Abstract
The prevalence of age-related diseases such as dementia and cognitive disorders is rapidly increasing. This study aimed to identify the dietary patterns associated with mild cognitive impairment (MCI) in adults aged over 50 years. This cross-sectional study investigated dietary patterns associated with cognitive function among older adults hospitalized in Gwangju province. Global cognitive function was assessed using the Mini-Mental State Examination. Diet information was obtained using a food frequency questionnaire with 112 food items and 24-h dietary recall. Using a principal component analysis, we identified three dietary patterns, “legumes and vegetables”, “beverage and nuts”, and “white rice”. The “beverage and nuts” pattern was inversely associated with the prevalence of high MCI after adjusting for covariates (third vs. first tertile, adjusted odds ratio: 0.333; 95% confidence interval: 0.133∼0.831; P<0.05). The white rice pattern was associated with the prevalence of MCI in the crude analysis. However, after adjusting for all confounding factors, no association was found. The “beverage and nuts” pattern was inversely associated with the prevalence of MCI. In the future, longitudinal population-based studies and randomized clinical trials are required to confirm the effect of potential dietary patterns on cognitive impairment and reveal the underlying mechanism of their association.
Keywords: diet, mild cognitive impairment, principal component analysis
INTRODUCTION
The prevalence of age-related diseases, such as dementia and cognitive impairment, is rapidly increasing worldwide. In 2013, the World Health Organization reported that there were about 47.5 million patients with dementia globally in 2010, with 7.7 million patients newly diagnosed each year (Wimo et al., 2013). As a result, the cost of dementia worldwide is estimated to be 604 billion dollars per year (Wimo et al., 2013). In a study of 9,485 Koreans conducted in 2010 and 2011, the prevalence of dementia and mild cognitive impairment (MCI) in participants aged over 65 years was 5.4% and 4.3%, respectively (Jang et al., 2014). MCI is considered to be the transitional state between the expected cognitive decline of normal aging and dementia progression (Albert and Blacker, 2006). Although people with MCI have a greater risk of dementia, many studies have reported that it is possible to prevent progression to dementia by controlling environmental factors such as dietary habits, exercise, and chronic disease management (Eshkoor et al., 2015; Jiang et al., 2017). Several studies have recently investigated the associations between cognitive function and dietary factors, including certain foods and nutrients (Panza et al., 2015; Jiang et al., 2017). Adequate consumption of omega-3 fatty acids (Cederholm et al., 2013), fruits and vegetables (Dong et al., 2016; Jiang et al., 2017), dairy products (Ogata et al., 2016), and moderate alcohol consumption (Xu et al., 2017) have been reported to have protective effects against disease. However, the association between dietary factors and the risk of cognitive impairment and dementia remains unclear (Panza et al., 2015; Kesse-Guyot et al., 2016; Smith and Blumenthal, 2016).
Recently, dietary patterns have been used to examine how diseases can be prevented and disease conditions improved (Ozawa et al., 2013; Kim et al., 2015; van de Rest et al., 2015; Shin et al., 2018). As we consume a number of different types of food, rather than a single type of food, it seems reasonable to investigate the effects of dietary patterns on disease. Thus, research using dietary patterns, considering the interaction and synergy of nutrients in foods, is valid for disease prevention studies (Hoffmann et al., 2004; Ozawa et al., 2013; Kim et al., 2015). Accelerated economic development and globalization have changed traditional Korean dietary patterns. This change has resulted in Koreans consuming fewer food crops, such as rice, but increased amounts of bread, meat, and seafood (Lee and Cho, 2014). Thus, over time, the diet of Koreans has become more westernized. Western dietary habits are known to affect the incidence of and mortality due to chronic diseases such as metabolic syndrome and cardiovascular disease (Lee and Cho, 2014). Thus, it is necessary to investigate the current daily dietary patterns of Koreans.
Factor analysis, cluster analysis, reduced rank regression, and partial least-squares regression have been used to identify dietary patterns. A factor analysis is a statistical technique that considers the correlation between variables, reduces the order of variables through common underlying dimensions, and generally uses a principal component analysis (PCA) (Hoffmann et al., 2004).
This study aimed to identify the dietary patterns of elderly Koreans with MCI using a PCA and determine their impact on cognitive function so as to contribute to the provision of healthy dietary guidelines.
MATERIALS AND METHODS
Study design and participants
Data of 324 older adults aged over 50 years hospitalized in Gwangju Sun-Han Hospital were collected through a face-to-face interview with questionnaires from July 2017 to March 2018. We excluded participants with very high or low total energy intake levels (<500 or >3,500 kcal), those who were on diet therapy within the last year (as this would change their daily dietary patterns), or those with a severe mental disorder, metabolic diseases, cancer, alcohol abuse, Parkinson’s disease, and/or Alzheimer’s disease. Two hundred and seventy-five participants, including 104 males and 171 females, completed all of the questionnaires, including a Mini-Mental State Examination (MMSE), short-form geriatric depression scales, 24-h dietary recall, and a semi-quantitative food frequency questionnaire (SQ-FFQ). This study complied with the tenets of the Declaration of Helsinki, and all procedures involving human participants were approved by the Institutional Review Board of Chonnam National University (1040198-180731-HR-071-01). All participants who participated in our study signed a consent form.
Dietary assessment
Data were obtained by trained dietitians who interviewed all the participants face-to-face. If necessary, patients’ caregivers helped with the completion of the dietary intake survey.
A food and nutrient intake survey was conducted using only the 24-h dietary recall method considering the age of the participants and SQ-FFQ with 112 food items. The FFQ examines the food intake of participants, assuming that their dietary habits do not change frequently. The 24-h dietary recall method provides more accurate information on the food that participants have consumed. It has been reported that using the two methods in parallel makes it possible to capture dietary habits more accurately (Freedman et al., 2018). The SQ-FFQ has been reported to be valid and reproducible previously (Feskanich et al., 1993). Participants were asked to check each of the nine frequency ranges from “none” to “three times a day” for food and beverages. Daily food intake derived from the FFQ was calculated by multiplying the food intake frequency of each standard serving size. The daily nutrient intake was calculated by multiplying the intake frequency and standard portion size according to CAN-PRO version 4.0 (Computer-Aided Nutritional Analysis Program, the Korea Nutrition Society, Seoul, Korea).
Cognitive function assessment
We used the MMSE tool, a global test (Huang et al., 2009), to measure cognitive function. The MMSE includes 30 items covering the following fields: time and place orientation, memory registration and recall, attention and calculation, language function, and understanding and judgment. Scores were corrected according to education level and ranged from 0 to 30. Higher MMSE scores indicate better cognitive function. Participants were assigned to the MCI group if their MMSE score was 19∼24 and to the normal group if their MMSE score was 25∼30, according to the MCI clinical diagnosis cut-off value mentioned in a previous study (Huang et al., 2009). The sensitivity and accuracy of a score below 24 on the MMSE, defined as cognitive impairment, is 80∼90% and 80∼100%, respectively (Tombaugh and McIntyre, 1992). Finally, the Sun-Han medical staff confirmed the diagnosis of the participants with MCI. The short geriatric depression scale (SGDS) developed in 1986 is a tool used for screening older adults for symptoms of depression (Greenberg, 2007). This self-reported screening tool consists of 15 questions that can be completed quickly using “yes” or “no” answers, making it useful in the community setting. A score of 0∼4 is not typically a cause for concern, 5∼8 suggests mild depression, 9∼11 suggests moderate depression, and 12∼15 suggests severe depression (Greenberg, 2007). The SGDS tool has been reported to identify 92% of people with depression (Sheikh and Yesavage, 1986).
PCA and identification of dietary patterns
Dietary patterns were generated by utilizing the PCA for 21 predefined food groups (Khosravi et al., 2015; Kim et al., 2015; Table 1). In this study, the food items were combined into food groups based on their nutrient contents and uses. Besides, we divided the vegetable group into salty vegetables and vegetables to consider whether the salt difference had any impact.
Table 1.
Food grouping used in the dietary intake analysis
| Food groups | Food items |
|---|---|
| White rice | Cooked white rice, fried rice, cooked rice with assorted mixtures, rice rolled in laver, curry and rice, cereal |
| Multigrain rice | Cooked rice with other grains and legumes |
| Flour-based foods | Instant noodles, instant cup noodles, noodles, kalguksu, udong, Chinese black bean noodles, spicy seafood noodle soup, cold noodles, dumpling (steamed or fried) |
| Rice-cake | Plain steamed rice-cake, steamed rice-cake with red bean, cubed rice-cake with soybean powder, plain cubed rice cake, seasoned bar rice-cake |
| Bread | Loaf bread, sweet red-beans buns, steamed sweet red-bean buns, cream buns, sponge cake (castella), cake, chocopie |
| Soup and stew | Rice-cake soup, beef born and meat potage, potato and pork rib soup, loach stew, frozen Alaska pollack stew, spicy seafood stew, sea mustard soup, dried Alaska pollack soup, beef soup, spicy beef soup, radish soup, bean paste soup, bean paste stew, fermented soybean stew, kimchi stew, stir-fried kimchi, spicy sausage stew, bean curd stew, soft bean curd stew |
| Legume | Bean curd, bean curd boiled in soy sauce, pan-fried bean curd, soybean boiled in soy sauce |
| Eggs | Fried egg, fried egg roll, boiled egg, steamed egg |
| Red meats and processed meats | Pizza, hamburger, sandwich, grilled pork belly, boiled pork, stir-fried pork (sweet, spicy), grilled pork ribs, steamed pork ribs, grilled beef, stir-fried beef, sweet and sour pork, pork cutlet, ham, pork roll |
| Poultry | Korean traditional chicken soup, stir-fried chicken, chicken boiled with soy sauce, fried chicken, grilled duck |
| Fish | Mackerel, saury (grill, boiled with soy sauce), hairtail, croaker (grill, boiled with soy sauce), anchovy, stir-fried anchovy, squid (raw, boiled, stir-fried), dried shredded squid (stir-fried, seasoned), dried squid, crab preserved in soy or spicy sauce, salted shrimp, squid and clam, fish ball (stir-fried, soup) |
| Vegetables | Stir-fried potatoes, potatoes boiled with soy sauce, steamed potatoes, grilled potatoes, steamed sweet potatoes, grilled sweet potatoes, steamed corn, grilled corn, bean sprout (seasoned, soup), seasoned mung bean sprout, seasoned spinach, seasoned bellflower (boiled or not), pumpkin (seasoned, pan-fried), seasoned other vegetables, cucumber (seasoned, raw), radish (seasoned, pickled, dried), vegetables salad, seasoned green onion, seasoned Chinese chive, raw vegetables (lettuce, sesame, Chinese cabbage, pumpkin leaf), green pepper, boiled broccoli, boiled cabbage, garlic, lotus roots boiled with soy sauce, burdock boiled with soy sauce, Korean pancake (Chinese chive pancake, kimchi pancake), stir-fried vegetable and noodles, stir-fried mushroom, soybean paste sauce |
| Salty vegetables | Korean cabbage kimchi, other kimchi, pickle |
| Seaweeds | Grilled laver, raw laver, seasoned laver, seasoned green laver, seasoned brown seaweed, stir-fried sea mustard stems |
| Fruits | Strawberry, tomato, cherry tomato, melon, water melon, peach, grape, apple, pear, persimmon, dried persimmon, tangerine, banana, orange, kiwi |
| Dairy products | Milk (low fat, normal), liquid type yogurt, curd type yogurt, soybean milk |
| Coffee and tea | Coffee, green tea |
| Beverages | Soft drink (cola, soda, fruit juice soda), fruit juice, grain powder beverage, rice beverage |
| Nuts | Peanut, chestnut |
| Snack | Snack, cookie, cracker, chocolate, ice cream, ices |
| Alcohol | Soju, beer, rice wine |
This study reorganized the foods containing similar nutrients into new groups based on previous studies (Khosravi et al., 2015; Kim et al., 2015).
A principal component and factor analysis is a nutritional epidemiology method that derives dietary patterns by distinguishing one or more factors based on foods that tend to (or are not) ingested by the same subject (Osler et al., 2002; Schulze et al., 2003). The PCA explains the frequency of various foods or food groups consumed by the individual as a linear function of the principal components. That is, the first principal component accounts for the maximum amount of variation among individuals. The second principal component is derived from the orthogonal rotation of the first principal component and accounts for the maximum amount of variance among the factors. Finally, the PCA identifies dietary patterns by analyzing the intake frequency based on the correlation matrix of the foods included in the survey (Schulze et al., 2003).
To extract the dietary patterns, we classified 112 food items into 21 food groups with reference to similar nutrient profiles and previous studies: white rice, multigrain rice, flour-based food, rice-cakes, bread, soup and stew, legumes, eggs, red meat and processed meat, poultry, fish, vegetables, salty vegetables, seaweed, fruit, dairy products, coffee and tea, beverages, nuts, snacks, and alcohol. The number of dietary patterns (referred to as derived factors) was determined using an eigenvalue of >1.25 and scree plot (Schulze et al., 2003). Furthermore, the factors were rotated with an orthogonal transformation using a varimax rotation to achieve a simpler structure with easier interpretability (Kline, 1994). We considered the food groups with an absolute factor loading >0.2 to be significant in the calculation of pattern scores because the food items included in these food groups appeared to have a strong association with the identified factors (Kline, 1994; McCann et al., 2001). The factor scores were calculated by summing each subject’s intake of the 21 food groups weighted by the factor loadings. Each dietary pattern score was categorized by tertile, with a higher tertile indicating better adherence. We labeled the dietary pattern according to the food with the highest factor loadings.
Energy and nutrient intake using the 24-h recall method
Nutrient intakes were estimated by multiplying the intake frequency and standardized portion size for each food. The amount of nutrients contained per gram of food was obtained from CAN-PRO version 4.0. Daily nutrient intakes of participants were the sum of their intake of the 112 food items. Macro- and micronutrient intakes were adjusted for in the total energy intake using the residual method. Considering the age of the participants, the dietary survey was performed using ancillary equipment such as a measuring cup, photographs of the prescribed amount of food, and tableware. The nutrient variables were used as continuous data of the daily intake of total energy (kcal/d), carbohydrates (g/1,000 kcal), fat (g/1,000 kcal), protein (g/1,000 kcal), saturated fatty acid (g/1,000 kcal), monounsaturated fatty acid (MUFA; g/1,000 kcal), polyunsaturated fatty acid (PUFA; g/1,000 kcal), fiber (g/1,000 kcal), water (g/1,000 kcal), β-carotene (mg retinol equivalent/1,000 kcal), vitamin E (mg/1,000 kcal), vitamin C (mg/1,000 kcal), thiamin (mg/1,000 kcal), niacin (mg/1,000 kcal), vitamin B6 (mg/1,000 kcal), folate (μg/1,000 kcal), vitamin B12 (mg/1,000 kcal), calcium (mg/1,000 kcal), and cholesterol (mg/1,000 kcal).
Covariates
We interviewed all the participants face-to-face. The participants were informed that their data would be handled confidentially. The survey was conducted as quickly as possible due to the age of the participants.
Participants’ general characteristics such as age, sex, education level, inhabitation, self-measured health status level, prescribed medications, self-reported dental condition level, and sleep duration were collected. Furthermore, the following information was collected: alcohol consumption status (if less than 12 times per year with less than one glass per drink then the participant was classified as no, former, and current drinkers was classified as a yes), smoking status (never was classified as no, former, and current smokers were classified as yes), physical activity in leisure time (no, usually, and yes), breakfast frequency/week, and nutritional supplements. Participants had standardized anthropometric measures taken by trained nurses. Body mass index was calculated as a participant’s body weight in kilograms divided by their height in meters squared. A trained nurse measured each participant’s blood pressure using an automatic blood pressure monitor (HBP-9020, Omron Healthcare Co., Ltd., Kyoto, Japan) after allowing the participant to rest for 5 min beforehand. Then, subject’s blood pressure was repeatedly measured, with their arms and back in a straight line and their arms in line with their heart.
Statistical analysis
Categorical variables were expressed as frequency and percentage (%), and continuous variables as mean±standard deviation. We investigated the association between cognitive function and dietary patterns using a logistic regression analysis. Dietary patterns were determined using a factor analysis and PCA. We considered the correlation between the measured variables and extracted the factors by examining the calculated correlation matrix. Factor loading was calculated from the extracted factors. To simplify the column of the factor matrix, varimax rotation was performed.
The effect of each dietary pattern on cognitive function as the tertile increases from T1 to T3 was estimated using the odds ratio. The confounding factors of the analysis were as follows: sex, age, inhabitation, education, self-reported dental condition, sleep duration, alcohol consumption status, smoking status, physical activity in leisure time, nutritional supplements, and the SGDS variable to analyze the risk of MCI with each dietary pattern score (Model 1). A P-value of <0.05 was considered statistically significant. All statistical analyses were performed using SPSS version 18.0 (IBM Corp., Armonk, NY, USA).
RESULTS
General and anthropometric characteristics of the participants according to the MMSE score
According to the MMSE score, the general and anthropometric characteristics of participants were analyzed and are presented in Table 2. Participants with MCI (70.5 years) tended to be older than normal participants (63.8 years). Normal participants were more highly educated than the participants with MCI. Furthermore, 75.5% of normal participants and 55.7% of the participants with MCI lived alone. In addition, 32.9% of participants with MCI responded that their health status was poor. Sleep duration was shorter in participants with MCI (4∼6 h/d) than normal participants (6∼8 h/d). Participants who self-reported SGDS≥12 were more likely to be in the MCI group (22.4%) than the normal group (3.1%). Systolic blood pressure was higher in the MCI group (120.1 mmHg) than the normal group (116.4 mmHg).
Table 2.
General characteristics of participants according to MMSE score
| Characteristics | MMSE | P-value | ||
|---|---|---|---|---|
| Total (n=275) |
19∼24 (n=79) |
≥25 (n=196) |
||
| Sex | 0.606 | |||
| Men | 104 (37.8) | 28 (35.4) | 76 (38.8) | |
| Women | 171 (62.2) | 51 (64.6) | 120 (61.2) | |
| Age (yrs) | 65.7±9.4 | 70.5±9.5 | 63.8±9.2 | <0.001 |
| 50∼64 | 130 (47.3) | 19 (24.1) | 111 (56.6) | |
| 65∼74 | 97 (35.3) | 35 (44.3) | 62 (31.6) | |
| ≥75 | 48 (17.5) | 25 (31.6) | 23 (11.7) | |
| Education | <0.001 | |||
| Illiterate | 115 (41.8) | 49 (62.0) | 66 (33.7) | |
| Junior high school | 42 (15.3) | 6 (7.6) | 36 (18.4) | |
| High school | 80 (29.1) | 19 (24.1) | 61 (31.1) | |
| Above | 38 (13.8) | 5 (6.3) | 33 (16.8) | |
| Inhabitation | 0.001 | |||
| Alone | 192 (69.8) | 44 (55.7) | 148 (75.5) | |
| With spouse | 83 (30.2) | 35 (44.3) | 48 (24.5) | |
| Self-reported health status1) | 0.024 | |||
| Poor | 64 (23.8) | 26 (32.9) | 38 (20.0) | |
| Good or fair | 205 (76.2) | 53 (67.1) | 152 (80.0) | |
| Medication (yes) | 205 (74.5) | 68 (86.1) | 137 (69.9) | 0.005 |
| Current disease (yes) | 195 (70.9) | 62 (78.5) | 133 (67.9) | 0.079 |
| Self-reported dental condition | 0.145 | |||
| Very good or good | 184 (66.9) | 58 (73.4) | 126 (64.3) | |
| Very poor or poor | 91 (33.1) | 21 (26.6) | 70 (35.7) | |
| Sleep duration (h/d) | 0.002 | |||
| <4 | 17 (6.2) | 11 (13.9) | 6 (3.1) | |
| 4∼6 | 126 (45.8) | 40 (50.6) | 86 (43.9) | |
| 6∼8 | 121 (44.0) | 26 (32.9) | 95 (48.5) | |
| ≥8 | 11 (4.0) | 2 (2.5) | 9 (4.6) | |
| Alcohol consumption (yes) | 107 (38.9) | 23 (29.1) | 86 (43.9) | 0.024 |
| Smoking (yes) | 213 (77.5) | 66 (83.5) | 147 (75.0) | 0.125 |
| Physical activity in leisure time | 0.083 | |||
| No | 131 (47.6) | 46 (58.2) | 85 (43.4) | |
| Usually | 88 (32.0) | 20 (25.3) | 68 (34.7) | |
| Yes | 56 (20.4) | 13 (16.5) | 43 (21.9) | |
| Breakfast frequency (weekly, times) | 0.969 | |||
| 5∼7 | 257 (93.5) | 74 (93.7) | 183 (93.4) | |
| 3∼4 | 10 (3.6) | 3 (3.8) | 7 (3.6) | |
| ≤2 | 8 (2.9) | 2 (2.5) | 6 (3.1) | |
| Nutritional supplements (usually or yes) | 229 (83.3) | 63 (79.7) | 166 (84.7) | 0.320 |
| SGDS1) | <0.001 | |||
| Normal (≤4) | 197 (76.4) | 32 (47.8) | 165 (86.4) | |
| Mild or moderate (5∼11) | 40 (15.5) | 20 (29.9) | 20 (10.5) | |
| Severe (≥12) | 21 (8.1) | 15 (22.4) | 6 (3.1) | |
| BMI (kg/m2) | 23.7±3.8 | 23.6±3.6 | 23.8±3.9 | 0.702 |
| SBP (mmHg) | 117.4±12.9 | 120.1±14.7 | 116.4±11.0 | 0.024 |
| DBP (mmHg) | 75.8±11.5 | 77.8±12.5 | 75.0±10.4 | 0.056 |
Values are expressed as the number of participants for each category (%) or mean±standard deviation.
MMSE, mini-mental state examination; SGDS, short geriatric depression scale; BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure.
1)The response base differs because there are cases of irrelevant responses or no responses.
P-values were obtained from chi-square test for categorical variables.
Factor loadings and dietary patterns from the PCA
Based on the scree plot, we derived three dietary patterns with eigenvalues of ≥1.6, 46.85% of the cumulative explained variation among the 21 food groups. Table 3 and Fig. 1 illustrate the factor loadings (≥|0.20|), which characterize each dietary pattern. The first dietary pattern, “legumes and vegetables”, was positively characterized by a high consumption of legumes, vegetables, seaweed, soup and stew, eggs, fish, poultry, red meat, and processed meat (Fig. 1). Furthermore, the second dietary pattern (mix of healthy and unhealthy food groups), “beverage and nuts”, was positively characterized by a high consumption of beverages, nuts, sweet foods, fruit, rice-cakes, coffee and tea, and bread (Fig. 1). The “white rice” pattern was characterized by a high consumption of white rice, flour-based food, and alcohol, and a low consumption of dairy products and multigrain rice (Fig. 1).
Table 3.
Factor loadings and variation in food groups, and dietary patterns from principal component analysis
| Food groups | Factor 11) | Factor 22) | Factor 33) |
|---|---|---|---|
| Legume | 0.835 | − | − |
| Vegetables | 0.775 | − | − |
| Seaweeds | 0.770 | − | − |
| Soup and stew | 0.711 | − | − |
| Eggs | 0.648 | − | − |
| Fish | 0.623 | − | − |
| Poultry | 0.564 | − | − |
| Red meats and processed meats | 0.513 | − | − |
| Beverages | − | 0.711 | − |
| Nuts | − | 0.609 | − |
| Snack | − | 0.604 | − |
| Fruits | − | 0.559 | − |
| Rice-cake | − | 0.474 | − |
| Coffee and tea | − | 0.393 | − |
| Bread | − | 0.298 | − |
| Salty vegetables | − | −0.257 | − |
| White rice | − | − | 0.662 |
| Flour-based foods | − | − | 0.629 |
| Alcohol | − | − | 0.563 |
| Dairy products | − | − | −0.485 |
| Multigrain rice | − | − | −0.430 |
| Eigenvalue | 6.137 | 2.041 | 1.661 |
| Cumulative explained variation | 21.347 | 35.302 | 46.854 |
Kaiser-Meyer-Olkin=0.821, Bartlett’s test results=2,270.582, and df=210, and Sig=0.000.
The following factors had loadings ≥|0.20| are shown in the table. The score for each dietary pattern was estimated from the 21 predefined food groups.
Legume and vegetables pattern include legume, vegetables, seaweeds, soup and stew, eggs, fish, poultry, red meats and processed meats.
1)“Legume and vegetables” pattern was positively characterized by high consumption of legume, vegetables, seaweeds, soup and stew, eggs, fish, poultry, and red meats and processed meat.
2)“Beverage and nuts” pattern was positively characterized by high consumption of beverages, nuts, sweet foods, fruits, rice-cake, coffee and tea, and bread.
3)“White rice” pattern was characterized by higher consumption of white rice, flour-based foods and alcohol and lower consumption of dairy products, and multigrain rice.
Fig. 1.
Radar graph of factor loadings characterizing 3 dietary patterns. Factor scores were calculated by summing the 21 food groups’ intake frequency weighted by the factor loading.
Characteristics of participants with different dietary patterns
Table 4 and Fig. 2 presents the characteristics of participants according to the derived dietary pattern score tertile. The level of education and physical activity increased across the tertiles of the “beverage and nuts” pattern. However, the self-perceived dental condition was very poor or poor in higher tertiles in this dietary pattern. Self-reported depressive symptom scores were lower in T3 (score: 3.4) than in T1 (score: 4.6), and participants with severe status (score: ≥12) were less prevalent in T3 (7.4%) than T1 (18.1%). The MMSE score was higher in higher tertiles (Tl score: 26.0 vs. T3 score: 28.1). As the tertile increased in the “white rice” pattern, the distribution of males and participants ≥75 years was augmented. The proportion of participants who slept <4 h/d increased from T1 to T3. The proportion of former and current smokers was higher in T1 (82.4%). As the tertile increased, the self-reported SGDS score (Tl score: 2.6 vs. T3 score: 4.5) increased, and the MMSE score (Tl score: 28.0 vs. T3 score: 25.9) decreased. The anthropometric characteristics of participants were not significant in all patterns.
Table 4.
General characteristics according to each dietary pattern score tertiles
| Characteristics | Legume and vegetables pattern | Beverage and nuts pattern | White rice pattern | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| T1 | T2 | T3 | Total | P | T1 | T2 | T3 | Total | P | T1 | T2 | T3 | Total | P | |||
| n | 91 | 93 | 91 | 275 | 92 | 92 | 91 | 275 | 91 | 92 | 92 | 275 | |||||
| Sex | 0.039 | 0.531 | <0.001 | ||||||||||||||
| Men | 43 (47.3) | 27 (29.0) | 34 (37.4) | 104 (37.8) | 31 (33.7) | 35 (38.0) | 38 (41.8) | 104 (37.8) | 23 (25.3) | 31 (33.7) | 50 (54.3) | 104 (37.8) | |||||
| Women | 48 (52.7) | 66 (71.0) | 57 (62.6) | 171 (62.2) | 61 (66.3) | 57 (62.0) | 53 (58.2) | 171 (62.2) | 68 (74.7) | 61 (66.3) | 42 (45.7) | 171 (62.2) | |||||
| Age (yrs) | 65.2±9.2 | 67.4±9.5 | 64.6±10.4 | 65.7±9.7 | 0.125 | 66.8±10.0 | 66.6±9.1 | 63.8±10.0 | 65.7±9.7 | 0.065 | 66.7±8.9 | 65.2±9.3 | 65.4±11.0 | 65.7±9.7 | 0.495 | ||
| 50∼64 | 43 (47.3) | 35 (37.6) | 52 (57.1) | 130 (47.3) | 0.040 | 39 (42.4) | 39 (42.4) | 52 (57.1) | 130 (47.3) | 0.252 | 35 (38.5) | 44 (47.8) | 51 (55.4) | 130 (47.3) | 0.039 | ||
| 65∼74 | 36 (39.6) | 39 (41.9) | 22 (24.2) | 97 (35.3) | 35 (38.0) | 36 (39.1) | 26 (28.6) | 97 (35.3) | 42 (46.2) | 33 (35.9) | 22 (23.9) | 97 (35.3) | |||||
| ≥75 | 12 (13.2) | 19 (20.4) | 17 (18.7) | 48 (17.5) | 18 (19.6) | 17 (18.5) | 13 (14.3) | 48 (17.5) | 14 (15.4) | 15 (16.3) | 19 (20.7) | 48 (17.5) | |||||
| Education | 0.941 | <0.001 | 0.350 | ||||||||||||||
| Illiterate | 37 (40.7) | 41 (44.1) | 37 (40.7) | 115 (41.8) | 56 (60.9) | 33 (35.9) | 26 (28.6) | 115 (41.8) | 36 (39.6) | 42 (45.7) | 37 (40.2) | 115 (41.8) | |||||
| Junior high school | 14 (15.4) | 16 (17.2) | 12 (13.2) | 42 (15.3) | 9 (9.8) | 20 (21.7) | 13 (14.3) | 42 (15.3) | 19 (20.9) | 14 (15.2) | 9 (9.8) | 42 (15.3) | |||||
| High school | 26 (28.6) | 26 (28.0) | 28 (30.8) | 80 (29.1) | 18 (19.6) | 26 (28.3) | 36 (39.6) | 80 (29.1) | 26 (28.6) | 25 (27.2) | 29 (31.5) | 80 (29.1) | |||||
| Above | 14 (15.4) | 10 (10.8) | 14 (15.4) | 38 (13.8) | 9 (9.8) | 13 (14.1) | 16 (17.6) | 38 (13.8) | 10 (11.0) | 11 (12.0) | 17 (18.5) | 38 (13.8) | |||||
| Inhabitation | 0.612 | 0.437 | 0.029 | ||||||||||||||
| Alone | 60 (65.9) | 67 (72.0) | 65 (71.4) | 192 (69.8) | 61 (66.3) | 63 (68.5) | 68 (74.7) | 192 (69.8) | 66 (72.5) | 71 (77.2) | 55 (59.8) | 192 (69.8) | |||||
| With spouse | 31 (34.1) | 26 (28.0) | 26 (28.6) | 83 (30.2) | 31 (33.7) | 29 (31.5) | 23 (25.3) | 83 (30.2) | 25 (27.5) | 21 (22.8) | 37 (40.2) | 83 (30.2) | |||||
| Self-reported health status1) | 0.445 | 0.616 | 0.240 | ||||||||||||||
| Poor | 22 (24.4) | 18 (19.6) | 24 (27.6) | 64 (23.8) | 19 (21.1) | 21 (23.1) | 24 (27.3) | 64 (23.8) | 23 (25.6) | 16 (17.8) | 25 (28.1) | 64 (23.8) | |||||
| Good or fair | 68 (75.6) | 74 (80.4) | 63 (72.4) | 205 (76.2) | 71 (78.9) | 70 (76.9) | 64 (72.7) | 205 (76.2) | 67 (74.4) | 74 (82.2) | 64 (71.9) | 205 (76.2) | |||||
| Medication (yes) | 66 (72.5) | 75 (80.6) | 64 (70.3) | 205 (74.5) | 0.238 | 66 (71.7) | 74 (80.4) | 65 (71.4) | 205 (74.5) | 0.282 | 70 (76.9) | 65 (70.7) | 70 (76.1) | 205 (74.5) | 0.571 | ||
| Current disease (yes) | 63 (69.2) | 75 (80.6) | 57 (62.6) | 195 (70.9) | 0.025 | 65 (70.7) | 64 (69.6) | 66 (72.5) | 195 (70.9) | 0.905 | 67 (73.6) | 62 (67.4) | 66 (71.7) | 195 (70.9) | 0.635 | ||
| Self-reported dental condition | 0.553 | 0.016 | 0.152 | ||||||||||||||
| Very good or good | 62 (68.1) | 65 (69.9) | 57 (62.6) | 184 (66.9) | 71 (77.2) | 61 (66.3) | 52 (57.1) | 184 (66.9) | 55 (60.4) | 68 (73.9) | 61 (66.3) | 184 (66.9) | |||||
| Very poor or poor | 29 (31.9) | 28 (30.1) | 34 (37.4) | 91 (33.1) | 21 (22.8) | 31 (33.7) | 39 (42.9) | 91 (33.1) | 36 (39.6) | 24 (26.1) | 31 (33.7) | 91 (33.1) | |||||
| Sleep duration (h/d) | 0.211 | 0.276 | 0.003 | ||||||||||||||
| <4 | 8 (8.8) | 2 (2.2) | 7 (7.7) | 17 (6.2) | 7 (7.6) | 6 (6.5) | 4 (4.4) | 17 (6.2) | 0 (0) | 5 (5.4) | 12 (13.0) | 17 (6.2) | |||||
| 4∼6 | 34 (37.4) | 51 (54.8) | 41 (45.1) | 126 (45.8) | 50 (54.3) | 38 (41.3) | 38 (41.8) | 126 (45.8) | 35 (38.5) | 46 (50.0) | 45 (48.9) | 126 (45.8) | |||||
| 6∼8 | 44 (48.4) | 37 (39.8) | 40 (44.0) | 121 (44.0) | 33 (35.9) | 45 (48.9) | 43 (47.3) | 121 (44.0) | 51 (56.0) | 38 (41.3) | 32 (34.8) | 121 (44.0) | |||||
| ≥8 | 5 (5.5) | 3 (3.2) | 3 (3.3) | 11 (4.0) | 2 (2.2) | 3 (3.3) | 6 (6.6) | 11 (4.0) | 5 (5.5) | 3 (3.3) | 3 (3.3) | 11 (4.0) | |||||
| Alcohol consumption (yes) | 49 (53.8) | 26 (28.0) | 34 (37.4) | 109 (39.6) | 0.001 | 31 (33.7) | 36 (39.1) | 42 (46.2) | 109 (39.6) | 0.225 | 28 (30.8) | 38 (41.3) | 43 (46.7) | 109 (39.6) | 0.081 | ||
| Smoking (yes) | 64 (70.3) | 81 (87.1) | 68 (74.7) | 213 (77.5) | 0.018 | 71 (77.2) | 70 (76.1) | 72 (79.1) | 213 (77.5) | 0.884 | 75 (82.4) | 77 (83.7) | 61 (66.3) | 213 (77.5) | 0.007 | ||
| Physical activity in leisure time | 0.635 | 0.017 | 0.256 | ||||||||||||||
| No | 43 (47.3) | 46 (49.5) | 42 (46.2) | 131 (47.6) | 52 (56.5) | 42 (45.7) | 37 (40.7) | 131 (47.6) | 37 (40.7) | 44 (47.8) | 50 (54.3) | 131 (47.6) | |||||
| Usually | 30 (33.0) | 32 (34.4) | 26 (28.6) | 88 (32.0) | 30 (32.6) | 32 (34.8) | 26 (28.6) | 88 (32.0) | 32 (35.2) | 33 (35.9) | 23 (25.0) | 88 (32.0) | |||||
| Yes | 18 (19.8) | 15 (16.1) | 23 (25.3) | 56 (20.4) | 10 (10.9) | 18 (19.6) | 28 (30.8) | 56 (20.4) | 22 (24.2) | 15 (16.3) | 19 (20.7) | 56 (20.4) | |||||
| Breakfast frequency (weekly, times) | 0.367 | 0.567 | 0.300 | ||||||||||||||
| 5∼7 | 82 (90.1) | 89 (95.7) | 86 (94.5) | 257 (93.5) | 3 (3.3) | 3 (3.3) | 2 (2.2) | 8 (2.9) | 87 (95.6) | 88 (95.7) | 82 (89.1) | 257 (93.5) | |||||
| 3∼4 | 6 (6.6) | 1 (1.1) | 3 (3.3) | 10 (3.6) | 4 (4.3) | 1 (1.1) | 5 (5.5) | 10 (3.6) | 2 (2.2) | 3 (3.3) | 5 (5.4) | 10 (3.6) | |||||
| ≤2 | 3 (3.3) | 3 (3.2) | 2 (2.2) | 8 (2.9) | 85 (92.4) | 88 (95.7) | 84 (92.3) | 257 (93.5) | 2 (2.2) | 1 (1.1) | 5 (5.4) | 8 (2.9) | |||||
| Nutritional supplements (usually or yes) | 82 (90.1) | 76 (81.7) | 71 (78.0) | 229 (83.3) | 0.081 | 84 (91.3) | 76 (82.6) | 69 (75.8) | 229 (83.3) | 0.019 | 71 (78.0) | 77 (83.7) | 81 (88.0) | 229 (83.3) | 0.190 | ||
| SGDS | 3.4±3.6 | 3.5±3.9 | 3.7±4.0 | 3.6±3.8 | 0.901 | 4.6±4.5 | 2.8±3.2 | 3.4±3.5 | 3.6±3.8 | 0.006 | 2.6±3.3 | 3.5±4.1 | 4.5±3.9 | 3.6±3.8 | 0.005 | ||
| Normal (≤4)1) | 15 (17.2) | 10 (11.9) | 15 (17.2) | 40 (15.5) | 0.511 | 16 (19.0) | 12 (13.8) | 12 (13.8) | 40 (15.5) | 0.014 | 9 (10.3) | 13 (14.6) | 18 (22.0) | 40 (15.5) | 0.119 | ||
| Mild or moderate (5∼11)1) | 5 (5.7) | 10 (11.9) | 6 (6.9) | 21 (8.1) | 13 (15.5) | 2 (2.3) | 6 (6.9) | 21 (8.1) | 4 (4.6) | 9 (10.1) | 8 (9.8) | 21 (8.1) | |||||
| Severe (≥12)1) | 10 (10.3) | 13 (14.1) | 9 (9.4) | 32 (11.2) | 17 (18.1) | 8 (8.2) | 7 (7.4) | 32 (11.2) | 14 (15.4) | 12 (12.0) | 6 (6.4) | 32 (11.2) | |||||
| MMSE score | 27.1±3.4 | 26.7±4.1 | 27.3±4.0 | 27.0±3.8 | 0.588 | 26.0±4.3 | 27.1±3.7 | 28.1±3.2 | 27.0±3.8 | 0.001 | 28.0±3.3 | 27.2±3.8 | 25.9±4.2 | 27.0±3.8 | 0.001 | ||
| BMI | 23.9±4.1 | 23.8±3.3 | 23.6±4.1 | 23.7±3.8 | 0.830 | 23.3±3.8 | 24.2±4.1 | 23.7±3.5 | 23.7±3.8 | 0.310 | 24.2±4.3 | 23.8±3.6 | 23.2±3.5 | 23.7±3.8 | 0.187 | ||
| SBP | 116.9±11.7 | 117.1±12.0 | 118.3±13.1 | 117.4±12.3 | 0.714 | 119.1±12.1 | 117.3±12.2 | 115.9±12.4 | 117.4±12.3 | 0.221 | 115.2±10.4 | 117.7±12.7 | 119.4±13.3 | 117.4±12.3 | 0.072 | ||
| DBP | 75.5±11.4 | 75.5±11.2 | 76.3±10.6 | 75.8±11.0 | 0.854 | 77.6±10.8 | 75.5±10.5 | 74.3±11.8 | 75.8±11.0 | 0.126 | 74.5±9.7 | 75.8±12.1 | 77.1±11.2 | 75.8±11.0 | 0.278 | ||
Values are expressed as the number of participants for each category (%) or mean±standard deviation.
P-values were obtained from chi-square test for categorical variables and from t-test for continuous variables.
T1, tertile1; T2, tertile2; T3, tertile3; SGDS, short geriatric depression scale; MMSE, mini-mental state examination; BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure.
1)The response base differs because there are cases of irrelevant responses or no responses.
Fig. 2.
Percentage of mild cognitive impairment prevalence across the tertiles of dietary pattern score. The prevalence of adult patients over aged 50 years with mild cognitive impairment decreased with an increase in the “beverage and nuts” pattern score, from the lowest tertile (42.4%) to the highest tertile (17.6%). However, as the white rice pattern score increased, the prevalence of mild cognitive impairment increased.
Energy and nutrient intake level according to the dietary pattern
Energy and nutrient intakes according to each dietary pattern score tertile are presented in Table 5. The nutrient intake of the legumes and vegetable pattern did not show any significant difference according to the tertile. β-Carotene, vitamin C, and folate significantly increased as the “beverage and nuts” pattern score increased from T1 to T3 (P<0.05). There was no significant difference in other nutrients by tertile in the white rice pattern except for thiamin.
Table 5.
Energy and nutrient intake using 24-h recall across the tertiles of each dietary patterns score
| Variables | Legume and vegetables pattern | Beverage and nuts pattern | White rice pattern | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| T1 | T2 | T3 | P | T1 | T2 | T3 | P | T1 | T2 | T3 | P | |||
| Energy (kcal/d) | 1,539±386 | 1,684±449 | 1,640±504 | 0.417 | 1,608±418 | 1,621±495 | 1,631±425 | 0.271 | 1,556±445 | 1,694±447 | 1,612±432 | 0.147 | ||
| Carbohydrate (g/1,000 kcal) | 151.4±14.9 | 155.1±16.9 | 1,501±17.8 | 0.387 | 151.6±14.2 | 150.9±20.0 | 154.6±16.2 | 0.096 | 151.4±14.9 | 150.1±17.7 | 155.1±16.9 | 0.057 | ||
| Fat (g/1000 kcal) | 24.6±5.8 | 24.8±6.1 | 25.6±5.7 | 0.384 | 25.1±6.0 | 25.6±6.3 | 24.3±5.3 | 0.246 | 24.6±5.8 | 25.6±5.7 | 24.8±6.1 | 0.478 | ||
| Protein (g/1,000 kcal) | 42.2±7.4 | 41.7±7.5 | 43.5±7.5 | 0.550 | 43.1±7.3 | 42.6±7.7 | 41.6±7.5 | 0.249 | 42.2±7.4 | 41.7±7.5 | 43.5±7.5 | 0.550 | ||
| MUFA (g/1,000 kcal) | 7.1±3.7 | 7.6±4.4 | 8.5±4.8 | 0.370 | 7.4±5.3 | 7.3±4.3 | 7.3±3.1 | 0.061 | 7.1±3.7 | 8.5±4.8 | 7.6±4.4 | 0.370 | ||
| PUFA (g/1,000 kcal) | 6.9±2.3 | 6.3±2.9 | 6.3±1.7 | 0.504 | 6.1±2.2 | 6.4±2.2 | 6.8±2.7 | 0.058 | 6.9±2.3 | 6.3±1.7 | 6.3±2.9 | 0.405 | ||
| Fiber (g/1,000 kcal) | 15.0±3.9 | 15.7±4.2 | 16.3±7.9 | 0.608 | 15.2±4.1 | 15.7±3.6 | 16.1±7.7 | 0.057 | 15.0±3.9 | 16.3±7.9 | 15.7±4.2 | 0.608 | ||
| Water (g/1,000 kcal) | 579.2±196.1 | 539.1±176.4 | 518.7±190.5 | 0.388 | 521.3±157.7 | 580.8±190.0 | 540.1±210.8 | 0.390 | 579.2±196.1 | 518.7±190.5 | 539.1±176.4 | 0.058 | ||
| β-Carotene (μg RE/1,000 kcal) | 3,496.7±2,421.1 | 3,656.2±2,080.7 | 4,111.9±2,995.7 | 0.562 | 3,243.6±2,016.9 | 3,540.3±2,855.6 | 4,623.6±2,369.3 | 0.047 | 626.2±408.6 | 653.1±332.5 | 728.4±492.1 | 0.556 | ||
| Vitamin E (mg/1,000 kcal) | 10.1±3.4 | 10.0±3.7 | 10.7±3.6 | 0.469 | 9.5±3.6 | 10.3±3.9 | 11.1±2.8 | 0.168 | 10.7±3.4 | 10.1±3.6 | 10.0±3.7 | 0.649 | ||
| Vitamin C (mg/1,000 kcal) | 71.6±38.4 | 77.7±37.7 | 81.9±42.3 | 0.550 | 68.8±36.2 | 79.4±44.1 | 84.7±35.7 | 0.024 | 81.9±42.3 | 71.6±38.4 | 77.7±37.7 | 0.550 | ||
| Thiamin (mg/1,000 kcal) | 0.9±0.3 | 0.9±0.2 | 1.5±3.5 | 0.331 | 0.9±0.3 | 0.9±0.2 | 0.9±0.3 | 0.412 | 0.9±0.3 | 1.5±3.5 | 0.9±0.2 | 0.031 | ||
| Niacin (mg/1,000 kcal) | 9.7±2.1 | 9.4±2.2 | 11.4±7.5 | 0.113 | 10.0±2.6 | 10.3±7.2 | 9.7±2.0 | 0.582 | 9.4±2.1 | 11.4±7.5 | 9.4±2.2 | 0.113 | ||
| Vitamin B6 (mg/1,000 kcal) | 1.2±0.8 | 1.0±0.2 | 1.7±3.4 | 0.370 | 1.0±0.2 | 1.1±0.3 | 1.0±0.2 | 0.209 | 1.2±0.8 | 1.7±3.4 | 1.0±0.2 | 0.070 | ||
| Folate (mg /1,000 kcal) | 384.5±148.9 | 388.5±136.2 | 430.5±219.0 | 0.445 | 356.9±114.6 | 411.5±216.1 | 440.1±152.8 | 0.049 | 384.5±148.9 | 4305±219.0 | 388.5±136.2 | 0.445 | ||
| Vitamin B12 (mg/1,000 kcal) | 6.0±3.1 | 6.5±3.5 | 6.8±8.8 | 0.587 | 6.9±3.3 | 7.5±8.2 | 7.7±2.8 | 0.070 | 6.0±3.1 | 6.8±8.8 | 6.5±3.5 | 0.587 | ||
| Calcium (mg/1,000 kcal) | 379.2±140.4 | 380.1±161.6 | 370.4±156.9 | 0.597 | 372.7±149.6 | 378.8±175.1 | 379.6±130.0 | 0.399 | 379.2±140.4 | 370.4±157.0 | 380.1±161.6 | 0.597 | ||
| Cholesterol (mg/1,000 kcal) | 169.1±83.7 | 154.8±85.3 | 176.6±97.5 | 0.358 | 163.8±76.8 | 172.2±105.2 | 160.7±81.8 | 0.468 | 169.1±83.7 | 176.6±97.5 | 154.8±85.3 | 0.358 | ||
Values are expressed as mean±standard deviation.
P-values were obtained from t-test for continuous variables.
T1, tertile1; T2, tertile2; T3, tertile3; MUFA, monounsaturated fatty acid; PUFA, polyunsaturated fatty acid; RE, retinol equivalent.
Intake frequency of food groups and food items according to the dietary pattern
Table 6 shows the intake level over the last year by food group as surveyed using the SQ-FFQ as the tertile of the dietary pattern score. In the legumes and vegetable pattern, the intake of white rice, rice-cake, soup and stew, legumes, eggs, red meat and processed meat, poultry, fish, vegetables, seaweed, fruit, dairy products, and nuts increased significantly in higher tertiles. In the “beverage and nuts” pattern, the intake of 20 food groups except for vegetables showed a significant difference according to the pattern score tertile. The subjects of the “beverage and nuts” pattern had a low level of vegetables intake, then the intake of salty vegetables was low according to tertile increased. Except for white rice, soup and stew, and legumes, the food group intake frequency was increased significantly between T1 to T3. This pattern was characterized by intake snacks such as drinks, nuts, sweets, fruits, rice cakes, coffee, tea, and bread, which resulted in a decrease of salty vegetables with high salt content as tertile increased. In the white rice pattern, the intake frequency of white rice, flour-based food, eggs, red meat and processed meat, poultry, and fish increased significantly with increasing tertile. On the other hand, the intake frequency of multigrain rice, fruit, and dairy products, decreased significantly as the tertile increased from T1 to T3.
Table 6.
Intake frequency of food using SQ-FFQ according to each dietary patterns score tertiles
| Food | Legume and vegetables pattern | Beverage and nuts pattern | White rice pattern | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| T1 | T2 | T3 | P | T1 | T2 | T3 | P | T1 | T2 | T3 | P | |||
| White rice | 0.17±0.17 | 0.21±0.17 | 0.27±0.25 | 0.003 | 0.26±0.19 | 0.16±0.16 | 0.23±0.24 | 0.005 | 0.09±0.11 | 0.17±0.12 | 0.40±0.21 | <0.001 | ||
| Multigrain rice | 1.23±1.10 | 0.99±0.98 | 1.07±0.99 | 0.262 | 0.66±0.83 | 1.26±1.09 | 1.37±1.00 | <0.001 | 1.75±1.04 | 1.01±0.91 | 0.54±0.72 | <0.001 | ||
| Flour-based foods | 0.07±0.17 | 0.04±0.07 | 0.17±0.24 | <0.001 | 0.02±0.04 | 0.07±0.12 | 0.20±0.26 | <0.001 | 0.03±0.06 | 0.04±0.07 | 0.21±0.27 | <0.001 | ||
| Rice-cake | 0.04±0.09 | 0.04±0.07 | 0.18±0.27 | <0.001 | 0.02±0.04 | 0.06±0.11 | 0.18±0.26 | <0.001 | 0.07±0.18 | 0.06±0.14 | 0.12±0.21 | 0.060 | ||
| Bread | 0.17±1.16 | 0.06±0.11 | 0.20±0.27 | 0.369 | 0.03±0.08 | 0.08±0.14 | 0.33±1.16 | 0.007 | 0.18±1.16 | 0.07±0.16 | 0.17±0.25 | 0.490 | ||
| Soup and stew | 0.11±0.08 | 0.20±0.19 | 0.51±0.44 | <0.001 | 0.30±0.45 | 0.19±0.17 | 0.33±0.29 | 0.012 | 0.24±0.36 | 0.24±0.24 | 0.33±0.37 | 0.112 | ||
| Legume | 0.05±0.07 | 0.17±0.14 | 0.52±0.30 | <0.001 | 0.29±0.32 | 0.18±0.22 | 0.28±0.27 | 0.011 | 0.20±0.28 | 0.25±0.27 | 0.30±0.27 | 0.055 | ||
| Eggs | 0.14±0.17 | 0.26±0.22 | 0.53±0.34 | <0.001 | 0.29±0.25 | 0.25±0.27 | 0.39±0.35 | 0.005 | 0.21±0.23 | 0.32±0.30 | 0.40±0.33 | <0.001 | ||
| Red meats and processed meats | 0.06±0.08 | 0.08±0.09 | 0.24±0.25 | <0.001 | 0.08±0.12 | 0.11±0.14 | 0.20±0.23 | <0.001 | 0.05±0.08 | 0.11±0.16 | 0.22±0.22 | <0.001 | ||
| Poultry | 0.04±0.07 | 0.06±0.08 | 0.26±0.29 | <0.001 | 0.05±0.10 | 0.10±0.17 | 0.21±0.27 | <0.001 | 0.05±0.10 | 0.10±0.17 | 0.21±0.26 | <0.001 | ||
| Fish | 0.07±0.07 | 0.14±0.11 | 0.33±0.26 | <0.001 | 0.14±0.15 | 0.15±0.15 | 0.25±0.25 | <0.001 | 0.14±0.15 | 0.16±0.19 | 0.24±0.23 | 0.001 | ||
| Vegetables | 0.15±0.12 | 0.27±0.16 | 0.60±0.31 | <0.001 | 0.32±0.29 | 0.31±0.25 | 0.39±0.30 | 0.084 | 0.39±0.33 | 0.32±0.27 | 0.31±0.25 | 0.177 | ||
| Salty vegetables | 0.83±0.58 | 0.86±0.67 | 0.93±0.55 | 0.563 | 1.10±0.67 | 0.85±0.56 | 0.68±0.49 | <0.001 | 0.82±0.61 | 0.85±0.52 | 0.96±0.67 | 0.269 | ||
| Seaweeds | 0.06±0.07 | 0.18±0.20 | 0.57±0.41 | <0.001 | 0.24±0.40 | 0.21±0.26 | 0.34±0.34 | 0.032 | 0.32±0.43 | 0.26±0.31 | 0.21±0.26 | 0.081 | ||
| Fruits | 0.13±0.24 | 0.25±0.25 | 0.40±0.30 | <0.001 | 0.11±0.15 | 0.20±0.20 | 0.47±0.34 | <0.001 | 0.33±0.33 | 0.23±0.26 | 0.22±0.26 | 0.009 | ||
| Dairy products | 0.21±0.21 | 0.24±0.26 | 0.35±0.29 | 0.001 | 0.14±0.15 | 0.26±0.24 | 0.40±0.30 | <0.001 | 0.44±0.30 | 0.22±0.21 | 0.14±0.16 | <0.001 | ||
| Coffee and tea | 0.41±0.54 | 0.33±0.41 | 0.46±0.47 | 0.173 | 0.20±0.35 | 0.41±0.47 | 0.59±0.52 | <0.001 | 0.39±0.47 | 0.31±0.37 | 0.50±0.56 | 0.023 | ||
| Soft drinks and beverages | 0.12±0.29 | 0.03±0.07 | 0.12±0.19 | 0.003 | 0.01±0.04 | 0.04±0.09 | 0.21±0.32 | <0.001 | 0.09±0.21 | 0.06±0.14 | 0.11±0.26 | 0.281 | ||
| Nuts | 0.05±0.17 | 0.06±0.16 | 0.19±0.26 | <0.001 | 0.02±0.07 | 0.03±0.08 | 0.26±0.29 | <0.001 | 0.12±0.23 | 0.06±0.16 | 0.12±0.23 | 0.068 | ||
| Snack | 0.10±0.38 | 0.04±0.10 | 0.14±0.22 | 0.028 | 0.02±0.07 | 0.04±0.10 | 0.22±0.41 | <0.001 | 0.12±0.38 | 0.06±0.14 | 0.10±0.21 | 0.258 | ||
| Alcohol | 0.10±0.30 | 0.04±0.09 | 0.13±0.30 | 0.046 | 0.02±0.06 | 0.04±0.13 | 0.20±0.39 | <0.001 | 0.03±0.09 | 0.03±0.07 | 0.20±0.40 | <0.001 | ||
Values are expressed as mean±standard deciation.
P-values were obtained from t-test for continuous variables.
SQ-FFQ, semi-quantitative food frequency questionnaire; T1, tertile1; T2, tertile2; T3, tertile3.
Adjusted odds ratio (AORs) for MCI by tertile of each dietary pattern score
The AOR and the 95% CI for MCI by the tertile of each dietary pattern score are shown in Table 7. The “legumes and vegetable” pattern was not significantly associated with the risk of developing MCI in the crude or fully adjusted Model 1 (adjusted for sex, age, inhabitation, education, current disease, self-reported dental condition, sleep duration, alcohol consumption status, smoking status, physical activity in leisure time, nutritional supplements, and SGDS). The “beverage and nuts” pattern was associated with reduced odds of high MCI after fully adjusting for covariates (Model 1) [T3 vs. T1, AOR: 0.333; 95% confidence interval (CI): 0.133∼0.831; P<0.05]. The white rice pattern was associated with increased odds of high MCI in the crude analysis (T3 vs. T1, odd ratio: 2.984; 95% CI: 1.541∼5.780; P<0.01).
Table 7.
Adjusted odds ratios (AOR) for mild cognitive impairment
| Dietary patterns | MCI (n)/Total (n) | Crude | Model 1 | |||
|---|---|---|---|---|---|---|
| OR1)2) | 95% CI1) | AOR1)3) | 95% CI1) | |||
| Legume and vegetables pattern | ||||||
| Tertile1 | 24/91 | Reference | Reference | |||
| Tertile2 | 32/93 | 1.464 | 0.778∼2.757 | 1.175 | 0.587∼2.351 | |
| Tertile3 | 23/91 | 0.944 | 0.486∼1.834 | 0.949 | 0.466∼1.935 | |
| P for trend | 0.870 | 0.931 | ||||
| Beverage and nuts pattern | ||||||
| Tertile1 | 39/92 | Reference | Reference | |||
| Tertile2 | 24/92 | 0.480* | 0.257∼0.894 | 0.833 | 0.370∼1.876 | |
| Tertile3 | 16/91 | 0.290*** | 0.147∼0.572 | 0.333* | 0.133∼0.831 | |
| P for trend | <0.001 | 0.014 | ||||
| White rice pattern | ||||||
| Tertile1 | 18/91 | Reference | Reference | |||
| Tertile2 | 22/92 | 1.275 | 0.630∼2.577 | 0.975 | 0.399∼2.382 | |
| Tertile3 | 39/92 | 2.984** | 1.541∼5.780 | 1.876 | 0.750∼4.690 | |
| P for trend | 0.001 | 0.094 | ||||
1)Logistic regression analysis were used to estimate the OR and 95% CI of MCI based on increasing the pattern score tertiles.
2)OR: without adjusting (crude).
3)AOR: adjusted for sex, age, inhabitation, education, self-reported dental condition, sleep duration, alcohol consumption status, smoking status, physical activity in leisure time, nutritional supplement, short geriatric depression scale (SGDS) (Model 1).
*P<0.05, **P<0.01, ***P<0.001.
MCI, mild cognitive impairment; OR, odds ratio; CI, confidence interval.
DISCUSSION
We identified the “legumes and vegetables”, “beverage and nuts”, and “white rice” patterns among participants aged ≥50 years. The “beverage and nuts” pattern was negatively associated with the prevalence of high MCI, independent of education, self-reported dental condition, physical activity in leisure time, nutritional supplements, and SGDS. In contrast, the white rice pattern was positively associated with a risk of mild impairment, independent of sex, age, inhabitation, sleep duration, smoking status, and SGDS.
It has become increasingly important to consider the relevance of dietary patterns that reflect overall diet and dietary behavior to prevent and delay age-related cognitive decline. Previous systematic reviews and meta-analyses have shown the role of dietary patterns in cognitive function (Allès et al., 2012; Singh et al., 2014; van de Rest et al., 2015; Petersson and Philippou, 2016). Fur-thermore, Mediterranean diet (Valls-Pedret et al., 2015), Mediterranean-Dietary Approaches to Stop Hypertension (DASH) and Mediterranean-DASH Intervention for Neu-rodegenerative Delay diets (McEvoy et al., 2017) are associated with significantly better cognitive function and reduced risk of cognitive impairment. In the Melbourne Collaborative Cohort Study, fruit intake was positively associated with successful aging, including mental health and physical function, while meat/fat patterns were negatively associated (Hodge et al., 2014).
Based on these previous studies, the dietary patterns that affect cognitive function using multiple approaches were derived. In general, intake of more fruit, vegetables, fish, nuts, and higher fat dairy products have been found to have a beneficial effect on cognitive function.
The Whitehall II prospective cohort study evaluated that inflammatory diet patterns were associated with increased cognitive decline (Ozawa et al., 2017). Previous studies have assessed the role of these food groups on cognitive function (Gómez-Pinilla, 2008; Barbour et al., 2014; Solfrizzi et al., 2017). Flavonoid-rich fruits (Polidori et al., 2009) and nuts rich (in vitamins, minerals, MUFA, and PUFA (Barbour et al., 2014; Solfrizzi et al., 2017) that affect glucose metabolism, insulin resistance, and inflammatory mediators have been reported to have an impact on overall cognitive performance. Thus, the effect of fruit on cognitive function is not consistent. A study reported that fruit intake is associated with an increased risk of cognitive impairment due to high glycemic index and presence of simple sugars (Staubo et al., 2017).
In our study, “beverage and nuts” pattern, which is characterized by a high consumption of beverages, nuts, sweet foods, fruit, rice-cakes, coffee, tea, and bread, consisted of a combination of healthy and unhealthy food groups, such as in the study by Chan et al. (2013). At the current research level, it is not easy to interpret the relevance of our “beverage and nuts” pattern on cognitive function.
A recent systematic review of several cross-sectional studies and longitudinal population-based studies suggested that coffee and tea intake had a protective effect on cognitive impairment in older people. Although there were some limitations (such as using a dose-response analysis and cognitive domains), this review reported that this association was stronger in females than in males (Panza et al., 2015). Barbour et al. (2014) examined the effects of nut consumption on blood pressure, glucose regulation, endothelial vasodilator function, arterial compliance, inflammatory biomarkers, and cognitive function through several epidemiological or intervention studies. The effect of nut intake on cognitive function was found to be limited (Barbour et al., 2014). Therefore, we consider that more evidence from controlled intervention clinical trials is needed before determining whether nuts are beneficial. As is known, beverages such as soft drinks (cola, soda, and fruit juice soda), fruit juice, grain powder beverages, and rice beverages and snacks, such as cookies, crackers, chocolate, and ice cream, have a high sugar content. So far, there have been controversial results between studies on the effect that the consumption of beverages on cognitive function (Kakutani et al., 2019). An in-depth investigation is needed that takes into account different types of beverage.
As reviewed by Stephan et al. (2010) metabolic changes increase the risk of metabolic syndrome and may eventually increase cognitive decline (Yaffe et al., 2004). These results show that the positive effects of the “beverage and nuts” pattern on cognitive impairment might be due to the combined and synergistic results of various components, rather than simply a food component.
As shown Table 5, compared to the two other dietary patterns, the “beverage and nuts” pattern showed that β-carotene, vitamin C, and folate intake were significantly increased as the pattern score grows. The intake levels of β-carotene, vitamin C, and folate in the “beverage and nuts” pattern met the dietary intake levels recommended in the Dietary Reference Intakes for Koreans (Kim et al., 2015). A previous study reported that vitamin B and folic acid intake, which lowers plasma homocysteine levels, is associated with improved overall cognitive function and memory (Kim et al., 2014; Agnew-Blais et al., 2015). Staubo et al. (2017) confirmed that β-carotene intake is associated with cognitive function using dorsolateral, prefrontal, and temporal pole computed tomography. Li et al. (2012) also demonstrated that vitamin C and β-carotene have protective effects against the risk of Alzheimer’s disease. However, since not all of the food consumed is absorbed into the body, further studies are warranted to explore the relationship between the intake of antioxidant nutrients (vitamin C and β-carotene), which increases in concentration with the rising “beverage and nuts” pattern and plasma concentration.
In our study, the white rice pattern was found to be positively associated with increased cognitive decline in the crude analysis, but not after being fully adjusted. According to Korczak et al. (2016) inadequate intake of grain-based foods (namely, higher white rice intake and lower whole-grain intake) results in unbalanced mineral levels and insufficient intake of antioxidant nutrients, which is associated with an increased risk of developing MCI. It is believed that Koreans have unique dietary patterns, and the types of foods that make up the patterns are so diverse that it may be difficult to obtain consistent results on disease effects. We found no association between the legumes and vegetable pattern and cognitive impairment.
Our study has several limitations. First, we conducted a cross-sectional study that examined the dietary pattern and cognitive function for a specific period using a PCA analysis (a posteriori approach). In brief, cross-sectional studies cannot include all possible diet categories and cannot measure all aspects of the diet with absolute precision. We calibrated residual confounding factors in the analysis to minimize potential limitations. Second, our results cannot be generalized as our study participants were not a representative sample of Koreans over 50 years old. Despite the limitations stated, our study is meaningful as it is the first to analyze the relationship between cognitive status and dietary patterns of participants over 50 years old living in Gwangju province. Moreover, PCA analysis used in our study is widely used to derive dietary patterns in nutrition epidemiology, and our dietary patterns were similar to those obtained in previous studies that used a PCA analysis (Chan et al., 2013; Kim et al., 2015).
In conclusion, the present cross-sectional study identified three dietary patterns, “legumes and vegetables”, “beverages and nuts”, and “white rice”. The “beverage and nuts” pattern, which is characterized by a high consumption of beverages, nuts, sweet foods, fruit, rice-cakes, coffee, tea, and bread, was negatively associated with the prevalence of high MCI among Korean adults over 50 years old. In the future, longitudinal population-based studies and randomized clinical trials are required to confirm the effect of potential dietary patterns on cognitive impairment and to reveal the underlying mechanism of their association.
Footnotes
AUTHOR DISCLOSURE STATEMENT
The authors declare no conflict of interest.
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