Abstract
Reduced skeletal muscle mass in older populations is independently associated with functional impairment and disability, resulting in increased risk of mortality and various comorbidities. This study aimed to examine the association between major dietary pattern and low muscle mass among Korean middle-aged and elderly populations. A total of 8136 participants aged ≥50 years were included from a cross-sectional study based on the 2008–2011 Korea National Health and Nutrition Examination Survey. The following four distinct dietary patterns were derived using factor analysis: “Condiment, vegetables, and meats”; “wheat flour, bread, fruits, milk, and dairy products”; “white rice, fish, and seaweeds”; and “whole grain, bean products, and kimchi”. A higher “white rice, fish, and seaweeds” pattern score was associated with a lower prevalence of low muscle mass in both men and women, whereas a higher “condiment, vegetables, and meats” pattern score was associated with a higher prevalence of low muscle mass in men. A dietary pattern based on white rice, fish, and seaweeds can be helpful in protecting against loss of skeletal muscle mass in Korean middle-aged and elderly populations. Future research is paramount to confirm the causal association between dietary pattern and the risk of low muscle mass.
Keywords: dietary pattern, low muscle mass, skeletal muscle, sarcopenia
1. Introduction
Due to declining fertility rates and remarkable increases in life expectancy, the number of people aged 65 years or older is projected to grow from an estimated 524 million in 2010 to nearly 1.5 billion in 2050, globally [1]. Population aging is one of the most important global public health problems in modern society. Aging naturally involves various physiological changes, such as a decrease in skeletal muscle mass and increase in fat mass [2]. Reduced skeletal muscle mass in older populations is independently associated with functional impairment and disability, sequentially resulting in increased risk of mortality and various comorbidities [3,4,5,6].
Sarcopenia is a complex geriatric syndrome that is associated with various adverse health outcomes, such as physical disability, poor quality of life, and death [7,8]. Previously, loss of muscle mass associated with aging was commonly used to define sarcopenia [9]; however, more recent definitions have recommended using the presence of both low muscle mass and low muscle function (strength or performance) for the diagnosis of sarcopenia [10,11]. In brief, sarcopenia is characterized by progressive loss of skeletal muscle mass and strength; hence, low muscle mass is a sufficient condition for sarcopenia.
Sarcopenia and loss of muscle mass can arise from multifactorial pathogenesis, including neuromuscular degeneration, changes in muscle protein turnover, changes in hormone levels and sensitivity, chronic inflammation, oxidative stress, and behavior/lifestyle factors [8]. Among these risk factors, lifestyle factors, such as physical activity and diet, are the most reversible and modifiable [8]. Exercise (both resistance and aerobic), in combination with nutritional strategy, has been recommended as a key component in the prevention and management of sarcopenia [12]. In particular, the main nutritional strategies proposed for the treatment of sarcopenia or low muscle mass include the increased intakes of protein; vitamin D supplementation; and antioxidants, such as selenium, vitamin A, vitamin C, vitamin E, and β-carotene [8].
Because people consume holistic meals, rather than single-nutrient or single-food diets, on a daily basis, the dietary pattern approach is often recommended to examine the association between diet and diet-related disease. The dietary pattern approach has been widely used to examine intricate interactions of nutrients and foods with various diseases as well as their synergistic effects on the same [13]. Dietary patterns conceptually indicate a broader picture of the overall diet; therefore, examining dietary patterns may be more predictive of disease risk than individual nutrients or foods [13].
Population aging in Korea is expected to accelerate sharply in the next three decades, faster than in other Organization for Economic Co-operation and Development (OECD) member countries [14]. In addition, Korean people who traditionally consume rice-based high-carbohydrate, low-protein, and low-fat diets may be more prone to low muscle mass. In this respect, establishing a nutritional strategy that prevents and manages age-related health problems of the elderly population is one of the most practical and effective plans to alleviate the social burden of the elderly society in the future. In particular, understanding the dietary pattern of people with higher or lower risk of low muscle mass can provide evidence to develop practical guidelines for preventing and managing low muscle mass. Therefore, in the present study, we aimed to examine the association between major dietary pattern and low muscle mass among Korean middle-aged and elderly populations.
2. Materials and Methods
2.1. Study Population
The data used in the current study were based on the 2008–2011 Korea National Health and Nutrition Examination Survey (KNHANES). The KNHANES is a cross-sectional, nationally representative survey in South Korea annually conducted by the Korea Centers for Disease Control and Prevention (KCDC). It consists of a health examination survey, health behavioral survey, and nutritional survey, and it occasionally involves body composition measurements. A flow diagram of the selection of study participants is shown in Figure 1. To date, body composition measurements were conducted between 2008 and 2011. Among participants who underwent health examinations and body composition measurements (n = 21,303), those aged ≥50 years or postmenopausal women were selected (n = 9677). Among them, we excluded those who did not have sufficient information on body composition (n = 380) and 24-h recall data (n = 807). We further excluded those with implausible energy intakes (<500 or >5000 kcal/day; n = 101) and those who had lost or gained more than 6kg in body weight over the past year and consumed an unusual diet on the day of the survey for the purpose of weight control (n = 253). Finally, a total of 8136 participants (3333 men and 4803 women) were included in this study. The present study was conducted according to the guidelines laid down in the Declaration of Helsinki. All procedures involved in the KNHANES were approved by the KCDC Institutional Review Board (IRB No: 2008-04EXP-01-C, 2009-01CON-03-2C, 2010-02CON-21-C, and 2011-02CON-06-C), and all participants provided written informed consent.
Figure 1.
Flow diagram of the selection of study participants: the KNHANES (2008–2011).
2.2. Dietary Assessment and Dietary Pattern Analysis
Dietary intake was assessed using a one-day 24-h dietary recall method. Nutrient-intake calculations were based on the KNHANES nutrient database. In total, 657 food items were reported in this study, and they were categorized into 22 food groups based on the Korean Nutrition Database and previous studies on dietary patterns in Korea [15,16] (Figure 2). Since white rice is the staple food of Koreans, it was isolated from the grain group. Similarly, since kimchi is typically one of the most frequently consumed foods in Korea, it was also separated from other vegetables. The average energy intake of each of the 22 food groups was calculated. We subsequently conducted a factor analysis to identify the major dietary patterns based on the total daily energy intake from the 22 food groups. The factors were rotated by an orthogonal transformation to achieve a simpler structure with greater interpretability. To determine the number of factors, we considered eigenvalues, scree plot, and the interpretability of the derived patterns. The derived patterns were named from foods loaded most positively on each pattern. Participants had their own factor score for each identified pattern, and they were categorized by sex into tertiles for every pattern.
Figure 2.
Factor loading matrix of food groups for the four dietary patterns identified from the 24-h dietary recall. (a) the “condiment, vegetables, and meats” pattern; (b) the “wheat flour, breads, fruits, milk, and dairy products” pattern; (c) the “white rice, fish, and seaweeds” pattern; and (d) the “whole grain, bean products, and kimchi” pattern. The top three food groups with the highest factor loading value were used to name each dietary pattern. As an exception, oils, fermented paste, sauce, and seasoning, and sweets were grouped into condiments and used for naming the “condiment, vegetables, and meats” pattern. F1: white rice, F2: whole grain, F3: noodles and dumpling, F4: wheat flour and bread, F5: potatoes and corn, F6: sweets, F7: fermented paste, sauce, and seasoning, F8: bean, tofu, and soymilk, F9: nuts and seeds, F10: vegetables, F11: kimchi, F12: mushroom, F13: fruits, F14: meat and its product, F15: eggs, F16: fish and shellfish, F17: seaweeds, F18: milk and dairy products, F19: oil, F20: beverage, F21: alcohol, F22: coffee and tea.
2.3. Body Composition Measurement
Body weight (kg) and height (cm) were measured according to standard protocol, with the participant in light clothing and without shoes. Body mass index (BMI) was calculated as follows: weight divided by the height squared (kg/m2).
Body composition was measured using dual-energy X-ray absorptiometry (DEXA, Discovery QDR 4500; Hologic, Inc., Waltham, MA, USA) at the health examination center on the same day when the participants took anthropometric measurement and blood test after 8 h of fasting. Appendicular skeletal muscle mass (ASMM, kg) was calculated as the sum of muscle mass in the arms and legs, assuming that all non-fat and non-bone tissue is skeletal muscle, in accordance with previous studies [17,18,19]. According to the definition proposed in a previous study [20], we used the weight-adjusted ASMM (ASMM/weight × 100 kg/m2). To establish the cut-off value for low muscle mass, the gender-specific mean (33.92 in men, 26.35 in women) and standard deviation (SD) (2.72 in men, 2.30 in women) of the weight-adjusted ASMM of the young-adult reference group (healthy men and women aged 20–39 years) were used. Individuals whose weight-adjusted ASMM was higher than 1SD below the gender-specific mean for the young reference group were considered normal according to each definition. Class I low muscle mass was indicated by definition in participants whose weight-adjusted ASMM was between the gender-specific mean for the young reference group, 1 SD, and the mean for young adults, 2 SD. Class II low muscle mass was indicated by definition in participants whose weight-adjusted ASMM was below the mean for young adults, 2 SD [3].
2.4. Assessment of Other Variables
Demographic characteristics, including age and household income, were acquired from a self-report questionnaire. Household income was categorized into quartiles. Lifestyle factors included smoking (never smoked, past smoker, current smoker), alcohol drinking (current alcohol drinker, non-alcohol drinker), and physical activity.
Physical activity was estimated using the Korean version of the International Physical Activity Questionnaire (IPAQ) [21]. The duration (in minutes) of physical activity was then converted into metabolic equivalents (MET) [22], and our participants were subsequently categorized into the following 3 groups on the basis of the IPAQ guidelines: “High”, “moderate”, or “low” [23]. The “high” group included (i) those who performed vigorous-intensity activity at least three days a week, achieving a minimum total physical activity of 1500 MET-min/week or (ii) those who engaged in seven or more days of any combination of walking, moderate-intensity, or vigorous-intensity activities, achieving a minimum total physical activity of 3000 MET-min/week. The “moderate” group comprised individuals who performed (i) three or more days of vigorous-intensity activity of at least 20 min/day, (ii) five or more days of moderate-intensity activity and/or walking of at least 30 min/day, or (iii) five or more days of any combination of walking, moderate-intensity, or vigorous-intensity activities, achieving a minimum total physical activity of 600 MET-min/week. Individuals who did not meet the criteria for the aforementioned categories were placed in the “low” group.
The serum 25-hydroxyvitamin D (25[OH]D) level was measured by radioimmunoassay (DiaSorin Inc., Stillwater, MN, USA) using a gamma counter (1470 Wizard; PerkinElmer, Turku, Finland).
2.5. Statistical Analysis
The participants were divided into tertile groups according to each of the four dietary pattern scores. Differences in the general characteristics of participants across the tertile groups of each dietary pattern score were determined using the chi-square test for categorical variables and the generalized linear model for continuous variables. Multivariable-adjusted logistic regression analysis was conducted to compare the odds ratios (ORs) and 95% confidence intervals (CIs) for low muscle mass among tertiles of each dietary pattern score. Logistic regression models were adjusted for age (continuous), BMI (continuous), energy intake (continuous), smoking status (never, past, and current), alcohol consumption (non-current, current), physical activity (low, moderate, and high), household income (low, middle-low, middle-high, and high), and serum vitamin D (continuous). In general, because the correlation between educational and household income levels was high, only household income level was selected as an adjustment variable. All statistical analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC, USA). Statistical significance was defined as p < 0.05.
3. Results
Four major dietary patterns were identified from the factor analysis (Figure 2), and they were named after foods or food groups with high factor loading values. These four dietary patterns accounted for 27.8% of the total variance: 10.0%, 6.5%, 6.0%, and 5.3%, respectively. The “condiment, vegetables, and meats” pattern was characterized by a high consumption of condiments, including oil, sweets, fermented paste, sauce, and seasoning as well as vegetables, meat and its products, fish and shellfish, eggs, and alcohol. The “wheat flour, breads, fruits, milk, and dairy products” pattern had positive factor loadings for milk and dairy products, wheat flour and breads, fruits, potatoes and corn, oil, sweets, eggs, and whole grains; however, it had negative loadings for white rice, kimchi, and alcohol. The “white rice, fish, and seaweeds” pattern featured a high consumption of white rice, fish, seaweeds, kimchi, and fruits as well as a low consumption of noodles and dumplings, meat and its products, and alcohol. The “whole grain, bean products, and kimchi” pattern showed high positive factor loadings for whole grain, bean products, kimchi, vegetables, and mushroom as well as negative factor loadings for beverages, coffee and tea, and sweets.
The general characteristics of study participants according to the tertiles of each dietary pattern score by sex are shown in Table 1. People with higher pattern scores for the “condiment, vegetables, and meats” pattern tended to be younger, have higher body fat mass and % body fat, have higher household income levels, and be alcohol drinkers compared to those with lower pattern scores (all p < 0.01). A higher “wheat flour, breads, fruits, milk, and dairy products” pattern score was associated with participants’ higher body fat mass as well as higher household income levels (all p < 0.05). People with higher “white rice, fish, and seaweeds” pattern scores were more likely to have lower body fat mass and % body fat compared to those with lower pattern scores (all p < 0.01). People with higher pattern scores for the “whole grain, bean products, and kimchi” pattern tended to have lower % body fat, be currently non-smokers, earners of higher household income levels, and more physically active compared to those with lower pattern scores (all p < 0.01).
Table 1.
General characteristics of study participants according to the tertiles of each dietary pattern score by sex.
Tertile of Each Pattern Score | ||||||||
---|---|---|---|---|---|---|---|---|
Men | Women | |||||||
T1 | T2 | T3 | p Value 1 | T1 | T2 | T3 | p Value 1 | |
Condiment, vegetables, and meats | ||||||||
Age (year) | 67.3 ± 8.6 | 63.9 ± 8.2 | 60.8 ± 7.8 | <0.001 | 66.1 ± 9.2 | 62.9 ± 9.3 | 60.1 ± 8.6 | <0.001 |
BMI (kg/m2) | 23.2 ± 3.0 | 23.6 ± 2.9 | 24.2 ± 2.8 | <0.001 | 24.1 ± 3.3 | 24.3 ± 3.3 | 24.3 ± 3.1 | 0.090 |
Obesity prevalence, n (%) | 300 (27.0) | 352 (31.7) | 404 (36.4) | <0.001 | 582 (36.4) | 609 (38.0) | 608 (38.0) | 0.535 |
Lean body mass (kg) 2 | 50.4 ± 0.3 | 50.6 ± 0.3 | 50.4 ± 0.3 | 0.367 | 36.9 ± 0.2 | 37.1 ± 0.2 | 36.8 ± 0.2 | 0.037 |
Appendicular skeletal muscle mass (kg) 2 | 20.5 ± 0.2 | 20.6 ± 0.2 | 20.5 ± 0.2 | 0.424 | 14.0 ± 1.0 | 14.1 ± 1.0 | 13.9 ± 1.0 | 0.018 |
Body fat mass (kg) 2 | 14.7 ± 0.2 | 14.9 ± 0.2 | 15.3 ± 0.2 | <0.001 | 19.4 ± 0.2 | 19.5 ± 0.2 | 19.8 ± 0.2 | 0.004 |
% Body fat (%) 2 | 22.2 ± 0.3 | 22.3 ± 0.3 | 22.8 ± 0.3 | 0.005 | 33.9 ± 0.2 | 33.9 ± 0.2 | 34.4 ± 0.3 | 0.001 |
Serum vitamin D (ng/mL) | 20.8 ± 7.3 | 21.5 ± 7.5 | 21.5 ± 7.0 | 0.033 | 18.7 ± 7.0 | 18.6 ± 6.8 | 18.7 ± 6.8 | 0.682 |
Household income 3, n (%) | ||||||||
Low | 476 (42.8) | 317 (28.5) | 205 (18.5) | <0.001 | 721 (45.0) | 566 (35.4) | 406 (25.4) | <0.001 |
Middle-low | 297 (26.7) | 310 (27.9) | 266 (23.9) | 377 (23.6) | 438 (27.4) | 391 (24.4) | ||
Middle-high | 179 (16.1) | 237 (21.3) | 290 (26.1) | 255 (15.9) | 302 (18.9) | 369 (23.1) | ||
High | 145 (13.1) | 240 (21.6) | 339 (30.5) | 223 (13.9) | 268 (16.7) | 414 (25.9) | ||
Current smoking status 3 | ||||||||
Non-smoker | 213 (19.2) | 184 (16.6) | 165 (14.9) | 0.003 | 1426 (89.1) | 1473 (92.0) | 1470 (91.8) | 0.057 |
Past smoker | 575 (51.8) | 574 (51.7) | 547 (49.2) | 80 (5.0) | 58 (3.6) | 56 (3.5) | ||
Current smoker | 312 (28.1) | 348 (31.3) | 394 (35.5) | 78 (4.9) | 57 (3.6) | 66 (4.1) | ||
Alcohol consumption 3 | ||||||||
Non-drinker | 486 (43.7) | 342 (30.8) | 279 (25.1) | <0.001 | 1274 (79.6) | 1189 (74.3) | 1088 (68.0) | <0.001 |
Current drinker | 611 (55.0) | 763 (68.7) | 824 (74.2) | 305 (19.1) | 396 (24.7) | 498 (31.1) | ||
Physical activity 3 | ||||||||
Low | 451 (40.6) | 436 (39.2) | 456 (41.0) | 0.005 | 728 (45.5) | 775 (48.4) | 765 (47.8) | 0.104 |
Moderate | 359 (32.3) | 369 (33.2) | 319 (28.7) | 552 (34.5) | 516 (32.2) | 495 (30.9) | ||
High | 285 (25.7) | 302 (27.2) | 331 (29.8) | 298 (18.6) | 296 (18.5) | 328 (20.5) | ||
Wheat flour, breads, fruits, milk, and dairy products | ||||||||
Age (year) | 64.0 ± 8.4 | 65.0 ± 8.7 | 63.1 ± 8.5 | <0.001 | 65.5 ± 9.2 | 63.4 ± 9.2 | 60.2 ± 8.9 | <0.001 |
BMI (kg/m2) | 23.5 ± 3.0 | 23.5 ± 2.9 | 24.0 ± 2.9 | <0.001 | 24.1 ± 3.4 | 24.3 ± 3.2 | 24.2 ± 3.1 | 0.121 |
Obesity prevalence, n (%) | 336 (30.2) | 326 (29.3) | 394 (35.5) | 0.004 | 589 (36.8) | 632 (39.5) | 578 (36.1) | 0.114 |
Lean body mass (kg) | 50.3 ± 0.3 | 50.5 ± 0.3 | 50.4 ± 0.3 | 0.688 | 36.7 ± 0.2 | 36.9 ± 0.2 | 37.2 ± 0.2 | 0.002 |
Appendicular skeletal muscle mass (kg) | 20.5 ± 0.2 | 20.6 ± 0.2 | 20.5 ± 0.2 | 0.613 | 13.9 ± 1.0 | 14.0 ± 1.0 | 14.1 ± 1.0 | 0.024 |
Body fat mass (kg) | 14.8 ± 0.2 | 15.0 ± 0.2 | 15.1 ± 0.2 | 0.018 | 19.2 ± 0.2 | 19.6 ± 0.2 | 19.8 ± 0.2 | <0.001 |
% Body fat (%) | 22.2 ± 0.3 | 22.5 ± 0.3 | 22.6 ± 0.3 | 0.099 | 33.7 ± 0.2 | 34.2 ± 0.2 | 34.2 ± 0.2 | <0.001 |
Serum vitamin D (ng/mL) | 22.2 ± 7.7 | 21.0 ± 7.2 | 20.6 ± 6.8 | <0.001 | 19.0 ± 7.0 | 18.4 ± 6.9 | 18.6 ± 6.7 | 0.024 |
Household income, n (%) | ||||||||
Low | 386 (34.7) | 352 (31.7) | 260 (23.4) | <0.001 | 715 (44.7) | 599 (37.4) | 379 (23.7) | <0.001 |
Middle-low | 310 (27.9) | 296 (26.6) | 267 (24.0) | 407 (25.4) | 413 (25.8) | 386 (24.1) | ||
Middle-high | 196 (17.6) | 242 (21.8) | 268 (24.1) | 254 (15.9) | 306 (19.1) | 366 (22.9) | ||
High | 212 (19.1) | 207 (18.6) | 305 (27.5) | 196 (12.2) | 260 (16.2) | 449 (28.0) | ||
Current smoking status | ||||||||
Non-smoker | 150 (13.5) | 195 (17.6) | 217 (19.5) | <0.001 | 1445 (90.3) | 1456 (90.9) | 1468 (91.7) | 0.546 |
Past smoker | 534 (48.1) | 578 (52.0) | 584 (52.6) | 66 (4.1) | 64 (4.0) | 64 (4.0) | ||
Current smoker | 422 (38.0) | 328 (29.5) | 304 (27.4) | 79 (4.9) | 67 (4.2) | 55 (3.4) | ||
Alcohol consumption | ||||||||
Non-drinker | 260 (23.4) | 405 (36.5) | 442 (39.8) | <0.001 | 1185 (74.0) | 1198 (74.8) | 1168 (73.0) | 0.498 |
Current drinker | 845 (76.1) | 694 (62.5) | 659 (59.3) | 403 (25.2) | 384 (24.0) | 412 (25.7) | ||
Physical activity | ||||||||
Low | 445 (40.1) | 454 (40.9) | 444 (40.0) | 0.001 | 769 (48.0) | 779 (48.7) | 720 (45.0) | 0.202 |
Moderate | 314 (28.3) | 374 (33.7) | 359 (32.3) | 500 (31.2) | 519 (32.4) | 544 (34.0) | ||
High | 348 (31.3) | 269 (24.2) | 301 (27.1) | 318 (19.9) | 283 (17.7) | 321 (20.1) | ||
White rice, fish, and seaweeds | ||||||||
Age (year) | 63.3 ± 8.7 | 65.2 ± 8.7 | 63.5 ± 8.3 | <0.001 | 62.6 ± 9.6 | 63.8 ± 9.4 | 62.8 ± 9.0 | <0.001 |
BMI (kg/m2) | 23.7 ± 2.9 | 23.5 ± 2.9 | 23.8 ± 2.9 | 0.209 | 24.1 ± 3.2 | 24.2 ± 3.2 | 24.3 ± 3.2 | 0.579 |
Obesity prevalence, n (%) | 354 (31.9) | 333 (30.0) | 369 (33.2) | 0.257 | 600 (37.5) | 604 (37.7) | 595 (37.2) | 0.947 |
Lean body mass (kg) | 50.3 ± 0.3 | 50.5 ± 0.3 | 50.6 ± 0.3 | 0.126 | 36.9 ± 0.2 | 36.9 ± 0.2 | 37.0 ± 0.2 | 0.730 |
Appendicular skeletal muscle mass (kg) | 20.5 ± 0.2 | 20.6 ± 0.2 | 20.7 ± 0.2 | 0.059 | 13.9 ± 1.0 | 14.0 ± 1.0 | 14.0 ± 1.0 | 0.330 |
Body fat mass (kg) | 15.2 ± 0.2 | 15.0 ± 0.2 | 14.7 ± 0.2 | <0.001 | 19.7 ± 0.2 | 19.5 ± 0.2 | 19.4 ± 0.2 | 0.005 |
% Body fat (%) | 22.7 ± 0.3 | 22.5 ± 0.3 | 22.0 ± 0.3 | <0.001 | 34.3 ± 0.2 | 34.1 ± 0.2 | 33.8 ± 0.2 | 0.009 |
Serum vitamin D (ng/mL) | 21.2 ± 7.2 | 21.3 ± 7.3 | 21.5 ± 7.4 | 0.653 | 18.4 ± 6.7 | 18.7 ± 7.0 | 18.8 ± 6.9 | 0.212 |
Household income, n (%) | ||||||||
Low | 317 (28.5) | 360 (32.4) | 321 (28.9) | 0.104 | 540 (33.7) | 599 (37.4) | 554 (34.6) | 0.010 |
Middle-low | 269 (24.2) | 296 (26.6) | 308 (27.7) | 398 (24.9) | 409 (25.6) | 399 (24.9) | ||
Middle-high | 247 (22.2) | 227 (20.4) | 232 (20.9) | 320 (20.0) | 273 (17.1) | 333 (20.8) | ||
High | 266 (23.9) | 216 (19.4) | 242 (21.8) | 325 (20.3) | 285 (17.8) | 295 (18.4) | ||
Current smoking status | ||||||||
Non-smoker | 168 (15.1) | 188 (16.9) | 206 (18.5) | <0.001 | 1427 (89.1) | 1463 (91.4) | 1479 (92.4) | 0.011 |
Past smoker | 530 (47.7) | 606 (54.6) | 560 (50.4) | 71 (4.4) | 71 (4.4) | 52 (3.3) | ||
Current smoker | 402 (36.2) | 312 (28.1) | 340 (30.6) | 87 (5.4) | 59 (3.7) | 55 (3.4) | ||
Alcohol consumption | ||||||||
Non-drinker | 282 (25.4) | 409 (36.8) | 416 (37.4) | <0.001 | 1144 (71.5) | 1212 (75.7) | 1195 (74.6) | 0.078 |
Current drinker | 814 (73.3) | 693 (62.4) | 691 (62.2) | 436 (27.2) | 374 (23.4) | 389 (24.3) | ||
Physical activity | ||||||||
Low | 486 (43.7) | 452 (40.7) | 405 (36.5) | 0.012 | 785 (49.0) | 746 (46.6) | 737 (46.0) | 0.430 |
Moderate | 328 (29.5) | 347 (31.2) | 372 (33.5) | 492 (30.7) | 543 (33.9) | 528 (33.0) | ||
High | 285 (25.7) | 304 (27.4) | 329 (29.6) | 310 (19.4) | 295 (18.4) | 317 (19.8) | ||
Whole grain, bean products, and kimchi | ||||||||
Age (year) | 64.1 ± 9.0 | 64.5 ± 8.7 | 63.3 ± 8.0 | 0.005 | 63.9 ± 9.7 | 63.0 ± 9.4 | 62.2 ± 8.8 | <0.001 |
BMI (kg/m2) | 23.4 ± 3.0 | 23.8 ± 2.8 | 23.9 ± 2.9 | <0.001 | 24.1 ± 3.3 | 24.3 ± 3.2 | 24.3 ± 3.2 | 0.088 |
Obesity prevalence, n (%) | 326 (29.3) | 353 (31.8) | 377 (33.9) | 0.067 | 578 (36.1) | 622 (38.9) | 599 (37.4) | 0.275 |
Lean body mass (kg) | 50.4 ± 0.3 | 50.3 ± 0.3 | 50.6 ± 0.3 | 0.194 | 36.9 ± 0.2 | 36.9 ± 0.2 | 37.1 ± 0.2 | 0.390 |
Appendicular skeletal muscle mass (kg) | 20.6 ± 0.2 | 20.5 ± 0.2 | 20.6 ± 0.2 | 0.451 | 14.0 ± 1.0 | 14.0 ± 1.0 | 14.0 ± 1.0 | 0.805 |
Body fat mass (kg) | 14.9 ± 0.2 | 15.0 ± 0.2 | 15.1 ± 0.2 | 0.305 | 19.4 ± 0.2 | 19.6 ± 0.2 | 19.7 ± 0.2 | 0.015 |
% Body fat (%) | 22.7 ± 0.3 | 22.5 ± 0.3 | 22.0 ± 0.3 | <0.001 | 34.3 ± 0.2 | 34.1 ± 0.2 | 33.8 ± 0.2 | 0.009 |
Serum vitamin D (ng/mL) | 21.5 ± 7.1 | 21.0 ± 7.4 | 21.4 ± 7.3 | 0.203 | 18.8 ± 7.0 | 18.6 ± 6.7 | 18.6 ± 6.9 | 0.571 |
Household income, n (%) | ||||||||
Low | 375 (33.8) | 335 (30.2) | 288 (25.9) | 0.003 | 638 (39.9) | 551 (34.4) | 504 (31.5) | <0.001 |
Middle-low | 284 (25.6) | 288 (25.9) | 301 (27.1) | 424 (26.5) | 404 (25.2) | 378 (23.6) | ||
Middle-high | 233 (21.0) | 232 (20.9) | 241 (21.7) | 272 (17.0) | 317 (19.8) | 337 (21.1) | ||
High | 206 (18.5) | 244 (22.0) | 274 (24.7) | 244 (15.2) | 300 (18.7) | 361 (22.6) | ||
Current smoking status | ||||||||
Non-smoker | 150 (13.5) | 189 (17.0) | 223 (20.1) | <0.001 | 1397 (87.3) | 1477 (92.3) | 1495 (93.4) | <0.001 |
Past smoker | 513 (46.2) | 587 (52.8) | 596 (53.7) | 81 (5.1) | 58 (3.6) | 55 (3.4) | ||
Current smoker | 438 (39.4) | 328 (29.5) | 288 (25.9) | 109 (6.8) | 53 (3.3) | 39 (2.4) | ||
Alcohol consumption | ||||||||
Non-drinker | 400 (36.0) | 353 (31.8) | 354 (31.9) | 0.083 | 1151 (71.9) | 1179 (73.6) | 1221 (76.3) | 0.079 |
Current drinker | 699 (62.9) | 748 (67.3) | 751 (67.6) | 432 (27.0) | 405 (25.3) | 362 (22.6) | ||
Physical activity | ||||||||
Low | 490 (44.1) | 464 (41.8) | 389 (35.0) | <0.001 | 810 (50.6) | 739 (46.2) | 719 (44.9) | 0.007 |
Moderate | 341 (30.7) | 333 (30.0) | 373 (33.6) | 460 (28.7) | 540 (33.7) | 563 (35.2) | ||
High | 267 (24.0) | 306 (27.5) | 345 (31.1) | 314 (19.6) | 304 (19.0) | 304 (19.0) |
T: tertile, BMI: Body mass index. 1 p values were calculated using a generalized linear model for continuous variables and χ2 test for categorical variables; 2 Body composition variables, including lean body mass, appendicular skeletal muscle mass, body fat mass, % body fat, were presented as least squares means (LSmeans) ± standard errors adjusted for age (continuous), BMI (continuous), energy intake (continuous), smoking status (never, past, current), alcohol consumption (non-current, current), physical activity (low, moderate, and high), household income (low, middle-low, middle-high, and high), and serum vitamin D (continuous); 3 Numbers of missing values were 105, 60, 81 and 75 for household income, current smoking status, alcohol consumption, and physical activity, respectively.
Table 2 displays nutrient intakes of study participants according to the tertiles of each dietary pattern score by sex. The “condiment, vegetables, and meats” and “whole grain, bean products, and kimchi” pattern scores were positively associated with energy intake and other nutrient intakes, including percentage of energy from protein and fat, fiber, calcium, phosphorus, iron, sodium, potassium, vitamin A, carotenoid, thiamin, riboflavin, niacin, and vitamin C, except percentage of energy from carbohydrates (all p < 0.001). The “wheat flour, breads, fruits, milk, and dairy products” pattern score was positively associated with the percentage of energy intake from protein and fat (all p < 0.001), whereas the “white rice, fish, and seaweeds” pattern score was positively associated with percentage of energy from carbohydrates, fiber, calcium, iron, carotenoid, and vitamin C intake (all p < 0.001).
Table 2.
Nutrient intakes of study participants according to the tertiles of each dietary pattern score by sex.
Tertile of Each Pattern Score | ||||||||
---|---|---|---|---|---|---|---|---|
Men | Women | |||||||
T1 | T2 | T3 | p Value | T1 | T2 | T3 | p Value | |
Condiment, vegetables, and meats | ||||||||
Energy intake (kcal) | 1522.7 ± 406.5 | 1981.9 ± 464.8 | 2703.1 ± 685.4 | <0.001 | 1201.8 ± 395.5 | 1516.9 ± 413.2 | 1980.7 ± 558.7 | <0.001 |
% energy from carbohydrate | 77.1 ± 8.7 | 69.8 ± 10.5 | 59.2 ± 13.3 | <0.001 | 80.4 ± 7.6 | 76.1 ± 8.5 | 68.6 ± 10.8 | <0.001 |
% energy from protein | 12.0 ± 3.0 | 13.9 ± 3.5 | 15.2 ± 4.0 | <0.001 | 11.5 ± 2.9 | 13.1 ± 3.2 | 15.0 ± 4.0 | <0.001 |
% energy from fat | 9.8 ± 5.5 | 13.0 ± 6.0 | 18.1 ± 7.9 | <0.001 | 9.0 ± 5.7 | 11.9 ± 6.0 | 16.9 ± 7.4 | <0.001 |
Fiber (g) | 6.2 ± 3.9 | 8.6 ± 5.2 | 10.4 ± 6.5 | <0.001 | 5.1 ± 4.5 | 7.1 ± 5.3 | 9.2 ± 6.0 | <0.001 |
Calcium (mg) | 363.6 ± 235.8 | 538.2 ± 335.6 | 702.3 ± 407.0 | <0.001 | 285.6 ± 212.6 | 413.2 ± 251.5 | 573.8 ± 469.1 | <0.001 |
Phosphorus (mg) | 893.2 ± 296.4 | 1213.4 ± 358.3 | 1625.8 ± 498.2 | <0.001 | 695.7 ± 271.5 | 919.4 ± 293.7 | 1251.0 ± 430.4 | <0.001 |
Iron (mg) | 10.7 ± 7.5 | 16.4 ± 12.0 | 21.7 ± 15.6 | <0.001 | 8.9 ± 13.5 | 12.8 ± 8.7 | 18.2 ± 16.3 | <0.001 |
Sodium (mg) | 3503.2 ± 2039.7 | 5306.3 ± 2786.6 | 7188.4 ± 3491.6 | <0.001 | 2391.9 ± 1493.8 | 3786.6 ± 2111.2 | 5355.5 ± 2968.2 | <0.001 |
Potassium (mg) | 2254.2 ± 1055.4 | 3180.4 ± 1267.5 | 4156.0 ± 1535.6 | <0.001 | 1880.7 ± 1198.0 | 2533.5 ± 1182.8 | 3477.9 ± 1496.2 | <0.001 |
Vitamin A (μgRE) | 505.8 ± 643.3 | 787.4 ± 709.6 | 1100.0 ± 922.8 | <0.001 | 427.4 ± 651.2 | 637.4 ± 680.9 | 990.3 ± 1002.1 | <0.001 |
Carotenoid (μg) | 2735.4 ± 3377.0 | 4289.4 ± 4134.8 | 5681.9 ± 4606.1 | <0.001 | 2367.6 ± 3874.4 | 3524.4 ± 4029.1 | 5204.0 ± 5298.6 | < 0.001 |
Thiamin (mg) | 0.9 ± 0.4 | 1.2 ± 0.5 | 1.8 ± 0.8 | <0.001 | 0.7 ± 0.3 | 0.9 ± 0.4 | 1.3 ± 0.6 | < 0.001 |
Riboflavin (mg) | 0.7 ± 0.4 | 1.1 ± 0.5 | 1.6 ± 0.7 | <0.001 | 0.6 ± 0.4 | 0.8 ± 0.4 | 1.2 ± 0.6 | < 0.001 |
Niacin (mg) | 10.8 ± 3.8 | 16.1 ± 5.5 | 24.2 ± 9.2 | <0.001 | 8.2 ± 3.6 | 11.5 ± 4.0 | 17.5 ± 7.1 | < 0.001 |
Vitamin C (mg) | 75.3 ± 70.3 | 106.3 ± 79.3 | 133.4 ± 97.4 | <0.001 | 68.0 ± 80.2 | 92.4 ± 73.3 | 127.9 ± 98.8 | < 0.001 |
Wheat flour, breads, fruits, milk, and dairy products | ||||||||
Energy intake(kcal) | 2270.8 ± 740.9 | 1823.0 ± 620.0 | 2114.0 ± 723.2 | <0.001 | 1564.8 ± 502.9 | 1400.4 ± 501.1 | 1734.2 ± 621.9 | <0.001 |
% energy from carbohydrate | 64.8 ± 16.2 | 71.7 ± 11.3 | 69.6 ± 10.4 | <0.001 | 76.8 ± 10.7 | 75.4 ± 9.4 | 72.9 ± 10.2 | <0.001 |
% energy from protein | 13.1 ± 4.0 | 13.6 ± 3.5 | 14.4 ± 3.7 | <0.001 | 12.5 ± 3.6 | 13.3 ± 3.6 | 13.9 ± 3.8 | <0.001 |
% energy from fat | 11.9 ± 7.6 | 12.5 ± 6.2 | 16.5 ± 7.2 | <0.001 | 10.0 ± 7.0 | 12.2 ± 6.4 | 15.6 ± 7.1 | <0.001 |
Fiber (g) | 8.7 ± 5.1 | 7.5 ± 4.6 | 9.0 ± 6.7 | <0.001 | 6.6 ± 4.7 | 6.2 ± 4.3 | 8.7 ± 7.0 | <0.001 |
Calcium (mg) | 523.9 ± 383.0 | 467.0 ± 330.9 | 613.2 ± 352.5 | <0.001 | 367.1 ± 425.7 | 358.5 ± 254.9 | 547.0 ± 318.5 | <0.001 |
Phosphorus (mg) | 1266.8 ± 485.4 | 1110.9 ± 443.7 | 1354.7 ± 521.1 | <0.001 | 898.1 ± 361.0 | 848.3 ± 354.5 | 1119.7 ± 451.3 | <0.001 |
Iron (mg) | 16.8 ± 14.0 | 14.3 ± 9.8 | 17.7 ± 14.4 | <0.001 | 12.1 ± 11.6 | 11.8 ± 10.5 | 16.1 ± 17.7 | <0.001 |
Sodium (mg) | 6172.2 ± 3621.6 | 4886.1 ± 2936.0 | 4939.6 ± 2849.4 | <0.001 | 4214.6 ± 2811.5 | 3497.5 ± 2347.5 | 3821.9 ± 2494.9 | <0.001 |
Potassium (mg) | 3145.8 ± 1403.0 | 2840.7 ± 1328.6 | 3604.1 ± 1691.1 | <0.001 | 2292.1 ± 1170.3 | 2304.8 ± 1158.5 | 3295.1 ± 1728.9 | <0.001 |
Vitamin A (μgRE) | 764.8 ± 772.8 | 705.2 ± 750.5 | 923.1 ± 871.7 | <0.001 | 575.3 ± 674.2 | 605.6 ± 688.5 | 874.2 ± 1034.9 | <0.001 |
Carotenoid (μg) | 4166.8 ± 3937.1 | 3783.4 ± 3877.9 | 4756.4 ± 4800.6 | <0.001 | 3197.5 ± 3715.8 | 3265.1 ± 3623.5 | 4633.4 ± 5927.9 | <0.001 |
Thiamin (mg) | 1.4 ± 0.8 | 1.1 ± 0.6 | 1.4 ± 0.6 | <0.001 | 0.9 ± 0.5 | 0.9 ± 0.5 | 1.2 ± 0.6 | <0.001 |
Riboflavin (mg) | 1.1 ± 0.6 | 1.0 ± 0.6 | 1.4 ± 0.6 | <0.001 | 0.7 ± 0.4 | 0.8 ± 0.4 | 1.2 ± 0.6 | <0.001 |
Niacin (mg) | 18.2 ± 9.2 | 15.1 ± 7.5 | 17.8 ± 8.6 | <0.001 | 11.8 ± 5.9 | 11.3 ± 5.8 | 14.2 ± 7.1 | <0.001 |
Vitamin C (mg) | 98.3 ± 71.6 | 94.9 ± 87.2 | 121.8 ± 96.2 | <0.001 | 74.8 ± 59.0 | 84.6 ± 72.9 | 128.8 ± 113.7 | <0.001 |
White rice, fish, and seaweeds | ||||||||
Energy intake(kcal) | 2103.1 ± 812.4 | 1819.5 ± 598.4 | 2285.1 ± 656.9 | <0.001 | 1379.2 ± 573.4 | 1429.1 ± 438.7 | 1891.1 ± 515.6 | <0.001 |
% energy from carbohydrate | 60.4 ±15.0 | 71.9 ± 10.2 | 73.8 ± 9.5 | <0.001 | 71.1 ± 11.8 | 76.6 ± 8.8 | 77.4 ± 8.8 | <0.001 |
% energy from protein | 13.8 ± 3.9 | 13.5 ± 3.5 | 13.9 ± 3.8 | 0.054 | 13.8 ± 3.8 | 12.9 ± 3.5 | 13.0 ± 3.8 | <0.001 |
% energy from fat | 16.3 ± 8.5 | 12.6 ± 6.6 | 12.1 ± 6.0 | <0.001 | 15.2 ± 8.2 | 11.6 ± 6.5 | 11.0 ± 6.1 | <0.001 |
Fiber (g) | 7.6 ± 4.6 | 7.7 ± 5.2 | 9.9 ± 6.4 | <0.001 | 6.4 ± 5.6 | 6.6 ± 5.5 | 8.5 ± 5.3 | <0.001 |
Calcium (mg) | 470.9 ± 300.2 | 484.8 ± 336.8 | 648.5 ± 410.2 | <0.001 | 363.9 ± 254.9 | 389.0 ± 268.6 | 519.7 ± 468.1 | <0.001 |
Phosphorus (mg) | 1149.4 ± 481.1 | 1115.8 ± 433.2 | 1467.2 ± 490.0 | <0.001 | 832.9 ± 401.7 | 876.6 ± 341.2 | 1156.6 ± 402.4 | <0.001 |
Iron (mg) | 14.4 ± 9.9 | 14.8 ± 12.6 | 19.6 ± 15.2 | <0.001 | 11.4 ± 16.1 | 11.7 ± 8.5 | 16.8 ± 14.7 | <0.001 |
Sodium (mg) | 5291.9 ± 3229.7 | 4647.0 ± 2897.1 | 6059.0 ± 3330.3 | <0.001 | 3542.0 ± 2522.2 | 3289.5 ± 2277.3 | 4702.6 ± 2685.9 | <0.001 |
Potassium (mg) | 2938.6 ± 1398.3 | 2866.9 ± 1418.1 | 3785.1 ± 1549.4 | <0.001 | 2349.4 ± 1449.5 | 2382.4 ± 1261.9 | 3160.3 ± 1499.5 | <0.001 |
Vitamin A (μgRE) | 685.3 ± 651.5 | 681.6 ± 739.8 | 1026.2 ± 946.3 | <0.001 | 550.2 ± 669.7 | 580.4 ± 622.1 | 924.5 ± 1063.9 | <0.001 |
Carotenoid (μg) | 3528.2 ± 3397.5 | 3595.0 ± 3494.6 | 5583.5 ± 5251.7 | <0.001 | 2834.0 ± 3311.8 | 3144.2 ± 3550.0 | 5117.8 ± 6062.1 | <0.001 |
Thiamin (mg) | 1.4 ± 0.8 | 1.1 ± 0.6 | 1.4 ± 0.6 | <0.001 | 0.9 ± 0.6 | 0.9 ± 0.5 | 1.1 ± 0.5 | <0.001 |
Riboflavin (mg) | 1.1 ± 0.6 | 1.0 ± 0.6 | 1.3 ± 0.6 | <0.001 | 0.8 ± 0.5 | 0.8 ± 0.5 | 1.1 ± 0.6 | <0.001 |
Niacin (mg) | 16.7 ± 9.2 | 14.7 ± 7.0 | 19.7 ± 8.7 | <0.001 | 11.3 ± 6.6 | 11.2 ± 5.5 | 14.8 ± 6.5 | <0.001 |
Vitamin C (mg) | 90.3 ± 71.7 | 97.0 ± 91.4 | 127.7 ± 90.2 | <0.001 | 85.2 ± 81.5 | 86.9 ± 73.1 | 116.1 ± 103.9 | <0.001 |
Whole grain, bean products, and kimchi | ||||||||
Energy intake(kcal) | 1987.6 ± 737.7 | 1985.9 ± 675.8 | 2234.2 ± 719.8 | <0.001 | 1466.6 ± 556.8 | 1490.3 ± 521.0 | 1742.4 ± 564.3 | <0.001 |
% energy from carbohydrate | 68.9 ± 13.0 | 68.7 ± 13.6 | 68.5 ± 13.0 | 0.738 | 74.8 ± 10.8 | 75.4 ± 10.2 | 74.8 ± 9.8 | 0.142 |
% energy from protein | 12.9 ± 3.9 | 13.6 ± 3.7 | 14.6 ± 3.5 | <0.001 | 12.4 ± 3.9 | 13.0 ± 3.6 | 14.2 ± 3.4 | <0.001 |
% energy from fat | 13.2 ± 7.2 | 13.3 ± 7.4 | 14.5 ± 7.4 | <0.001 | 12.0 ± 7.5 | 12.4 ± 7.2 | 13.3 ± 6.9 | <0.001 |
Fiber (g) | 6.1 ± 3.7 | 7.9 ± 5.4 | 11.1 ± 6.0 | <0.001 | 5.0 ± 4.2 | 6.8 ± 5.0 | 9.7 ± 6.2 | <0.001 |
Calcium (mg) | 431.7 ± 326.9 | 507.3 ± 328.3 | 665.2 ± 385.0 | <0.001 | 341.5 ± 413.7 | 402.8 ± 273.2 | 528.3 ± 326.1 | <0.001 |
Phosphorus (mg) | 1100.5 ± 475.0 | 1181.0 ± 458.1 | 1451.0 ± 481.2 | <0.001 | 816.3 ± 367.6 | 894.7 ± 358.5 | 1155.2 ± 418.1 | <0.001 |
Iron (mg) | 13.2 ± 11.6 | 15.3 ± 10.2 | 20.4 ± 15.5 | <0.001 | 10.3 ± 11.5 | 12.4 ± 9.2 | 17.2 ± 18.0 | <0.001 |
Sodium (mg) | 4387.4 ± 2581.3 | 5100.7 ± 2787.9 | 6509.8 ± 3760.9 | <0.001 | 3127.1 ± 2171.8 | 3697.9 ± 2246.4 | 4709.0 ± 2975.0 | <0.001 |
Potassium (mg) | 2662.9 ± 1266.7 | 3028.8 ± 1376.9 | 3899.0 ± 1606.7 | <0.001 | 2033.2 ± 1102.5 | 2489.8 ± 1257.9 | 3369.2 ± 1625.7 | <0.001 |
Vitamin A (μgRE) | 634.2 ± 674.9 | 757.6 ± 707.4 | 1001.3 ± 959.1 | <0.001 | 497.5 ± 622.0 | 665.2 ± 764.3 | 892.4 ± 1002.1 | <0.001 |
Carotenoid (μg) | 3206.7 ± 3143.1 | 4050.9 ± 3674.1 | 5449.1 ± 5302.8 | <0.001 | 2573.1 ± 3097.4 | 3576.4 ± 4082.6 | 4946.5 ± 5855.6 | <0.001 |
Thiamin (mg) | 1.1 ± 0.6 | 1.2 ± 0.6 | 1.5 ± 0.7 | <0.001 | 0.8 ± 0.5 | 0.9 ± 0.5 | 1.2 ± 0.6 | <0.001 |
Riboflavin (mg) | 1.0 ± 0.6 | 1.1 ± 0.6 | 1.3 ± 0.7 | <0.001 | 0.7 ± 0.5 | 0.9 ± 0.5 | 1.1 ± 0.6 | <0.001 |
Niacin (mg) | 16.0 ± 8.7 | 16.2 ± 7.9 | 18.9 ± 8.8 | <0.001 | 11.1 ± 6.3 | 11.8 ± 6.2 | 14.4 ± 6.3 | <0.001 |
Vitamin C (mg) | 77.5 ± 63.3 | 103.9 ± 91.3 | 133.6 ± 92.1 | <0.001 | 67.3 ± 62.1 | 92.5 ± 78.7 | 128.4 ± 107.0 | <0.001 |
T: tertile.
Table 3 shows the ORs and 95% CIs for risk of low muscle mass according to the tertiles of each dietary pattern score by sex. In men, a higher “condiment, vegetables, and meats” pattern score was associated with a higher OR for class II low muscle mass (OR 1.51, 95% CI 1.05–2.18, p for trend = 0.030). On the other hand, a higher “white rice, fish, and seaweeds” pattern score was associated with a lower OR for class I low muscle mass in both men and women (men: OR 0.72, 95% CI 0.59–0.88, p for trend = 0.001; women: OR 0.76, 95% CI 0.63–0.91, p for trend = 0.003). No significant association was observed between each of the “wheat flour, breads, fruits, milk, and dairy products” and “whole grain, bean products, and kimchi” patterns and low muscle mass.
Table 3.
Odds ratios and 95% confidence intervals for risk of low muscle mass according to the tertiles of each dietary pattern score by sex.
Tertile of Each Pattern Score | ||||||||
---|---|---|---|---|---|---|---|---|
Men | Women | |||||||
T1 | T2 | T3 | p for Trend 1 | T1 | T2 | T3 | p for Trend 1 | |
Condiment, vegetables, and meats | ||||||||
Class I low muscle mass 2 | ||||||||
Cases/n | 402/1111 | 361/1111 | 367/1111 | 465/1601 | 470/1601 | 454/1601 | ||
OR (95% CI) 3 | 1.00 | 0.97 (0.78–1.20) | 1.23 (0.93–1.61) | 0.104 | 1.00 | 1.02 (0.85–1.21) | 1.11 (0.90–1.37) | 0.302 |
Class II low muscle mass 2 | ||||||||
Cases/n | 169/1111 | 148/1111 | 128/1111 | 188/1601 | 157/1601 | 159/1601 | ||
OR (95% CI) 3 | 1.00 | 1.25 (0.94–1.65) | 1.51 (1.05–2.18) | 0.030 | 1.00 | 0.87 (0.68–1.13) | 1.20 (0.89–1.61) | 0.156 |
Wheat flour, breads, fruits, milk, and dairy products | ||||||||
Class I low muscle mass | ||||||||
Cases/n | 360/1111 | 390/1111 | 380/1111 | 435/1601 | 489/1601 | 465/1601 | ||
OR (95% CI) | 1.00 | 0.97 (0.79–1.20) | 0.98 (0.79–1.20) | 0.825 | 1.00 | 1.10 (0.93–1.31) | 1.12 (0.94–1.34) | 0.239 |
Class II low muscle mass | ||||||||
Cases/n | 129/1111 | 153/1111 | 163/1111 | 163/1601 | 184/1601 | 157/1601 | ||
OR (95% CI) | 1.00 | 0.97 (0.73–1.29) | 1.09 (0.82–1.44) | 0.483 | 1.00 | 1.06 (0.83–1.35) | 1.10 (0.85–1.42) | 0.487 |
White rice, fish, and seaweeds | ||||||||
Class I low muscle mass | ||||||||
Cases/n | 405/1111 | 379/1111 | 346/1111 | 502/1601 | 463/1601 | 424/1601 | ||
OR (95% CI) | 1.00 | 0.81 (0.66–0.99) | 0.72 (0.59–0.88) | 0.001 | 1.00 | 0.84 (0.71–1.00) | 0.76 (0.63–0.91) | 0.003 |
Class II low muscle mass | ||||||||
Cases/n | 157/1111 | 164/1111 | 124/1111 | 181/1601 | 168/1601 | 155/1601 | ||
OR (95% CI) | 1.00 | 0.89 (0.68–1.16) | 0.77 (0.58–1.02) | 0.067 | 1.00 | 0.92 (0.72–1.17) | 0.93 (0.71–1.22) | 0.568 |
Whole grain, bean products, and kimchi | ||||||||
Class I low muscle mass | ||||||||
Cases/n | 373/1111 | 393/1111 | 364/1111 | 445/1601 | 451/1601 | 493/1601 | ||
OR (95% CI) | 1.00 | 1.06 (0.87–1.29) | 0.97 (0.79–1.19) | 0.677 | 1.00 | 0.97 (0.82–1.15) | 1.17 (0.98–1.39) | 0.058 |
Class II low muscle mass | ||||||||
Cases/n | 131/1111 | 168/1111 | 146/1111 | 168/1601 | 175/1601 | 161/1601 | ||
OR (95% CI) | 1.00 | 1.21 (0.92–1.58) | 1.14 (0.86–1.52) | 0.420 | 1.00 | 1.01 (0.79–1.28) | 0.99 (0.77–1.27) | 0.903 |
T: tertile; OR: odds ratio; CI: confidence interval; 1 Linear trends across tertiles of each pattern were tested using the median value for each tertile as a continuous variable; 2 By definition, class I low muscle mass was indicated by definition in participants whose weight-adjusted ASMM was between the gender-specific mean for young reference group-1 SD and the mean for young adults-2 SD. Class II low muscle mass was indicated by definition in participants whose weight-adjusted ASMM was below the mean for young adults-2 SD. 3 Adjusted for age (continuous), BMI (continuous), energy intake (continuous), smoking status (never, past, current), alcohol consumption (non-current, current), physical activity (low, moderate, and high), household income (low, middle-low, middle-high, and high), and serum vitamin D (continuous).
4. Discussion
This cross-sectional study, conducted on a representative sample in Korea, showed that a higher “white rice, fish, and seaweeds” pattern score was associated with a lower prevalence of low muscle mass in both men and women, whereas a higher “condiment, vegetables, and meats” pattern score was associated with a higher prevalence of low muscle mass in men.
In the present study, the following four major dietary patterns were derived from Korean middle-aged and elderly populations: the “condiment, vegetables, and meats” pattern; “wheat flour, breads, fruits, milk, and dairy products” pattern; “white rice, fish, and seaweeds” pattern; and “whole grain, bean products, and kimchi” pattern. These dietary patterns were distinguished from those of previous Korean studies that examined the association between dietary pattern and muscle mass or muscle strength [24,25]. In a previous cross-sectional study that investigated the association between dietary patterns and ASMM in the Korean older population, two dietary patterns were identified: “Healthy” and “Western” [24]. The “healthy” dietary pattern, which was characterized by a high intake of vegetables, fish, fruits, seaweed, legumes, mushrooms, whole grains, potatoes, eggs, dairy products, and red meat, was associated with a higher ASMM in men aged ≥60 years [24]. Moreover, another cross-sectional study that investigated the association between dietary patterns and handgrip strength identified two dietary patterns: “Prudent” and “Western” [25]. The study revealed a significantly positive association between handgrip strength and the “prudent” dietary pattern, characterized by higher intakes of vegetables, potatoes, fish, mushroom, fruits, nuts, legumes, and mixed grains [25]. The differences in derived dietary patterns and their associations with muscle mass or muscle strength between previous studies and the present one may be primarily due to the difference in dietary assessment methods. Previous studies used food frequency questionnaires (FFQs) to assess the participants’ diets, whereas the present study used the 24-h dietary recall method. The FFQ consists of a predefined list of foods, whereas 24-h dietary recall is open-ended [26]. Open-ended questions, such as those in 24-h dietary recall, may be more appropriate for collecting a variety of detailed dietary information from participants than closed-ended ones, such as those in the FFQ [26], since the dietary pattern approach focuses on the combined and synergetic effects of various foods.
This study found that the “white rice, fish, and seaweeds” pattern was associated with a lower prevalence of low muscle mass in both men and women. Additionally, the mean appendicular skeletal muscle mass of the highest “white rice, fish, and seaweeds” pattern score group (men: 20.7 kg, women: 14.0 kg) is higher than that of the lowest pattern score group (men: 20.5 kg, women: 13.9 kg), though it was not statistically significant. The underlying mechanism can be explained by the role of various nutrients predominant in fish and seaweeds, such as protein, n-3 polyunsaturated fatty acid (PUFA), vitamin D, magnesium, and carnitine, which can be involved positively in muscle metabolism [27]. First, protein intake is crucial for maintaining skeletal muscle because skeletal muscle is the main reservoir of amino acids, containing 50–75% of all proteins in the human body [28]. Amino acids, especially leucine and insulin-like growth factor 1, are anabolic stimuli for muscle metabolism [29]. Regarding the protein source, fish protein can increase skeletal muscle weight in rats [30]; however, very few studies have focused on the effects of fish proteins on muscle mass in humans. Second, n-3 PUFA, predominant in fish, can mediate an increase in muscle protein synthesis. It is incorporated into the cellular membranes of various body tissues, including skeletal muscle, and may enhance membrane fluidity, thus improving the uptake of amino acids and, consequently, making the cells more responsive to muscle protein synthesis [31,32]. Finally, combining several anabolic nutrients, such as amino acids, n-3 PUFA, vitamin D, and magnesium, could increase protein synthesis and finally promote muscle mass gain [33,34].
In the present study, the “condiment, vegetables, and meats” pattern was associated with a higher prevalence of class II low muscle mass in men. Men with a higher “condiment, vegetables, and meats” pattern score (2703.1 kcal/day) consumed 1.8 times more calories per day than those with a lower one (1522.7 kcal/day). Moreover, men in the highest “condiment, vegetables, and meats” pattern score group had higher BMI, body fat mass, and % body fat, and higher prevalence of obesity compared to the lowest group (Table 1). This excessive calorie intake and higher BMI, body fat mass, and % body fat, and higher prevalence of obesity suggests the possibility of obesity in people who adhere to the “condiment, vegetables, and meats” pattern. Thus, low muscle mass is possibly associated with sarcopenic obesity, which involves the coexistence of age-related physical changes, such as a decrease in skeletal muscle mass and function (sarcopenia) as well as an increase in fat mass (obesity) [34]. In addition to sarcopenia and obesity having similar pathological pathways, obesity could be a risk factor for the development of sarcopenia [35]. The increase in intramuscular fat involved in obesity can affect the signaling pathways that are engaged in muscle protein synthesis and thereby increase the risk for sarcopenia [34,36].
In this study, the “condiment, vegetables, and meats” pattern was associated with an increased prevalence of class II low muscle mass in men, not in women. This sex difference can be explained by the unhealthy lifestyle of men compared to women. The highest “condiment, vegetables, and meats” pattern score group in men showed a much higher percentage of current smokers (men: 35.5%, women: 4.1%) and current drinkers (men: 74.2%, women: 31.1%) than that of women (Table 1). The results of a meta-analysis demonstrate that cigarette smoking is an isolated factor, which may contribute to the development of sarcopenia [37]. Alcohol consumption has not been reported as a direct cause of sarcopenia; however, previous evidence suggests that chronic alcohol consumption may promote loss of muscle mass in older people [38]. Although these lifestyle factors were statistically adjusted in the present analysis, these unhealthy lifestyles might exert combined negative effects on low muscle mass in men.
Findings from the present study showed that people adhering to the “white rice, fish, and seaweeds” pattern were less likely to have low muscle mass, whereas men who adhered to the “condiment, vegetables, and meats” pattern were more likely to have low muscle mass. To prevent and manage age-related loss of skeletal muscle mass, it may be recommended to adhere to a dietary pattern based on white rice, fish, and seaweed and avoid one with excessive calories, such as that consisting of mainly oil, sugar, and various sauces or seasoning. To design nutritional strategies that prevent low muscle mass, dietary patterns that ensure optimal nutrient intake should be developed to not only increase skeletal muscle mass or prevent muscle mass loss but also decrease excess fat mass, thereby preventing sarcopenic obesity. Additionally, to maximize the benefits of dietary pattern on muscle mass, adequate physical activity should be taken into consideration [38].
To the best of our knowledge, this study is the first to use 24-h dietary recall in investigating the association between major dietary pattern and the prevalence of low muscle mass among Korean middle-aged and elderly populations. Compared to previous studies that used the FFQ to derive dietary patterns among the Korean older population, the present one could derive more detailed and distinctive dietary patterns of Korean middle-aged and elderly populations.
However, several limitations should be considered when interpreting the results. First, due to the nature of the cross-sectional design, causal association between dietary pattern and the risk of low muscle mass cannot be confirmed from the present study’s results. Second, using the one-day 24-h dietary recall method may not reflect the participant’s usual intake. Finally, the factor analysis approach entails arbitrary yet important decisions in some processes, including the classification of food items into food groups, the number of factors to derive, the method of factor rotation, and even the labelling of the derived factors [39]. Therefore, the dietary pattern approach can be somewhat subjective, and the results may be difficult to replicate in other populations. Future research will be needed to confirm the causal association between dietary pattern and the risk of low muscle mass or muscle function in a large-scaled prospective cohort or randomized clinical trials.
5. Conclusions
The large-scaled cross-sectional study in Korea demonstrated that a dietary pattern based on white rice, fish, and seaweeds is associated with a lower prevalence of low muscle mass in middle-aged and elderly populations. Further, the aforementioned dietary pattern can be helpful in protecting against loss of skeletal muscle mass in the same populations.
Author Contributions
Conceptualization, S.S. and J.H.; formal analysis, S.-A.K.; writing—Original draft preparation, S.-A.K. and J.H.; writing—Review and editing, S.-A.K. and S.S.; visualization, B.L. and J.-M.K.; supervision, S.S.; funding acquisition, J.-M.K. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by National Research Foundation of Korea (NRF-2018R1A6A1A03025159).
Conflicts of Interest
The authors declare no conflict of interest.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Global Health and Aging. National Institute on Aging, National Institutes of Health, U.S. Department of Health and Human Services, and World Health Organization. [(accessed on 2 September 2020)]; Available online: https://www.who.int/ageing/publications/global_health.pdf.
- 2.Tyrovolas S., Koyanagi A., Olaya B., Ayuso-Mateos J.L., Miret M., Chatterji S., Tobiasz-Adamczyk B., Koskinen S., Leonardi M., Haro J.M. Factors associated with skeletal muscle mass, sarcopenia, and sarcopenic obesity in older adults: A multi-continent study. J. Cachexia Sarcopenia Muscle. 2016;7:312–321. doi: 10.1002/jcsm.12076. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Janssen I., Heymsfield S.B., Ross R. Low relative skeletal muscle mass (sarcopenia) in older persons is associated with functional impairment and physical disability. J. Am. Geriatr. Soc. 2002;50:889–896. doi: 10.1046/j.1532-5415.2002.50216.x. [DOI] [PubMed] [Google Scholar]
- 4.Harada K., Suzuki S., Ishii H., Aoki T., Hirayama K., Shibata Y., Negishi Y., Sumi T., Kawashima K., Kunimura A. Impact of skeletal muscle mass on long-term adverse cardiovascular outcomes in patients with chronic kidney disease. Am. J. Cardiol. 2017;119:1275–1280. doi: 10.1016/j.amjcard.2017.01.003. [DOI] [PubMed] [Google Scholar]
- 5.Park B.S., Yoon J.S. Relative skeletal muscle mass is associated with development of metabolic syndrome. Diabetes Metab. J. 2013;37:458–464. doi: 10.4093/dmj.2013.37.6.458. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Chuang S.-Y., Chang H.-Y., Lee M.-S., Chen R.C.-Y., Pan W.-H. Skeletal muscle mass and risk of death in an elderly population. Nutr. Metab. Cardiovasc. Dis. 2014;24:784–791. doi: 10.1016/j.numecd.2013.11.010. [DOI] [PubMed] [Google Scholar]
- 7.Beaudart C., Zaaria M., Pasleau F., Reginster J.-Y., Bruyère O. Health outcomes of sarcopenia: A systematic review and meta-analysis. PLoS ONE. 2017;12:e0169548. doi: 10.1371/journal.pone.0169548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Liguori I., Russo G., Aran L., Bulli G., Curcio F., Della-Morte D., Gargiulo G., Testa G., Cacciatore F., Bonaduce D. Sarcopenia: Assessment of disease burden and strategies to improve outcomes. Clin. Interv. Aging. 2018;13:913. doi: 10.2147/CIA.S149232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Evans W. What is sarcopenia? J. Gerontol. Ser. A Biol. Sci. Med. Sci. 1995;50:5–8. doi: 10.1093/gerona/50A.Special_Issue.5. [DOI] [PubMed] [Google Scholar]
- 10.Cruz-Jentoft A.J., Baeyens J.P., Bauer J.M., Boirie Y., Cederholm T., Landi F., Martin F.C., Michel J.-P., Rolland Y., Schneider S.M. Sarcopenia: European consensus on definition and diagnosisReport of the European Working Group on Sarcopenia in Older People. Age Ageing. 2010;39:412–423. doi: 10.1093/ageing/afq034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Cederholm T., Morley J.E. Sarcopenia: The new definitions. Curr. Opin. Clin. Nutr. Metab. Care. 2015;18:1–4. doi: 10.1097/MCO.0000000000000119. [DOI] [PubMed] [Google Scholar]
- 12.Morley J.E., Argiles J.M., Evans W.J., Bhasin S., Cella D., Deutz N.E., Doehner W., Fearon K.C., Ferrucci L., Hellerstein M.K. Nutritional recommendations for the management of sarcopenia. J. Am. Med. Dir. Assoc. 2010;11:391–396. doi: 10.1016/j.jamda.2010.04.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hu F.B. Dietary pattern analysis: A new direction in nutritional epidemiology. Curr. Opin. Lipidol. 2002;13:3–9. doi: 10.1097/00041433-200202000-00002. [DOI] [PubMed] [Google Scholar]
- 14.OECD . Preventing Ageing Unequally. OECD Publishing; Paris, France: 2017. [DOI] [Google Scholar]
- 15.Kim J., Jo I., Joung H. Dietetics. A rice-based traditional dietary pattern is associated with obesity in Korean adults. J. Acad. Nutr. Diet. 2012;112:246–253. doi: 10.1016/j.jada.2011.10.005. [DOI] [PubMed] [Google Scholar]
- 16.Hong S., Song Y., Lee K.H., Lee H.S., Lee M., Jee S.H., Joung H. A fruit and dairy dietary pattern is associated with a reduced risk of metabolic syndrome. Metabolism. 2012;61:883–890. doi: 10.1016/j.metabol.2011.10.018. [DOI] [PubMed] [Google Scholar]
- 17.Lee S.Y., Ahn S., Kim Y.J., Ji M.J., Kim K.M., Choi S.H., Jang H.C., Lim S. Comparison between dual-energy X-ray absorptiometry and bioelectrical impedance analyses for accuracy in measuring whole body muscle mass and appendicular skeletal muscle mass. Nutrients. 2018;10:738. doi: 10.3390/nu10060738. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Heymsfield S.B., Smith R., Aulet M., Bensen B., Lichtman S., Wang J.P.R.J., Pierson R.N. Appendicular skeletal muscle mass: Measurement by dual-photon absorptiometry. Am. J. Clin. Nutr. 1990;52:214–218. doi: 10.1093/ajcn/52.2.214. [DOI] [PubMed] [Google Scholar]
- 19.Wang Z., Visser M., Ma R., Baumgartner R.N., Kotler D., Gallagher D., Heymsfield S.B. Skeletal muscle mass: Evaluation of neutron activation and dual-energy X-ray absorptiometry methods. J. Appl. Physiol. 1996;80:824–831. doi: 10.1152/jappl.1996.80.3.824. [DOI] [PubMed] [Google Scholar]
- 20.Chen L.-K., Lee W.-J., Peng L.-N., Liu L.-K., Arai H., Akishita M., Asian Working Group for Sarcopenia Recent advances in sarcopenia research in Asia: 2016 update from the Asian Working Group for Sarcopenia. J. Am. Med. Dir. Assoc. 2016;17:767.e1–767.e7. doi: 10.1016/j.jamda.2016.05.016. [DOI] [PubMed] [Google Scholar]
- 21.Yeom H.-A., Jung D., Choi M. Adherence to physical activity among older adults using a geographic information system: Korean national health and nutrition examinations survey IV. Asian Nurs. Res. 2011;5:118–127. doi: 10.1016/S1976-1317(11)60020-0. [DOI] [PubMed] [Google Scholar]
- 22.Ainsworth B.E., Haskell W.L., Whitt M.C., Irwin M.L., Swartz A.M., Strath S.J., Brien W.L., Bassett D.R., Schmitz K.H., Emplaincourt P.O., et al. Compendium of physical activities: An update of activity codes and MET intensities. Med. Sci. Sports Exerc. 2000;32:S498–S504. doi: 10.1097/00005768-200009001-00009. [DOI] [PubMed] [Google Scholar]
- 23.Guidelines for Data Processing and Analysis of the International Physical Activity Questionnaire (IPAQ)–Short and Long Forms. The IPAQ Group. [(accessed on 7 September 2020)]; Available online: https://docs.google.com/viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnx0aGVpcGFxfGd4OjE0NDgxMDk3NDU1YWRlZTM.
- 24.Lee J.Y., Lee S. Dietary patterns related to appendicular skeletal muscle mass: The Korea National Health and Nutrition Examination Survey 2008–2011. J. Am. Coll. Nutr. 2019;38:358–363. doi: 10.1080/07315724.2018.1523759. [DOI] [PubMed] [Google Scholar]
- 25.Lee S. Associations between dietary patterns and handgrip strength: The Korea national health and nutrition examination survey 2014–2016. J. Am. Coll. Nutr. 2020;39:488–494. doi: 10.1080/07315724.2019.1691955. [DOI] [PubMed] [Google Scholar]
- 26.Shim J.-S., Oh K., Kim H.C. Dietary assessment methods in epidemiologic studies. Epidemiol. Health. 2014;36:e2014009. doi: 10.4178/epih/e2014009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Rondanelli M., Rigon C., Perna S., Gasparri C., Iannello G., Akber R., Alalwan T.A., Freije A.M. Novel Insights on Intake of Fish and Prevention of Sarcopenia: All Reasons for an Adequate Consumption. Nutrients. 2020;12:307. doi: 10.3390/nu12020307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Timmerman K.L., Volpi E. Amino acid metabolism and regulatory effects in aging. Curr. Opin. Clin. Nutr. Metab. Care. 2008;11:45. doi: 10.1097/MCO.0b013e3282f2a592. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Drummond M.J., Rasmussen B.B. Leucine-enriched nutrients and the regulation of mTOR signalling and human skeletal muscle protein synthesis. Curr. Opin. Clin. Nutr. Metab. Care. 2008;11:222. doi: 10.1097/MCO.0b013e3282fa17fb. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Kawabata F., Mizushige T., Uozumi K., Hayamizu K., Han L., Tsuji T., Kishida T. Fish protein intake induces fast-muscle hypertrophy and reduces liver lipids and serum glucose levels in rats. Biosci. Biotechnol. Biochem. 2015;79:109–116. doi: 10.1080/09168451.2014.951025. [DOI] [PubMed] [Google Scholar]
- 31.Smith G.I., Atherton P., Reeds D.N., Mohammed B.S., Rankin D., Rennie M.J., Mittendorfer B. Dietary omega-3 fatty acid supplementation increases the rate of muscle protein synthesis in older adults: A randomized controlled trial. Am. J. Clin. Nutr. 2011;93:402–412. doi: 10.3945/ajcn.110.005611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Rossato L.T., Schoenfeld B.J., de Oliveira E.P. Is there sufficient evidence to supplement omega-3 fatty acids to increase muscle mass and strength in young and older adults? Clin. Nutr. 2020;39:23–32. doi: 10.1016/j.clnu.2019.01.001. [DOI] [PubMed] [Google Scholar]
- 33.Chanet A., Verlaan S., Salles J., Giraudet C., Patrac V., Pidou V., Pouyet C., Hafnaoui N., Blot A., Cano N. Supplementing breakfast with a vitamin D and leucine–enriched whey protein medical nutrition drink enhances postprandial muscle protein synthesis and muscle mass in healthy older men. J. Nutr. 2017;147:2262–2271. doi: 10.3945/jn.117.252510. [DOI] [PubMed] [Google Scholar]
- 34.Trouwborst I., Verreijen A., Memelink R., Massanet P., Boirie Y., Weijs P., Tieland M. Exercise and nutrition strategies to counteract sarcopenic obesity. Nutrients. 2018;10:605. doi: 10.3390/nu10050605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Rolland Y., Czerwinski S., Van Kan G.A., Morley J., Cesari M., Onder G., Woo J., Baumgartner R., Pillard F., Boirie Y., et al. Sarcopenia: Its assessment, etiology, pathogenesis, consequences and future perspectives. J. Nutr. Health Aging. 2008;12:433–450. doi: 10.1007/BF02982704. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Hilton T.N., Tuttle L.J., Bohnert K.L., Mueller M.J., Sinacore D.R. Excessive adipose tissue infiltration in skeletal muscle in individuals with obesity, diabetes mellitus, and peripheral neuropathy: Association with performance and function. Phys. Ther. 2008;88:1336–1344. doi: 10.2522/ptj.20080079. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Steffl M., Bohannon R.W., Petr M., Kohlikova E., Holmerova I. Relation between cigarette smoking and sarcopenia: Meta-analysis. Physiol. Res. 2015;64:419. doi: 10.33549/physiolres.932802. [DOI] [PubMed] [Google Scholar]
- 38.Rom O., Kaisari S., Aizenbud D., Reznick A.Z. Lifestyle and sarcopenia—etiology, prevention, and treatment. Rambam Maimonides Med. J. 2012;3:e0024. doi: 10.5041/RMMJ.10091. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Martinez M.E., Marshall J.R., Sechrest L. Invited commentary: Factor analysis and the search for objectivity. Am. J. Epidemiol. 1998;148:17–19. doi: 10.1093/oxfordjournals.aje.a009552. [DOI] [PubMed] [Google Scholar]