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Article

Lower-Limb Muscle Power Is Negatively Associated with Protein Intake in Older Adults: A Cross-Sectional Study

by
Hélio José Coelho-Júnior
1,*,
Domenico Azzolino
2,3,
Riccardo Calvani
4,
Ivan de Oliveira Gonçalves
5,
Matteo Tosato
1,
Francesco Landi
1,4,
Matteo Cesari
2,3,
Anna Picca
4,6 and
Emanuele Marzetti
1,4
1
Department of Geriatrics and Orthopedics, Università Cattolica del Sacro Cuore, 00168 Rome, Italy
2
Department of Clinical and Community Sciences, University of Milan, 20122 Milan, Italy
3
Geriatric Unit, IRCCS Istituti Clinici Scientifici Maugeri, 20138 Milan, Italy
4
Fondazione Policlinico Universitario “Agostino Gemelli” IRCCS, 00168 Rome, Italy
5
Department of Health, Piaget University, Suzano 08673-010, Brazil
6
Department of Medicine and Surgery, LUM University, 70100 Casamassima, Italy
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(21), 14579; https://doi.org/10.3390/ijerph192114579
Submission received: 6 October 2022 / Revised: 27 October 2022 / Accepted: 2 November 2022 / Published: 7 November 2022

Abstract

:
The present study examined the association between lower-limb muscle power and protein-related parameters in older adults. This study followed a cross-sectional design. Participants were community-dwelling older adults. Candidates were considered eligible if they were 60 years or older, lived independently, and possessed sufficient physical and cognitive abilities to perform all the measurements required by the protocol. The 5 times sit-to-stand (5STS) test was performed as fast as possible according to a standard protocol. Absolute, relative, and allometric muscle power measures were estimated using 5STS-based equations. Diet was assessed by 24-h dietary recall and diet composition was estimated using a nutritional software. One-hundred and ninety-seven older adults participated to the present study. After adjustment for covariates, absolute and allometric muscle power were negatively associated with body weight-adjusted protein intake. Our findings indicate that absolute and allometric muscle power estimated through a simple equation are negatively associated with body weight-adjusted protein intake in community-dwelling older adults.

1. Introduction

Physical function refers to a large construct that involves numerous motor tasks that allow an individual to interact with the environment [1,2]. Physical function changes during the life course, such that it commonly increases during childhood, remains stable in adulthood, and decreases significantly past the fifth decade of life [1,3,4]. This scenario demands special attention because the preservation of physical function is a core element for maintaining independence and remaining engaged in social activities in advanced age [5,6]. Indeed, significant losses in physical function increase the risk of numerous negative outcomes, including cognitive decline, poor mobility, and death [7,8,9,10], have a central role in the development of frailty and sarcopenia [11,12], and negatively impact the prognosis of many diseases [13,14,15].
Muscle power is a type of physical function that encompasses the capacity of generating strength as quickly as possible [16,17]. In recent decades, studies have repeatedly indicated that muscle power declines earlier and faster with age than other important aspects of physical function (e.g., muscle strength) [18,19,20]. Furthermore, reduced muscle power is a strong, independent predictor of incident disability [20]. This evidence indicates that muscle power should be actively monitored during aging, and that strategies to maintain or even improve muscle power are urgently required [16,17].
The assessment of muscle power involves laboratory-based tests that are not completely adapted to the old population [21]. Available tests also lack standardized protocols, have high costs, and may possibly be harmful for older adults [21]. These limitations hamper the clinical assessment of muscle power in older adults. Recently, a simple equation was proposed by Alcazar et al. [22] to estimate lower-limb muscle power based on the time to complete the 5 times sit-to-stand (5STS) test, chair height, and the test person’s body weight (BW) and height. Muscle power estimates were validated against values obtained on a test performed in a leg press resistance machine [22]. Muscle power values estimated through the equation have been associated with quality of life, cognitive function, physical performance, and sarcopenia [22,23]. Although such associations were only tested cross-sectionally and need to be confirmed in longitudinal studies, 5STS-based muscle power estimation appears to be a feasible approach to assess lower-limb muscle power in clinical settings.
Nutrition is a modifiable lifestyle factor that may be harnessed to foster active and healthy aging [24,25]. In particular, protein intake greater than the current recommended dietary allowance (0.8 g/kg BW per day; RDA) may be proposed as a strategy to preserve physical function in advanced age [26,27,28,29]. More specifically, physically inactive older adults should be advised to ingest at least 0.8 g of protein/kg of BW/day, while a minimal intake of 1.2–1.5 g/kg of BW/day, depending on the type of physical exercise, is recommended to physically active people over 65 years [26]. These recommendations are supported by several studies showing that older adults with a high protein intake (HPI) have better performance on a set of physical performance tests, including the Short Physical Performance Battery (SPPB), greater lower-limb muscle strength, faster walking speed, and better balance than those who consume ≤0.8 g of protein/kg of BW/day [30,31].
The impact of protein intake on physical function is thought to be mediated, at least partly, by the anabolic action of branched-chain amino acids (BCAAs) on skeletal muscle [32]. In fact, adequate amounts of BCAAs, in particular leucine, are essential to optimally stimulate muscle protein synthesis (MPS) [32,33,34]. Recent evidence also suggests that the distribution of protein across the main meals might be more important than the total amount of protein ingested during the day [35,36,37].
To the best of our knowledge, only one study examined the association between protein intake and muscle power in older people [37]. The cross-sectional study involved 97 German healthy community-dwelling older adults without functional limitations and included measures of lower-limb muscle power, assessed using a pneumatic resistance seated leg press machine, and dietary intake, using 7-day food record. The authors reported that lower-limb muscle power was not significantly associated with mean daily protein intake, protein distribution across the meals, or number of meals providing at least 0.4 g of protein/kg of BW/per day [37].
To increase the knowledge on the subject, the present study examined the cross-sectional association between protein intake and measures of lower-limb muscle power (i.e., absolute, allometric, and relative) estimated using the equation proposed by Alcazar et al. [22] in community-dwelling Brazilian older adults. Our hypothesis was that muscle power and protein intake would be positively and significantly correlated.

2. Materials and Methods

This was a cross-sectional study that investigated the association between lower-limb muscle power estimates and protein-related parameters in community-dwelling Brazilian older adults. Lower-limb muscle power was estimated using 5STS-based equations [22] and food intake was assessed by 24-h dietary recall.
The study was approved by the Research Ethics Committee of the University of Mogi das Cruzes (UMC, São Paulo, Brazil). All study procedures were conducted in compliance with the Declaration of Helsinki and the Resolution 196/96 of the National Health Council. The manuscript was prepared in compliance with the STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) guidelines for observational studies [38].

2.1. Participants

Participants were recruited between January 2015 and January 2018 in a community senior center located in the metropolitan area of São Paulo, Brazil. This study was advertised through posters placed in public sites (e.g., parks, city hall, public offices, bus stops, train stations), local radios, and newspapers. People were also invited to participate by direct contact. Candidates were considered eligible if they were 60+ year-old, lived independently, and possessed sufficient physical and cognitive abilities to perform all measurements required by the protocol. All participants provided written informed consent prior to enrolment.

2.2. Anthropometric Measures

An analog weight scale with a stadiometer (Filizola, Brazil) was used to measure BW and height. The body mass index (BMI) was calculated as the ratio between BW (kg) and the square of height (m2). Participants were classified as underweight, normal weight, or overweight according to the following cut-points: <22 kg/m2, 22–27 kg/m2, and >27 kg/m2 [39].

2.3. The 5 Times Sit-to-Stand Test

Participants were instructed to rise from a chair five times as quickly as possible with their arms folded across their chest. Timing began when participants raised their buttocks off the chair and was stopped when they were seated at the end of the fifth stand [1]. Absolute, relative, and allometric muscle power were estimated according to the equations proposed by Alcazar et al. [22]:
(1)
Absolute muscle power: ([Body weight × 0.9 × g × (height × 0.5 − chair height)])/(5STS (s) × 0.1);
(2)
Allometric muscle power: Absolute muscle power/height2;
(3)
Relative muscle power: Allometric muscle power/BMI.

2.4. Dietary Assessment

Food intake was assessed by 24-h dietary recall [40]. The method uses an open-ended questionnaire to provide a quantitative and subjective estimation of actual food consumption. In the present study, two trained researchers (H.J.C.-J. and I.O.G.) asked the participants to recall in detail all foods they consumed on a meal-by-meal basis, including snacks, during the previous 24 h. Interviews occurred on Tuesdays, Wednesdays, Thursdays, and Fridays to avoid possible biases associated with the weekend. Participants were requested to provide details about cooking methods (e.g., fried, grilled, and roasted), serving and portion sizes, product brands, sauces, spices, and condiments consumed, and the eventual use of dietary supplements. Amounts of beverages consumed were also recorded, and participants were asked to specify if and how beverages were sweetened. Two-dimensional aids (e.g., photos), household utensils (e.g., standard measuring cups and spoons), and food models were used to facilitate assessment of portion sizes. Diet composition was estimated using the NutWin software, version 1.5 (Federal University of São Paulo, Brazil) [41].

2.5. Statistical Analysis

Continuous variables are expressed as the mean ± standard deviation (SD) or absolute numbers (percentage). Pearson’s correlation analysis was conducted to investigate the association between muscle power- and protein-related parameters. Associations with a p-value lower than 0.05 were included in the regression analyses. The final model was adjusted for sex, age, BMI (continuous and categorical), and total kilocalories consumed per day. Significance was set at 5% (p value < 0.05) for all tests. All analyses were performed using the SPSS software (version 23.0, SPSS Inc., Chicago, IL, USA).

3. Results

3.1. Study Participants

Two-hundred and fifty-four candidates agreed to be evaluated for inclusion. Of these, 46 were younger than 60 years, nine had missing data for the 5STS test, and two had missing data for diet, leaving a total of 197 participants for the analysis. The main characteristics of study participants are shown in Table 1. The study population was mostly composed of female (83%) “young-older” adults (mean age: 68.3 years, range: 60 to 99 years). Most participants were overweight, regardless of sex (Supplementary material [Table S1]) [39]. Mean 5STS performance scores were borderline to cutoff values for dynapenia [42]. Mean BW-adjusted protein intake was higher than the RDA (mean protein consumption = 1.5 g of protein /kg/BW per day). The majority of dietary protein was ingested at lunch.

3.2. Pearson’s Correlation Analysis

Results of Pearson’s correlation analysis are shown in Table 2. Absolute and allometric muscle power values were negatively and significantly associated with BW-adjusted protein intake and protein consumption at lunch. Relative muscle power was not significantly associated with either BW-adjusted protein intake or protein consumption at lunch. No significant associations were observed between any muscle power parameter and energy intake, absolute protein intake, protein intake at breakfast, lunch and dinner, or valine, isoleucine, and leucine intake.

3.3. Linear Regression Analysis

Results of the linear regression analysis are shown in Table 3. Unadjusted analyses indicated that BW-adjusted protein and protein intake at lunch were significantly associated with absolute muscle power. After adjusting the analysis according to age, sex, BMI (continuous), and mean daily energy intake, only BW-adjusted protein intake remained significantly associated with absolute muscle power. No protein-related parameter was significantly associated with allometric muscle power. When the analysis was run using BMI as a categorical variable (Table S2), similar results were observed, given that BW-adjusted protein intake was significantly associated with absolute muscle power. However, BW-adjusted protein intake became significantly associated with allometric muscle power.

4. Discussion

The main findings of the present study indicate that lower-limb absolute muscle power was negatively associated with BW-adjusted protein in older adults, regardless of whether BMI was treated as a continuous or categorical covariable. No significant associations were observed between protein intake at lunch and absolute muscle power, or between protein-related parameters and allometric muscle power. A significant association was found between BW-adjusted protein and allometric muscle power when BMI was analyzed as a categorical variable.
Only a few studies have investigated the association between protein intake and muscle power in older adults; and, to the best of our knowledge, ours is the first investigation that examined this relationship using the recently validated equation of Alcazar et al. [22]. In contrast to our findings, Gingrich et al. [37] did not observe significant associations between BW-adjusted protein intake and lower-limb muscle power, assessed using a pneumatic resistance seated leg press machine, in German healthy community-dwelling older adults.
Our findings are quite unexpected. Adequate protein consumption is a major regulator of muscle metabolism, avoiding, or at least reducing muscle catabolism, by providing essential amino acids (AAs) equivalent to body demands [27,29,43]. AAs stimulate MPS through the activation of the mammalian target of rapamycin and its downstream proteins: ribosomal protein kinase S6 and 4E-binding protein 1 [44,45]. Insufficient MPS predisposes to loss of muscle mass, with a major impact on type II, fast-twitch fibers [46,47,48]. These fibers are rich in myosin ATPase and glycolytic enzymes with high catalytic activity [46,47,48], allowing them to generate strength rapidly. Hence, it is reasonable to assume that protein intake could be associated with physical performance, and therefore muscle power.
However, this view has not been consistently supported. Isanejad et al. [49] found that a set of physical performance tests, including 5STS, balance, and walking speed, were not associated with protein intake after adjusting the analysis for several covariables. Ten Haaf et al. [36] observed that daily protein intake was not associated with SPPB scores, walking speed, chair rise ability, or isometric handgrip strength. Coelho-Junior et al. [50] found that BW-adjusted daily protein intake was not associated with 5STS performance in Italian older adults. A recent meta-analysis reported that protein intake higher than the RDA was cross-sectionally, but not longitudinally associated with walking speed [31]. These findings are in keeping with our observations, given that mobility, chair rise ability, and balance tests have a high muscle power component [19,51,52,53,54,55].
A potential explanation for our results is based on the pattern of protein distribution. The optimal strategy to provide the required amounts of AAs necessary to properly stimulate MPS is still under debate. Some authors have proposed that a pulse-feeding protein intake through the consumption of a high-protein meal, might saturate the splenic sequestration of AAs, thereby increasing their availability for MPS [36]. However, AA bioavailability seems to reach a plateau at approximately 30 g of protein per meal, after which AAs are oxidated [56,57]. Hence, other researchers argued that a spread feeding pattern with at least 30 g of dietary protein during the main meals could be a more effective strategy to sustain muscle anabolism [36].
In this regard, Farsijani et al. [35] found that older adults with a more spread protein distribution across the main meals were stronger and had better mobility than those with a pulse-feeding intake. Similar findings were reported by Ten Haff et al. [36] in Dutch older adults. In the present study, protein was mostly consumed at lunch, with a smaller percentage ingested at dinner and an even smaller amount at breakfast.
Taken together, these observations suggest that a large and disproportional consumption of proteins at lunch might contribute to whole-body protein oxidation and muscle protein breakdown, consequently favoring muscle atrophy and loss of muscle power. Notably, not all studies support an association between protein distribution and physical function [37,58]. Moreover, a further analysis was conducted to examine the association between protein distribution and power-related parameters (Figure S1), finding no significant associations. Additional studies are necessary to confirm our speculations.
Our sample was prevalently composed of overweight people with a high consumption of protein. Excess protein consumption has long been investigated as a possible risk factor for chronic kidney disease (CKD) [59]. It is suggested that a high intake of protein might enhance glomerular filtration rate, sharply increasing the glomerular pressure and/or causing renal hypertrophy and predisposing to the development of renal damage and CKD [59,60]. In this context, the negative association found between lower-limb muscle power measures and BW-adjusted protein might be the result of long-term impairments of kidney function leading to muscle atrophy and dynapenia [61].
However, longitudinal studies have reported that long-term exposure to HPI has no harmful effects on kidney function in healthy people. Herber-Gast et al. [62] examined more than 3,500 Dutch people and did not observe significant longitudinal associations between protein intake and changes in renal function. Rebholz et al. [63] followed 15,055 North American adults for 21 years. The authors observed that dietary acid load—the balance between acid-inducing and base-inducing foods—was significantly associated with the occurrence of CKD. When the analyses were conducted according to the individual components of the dietary acid load, a higher intake of protein was not associated with CKD. Given that none of the participants of our study reported kidney problems on recruitment, our results are unlikely to be explained by renal damage.
The fact that allometric muscle power was associated with BW-adjusted protein intake when data were analyzed using BMI as a categorical variable suggests that other protein-related aspects might underpin the results of our study. In overweight people, increased ingestion of protein might be associated with the intake of other macronutrients that impact neuromuscular function. For instance, high-fat diets significantly reduce the number of synaptic branches, satellite cell abundance, muscle cross-sectional area, and muscle strength in preclinical models [64,65]. Such a scenario suggests that high-fat/high-protein diets could affect the functional and structural components of the neuromuscular system, causing first impairment of allometric muscle power, which represents acceleration, and then of absolute muscle power. However, no data are available to explore this hypothesis.
Our study is not free of limitations. First, no muscle mass measures were collected, which precluded estimation of specific muscle power. Second, participants were not screened for sarcopenia [11] or frailty [12]. Third, only community-dwelling older adults were examined, and extrapolations to other contexts (e.g., institutionalized older adults) should be made with caution. Fourth, regression analysis was not corrected for covariables that might influence the association between muscle power and protein intake, including physical activity levels, diet quality, and sleep. Fifth, the studied population was relatively small, young, physically active, and with a high prevalence of participants whose protein and BCAA intakes were higher than RDA values. Sixth, the 5STS equation has received some criticism [66], and its predictive value toward health parameters and negative events still needs to be established. Seventh, protein sources might impact the association between physical function and protein-related parameters [41]. Animal-based proteins are thought to provide larger amounts of BCAAs than those of vegetable origin [67], thereby producing greater effects on muscle mass and strength. However, studies found a significant association between plant-based protein and physical function [41], which may be mediated by the amount of plant protein consumed. Hence, future studies should examine the impact of protein sources on muscle power. Finally, the results shown in this work are derived from cross-sectional observations.

5. Conclusions

Our findings indicate that absolute and allometric muscle power are negatively associated with BW-adjusted protein intake in community-dwelling older adults.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijerph192114579/s1, Table S1: Participant distribution according to body mass index categories; Table S2: Linear regression for the association between power and protein-related parameters. Figure S1: Association between the coefficient of variation of protein intake and power-related parameters.

Author Contributions

Conceptualization, H.J.C.-J., D.A., R.C., M.T., F.L., I.d.O.G., A.P., M.C. and E.M.; methodology, H.J.C.-J., D.A., R.C., M.T., F.L., I.d.O.G., A.P., M.C. and E.M.; formal analysis, H.J.C.-J. and D.A.; investigation, H.J.C.-J. and I.d.O.G.; resources, H.J.C.-J. and I.d.O.G.; data curation, H.J.C.-J., D.A., R.C., M.C. and A.P.; writing—original draft preparation, H.J.C.-J., D.A., R.C., M.T., I.d.O.G., F.L. and A.P.; writing—review and editing, H.J.C.-J., M.C., F.L. and E.M.; supervision, M.C. and E.M.; funding acquisition, E.M. All authors have read and agreed to the published version of the manuscript.

Funding

This work was partly funded by the Università Cattolica del Sacro Cuore (linea D1.2020 and D1.2022) and the nonprofit research foundation “Centro Studi Achille e Linda Lorenzon”.

Institutional Review Board Statement

This study was conducted in accordance with the Declaration of Helsinki, and approved by the Ethics Committee of the University of Mogi das Cruzes (621.614).

Informed Consent Statement

Informed consent was obtained from all subjects involved in this study.

Data Availability Statement

Data are available upon request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Coelho-Junior, H.J.; Uchida, M.C.; Gonçalves, I.O.; Calvani, R.; Rodrigues, B.; Picca, A.; Onder, G.; Landi, F.; Bernabei, R.; Marzetti, E. Age-And Gender-Related Changes in Physical Function in Community-Dwelling Brazilian Adults Aged 50 to 102 Years. J. Geriatr. Phys. Ther. 2021, 44, E123–E131. [Google Scholar] [CrossRef] [PubMed]
  2. Leversen, J.S.R.; Haga, M.; Sigmundsson, H. From Children to Adults: Motor Performance across the Life-Span. PLoS ONE 2012, 7, e38830. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Landi, F.; Calvani, R.; Martone, A.M.; Salini, S.; Zazzara, M.B.; Candeloro, M.; Coelho-Junior, H.J.; Tosato, M.; Picca, A.; Marzetti, E. Normative Values of Muscle Strength across Ages in a “Real World” Population: Results from the Longevity Check-up 7+ Project. J. Cachexia Sarcopenia Muscle 2020, 11, 1562–1569. [Google Scholar] [CrossRef] [PubMed]
  4. Marzetti, E.; Hwang, A.-C.; Tosato, M.; Peng, L.-N.; Calvani, R.; Picca, A.; Chen, L.-K.; Landi, F. Age-Related Changes of Skeletal Muscle Mass and Strength among Italian and Taiwanese Older People: Results from the Milan EXPO 2015 Survey and the I-Lan Longitudinal Aging Study. Exp. Gerontol. 2018, 102, 76–80. [Google Scholar] [CrossRef]
  5. Liffiton, J.A.; Horton, S.; Baker, J.; Weir, P.L. Successful Aging: How Does Physical Activity Influence Engagement with Life? Eur. Rev. Aging Phys. Act. 2012, 9, 103–108. [Google Scholar] [CrossRef] [Green Version]
  6. Lowry, K.A.; Vallejo, A.N.; Studenski, S.A. Successful Aging as a Continuum of Functional Independence: Lessons from Physical Disability Models of Aging. Aging Dis. 2012, 3, 5–15. [Google Scholar]
  7. Rosano, C.; Simonsick, E.M.; Harris, T.B.; Kritchevsky, S.B.; Brach, J.; Visser, M.; Yaffe, K.; Newman, A.B. Association between Physical and Cognitive Function in Healthy Elderly: The Health, Aging and Body Composition Study. Neuroepidemiology 2005, 24, 8–14. [Google Scholar] [CrossRef]
  8. Abellan van Kan, G.; Rolland, Y.; Andrieu, S.; Bauer, J.; Beauchet, O.; Bonnefoy, M.; Cesari, M.; Donini, L.M.; Gillette Guyonnet, S.; Inzitari, M.; et al. Gait Speed at Usual Pace as a Predictor of Adverse Outcomes in Community-Dwelling Older People an International Academy on Nutrition and Aging (IANA) Task Force. J. Nutr. Health Aging 2009, 13, 881–889. [Google Scholar] [CrossRef]
  9. Studenski, S.; Perera, S.; Patel, K.; Rosano, C.; Faulkner, K.; Inzitari, M.; Brach, J.; Chandler, J.; Cawthon, P.; Connor, E.B.; et al. Gait Speed and Survival in Older Adults. JAMA 2011, 305, 50–58. [Google Scholar] [CrossRef] [Green Version]
  10. Pavasini, R.; Guralnik, J.; Brown, J.C.; di Bari, M.; Cesari, M.; Landi, F.; Vaes, B.; Legrand, D.; Verghese, J.; Wang, C.; et al. Short Physical Performance Battery and All-Cause Mortality: Systematic Review and Meta-Analysis. BMC Med. 2016, 14, 215. [Google Scholar] [CrossRef] [Green Version]
  11. Cruz-Jentoft, A.J.; Sayer, A.A. Sarcopenia. Lancet 2019, 393, 2636–2646. [Google Scholar] [CrossRef]
  12. Hoogendijk, E.O.; Afilalo, J.; Ensrud, K.E.; Kowal, P.; Onder, G.; Fried, L.P. Frailty: Implications for Clinical Practice and Public Health. Lancet 2019, 394, 1365–1375. [Google Scholar] [CrossRef]
  13. Belkin, M.D.; Doerfler, R.M.; Wagner, L.-A.; Zhan, M.; Fink, J.C. Associations of Performance-Based Functional Assessments and Adverse Outcomes in CKD. Kidney360 2021, 2, 629–638. [Google Scholar] [CrossRef]
  14. Choi, J.H.; Kim, B.R.; Kim, S.R.; Nam, K.W.; Lee, S.Y.; Suh, M.J. Performance-Based Physical Function Correlates with Walking Speed and Distance at 3 Months Post Unilateral Total Knee Arthroplasty. Gait Posture 2021, 87, 163–169. [Google Scholar] [CrossRef]
  15. Almugbel, F.A.; Timilshina, N.; Papadopoulos, E.; Al-Showbaki, L.; Alibhai, S.M.H. The Role of Grip Strength and Short Physical Performance Battery Test in Predicting Chemotherapy-Related Outcomes in Older Adults with Cancer. J. Geriatr. Oncol. 2022, 13, 318–324. [Google Scholar] [CrossRef]
  16. Cadore, E.L.; Izquierdo, M. Muscle Power Training: A Hallmark for Muscle Function Retaining in Frail Clinical Setting. J. Am. Med. Dir. Assoc. 2018, 19, 190–192. [Google Scholar] [CrossRef]
  17. Izquierdo, M.; Cadore, E.L. Muscle Power Training in the Institutionalized Frail: A New Approach to Counteracting Functional Declines and Very Late-Life Disability. Curr. Med. Res. Opin. 2014, 30, 1385–1390. [Google Scholar] [CrossRef]
  18. Suzuki, T.; Bean, J.F.; Fielding, R.A. Muscle Power of the Ankle Flexors Predicts Functional Performance in Community-Dwelling Older Women. J. Am. Geriatr. Soc. 2001, 49, 1161–1167. [Google Scholar] [CrossRef]
  19. Bean, J.F.; Leveille, S.G.; Kiely, D.K.; Bandinelli, S.; Guralnik, J.M.; Ferrucci, L. A Comparison of Leg Power and Leg Strength Within the InCHIANTI Study: Which Influences Mobility More? J. Gerontol. A Biol. Sci. Med. Sci. 2003, 58, M728–M733. [Google Scholar] [CrossRef]
  20. Lauretani, F.; Russo, C.R.; Bandinelli, S.; Bartali, B.; Cavazzini, C.; Di Iorio, A.; Corsi, A.M.; Rantanen, T.; Guralnik, J.M.; Ferrucci, L. Age-Associated Changes in Skeletal Muscles and Their Effect on Mobility: An Operational Diagnosis of Sarcopenia. J. Appl. Physiol. 2003, 95, 1851–1860. [Google Scholar] [CrossRef] [Green Version]
  21. Alcazar, J.; Guadalupe-Grau, A.; García-García, F.J.; Ara, I.; Alegre, L.M. Skeletal Muscle Power Measurement in Older People: A Systematic Review of Testing Protocols and Adverse Events. J. Gerontol. A Biol. Sci. Med. Sci. 2018, 73, 914–924. [Google Scholar] [CrossRef]
  22. Alcazar, J.; Losa-Reyna, J.; Rodriguez-Lopez, C.; Alfaro-Acha, A.; Rodriguez-Mañas, L.; Ara, I.; García-García, F.J.; Alegre, L.M. The Sit-to-Stand Muscle Power Test: An Easy, Inexpensive and Portable Procedure to Assess Muscle Power in Older People. Exp. Gerontol. 2018, 112, 38–43. [Google Scholar] [CrossRef]
  23. Losa-Reyna, J.; Alcazar, J.; Rodríguez-Gómez, I.; Alfaro-Acha, A.; Alegre, L.M.; Rodríguez-Mañas, L.; Ara, I.; García-García, F.J. Low Relative Mechanical Power in Older Adults: An Operational Definition and Algorithm for Its Application in the Clinical Setting. Exp. Gerontol. 2020, 142, 111141. [Google Scholar] [CrossRef]
  24. Chen, L.; Arai, H.; Assantachai, P.; Akishita, M.; Chew, S.T.H.; Dumlao, L.C.; Duque, G.; Woo, J. Roles of Nutrition in Muscle Health of Community-dwelling Older Adults: Evidence-based Expert Consensus from Asian Working Group for Sarcopenia. J. Cachexia Sarcopenia Muscle 2022, 13, 1653–1672. [Google Scholar] [CrossRef]
  25. Calvani, R.; Miccheli, A.; Landi, F.; Bossola, M.; Cesari, M.; Leeuwenburgh, C.; Sieber, C.C.; Bernabei, R.; Marzetti, E. Current Nutritional Recommendations and Novel Dietary Strategies to Manage Sarcopenia. J. Frailty Aging 2013, 2, 38–53. [Google Scholar] [CrossRef]
  26. Bauer, J.; Biolo, G.; Cederholm, T.; Cesari, M.; Cruz-Jentoft, A.J.; Morley, J.E.; Phillips, S.; Sieber, C.; Stehle, P.; Teta, D.; et al. Evidence-Based Recommendations for Optimal Dietary Protein Intake in Older People: A Position Paper from the Prot-Age Study Group. J. Am. Med. Dir. Assoc. 2013, 14, 542–559. [Google Scholar] [CrossRef]
  27. Coelho-Junior, H.J.; Marzetti, E.; Picca, A.; Cesari, M.; Uchida, M.C.; Calvani, R. Protein Intake and Frailty: A Matter of Quantity, Quality, and Timing. Nutrients 2020, 12, 2915. [Google Scholar] [CrossRef]
  28. Deer, R.R.; Volpi, E. Protein Intake and Muscle Function in Older Adults. Curr. Opin. Clin. Nutr. Metab. Care 2015, 18, 248–253. [Google Scholar] [CrossRef] [Green Version]
  29. Landi, F.; Calvani, R.; Tosato, M.; Martone, A.M.; Ortolani, E.; Savera, G.; D’Angelo, E.; Sisto, A.; Marzetti, E. Protein Intake and Muscle Health in Old Age: From Biological Plausibility to Clinical Evidence. Nutrients 2016, 8, 295. [Google Scholar] [CrossRef]
  30. Coelho-Júnior, H.; Milano-Teixeira, L.; Rodrigues, B.; Bacurau, R.; Marzetti, E.; Uchida, M. Relative Protein Intake and Physical Function in Older Adults: A Systematic Review and Meta-Analysis of Observational Studies. Nutrients 2018, 10, 1330. [Google Scholar] [CrossRef] [Green Version]
  31. Coelho-Júnior, H.J.; Calvani, R.; Tosato, M.; Landi, F.; Picca, A.; Marzetti, E. Protein Intake and Physical Function in Older Adults: A Systematic Review and Meta-Analysis. Ageing Res. Rev. 2022, 81, 101731. [Google Scholar] [CrossRef]
  32. Xu, Z.; Tan, Z.; Zhang, Q.; Gui, Q.; Yang, Y. The Effectiveness of Leucine on Muscle Protein Synthesis, Lean Body Mass and Leg Lean Mass Accretion in Older People: A Systematic Review and Meta-Analysis. Br. J. Nutr. 2015, 113, 25–34. [Google Scholar] [CrossRef] [Green Version]
  33. Katsanos, C.S.; Kobayashi, H.; Sheffield-Moore, M.; Aarsland, A.; Wolfe, R.R. A High Proportion of Leucine Is Required for Optimal Stimulation of the Rate of Muscle Protein Synthesis by Essential Amino Acids in the Elderly. Am. J. Physiol. Metab. 2006, 291, E381–E387. [Google Scholar] [CrossRef] [Green Version]
  34. Paddon-Jones, D.; Rasmussen, B.B. Dietary Protein Recommendations and the Prevention of Sarcopenia. Curr. Opin. Clin. Nutr. Metab. Care 2009, 12, 86–90. [Google Scholar] [CrossRef] [Green Version]
  35. Farsijani, S.; Payette, H.; Morais, J.A.; Shatenstein, B.; Gaudreau, P.; Chevalier, S. Even Mealtime Distribution of Protein Intake Is Associated with Greater Muscle Strength, but Not with 3-y Physical Function Decline, in Free-Living Older Adults: The Quebec Longitudinal Study on Nutrition as a Determinant of Successful Aging (NuAge Study). Am. J. Clin. Nutr. 2017, 106, 113–124. [Google Scholar] [CrossRef] [Green Version]
  36. Ten Haaf, D.S.; Van Dongen, E.J.; Nuijten, M.A.; Eijsvogels, T.M.; De Groot, L.C.; Hopman, M.T. Protein Intake and Distribution in Relation to Physical Functioning and Quality of Life in Community-Dwelling Elderly People: Acknowledging the Role of Physical Activity. Nutrients 2018, 10, 506. [Google Scholar] [CrossRef] [Green Version]
  37. Gingrich, A.; Spiegel, A.; Kob, R.; Schoene, D.; Skurk, T.; Hauner, H.; Siebe, C.C.; Volkert, D.; Kiesswetter, E. Amount, Distribution, and Quality of Protein Intake Are Not Associated with Muscle Mass, Strength, and Power in Healthy Older Adults without Functional Limitations—An Enable Study. Nutrients 2017, 9, 1358. [Google Scholar] [CrossRef] [Green Version]
  38. von Elm, E.; Altman, D.G.; Egger, M.; Pocock, S.J.; Gøtzsche, P.C.; Vandenbroucke, J.P. STROBE Initiative The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies. Lancet 2007, 370, 1453–1457. [Google Scholar] [CrossRef] [Green Version]
  39. Lipschitz, D.A. Screening for Nutritional Status in the Elderly. Prim. Care 1994, 21, 55–67. [Google Scholar] [CrossRef]
  40. Coulston, A.M.; Boushey, C.; Ferruzzi, M.G.; Delahanty, L.M.; Linda, M. Nutrition in the Prevention and Treatment of Disease; Elsevier: Amsterdam, The Netherlands; ISBN 9780128029473.
  41. Coelho-Junior, H.J.; Calvani, R.; Gonçalves, I.O.; Rodrigues, B.; Picca, A.; Landi, F.; Bernabei, R.; Uchida, M.C.; Marzetti, E. High Relative Consumption of Vegetable Protein Is Associated with Faster Walking Speed in Well-Functioning Older Adults. Aging Clin. Exp. Res. 2019, 31, 837–844. [Google Scholar] [CrossRef]
  42. Cruz-Jentoft, A.J.; Bahat, G.; Bauer, J.; Boirie, Y.; Bruyère, O.; Cederholm, T.; Cooper, C.; Landi, F.; Rolland, Y.; Sayer, A.A.; et al. Sarcopenia: Revised European Consensus on Definition and Diagnosis. Age Ageing 2018, 48, 16–31. [Google Scholar] [CrossRef]
  43. Bohé, J.; Low, A.; Wolfe, R.R.; Rennie, M.J. Human Muscle Protein Synthesis Is Modulated by Extracellular, Not Intramuscular Amino Acid Availability: A Dose-Response Study. J. Physiol. 2003, 552, 315–324. [Google Scholar] [CrossRef]
  44. Greenhaff, P.L.; Karagounis, L.G.; Peirce, N.; Simpson, E.J.; Hazell, M.; Layfield, R.; Wackerhage, H.; Smith, K.; Atherton, P.; Selby, A.; et al. Disassociation between the Effects of Amino Acids and Insulin on Signaling, Ubiquitin Ligases, and Protein Turnover in Human Muscle. Am. J. Physiol. Endocrinol. Metab. 2008, 295, E595–E604. [Google Scholar] [CrossRef] [Green Version]
  45. Wilkinson, D.J.; Hossain, T.; Hill, D.S.; Phillips, B.E.; Crossland, H.; Williams, J.; Loughna, P.; Churchward-Venne, T.A.; Breen, L.; Phillips, S.M.; et al. Effects of Leucine and Its Metabolite β-Hydroxy-β-Methylbutyrate on Human Skeletal Muscle Protein Metabolism. J. Physiol. 2013, 591, 2911–2923. [Google Scholar] [CrossRef]
  46. Lexell, J.; Taylor, C.C.; Sjöström, M. What Is the Cause of the Ageing Atrophy? Total Number, Size and Proportion of Different Fiber Types Studied in Whole Vastus Lateralis Muscle from 15- to 83-Year-Old Men. J. Neurol. Sci. 1988, 84, 275–294. [Google Scholar] [CrossRef]
  47. Klitgaard, H.; Mantoni, M.; Schiaffino, S.; Ausoni, S.; Gorza, L.; Laurent-Winter, C.; Schnohr, P.; Saltin, B. Function, Morphology and Protein Expression of Ageing Skeletal Muscle: A Cross-Sectional Study of Elderly Men with Different Training Backgrounds. Acta Physiol. Scand. 1990, 140, 41–54. [Google Scholar] [CrossRef]
  48. Nilwik, R.; Snijders, T.; Leenders, M.; Groen, B.B.L.; van Kranenburg, J.; Verdijk, L.B.; Van Loon, L.J.C. The Decline in Skeletal Muscle Mass with Aging Is Mainly Attributed to a Reduction in Type II Muscle Fiber Size. Exp. Gerontol. 2013, 48, 492–498. [Google Scholar] [CrossRef]
  49. Isanejad, M.; Mursu, J.; Sirola, J.; Kröger, H.; Rikkonen, T.; Tuppurainen, M.; Erkkilä, A.T. Dietary Protein Intake Is Associated with Better Physical Function and Muscle Strength among Elderly Women. Br. J. Nutr. 2016, 115, 1281–1291. [Google Scholar] [CrossRef] [Green Version]
  50. Coelho-Junior, H.J.; Calvani, R.; Picca, A.; Gonçalves, I.O.; Landi, F.; Bernabei, R.; Cesari, M.; Uchida, M.C.; Marzetti, E. Association between Dietary Habits and Physical Function in Brazilian and Italian Older Women. Nutrients 2020, 12, 1635. [Google Scholar] [CrossRef]
  51. Orr, R.; de Vos, N.J.; Singh, N.A.; Ross, D.A.; Stavrinos, T.M.; Fiatarone-Singh, M.A. Power Training Improves Balance in Healthy Older Adults. J. Gerontol. A Biol. Sci. Med. Sci. 2006, 61, 78–85. [Google Scholar] [CrossRef] [Green Version]
  52. Cuoco, A.; Callahan, D.M.; Sayers, S.; Frontera, W.R.; Bean, J.; Fielding, R.A. Impact of Muscle Power and Force on Gait Speed in Disabled Older Men and Women. J. Gerontol. A Biol. Sci. Med. Sci. 2004, 59, 1200–1206. [Google Scholar] [CrossRef] [PubMed]
  53. Orr, R.; Raymond, J.; Fiatarone Singh, M. Efficacy of Progressive Resistance Training on Balance Performance in Older Adults: A Systematic Review of Randomized Controlled Trials. Sport. Med. 2008, 38, 317–343. [Google Scholar] [CrossRef] [PubMed]
  54. Alotaibi, M.M.; Almutairi, M.K.; Singh, H.; Ithurburn, M.P.; Lein, D.H. 30-Second Chair Stand Test Predicts Countermovement Jump Performance in Young Adults. Sports Health, 2022; 19417381221105040, online ahead of print. [Google Scholar] [CrossRef]
  55. Baltasar-Fernandez, I.; Alcazar, J.; Rodriguez-Lopez, C.; Losa-Reyna, J.; Alonso-Seco, M.; Ara, I.; Alegre, L.M. Sit-to-Stand Muscle Power Test: Comparison between Estimated and Force Plate-Derived Mechanical Power and Their Association with Physical Function in Older Adults. Exp. Gerontol. 2021, 145, 111213. [Google Scholar] [CrossRef] [PubMed]
  56. Moore, D.R.; Robinson, M.J.; Fry, J.L.; Tang, J.E.; Glover, E.I.; Wilkinson, S.B.; Prior, T.; Tarnopolsky, M.A.; Phillips, S.M. Ingested Protein Dose Response of Muscle and Albumin Protein Synthesis after Resistance Exercise in Young Men. Am. J. Clin. Nutr. 2009, 89, 161–168. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Symons, T.B.; Sheffield-Moore, M.; Wolfe, R.R.; Paddon-Jones, D. A Moderate Serving of High-Quality Protein Maximally Stimulates Skeletal Muscle Protein Synthesis in Young and Elderly Subjects. J. Am. Diet. Assoc. 2009, 109, 1582–1586. [Google Scholar] [CrossRef] [Green Version]
  58. Højfeldt, G.; Nishimura, Y.; Mertz, K.; Schacht, S.R.; Lindberg, J.; Jensen, M.; Hjulmand, M.; Lind, M.V.; Jensen, T.; Jespersen, A.P.; et al. Daily Protein and Energy Intake Are Not Associated with Muscle Mass and Physical Function in Healthy Older Individuals—A Cross-Sectional Study. Nutrients 2020, 12, 2794. [Google Scholar] [CrossRef]
  59. Martin, W.F.; Armstrong, L.E.; Rodriguez, N.R. Dietary Protein Intake and Renal Function. Nutr. Metab. 2005, 2, 25. [Google Scholar] [CrossRef] [Green Version]
  60. Ko, G.-J.; Rhee, C.M.; Kalantar-Zadeh, K.; Joshi, S. The Effects of High-Protein Diets on Kidney Health and Longevity. J. Am. Soc. Nephrol. 2020, 31, 1667–1679. [Google Scholar] [CrossRef]
  61. Troutman, A.D.; Arroyo, E.; Lim, K.; Moorthi, R.N.; Avin, K.G. Skeletal Muscle Complications in Chronic Kidney Disease. Curr. Osteoporos. Rep. 2022; online ahead of print. [Google Scholar] [CrossRef]
  62. Herber-Gast, G.-C.M.; Biesbroek, S.; Verschuren, W.M.; Stehouwer, C.D.A.; Gansevoort, R.T.; Bakker, S.J.; Spijkerman, A.M. Association of Dietary Protein and Dairy Intakes and Change in Renal Function: Results from the Population-Based Longitudinal Doetinchem Cohort Study. Am. J. Clin. Nutr. 2016, 104, 1712–1719. [Google Scholar] [CrossRef]
  63. Rebholz, C.M.; Coresh, J.; Grams, M.E.; Steffen, L.M.; Anderson, C.A.M.; Appel, L.J.; Crews, D.C. Dietary Acid Load and Incident Chronic Kidney Disease: Results from the ARIC Study. Am. J. Nephrol. 2015, 42, 427–435. [Google Scholar] [CrossRef] [Green Version]
  64. Lee, S.-R.; Khamoui, A.V.; Jo, E.; Park, B.-S.; Zourdos, M.C.; Panton, L.B.; Ormsbee, M.J.; Kim, J.-S. Effects of Chronic High-Fat Feeding on Skeletal Muscle Mass and Function in Middle-Aged Mice. Aging Clin. Exp. Res. 2015, 27, 403–411. [Google Scholar] [CrossRef] [PubMed]
  65. Martinez-Pena, Y.; Valenzuela, I.; Akaaboune, M. The Disassembly of the Neuromuscular Synapse in High-Fat Diet-Induced Obese Male Mice. Mol. Metab. 2020, 36, 100979. [Google Scholar] [CrossRef] [PubMed]
  66. Fabrica, G.; Biancardi, C.M. Commentary: The Sit-to-Stand Muscle Power Test: An Easy, Inexpensive and Portable Procedure to Assess Muscle Power in Older People. Exp. Gerontol. 2022, 158, 111652. [Google Scholar] [CrossRef] [PubMed]
  67. Berrazaga, I.; Micard, V.; Gueugneau, M.; Walrand, S. The Role of the Anabolic Properties of Plant-versus Animal-Based Protein Sources in Supporting Muscle Mass Maintenance: A Critical Review. Nutrients 2019, 11, 1825. [Google Scholar] [CrossRef] [PubMed]
Table 1. Main characteristics of study participants (n = 197).
Table 1. Main characteristics of study participants (n = 197).
VariablesMean, Absolute NumberSD,
Percentage
MinMax
Age, y68.36.86099
Female n (%)16383
Weight, kg68.912.040.8108.0
Height, m154.78.1139.0184.0
Educational level
  Primary school (4 years)3618.3
  Middle school (8 years)5628.4
  Secondary school (11 years)4221.3
  Undergraduate (14–15 years)4824.4
  Graduate (18–21 years)157.6
BMI, kg/m228.75.015.243.1
Underweight, n (%)179
Normal weight, n (%)5226
Overweight, n (%)12865
5STS, s14.36.53.070.0
Absolute muscle power, W154.967.018.0648.0
Relative muscle power, W/BMI0.020.0080.0000.10
Allometric muscle power, W/m20.640.260.092.70
Energy intake, kcal1846.1545.1636.64490.1
Protein, g106.140.930.7228.2
Protein, g/kg1.580.650.44.0
Protein at breakfast, g/kg0.180.1100.6
Protein at lunch, g/kg0.830.4202.3
Protein at dinner, g/kg0.350.4101.8
Valine, g/kg5.32.11.611.4
Isoleucine, g/kg4.72.30.210.9
Leucine, g/kg8.03.12.317.3
5STS = sit-to-stand test; BMI = body mass index; SD = standard deviation.
Table 2. Person’s correlation analysis for the association between muscle power and protein-related parameters (n = 197).
Table 2. Person’s correlation analysis for the association between muscle power and protein-related parameters (n = 197).
VariablesAbsolute Muscle PowerRelative Muscle PowerAllometric Muscle Power
Kilocalories−0.039−0.049−0.055
Protein−0.011−0.031−0.028
Protein/kg body weight−0.241 *−0.120−0.233 *
Protein at breakfast−0.134−0.111−0.132
Protein at lunch−0.210 *−0.092−0.201 *
Protein at dinner−0.0440.018−0.047
Valine0.010−0.009−0.008
Isoleucine0.003−0.0160.004
Leucine0.004−0.015−0.014
* p < 0.05.
Table 3. Linear regression analysis for the association between muscle power and protein-related parameters (n = 197).
Table 3. Linear regression analysis for the association between muscle power and protein-related parameters (n = 197).
Absolute Muscle Power
UnadjustedAdjusted *
VariablesUnstandardized Coefficientsp Value95% CIUnstandardized Coefficientsp Value95% CI
Protein intake/body weight−23.20.005−39.2, −7.2−27.80.01−50.0, −5.5
Lunch protein intake−25.70.04−50.3, −1.0−12.30.37−39.8, 15.1
Allometric Muscle Power
UnadjustedAdjusted *
VariablesUnstandardized CoefficientspValue95% CIUnstandardized CoefficientspValue95% CI
Protein intake/body weight−0.080.007−0.151, −0.024−0.080.05−0.174, 0.01
Lunch protein intake−0.090.06−0.191, 0.004−0.030.48−0.14, 0.96
* Adjusted for age, body mass index, sex, and kilocalories; CI = confidence interval.
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Coelho-Júnior, H.J.; Azzolino, D.; Calvani, R.; Gonçalves, I.d.O.; Tosato, M.; Landi, F.; Cesari, M.; Picca, A.; Marzetti, E. Lower-Limb Muscle Power Is Negatively Associated with Protein Intake in Older Adults: A Cross-Sectional Study. Int. J. Environ. Res. Public Health 2022, 19, 14579. https://doi.org/10.3390/ijerph192114579

AMA Style

Coelho-Júnior HJ, Azzolino D, Calvani R, Gonçalves IdO, Tosato M, Landi F, Cesari M, Picca A, Marzetti E. Lower-Limb Muscle Power Is Negatively Associated with Protein Intake in Older Adults: A Cross-Sectional Study. International Journal of Environmental Research and Public Health. 2022; 19(21):14579. https://doi.org/10.3390/ijerph192114579

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Coelho-Júnior, Hélio José, Domenico Azzolino, Riccardo Calvani, Ivan de Oliveira Gonçalves, Matteo Tosato, Francesco Landi, Matteo Cesari, Anna Picca, and Emanuele Marzetti. 2022. "Lower-Limb Muscle Power Is Negatively Associated with Protein Intake in Older Adults: A Cross-Sectional Study" International Journal of Environmental Research and Public Health 19, no. 21: 14579. https://doi.org/10.3390/ijerph192114579

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