessed. Diagnosis of sarcopenia was based on the 2019 revised Asian Working Group for Sarcopenia cut-offs. Agreement analysis was performed to cross-validate ASM measurements by BIA and DXA. Multiple regression was used to explore contribution of measured parameters in predicting DXA ASM from BIA.

Results: A total of 1587 participants (age = 72 ± 12 years) were recruited; 1065 participants were screened by BIA (InBody 120) with 18 followed up by DXA, while the remaining 522 participants were assessed by the BIA (InBody 720) and DXA. The appendicular skeletal muscle mass index (ASMI) evaluated by BIA showed a mean difference of 2.89 ± 0.38 kg/m2 (InBody 120) and 2.97 ± 0.45 kg/m2 (InBody 720) against DXA gold standard. A significant overestimation of muscle mass was measured by BIA compared with DXA (P < 0.005). BIA data were adjusted using prediction equation and mean difference reduced to -0.02 ± 0.31 kg/m2 in cross-validation. Prevalence of sarcopenia in older adults ≥65 ranged from 39.4% (based on ASMI by DXA) to 40.8% (based on predicted DXA ASMI from BIA). Low ASMI by DXA was found in 68.5% of the older adults screened. The percentage of older adults exhibited low handgrip strength ranged from 31.3% to 56%, while 49% showed low gait speed.

Conclusions: Bioimpedance analysis was found to overestimate skeletal muscle mass compared with DXA. With adjustment equations, BIA can be used as a quick and reliable tool for screening sarcopenia in community and clinical settings with limited access to better options.

Keywords: Bioimpedance analysis (BIA); Diagnosis; Dual-energy X-ray absorptiometry (DXA); Sarcopenia; Skeletal muscle mass.

Conflict of interest statement

None declared.

© 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

Figures

Figure 1
Figure 1
Definition of sarcopenia used in this study based on the Asian Working Group for Sarcopenia (AWGS) 2019 guidelines, where ‘sarcopenia’ is defined as ‘low appendicular skeletal muscle mass index (ASMI) with either low muscle strength or low physical performance’, while ‘severe sarcopenia’ is defined as ‘low ASMI with low muscle strength and low physical performance’. DXA, dual‐energy X‐ray absorptiometry.
Figure 2
Figure 2
Appendicular skeletal muscle mass index (ASMI, kg/m2) evaluated by (BIA) and dual‐energy X‐ray absorptiometry (DXA). Top and bottom lines indicate ±1.96 SD. (A) BIA (InBody 120) ASMI vs. age in Dataset120 (n = 1065). (B) BIA (InBody 720) ASMI vs. age in Dataset720 (n = 522). (C) DXA ASMI vs. age in Dataset120 (n = 18). (D) DXA ASMI vs. age in Dataset720 (n = 522). (E) Correlation between DXA and BIA ASMI in Dataset120 (r2 = 0.867, n = 18, P < 0.05). (F) Correlation between DXA and BIA ASMI in Dataset720 (r2 = 0.893, n = 522, P < 0.05).
Figure 3
Figure 3
Appendicular skeletal muscle mass (ASMI, kg/m2) as evaluated by dual‐energy X‐ray absorptiometry (DXA). Top and bottom lines on (C) and (D) indicate ±1.96 SD. (A) Flow chart showing the breakdown of different tests and number of subjects in each dataset. (B) ASMI vs. age coloured by gender (n = 540). (C) Male DXA ASMI vs. age (n = 299). (D) Female DXA ASMI vs. age (n = 241). BIA, bioimpedance analysis.
Figure 4
Figure 4
Handgrip strength measured by dynamometer in kilograms (kg) and gait speed by 6 m walk test measured in seconds (s) plotted against age separated by gender. Top and bottom lines indicate ±1.96 SD. (A) Female handgrip strength by age (n = 1160). (B) Male handgrip strength by age (n = 427). (C) Six metre walk time for female gait speed by age (n = 226). (D) Six metre walk time for male gait speed by age (n = 296).
Figure 5
Figure 5
Bland–Altman plot comparing appendicular skeletal muscle mass (ASM) and appendicular skeletal muscle mass index (ASMI) measured between bioimpedance analysis (BIA) and dual‐energy X‐ray absorptiometry (DXA) in Dataset120 (n = 18) and Dataset720 (n = 522). Top and bottom reference lines indicate 95% confidence interval. (A) ASM mean difference = 6.77 ± 1.24 kg, limits of agreement = 4.35, 9.20. (B) ASM mean difference = 8.25 ± 1.80 kg, limits of agreement = 4.73, 11.77. (C) ASMI mean difference = 2.89 ± 0.38 kg/m2, limits of agreement = 2.15, 3.63. (D) ASMI mean difference = 3.11 ± 0.45 kg/m2, limits of agreement = 2.22, 4.00.
Figure 6
Figure 6
Bland–Altman plot comparing predicted appendicular skeletal muscle mass (ASM) and appendicular skeletal muscle mass index (ASMI) vs. actual dual‐energy X‐ray absorptiometry (DXA) measurements in one‐third (n = 174) of Dataset720 after deriving regression model with the remaining two‐thirds. Top and bottom reference lines indicate 95% confidence interval. (A) ASM mean difference = −0.04 ± 0.82, limits of agreement = 1.57, −1.65. (B) ASMI mean difference = −0.02 ± 0.31, limits of agreement = 0.58, −0.61.
Figure 7
Figure 7
Recommended application workflow of bioimpedance analysis (BIA) for sarcopenia screening. (A) Skeletal muscle mass (SMM) can be taken directly from the report of a commercially available BIA device (InBody 120 or 720) and used as the appendicular skeletal muscle mass (ASM) as defined by European Working Group on Sarcopenia in Older People or Asian Working Group for Sarcopenia. (B, C) The SMM or ASM measured by BIA can be substituted into the relevant equations along with other parameters of weight, height, gender, or body mass index for the estimation of predicted ASM (which is the expected ASM from a DXA measurement). (B) Prediction equation from InBody 120 measurement. (C) Prediction equation from InBody 720 measurement. (D) This predicted ASM (ASMpredicted) can be directly compared with the DXA cut‐off values defined by the European Working Group on Sarcopenia in Older People or Asian Working Group for Sarcopenia for male or female for the diagnosis of low muscle mass content. Suggested BIA application for muscle mass evaluation in community settings.

References

    1. Cruz‐Jentoft AJ, Sayer AA. Sarcopenia. Lancet 2019;393:2636–2646.
    1. Cao L, Morley JE. Sarcopenia is recognized as an independent condition by an International Classification of Disease, Tenth Revision, Clinical Modification (ICD‐10‐CM) code. J Am Med Dir Assoc 2016;17:675–677.
    1. Cruz‐Jentoft AJ, Baeyens JP, Bauer JM, Boirie Y, Cederholm T, Landi F, et al. Sarcopenia: European consensus on definition and diagnosis: report of the European Working Group on Sarcopenia in Older People. Age Ageing 2010;39:412–423.
    1. Cruz‐Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyere O, Cederholm T, et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 2019;48:16–31.
    1. Chen LK, Liu LK, Woo J, Assantachai P, Auyeung TW, Bahyah KS, et al. Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia. J Am Med Dir Assoc 2014;15:95–101.
    1. Chen LK, Woo J, Assantachai P, Auyeung TW, Chou MY, Iijima K, et al. Asian Working Group for Sarcopenia: 2019 consensus update on sarcopenia diagnosis and treatment. J Am Med Dir Assoc 2020;21:300–307.e2.
    1. Woo J, Leung J, Morley JE. Defining sarcopenia in terms of incident adverse outcomes. J Am Med Dir Assoc 2015;16:247–252.
    1. Wong RMY, Wong H, Zhang N, Chow SKH, Chau WW, Wang J, et al. The relationship between sarcopenia and fragility fracture—a systematic review. Osteoporos Int 2019;30:541–553.
    1. Yu R, Leung J, Woo J. Incremental predictive value of sarcopenia for incident fracture in an elderly Chinese cohort: results from the Osteoporotic Fractures in Men (MrOs) Study. J Am Med Dir Assoc 2014;15:551–558.
    1. Sánchez‐Castellano C, Martín‐Aragón S, Bermejo‐Bescós P, Vaquero‐Pinto N, Miret‐Corchado C, Merello de Miguel A, et al. Biomarkers of sarcopenia in very old patients with hip fracture. J Cachexia Sarcopenia Muscle 2020;11:478–486.
    1. Buehring B, Krueger D, Binkley N. Effect of including historical height and radius BMD measurement on sarco‐osteoporosis prevalence. J Cachexia Sarcopenia Muscle 2013;4:47–54.
    1. Malmstrom TK, Morley JE. SARC‐F: a simple questionnaire to rapidly diagnose sarcopenia. J Am Med Dir Assoc 2013;14:531–532.
    1. Woo J, Leung J, Morley JE. Validating the SARC‐F: a suitable community screening tool for sarcopenia? J Am Med Dir Assoc 2014;15:630–634.
    1. Cruz‐Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyere O, Cederholm T, et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 2019;48:601.
    1. Bosy‐Westphal A, Schautz B, Later W, Kehayias JJ, Gallagher D, Muller MJ. What makes a BIA equation unique? Validity of eight‐electrode multifrequency BIA to estimate body composition in a healthy adult population. Eur J Clin Nutr 2013;67:S14–S21.
    1. Gonzalez MC, Heymsfield SB. Bioelectrical impedance analysis for diagnosing sarcopenia and cachexia: what are we really estimating? J Cachexia Sarcopenia Muscle 2017;8:187–189.
    1. Chow SK, Chim YN, Cheng KY, Ho CY, Ho WT, Cheng KC, et al. Elastic‐band resistance exercise or vibration treatment in combination with hydroxymethylbutyrate (HMB) supplement for management of sarcopenia in older people: a study protocol for a single‐blinded randomised controlled trial in Hong Kong. BMJ Open 2020;10:e034921.
    1. Aleixo GFP, Shachar SS, Nyrop KA, Muss HB, Battaglini CL, Williams GR. Bioelectrical impedance analysis for the assessment of sarcopenia in patients with cancer: a systematic review. Oncologist 2020;25:170–182.
    1. Wang H, Hai S, Cao L, Zhou J, Liu P, Dong B‐R. Estimation of prevalence of sarcopenia by using a new bioelectrical impedance analysis in Chinese community‐dwelling elderly people. BMC Geriatr 2016;16:216.
    1. Ling CH, de Craen AJ, Slagboom PE, Gunn DA, Stokkel MP, Westendorp RG, et al. Accuracy of direct segmental multi‐frequency bioimpedance analysis in the assessment of total body and segmental body composition in middle‐aged adult population. Clin Nutr 2011;30:610–615.
    1. Kim H, Hirano H, Edahiro A, Ohara Y, Watanabe Y, Kojima N, et al. Sarcopenia: prevalence and associated factors based on different suggested definitions in community‐dwelling older adults. Geriatr Gerontol Int 2016;16:110–122.
    1. Achamrah N, Colange G, Delay J, Rimbert A, Folope V, Petit A, et al. Comparison of body composition assessment by DXA and BIA according to the body mass index: a retrospective study on 3655 measures. PLoS ONE 2018;13:e0200465‐e.
    1. Lee SY, Ahn S, Kim YJ, Ji MJ, Kim KM, Choi SH, et al. Comparison between dual‐energy X‐ray absorptiometry and bioelectrical impedance analyses for accuracy in measuring whole body muscle mass and appendicular skeletal muscle mass. Nutrients 2018;10.
    1. Scott D, Park MS, Kim TN, Ryu JY, Hong HC, Yoo HJ, et al. Associations of low muscle mass and the metabolic syndrome in Caucasian and Asian middle‐aged and older adults. J Nutr Health Aging 2016;20:248–255.
    1. Reiss J, Iglseder B, Kreutzer M, Weilbuchner I, Treschnitzer W, Kassmann H, et al. Case finding for sarcopenia in geriatric inpatients: performance of bioimpedance analysis in comparison to dual X‐ray absorptiometry. BMC Geriatr 2016;16:52.
    1. Anderson LJ, Erceg DN, Schroeder ET. Utility of multifrequency bioelectrical impedance compared with dual‐energy x‐ray absorptiometry for assessment of total and regional body composition varies between men and women. Nutr Res 2012;32:479–485.
    1. Yu R, Wong M, Leung J, Lee J, Auyeung TW, Woo J. Incidence, reversibility, risk factors and the protective effect of high body mass index against sarcopenia in community‐dwelling older Chinese adults. Geriatr Gerontol Int 2014;14:15–28.
    1. Makizako H, Nakai Y, Tomioka K, Taniguchi Y. Prevalence of sarcopenia defined using the Asia Working Group for Sarcopenia criteria in Japanese community‐dwelling older adults: a systematic review and meta‐analysis. Phys Ther Res 2019;22:53–57.
    1. Chang HK, Lee JY, Gil CR, Kim MK. Prevalence of sarcopenia in community‐dwelling older adults according to simplified algorithms for sarcopenia consensus based on Asian Working Group for Sarcopenia. Clin Interv Aging 2020;15:2291–2299.
    1. von Haehling S, Morley JE, Coats AJS, Anker SD. Ethical guidelines for publishing in the Journal of Cachexia, Sarcopenia and Muscle: update 2019. J Cachexia Sarcopenia Muscle 2019;10:1143–1145.

Source: PubMed

3
Tilaa