Abstract
Background
A loss of muscle mass may be influenced by multiple factors. Insulin sensitivity and metabolic acidosis are associated with muscle wasting and may be improved with potassium intake. This study evaluated the association between dietary potassium intake and skeletal muscle mass.
Methods
We performed a cross-sectional study with data obtained from the Korean National Health and Nutrition Examination Survey (KNHANES) (2008–2011). Participant’s daily food intake was assessed using a 24-h recall method. Appendicular skeletal muscle mass (ASM) was calculated as the sum of muscle mass in both arms and legs, measured using dual energy X-ray absorptiometry. The skeletal muscle index (SMI) was calculated as ASM divided by height2 (kg/m2). Low muscle mass was defined as a SMI < 7.0 kg/m2 for men and < 5.4 kg/m2 for women.
Results
Data from 16,558 participants (age ≥ 19 years) were analyzed. Participants were categorized into quintiles according to their potassium intake. Sex-specific differences were found in the association between potassium intake and muscle mass (PInteraction < 0.001). In men, higher potassium intake was associated with lower odds for low muscle mass; the fully adjusted odds ratios (95% confidence intervals) were 0.78 (0.60–1.03), 0.71 (0.54–0.93), 0.68 (0.51–0.90), and 0.71 (0.51–0.98) for the top four quintiles (referenced against the lowest quintile), respectively. However, this association was attenuated in women after adjusting for total energy intake. Higher potassium intakes were also associated with a greater SMI.
Conclusions
Higher dietary potassium intake decreased the odds of low muscle mass in men but not in women.
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Introduction
Skeletal muscle mass is a body tissue that play an important role in metabolic regulation, movement, and strength [1, 2]. Muscle mass decreases as much as 3–8% each decade after the age of 30–40 years and the rate of loss increases to 15% each decade after the age of 70 years [3]. A loss of muscle mass and strength resulting in impaired physical function, a condition called sarcopenia, is now recognized as a clinical concern for public health, especially in the aging population [4, 5]. Low muscle mass leads to reduced muscle function, [6] which may be associated with an increased risk of adverse health outcomes such as type 2 diabetes, metabolic syndrome, cardiovascular disease, frailty, and reduced quality of life [7,8,9,10]. Therefore, for overall health it is important to maintain optimal muscle mass across the lifespan.
Although a loss of muscle mass usually occurs with aging, the degree or rate of decrease in muscle mass varies across the population, indicating that the loss of muscle mass may be influenced by multiple factors [11]. In particular, loss of muscle mass is thought to be faster in men than in women, which may be mainly mediated by hormonal factors [12]. In addition, lack of physical activity, malnutrition, chronic diseases, insulin resistance or mild metabolic acidosis can be associated with muscle wasting [13,14,15,16].
Potassium is a vital element that plays an important role in maintaining cell function, particularly in muscles and nerves and has various health benefits; increased potassium intake has proved to be effective in reducing blood pressure [17] and was associated with a reduced risk of stroke [18]. As a result, the World Health Organization recommends an increase in potassium intake from food for reducing blood pressure and the risks of cardiovascular disease and stroke in adults [19]. Dietary potassium intake may also have a beneficial effect on bone health and insulin sensitivity [20, 21]. Higher potassium intake was associated with enhanced bone mineral density, probably by neutralizing acid load and consequently reducing calcium loss from the bone [20, 22, 23]. Lower potassium intake was associated with lower insulin sensitivity [21, 24].
The proposed methods to prevent a loss of muscle mass in the elderly are mainly protein intake and exercise [25, 26]. However, there have been little evidence of the effectiveness of other dietary approaches on muscle mass. Although some studies show an association between the intake of minerals, such as calcium and magnesium, and muscle mass, there are few studies on the role of potassium intake on muscle mass [27,28,29]. Given any association between factors that may be associated with muscle loss, such as insulin resistance or mild metabolic acidosis, and the beneficial effects of potassium on these factors, we sought to examine the association between dietary potassium intake and muscle mass. Furthermore, given that loss of muscle mass is different between men and women, we sought to evaluate the association of dietary potassium intake with loss of muscle mass according to sex.
Materials and methods
Study subjects
We extracted and examined data obtained from the fourth and fifth Korean National Health and Nutrition Examination Survey (KNHANES), conducted by the Korean Centers for Disease Control and Prevention (KCDC) from 2008 to 2011. This survey used a stratified, multistage clustered probability sampling method to collect a representative sample of the noninstitutionalized Korean population. A total of 9744; 10,533; 8958; and 8518 participants were recruited in KNHANES in 2008, 2009, 2010, and 2011, respectively, and the response rates were 77.8, 82.8, 81.9, and 80.4%, respectively. The survey was composed of a health interview, health examination, and nutrition survey.
All participants signed a written informed consent form and the protocols for KNHANES were approved by the Institutional review board of the KCDC. The KNHANES database is publicly available at the KNHANES website (http://knhanes.cdc.go.kr).
Demographic and laboratory measurements
Demographic factors (age and sex), history of diabetes and hypertension, and smoking status (current, past, or never) were obtained from the datasets. Blood samples were collected from participants after they had fasted for 8 h. Samples were then transported to a central laboratory (Neodin Medical Institute, Seoul, South Korea) and analyzed within 24 h. White blood cell count (WBC), serum hemoglobin, fasting glucose, total cholesterol, and serum creatinine (sCr) values were used for analyses. Estimated glomerular filtration rate (eGFR) was calculated using the Chronic Kidney Disease Epidemiology Collaboration equation [30] as follows:
eGFR (mL/min/1.73 m2) = 141 × min (sCr/κ, 1)α × max (sCr/κ, 1)–1.209 × 0.993Age (× 1.018 if female) (× 1.159 if black), where κ is 0.7 for women and 0.9 for men, α is − 0.329 for women and − 0.411 for men, min (sCr/κ, 1) is the minimum of sCr/κ or 1, and max (sCr/κ, 1) is the maximum of sCr/κ or 1.
Anthropometric measurement and assessment of physical activity
Height and weight were measured directly by a trained investigator using a stadiometer and scale while the participants were wearing light clothing without shoes. Body mass index (BMI) was calculated as the individual’s weight (in kg) divided by their height (in meters squared) (kg/m2). Physical activity was evaluated by asking participants their physical activity level during each week using the Korean version of the International Physical Activity Questionnaire [31]. Physical activity levels were categorized as high, moderate, or low. High physical activity was defined as ≥20 min at a time of vigorous-intensity activity on at least 3 days per week. Moderate physical activity was defined as ≥30 min at a time of moderate-intensity activity on at least 5 days per week. Other physical activity was defined as all remaining intensities and volumes of activity.
Assessment of dietary nutrient intake
Dietary intake was surveyed in a face-to-face interview at the participant’s home. The food intake questionnaire is an open-ended survey using a 24-h recall method with various measuring aids to determine the participant’s intake of various dishes and foods. Survey staff members completed an intensive training course and conducted supervised practice interviews before conducting a survey with a participant. Survey staff were retrained five to six times a year to ensure they followed proper techniques and protocols. The types and quantities of food examined were coded by computerized methods and nutrient intake levels were determined from this data using various databases and formulas. The details of the nutrition survey protocol are described on the KNHANES website (http://knhanes.cdc.go.kr).
Measurements of skeletal muscle mass index
Bone mineral contents and body composition were measured by licensed technicians using dual energy X-ray absorptiometry (DXA) (Discovery QDR 4500 W, Hologic Inc., Belford, MA, USA). Participants fasted prior to the assessment and were in the supine position during the assessment. All non-fat and non-bone tissue was assumed to be skeletal muscle. Appendicular skeletal muscle mass (ASM) was calculated as the sum of skeletal muscle mass in both arms and legs, as measured by DXA. The subject’s skeletal muscle mass index (SMI) was calculated as their ASM (kg) divided by their height in meters squared (m2). Low muscle mass was defined as SMI values < 7.0 kg/m2 for men and < 5.4 kg/m2 for women, as recommended by the Asian Working Group for Sarcopenia [32].
Statistical methods
Characteristics of participants were described across potassium intake quintiles and trends across categories were evaluated using either a Wilcoxon-type non-parametric trend test or a linear regression model, as appropriate. The association between categorized potassium intake and low muscle mass was assessed with logistic regression models, using the lowest quintile as a reference. Four hierarchical models were examined: (1) adjusted for age and sex (Model 1); (2) adjusted for additional comorbidities (diabetes and hypertension), BMI, smoking status, number of days of weight training per week, physical activity (high, moderate, or other), WBC, hemoglobin, and total cholesterol (Model 2); (3) adjusted for the variables included in Model 2, eGFR, and protein intake (Model 3); and (4) adjusted for the variables included in Model 3 and total energy intake (Model 4). Effect modification by sex was examined by adding the interaction terms into the logistic regression models, followed by subgroup analyses (man or woman). A receiver operating characteristic (ROC) curve was constructed to assess the ability of dietary potassium intake to predict low muscle mass. The association between potassium intake, as a continuous variable, and low muscle mass, adjusted as previously mentioned, was examined. A restricted cubic spline model with four knots was also used to examine the association of potassium intake with low muscle mass. In sensitivity analysis, the association between potassium intake and SMI was assessed using a linear regression model with the four aforementioned adjustment levels.
We assessed missing data in our covariates and found that hypertension, BMI, smoking status, number of days of weight training per week, physical activity, WBC, hemoglobin, cholesterol, and protein intake had missing data in < 5% of our cohort, except for diabetes (6.8%). We performed multiple imputations using a multivariate normal distribution. We included the variables including age, sex, hypertension, diabetes, BMI, smoking status, number of days of weight training per week, physical activity, WBC, hemoglobin, cholesterol, eGFR, protein intake, total energy intake, and SMI in the imputation model using 10 imputed datasets. The estimates were combined using Rubin’s rules [33]. Statistical analyses were conducted using STATA, version 13.1 (StataCorp LP, College Station, TX, USA).
Results
Patient characteristics
Among the 37,753 participants included in the KNHANES, the 17,059 subjects aged ≥19 years whose surveys included DXA and 24-h dietary recall data were included in this cross-sectional study. Of those potential subjects, 501 subjects without data on SMI were excluded from the analysis (Fig. 1). Thus, a total of 16,558 participants were finally analyzed in this study. The participants were categorized into quintiles according to their daily potassium intake; the median (interquartile range [IQR]) potassium intake of each quintile was 1.4 (1.1–1.6), 2.1 (1.9–2.2), 2.7 (2.5–2.9), 3.5 (3.2–3.7), and 4.9 (4.4–5.8) g/day. The baseline characteristics of the study participants across quintiles of potassium intake are described in Table 1. In the overall cohort, the mean age was 50 ± 16 years and 40% were men. Median (IQR) potassium intake was 2.7 (1.9–3.7) g/day. Median (IQR) SMI was 6.6 kg/m2. Mean ± SD baseline eGFR was 96 ± 17 mL/min/1.73 m2. The proportion of participants with eGFR < 30 mL/min/1.73 m2 was less than 0.2%. Subjects with higher potassium intakes tended to be men. Subjects with higher potassium intakes also had a larger SMI, higher protein intake, and lower prevalence of hypertension.
Association between potassium intake and low muscle mass according to sex
In our cohort, 4174 (25.2%) subjects met diagnostic criteria for low muscle mass (24% of men and 26% of women). Higher dietary potassium intake tended to be associated with decreased odds for low muscle mass, but the association was attenuated after adjusting for total energy intake (Supplementary Fig. 1). The association between potassium intake and low muscle mass was significantly modified by sex (PInteraction < 0.001). For men, higher dietary potassium intake decreased the odds for low muscle mass across all adjustment levels. In a fully adjusted model, the highest quintile of potassium intake was associated with 29% lower odds of low muscle mass compared to the lowest quintile of potassium intake; the fully adjusted odds ratio (OR) and 95% confidence interval (CI) for the second to fifth quintiles were 0.78 (0.60–1.03), 0.71 (0.54–0.93), 0.68 (0.51–0.90), and 0.71 (0.51–0.98). However, for women, the association of higher potassium intake with lower odds for low muscle mass was attenuated after adjusting for total energy intake (Table 2). In restricted cubic spline models, the association between higher potassium intake (as a continuous variable) and low muscle mass similarly showed sex-specific differences; the association was attenuated in women (Fig. 2a and b).
In a sensitivity analysis of the association between potassium intake and SMI, higher quintiles of potassium intake were associated with a graded increase of SMI compared to the lowest quintile of potassium intake in all adjusted models, with some attenuation after adjusting for energy intake (Fig. 3). Restricted cubic spline models for the association between potassium intake as a continuous variable and SMI also showed sex-specific differences (Fig. 4a and b).
Linear regression analyses with four levels adjustment showing the association between dietary potassium intake and skeletal muscle mass index among 16,558 Korean general population. Model 1 is adjusted for age and sex. Model 2 is adjusted for all variables included in Model 1, diabetes, hypertension, body mass index, smoking status, physical activity, white blood cell count, hemoglobin, and total cholesterol. Model 3 is adjusted for all variables included in Model 2, estimated glomerular filtration rate, and protein intake. Model 4 is adjusted for all variables included in Model 3 and total energy intake
Discussion
In this study, we found a trend toward decreased odds for low muscle mass across higher dietary potassium intake in the general population but the association was attenuated after adjusting for total energy intake. Interestingly, sex was observed to be a potential effect modifier of the association between potassium intake and low muscle mass. The association between higher potassium intake and low muscle mass remained robust even after adjusting for energy intake in men but not in women. These findings indicate that dietary potassium intake may affect skeletal muscle mass independent of total energy intake in men but that total energy intake rather than potassium intake per se may affect muscle mass in women.
A previous study showed a favorable effect of alkaline diets on lean tissue mass in adults ≥65 years old by assessing the association between 24-h urinary potassium and the percentage of lean tissue mass [29]. The finding of our study is in line with that of this previous study. The beneficial effects of potassium on skeletal muscle mass may be partially explained by acid-base theory [14, 34]. Chronic metabolic acidosis in chronic kidney disease is associated with protein-energy wasting and loss of muscle mass [14, 35]. Treatment of metabolic acidosis in dialysis patients ameliorates protein-energy wasting [34, 36]. In normal adults, metabolic acidosis also stimulates nitrogen loss due to accelerated degradation of muscle protein [37, 38]. A diet that is high in meats and grains promotes low-grade metabolic acidosis [39]. Treatment with potassium bicarbonate was shown to improve the nitrogen balance in postmenopausal women with mild metabolic acidosis [40]. Therefore, alkaline potassium salts produced from vegetables and fruits may have a protective effect against a loss of muscle mass by neutralizing an acidic condition [41, 42].
Another putative mechanism for the association between potassium intake and muscle mass is their relationship to insulin sensitivity and inflammation. Impaired insulin signaling in cultured muscle cells stimulated proteolysis, causing muscle atrophy [15]. Insulin resistance in patients without diabetes receiving dialysis was associated with skeletal muscle protein breakdown [43]. High potassium intake was associated with a reduced risk for developing insulin resistance or diabetes mellitus [44]. Moreover, chronic inflammation is also a well-known risk factor for loss of muscle mass [45]. Low dietary potassium is known to be pro-inflammatory and associated with increased free radical generation [46]. Therefore, improved insulin resistance and a lower inflammatory state resulting from high potassium intake may help reduce muscle protein breakdown.
The underlying mechanism for the sex-specific difference in the association between potassium intake and muscle mass is unclear. Although the prevalence of sarcopenia was higher for women in that absolute muscle mass was smaller to start with, the rate of loss of muscle mass was higher in men than women in previous longitudinal studies [12]. However, the anabolic response of muscle to nutrition with or without exercise was subtle in older women [47]. Likewise, the benefits of sex hormones such as testosterone on preserving muscle mass also differed by sex; the effects were minimal or unknown in women [12]. Sex-specific differences in muscle protein metabolism, which is thought to be primarily associated with hormone profiles, may exist and may consequently lead to differences in therapeutic effects [48]. Another possible explanation is sex difference in insulin resistance. Insulin resistance is higher in men than women, possibly associated with differences in adipokines and sex hormones [49]. Improved insulin sensitivity in men may benefit more from high potassium intake than in women.
We acknowledge several limitations in our study. First, although we adjusted for potential confounders to investigate the association of dietary potassium intake with low muscle mass, there may be other unmeasured confounding factors. In particular, it might be that adults with higher potassium intakes are those who eat more, are heavier, and have more muscle mass. However, the association between dietary potassium intake and muscle mass remained robust even after adjusting for total energy intake in men. In addition, we could not prove a temporal relationship with our results due to the cross-sectional design of the study. Second, the KNHANES used a 24-h dietary recall method with various measuring aids to assess potassium intake, which might lead to a measurement error. This method, in particular, did not reflect seasonal variations which may underestimate mean potassium intake and attenuate the true association of potassium intake with health outcomes [50]. However, this effect may bias our results toward the null. Furthermore, we used self-reported physical activity. Although the questionnaire was validated, the assessment of physical activity by self-reporting can lead to response bias, thus overestimating actual activity. However, even after the effect of physical activity as a confounding variable was adjusted in our study, the association between primary exposure and outcome was not affected. Third, the mean eGFR in our cohort was 96 mL/min/1.73 m2. The proportion of participants with eGFR < 30 mL/min/1.73 m2 was only < 0.2%. High potassium intake can cause hyperkalemia and subsequently poor outcomes in patients with decreased renal function. Therefore, the ability to extrapolate our study findings to adults with decreased renal function is limited. Lastly, as data on muscle strength was not available, we could not address whether higher potassium intake was associated with greater muscle strength.
Conclusions
We demonstrated a positive association of higher potassium intake with lower odds of low muscle mass for men but not for women. Based on our findings, future clinical trials are needed to establish not only a causal relationship between potassium intake and preservation of muscle mass and function, but also an effect modification on that association by sex. Moreover, in further studies, the use of more objective tools for assessment of variables such as potassium intake, muscle mass and function, and physical activity may be more helpful in proving the results of the study.
Availability of data and materials
The KNHANES database is publicly available at the KNHANES website (http://knhanes.cdc.go.kr).
Abbreviations
- ASM:
-
Appendicular skeletal muscle mass
- BMI:
-
Body mass index
- DXA:
-
Dual energy X-ray absorptiometry
- eGFR:
-
Estimated glomerular filtration rate
- IQR:
-
Interquartile range
- ROC:
-
Receiver operating characteristic
- sCr:
-
Serum creatinine
- SMI:
-
Skeletal muscle index
- WBC:
-
White blood cell count
References
Mukund K, Subramaniam S. Skeletal muscle: a review of molecular structure and function, in health and disease. Wiley Interdiscip Rev Syst Biol Med. 2020;12:e1462.
Srikanthan P, Karlamangla AS. Relative muscle mass is inversely associated with insulin resistance and prediabetes. Findings from the third National Health and nutrition examination survey. J Clin Endocrinol Metab. 2011;96:2898–903.
McCormick R, Vasilaki A. Age-related changes in skeletal muscle: changes to life-style as a therapy. Biogerontology. 2018;19:519–36.
Cruz-Jentoft AJ, Landi F, Schneider SM, Zuniga C, Arai H, Boirie Y, Chen LK, Fielding RA, Martin FC, Michel JP, et al. Prevalence of and interventions for sarcopenia in ageing adults: a systematic review. Report of the international sarcopenia initiative (EWGSOP and IWGS). Age Ageing. 2014;43:748–59.
Marty E, Liu Y, Samuel A, Or O, Lane J. A review of sarcopenia: enhancing awareness of an increasingly prevalent disease. Bone. 2017;105:276–86.
Charlier R, Mertens E, Lefevre J, Thomis M. Muscle mass and muscle function over the adult life span: a cross-sectional study in Flemish adults. Arch Gerontol Geriatr. 2015;61:161–7.
Yuki A, Ando F, Otsuka R, Shimokata H. Sarcopenia based on the Asian working Group for Sarcopenia criteria and all-cause mortality risk in older Japanese adults. Geriatr Gerontol Int. 2017;17:1642–7.
Kim JK, Kim SG, Oh JE, Lee YK, Noh JW, Kim HJ, Song YR. Impact of sarcopenia on long-term mortality and cardiovascular events in patients undergoing hemodialysis. Korean J Intern Med. 2019;34:599–607.
Greco EA, Pietschmann P, Migliaccio S. Osteoporosis and sarcopenia increase frailty syndrome in the elderly. Front Endocrinol (Lausanne). 2019;10:255.
Son JW, Lee SS, Kim SR, Yoo SJ, Cha BY, Son HY, Cho NH. Low muscle mass and risk of type 2 diabetes in middle-aged and older adults: findings from the KoGES. Diabetologia. 2017;60:865–72.
Walston JD. Sarcopenia in older adults. Curr Opin Rheumatol. 2012;24:623–7.
Anderson LJ, Liu H, Garcia JM. Sex differences in muscle wasting. Adv Exp Med Biol. 2017;1043:153–97.
Wang XH, Mitch WE. Mechanisms of muscle wasting in chronic kidney disease. Nat Rev Nephrol. 2014;10:504–16.
Caso G, Garlick PJ. Control of muscle protein kinetics by acid-base balance. Curr Opin Clin Nutr Metab Care. 2005;8:73–6.
Wang X, Hu Z, Hu J, Du J, Mitch WE. Insulin resistance accelerates muscle protein degradation: activation of the ubiquitin-proteasome pathway by defects in muscle cell signaling. Endocrinology. 2006;147:4160–8.
Fung FY, Koh YLE, Malhotra R, Ostbye T, Lee PY, Shariff Ghazali S, Tan NC. Prevalence of and factors associated with sarcopenia among multi-ethnic ambulatory older Asians with type 2 diabetes mellitus in a primary care setting. BMC Geriatr. 2019;19:122.
Poorolajal J, Zeraati F, Soltanian AR, Sheikh V, Hooshmand E, Maleki A. Oral potassium supplementation for management of essential hypertension: a meta-analysis of randomized controlled trials. PLoS One. 2017;12:e0174967.
Vinceti M, Filippini T, Crippa A, de Sesmaisons A, Wise LA, Orsini N. Meta-analysis of potassium intake and the risk of stroke. J Am Heart Assoc. 2016;5:e004210.
WHO. Guideline: Potassiium Intake for Adults and Chldren. Geneva: World Health Organization (WHO); 2012.
Kong SH, Kim JH, Hong AR, Lee JH, Kim SW, Shin CS. Dietary potassium intake is beneficial to bone health in a low calcium intake population: the Korean National Health and nutrition examination survey (KNHANES) (2008-2011). Osteoporos Int. 2017;28:1577–85.
Park YM, Kwock CK, Park S, Eicher-Miller HA, Yang YJ. An association of urinary sodium-potassium ratio with insulin resistance among Korean adults. Nutr Res Pract. 2018;12:443–8.
Sebastian A, Morris RC Jr. Improved mineral balance and skeletal metabolism in postmenopausal women treated with potassium bicarbonate. N Engl J Med. 1994;331:279.
Barzel US. The skeleton as an ion exchange system: implications for the role of acid-base imbalance in the genesis of osteoporosis. J Bone Miner Res. 1995;10:1431–6.
Chatterjee R, Biggs ML, de Boer IH, Brancati FL, Svetkey LP, Barzilay J, Djousse L, Ix JH, Kizer JR, Siscovick DS, et al. Potassium and glucose measures in older adults: the cardiovascular health study. J Gerontol A Biol Sci Med Sci. 2015;70:255–61.
Anton SD, Hida A, Mankowski R, Layne A, Solberg LM, Mainous AG, Buford T. Nutrition and exercise in sarcopenia. Curr Protein Pept Sci. 2018;19:649–67.
Liao CD, Chen HC, Huang SW, Liou TH. The role of muscle mass gain following protein supplementation plus exercise therapy in older adults with sarcopenia and frailty risks: a systematic review and meta-regression analysis of randomized trials. Nutrients. 2019;11:1713.
van Dronkelaar C, van Velzen A, Abdelrazek M, van der Steen A, Weijs PJM, Tieland M. Minerals and sarcopenia; the role of calcium, Iron, magnesium, phosphorus, potassium, selenium, sodium, and zinc on muscle mass, muscle strength, and physical performance in older adults: a systematic review. J Am Med Dir Assoc. 2018;19:6–11 e13.
Welch AA, MacGregor AJ, Skinner J, Spector TD, Moayyeri A, Cassidy A. A higher alkaline dietary load is associated with greater indexes of skeletal muscle mass in women. Osteoporos Int. 2013;24:1899–908.
Dawson-Hughes B, Harris SS, Ceglia L. Alkaline diets favor lean tissue mass in older adults. Am J Clin Nutr. 2008;87:662–5.
Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF 3rd, Feldman HI, Kusek JW, Eggers P, Van Lente F, Greene T, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150:604–12.
Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003;35:1381–95.
Chen LK, Liu LK, Woo J, Assantachai P, Auyeung TW, Bahyah KS, Chou MY, Chen LY, Hsu PS, Krairit O, et al. Sarcopenia in Asia: consensus report of the Asian working Group for Sarcopenia. J Am Med Dir Assoc. 2014;15:95–101.
Rubin DB. Multiple imputation for nonresponse in surveys. New York: Wiley; 1987.
Graham KA, Reaich D, Channon SM, Downie S, Goodship TH. Correction of acidosis in hemodialysis decreases whole-body protein degradation. J Am Soc Nephrol. 1997;8:632–7.
Fahal IH. Uraemic sarcopenia: aetiology and implications. Nephrol Dial Transplant. 2014;29:1655–65.
Graham KA, Reaich D, Channon SM, Downie S, Gilmour E, Passlick-Deetjen J, Goodship TH. Correction of acidosis in CAPD decreases whole body protein degradation. Kidney Int. 1996;49:1396–400.
Reaich D, Channon SM, Scrimgeour CM, Goodship TH. Ammonium chloride-induced acidosis increases protein breakdown and amino acid oxidation in humans. Am J Physiol. 1992;263:E735–9.
Ballmer PE, McNurlan MA, Hulter HN, Anderson SE, Garlick PJ, Krapf R. Chronic metabolic acidosis decreases albumin synthesis and induces negative nitrogen balance in humans. J Clin Invest. 1995;95:39–45.
Frassetto LA, Todd KM, Morris RC Jr, Sebastian A. Estimation of net endogenous noncarbonic acid production in humans from diet potassium and protein contents. Am J Clin Nutr. 1998;68:576–83.
Frassetto L, Morris RC Jr, Sebastian A. Potassium bicarbonate reduces urinary nitrogen excretion in postmenopausal women. J Clin Endocrinol Metab. 1997;82:254–9.
Remer T. Influence of diet on acid-base balance. Semin Dial. 2000;13:221–6.
Demigne C, Sabboh H, Remesy C, Meneton P. Protective effects of high dietary potassium: nutritional and metabolic aspects. J Nutr. 2004;134:2903–6.
Siew ED, Pupim LB, Majchrzak KM, Shintani A, Flakoll PJ, Ikizler TA. Insulin resistance is associated with skeletal muscle protein breakdown in non-diabetic chronic hemodialysis patients. Kidney Int. 2007;71:146–52.
Chatterjee R, Colangelo LA, Yeh HC, Anderson CA, Daviglus ML, Liu K, Brancati FL. Potassium intake and risk of incident type 2 diabetes mellitus: the coronary artery risk development in young adults (CARDIA) study. Diabetologia. 2012;55:1295–303.
Dalle S, Rossmeislova L, Koppo K. The role of inflammation in age-related sarcopenia. Front Physiol. 2017;8:1045.
Yang BC, Li DY, Weng YF, Lynch J, Wingo CS, Mehta JL. Increased superoxide anion generation and altered vasoreactivity in rabbits on low-potassium diet. Am J Physiol. 1998;274:H1955–61.
Bukhari SS, Phillips BE, Wilkinson DJ, Limb MC, Rankin D, Mitchell WK, Kobayashi H, Greenhaff PL, Smith K, Atherton PJ. Intake of low-dose leucine-rich essential amino acids stimulates muscle anabolism equivalently to bolus whey protein in older women at rest and after exercise. Am J Physiol Endocrinol Metab. 2015;308:E1056–65.
Markofski MM, Volpi E. Protein metabolism in women and men: similarities and disparities. Curr Opin Clin Nutr Metab Care. 2011;14:93–7.
Geer EB, Shen W. Gender differences in insulin resistance, body composition, and energy balance. Gend Med. 2009;6(Suppl 1):60–75.
Va P, Dodd KW, Zhao L, Thompson-Paul AM, Mercado CI, Terry AL, Jackson SL, Wang CY, Loria CM, Moshfegh AJ, et al. Evaluation of measurement error in 24-hour dietary recall for assessing sodium and potassium intake among US adults - National Health and nutrition examination survey (NHANES), 2014. Am J Clin Nutr. 2019;109:1672–82.
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YL, SC, and SRK designed research; YL, ML, YMW, SC, and SRK conducted research; YL, ML, and YMW analyzed data; YL wrote paper; YL, ML, YMW, SC, and SRK reviewed paper; YL had primary responsibility for final content. The authors read and approved the final manuscript.
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Additional file 1.
Odds ratios for low muscle mass with four levels of adjustment based upon baseline dietary potassium intake among 16,558 Korean general population. Model 1 is adjusted for age and sex. Model 2 is adjusted for variables included in Model 1, diabetes, hypertension, body mass index, smoking status, physical activity, white blood cell count, hemoglobin, and total cholesterol. Model 3 is adjusted for all variables included in Model 2, estimated glomerular filtration rate, and protein intake. Model 4 is adjusted for all variables included in Model 3 and total energy intake.
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Lee, YJ., Lee, M., Wi, Y.M. et al. Potassium intake, skeletal muscle mass, and effect modification by sex: data from the 2008–2011 KNHANES. Nutr J 19, 93 (2020). https://doi.org/10.1186/s12937-020-00614-z
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Accepted:
Published:
DOI: https://doi.org/10.1186/s12937-020-00614-z