Abstract

Objective

Thresholds for overweight and obesity are currently defined by body mass index (BMI), a poor surrogate marker of actual adiposity (percent body fat [%BF]). Practical modern technologies provide estimates of %BF but medical providers need outcome-based %BF thresholds to guide patients. This analysis determines %BF thresholds based on key obesity-related comorbidities, exhibited as metabolic syndrome (MetSyn). These limits were compared to existing BMI thresholds of overweight and obesity.

Design

Correlational analysis of data from cross sectional sampling of 16 918 adults (8734 men and 8184 women) from the US population, accessed by the National Health and Nutrition Examination Survey public use datasets.

Results

Individuals measured by BMI as overweight (BMI > 25 kg/m2) and with obesity (BMI > 30 kg/m2) included 5% and 35% of individuals with MetSyn, respectively. For men, there were no cases of MetSyn below 18%BF, %BF equivalence to “overweight” (ie, 5% of MetSyn individuals) occurred at 25%BF, and “obesity” (ie, 35% of MetSyn individuals) corresponded to 30%BF. For women, there were no cases of MetSyn below 30%BF, “overweight” occurred at 36%BF, and “obesity” corresponded to 42%BF. Comparison of BMI to %BF illustrates the wide range of variability in BMI prediction of %BF, highlighting the potential importance of using more direct measures of adiposity to manage obesity-related disease.

Conclusion

Practical methods of body composition estimation can now replace the indirect BMI assessment for obesity management, using threshold values provided from this study. Clinically relevant “overweight” can be defined as 25% and 36% BF for men and women, respectively, and “obesity” is defined as 30% and 42% BF for men and women.

Clinical health standards currently define thresholds for healthy, overweight, and obesity by body mass index (BMI; kg/m2). Although BMI has long been the primary metric in clinical weight management, it has also been well recognized to be a poor surrogate marker of actual adiposity or relative body fat (%BF) (1). Practical modern technologies are beginning to provide more reliable estimates of %BF but for these to be useful, medical providers require outcome-based %BF thresholds to help guide patient health. These %BF metrics to advise patients about obesity-related health risks require direct derivation from clinical health outcomes. Previous attempts to derive %BF health risk thresholds from BMI are problematic because of the imprecise relationship and the relationship is further affected by factors such as age, sex, nutrition, and fitness habits (2, 3).

Obesity-related diseases have been defined on the basis of excess adiposity, primarily via deposition of lipids in liver and muscle and decreases in whole-body insulin sensitivity (4). However, instead of targeting the association of %BF with obesity-related diseases, “ideal weight” recommendations for Americans have been generalized to associations with all-cause mortality. This strategy began with the 1912 height-weight tables that were derived from mortality statistics of the insured population, and it continued with later updates such as the Metropolitan Life ideal weight tables in 1959 and 1983 (5). In an attempt to check the rising prevalence of obesity, the 1985 National Institutes of Health Obesity Consensus panel simply provided arbitrary weight targets for the country, calculated from the 85th percentile of the BMI of men and women in the National Health and Nutrition Examination Survey (NHANES) II (27.8 and 27.3 kg/m2, respectively) (6). Finally, the 1998 National Heart, Lung, and Blood Institute expert panel developed the current definitions of “overweight” established as BMI > 25 kg/m2 and “obese” as BMI > 30 kg/m2, roughly based on BMI inflection points for various obesity-related disease risks. However, there is a continued focus on the association between BMI thresholds and all-cause mortality (7, 8). These thresholds were based on simple anthropometrics (BMI and waist circumference) because these were the only practical metrics available on which to base national health goals. The National Institutes of Health expert panel review of bioelectrical impedance technologies held out hope for the future maturity of practical methods for %BF estimation to more effectively target obesity disease management (9). Today, practical methods to estimate %BF, such as multifrequency bioelectrical impedance, are maturing and may find an important role in preventive medicine.

Metabolic syndrome (MetSyn), affecting an estimated one third of adult Americans, has a plausible mechanistic relationship to %BF (4, 10, 11). On this basis, the use of %BF metrics could be more useful than body size (BMI) in guiding patients because excess fat is either a key marker or a direct cause of metabolic disease. The Adult Treatment Panel III from the National Cholesterol Education Program, classified MetSyn when 3 or more of the 5 key markers are present. The Adult Treatment Panel III criteria used for MetSyn includes waist circumference >101.6 cm (men), >88.9 cm (women); high-density lipoprotein cholesterol < 40 mg/dL (men), <50 mg/dL (women); fasting glucose ≥ 100 mg/dL; blood pressure > 130/85 mm Hg; and triglycerides ≥ 150 mg/dL (12).

This analysis uses a large diverse sample of data to provide sex-specific thresholds of %BF based on key obesity-related comorbidities, exhibited as MetSyn. These upper limits of %BF to categorize men and women were compared to existing BMI thresholds of overweight and obesity. The concept was to derive %BF thresholds directly from the MetSyn outcomes instead of less directly by translation from BMI. The thresholds were established based on equivalent MetSyn population outcomes for the 2 commonly used BMI-based definitions of “overweight” and “obesity.” Use of these measures of %BF may be more clinically relevant markers for metabolic health across the general population than body size (ie, BMI).

Materials and Methods

Study Design and Sample Population

This is a correlational analysis of data from cross sectional sampling of the US population via the NHANES public use datasets (13). NHANES provides a demographically representative sampling of the US population that is collected continuously and collated into 2-year datasets.

Individual participant data were obtained from the NHANES (13, 14). The NHANES has been approved by the National Center for Health Statistics Research Ethics Review Board; therefore, the present analyses did not require a separate regulatory approval. Each participant within the NHANES study provided written informed consent before assessments (13).

The present analyses include data from 16 918 adults (8734 men and 8184 women), ages 18 to 85 years, from NHANES 1999-2018. Data were obtained for individual demographics (age, race/ethnicity), laboratory measures: fasting glucose (mg/dL), triglycerides (mg/dL), high-density lipoprotein-C (mg/dL), and blood pressure (mm Hg), body measures (height, weight, waist circumference, and BMI), and from whole-body dual-energy x-ray absorptiometry (DXA) assessments (Hologic, Inc., Bedford, Massachusetts). Individual data were included if associated DXA measures were available; as a result, two survey periods with no recorded DXA measures (2007-2008 and 2009-2010) were not included. For the present analysis, classification for metabolic health outcomes for each individual was made based on meeting the criteria for MetSyn (≥3 markers) (12). The CONSORT flow diagram is presented in Fig. 1.

CONSORT flow diagram for study participant data selection.
Figure 1.

CONSORT flow diagram for study participant data selection.

Statistical Analyses

Statistical analyses were conducted using a combination of SAS version 9.4 (SAS Institute), SPSS version 28.01.1 (IBM Corporation), and Excel (Microsoft Corporation). Descriptive statistics are shown as mean ± standard deviation or by number of incidences.

Results

Data analyses were conducted on 16 918 adults (8734 men, mean age 41.6 years; 8184 women, mean age 42.6 years), including self-reported race/ethnicity as 39% non-Hispanic White, 27% Hispanic, 21% non-Hispanic Black, 8% non-Hispanic Asian, and 4% non-Hispanic multiple (0.4% no answer). Descriptive statistics are shown in Tables 1-3.

Table 1.

Study descriptive statistics

 MenWomen
n87348184
Age (y)41.6 ± 16.542.6 ± 16.4
BMI (kg/m2)28.7 ± 6.529.3 ± 7.7
LBM (kg)62.7 ± 11.245.4 ± 9.2
BMC (kg)2.64 ± 0.452.09 ± 0.36
BMD (cm3)1.17 ± 0.121.08 ± 0.12
BF (%)27.8 ± 6.539.7 ± 6.5
MetSyn (n,%)3353 (38.4%)2375 (29.0%)
 MenWomen
n87348184
Age (y)41.6 ± 16.542.6 ± 16.4
BMI (kg/m2)28.7 ± 6.529.3 ± 7.7
LBM (kg)62.7 ± 11.245.4 ± 9.2
BMC (kg)2.64 ± 0.452.09 ± 0.36
BMD (cm3)1.17 ± 0.121.08 ± 0.12
BF (%)27.8 ± 6.539.7 ± 6.5
MetSyn (n,%)3353 (38.4%)2375 (29.0%)

Abbreviations: BF, body fat; BMC, bone mineral content; BMD, bone mineral density; BMI, body mass index; LBM, lean body mass; MetSyn, metabolic syndrome.

Table 1.

Study descriptive statistics

 MenWomen
n87348184
Age (y)41.6 ± 16.542.6 ± 16.4
BMI (kg/m2)28.7 ± 6.529.3 ± 7.7
LBM (kg)62.7 ± 11.245.4 ± 9.2
BMC (kg)2.64 ± 0.452.09 ± 0.36
BMD (cm3)1.17 ± 0.121.08 ± 0.12
BF (%)27.8 ± 6.539.7 ± 6.5
MetSyn (n,%)3353 (38.4%)2375 (29.0%)
 MenWomen
n87348184
Age (y)41.6 ± 16.542.6 ± 16.4
BMI (kg/m2)28.7 ± 6.529.3 ± 7.7
LBM (kg)62.7 ± 11.245.4 ± 9.2
BMC (kg)2.64 ± 0.452.09 ± 0.36
BMD (cm3)1.17 ± 0.121.08 ± 0.12
BF (%)27.8 ± 6.539.7 ± 6.5
MetSyn (n,%)3353 (38.4%)2375 (29.0%)

Abbreviations: BF, body fat; BMC, bone mineral content; BMD, bone mineral density; BMI, body mass index; LBM, lean body mass; MetSyn, metabolic syndrome.

Table 2.

Study sex and age group distribution

Age group (y)MenWomenTotal (proportion %)MetSyn cases (% of age group)
n8734818416 9185728 (33.9%)
18-29243520994534 (26.8%)610 (13.5%)
30-39173115323263 (19.3%)920 (28.2%)
40-49176517763541 (20.9%)1319 (37.2%)
50-59161516093224 (19.1%)1454 (45.1%)
60-696416421283 (7.6%)785 (61.2%)
70-79343293636 (3.8%408 (64.2%)
≥80204233437 (2.6%)232 (53.1%)
Age group (y)MenWomenTotal (proportion %)MetSyn cases (% of age group)
n8734818416 9185728 (33.9%)
18-29243520994534 (26.8%)610 (13.5%)
30-39173115323263 (19.3%)920 (28.2%)
40-49176517763541 (20.9%)1319 (37.2%)
50-59161516093224 (19.1%)1454 (45.1%)
60-696416421283 (7.6%)785 (61.2%)
70-79343293636 (3.8%408 (64.2%)
≥80204233437 (2.6%)232 (53.1%)

Abbreviation: MetSyn, metabolic syndrome.

Table 2.

Study sex and age group distribution

Age group (y)MenWomenTotal (proportion %)MetSyn cases (% of age group)
n8734818416 9185728 (33.9%)
18-29243520994534 (26.8%)610 (13.5%)
30-39173115323263 (19.3%)920 (28.2%)
40-49176517763541 (20.9%)1319 (37.2%)
50-59161516093224 (19.1%)1454 (45.1%)
60-696416421283 (7.6%)785 (61.2%)
70-79343293636 (3.8%408 (64.2%)
≥80204233437 (2.6%)232 (53.1%)
Age group (y)MenWomenTotal (proportion %)MetSyn cases (% of age group)
n8734818416 9185728 (33.9%)
18-29243520994534 (26.8%)610 (13.5%)
30-39173115323263 (19.3%)920 (28.2%)
40-49176517763541 (20.9%)1319 (37.2%)
50-59161516093224 (19.1%)1454 (45.1%)
60-696416421283 (7.6%)785 (61.2%)
70-79343293636 (3.8%408 (64.2%)
≥80204233437 (2.6%)232 (53.1%)

Abbreviation: MetSyn, metabolic syndrome.

Table 3.

Study sex and race/ethnicity group distribution

 MenWomenTotal (proportion %)MetSyn Cases (% of subgroup)
n8734818416 918
Hispanic237622544630 (27.4%)1272 (38.8%)
Non-Hispanic White352731646691 (39.5%)456 (37.0%)
Non-Hispanic Black173117903521 (20.8%)2477 (28.7%)
Non-Hispanic Asian6976281325 (7.8%)246 (18.6%)
Non-Hispanic multiple370320690 (4.1%)217 (31.4%)
No answer332861 (0.4%)51 (83.6%)
 MenWomenTotal (proportion %)MetSyn Cases (% of subgroup)
n8734818416 918
Hispanic237622544630 (27.4%)1272 (38.8%)
Non-Hispanic White352731646691 (39.5%)456 (37.0%)
Non-Hispanic Black173117903521 (20.8%)2477 (28.7%)
Non-Hispanic Asian6976281325 (7.8%)246 (18.6%)
Non-Hispanic multiple370320690 (4.1%)217 (31.4%)
No answer332861 (0.4%)51 (83.6%)

Abbreviation: MetSyn, metabolic syndrome.

Table 3.

Study sex and race/ethnicity group distribution

 MenWomenTotal (proportion %)MetSyn Cases (% of subgroup)
n8734818416 918
Hispanic237622544630 (27.4%)1272 (38.8%)
Non-Hispanic White352731646691 (39.5%)456 (37.0%)
Non-Hispanic Black173117903521 (20.8%)2477 (28.7%)
Non-Hispanic Asian6976281325 (7.8%)246 (18.6%)
Non-Hispanic multiple370320690 (4.1%)217 (31.4%)
No answer332861 (0.4%)51 (83.6%)
 MenWomenTotal (proportion %)MetSyn Cases (% of subgroup)
n8734818416 918
Hispanic237622544630 (27.4%)1272 (38.8%)
Non-Hispanic White352731646691 (39.5%)456 (37.0%)
Non-Hispanic Black173117903521 (20.8%)2477 (28.7%)
Non-Hispanic Asian6976281325 (7.8%)246 (18.6%)
Non-Hispanic multiple370320690 (4.1%)217 (31.4%)
No answer332861 (0.4%)51 (83.6%)

Abbreviation: MetSyn, metabolic syndrome.

Redefined Overweight and Obesity on the Basis of Relative Body fat (%BF)

The percentage of individuals with MetSyn at BMI-defined limits of overweight (BMI >25 kg/m2) and obesity (BMI ≥30 kg/m2) were 5% and 35% (Fig. 2). These rates of MetSyn were then used to define %BF thresholds for comparable definitions of %BF-defined “overweight” and “obesity” for both men and women.

Prevalence of men and women in the NHANES data with ≥3 markers of metabolic syndrome by BMI.
Figure 2.

Prevalence of men and women in the NHANES data with ≥3 markers of metabolic syndrome by BMI.

The prevalence rates of MetSyn that corresponded to overweight and obese BMI thresholds (5% and 35%) were associated with 25% and 30%BF for men, and 36% and 42%BF for women, respectively (Fig. 3).

Prevalence of men and women in the NHANES data with ≥3 markers of metabolic syndrome by relative %BF.
Figure 3.

Prevalence of men and women in the NHANES data with ≥3 markers of metabolic syndrome by relative %BF.

Prevalence in Overweight and Obesity Based on Relative Body fat (%BF)

Based on conventional BMI thresholds, 29.5% of men and 33.1% of women were of healthy weight, 35.0% of men and 26.2% of women met the criteria for being overweight, and 35.5% of men and 40.7% of women for obesity. Using the %BF thresholds derived in this study, 27.7% of men and 27.2% of women had healthy weights, 34.0% of men and 33.5% of women were overweight, and 38.3% of men and 39.3% of women met the proposed %BF criteria for obesity.

Relationship Between BMI and %BF

The BMI and %BF thresholds for MetSyn were independently established from the symptom-defined outcomes but similar agreement was observed for %BF predicted indirectly from BMI. Nevertheless, the poor predictive value of BMI for adiposity at the individual level was highlighted by the high scatter in a curvilinear relationship between BMI and %BF. The curvilinear relationship and the large scatter for individuals plotted by BMI vs %BF (Fig. 4) highlights one of the problems in using BMI to represent %BF. Although of BMI 25 kg/m2 and 30 kg/m2 correspond to mean %BF values very close to those associated with 5% and 35% prevalence of MetSyn in the current analysis, at an individual level, a different set of individuals will be identified at risk using the %BF metrics instead of BMI. Additionally, there is an obvious difference between how BMI to %BF tracks for men and women. This systemic difference in how BMI represents adiposity in women poses a number of potential problems when used to evaluate health outcomes.

Comparison of BMI (kg/m2) to measured relative %BF for men and women in the NHANES data (1999-2018).
Figure 4.

Comparison of BMI (kg/m2) to measured relative %BF for men and women in the NHANES data (1999-2018).

Discussion

Until recently, only anthropometric predictions of body composition were practical for population-wide obesity metrics. Direct assessments of %BF using emerging technologies such as multifrequency bioelectrical impedance (MF-BIA) are increasing in reliability and affordability, opening the door to more effective personalized obesity management. There is still a wide range in validity and precision of %BF-derived from bioelectrical impedance devices, methods, and predictive equations in comparison to criterion methods such as DXA (15-18). A large step in this direction is a policy-based adoption of these types of systems within the US Department of Defense for evaluation of their own body composition standards (15, 19, 20). This will surely also lead the way to wider use in clinical practices, with creation of epidemiological data with clinical outcomes to further refine %BF associations with disease. Receiver operating characteristic and area under the curve statistics were similar between BMI and %BF for both men (0.83 and 0.80) and women (0.75 and 0.71), highlighting sex differences in the general accuracy for both methods. In this study, the similarity of MetSyn receiver operating characteristic and area under the curve statistics for BMI and %BF indicate that there is more to be learned about the relationships between body composition and metabolic disease. Like BMI, the relative amount of stored fat may itself be only a proxy for more dynamic nutrition and exercise influences on metabolic disease as proposed by Blair et al (21, 22).

Obesity-related diseases may be more effectively managed by finally moving away from anthropometric estimations of adiposity to direct measurement of the fat component, generally expressed as relative fat (%BF) or fat mass index (fat mass/height2); we chose to use %BF in our analysis. This analysis suggests %BF thresholds for patient guidance; these metrics align with “overweight” (5% of MetSyn individuals) and “obesity” (35% of MetSyn individuals) in a large nationally representative sample. The %BF thresholds produced in this current analysis are in line with previously reported guideline estimates made from indirect analyses based on BMI relationship to %BF (2, 3). This is also relatively consistent with health-related %BF standards (26% for men and 36% for women) established by the US Army for the oldest category of soldiers (age 40+) on the basis of equivalence to BMI 25 kg/m2 for a large sample of soldiers assessed by underwater weighing in 1984 and 1985 (23).

Although BMI can be helpful as a first-level screening criteria, it is not an accurate method for determining body composition and, in fact, does not provide accurate information about fat and lean components. This point is well illustrated in Fig. 4, where the wide variation in the relationship between %BF and BMI is apparent for both men and women. This can be most problematic at both the lower and upper ranges of BMI because a person with an apparently healthy BMI (≤25 kg/m2) can have excess body fat (metabolically obese normal weight, “skinny fat”) (24, 25) and individuals with higher BMIs (>25 kg/m2) may carry high lean mass and not have excess relative fat (eg, athletes, military) (26-28). Further technological improvements in body composition assessments such as refinement of mathematical models for MF-BIA technologies to produce increasingly more accurate intraabdominal fat content may lead to the next generation of clinically relevant metrics of body health. Currently available methods such as DXA provide estimates of intraabdominal fat and other information about soft tissue lean mass and bone mineral content with emerging relationships to all-cause mortality (29), whereas MF-BIA systems also provide some of these other components of body composition with clinical utility and are continuing to evolve. Endorsement of body composition assessments by medical societies will help to encourage better insurance coverage to lower out-of-pocket expenses for patients and will facilitate greater use and application of these useful technologies.

Acknowledgments

The authors are grateful to Dr. Roy Vigneulle, Military Operational Medicine Research Program, Fort Detrick, Maryland, for supporting the initial research initiative on metabolic performance.

Funding

Research was funded by the U.S. Army Medical Research and Development Command, Military Operational Medicine Research Program, Fort Detrick, MD. Funding source had no role in study design; collection, analysis, and interpretation of data; writing of the report; and has no restrictions regarding the submission of the report for publication.

Author Contributions

A.W.P. and K.E.F. designed the research; A.W.P. analyzed data; and A.W.P., G.C.C., D.P.L., and K.E.F. wrote the paper. A.W.P. had primary responsibility for final content. All authors read and approved the final manuscript.

Disclosures

The authors have no conflicts of interest to disclose. The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Army or the Department of Defense. Citations of commercial organizations and trade names in this report do not constitute an official Department of the Army endorsement or approval of the products or services of these organizations.

Data Availability

Data from this analysis is openly available to anyone under NHANES, found here: https://www.cdc.gov/nchs/nhanes/about_nhanes.htm.

References

1

Prentice
AM
,
Jebb
SA
.
Beyond body mass index
.
Obes Rev
.
2001
;
2
(
3
):
141
147
.

2

Gallagher
D
,
Heymsfield
SB
,
Heo
M
,
Jebb
SA
,
Murgatroyd
PR
,
Sakamoto
Y
.
Healthy percentage body fat ranges: an approach for developing guidelines based on body mass index
.
Am J Clin Nutr
.
2000
;
72
(
3
):
694
701
.

3

Heo
M
,
Faith
MS
,
Pietrobelli
A
,
Heymsfield
SB
.
Percentage of body fat cutoffs by sex, age, and race-ethnicity in the US adult population from NHANES 1999–2004
.
Am J Clin Nutr
.
2012
;
95
(
3
):
594
602
.

4

Sakers
A
,
De Siqueira
MK
,
Seale
P
,
Villanueva
CJ
.
Adipose-tissue plasticity in health and diseases
.
Cell
.
2022
;
185
(
3
):
419
446
.

5

Dwight
EW
,
Rogers Oscar
H
,
Root Edward
K
, et al.
Medico-actuarial mortality investigation. The association of life insurance medical directors and the actuarial society of America. 1913
.
Obes Res
.
1995
;
3
(
1
):
100
106
.

6

National Institutes of Health Consensus Development Panel on the Health Implications of Obesity
.
Health implications of obesity: national institutes of health consensus development conference statement
.
Ann Int Med
.
1985
;
103
(
6_Part_2
):
1073
1077
.

7

National Heart, Lung, and Blood Institute
.
Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults: the Evidence Report
.
National Heart, Lung, and Blood Institute
;
1998
.

8

Flegal
KM
,
Graubard
BI
,
Williamson
DF
,
Gail
MH
.
Excess deaths associated with underweight, overweight, and obesity
.
J Am Med Assoc
.
2005
;
293
(
15
):
1861
1867
.

9

Ellis
KJ
,
Bell
SJ
,
Chertow
GM
, et al.
Bioelectrical impedance methods in clinical research: a follow-up to the NIH technology assessment conference
.
Nutr
.
1999
;
15
(
11-12
):
874
880
.

10

Hirode
G
,
Wong
RJ
.
Trends in the prevalence of metabolic syndrome in the United States, 2011–2016
.
J Am Med Assoc
.
2020
;
323
(
24
):
2526
2528
.

11

Pi-Sunyer
FX
.
Medical hazards of obesity
.
Ann Int Med
.
1993
;
119
(
7_Part_2
):
655
660
.

12

Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults
.
Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III)
.
J Am Med Assoc
.
2001
;
285
(
19
):
2486
2497
.

13

National Center for Health Statistics
.
Centers for Disease Control and Prevention. National Health and Nutrition Examination Survey. Last reviewed: November 6,
2015
. https://www.cdc.gov/nchs/nhanes/genetics/genetic_participants.htm

14

Ahluwalia
N
,
Dwyer
J
,
Terry
A
,
Moshfegh
A
,
Johnson
C
.
Update on NHANES dietary data: focus on collection, release, analytical considerations, and uses to inform public policy
.
Adv Nutr
.
2016
;
7
(
1
):
121
134
.

15

Potter
AW
,
Nindl
LJ
,
Soto
LD
, et al.
High precision but systematic offset in a standing bioelectrical impedance analysis (BIA) compared with dual-energy X-ray absorptiometry (DXA)
.
BMJ Nutr Prev Health
.
2022
;
5
(
2
):
254
262
.

16

Ward
LC
.
Bioelectrical impedance analysis for body composition assessment: reflections on accuracy, clinical utility, and standardisation
.
Eur J Clin Nutr
.
2019
;
73
(
2
):
194
199
.

17

McLester
CN
,
Nickerson
BS
,
Kliszczewicz
BM
,
McLester
JR
.
Reliability and agreement of various InBody body composition analyzers as compared to dual-energy X-ray absorptiometry in healthy men and women
.
J Clin Densitom
.
2020
;
23
(
3
):
443
450
.

18

Schoenfeld
BJ
,
Nickerson
BS
,
Wilborn
CD
, et al.
Comparison of multifrequency bioelectrical impedance vs. dual-energy X-ray absorptiometry for assessing body composition changes after participation in a 10-week resistance training program
.
J Strength Cond Res
.
2020
;
34
(
3
):
678
688
.

19

Marine corps bulletin 6110
.
Marine Corps Body Composition and Military Appearance
.
Commandant of the Marine Corps
;
2022
.

20

All Army Activities Memorandum (ALARACT)
.
Notification of new army body fat assessment for army body composition program. 046/2023
. June
2023
.

21

Blair
SN
.
Physical inactivity: the biggest public health problem of the 21st century
.
Brit J Sports Med
.
2009
;
43
(
1
):
1
2
.

22

LaMonte
MJ
,
Barlow
CE
,
Jurca
R
,
Kampert
JB
,
Church
TS
,
Blair
SN
.
Cardiorespiratory fitness is inversely associated with the incidence of metabolic syndrome: a prospective study of men and women
.
Circulation
.
2005
;
112
(
4
):
505
512
.

23

Friedl
KE
.
Body composition and military performance—many things to many people
.
J Strength Cond Res
.
2012
;
26
(Supplement 2):
S87
S100
.

24

Ding
C
,
Chan
Z
,
Magkos
F
.
Lean, but not healthy: the ‘metabolically obese, normal-weight’ phenotype
.
Curr Opin Clin Nutr Metab Care
.
2016
;
19
(
6
):
408
417
.

25

Foulis
SA
,
Hughes
JM
,
Friedl
KE
.
New concerns about military recruits with metabolic obesity but normal weight (“skinny fat”)
.
Obesity
.
2020
;
28
(
2
):
223
.

26

Potter
AW
,
Soto
LD
,
Friedl
KE
.
Body composition of extreme performers in the US marine corps
.
BMJ Mil Health
.
Published online November 2, 2022. Doi: 10.1136/military-2022-002189

27

Kraemer
WJ
,
Caldwell
LK
,
Post
EM
, et al.
Body composition in elite strongman competitors
.
J Strength Cond Res
.
2020
;
34
(
12
):
3326
3330
.

28

Bosch
TA
,
Carbuhn
A
,
Stanforth
PR
,
Oliver
JM
,
Keller
KA
,
Dengel
DR
.
Body composition and bone mineral density of division 1 collegiate football players, a consortium of college athlete research (C-CAR) study
.
J Strength Cond Res
.
2019
;
33
(
5
):
1339
1346
.

29

Sedlmeier
AM
,
Baumeister
SE
,
Weber
A
, et al.
Relation of body fat mass and fat-free mass to total mortality: results from 7 prospective cohort studies
.
Am J Clin Nutr
.
2021
;
113
(
3
):
639
646
.

Abbreviations

     
  • %BF

    percent body fat

  •  
  • BMI

    body mass index

  •  
  • DXA

    dual-energy x-ray absorptiometry

  •  
  • MetSyn

    metabolic syndrome

  •  
  • MF-BIA

    multifrequency bioelectrical impedance

  •  
  • NHANES

    National Health and Nutrition Examination Survey

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. See the journal About page for additional terms.