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Association between Healthy Eating Index-2015 scores and probable sarcopenia in community-dwelling Iranian older adults: a cross-sectional study

Published online by Cambridge University Press:  25 March 2021

Zahra Esmaeily
Affiliation:
Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Zahra Tajary
Affiliation:
Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Sharzad Daei
Affiliation:
Department of Nutrition, Science and Research Branch, Islamic Azad University, Tehran, Iran
Mahshid Rezaei
Affiliation:
Department of Nutrition, Science and Research Branch, Islamic Azad University, Tehran, Iran
Atefeh Eyvazkhani
Affiliation:
Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Ahmad Reza Dorosty Motlagh*
Affiliation:
Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Andriko Palmowski
Affiliation:
Department of Rheumatology and Clinical Immunology, Charité – University Medicine Berlin, Berlin, Germany
*
*Corresponding author. Ahmad R. Dorosty, fax 98-21-8897-4462, email [email protected]

Abstract

Sarcopenia is associated with frailty and disability in older adults. Adherence to current dietary guidelines in addition to physical activity could prevent muscle wasting and weakness. The Healthy Eating Index-2015 (HEI) is a tool to assess diet quality. We aimed to investigate the association between HEI scores and probable sarcopenia (PS) among older adults in Tehran. 201 randomly selected older adults were included in this cross-sectional study between May and October 2019 in Tehran, Iran. A previously validated semi-quantitative food frequency questionnaire was used to estimate HEI scores and dietary intake. Handgrip strength (HGS) was measured to evaluate the PS. Statistical evaluation included descriptive analysis, logistic and linear regression. Those probably suffering from sarcopenia had significantly lower HEI scores (P=0⋅02). After adjusting for confounders, HEI scores and HGS were still significantly associated (adjusted R2=0⋅56, slope β=0⋅03, P=0⋅09). Older adults with a low PS had a higher ratio of monounsaturated and polyunsaturated to saturated fatty acids (P= 0⋅06) and ingested less added sugars and saturated fats (P=0⋅01 and P=0⋅02, respectively). Furthermore, consuming more total protein foods correlated positively with muscle strength (P=0⋅01, R=0⋅18). To sum up, HEI scores were associated with PS, measured by HGS, indicating that adhering to the HEI might improve muscle strength in aging individuals.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press in association with The Nutrition Society

As life expectancy is increasing, there is a need for studies on health problems of the aging population(Reference Hashemi, Shafiee and Motlagh1). Aging goes hand in hand with physical changes which may lead to both decreased muscle mass and decreased physical function. In pathologic form, this is called sarcopenia(Reference Abdelmawgoud, Brown and Sui2). According to the European Working Group of Sarcopenia in Older People (EWGSOP), sarcopenia can be defined as a decrease of muscle mass and physical activity or a low muscle mass with decreased muscle strength in older adults. Probable sarcopenia (PS) can be estimated by evaluating muscle strength(Reference Cruz-Jentoft, Bahat and Bauer3). Decreasing muscle strength starts to occur gradually in the thirties and further accelerates by the age of fifty(Reference Keller and Engelhardt4). Sarcopenia has different causes, which include some diseases, decreased calorie intake, lack of physical activity, low muscle perfusion, mitochondrial dysfunction, decreased anabolic hormones and increased pro-inflammatory cytokines(Reference Morley, Anker and von Haehling5). It can lead to major health problems in older adults, e.g., muscle weakness increases the odds of falling(Reference Van Ancum, Pijnappels and Jonkman6).

Several studies have been published concerning the role of nutrient intake and muscle weakness or sarcopenia. However, assessing a nutrient by itself may give only a little information about diet quality(Reference Esmaili, Mohd Yusof and Abu Saad7,Reference Lockheart, Steffen and Rebnord8) . Few other studies have focused on dietary patterns rather than on a particular nutrient to examine relationships between diet and health status(Reference Brown, Harhay and Harhay9Reference Smee, Pumpa and Falchi11).

Assessing dietary pattern quality is one way to demonstrate a person's dietary status. The Healthy Eating Index (HEI) was developed by the United States Department of Agriculture (USDA) and is based on Dietary Guidelines for Americans (DGAs)(Reference Krebs-Smith, Pannucci and Subar12). Higher HEI scores indicate better adherence to the DGAs(Reference Reedy, Lerman and Krebs-Smith13).

Previous studies have evaluated associations between HEI scores and the risk of several morbidities. The prevalence of metabolic syndrome decreased and bone mineral density increased in Iranian women with high HEI scores. In a case-control study by Varkaneh et al., high HEI scores were associated with a decreased risk of breast cancer(Reference Bagheri, Soltani and Hashemi14Reference Kord-Varkaneh, Salehi-Sahlabadi and Zarezade16). Also, several dietary patterns have already been studied in the field of sarcopenia and muscle weakness. Studies showed that a Mediterranean diet is significantly associated with low odds of sarcopenia progression in contrast to pro-inflammatory diets(Reference Hashemi, Motlagh and Heshmat10,Reference Bagheri, Soltani and Hashemi14) . Other studies suggested that adherence to the HEI and Mediterranean diets might play a role in preventing muscle weakness in the elderly(Reference Kim and Kwon17,Reference Barrea, Muscogiuri and Di Somma18) . Given that the scarce number of Iranian studies on the association of diet with sarcopenia and abnormal handgrips strength, and the necessity of studies about improving lifestyle factors of older adults, the present study aimed to investigate the association of HEI values with PS in community-dwelling Iranian older adults in the Tehran district of Iran.

Methods

Data collection

This cross-sectional study was conducted between May and October 2019 in randomly selected older adults (≥60) residents of Tehran, Iran. Eligible participants were people with no changes in their dietary habits during last year, who could walk without any helping equipment, with no artificial or prosthetic limbs and with no history of congestive heart failure, chronic obstructive pulmonary disease, chronic renal failure, cirrhosis or active cancer.

A pilot study was conducted in 100 older adults to check the reliability of questionnaires and also to calculate the sample size, which was calculated as follows with a type I error (α)=0⋅05 and type II error )=80 %:

$$n = \displaystyle{{2\;{\left({Z_{1-{\alpha \over 2}} + Z_{1-\beta }} \right)}^2 [ {\bar{P}\lpar {1-\bar{P}} \rpar } ] } \over {{\lpar P_1-P_2\rpar }^2}} = \displaystyle{{2 \times {\lpar {1.96 + 0.84} \rpar }^2 + \lpar {0.723\;\times 0.277} \rpar } \over {{\lpar {0.641-0.805} \rpar }^2}} = 117$$

To include 117 participants with a high PS, 191 overall participants were originally needed. We sought to include 235 older adults to further increase statistical power. After asking about their dietary habits, physical and medical situations, 34 of the 235 individuals did not meet the inclusion criteria; therefore, 201 subjects eventually took part in the present study.

For sampling, Tehran was divided into five regions: East, West, North, South and city centre. Sampling was done in two stages. Firstly, a list of health centres – which participants attend for routine check-ups – was collected from every region and centres were selected by cluster sampling. Secondly, sampling was started in the first centre and continued until we found enough older adults with a high PS. We took written consent from the participants and gathered information on demographics, physical activities and socioeconomic and medical status. The amount of physical activity was estimated by asking participants about the daily average time used to exercise, jog or do other sports. Socioeconomic status was ascertained by gathering data about education and participants’ economic status. For determining the economic status, we used a 9-item questionnaire (possession of house, car, side-by-side refrigerator, washing machine, dishwasher, laptop/personal computer, sofa, microwave and handmade carpet)(Reference Safarpour, Dorosty Motlagh and Hosseini19) and asked about house and car ownership as we suspected to encounter refusals to declare monthly income. The participants’ economic status was categorised as Very bad: ≤3 items without any personal home and car. Bad: ≤3 items with personal home or car. 4–6 items without personal home and car. Average: 4–6 items with personal home or car. 7 items ≤ without a personal home and car. Good: 7 ≤ items with personal home or car. Very good: 7 items ≤ with personal home and car.

The present study was approved by the ethics committee of Tehran University of Medical Sciences. The protocol number of the local ethics committee was IR.TUMS.VCR.REC.1398.476.

Anthropometric measurements

Measurements included waist, hip and mid-upper arm circumferences (MUAC), height and weight. Considering these measurements, body mass index (BMI), waist-to-hip ratio (WHR) and waist-to-height ratio (WHtR) were calculated. Subjects were considered underweight and overweight/obese if their BMI values were lower than 23⋅5 and higher than 30⋅9 kg/m2, respectively(Reference Winter, MacInnis and Wattanapenpaiboon20). Abdominal obesity was defined as waist circumference higher than 102 and 88 cm in men and women, respectively. Besides, women with a WHR higher than 0⋅85 and subjects with WHtR higher than 0⋅6 were considered abdominally obese(Reference Schneider, Friedrich and Klotsche21,Reference Organization22) . Of note, WHR was not used for men because of cultural and religious issues. Weight (kg) and height (cm) were measured with light clothes and no shoes on with a Camry EB9011 scale (Camry Co) and a Fibre-Glass tape measure, respectively. Waist circumference was the midway between the lowest rib and the iliac crest; hip circumference was the maximum circumference of the hip when a participant stood firmly. The circumference of the mid-upper arm was measured on the non-dominant side with the elbow flexed by 90° midway between scapula and olecranon. Circumferences were measured by a Fibre-Glass tape measure as well.

Dietary data collection

In the present study, we used a previously validated semi-quantitative food frequency questionnaire (FFQ) with 147 items(Reference Mirmiran, Esfahani and Azizi23) for assessing dietary intake during the last year. Main items included intake of bread and grains, legumes, meat and meat-derived products, poultry, fish, eggs, dairies, kinds of butter, vegetables, pickles, fruits and fruit juices, oils, seeds and nuts, added sugar, drinks, spices and salt. Both frequencies and quantities of every item were asked. Questionnaires were completed by trained dietitians.

Calculation of HEI-2015 scores

A simple HEI scoring algorithm method was used in the present study. In this method, thirteen components containing total fruits, whole fruit, total vegetables, greens and beans, whole grains, dairy, total protein foods, seafood/plant proteins, fatty acids, refined grains, sodium, added sugars and saturated fats (including two categories for adequacy and moderation) receive scores. Every component has a minimum score of 0 and a maximum score of 5 or 10; amounts for gaining these scores have been reported elsewhere(Reference Krebs-Smith, Pannucci and Subar12). After scoring each component, the scores were summed up to obtain every individual's final score (ranging between 0 and 100). Reported amounts were converted to cups or ounces according to the scoring system. For converting to ounce, we divided it by 28⋅35; for converting to cup, we used the Food Patterns Equivalent Database (FPED)(Reference Bowman, Clemens and Shimizu24).

Probable sarcopenia

According to the EWGSOP2, the presence of PS was surrogately measured by handgrip strength (HGS)(Reference Cruz-Jentoft, Bahat and Bauer3). HGS was quantified by a squeeze dynamometer (Saehan SH5008, Co, Seoul, Korea). Participants sat on a chair with the arm flexed at 90° and pressed the dynamometer three times with each hand with maximum power and held it for 10 s. 30 s of rest were allowed between every attempt. Finally, the average maximum strength of each hand was defined to be the participant's HGS. The above-mentioned dynamometer has not been used in previous studies; thus, for assessing its accuracy, it was tested against a Jamar dynamometer, which is the gold standard also included in the EWGSOP2 standards(Reference Cruz-Jentoft, Bahat and Bauer3). Results of this comparison indicated that by multiplication by 1⋅6, we yielded the value estimated by the Jamar dynamometer. Consequently, participants were defined to have a high probability of PS if their HGS was <16⋅5 kg (men) and <10 kg (women).

Statistical analysis

IBM SPSS software, version 16, was used for statistical analysis. The Kolmogorov–Smirnov test was performed to assess if variables were normally distributed. Mean ± standard deviation (sd) and frequencies (%) are reported for continuous and nominal variables, respectively. HEI-2015 was divided into quartiles for assessing dietary quality. Student's t test and analysis of covariance (ANCOVA) were used to test for statistically significant differences in continuous variables between probably sarcopenic and non-sarcopenic participants; the χ2 test for assessing differences of participants in the HEI quartiles. Binary logistic regression was performed for evaluating the association between HEI and PS and odds ratio (OR) calculation. Finally, a multiple linear regression model was used to adjust for confounders of HGS to assess the actual relationship between HEI and HGS. The level of statistical significance α was set at 0⋅1 for the multiple linear regression and 0⋅05 for other tests.

Result

Participant characteristics

We finally included 201 participants. In Table 1, we summarised the main characteristics of these participants. They were on average 66 years old, had a daily physical activity of 32 min, and a BMI of 29 kg/m2. 46 (23 %) participants were men, 155 (77 %) were women. Cardiovascular diseases and skeletal disorders were the most prevalent diseases. 123 (61 %) subjects were considered to be probably sarcopenic judging from HGS. Participants with a high PS were significantly older (67⋅54 v. 63⋅9 years, P < 0⋅0001) and had a significantly worse economic status compared with subjects with normal HGS (P=0⋅002). Furthermore, subjects with a history of cardiovascular disorders and those taking cardiovascular medication tended to be more often probably sarcopenic than those without (P=0⋅004 and P < 0⋅0001, respectively).

Table 1. Participant characteristic

HGS, handgrip strength; sd, standard deviation; MUAC, mid-upper arm circumference; BMI, body mass index; WC, waist circumference; WHtR, waist to hight ratio; WHR, waist to hip ratio.

a Calculated in women.

* P < 0.05; Student's t test was used for comparing mean differences of quantitative variables, and χ2 test was used for qualitative variables.

HEI-2015 and handgrip strength

Mean HEI scores differed significantly between normal [60⋅55 (±9⋅85)] and probably sarcopenic [56⋅88 (±11⋅48)] groups by 3⋅67 (P=0⋅02). Associations between HEI components and PS are shown in Table 2. The probable-sarcopenic subjects had significantly lower scores of added sugars and saturated fatty acids. The assessment of the correlation between components of the HEI and HGS showed that there is a positive correlation between the scores of total protein foods (R=0⋅18, P=0⋅01), fatty acids (R=0⋅17, P=0⋅02), added sugars (R=0⋅13, P=0⋅06) and saturated fats (R=0⋅17, P=0⋅02) – participants with higher intake of total protein foods, poly- and monounsaturated fatty acids (PUFAs and MUFAs), and low intake of added sugars and saturated fats had significantly higher HGS. There was no statistically significant association between HEI quartiles and PS (Table 3). However, we found a reduction in proportions of probable-sarcopenic participants from 72⋅5 % in the lowest quartile to 54 % in the highest quartile. Those in the top HEI quartile were 59 and 69 % less likely to have PS in crude and adjusted models, respectively, in comparison to those in the lowest quartile (Table 4).

Table 2. HEI-2015 and the component scores across probable and non-sarcopenic subjects

HGS, handgrip strength; sd, standard deviation.

a All forms of fruits include whole fruits and fruit juices.

b All forms except juices.

c Includes legumes (beans and peas), dark-green vegetables and all other vegetables.

d Legumes (beans and peas).

e Meat, poultry, eggs, seafood, nuts, seeds and soy products.

f Seafood, nuts, seeds, soy products (other than beverages) and legumes (beans and peas).

g Ratio of PUFAs and MUFAs to saturated fatty acids.

* P ≤ 0·05, Student's t test.

** P ≤ 0·05, analysis of covariance (ANCOVA); Adjusted for age, family number, gender, CVD medication, height and physical activity.

Table 3. Association between HGS and quartiles of HEI-2015

HGS, handgrip strength; Q, quartile.

* P < 0·05; X2 test.

Table 4. Logistic regression: PS

a All forms of fruits include whole fruits and fruit juices.

b All forms except juices.

c Includes legumes (beans and peas), dark-green vegetables and all other vegetables.

d Legumes (beans and peas).

e Meat, poultry, eggs, seafood, nuts, seeds and soy products.

f Seafood, nuts, seeds, soy products (other than beverages) and legumes (beans and peas).

g Ratio of PUFAs and MUFAs to saturated fatty acids.

* Adjusted for age and gender.

** Adjusted for age, family number, gender, CVD medication, height and physical activity.

HEI-2015, handgrip strength and confounders

Multiple linear regression models evaluating HGS and HEI scores are shown in Table 5. There was a statistically significant positive association between HEI scores and HGS in both the unadjusted (P=0⋅04) and adjusted (P=0⋅02 and=0⋅09) models.

Table 5. Multiple linear regression for the association of handgrip strength with HEI-2015 and component scores

a All forms of fruits include whole fruits and fruit juices.

b All forms except juices.

c Includes legumes (beans and peas), dark-green vegetables and all other vegetables.

d Legumes (beans and peas).

e Meat, poultry, eggs, seafood, nuts, seeds and soy products.

f Seafood, nuts, seeds, soy products (other than beverages) and legumes (beans and peas).

g Ratio of PUFAs and MUFAs to saturated fatty acids.

Adjusted for age and gender.

Adjusted for age, family number, gender, CVD medication, height and physical activity.

* P < 0·1.

Discussion

The present results show that there is a statistically significant association between diet quality and PS. Participants with PS had lower HEI scores compared with healthy controls. Even after adjusting HGS – our surrogate parameter for PS – for several covariates, it was still significantly associated with HEI scores.

While the HEI has not yet been validated in an Iranian population, the main components of Iranian food are comparable to the US, Europe and the Middle East: refined grains like white rice and bread, potatoes and hydrogenated fats(Reference Esmaillzadeh and Azadbakht25), so HEI could be used as a good indicator of dietary intake status in the Iranian population. Based on our knowledge, this is the first study to assess the relationship between HEI and PS. In the present study, we used EWGSOP2 cutoff-values, which have been reported to be good indicators in Iranian populations(Reference Shafiee, Heshmat and Ostovar26).

According to Xu et al. (Reference Xu, Houston and Locher27), diet quality evaluated by HEI-2005 also had a significant association with enhanced physical performance. Consistent with our findings, Rahi et al. (Reference Rahi, Morais and Dionne28) found that adherence to the Canadian-HEI in addition to an active lifestyle might prevent muscle strength reduction in diabetic patients. Hashemi et al. (Reference Hashemi, Motlagh and Heshmat10) suggest that a Mediterranean dietary pattern is associated with low odds of sarcopenia in older adults. The Mediterranean diet is based on the consumption of high sources of antioxidants like MUFAs, and more fruits and vegetables that contribute to a reduction of oxidative stress, the main mechanism of sarcopenia pathogenesis(Reference Semba, Lauretani and Ferrucci29). Our findings in fruit and vegetable consumption demonstrated that PS participants consumed less than healthy older adults. The lack of statistical significance in assessing the association of fruits and vegetables with PS might be clarified by the HEI algorithm, in which consuming higher amounts of these components against what is supposed for getting maximum scores remain unconsidered.

No exact mechanisms in the relationship between HEI and PS have been described yet, but it could be mediated by physical activity as well. Most older adults adhering to a high-quality diet tend to maintain a generally healthier lifestyle and are more regularly physically active. Thus, they are less susceptible to obesity and decreased muscle strength(Reference Kim and Kwon17).

Other findings of the present study were the significant association between lower muscle strength and higher intake of added sugars and saturated fats. In aging individuals, there is an elevation of pro-inflammatory cytokines like TNF-α, IL-6 and CRP. Studies show that there is a significant association between these cytokines and low muscle mass and muscle strength(Reference Taaffe, Harris and Ferrucci30). Furthermore, NF-kB might play a role as well(Reference Thoma and Lightfoot31). Saturated fat is one of the nutrients which stimulating inflammatory responses through the NF-kB pathway and people with a high intake of saturated fats might experience low muscle mass and weak muscle strength in comparison with those who consume high amounts of PUFAs or MUFAs as anti-inflammatory nutrients(Reference Sears and Ricordi32).

Another study showed that consumption of sugar-sweetened beverages, which has increased over the last decades, causes the elevation of Homeostatic Model Assessment for Insulin Resistance (HOMA-IR), i.e., insulin resistance(Reference Bremer, Auinger and Byrd33). Aging is associated with insulin resistance as well. This may link with impaired muscle glucose uptake that leads to impaired intracellular energy production and, as a result, muscle weakness might occur(Reference Abbatecola, Ferrucci and Ceda34). Gatineau et al. found that feeding aging rats sucrose causes a reduction in muscle mass(Reference Gatineau, Savary-Auzeloux and Migne35). Similar to the present study, others also found that the simultaneous effect of aging and added sugar consumption may be a cause of low HGS(Reference Pasdar, Moradi and Moradinazar36).

In the present study, healthy people consumed more total protein foods compared with PS subjects. Total protein foods correlated positively with muscle strength; however, this association vanished after adjustment for covariates. This lack of statistical significance might be explained in part by the imperfect HEI scoring system: as 2⋅5 ounces of total protein foods per 1000 kcal already receive the highest attainable score, further intake is going unnoticed. Various studies have already shown that people with a low intake of total protein have a lower average muscle mass and strength(Reference Isanejad, Mursu and Sirola37Reference Suga and Hashimoto39). Decreased protein synthesis as a result of poor dietary intake might cause muscle fibre atrophy and a reduction of muscle mass leading to weak muscle strength, possibly providing the link of causality between low protein intake and low HGS(Reference Tak, Lee and Yi40); however, there is a controversy about the association between improvement of muscle mass or weakness with dietary protein intake in many studies(Reference Tak, Lee and Yi40Reference Zhu, Kerr and Meng44), which warrants further research.

A strength of the present study is that participants were selected from all of Tehran's regions, thereby providing a good representation of Tehran's older adults. Furthermore, PS was detected by using the newest EWGSOP definition. Still, the present study had some limitations. First and foremost, the squeeze dynamometer used in the present study has a lower accuracy in comparison to digital ones. We used FFQ to evaluate dietary intake, and reported amounts are based on participants’ memories (which can cause both underestimation and overestimation). Finally, the present study is a cross-sectional study that cannot prove any causality, that is, it cannot determine the direct role of diet in PS.

In conclusion, giving serious consideration to adhere to dietary recommendations such as the DGAs, which we measured with the HEI-2015, might improve muscle strength in aging individuals. This finding warrants confirmation in high-quality interventional studies.

Acknowledgments

The present study was supported by the Tehran University of Medical Science, Iran, Tehran. We would like to express our gratitude to the research deputy of the School of Nutritional Sciences and Dietetics and Dietitians who helped us collect the data, and especially, the health centres and subjects who participated in the present study.

Z. E.: conceptualisation, methodology, formal analysis, investigation, resources and writing – original draft. Z. T., S. D., M. R. and A. E.: investigation and resources. A. P.: writing – editing and interpretation of data. A. D. M.: conceptualisation, methodology, supervision and project administration.

There are no conflicts of interest.

References

Hashemi, R, Shafiee, G, Motlagh, AD, et al. (2016) Sarcopenia and its associated factors in Iranian older individuals: results of SARIR study. Arch Gerontol Geriatr 66, 1822.CrossRefGoogle ScholarPubMed
Abdelmawgoud, A, Brown, CJ, Sui, X, et al. (2015) Relationship of physical activity and healthy eating with mortality and incident heart failure among community-dwelling older adults with normal body mass index. ESC Heart Fail 2, 2024.CrossRefGoogle ScholarPubMed
Cruz-Jentoft, AJ, Bahat, G, Bauer, J, et al. (2019) Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 48, 1631.CrossRefGoogle ScholarPubMed
Keller, K & Engelhardt, M (2013) Strength and muscle mass loss with aging process. Age and strength loss. Muscles Ligaments Tendons J 3, 346350.CrossRefGoogle ScholarPubMed
Morley, JE, Anker, SD & von Haehling, S (2014) Prevalence, incidence, and clinical impact of sarcopenia: facts, numbers, and epidemiology – update 2014. J Cachexia Sarcopenia Muscle 5, 253259.CrossRefGoogle ScholarPubMed
Van Ancum, JM, Pijnappels, M, Jonkman, NH, et al. (2018) Muscle mass and muscle strength are associated with pre- and post-hospitalization falls in older male inpatients: a longitudinal cohort study. BMC Geriatr 18, 116.CrossRefGoogle ScholarPubMed
Esmaili, H, Mohd Yusof, R, Abu Saad, H, et al. (2015) Association of dietary patterns with sociodemographic and health-related factors among coronary artery disease (CAD) patients. Ecol Food Nutr 54, 419.CrossRefGoogle ScholarPubMed
Lockheart, MS, Steffen, LM, Rebnord, HM, et al. (2007) Dietary patterns, food groups and myocardial infarction: a case-control study. Br J Nutr 98, 380387.CrossRefGoogle ScholarPubMed
Brown, JC, Harhay, MO & Harhay, MN (2017) Physical activity, diet quality, and mortality among sarcopenic older adults. Aging Clin Exp Res 29, 257263.CrossRefGoogle ScholarPubMed
Hashemi, R, Motlagh, AD, Heshmat, R, et al. (2015) Diet and its relationship to sarcopenia in community dwelling Iranian elderly: a cross sectional study. Nutrition 31, 97104.CrossRefGoogle ScholarPubMed
Smee, D, Pumpa, K, Falchi, M, et al. (2015) The relationship between diet quality and falls risk, physical function and body composition in older adults. J Nutr Health Aging 19, 10371042.CrossRefGoogle ScholarPubMed
Krebs-Smith, SM, Pannucci, TE, Subar, AF, et al. (2018) Update of the Healthy Eating Index: HEI-2015. J Acad Nutr Diet 118, 15911602.CrossRefGoogle ScholarPubMed
Reedy, J, Lerman, JL, Krebs-Smith, SM, et al. (2018) Evaluation of the Healthy Eating Index-2015. J Acad Nutr Diet 118, 16221633.CrossRefGoogle ScholarPubMed
Bagheri, A, Soltani, S, Hashemi, R, et al. (2020) Inflammatory potential of the diet and risk of sarcopenia and its components. Nutr J 19, 129.CrossRefGoogle ScholarPubMed
Hassani Zadeh, S, Nadjarzadeh, A, Mirzaei, M, et al. (2020) Adherence to Healthy Eating Index-2015 and metabolic syndrome in a large sample of Iranian adults.[ahead-of-print]CrossRefGoogle Scholar
Kord-Varkaneh, H, Salehi-Sahlabadi, A, Zarezade, M, et al. (2020) Association between Healthy Eating Index-2015 and breast cancer risk: a case-control study. Asian Pac J Cancer Prev 21, 13631367.CrossRefGoogle ScholarPubMed
Kim, H & Kwon, O (2019) Higher diet quality is associated with lower odds of low hand grip strength in the Korean elderly population. Nutrients 11, 1487.CrossRefGoogle ScholarPubMed
Barrea, L, Muscogiuri, G, Di Somma, C, et al. (2019) Association between Mediterranean diet and hand grip strength in older adult women. Clin Nutr 38, 721729.CrossRefGoogle ScholarPubMed
Safarpour, M, Dorosty Motlagh, A, Hosseini, SM, et al. (2014) Prevalence and outcomes of food insecurity and its relationship with some socioeconomic factors. Knowl Health 8, 193198.Google Scholar
Winter, JE, MacInnis, RJ, Wattanapenpaiboon, N, et al. (2014) BMI and all-cause mortality in older adults: a meta-analysis. Am J Clin Nutr 99, 875890.CrossRefGoogle ScholarPubMed
Schneider, HJ, Friedrich, N, Klotsche, J, et al. (2010) The predictive value of different measures of obesity for incident cardiovascular events and mortality. J Clin Endocrinol Metab 95, 17771785.CrossRefGoogle ScholarPubMed
Organization, WH (2011) Waist circumference and waist-hip ratio: report of a WHO expert consultation, Geneva, 8–11 December 2008.Google Scholar
Mirmiran, P, Esfahani, F & Azizi, F (2009) Relative validity and reliability of the food frequency questionnaire used to assess nutrient intakes: Tehran lipid and glucose study. Iran J Diabetes Lipid 9, 185197.Google Scholar
Bowman, S, Clemens, J, Shimizu, M, et al. (2018) Food Patterns Equivalents Database 2015–2016: Methodology and User Guide; available at http://www.ars.usda.gov/nea/bhnrc/fsrg.Google Scholar
Esmaillzadeh, A & Azadbakht, L (2008) Major dietary patterns in relation to general obesity and central adiposity among Iranian women. J Nutr 138, 358363.CrossRefGoogle ScholarPubMed
Shafiee, G, Heshmat, R, Ostovar, A, et al. (2020) Comparison of EWGSOP-1and EWGSOP-2 diagnostic criteria on prevalence of and risk factors for sarcopenia among Iranian older people: the Bushehr Elderly Health (BEH) program. J Diabetes Metab Disord 19, 727734.CrossRefGoogle ScholarPubMed
Xu, B, Houston, DK, Locher, JL, et al. (2012) Higher Healthy Eating Index-2005 scores are associated with better physical performance. J Gerontol A Biol Sci Med Sci 67, 9399.CrossRefGoogle ScholarPubMed
Rahi, B, Morais, JA, Dionne, IJ, et al. (2014) The combined effects of diet quality and physical activity on maintenance of muscle strength among diabetic older adults from the NuAge cohort. Exp Gerontol 49, 4046.CrossRefGoogle ScholarPubMed
Semba, RD, Lauretani, F & Ferrucci, L (2007) Carotenoids as protection against sarcopenia in older adults. Arch Biochem Biophys 458, 141145.CrossRefGoogle ScholarPubMed
Taaffe, DR, Harris, TB, Ferrucci, L, et al. (2000) Cross-sectional and prospective relationships of interleukin-6 and C-reactive protein with physical performance in elderly persons: Macarthur studies of successful aging. J Gerontol A Biol Sci Med Sci 55, M709M715.CrossRefGoogle ScholarPubMed
Thoma, A & Lightfoot, AP (2018) NF-kB and inflammatory cytokine signalling: role in skeletal muscle atrophy. Adv Exp Med Biol 1088, 267279.CrossRefGoogle ScholarPubMed
Sears, B & Ricordi, C (2011) Anti-inflammatory nutrition as a pharmacological approach to treat obesity. J Obes 2011, 431985.CrossRefGoogle ScholarPubMed
Bremer, AA, Auinger, P & Byrd, RS (2010) Sugar-sweetened beverage intake trends in US adolescents and their association with insulin resistance-related parameters. J Nutr Metab 2010, 196476.CrossRefGoogle ScholarPubMed
Abbatecola, AM, Ferrucci, L, Ceda, G, et al. (2005) Insulin resistance and muscle strength in older persons. J Gerontol A Biol Sci Med Sci 60, 12781282.CrossRefGoogle ScholarPubMed
Gatineau, E, Savary-Auzeloux, I, Migne, C, et al. (2015) Chronic intake of sucrose accelerates sarcopenia in older male rats through alterations in insulin sensitivity and muscle protein synthesis. J Nutr 145, 923930.CrossRefGoogle ScholarPubMed
Pasdar, Y, Moradi, S, Moradinazar, M, et al. (2020) Better muscle strength with healthy eating. Eat Weight Disord 26, 367374.CrossRefGoogle ScholarPubMed
Isanejad, M, Mursu, J, Sirola, J, et al. (2016) Dietary protein intake is associated with better physical function and muscle strength among elderly women. Br J Nutr 115, 12811291.CrossRefGoogle ScholarPubMed
Kuczmarski, MF, Pohlig, RT, Stave Shupe, E, et al. (2018) Dietary protein intake and overall diet quality are associated with handgrip strength in African American and white adults. J Nutr Health Aging 22, 700709.CrossRefGoogle Scholar
Suga, H & Hashimoto, H (2018) Age threshold for recommending higher protein intake to prevent age-related muscle weakness: a cross-sectional study in Japan. PLoS One 13, e0208169.CrossRefGoogle ScholarPubMed
Tak, YJ, Lee, JG, Yi, YH, et al. (2018) Association of handgrip strength with dietary intake in the Korean population: findings based on the seventh Korea national health and nutrition examination survey (KNHANES VII-1), 2016. Nutrients 10, 1180.CrossRefGoogle ScholarPubMed
Alemán-Mateo, H, Carreón, VR, Macías, L, et al. (2014) Nutrient-rich dairy proteins improve appendicular skeletal muscle mass and physical performance, and attenuate the loss of muscle strength in older men and women subjects: a single-blind randomized clinical trial. Clin Interv Aging 9, 15171525.CrossRefGoogle ScholarPubMed
Campbell, WW, Crim, MC, Young, VR, et al. (1995) Effects of resistance training and dietary protein intake on protein metabolism in older adults. Am J Physiol 268, E1143E1153.Google ScholarPubMed
Welle, S & Thornton, CA (1998) High-protein meals do not enhance myofibrillar synthesis after resistance exercise in 62- to 75-yr-old men and women. Am J Physiol 274, E677E683.Google Scholar
Zhu, K, Kerr, DA, Meng, X, et al. (2015) Two-year whey protein supplementation did not enhance muscle mass and physical function in well-nourished healthy older postmenopausal women. J Nutr 145, 25202526.CrossRefGoogle Scholar
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Table 1. Participant characteristic

Figure 1

Table 2. HEI-2015 and the component scores across probable and non-sarcopenic subjects

Figure 2

Table 3. Association between HGS and quartiles of HEI-2015

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Table 4. Logistic regression: PS

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Table 5. Multiple linear regression for the association of handgrip strength with HEI-2015 and component scores