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Predicted versus measured thoracic gas volume in estimating body fat percentage among male college athletes and sedentary controls: A cross-sectional observational study
*Corresponding author: Simran Obhrai, MYAS-GNDU Department of Sports Sciences and Medicine, Guru Nanak Dev University, Amritsar, Punjab, India. simranobhrai.sj@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Obhrai S, Ghole SS, Shenoy S. Predicted versus measured thoracic gas volume in estimating body fat percentage among male college athletes and sedentary controls: A cross-sectional observational study. Indian J Physiol Pharmacol. doi: 10.25259/IJPP_531_2025
Abstract
Objectives:
Despite established discrepancies between predicted thoracic gas volume (TGVp) and measured thoracic gas volume (TGVm) in Body Composition Pod (BOD POD) assessments, the influence of training modality on measurement accuracy remains unclear. This study examined whether TGVp provides an accurate body fat percentage (BF%) estimation compared to TGVm across different training modalities.
Materials and Methods:
In this cross-sectional study, sixty-six male participants (age 20–25 years) were categorized into three groups: sedentary individuals, anaerobic athletes (sprinters, weightlifters, throwers), and intermittent sport athletes (football, basketball, hockey) (n = 22 each). Body composition was assessed via Air Displacement Plethysmography (ADP; BOD POD), with BF% calculated using both TGVp (demographic equations) and TGVm (direct measurement). Agreement patterns were evaluated using Bland–Altman analysis and proportional bias assessments.
Results:
TGVm significantly exceeded TGVp in sedentary individuals (4.67 ± 0.16 vs. 4.13 ± 0.21 L, d = −3.64), anaerobic athletes (5.02 ± 0.44 vs. 4.60 ± 0.52 L, d = −3.24), and intermittent sport athletes (6.27 ± 1.10 vs. 5.98 ± 0.92 L, d = −0.66; all p ≤ 0.006). Consequently, TGVp significantly underestimated BF% by 2.12 ± 0.44% in sedentary, 2.52 ± 1.31% in anaerobic, and 2.02 ± 0.65% in intermittent sport athletes (all p < 0.001). Bland–Altman analysis revealed proportional bias in anaerobic athletes for TGV (β = 0.158, p = 0.005) and strong proportional bias in intermittent sport athletes for BF% (β = 0.510, R2 = 0.839, p < 0.001), indicating that measurement errors vary with the magnitude of the measurement rather than remaining constant.
Conclusion:
TGVp systematically underestimates BF% by 2.0–2.5% across all populations. Furthermore, the presence of proportional bias in athletic groups precludes the use of simple correction factors. Direct TGV measurement is essential for accurate body composition assessment, particularly in athletes, where training-induced adaptations create variable and unpredictable prediction errors.
Keywords
Air displacement plethysmography
BOD POD
Body composition
Lung volume
Thoracic gas volume
INTRODUCTION
Body composition assessment is essential in sports science, and accurately measuring body fat percentage (BF%) is crucial for optimising athletic performance, training plans and monitoring health. The fat-to-lean mass ratio in athletic populations directly correlates with performance outcomes, though optimal ratios vary considerably across sports disciplines.[1,2] In competitive sports, accurate body composition measurement is particularly important, as even minor measurement errors can significantly impact training decisions, performance evaluation and athlete classification, especially when athletes are near critical thresholds for weight categories or team selection.
Air displacement plethysmography (ADP) via the Body Composition Pod (BOD POD) has become a widely adopted body composition assessment tool because it is non-invasive, rapid, and demonstrates high test-retest reliability compared with conventional methods such as hydrostatic weighing and skinfold measurements.[3,4] The BOD POD determines body composition by measuring body volume through air displacement in a sealed chamber, calculating body density and subsequently estimating BF%. However, the accuracy of these calculations critically depends on thoracic gas volume (TGV), which represents the air volume within the lungs and airways during measurement. TGV can be either predicted using demographic equations (TGVp) based on age, sex, height and weight or directly measured (TGVm) through spirometric assessment during controlled breathing manoeuvres against an occluded airway.
Previous studies have consistently demonstrated substantial discrepancies between these methods, with TGVm exceeding TGVp, particularly in athletic populations. Miller et al.[5] reported that male college athletes had significantly higher TGVm than TGVp (4.59 ± 0.88 L vs. 4.11 ± 0.45 L, p < 0.001), leading to systematic BF% underestimation of 1.2 ± 1.8% when using predicted values. Similarly, Ducharme et al.[6] found that TGVp underestimated TGVm by 0.49 ± 0.7 L in trained men, resulting in BF% underestimation of 1.3 ± 1.8%. These findings suggest that prediction equations developed on general populations may not adequately account for training-induced respiratory adaptations in athletes.
Despite these established discrepancies, critical gaps remain in understanding how different training modalities influence TGV prediction accuracy. Most existing studies have either examined heterogeneous athletic populations without distinguishing between training types or focused on single sports.[6-9] This limitation is significant because different training modalities induce distinct physiological adaptations. Anaerobic training, encompassing sports such as sprinting, weightlifting and throwing events, primarily promotes muscular hypertrophy, phosphocreatine system development and neuromuscular power adaptations.[10,11] In contrast, intermittent sports requiring repeated high-intensity efforts with recovery periods, such as football, basketball and hockey, induce mixed adaptations including enhanced aerobic capacity, anaerobic power and specific respiratory muscle endurance.[12] These differential adaptations likely result in varying patterns of lung volume changes that could affect prediction equation accuracy differently across athlete types.
Furthermore, no studies have systematically examined whether measurement errors exhibit constant bias (consistent underestimation across all values) or proportional bias (errors that vary with measurement magnitude) across different training modalities. This distinction has important practical implications: constant bias might be correctable with simple adjustment factors, while proportional bias would require measurement-specific corrections or mandate direct TGV measurement for accurate assessment.
Therefore, this study aimed to determine whether TGVp provides accurate BF% estimation compared to TGVm in sedentary individuals, anaerobic athletes and intermittent sport athletes using BOD POD measurements. Specifically, we examined: (1) The magnitude of difference between TGVp and TGVm across groups; (2) The resulting impact on BF% estimation accuracy; and (3) Whether measurement errors demonstrate constant or proportional bias patterns. We hypothesised that TGVm would significantly exceed TGVp in both athletic groups, with both the magnitude and pattern of difference varying by training modality. We further hypothesised that athletic populations would exhibit proportional bias, where prediction equation accuracy deteriorates as physiological adaptations increasingly deviate from population norms. These findings will provide evidence-based guidance for optimising body composition assessment protocols and identifying when direct TGV measurement is essential versus when predicted values might suffice for different populations.
MATERIALS AND METHODS
Study design and participants
This cross-sectional observational study recruited 66 healthy male participants aged 20–25 years from a university population between September 2024 and March 2025. Participants were stratified into three groups (n = 22 each) based on training status and sport participation: sedentary individuals, anaerobic athletes and intermittent sport athletes.
The sedentary group comprised individuals with no structured exercise participation for at least 12 months before testing and self-reported physical activity levels below 150 min/week of moderate-intensity exercise. These participants were recruited from academic programs with no sports requirements.
Athletes were classified based on their primary sport’s metabolic demands. The anaerobic group (n = 22) included athletes whose sports demand predominantly phosphocreatine and glycolytic energy systems: sprinters (100–400 m track events, n = 9), weightlifters (Olympic and powerlifting, n = 10) and javelin throwers (n = 3). The intermittent sport group (n = 22) comprised athletes from team sports requiring repeated high-intensity efforts interspersed with recovery periods: football (n = 9), basketball (n = 5) and field hockey (n = 8). These sports typically involve mixed energy system contributions with 60–80% aerobic and 20–40% anaerobic metabolism during competition.
All athletes met the following inclusion criteria: (1) Minimum 2 years of structured training in their respective sport; (2) Current training volume of 8–12 h/week (2–3 h/day, 4–5 days/week); (3) Active competitive participation at collegiate level or above; and (4) No injury preventing normal training for the past 3 months. Exclusion criteria for all participants included: history of pulmonary or cardiovascular disease, current respiratory infection, claustrophobia (which could affect BOD POD testing), use of medications affecting metabolism or body composition and body mass exceeding 136 kg (BOD POD weight limit).
Sample size determination
A priori power analysis was conducted using G*Power 3.0.10 with the primary outcome of TGV difference (TGVm−TGVp). Based on a previous study Miller et al.,[5] who reported a mean TGV difference of 0.48 L (d = 0.77) in male college athletes, we conservatively assumed a medium effect size (d = 0.5) to account for potential variability across different training modalities. With α = 0.05 and power = 0.95, 22 participants per group were required for within-group paired t-tests. This sample size also provided 95% power for between-group one-way Analysis of Variance (ANOVA) comparisons (f = 0.5, three groups) and >90% power for post hoc tests detecting large effects, though analyses may be underpowered for small to medium between-group differences.
Ethical considerations
The study protocol was approved by the Institutional Ethics Committee (No. 2723/HG, dated 13 May 2024) in accordance with the Indian Council of Medical Research guidelines[13] and the Declaration of Helsinki.[14] All participants provided written informed consent after receiving comprehensive information about study procedures, potential risks and benefits, data confidentiality measures and their right to withdraw at any time without penalty. Participant data were anonymised using numerical codes and stored in password-protected databases accessible only to the research team.
Body composition assessment
Testing was conducted in the Human Performance Laboratory between 9:00 and 11:00 AM to minimise circadian variation. Upon arrival, participants confirmed adherence to pre-test requirements: ≥2-h fast from food and exercise (water permitted), no alcohol or caffeine for 12 h and normal hydration status. Non-compliant participants were rescheduled. Height was measured to the nearest 0.1 cm using a wall-mounted stadiometer.
The BOD POD (COSMED, Rome, Italy) was calibrated before each testing session using the standard 50.28-L calibration cylinder according to manufacturer’s specifications. Room temperature was maintained at 21–25°C with relative humidity <60%. Participants wore minimal, form-fitting swimwear or compression shorts and a Lycra swim cap to minimise air trapped in clothing and hair. Body mass was measured using the BOD POD’s integrated electronic scale (precision: ±0.01 kg, range: 0–250 kg).
Each participant underwent two assessment protocols in fixed order:
Protocol 1 (TGVp): Body volume was measured using standard BOD POD procedures. Two consecutive measurements were performed; if these differed by >150 mL, a third measurement was obtained. The mean of the two closest measurements was used for analysis. Body density was calculated using body mass and volume, and BF% was estimated using the Siri equation (BF% = [495/body density]−450) with TGV predicted from demographic equations incorporated in the BOD POD software.
Protocol 2 (TGVm): Identical body volume measurements were performed. Following volume assessment, participants performed the direct TGV measurement procedure. While seated in the BOD POD, participants breathed normally through a disposable breathing tube with a nose clip applied. Following instructions displayed on the interior monitor, they performed a breathing manoeuvre at functional residual capacity (mid-exhalation): Three gentle panting breaths (huffing) at approximately 0.5– 1.0 Hz frequency against an occluded airway for 3 s. The BOD POD software calculated TGV from airway pressure changes and known chamber pressure-volume relationships using Boyle’s Law. If the measurement was flagged as unacceptable by the software (coefficient of variation >5% or irregular breathing pattern detected), the procedure was repeated up to five attempts. The measurement was used to recalculate body density and BF% using the same Siri equation but with measured TGV values.
Statistical analysis
Data were analysed using IBM Statistical Package for the Social Sciences Statistics version 26.0 (IBM Corp., Armonk, NY, USA). All continuous variables were assessed for normality using the Shapiro–Wilk test and visual inspection of Q-Q plots. Homogeneity of variance was tested using Levene’s test. Data are presented as mean ± standard deviation.
Within-group comparisons between TGVp and TGVm (and corresponding BF% values) were performed using paired-samples t-tests. Cohen’s d effect sizes were calculated as mean difference divided by the standard deviation of differences, with interpretations of 0.2 = small, 0.5 = medium, 0.8 = large and >1.3 = very large effect.
Between-group comparisons were conducted using one-way ANOVA for normally distributed variables with homogeneous variances. For variables violating homogeneity assumptions (TGV measures), Welch’s ANOVA was employed with Games–Howell post hoc tests, which do not assume equal variances. Effect sizes for ANOVA were reported as partial eta-squared (η2p) with interpretations of 0.01 = small, 0.06 = medium and 0.14 = large effect.
Agreement analysis between TGVp and TGVm was evaluated using Bland–Altman methodology. For each group, mean bias (TGVp−TGVm) and 95% limits of agreement (mean bias ± 1.96 × standard deviation of differences) were calculated. Proportional bias was assessed using linear regression of the difference (TGVp−TGVm) against the mean ([TGVp+TGVm]/2), with significant regression coefficients (p < 0.05) indicating proportional bias.
Sensitivity analyses included non-parametric Kruskal– Wallis tests for between-group comparisons when normality assumptions were violated, with Bonferroni-adjusted pairwise comparisons. To control for Type I error inflation from multiple comparisons, the Bonferroni correction was applied to the primary outcomes (adjusted α = 0.017 for three group comparisons).
Statistical significance was set at p < 0.05 for all tests. Assumptions of statistical tests were verified and reported when violations occurred, with appropriate alternative analyses employed.
RESULTS
Participant characteristics
Sixty-six male participants completed the study protocol with no dropouts or missing data. Baseline characteristics are presented in Table 1. Groups were similar in age (p = 0.632) and height (p = 0.243). However, anaerobic athletes had significantly greater body mass (80.6 ± 8.5 kg) than both intermittent sport athletes (74.4 ± 10.1 kg) and sedentary individuals (69.6 ± 5.6 kg, p < 0.001). All athletes met the inclusion criteria of minimum 2 years of structured training experience and a current training volume of 8–12 h/week.
| Variable | Sedentary (n=22) | Anaerobic (n=22) | Intermittent (n=22) | p-value |
|---|---|---|---|---|
| Age (years) | 22.5±1.8 | 22.5±1.7 | 23.0±1.7 | 0.632 |
| Height (cm) | 174.5±6.3 | 175.8±3.2 | 177.4±7.1 | 0.243 |
| Weight (kg) | 69.6±5.6a | 80.6±8.5b | 74.4±10.1a | <0.001*** |
| BMI (kg/m2) | 22.8±1.4a | 26.1±2.3b | 23.6±2.8a | <0.001*** |
Statistical significance was set at p < 0.05 Data presented as mean ± standard deviation. p-values derived from one-way Analysis of Variance. Statistical significance denoted as: *** p < 0.001. Means in the same row with different superscript letters (a, b) are significantly different from each other (p < 0.05, Tukey Honestly significant difference post-hoc test). BMI: Body mass index.
Assumption testing and statistical approach
Shapiro–Wilk tests revealed violations of normality for TGVm in the intermittent (W = 0.782, p < 0.001) and anaerobic groups (W = 0.853, p = 0.004). Levene’s test indicated heterogeneous variances for TGV measures (TGVp: F[2,63] = 28.68, p < 0.001; TGVm: F[2,63] = 40.93, p < 0.001) but homogeneous variances for BF%. Given the equal sample sizes and robustness of t-tests to moderate violations, parametric analyses were retained with Welch’s correction applied for between-group TGV comparisons.
Within-group comparisons: TGV differences
Paired t-tests revealed significant underestimation of TGVm by TGVp across all groups [Table 2]. The sedentary group showed the largest absolute difference (−0.54 ± 0.15 L, t(21) = −17.05, p < 0.001, Cohen’s d = −3.64), followed by the anaerobic group (−0.42 ± 0.13 L, t(21) = −15.20, p < 0.001, d = −3.24). The intermittent sport group demonstrated the smallest but still significant difference (−0.29 ± 0.44 L, t[21] = −3.08, p = 0.006, d = −0.66).
| Group | TGVp (L) | TGVm (L) | Mean Diff (L) | 95% CI | t | p-value | Cohen’s d |
|---|---|---|---|---|---|---|---|
| Sedentary | 4.13±0.21 | 4.67±0.16 | −0.54±0.15 | −0.60–−0.47 | −17.05 | <0.001*** | −3.64 |
| Anaerobic | 4.60±0.52 | 5.02±0.44 | −0.42±0.13 | −0.48–−0.36 | −15.20 | <0.001*** | −3.24 |
| Intermittent | 5.98±0.92 | 6.27±1.10 | −0.29±0.44 | −0.48–−0.09 | −3.08 | 0.006** | −0.66 |
Statistical significance was set at p < 0.05. Data presented as mean ± standard deviation. TGVp: Predicted thoracic gas volume; TGVm: Measured thoracic gas volume; CI: Confidence interval. Mean difference = TGVp − TGVm (negative values indicate underestimation by the predicted method). Statistics from paired-samples t-tests (df = 21 for all groups). Statistical significance denoted as: **p < 0.01, ***p < 0.001.
Within-group comparisons: BF%
The systematic underestimation of TGV translated to a substantial underestimation of BF% across all groups [Table 3]. All groups showed very large effect sizes for BF% differences, with the sedentary group demonstrating the largest effect (difference: −2.12 ± 0.44%, t[21] = −22.80, p < 0.001, d = −4.86). The anaerobic group showed −2.52 ± 1.31% difference (t[21] = −9.02, p < 0.001, d = −1.92), while the intermittent sport group showed −2.02 ± 0.65% difference (t[21] = −14.58, p < 0.001, d = −3.11).
| Group | BFp (%) | BFm (%) | Mean difference (%) | 95% CI | t | p-value | Cohen’s d |
|---|---|---|---|---|---|---|---|
| Sedentary | 17.8±1.2 | 19.9±1.1 | −2.12±0.44 | −2.32–−1.93 | −22.80 | <0.001*** | −4.86 |
| Anaerobic | 9.7±1.3 | 12.2±1.0 | −2.52±1.31 | −3.10–−1.94 | −9.02 | <0.001*** | −1.92 |
| Intermittent | 9.3±1.5 | 11.4±0.9 | −2.02±0.65 | −2.31– −1.73 | −14.58 | <0.001*** | −3.11 |
Statistical significance was set at p < 0.05. Data presented as mean ± standard deviation. BFp: Body fat percentage calculated using predicted TGV; BFm: Body fat percentage calculated using measured TGV; CI: Confidence interval; TGV: Thoracic gas volume. Mean difference = BFp − BFm (negative values indicate underestimation by the predicted method). Statistics from paired-samples t-tests (df = 21 for all groups). Statistical significance denoted as: *** p < 0.001.
Between-group comparisons
Welch’s ANOVA revealed significant between-group differences for both TGV measures and BF% variables [Table 4] (TGVp: Welch’s F[2,33.19] = 46.57, p < 0.001; TGVm: Welch’s F[2,31.69] = 27.22, p < 0.001; BF% predicted: Welch’s F[2,41.78] = 301.56, p < 0.001; BF% measured: Welch’s F[2,41.62] = 461.47, p < 0.001).
| Variable | Standard ANOVA | Welch’s ANOVA | |||||
|---|---|---|---|---|---|---|---|
| F (2,63) | p | η2p | Welch’s F | df1, df2 | p-value | ||
| TGV predicted | 52.96 | <0.001 | 0.627 | 46.57 | 2, 33.19 | <0.001*** | |
| TGV measured | 32.47 | <0.001 | 0.507 | 27.22 | 2, 31.69 | <0.001*** | |
| BF% predicted | 279.71 | <0.001 | 0.899 | 301.56 | 2, 41.78 | <0.001*** | |
| BF% measured | 490.60 | <0.001 | 0.940 | 461.47 | 2, 41.62 | <0.001*** | |
Statistical significance was set at p < 0.05. η2p: Partial eta squared. Welch’s ANOVA was performed due to violation of homogeneity of variances (Levene’s test, p < 0.001). Standard ANOVA results are provided for comparison; Welch’s ANOVA values were used for primary interpretation. Statistical significance denoted as: *** p < 0.001. ANOVA: Analysis of Variance; TGV: Thoracic gas volume; BF%: Body fat percentage.
Bland–Altman agreement analysis
Furthermore, post-hoc pairwise comparisons confirmed significant differences in TGVm and BFm between all groups [Supplementary Table 1]. After- Bland-Altman Agreement Analysis Agreement analysis revealed varying patterns across groups [Table 5; complete Bland-Altman plots in Supplementary Figures 1-2]. The sedentary group showed the narrowest 95% limits of agreement for TGV (−0.83–−0.25 L) with no proportional bias (β=0.334, p = 0.070). The anaerobic group demonstrated significant proportional bias for TGV (β = 0.158, p = 0.005), indicating increasing error with larger lung volumes. Most notably, the intermittent sport group showed significant proportional bias for both TGV (β = −0.191, p = 0.045) and strong proportional bias for BF% (β = 0.510, p < 0.001, R2 = 0.839).
| Group | Measure | (Predicted−Measured | Proportional bias test | |||
|---|---|---|---|---|---|---|
| Mean bias±SD | 95% LoA | β | R2 | p-value | ||
| Sedentary | TGV (L) | −0.54±0.15 | −0.83–−0.25 | 0.334 | 0.154 | 0.070 |
| BF (%) | −2.12±0.44 | −2.98–−1.26 | 0.134 | 0.120 | 0.114 | |
| Anaerobic | TGV (L) | −0.42±0.13 | −0.68–−0.17 | 0.158 | 0.335 | 0.005** |
| BF (%) | −2.52±1.31 | −5.09–0.05 | 0.347 | 0.072 | 0.227 | |
| Intermittent | TGV (L) | −0.29±0.44 | −1.15–0.57 | −0.191 | 0.186 | 0.045** |
| BF (%) | −2.02±0.65 | −3.29–−0.75 | 0.510 | 0.839 | <0.001*** | |
Statistical significance was set at p < 0.05. 95% LoA = 95% Limits of Agreement (Mean bias ± 1.96×SD), SD: Standard deviation, β = regression coefficient from Bland-Altman regression analysis, Statistical significance denoted as: ** p < 0.01, *** p < 0.001, indicates measurement error varies with magnitude.
Relationship between TGV and BF% errors
Pearson correlations between TGV_Diff and BF_Diff were non-significant across all groups (sedentary: r = 0.175, p = 0.437; anaerobic: r = 0.172, p = 0.445; intermittent: r = 0.226, p = 0.312), indicating that the magnitude of TGV prediction error did not directly predict the magnitude of BF% error at the individual level.
Sensitivity analysis
Non-parametric Kruskal–Wallis tests confirmed significant between-group differences in TGV measurement discrepancies (H[2] = 10.61, p = 0.005). After Bonferroni correction, pairwise comparisons showed significant differences between intermittent and sedentary groups (p = 0.005) but no other pairs. Notably, while TGV errors varied significantly across groups, the resulting BF% errors did not differ significantly in non-parametric analysis (H[2] = 3.39, p = 0.184), suggesting that despite varying TGV prediction errors, the clinical impact on body fat assessment remains consistent across training modalities.
DISCUSSION
This study examined the accuracy of TGVm versus TGVp in body composition assessment across different training modalities. Our primary finding was that TGVp systematically underestimated TGVm in all groups, leading to a clinically significant BF% underestimation of 2.0–2.5%. However, the relationship between training modality and prediction accuracy proved more complex than anticipated, with distinct patterns of constant versus proportional bias emerging across groups. These findings have important implications for body composition assessment protocols in athletic populations.
A particularly striking discovery was the presence of proportional bias in athletic groups but not in sedentary individuals. The sedentary group exhibited constant bias across all measurement ranges (β = 0.334, p = 0.070), suggesting that a simple correction factor might suffice for this population. In contrast, the anaerobic group demonstrated significant proportional bias for TGV (β = 0.158, p = 0.005, R2 = 0.335), indicating that prediction error increased with larger lung volumes. This pattern suggests that as anaerobic athletes develop greater lung capacity, potentially through training-induced respiratory muscle strengthening, the prediction equations become progressively less accurate.
Most remarkably, the intermittent sport group showed complex bias patterns: negative proportional bias for TGV (β = −0.191, p = 0.045) but strong positive proportional bias for BF% (β = 0.510, p < 0.001, R2 = 0.839). The negative TGV coefficient represents an unexpected phenomenon where prediction accuracy actually improved for athletes with larger lung volumes. We hypothesise this may reflect sport-specific adaptations in intermittent athletes that coincidentally align with prediction model assumptions at higher lung volumes. However, the strong proportional bias in BF% indicates that, despite this apparent TGV improvement, the error in final body composition estimates varies dramatically across the body fat spectrum. Athletes with lower body fat show different prediction errors than those with higher body fat, potentially leading to misclassification near critical thresholds for team selection or weight categories.
The differential bias patterns across training modalities likely reflect distinct physiological adaptations. Anaerobic training induces adaptations that may influence TGV measurement accuracy through mechanisms that remain incompletely understood.[15] The proportional bias observed in anaerobic athletes (β = 0.158, p = 0.005) suggests that prediction errors increase with larger lung volumes, possibly reflecting training-induced changes in respiratory muscle function or breathing patterns not accounted for in standard prediction equations. However, the specific physiological mechanisms underlying this bias require further investigation. These changes may affect the pressure–volume relationships assumed by prediction equations, which were developed using general populations. The proportional nature of the bias suggests these effects amplify with greater muscular development.
Intermittent sport athletes demonstrated the highest absolute TGVm values (6.27 ± 1.10 L) among the three groups. This finding aligns with research showing that sports requiring repeated high-intensity efforts can induce substantial respiratory adaptations, including enhanced respiratory muscle endurance and increased lung volumes.[12] The mixed metabolic demands of sports such as basketball, football and hockey, combining sustained moderate activity with repeated sprints, may stimulate unique respiratory adaptations not captured by traditional aerobic-anaerobic classifications. The large standard deviation in this group (±1.10 L) suggests considerable heterogeneity, possibly reflecting positional differences, varying playing time or individual training emphasis.
Our findings both confirm and extend previous research. The overall magnitude of TGV underestimation (0.29–0.54 L) and resulting BF% errors (2.0–2.5%) align with previous findings.[5,6] However, our training-modality-specific analysis reveals previously unrecognised complexity. Wagner et al.[9] noted that prediction errors could vary substantially among individuals, our study is the first to demonstrate systematic proportional bias patterns that differ by training type.
The finding that all groups, including sedentary individuals, showed significant BF% underestimation challenges the assumption that prediction equations work adequately for non-athletic populations. Even our sedentary group, presumably most similar to the populations used to develop prediction equations, showed very large effect sizes (Cohen’s d = −3.64 for TGV, d = −4.86 for BF%). This suggests fundamental limitations in current prediction models that extend beyond athletic adaptations.
The presence of proportional bias has critical implications for practitioners. For anaerobic athletes and especially intermittent sport athletes, no single correction factor can address prediction errors across all individuals. The strong proportional bias in BF% for intermittent athletes (R2 = 0.839) means errors vary predictably but dramatically with body composition level. An athlete with 8% body fat might have a different magnitude of error than a teammate with 15% body fat, despite identical measurement protocols.
These findings strongly support universal adoption of measured TGV for individual athlete assessment. The magnitude of error we observed (2.0–2.5% BF% underestimation) exceeds the typical measurement precision of BOD POD itself (±1–2%), effectively doubling the potential error in body composition assessment. This degree of inaccuracy has substantial practical implications across multiple domains of sports medicine and performance management. In clinical settings, such errors could lead to misclassification of athletes relative to body composition thresholds, potentially missing cases of relative energy deficiency in sport or inappropriately clearing athletes with suboptimal body composition. For weight-class sports, where athletes often manipulate body composition to compete in specific categories, a 2–2.5% underestimation could mask dangerous weight-cutting practices or result in suboptimal category selection. The impact extends to rehabilitation contexts, where accurate body composition monitoring is essential for tracking muscle mass preservation during injury recovery and determining readiness for return to play. Furthermore, coaches and sports scientists relying on body composition trends to evaluate training effectiveness may draw incorrect conclusions about program efficacy, potentially leading to unnecessary or counterproductive training modifications. The consistency of BF% underestimation across all groups, despite varying mechanisms of error as confirmed by our Kruskal–Wallis analysis (H[2] = 3.39, p = 0.184), underscores that this is not merely a concern for elite athletes but represents a systematic measurement issue affecting all populations assessed with predicted TGV.
Our use of Welch’s ANOVA and Games–Howell post hoc tests to address heterogeneous variances strengthens our conclusions. The violation of homogeneity assumptions itself provides valuable information-the greater variance in TGV measures among athletic groups (particularly intermittent athletes) suggests that training induces not just mean changes but also increased individual variability in lung adaptations. This heterogeneity further supports individualised measurement rather than population-based predictions.[3]
The lack of significant correlation between TGV errors and BF% errors within groups (all r < 0.23, p > 0.31) indicates that the relationship between lung volume prediction error and body composition error is complex and likely mediated by body density calculations. This finding underscores that even small TGV errors can have unpredictable effects on final BF% estimates.
Several limitations of the paper should also be discussed. First, our sample comprised only college-aged males, limiting generalisability to females, younger athletes or elite competitors. Sex differences in body composition and respiratory function may yield different bias patterns. Second, while all athletes met minimum training criteria (≥2 years, 8–12 h/week), we lacked detailed training history data that might explain within-group variability. Third, our cross-sectional design cannot determine whether bias patterns change with training progression or detraining.
In addition, while we identified proportional bias, we cannot definitively explain the physiological mechanisms. The negative proportional bias in intermittent athletes’ TGV remains particularly puzzling and warrants further investigation. Finally, we compared predicted versus measured TGV but did not validate against a four-compartment model, meaning our ‘accuracy’ assessments are relative rather than absolute.
Our findings suggest several research priorities. The development of training-specific prediction equations could improve accuracy, though our proportional bias results suggest simple adjustments may be insufficient. Machine learning approaches incorporating multiple anthropometric and training variables might better capture the complex relationships we observed. Longitudinal studies tracking athletes through training cycles could identify when prediction equations begin failing and whether bias patterns are stable within individuals.
Investigation of sex differences in training-related bias patterns is essential for extending these findings to female athletes. Similarly, examining elite athletes would determine whether bias patterns intensify with higher training volumes or reach a plateau. Understanding the physiological basis for negative proportional bias in intermittent athletes could reveal important insights about respiratory adaptations in team sports.
CONCLUSION
This study demonstrates that the relationship between training modality and TGV prediction accuracy is more complex than previously recognised, with distinct patterns of constant and proportional bias emerging across different athletic populations. While TGVp consistently underestimated TGVm by 0.29–0.54 L across all groups, leading to clinically significant BF% errors of 2.0–2.5%, the nature of these errors varied substantially. Sedentary individuals showed constant bias, anaerobic athletes demonstrated proportional bias in TGV, and intermittent sport athletes exhibited strong proportional bias in BF% (R2 = 0.839). These findings indicate that predicted TGV should not be used for individual body composition assessment in any population, but particularly not in athletes, where proportional bias makes corrections more complicated. Direct measurement of TGV is essential for accurate body composition assessment, regardless of training status or apparent prediction accuracy.
Ethical approval:
The research/study was approved by the Institutional Review Board at Guru Nanak Dev University, approval number 2723/HG, dated 13th May 2024.
Declaration of participant consent:
The authors certify that they have obtained all appropriate informed consent forms from the participants. The participants have given consent for their anonymized data to be reported in the journal. It has been communicated that names and initials will not be published and efforts will be made to maintain confidentiality.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript, and no images were manipulated using AI.
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