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Body composition reference values in Singaporean adults using dual-energy X-ray absorptiometry—The Yishun study

  • BaoLin Pauline Soh ,

    Contributed equally to this work with: BaoLin Pauline Soh, Shuen Yee Lee, Shiou-Liang Wee

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Resources, Software, Validation, Visualization, Writing – original draft

    weeshiouliang@gmail.com (SLW); pauline.soh@singaporetech.edu.sg (BPS)

    Affiliation Health and Social Sciences Cluster, Singapore Institute of Technology, Singapore, Singapore

  • Shuen Yee Lee ,

    Contributed equally to this work with: BaoLin Pauline Soh, Shuen Yee Lee, Shiou-Liang Wee

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Software, Visualization, Writing – review & editing

    Affiliation Health and Social Sciences Cluster, Singapore Institute of Technology, Singapore, Singapore

  • Wai Yin Wong ,

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Validation, Visualization, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliations Department of Nuclear Medicine and Molecular Imaging, Singapore General Hospital, Singapore, Singapore, Duke-NUS Medical School, Singapore, Singapore

  • Benedict Wei Jun Pang ,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Geriatric Education and Research Institute (GERI), Singapore, Singapore

  • Lay Khoon Lau ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Project administration, Software, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Geriatric Education and Research Institute (GERI), Singapore, Singapore

  • Khalid Abdul Jabbar ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Project administration, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Geriatric Education and Research Institute (GERI), Singapore, Singapore

  • Wei Ting Seah ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Project administration, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Geriatric Education and Research Institute (GERI), Singapore, Singapore

  • Kexun Kenneth Chen ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Project administration, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Geriatric Education and Research Institute (GERI), Singapore, Singapore

  • Sivasubramanian Srinivasan ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliation Diagnostic Radiology, Khoo Teck Puat Hospital, Singapore, Singapore

  • Tze Pin Ng ,

    Roles Conceptualization, Data curation, Investigation, Methodology, Supervision, Validation, Writing – review & editing

    ‡ WYW, BWJP, LKL, KAJ, WTS, KKC, SS and TPN also contributed equally to this work.

    Affiliations Geriatric Education and Research Institute (GERI), Singapore, Singapore, Department of Psychological Medicine, National University of Singapore, Singapore, Singapore

  • Shiou-Liang Wee

    Contributed equally to this work with: BaoLin Pauline Soh, Shuen Yee Lee, Shiou-Liang Wee

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Supervision, Validation, Visualization, Writing – review & editing

    weeshiouliang@gmail.com (SLW); pauline.soh@singaporetech.edu.sg (BPS)

    Affiliations Health and Social Sciences Cluster, Singapore Institute of Technology, Singapore, Singapore, Geriatric Education and Research Institute (GERI), Singapore, Singapore

Abstract

Objectives

This study establishes age- and sex-specific reference values for fat mass index (FMI), lean mass index (LMI), appendicular LMI (aLMI), and body fat distribution indices including Android/Gynoid % fat ratio and Trunk/Limb % fat ratio in multi-ethnic Singaporean adults.

Methods

A population-based cross-sectional study using dual-energy X-ray absorptiometry (Hologic Discovery Wi) was carried out to measure whole body and regional fat and lean mass in community-dwelling adults. A total of 537 adults (57.5% women), aged from 21 to 90 years, were recruited from the large north-eastern residential town of Yishun. Age- and sex-specific percentile reference values were generated for FMI, LMI, aLMI, Android/Gynoid % fat ratio and Trunk/Limb % fat ratio using the Lambda–Mu–Sigma method. The relationship between the parameters and age were assessed through the Pearson’s correlation coefficient.

Results

All parameters demonstrated significant correlation with age (p < 0.05) for both men and women, except for LMI in women, with the strength of r ranging from 0.12 (weak correlation) to 0.54 (strong correlation). LMI (r = −0.45) and appendicular LMI (r = −0.54) were negatively associated with age in men while none (r = −0.06) to weak correlation (r = −0.14) were shown in women for the same parameters respectively. The Android/Gynoid % fat ratio and Trunk/Limb % fat ratio were positively related to age for both men (r = 0.37 & 0.43, p < 0.001) and women (r = 0.52 & 0.48, p < 0.001).

Conclusion

We have established DXA-based body composition reference data for the Singapore adult population. These reference data will be particularly useful in geriatric, obesity and oncology clinics, enabling the prescription of appropriate therapy to individuals at risk of morbidity from unfavorable body composition phenotypes. It also adds on to the limited reference database on Southeast Asian body composition.

Introduction

Body composition (BC) is closely related to health and includes parameters that define diseases/conditions such as sarcopenia, obesity, and low bone mass. These conditions in turn predict other diseases or adverse health, e.g. diabetes, cardio/cerebro-vascular diseases, cancers, fractures and functional disability that increase healthcare cost, reduce health span and lower quality of life [18]. While body mass index (BMI, total mass/height2), an anthropometric index, has been widely used in research and clinically as an indicator of adiposity, it is only a surrogate measure for obesity since it cannot differentiate between lean and fat mass [911]. BMI has also been used clinically to determine underweight and overweight status. Nevertheless, body composition is made up of components including muscle, fat, bone and water, hence expressing it using body weight relative to height meant that individuals with same BMI can have significantly different compositions, which can lead to the misclassification of persons carrying more weight in lean tissues as someone with excess body fat (high BMI) [12]. To overcome this limitation, more specific BC measures are necessary.

Dual X-ray absorptiometry (DXA), a non-invasive imaging modality that utilizes very low dose X-rays with two distinct energy peaks to image the soft tissue and bones of the human body, is considered the gold standard technique in the assessment of BC due to its precision and accuracy. It is capable of providing three BC measurements, namely: fat mass (FM), lean mass (LM) and bone mineral density (BMD), regionally and for the whole-body [13]. Although FM and LM measurements can accurately reflect body composition, it does not take a person’s height into account which in turn limit the comparisons between individuals, and therefore, the use of height adjusted fat mass index (FMI) and lean mass index (LMI) were proposed [14]. FMI was found to be more predictive of metabolic syndrome [11, 15] compared to BMI and is a better screening tool for obesity-related diseases including cardiovascular diseases, hypertension, stroke, type 2 diabetes mellitus, and some cancer types [1621], while appendicular LMI (aLMI) is a key component for sarcopenia diagnosis [2224]. Furthermore, the association between obesity and cardiovascular, as well as metabolic diseases is dependent on body fat distribution rather than total fat mass [25].

BC varies with age, sex and ethnicity, and so reference values should be population-specific and consider age, sex, and ethnicity [26, 27]. The National Health and Nutrition Examination Survey (NHANES) dataset, which is the most commonly used reference for body composition were developed from a cohort across the United States and provides reference BC values for Non-Hispanic Whites, Non-Hispanic Blacks and Mexican Americans. Therefore its application to Asians may not be appropriate [28, 29]. While there have been many reference value developed for the Western population [3033], only a limited number were established for diverse Asian populations [3437]. To our knowledge, a body composition reference database for multi-ethnic population in Singapore has yet to be established. Our study provides age- and sex-specific reference values for FMI, LMI, aLMI, and body fat indices (Trunk/Limb % fat ratio and Android/Gynoid % fat ratio) in a multi-ethnic Singaporean adult population using DXA. This enables meaningful interpretation of an individual’s BC result, giving an indication of his/her BC status relative to the average community dweller of the same age and sex.

Methods

Study design and participants

Community-dwelling adults aged ≥21 years old from Yishun, a large north-eastern residential town in Singapore comprising population of 220,320 (49.4% men), with 12.2% aged ≥65 years, were invited to participate in this study [38]. This is similar to the overall Singapore residential population consisting of 4.02 million (48.9% men), with 14.4% aged ≥65 years [38].

Recruitment within the Yishun region was conducted in two phases: between 1) October 2017 and February 2019; and 2) March and November 2019. A two-stage random sampling method was utilized in the first phase with 50% of all the housing blocks being randomly selected, followed by a random invitation of 20% of the units from those blocks to participate in the study. In the second phase, to increase the recruitment yield, 50% of the remaining housing blocks were randomly selected, and all the units within those blocks were invited to participate in the study. To achieve a representative sample of approximately 300 men and 300 women, a random sampling strategy was performed by filling quotas of 20–40 participants in each sex and age group (based on 10-year age groups between 21 and 60 years old; 5-year age-groups after 60 years old). This approach fulfilled the conventional recommendation of a minimum sample size of 30 per age-group for normative measures [39].

Door-to-door recruitment were conducted with up to three eligible members per household unit invited to participate in the study. Units with no response during the first home visit were contacted again at a different time of day on a later date. Recruitment of older individuals aged above 75 years old were extended to surrounding community including four senior activity centres. Exclusion criteria for recruitment include individuals with disabilities, injuries, fractures, or surgeries that affected function, neuromuscular, neurological, and cognitive impairments, or more than five poorly controlled comorbidities. Women who are pregnant or planning for pregnancy were also excluded. Ethics approval was obtained from the National Healthcare Group DSRB (2017/00212), in accordance with the relevant guidelines and regulations by the Declaration of Helsinki and the ethical principles in the Belmont Report. All participants gave written informed consent to participate in the study.

Data collection

Participants self-reported their medical conditions and comorbidities. All assessments were based on standardised protocols and administered by trained researchers at the Geriatric Education & Research Institute Lab on Yishun Health Campus, mostly within one visit.

Anthropometry.

Body weight and height were measured using an electronic scale and stadiometer, respectively (SECA, Hamburg, Germany). Body mass index was calculated as body weight (kg, measured to the nearest 0.1 kg) divided by height (m, measured to the nearest millimetre) squared.

Body composition measurement.

Whole body scans were conducted using Hologic Discovery Wi (Hologic, Marlborough, MA, USA) Dual X-ray absorptiometry (DXA) scanner. The scan was performed by experienced radiography technologists (six technologists with each having experience of 3–6 years), using standardized protocol recommended by the manufacturer (Hologic). Prior to the examination, participants were asked to remove all garments and removable metal objects such as jewellery and watches and to change into a standard hospital gown that is free from zippers and buttons that would potentially interfere with the scan. Quality check and cross calibrations were regularly performed before each scanning session. The body composition parameters were analyzed using the Hologic APEX analysis software [40]. Due to the DXA scan table limitations, participants who were more than 136 kilograms or greater than 1.96 metres in height were excluded.

For this analysis, whole body (including the head) and regional (including limbs, trunk, android, and gynoid) FM (in kg) and LM (in kg) were obtained from the DXA dataset. From these measurements, the following parameters were calculated: FMI (total fat mass/height2); LMI (total lean mass/height2); appendicular FMI (aFMI, appendicular fat mass/height2); aLMI (appendicular lean mass/height2); Trunk/Limb % fat ratio; Android/Gynoid % fat ratio; and % FM (total body fat mass/weight × 100%). The appendicular region refers to both upper and lower limbs. Trunk/Limb % fat ratio and Android/Gynoid % fat ratio were included as indices of body fat distribution.

Statistical analysis

All statistical analyses were performed using R V.3.6.2 (R Foundation for statistical computing, Vienna, Austria). For the descriptive analysis of participants’ characteristics, continuous variables were presented using means and SDs after dataset was stratified by sex and divided into the following age groups: 21–30; 31–40; 41–50; 51–60; 61–65; 66–70; 71–75; 76–80; > 80 years. Participant characteristics within each age group were analysed using independent samples t-test to assess potential differences between men and women. Age- and sex-specific reference values for body composition parameters were generated using the Lamda Mu Sigma (LMS) method of Cole and Green, as an extension of the normal distribution that adjusts for skewness, embedded in Generalized Additive Models for Location Scale and Shape (GAMLSS package version 5.2.0), for FMI, LMI, aLMI, Trunk/Limb % fat ratio and Android/Gynoid % fat ratio. The LMS method is equivalent to Box-Cox Cole and Green distribution (BCCG), and BCCG parameters (μ, σ, υ) are the approximate median, coefficient of variation and skewness parameters of the distribution of the response variable [41, 42]. That is, μ controls the location, σ controls the scale and υ controls the skewness of the distribution with age [41]. Generalized Akaike information criterion (GAIC) was used to determine the appropriate degrees of freedom [43]. The final GAMLSS model parameters were used to construct centiles tables for each sex and anthropometric measure of interest. Sex-stratified natural regression spline curves were also generated with 4 knots for FMI, LMI, aLMI, Trunk/Limb % fat ratio and Android/Gynoid % fat ratio. The relationships between each parameter and age were assessed separately in men and women using Pearson’s correlation coefficient (r). Correlation coefficient can range from -1.0 to +1.0 where the sign (+/-) indicates the direction and the numeric value representing the strength of the relationship. In terms of strength, a value of 0.5 or greater represented strong correlation; a value of 0.3 to less than 0.5, moderate correlation; and a value of 0.1 to less than 0.3, weak correlation [44]. The level of significance was set at p < 0.05.

Results

The overall response rate was 39.0%. A total of 537 participants (57.5% women) aged from 21 to 90 years were recruited with the ethnic composition of 81.6% Chinese, 8.9% Malay, 6.7% Indians, and 2.8% others.

Table 1 showed participants’ characteristics. Within the same age group, significant differences (p < 0.05) were shown between men and women for all anthropometric characteristics and body composition parameters except for BMI (for age group 41–50; 51–60; 61–65; 66–70; 71–75; 76–80; and >80), FM (for age group 21–30; 31–40; 41–50; 71–75; and >80), FMI (for age group 21–30 and 31–40) and aFMI (for age group 21–30; and 31–40) (Table 1). Men had higher indices of body fat distribution (Android/Gynoid % fat ratio and Trunk/Limb % fat ratio) and all parameters associated with lean mass (LM, %LM, LMI, and aLMI) while women had higher indices in parameters associated with fat mass (FM, %FM, FMI, and aFMI) (p < 0.05; Table 1).

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Table 1. Mean (SD) of baseline participant characteristics stratified by age groups for overall, male and females respectively.

https://doi.org/10.1371/journal.pone.0276434.t001

Using the LMS method, sex-stratified values for 3rd, 10th 50th, 90th, and 97th percentiles for individuals aged 21–90 years were generated for FMI, LMI, aLMI, Android/Gynoid % fat ratio and Trunk/Limb % fat ratio (Tables 26), with the age in each table representing the age point for the predicted centile LMS values generated using GAMLSS. The differences between the sexes were also demonstrated in the Spline regression plots where LMI, aLMI, Android/Gynoid % fat ratio and Trunk/Limb % fat ratio were consistently higher in men of all age groups compared to women (Figs 1 and 2). Significant correlation (p < 0.05) with age were shown for all variables for both men and women, except for LMI in women, with the strength of r ranging from 0.12 (weak correlation) to 0.54 (strong correlation) (Table 7). The LMI (r = −0.45, p < 0.001) and appendicular LMI (r = −0.54, p < 0.001) were negatively associated with age in general and decline started around 40 years of age in men (Table 7 and Fig 1). None (r = −0.06, p = 0.316) to weak correlation (r = −0.14, p = 0.012) were shown in women for the same parameters respectively (Table 7). The Android/Gynoid % fat ratio and Trunk/Limb % fat ratio were positively related to age for both men (r = 0.37 & 0.43, p < 0.001) and women (r = 0.52 & 0.48, p < 0.001) with the latter showing a steady increase with age (Table 7 and Fig 2).

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Fig 1. Natural spline regression by sex for FMI, LMI, and appendicular LMI in men and women aged 21–90 years.

FMI, fat mass index; LMI, lean mass index.

https://doi.org/10.1371/journal.pone.0276434.g001

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Fig 2. Natural spline regression by sex for Android/Gynoid % fat ratio and Trunk/Limb % fat ratio in men and women aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.g002

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Table 2. Sex-specific percentile values for fat mass index (FMI) in individuals aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.t002

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Table 3. Sex-specific percentile values for lean mass index (LMI) in individuals aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.t003

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Table 4. Sex-specific percentile values for appendicular lean mass index (aLMI) in individuals aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.t004

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Table 5. Sex-specific percentile values for Android/Gynoid % fat ratio in individuals aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.t005

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Table 6. Sex-specific percentile values for Trunk/Limb % fat ratio in individuals aged 21–90 years.

https://doi.org/10.1371/journal.pone.0276434.t006

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Table 7. List of reference values generated and correlation with age (years) in men and women respectively.

https://doi.org/10.1371/journal.pone.0276434.t007

Discussion

While it has been long established that BC reference values should be population-specific and take age, sex, and ethnicity into consideration [26, 27], the lack of local reference values has hitherto limited the adoption of BC screening in clinical practice. To our knowledge, this is the first study presenting age- and sex-specific reference values for FMI, LMI, aLMI, Android/Gynoid % fat ratio, and Trunk/Limb % fat ratio, based on a nationally and ethnically representative data set that were acquired using established DXA technology, equipment, and procedure.

FMI

FMI, which is calculated as the total body fat mass with height2 adjustment, is a direct adiposity measurement of the human body. This parameter has been proposed as a measure of abnormal fat mass level (low/excessive) and advocated for use in diagnosing clinical obesity although the appropriate cut-off point to diagnose obesity is still an ongoing debate [28, 45] FMI was shown to increase with age in both sexes from the Chinese and NHANES data [28, 34]. A Korean study on reference value demonstrated FMI trend amongst women similar to that of NHANES, however with no relationship was found in Korean men [36]. Interestingly, data from our study sample revealed a weakly correlated decrease in FMI with age, an effect in men that is opposite to the NHANES and Chinese data while women in our study are found to be consistent with previously reported trend. It has been shown that consumption of 113 grams of meat for five times a week helps in the prevention of sarcopenia [46]. Apart from diet, the contrasting evidence may also be attributed to differences in lifestyle between populations and future studies should examine this.

LMI and aLMI

aLMI has been widely used in sarcopenia diagnosis, which is a condition characterized by gradual and general loss of muscle mass and strength, and have been shown to be predict functional disability in older adults [23, 24, 47, 48]. Our data demonstrated significant sex differences in lean mass parameters, with men having greater LMI and aLMI for all age groups, supporting the need for sex-specific reference value. Consistent with the Chinese study, the LMI and aLMI for men in the present study were also negatively correlated with age, however with a decline observed from around 40 years of age instead of the fifth decade [34]. The same study found no relationship in both parameters with age in women, and while LMI in our work similarly showed no relationship, a weak negative correlation were demonstrated in aLMI. These findings are consistent with previous studies on Asian populations where men were shown to be more likely to develop sarcopenia compared to women [49, 50].

Body fat distribution

Body fat distribution has been shown to be a better predictor of health risk compared to total fat mass and therefore, Trunk/Limb % fat ratio and Android/Gynoid % fat ratio were included in our analysis [51, 52]. These indices were postulated to play a part in defining metabolic syndrome or lipodystrophy [53, 54]. Android adipose deposition was found to be associated with higher risk of cardiovascular and metabolic diseases, while fat accumulated around the gynoid is related to decreased risk of metabolic diseases and can potentially provide protection against harmful health effects in both sexes [51, 52, 55]. A linear relationship between sarcopenia and adiposity had also been suggested by another study [56].

From our dataset, there are indications of overall central fat accumulation with age in both sexes with the mean Android/Gynoid % fat ratio and Trunk/Limb % fat ratio increasing with age for the entire lifespan, except for Android/Gynoid % fat ratio in men which increased until 70 years of age. The men exhibited significantly higher central adiposity (Trunk/Limb % fat ratio, Android/Gynoid % fat ratio) compared to the women of all age groups although the latter have greater total body fat (% FM) in comparison to men. While the general trends are in line with previous studies [28, 30, 33, 36], other work have demonstrated higher central adiposity in Asian ethnicity compared to the Caucasian populations [57, 58]. Further work can elucidate the relationship between ethnicity, sex and central adiposity.

Strengths, limitations, and future works

To our knowledge, this is the first study to publish sex- and age-specific BC reference data in Singaporean adults. Although with a modest sample size, the subjects were randomly recruited from a population which is similar to the overall Singapore residential population in terms of gender and older adults (≥65 years) proportion, thereby contributing to the limited reference database on Southeast Asian body composition. There are, however, several limitations in this study that should be acknowledged. Firstly, our overall modest sample size did not allow for ethnic-specific reference values to be generated. Secondly, the number of male participants in the age groups below 60 years was slightly fewer than anticipated. Thus the normative distribution limits of BC parameters for males below 60 years may not be an exact reflection of true population parameters [59]. Thirdly, this study only excluded subjects with more than five poorly controlled comorbidities, which may affect some of the reported reference values. Lastly, this cross-sectional data across adult age spectrum do not represent changes with age and was not intended so. Future population-based longitudinal study with larger sample size can address these limitations. In addition, there is a further urgent need to develop ethnic-specific reference values for a more accurate clinical application. Nevertheless, the reference values reported here should provide a better representation of local population compared to the commonly used NHANES dataset which is based on Western population.

Conclusion

Our study presents the sex- and age-specific reference values in FMI, LMI, aLMI, and indices for body fat distribution, including Android/Gynoid % fat ratio and Trunk/Limb % fat ratio using DXA in multi-ethnic Singaporean adults. The importance of developing local reference values specific to our population is highlighted in this study. These reference data should prove useful for stratification of an individual’s BC result relative to persons of the same age and sex, and add on to the limited reference database on Southeast Asian body composition. This can inform future studies related to obesity, nutrition, and sarcopenia.

References

  1. 1. Öztürk ZA, Türkbeyler İH, Abiyev A, Kul S, Edizer B, Yakaryılmaz FD, et al. Health-related quality of life and fall risk associated with age-related body composition changes; sarcopenia, obesity and sarcopenic obesity. Intern Med J [Internet]. 2018 Aug 1 [cited 2021 Oct 12];48(8):973–81. Available from: https://pubmed.ncbi.nlm.nih.gov/29665258/ pmid:29665258
  2. 2. Goossens GH. The Metabolic Phenotype in Obesity: Fat Mass, Body Fat Distribution, and Adipose Tissue Function. Obes Facts [Internet]. 2017 Jul 1 [cited 2021 Oct 12];10(3):207–15. Available from: /pmc/articles/PMC5644968/ pmid:28564650
  3. 3. Yang W, Dall TM, Beronjia K, Lin J, Semilla AP, Chakrabarti R, et al. Economic costs of diabetes in the U.S. in 2017. Diabetes Care [Internet]. 2018 May 1 [cited 2021 Oct 12];41(5):917–28. Available from: https://pubmed.ncbi.nlm.nih.gov/29567642/ pmid:29567642
  4. 4. Yalcin G, Ozsoy E, Karabag T. The relationship of body composition indices with the significance, extension and severity of coronary artery disease. Nutr Metab Cardiovasc Dis [Internet]. 2020 Nov 27 [cited 2021 Oct 12];30(12):2279–85. Available from: https://pubmed.ncbi.nlm.nih.gov/32928627/ pmid:32928627
  5. 5. Karcher HS, Holzwarth R, Mueller HP, Ludolph AC, Huber R, Kassubek J, et al. Body fat distribution as a risk factor for cerebrovascular disease: An MRI-based body fat quantification study. Cerebrovasc Dis [Internet]. 2013 [cited 2021 Dec 10];35(4):341–8. Available from: https://pubmed.ncbi.nlm.nih.gov/23615579/ pmid:23615579
  6. 6. Avgerinos KI, Spyrou N, Mantzoros CS, Dalamaga M. Obesity and cancer risk: Emerging biological mechanisms and perspectives. Metabolism. 2019 Mar 1;92:121–35. pmid:30445141
  7. 7. Preuss HG, Bagchi M, Bagchi D, Kaats GR. Obesity and cancer. Oncologist [Internet]. 2010 Jan 1 [cited 2021 Dec 10];15(6):197–204. Available from: https://pubmed.ncbi.nlm.nih.gov/20507889/
  8. 8. Yeung SSY, Reijnierse EM, Pham VK, Trappenburg MC, Lim WK, Meskers CGM, et al. Sarcopenia and its association with falls and fractures in older adults: A systematic review and meta-analysis. J Cachexia Sarcopenia Muscle [Internet]. 2019 Jun 1 [cited 2021 Dec 10];10(3):485–500. Available from: /pmc/articles/PMC6596401/ pmid:30993881
  9. 9. Heymsfield SB, Gallagher D, Mayer L, Beetsch J, Pietrobelli A. Scaling of human body composition to stature: New insights into body mass index. Am J Clin Nutr [Internet]. 2007 Jul 1 [cited 2021 Oct 12];86(1):82–91. Available from: https://pubmed.ncbi.nlm.nih.gov/17616766/ pmid:17616766
  10. 10. Okorodudu DO, Jumean MF, Montori VM, Romero-Corral A, Somers VK, Erwin PJ, et al. Diagnostic performance of body mass index to identify obesity as defined by body adiposity: A systematic review and meta-analysis. Int J Obes [Internet]. 2010 May [cited 2021 Oct 12];34(5):791–9. Available from: https://pubmed.ncbi.nlm.nih.gov/20125098/ pmid:20125098
  11. 11. Blundell JE, Dulloo AG, Salvador J, Frühbeck G, BMI on behalf of the ESWG on. Beyond BMI—Phenotyping the Obesities. Obes Facts [Internet]. 2014 Nov 13 [cited 2021 Oct 12];7(5):322. Available from: /pmc/articles/PMC5644899/
  12. 12. Hull HR, Thornton J, Wang J, Pierson RN, Kaleem Z, Pi-Sunyer X, et al. Fat-free mass index: changes and race/ethnic differences in adulthood. Int J Obes (Lond) [Internet]. 2011 Jan [cited 2022 Sep 7];35(1):121–7. Available from: https://pubmed.ncbi.nlm.nih.gov/20531353/ pmid:20531353
  13. 13. Toombs RJ, Ducher G, Shepherd JA, De Souza MJ. The impact of recent technological advances on the trueness and precision of DXA to assess body composition. Obesity [Internet]. 2012 Jan [cited 2021 Oct 12];20(1):30–9. Available from: https://pubmed.ncbi.nlm.nih.gov/21760631/ pmid:21760631
  14. 14. VanItallie TB, Yang MU, Heymsfield SB, Funk RC, Boileau RA. Height-normalized indices of the body’s fat-free mass and fat mass: Potentially useful indicators of nutritional status. Am J Clin Nutr [Internet]. 1990 [cited 2021 Oct 12];52(6):953–9. Available from: https://pubmed.ncbi.nlm.nih.gov/2239792/ pmid:2239792
  15. 15. Bonikowske AR, Lara MIB, Koepp KE, Inojosa JRM, Squires RW, Lopez-Jimenez F, et al. Fat mass index better identifies metabolic syndrome: Insights from patients in early outpatient cardiac rehabilitation. J Clin Med [Internet]. 2019 Dec 1 [cited 2021 Oct 12];8(12). Available from: https://pubmed.ncbi.nlm.nih.gov/31817309/
  16. 16. Natsis M, Antza C, Doundoulakis I, Stabouli S, Kotsis V. Hypertension in Obesity: Novel Insights. Curr Hypertens Rev [Internet]. 2019 Apr 16 [cited 2021 Oct 12];16(1):30–6. Available from: https://pubmed.ncbi.nlm.nih.gov/30987571/
  17. 17. Hopkins BD, Goncalves MD, Cantley LC. Obesity and cancer mechanisms: Cancer metabolism. J Clin Oncol [Internet]. 2016 Dec 10 [cited 2021 Oct 12];34(35):4277–83. Available from: https://pubmed.ncbi.nlm.nih.gov/27903152/ pmid:27903152
  18. 18. Kachur S, Lavie CJ, De Schutter A, Milani R V., Ventura HO. Obesity and cardiovascular diseases. Minerva Med [Internet]. 2017 Jun 1 [cited 2021 Oct 12];108(3):212–28. Available from: https://pubmed.ncbi.nlm.nih.gov/28150485/ pmid:28150485
  19. 19. Lavie CJ, Milani R V., Ventura HO. Obesity and Cardiovascular Disease. Risk Factor, Paradox, and Impact of Weight Loss. J Am Coll Cardiol [Internet]. 2009 May 26 [cited 2021 Oct 12];53(21):1925–32. Available from: https://pubmed.ncbi.nlm.nih.gov/19460605/
  20. 20. Cho M, Jong SP, Nam J, Chul SK, Jae HN, Hai JK, et al. Association of abdominal obesity with atherosclerosis in type 2 diabetes mellitus (T2DM) in Korea. J Korean Med Sci [Internet]. 2008 Oct [cited 2021 Oct 12];23(5):781–8. Available from: https://pubmed.ncbi.nlm.nih.gov/18955782/ pmid:18955782
  21. 21. Kopelman PG. Obesity as a medical problem. Nature [Internet]. 2000 Apr 6 [cited 2021 Oct 12];404(6778):635–43. Available from: https://pubmed.ncbi.nlm.nih.gov/10766250/ pmid:10766250
  22. 22. Benton MJ, Silva-Smith AL. Accuracy of Body Mass Index Versus Lean Mass Index for Prediction of Sarcopenia in Older Women. J frailty aging [Internet]. 2018 Jan 1 [cited 2021 Oct 12];7(2):104–7. Available from: https://pubmed.ncbi.nlm.nih.gov/29741194/ pmid:29741194
  23. 23. Cruz-Jentoft AJ, Baeyens JP, Bauer JM, Boirie Y, Cederholm T, Landi F, et al. Sarcopenia: European consensus on definition and diagnosisReport of the European Working Group on Sarcopenia in Older PeopleA. J. Cruz-Gentoft et al. Age Ageing. 2010;39(4):412–23.
  24. 24. Baumgartner RN, Koehler KM, Gallagher D, Romero L, Heymsfield SB, Ross RR, et al. Epidemiology of sarcopenia among the elderly in New Mexico. Am J Epidemiol. 1998;147(8):755–63. pmid:9554417
  25. 25. Piché ME, Poirier P, Lemieux I, Després JP. Overview of Epidemiology and Contribution of Obesity and Body Fat Distribution to Cardiovascular Disease: An Update. Prog Cardiovasc Dis [Internet]. 2018 Jul 1 [cited 2021 Oct 12];61(2):103–13. Available from: https://pubmed.ncbi.nlm.nih.gov/29964067/ pmid:29964067
  26. 26. Morrison SA, Petri RM, Hunter HL, Raju D, Gower B. Comparison of the Lunar Prodigy and iDXA Dual-Energy X-ray Absorptiometers for Assessing Total and Regional Body Composition. J Clin Densitom. 2016;19(3):290–7. pmid:26209017
  27. 27. Bosy-Westphal A, Müller MJ. Identification of skeletal muscle mass depletion across age and BMI groups in health and disease—There is need for a unified definition. Int J Obes. 2015;39(3):379–86. pmid:25174451
  28. 28. Kelly TL, Wilson KE, Heymsfield SB. Dual energy X-ray absorptiometry body composition reference values from NHANES. PLoS One. 2009;4(9):2–9. pmid:19753111
  29. 29. Shuhart CR, Yeap SS, Anderson PA, Jankowski LG, Lewiecki EM, Morse LR, et al. Executive Summary of the 2019 ISCD Position Development Conference on Monitoring Treatment, DXA Cross-calibration and Least Significant Change, Spinal Cord Injury, Peri-prosthetic and Orthopedic Bone Health, Transgender Medicine, and Pediatrics. J Clin Densitom. 2019;22(4):453–71. pmid:31400968
  30. 30. Imboden MT, Welch WA, Swartz AM, Montoye AHK, Finch HW, Harber MP, et al. Reference standards for body fat measures using GE dual energy x-ray absorptiometry in Caucasian adults. 2017;1–12.
  31. 31. Ofenheimer A, Breyer-Kohansal R, Hartl S, Burghuber OC, Krach F, Schrott A, et al. Reference values of body composition parameters and visceral adipose tissue (VAT) by DXA in adults aged 18–81 years—results from the LEAD cohort. Eur J Clin Nutr [Internet]. 2020;74(8):1181–91. Available from: pmid:32123345
  32. 32. Clark P, Denova-Gutiérrez E, Ambrosi R, Szulc P, Rivas-Ruiz R, Salmerón J. Reference Values of Total Lean Mass, Appendicular Lean Mass, and Fat Mass Measured with Dual-Energy X-ray Absorptiometry in a Healthy Mexican Population. Calcif Tissue Int. 2016;99(5):462–71. pmid:27484026
  33. 33. Fan B, Shepherd JA, Levine MA, Steinberg D, Wacker W, Barden HS, et al. National Health and Nutrition Examination Survey Whole-Body Dual-Energy X-Ray Absorptiometry Reference Data for GE Lunar Systems. J Clin Densitom. 2014;17(3):344–77. pmid:24161789
  34. 34. Xiao Z, Guo B, Gong J, Tang Y, Shang J, Cheng Y, et al. Sex- and age-specific percentiles of body composition indices for Chinese adults using dual-energy X-ray absorptiometry. Eur J Nutr. 2017;56(7):2393–406. pmid:27473103
  35. 35. Rush EC, Freitas I, Plank LD. Body size, body composition and fat distribution: Comparative analysis of European, Maori, Pacific Island and Asian Indian adults. Br J Nutr. 2009;102(4):632–41. pmid:19203416
  36. 36. Hong S, Oh HJ, Choi H, Kim JG, Lim SK, Kim EK, et al. Characteristics of body fat, body fat percentage and other body composition for Koreans from KNHANES IV. J Korean Med Sci. 2011;26(12):1599–605. pmid:22147997
  37. 37. Park HW, Yoo HY, Kim CH, Kim H, Kwak BO, Kim KS, et al. Reference values of body composition indices: The korean national health and nutrition examination surveys. Yonsei Med J. 2015;56(1):95–102. pmid:25510752
  38. 38. DOS. Singapore Department of Statistics (DOS) | Singstat Website [Internet]. 2021 [cited 2021 May 24]. Available from: https://www.singstat.gov.sg/
  39. 39. Green PJ, Hogg R V., Tanis . Probability and Statistical Inference. 9th ed. Vol. 27, Applied Statistics. London: Pearson; 1978. 85 p.
  40. 40. Kelly TL, Scientist SP. The Body Composition Gold Standard: Hologic ‘ s approach to calibration for body composition measurements using DXA. 1997;
  41. 41. Stasinopoulos MD, Rigby RA, Bastiani F De. GAMLSS: A distributional regression approach. 2018;18(2012):248–73.
  42. 42. Cole TJ. The LMS method for constructing normalized growth standards. Eur J Clin Nutr. 1990 Jan 1;44(1):45–60. pmid:2354692
  43. 43. Cole TJ, Stanojevic S, Stocks J, Coates AL, Hankinson JL, Wade AM. Age- and size-related reference ranges: A case study of spirometry through childhood and adulthood. Stat Med [Internet]. 2009 Feb 28 [cited 2021 Dec 10];28(5):880–98. Available from: https://pubmed.ncbi.nlm.nih.gov/19065626/ pmid:19065626
  44. 44. Cohen J. Statistical Power Analysis for the Behavioral Sciences. Stat Power Anal Behav Sci. 2013;
  45. 45. Messina C, Albano D, Gitto S, Tofanelli L, Bazzocchi A, Ulivieri FM, et al. Body composition with dual energy X-ray absorptiometry: From basics to new tools. Quant Imaging Med Surg. 2020;10(8):1687–98. pmid:32742961
  46. 46. Rondanelli M, Perna S, Faliva MA, Peroni G, Infantino V, Pozzi R. Novel insights on intake of meat and prevention of sarcopenia: All reasons for an adequate consumption. Nutr Hosp. 2015;32(5):2136–43. pmid:26545670
  47. 47. Wulan SN, Westerterp KR, Plasqui G. Ethnic differences in body composition and the associated metabolic profile: a comparative study between Asians and Caucasians. Maturitas. 2010;65(4):315–9. pmid:20079586
  48. 48. Iannuzzi-Sucich M, Prestwood KM, Kenny AM. Prevalence of sarcopenia and predictors of skeletal muscle mass in healthy, older men and women. Journals Gerontol—Ser A Biol Sci Med Sci [Internet]. 2002 Dec 1 [cited 2021 Dec 7];57(12). Available from: https://pubmed.ncbi.nlm.nih.gov/12456735/ pmid:12456735
  49. 49. Sanada K, Miyachi M, Tanimoto M, Yamamoto K, Murakami H, Okumura S, et al. A cross-sectional study of sarcopenia in Japanese men and women: reference values and association with cardiovascular risk factors. Eur J Appl Physiol. 2010;110(1):57–65. pmid:20390291
  50. 50. Kim MK, Baek KH, Song KH, Il Kang M, Park CY, Lee WY, et al. Vitamin D deficiency is associated with sarcopenia in older Koreans, regardless of obesity: the Fourth Korea National Health and Nutrition Examination Surveys (KNHANES IV) 2009. J Clin Endocrinol Metab. 2011;96(10):3250–6. pmid:21832109
  51. 51. Pinnick KE, Nicholson G, Manolopoulos KN, McQuaid SE, Valet P, Frayn KN, et al. Distinct developmental profile of lower-body adipose tissue defines resistance against obesity-associated metabolic complications. Diabetes. 2014;63(11):3785–97. pmid:24947352
  52. 52. Lee MJ, Wu Y, Fried SK. Adipose tissue heterogeneity: implication of depot differences in adipose tissue for obesity complications. Mol Aspects Med. 2013;34(1):1–11. pmid:23068073
  53. 53. Law M, Puls R, Cheng AK, Cooper DA, Carr A. Evaluation of the HIV lipodystrophy case definition in a placebo-controlled, 144-week study in antiretroviral-naive adults. Antivir Ther. 2006;11(2):179. pmid:16640099
  54. 54. Bonnet E, Delpierre C, Sommet A, Marion-Latard F, Herve R, Aquilina C, et al. Total body composition by DXA of 241 HIV-negative men and 162 HIV-infected men: proposal of reference values for defining lipodystrophy. J Clin Densitom. 2005;8(3):287–92. pmid:16055958
  55. 55. Reis JP, Loria CM, Lewis CE, Powell-Wiley TM, Wei GS, Carr JJ, et al. Association between duration of overall and abdominal obesity beginning in young adulthood and coronary artery calcification in middle age. Jama. 2013;310(3):280–8. pmid:23860986
  56. 56. Perna S, Guido D, Grassi M, Rondanelli M. Association between muscle mass and adipo-metabolic profile: A cross-sectional study in older subjects. Clin Interv Aging. 2015;10:499–504. pmid:25759569
  57. 57. Kadowaki T, Sekikawa A, Murata K, Maegawa H, Takamiya T, Okamura T, et al. Japanese men have larger areas of visceral adipose tissue than Caucasian men in the same levels of waist circumference in a population-based study. Int J Obes. 2006;30(7):1163–5. pmid:16446744
  58. 58. Morimoto Y, Maskarinec G, Conroy SM, Lim U, Shepherd J, Novotny R. Asian ethnicity is associated with a higher trunk/peripheral fat ratio in women and adolescent girls. J Epidemiol. 2012;22(2):130–5. pmid:22327117
  59. 59. Gillette-Guyonnet S, Andrieu S, Nourhashemi F, Cantet C, Grandjean H, Vellas B. Comparison of bone mineral density and body composition measurements in women obtained from two DXA instruments. Mech Ageing Dev. 2003;124(3):317–21. pmid:12663129