Skip to main content
Journal of Physical Therapy Science logoLink to Journal of Physical Therapy Science
. 2025 Feb 1;37(2):77–83. doi: 10.1589/jpts.37.77

Relationship between 10 repetition maximum for chest press, leg press, and muscle mass measured using bioelectrical impedance analysis in healthy young adults

Hotaka Sugimoto 1,2, Masahito Taga 2,3, Kio Fukushima 2,4, Yuto Akashi 2,5, Kimito Momose 6,*
PMCID: PMC11787865  PMID: 39902303

Abstract

[Purpose] This study aimed to examine the relationship between bioelectrical impedance analysis measurements and 10 repetition maximum for chest press and leg press, and to develop a regression model to determine if bioelectrical impedance analysis can predict 10 repetition maximum in healthy young adults. [Participants and Methods] Ninety-four healthy adults participated in the study. Correlations between 10 repetition maximum and bioelectrical impedance analysis measurements were calculated, and simple linear regression was performed using bioelectrical impedance analysis measurements as independent variables to develop 10 repetition maximum prediction models. [Results] Significant correlations were found between 10 repetition maximum and bioelectrical impedance analysis measurements. The regression models for 10 repetition maximum for chest press based on upper limb muscle mass, skeletal muscle mass, and skeletal muscle mass index were Y=16.40X−13.27, Y=3.81X−36.78, and Y=20.51X−81.27, respectively. The regression models for 10 repetition maximum for leg press based on lower limb muscle mass, skeletal muscle mass, and skeletal muscle mass index were Y=12.60X−3.21, Y=8.09X−24.39, and Y=43.68X−119.60, respectively. [Conclusion] These findings may contribute to developing a safe and efficient method for measuring 10 repetition maximum, which can be useful in resistance training prescriptions.

Keywords: Muscle strength assessment, 10 repetition maximum, Bioelectrical impedance analysis

INTRODUCTION

Ten repetition maximum weight (10RM) is defined as the maximum weight that can be lifted in ten repetitions and is a loading intensity commonly used in clinical practice. In contrast, one-repetition maximum weight (1RM) is the most widely used strength index. When prescribing resistance training, load intensity is typically determined based on the expected number of repetitions at a given percentage of 1RM (%1RM)1). However, previous research has shown variability in the number of repetitions performed at load intensities derived from %1RM2). For example, the estimated number of repetitions at 85% 1RM in the leg press is 10.69, with a 95% confidence interval ranging from 6.98 to 16.37, indicating that overestimation or underestimation may occur when load intensity is indirectly determined from %1RM. Directly measuring load intensity with the 10RM test may provide a more accurate load than indirect estimation from %1RM. Furthermore, 1RM tests are time-consuming and involve heavy weights, which can place significant strain on muscles and joints, increasing the risk of injury for beginners, older adults, and patients. This has led to discussions on methodologies for indirectly estimating 1RM using alternative assessment measures3,4,5,6,7). However, estimated 1RM values naturally contain some degree of error, and furthermore, as mentioned above, using these estimates to determine loading intensity in %1RM can lead to large variations depending on the actual number of repetitions performed. Consequently, developing methodologies to estimate 10RM through other means could be clinically beneficial.

Bioelectrical impedance analysis (BIA) is a method for estimating muscle mass by applying a weak current through electrodes on the body and has gained wide usage in clinical and research settings. Since muscle strength is influenced by both morphological and neural factors8), evaluating morphological factors may be an effective means of assessing muscle function. BIA provides a safe and relatively low-cost estimation of muscle mass, offering a valid assessment compared to magnetic resonance imaging (MRI), computed tomography (CT), and dual-energy X-ray absorptiometry (DEXA). While MRI9,10,11), CT12), and DEXA13,14,15) can also estimate muscle mass with high accuracy, their clinical use is limited by time and equipment costs16, 17). Additionally, CT and DEXA pose restrictions due to radiation exposure16, 17). Therefore, it is necessary to clarify the relationship between BIA measurements and 10RM in order to develop a methodology for indirectly estimating 10RM using BIA.

Previous studies have reported significant relationships between BIA-measured values and muscle strength18,19,20). Sue et al. found significant positive correlations between dominant-leg skeletal muscle mass (SMM) and skeletal muscle index (SMI) measured by BIA and 1RM in the leg press (LP), suggesting the potential for predicting 1RM in the LP from BIA measurements7). However, no studies to date have investigated the relationship between BIA-measured values and 10RM. Thus, the aim of this study was to investigate the relationship between BIA measurements and 10RM for the chest press (CP) and LP in untrained, healthy young adults and to develop a regression model to determine whether BIA measurements can explain 10RM for CP and LP. Subgroup analyses were also conducted to examine correlations and assess the accuracy of sex differences in the BIA-based 10RM regression models.

PARTICIPANTS AND METHODS

Ninety-four healthy adults (43 males and 51 females) volunteered for this study. All participants were between 18 and 29 years of age and had not regularly performed resistance training in the past year. All participants were checked to ensure that they were not using performance-enhancing drugs or other medications that could affect the study and were not injured. This study (Approval No: 5556) was approved by the Ethics Committee, including approval for the use of data from a previous study that had been reviewed and approved by the Shinshu University Ethics Committee (Approval No: 4896). Written informed consent was obtained from all participants.

The test sessions lasted three days, with muscle mass measurement and familiarization on day 1, and 10RM testing on days 2 and 321). All tests were conducted by the same investigators.

All 10RM tests were first performed CP, and then for LP. In this study, a seated, weight-stacked chest press machine (TD-AR14, Hitachi Capital Corporation, Tokyo, Japan) was used for chest press exercises (Fig. 1), and a 45° leg press machine (LPM5-2, Super Sports Company, Osaka, Japan), with adjustable weight using detachable Olympic plates, was used for leg press exercises (Fig. 2). The participants completed familiarization sessions to receive instructions on proper techniques for CP and LP exercises22). The two exercises required the participants’ shoulders and buttocks to remain in contact with the bench during the exercise. The participants were instructed to start the CP with the elbows fully extended and move the handles until the elbows reached 90° before returning them to the original position. Similarly, the participants were instructed to start the LP with the knee fully extended and move the foot platform until the knees were at 90° before returning them to the original position. During the LP, the participants were instructed to keep their thighs parallel to each other. After a 5-minute warm-up on the ergometer and stretching of the major muscle groups, the participants performed three warm-up sets of 10 repetitions at approximately 50%, 70%, and 90% of the assumed 10RM. The load was then gradually increased until the participants could no longer lift in the correct form, allowing the participants to complete the 10RM test within five sets. Rest periods between the warm-up sets were 1 minute after the first set, 2 minutes after the second set, and 3 minutes after the third set, with a 3-minute rest between the main sets23). At least 48 h were left between the first and second 10RM tests, and the time periods were fixed as much as possible to minimize time zone effects. The representative value of the 10RM test was the largest of the two measurements.

Fig. 1.

Fig. 1.

Chest press machine.

Fig. 2.

Fig. 2.

Leg press machine.

Muscle mass was assessed using segmental multifrequency bioimpedance analysis (InBody 430; Biospace, Seoul, South Korea). The participants were instructed to refrain from eating and drinking for 4 h before the measurement and to avoid alcohol and strenuous exercise for 8 h prior to the measurement. Before the measurement, the participant’s palms and soles were wiped with alcohol cotton. Age, height, and sex, which were previously measured, were entered into the instrument. The participants then took a standing position on the platform of the instrument with bare feet and held the hand grips to perform the measurements. We used the upper limb muscle mass (ULMM), lower limb muscle mass (LLMM), SMM, and skeletal muscle mass index (SMI). ULMM was defined as the total muscle mass of the left and right upper limbs, and LLMM was defined as the total muscle mass of the left and right lower limbs. The SMI was calculated by dividing the SMM by the squared height.

Descriptive data were presented medians and interquartile ranges. As most measurement variables were not normally distributed (confirmed by the ShapiroWilk test), non-parametric statistical procedures were performed. Spearman’s rank correlation coefficient was used to analyze the relationship between the 10RM for CP and ULMM, SMM, and SMI, as well as the relationship between the 10RM for LP and LLMM, SMM, and SMI. Simple linear regression analysis was performed with BIA measurements as independent variables to create a 10RM regression model. The R2 and standard error (SE) parameters were used to assess the accuracy of the model. The significance level for all analyses was set at p<0.05. Statistical calculations were performed using R version 4.2.3.

RESULTS

One participant dropped out during the test sessions, leaving 93 participants for the analysis. The physical characteristics of the participants are listed in Table 1. There were significant differences in the physical characteristics other than age by sex.

Table 1. Participants’ characteristics.

Characteristic All participants (n=93) Male (n=42) Female (n=51)
Age, years 21.0 (20.0, 22.0) 21.0 (20.0, 22.8) 20.0 (20.0, 22.0)
Height, cm 165.0 (157.8, 169.4) 170.4 (166.2, 173.3)* 158.7 (155.1, 162.1)
Weight, kg 54.6 (50.3, 59.3) 59.0 (55.3, 61.6)* 51.3 (47.1, 54.9)
10RM for chest press, kg 55.0 (40.0, 70.0) 70.0 (66.2, 80.0)* 40.0 (35.0, 50.0)
10RM for leg press, kg 170.0 (145.0, 205.0) 205.0 (181.2, 228.8)* 145.0 (120.0, 167.5)
ULMM, kg 4.1 (3.4, 5.0) 5.1 (4.8, 5.5)* 3.5 (3.0, 3.8)
LLMM, kg 18.2 (15.3, 20.9) 16.1 (15.1, 17.4)* 11.9 (10.9, 12.9)
SMM, kg 23.9 (20.8, 27.7) 28.1 (27.0, 30.1)* 21.1 (19.0, 22.6)
SMI, kg/m2 6.7 (6.1, 7.4) 7.4 (7.1, 7.7)* 6.1 (5.7, 6.4)
Whole body fat mass, kg 11.1 (8.3, 13.0) 8.4 (5.9, 11.1)* 12.3 (10.6, 15.1)

Data are presented as median (inter-quartile range). *p<0.001 statistically significant difference from female values. 10RM: 10 repetition maximum; ULMM: upper limb muscle mass; LLMM: lower limb muscle mass; SMM: skeletal muscle mass; SMI: skeletal muscle mass index.

The relationships between the 10RM for CP, LP, and muscle mass are shown in Table 2. Significant correlation coefficients were found between the 10RM for CP and BIA measurements in all the participants. Significant correlation coefficients were also observed between the 10RM for LP and LLMM, SMM, and SMI in all the participants.

Table 2. Correlation analyses between BIA measurements and the 10RM for chest press and leg press.

All participants (n=93) Male (n=42) Female (n=51)
10RM for chest press

ULMM 0.90** 0.61** 0.71**
SMM 0.89** 0.56** 0.69**
SMI 0.90** 0.67** 0.69**

10RM for leg press

LLMM 0.75** 0.53** 0.43*
SMM 0.81** 0.72** 0.56**
SMI 0.83** 0.80** 0.56**

*p<0.01, **p<0.001. 10RM: 10 repetition maximum; ULMM: upper limb muscle mass; LLMM: lower limb muscle mass; SMM: skeletal muscle mass; SMI: skeletal muscle mass index.

Table 3 presents the results of the simple linear regression analysis. The R2 values of the regression model for 10RM for CP using ULMM, SMM, and SMI in all participants were 0.80 (SE: 0.86, p<0.001), 0.77 (SE: 0.22, p<0.001) and 0.79 (SE: 1.11, p<0.001), respectively. In the 10RM regression model that analyzed sex, the R2 values for males were 0.44 (SE: 2.39, p<0.001) for ULMM, 0.33 (SE: 0.63, p<0.001) for SMM and 0.45 (SE: 3.04, p<0.001) for SMI. In females, the R2 values were 0.52 (SE: 1.80, p<0.001) for ULMM, 0.48 (SE: 0.47, p<0.001) for SMM and 0.48 (SE: 2.18, p<0.001) for SMI. Next, the R2 values of the regression model for 10RM for LP using LLMM, SMM, and SMI in all participants were 0.55 (SE: 1.20, p<0.001), 0.64 (SE: 0.63, p<0.001) and 0.66 (SE: 3.27, p<0.001), respectively. In the 10RM regression model that analyzed sex, the R2 values for males were 0.29 (SE: 3.10, p<0.001) for ULMM, 0.51 (SE: 1.51, p<0.001) for SMM and 0.55 (SE: 7.66, p<0.001) for SMI. In females, the R2 values were 0.18 (SE: 3.02, p=0.002) for ULMM, 0.29 (SE: 1.79, p<0.001) for SMM and 0.32 (SE: 8.11, p<0.001) for SMI.

Table 3. Regression models of the 10RM for chest press and leg press using bioelectrical impedance analysis (BIA) measurements.

Dependent variable Regression model R2 SE 95% CI p-value

Lower Upper
The 10RM for chest press

All participants ULMM Y=16.40X−13.27 0.80 0.86 14.68 18.11 **
(n=93) SMM Y=3.81X−36.78 0.77 0.22 3.38 4.24 **
SMI Y=20.51X−81.27 0.79 1.11 18.31 22.70 **
Male (n=42) ULMM Y=13.27X+4.42 0.44 2.39 8.45 18.09 **
SMM Y=2.82X−7.21 0.33 0.63 1.54 4.10 **
SMI Y=17.40X−56.39 0.45 3.04 11.26 23.54 **
Female (n=51) ULMM Y=13.02X−2.90 0.52 1.80 9.40 16.64 **
SMM Y=3.18X−24.76 0.48 0.47 2.23 4.13 **
SMI Y=14.78X−47.94 0.48 2.18 10.40 19.16 **

The 10RM for leg press

All participants LLMM Y=12.60X−3.21 0.55 1.20 10.22 14.98 **
(n=93) SMM Y=8.09X−24.39 0.64 0.63 6.84 9.35 **
SMI Y=43.68X−119.60 0.66 3.27 37.18 50.18 **
Male (n=42) LLMM Y=12.50X−0.020 0.29 3.10 6.23 18.77 **
SMM Y=9.75X−73.09 0.51 1.51 6.69 12.81 **
SMI Y=53.55X−193.82 0.55 7.66 38.07 69.02 **
Female (n=51) LLMM Y=9.89X+27.90 0.18 3.02 3.82 15.96 *
SMM Y=7.99X−21.08 0.29 1.79 4.39 11.59 **
SMI Y=38.86X−89.73 0.32 8.11 22.57 55.16 **

*p<0.01, **p<0.001. 10RM: 10 repetition maximum; ULMM: upper limb muscle mass; LLMM: lower limb muscle mass; SMM: skeletal muscle mass; SMI: skeletal muscle mass index; SE: standard error; CI: confidence interval.

DISCUSSION

The purpose of this study was to investigate the relationship between BIA measurements and the 10RM for CP and LP, and to further develop a regression model to determine whether BIA measurements can describe the 10RM for CP and LP in young healthy adults. This study had two main findings. First, a significant correlation was found between BIA measurements and the 10RM for CP and LP. Second, the 10RM for CP and LP can be described using BIA measurements.

When examining the relationship between BIA measurements and 10RM, it is essential to consider the distinct differences in energy supply and muscle fiber activation that differentiate between 1RM and 10RM24). As the 1RM test involves a single maximum force exertion, it primarily relies on the ATP-CP system for energy and is largely influenced by fast-twitch muscle fibers, according to the size principle. In contrast, the 10RM test, due to the prolonged exercise duration, depends mainly on the glycolytic system and engages both fast- and slow-twitch muscle fibers. The 10RM requires not only high-force exertion but also the endurance to sustain 10 consecutive repetitions. Thus, it is crucial to note that 10RM may be affected by endurance-related factors such as energy supply and muscle fiber activation patterns that cannot be fully captured through BIA alone.

The findings of the present study demonstrated significant correlations between BIA measurements and 10RM for CP and LP in healthy adults. Alizadehkhaiyat et al. found significant correlations between SMM using BIA and shoulder joint strength18), Sue et al. reported significant correlations between 1RM and both dominant-leg SMM and SMI for single-leg LP7), and Cataidi et al. reported a significant correlation between BIA measurements and isokinetic muscle strength20). Unlike isometric muscle strength, 1RM, and other strength indices used in previous studies, the 10RM in the current study is influenced by endurance-related factors, such as energy supply and muscle fiber type, which BIA cannot directly assess. Nevertheless, consistent with prior studies, our results showed a significant correlation between BIA measurements and muscle strength, making this, to our knowledge, the first study to specifically examine the correlation between BIA measurements and 10RM.

In this study, regression models were constructed to explain 10RM in CP and LP exercises. The coefficients of determination (R2) for the models describing 10RM in CP were 0.80 (p<0.001) using ULMM, 0.77 (p<0.001) using SMM, and 0.79 (p<0.001) using SMI. For the LP, the R2 values were 0.55 (p<0.001) using LLMM, 0.64 (p<0.001) using SMM, and 0.66 (p<0.001) using SMI. These results indicate that BIA measurements significantly contribute to the regression models explaining 10RM in both CP and LP, despite the possible influence of endurance factors that cannot be assessed by BIA. Previous studies primarily focused on developing regression models for 1RM using BIA measurements7). Our findings suggest that BIA measurements can also effectively describe muscle strength for 10RM. Furthermore, the differences in R2 values between the exercises highlight that the descriptive accuracy of BIA-based models may vary depending on the muscle group involved. This is in line with previous studies that reported different R2 values in regression models between different muscle groups, particularly between lower limb and trunk exercises20). Differences in R2 values between exercises may be attributed to factors that BIA cannot assess, such as the distribution of muscle fiber types25,26,27). Given these findings, further research is warranted to explore the reasons for these differences in the coefficients of determination between exercises. Such research could help refine the regression models and improve their applicability to different types of strength exercises.

The present study examined the relationship between BIA measurements and muscle strength according to sex and founding significant correlations in both males and females. However, previous studies have yielded inconsistent results on this topic7, 19, 20). Cataldi et al. reported significant correlations between free fat mass measured using BIA and isokinetic lower limb muscle strength in both male and female athletes20). Conversely, Hayashida et al. found a significant correlation between BIA measurements and muscle strength in older men, but not in older women, as a function of age19). Sue et al. observed a strong correlation between BIA measurements and 1RM of the unilateral LP in healthy adult men, but no significant correlation in women7). These inconsistencies can be attributed to several factors. First, several studies have reported sex differences in firing rate28) and variability in motor units29). BIA can assess morphological factors but not neurological factors, which could explain the varying results across sexes. Additionally, differences in target populations, age groups, and methods of muscle strength measurement among the studies may contribute to inconsistent findings. The relationship between BIA measurements and muscle strength by sex is complex and requires further investigation. Future studies should standardize the measurement methods and control for factors such as age and population characteristics to provide more conclusive results.

These results may assist athletic trainers, fitness professionals, and rehabilitation clinicians in developing indirect methods for estimating appropriate weights in resistance training. While this study indicates that BIA measurements can explain 10RM, it remains unclear whether estimating 10RM directly from BIA measurements may actually reduce variability in the number of repetitions performed compared to estimating 10RM using %1RM based on 1RM values indirectly derived from BIA measurements. Future research should focus on expanding the sample size, incorporating additional variables, further improving the model’s predictive accuracy, and exploring optimal methodologies for the indirect estimation of 10RM.

This study had several limitations. First, the participants were healthy young adults with no training experience, and the correlation and regression models used in this study may not be directly applicable if the individual are older or have training experience. To address this issue, a multivariate regression model adaptable to any population must be developed. Second, because absolute SMM values have been reported to vary across BIA, the correlation and accuracy of the regression models may differ from those of other BIA instruments16). Therefore, new regression models should be developed by using other types of equipment. Finally, the regression model used in this study cannot be directly adapted to the same training category because the absolute value of the muscle force varies depending on the machine used. For example, in a horizontal LP machine that uses cables and pulleys to lift a weight stack, the force to push the platform and the weight of the weight stack are almost the same; however, in the 45° LP machine that uses barbell plates, the force to push the platform and the weight of the barbell plates are different. Therefore, it is necessary to develop a regression model for each machine.

In conclusion, BIA measurements were significantly correlated with 10RM for CP and LP in young healthy the participants with no training experience, suggesting that 10RM can be explained by BIA measurements. These results may help in the development of a methodology to safely and efficiently measure 10RM when prescribing resistance training.

Conflicts of interest

None.

REFERENCES

  • 1.Sheppard JM, Triplett NT: Program design for resistance training. In: Haff GG, Triplett NT, eds. Essentials of strength training and conditioning. 4. Champaign: National Strength and Conditioning Association; 2016, p 452. [Google Scholar]
  • 2.Nuzzo JL, Pinto MD, Nosaka K, et al. : Maximal number of repetitions at percentages of the one repetition maximum: a meta-regression and moderator analysis of sex, age, training status, and exercise. Sports Med, 2024, 54: 303–321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Picerno P, Iannetta D, Comotto S, et al. : 1RM prediction: a novel methodology based on the force-velocity and load-velocity relationships. Eur J Appl Physiol, 2016, 116: 2035–2043. [DOI] [PubMed] [Google Scholar]
  • 4.Macht JW, Abel MG, Mullineaux DR, et al. : Development of 1RM prediction equations for bench press in moderately trained men. J Strength Cond Res, 2016, 30: 2901–2906. [DOI] [PubMed] [Google Scholar]
  • 5.Kanada Y, Sakurai H, Sugiura Y, et al. : Estimation of 1RM for knee extension based on the maximal isometric muscle strength and body composition. J Phys Ther Sci, 2017, 29: 2013–2017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Nakamura M, Kiyono R, Sato S, et al. : One-repetition maximum can be estimated with a handheld dynamometer and circumference in community-dwelling older adults. J Phys Ther Sci, 2020, 32: 669–673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Sue K, Kobayashi Y, Ito M, et al. : Bioelectrical impedance analysis to estimate one-repetition maximum measurement of muscle strength for leg press in healthy young adults. Sci Rep, 2022, 12: 17142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Suchomel TJ, Nimphius S, Bellon CR, et al. : The importance of muscular strength: training considerations. Sports Med, 2018, 48: 765–785. [DOI] [PubMed] [Google Scholar]
  • 9.Tanaka NI, Miyatani M, Masuo Y, et al. : Applicability of a segmental bioelectrical impedance analysis for predicting the whole body skeletal muscle volume. J Appl Physiol, 2007, 103: 1688–1695. [DOI] [PubMed] [Google Scholar]
  • 10.Oshima Y, Shiga T, Namba H, et al. : Estimation of whole-body skeletal muscle mass by bioelectrical impedance analysis in the standing position. Obes Res Clin Pract, 2010, 4: e1–e82. [DOI] [PubMed] [Google Scholar]
  • 11.Bosy-Westphal A, Jensen B, Braun W, et al. : Quantification of whole-body and segmental skeletal muscle mass using phase-sensitive 8-electrode medical bioelectrical impedance devices. Eur J Clin Nutr, 2017, 71: 1061–1067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Kim EY, Kim SR, Won DD, et al. : Multifrequency bioelectrical impedance analysis compared with computed tomography for assessment of skeletal muscle mass in primary colorectal malignancy: a predictor of short-term outcome after surgery. Nutr Clin Pract, 2020, 35: 664–674. [DOI] [PubMed] [Google Scholar]
  • 13.Kim M, Shinkai S, Murayama H, et al. : Comparison of segmental multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for the assessment of body composition in a community-dwelling older population. Geriatr Gerontol Int, 2015, 15: 1013–1022. [DOI] [PubMed] [Google Scholar]
  • 14.Lee SY, Ahn S, Kim YJ, et al. : Comparison between dual-energy X-ray absorptiometry and bioelectrical impedance analyses for accuracy in measuring whole body muscle mass and appendicular skeletal muscle mass. Nutrients, 2018, 10: 738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Fang WH, Yang JR, Lin CY, et al. : Accuracy augmentation of body composition measurement by bioelectrical impedance analyzer in elderly population. Medicine (Baltimore), 2020, 99: e19103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Lee K, Shin Y, Huh J, et al. : Recent issues on body composition imaging for sarcopenia evaluation. Korean J Radiol, 2019, 20: 205–217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Tagliafico AS, Bignotti B, Torri L, et al. : Sarcopenia: how to measure, when and why. Radiol Med, 2022, 127: 228–237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Alizadehkhaiyat O, Hawkes DH, Kemp GJ, et al. : Muscle strength and its relationship with skeletal muscle mass indices as determined by segmental bio-impedance analysis. Eur J Appl Physiol, 2014, 114: 177–185. [DOI] [PubMed] [Google Scholar]
  • 19.Hayashida I, Tanimoto Y, Takahashi Y, et al. : Correlation between muscle strength and muscle mass, and their association with walking speed, in community-dwelling elderly Japanese individuals. PLoS One, 2014, 9: e111810. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Cataldi D, Bennett JP, Wong MC, et al. : Accuracy and precision of multiple body composition methods and associations with muscle strength in athletes of varying hydration: the Da Kine Study. Clin Nutr, 2024, 43: 284–294. [DOI] [PubMed] [Google Scholar]
  • 21.Radaelli R, Fleck SJ, Leite T, et al. : Dose-response of 1, 3, and 5 sets of resistance exercise on strength, local muscular endurance, and hypertrophy. J Strength Cond Res, 2015, 29: 1349–1358. [DOI] [PubMed] [Google Scholar]
  • 22.NSCA -National Strength & Conditioning Association: Exercise technique manual for resistance training. Illinois: Human Kinetics, 2016. [Google Scholar]
  • 23.de Salles BF, Simão R, Miranda F, et al. : Rest interval between sets in strength training. Sports Med, 2009, 39: 765–777. [DOI] [PubMed] [Google Scholar]
  • 24.Kataoka R, Vasenina E, Hammert WB, et al. : Is there evidence for the suggestion that fatigue accumulates following resistance exercise? Sports Med, 2022, 52: 25–36. [DOI] [PubMed] [Google Scholar]
  • 25.Ørtenblad N, Nielsen J, Boushel R, et al. : The muscle fiber profiles, mitochondrial content, and enzyme activities of the exceptionally well-trained arm and leg muscles of elite cross-country skiers. Front Physiol, 2018, 9: 1031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Gejl KD, Andersson EP, Nielsen J, et al. : Effects of acute exercise and training on the sarcoplasmic reticulum Ca2+ release and uptake rates in highly trained endurance athletes. Front Physiol, 2020, 11: 810. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Gejl KD, Hvid LG, Andersson EP, et al. : Contractile properties of mhc i and ii fibers from highly trained arm and leg muscles of cross-country skiers. Front Physiol, 2021, 12: 682943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Peng YL, Tenan MS, Griffin L: Hip position and sex differences in motor unit firing patterns of the vastus medialis and vastus medialis oblique in healthy individuals. J Appl Physiol, 2018, 124: 1438–1446. [DOI] [PubMed] [Google Scholar]
  • 29.Inglis JG, Gabriel DA: Sex differences in the modulation of the motor unit discharge rate leads to reduced force steadiness. Appl Physiol Nutr Metab, 2021, 46: 1065–1072. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Physical Therapy Science are provided here courtesy of Society of Physical Therapy Science

RESOURCES