Abstract
The relationship between eating behaviors, food intake, and mental health and the occurrence of obesity in older adults has rarely been investigated. Therefore, the objective of this study was to establish the associative links of these factors with two measures of obesity: class I obesity as indicated by body mass index (OB-BMI; BMI ≥ 30kg/m2) and class I obesity as indicated by waist circumference (OB-WC; WC ≥ 43 inches for men and ≥ 42 inches for women). Older adults participating in the Older American’s Act (OAA) congregate meal program (N = 113, mean age = 74 years, 74% female, 45% African American) were assessed. Eating behaviors (cognitive restraint, uncontrolled eating, and emotional eating), food groups group choices (sweets, salty snacks, and fruits), and mental health indices (depression, anxiety, and stress) were recorded by questionnaire and related to measured occurrence of OB-BMI and OB-WC. In a series of multivariate logistical regression models, we found cognitive restraint to be consistently and robustly associated with both measures of obesity. In the fully adjusted model, cognitive restraint, consumption of sweets, anxiety, and lack of depression were associated with OB-WC. In summary, we found an association of obesity with abnormal eating behaviors, certain food group intakes, and mental health symptoms in this population. These findings may guide the development of future weight management interventions in a congregate meal setting.
INTRODUCTION
The prevalence of obesity is increasing in the older adult population; in 2003, 31.0% of older adults reported a BMI of > 30 kg/m2 compared to 35.4% in 2012.(1) In recent reviews of the literature, obesity was associated with numerous co-morbidities, which included not only physical health problems such as diabetes, cardiovascular disease, and physical frailty, but also mental health concerns (depression, anxiety, and stress). It is estimated that obese individuals are approximately 55% more likely to develop depression and 25% more likely to develop anxiety.(2–5) Dietary patterns and abnormal eating behaviors are also thought to be associated with obesity in older adults, but the findings, to date, from studies of these associations in this population are inconsistent (6) or limited (7–9).
The goal of the Older Americans Act Nutrition Programs (OAANP) is to reduce hunger and food insecurity, promote socialization, and support health and wellbeing.(10) In 2011, OAANP served 88.6 million congregate meals to more than 1.7 million seniors in community settings.(11) While the reduction of hunger is an important goal of the OAANP, obesity often paradoxically occurs along with food insecurity in older adults. Older adults participating in the OAANP have a high prevalence of obesity (12), obesity-related health problems (13), mental health conditions (8), poor nutritional status (14, 15), and food insecurity (12, 16).
Although the fact that OAANP targets a low-income and minority population may contribute to the relatively high prevalence of obesity seen in some studies of this group (12), it is also possible that other factors are important, such as inappropriate eating behaviors, including cognitive restraint (CR; conscious restriction of food intake to control body weight), uncontrolled eating (UE; eating more than usual because of a loss of control over intake), and emotional eating (EE; overeating during emotional mood state). For example, among Georgia’s congregate meal program participants, obesity was associated with inappropriate eating behaviors, especially CR and EE (9) and with a higher intake of sweets (17). However, the associations of obesity with eating fruits and salty snacks, UE, depression, anxiety, and stress were attenuated when controlled for potential confounders. Moreover, the findings differed depending upon how obesity was characterized (body mass index versus waist circumference). Therefore, the purpose of this study was to build on these previous efforts to identify the independent associations of eating behaviors, food patterns, and mental health symptoms with two measures of obesity in fully adjusted multiple regression models. The results of this study will be useful in developing healthy weight management programs that promote better eating behaviors and mental health among congregate meal participants.
METHODS
Sample
In this cross-sectional study, individuals 60 years of age and older were recruited from four Area Agency on Aging (AAA) senior centers in northeast Georgia that provided congregate meals and other services to older adults. The Institutional Review Boards on Human Subjects of the University of Georgia, the Georgia Department of Human Services, and the Athens Community Council on Aging approved questionnaires and procedures. Written, informed consent was obtained from participants. Procedures were explained and consent forms were read to participants. Excluded individuals comprised homebound participants or those unable to understand the informed consent and/or answer questions as determined by the interviewer. These recruitment procedures yielded 124 participants. Due to missing data (n = 11) this report focuses on the 113 participants who had responses for obesity (BMI and WC), eating behaviors (CR, UE, and EE), food group intakes (sweet, salty, fruit, vegetables, whole grains, and milk), mental health (depression, anxiety, and stress), physical activity, physical function, food insecurity, health (self-reported health, diabetes, heart disease, high blood pressure, and arthritis), and demographics (age, race, education, and gender). One hundred and six individuals who received one or more meals at the senior center declined to participate. Non-participants (n = 106) differed significantly from study participants (n = 113) in mean age (77 vs. 74 years, p = 0.05) and race (30% vs. 45% black, p = 0.05), but there was no significant difference in gender (67% and 75% female, p = 0.23).
Assessments
Body weight is less reflective of body composition in older compared to younger adults due to an age-related decline in lean muscle mass and increase in central adiposity. To improve precision, we assessed obesity by two measures; one based on body weight (BMI) and one more indicative of visceral adiposity (waist circumference). Body weight was measured to the nearest 0.1 pound using a portable digital scale (model HD-317; Tanita Inc., Tokyo, Japan), with clothes on and without shoes, while height was measured with a stadiometer (model IP0955; Invicta Plastics Limited, Leicester, England) according to standard guidelines, in either bare feet or wearing light socks.(8) BMI, defined as [(weight (pounds)/height (inches)2)×703] was then calculated and BMI categories were derived using the NIH clinical guidelines.(18) BMI was dichotomized into two categories, obese (OB-BMI) defined as a BMI ≥ 30 kg/m2 and non-obese BMI < 30 kg/m2. WC was measured with a tape measure to the nearest 0.1 inches by following NIH guidelines.(18) The WC threshold values used were validated BMI-specific cut-off measurements (19) and reflected BMI class I obesity (> 30 kg/m2). WC measurements ≥ 43 inches for men and ≥ 42 inches for women were categorized as obese (OB-WC) and measurements < 43 inches for men and < 42 inches for women as non-obese.
Eating behaviors, CR, UE, and EE were all assessed by one questionnaire: The Three Factor Eating Questionnaire R-18. This includes 18 questions (response categories: 1 = never; 2 = rarely; 3 = sometimes; 4 = always).(20) As previously reported (9), it was found that participants understood these one-word response categories better than the original categories (definitely false, mostly false, mostly true, and definitely true). All questions were changed from “I” to “you” because questionnaire was read to the participants. Item 1 was reworded from this original question, “When I smell a sizzling steak or juicy piece of meat, I find it very difficult to keep from eating, even if I have just finished a meal” and replaced with, “When you see any of your favorite foods, do you find it very difficult to keep from eating, even if you have just finished a meal?” These changes were incorporated to improve measurement of the difficulty of controlling dietary patterns when an external stimulus was present; de Lauzon et al, made similar changes and tested the reliability of the questionnaire in the general population.(7) The three eating behaviors’ summary scores were created by summing the responses to the questions that corresponded to CR (six questions), UE (nine questions), and EE (three questions). Each eating behavior was recoded as either low (= 0) or high (= 1), according to the median split.
The intake of sweets and salty snacks (adapted from the Block food frequency questionnaire), fruits and vegetables (21), whole grains (22) and milk (23) were assessed as follows: “How many times a day do you eat something sweet, such as candy, cookies, cakes, pie, donuts, ice cream?” (range = 0 to 7), “How many times a day do you eat a salty snack, such as chips, French Fries, pretzels?” (range = 0 to 7), “How many servings of fruits and 100% fruit juices do you usually have each day?” (range = 0 to 7), “How many servings of vegetables do you usually eat each day?” (range = 0 to 7), “How often do you eat whole wheat or whole grain bread, such as 100% whole wheat bread?” (range = 0 times per week to 3 times per day), “How often do you eat whole grain cereals, such as oatmeal, Cheerios®, bran flakes or bran cereals?” (range = 0 times per week to 3 times per day), “How often do you drink milk as a beverage including soy milk?” (range = 0 times per week to 3 times per day), and “How often do you eat milk on cereal including soy milk?” (range = 0 times per week to 3 times per day). Summary scores were created for total whole grain and milk intake by summing food categories and then dividing them by 7 to determine frequency of intake per day. Food group variables were dichotomized based on the distribution of the responses for each variable and/or nutritionally meaningful category into two groups, either the lowest two tertiles or the highest tertile.
Mental health was assessed with the Depression Anxiety Stress Scale-21; this instrument includes seven questions per variable to assess depression, anxiety, and stress in the past week (0 = did not apply to me at all; 1 = applied to me to some degree or some of the time; 2 = applied to me to a considerable degree or a good part of time; 3 = applied to me very much or most of the time).(24) A summary score was created for each indices and categorized into severity.(24) For the purposes of this study, participants’ findings were assigned to one of two categories (0 = low symptoms; 1 = had symptoms that were mild, moderate, or severe).
Physical activity was assessed using our previously established methods (8), using the Behavior Risk Factor Surveillance Survey (BRFSS) question, “How many days of the last seven days did you participate in at least 30 minutes of moderate physical activity?”. Responses were dichotomized (< 5 vs. ≥ 5 days per week). Participants’ physical function was assessed using the Short Physical Performance Battery as previously described (8) summary performance scores were defined as poor to moderate (0 to 9) and good (10 to 12).
Food insecurity was measured using the augmented 6-item US Household Food Security Survey Module.(25) One point was scored for affirmative responses to each statement; responses were summed to create a six-item summary score. Possible summary scores ranged from 0 to 6 and for the purpose of this study were categorized as “secure” for summary scores 0 to 1 and “insecure” for summary scores 2 to 6.
Confounding variables included self-reported health and chronic health conditions adapted from BRFSS.(26) Socio-demographic variables included age, gender, and education and are the same categories used in a previous study.(9)
Statistical Analyses
Data was analyzed using the Statistical Analysis System (SAS Institute, Cary, NC). Descriptive statistics including frequencies and means were calculated. Spearman correlation coefficients were used to assess the relationship of the continuous measures of BMI and WC with eating behaviors, food group intakes, and mental health indices (data not shown). BMI, WC, eating behaviors, food groups, mental health and other variables were dichotomized as previously described (9), and relationships with the two measures of obesity (OB-BMI and OB-WC) were assessed with chi-square analyses (Table 1).
TABLE 1.
BMI Class I Obesity | WC Class I Obesity | ||||
---|---|---|---|---|---|
< 30kg/m2 n = 52 |
≥ 30kg/m2 n = 61 |
Low risk n = 68 |
High risk n = 45 |
||
n | % | % | % | % | |
Age (years) | |||||
< 70 | 37 | 30 | 70‖ | 49 | 51‡ |
≥ 70 | 76 | 54 | 46 | 66 | 34 |
Gender | |||||
Male | 29 | 45 | 55 | 38 | 62‖ |
Female | 84 | 46 | 54 | 68 | 32 |
Race/ethnicity | |||||
White | 62 | 47 | 53 | 60 | 40 |
Black | 51 | 45 | 55 | 61 | 39 |
Education | |||||
< 8 years | 19 | 74 | 26‖ | 74 | 26 |
≥ 8 years | 94 | 40 | 60 | 57 | 43 |
Cognitive restraint | |||||
< 14 (median split) | 51 | 63 | 30¶ | 56 | 29‖ |
≥ 14 (median split) | 62 | 37 | 70 | 44 | 71 |
Uncontrolled eating | |||||
< 16 (median split) | 53 | 58 | 38§ | 56 | 33§ |
≥ 16 (median split) | 60 | 42 | 62 | 44 | 67 |
Emotional eating | |||||
< 6 (median split) | 48 | 60 | 28¶ | 49 | 33 |
≥ 6 (median split) | 65 | 40 | 72 | 51 | 67 |
Depression | |||||
No symptoms (0) | 91 | 83 | 79 | 81 | 80 |
Mild to extreme (1 to 5) | 22 | 17 | 21 | 19 | 20 |
Anxiety | |||||
No symptoms (0) | 89 | 87 | 72‡ | 88 | 64‖ |
Mild to extreme (1 to 5) | 24 | 13 | 28 | 12 | 36 |
Stress | |||||
No symptoms (0) | 106 | 94 | 93 | 96 | 91 |
Mild to extreme (1 to 5) | 7 | 6 | 7 | 4 | 9 |
Sweets | |||||
< 2 times/day | 84 | 75 | 74 | 86 | 62§ |
≥ 2 times/day | 29 | 25 | 26 | 18 | 38 |
Salty snacks | |||||
< 1 times/day | 72 | 65 | 62 | 68 | 58 |
≥ 1 times/day | 41 | 35 | 38 | 32 | 42 |
Fruit | |||||
< 3 servings/day | 77 | 69 | 67 | 62 | 78‡ |
≥ 3 servings /day | 36 | 31 | 33 | 38 | 22 |
Vegetables | |||||
< 4 servings /day | 82 | 81 | 66‡ | 74 | 71 |
≥ 4 servings /day | 31 | 19 | 34 | 26 | 29 |
Whole grains | |||||
< 2 times/day | 65 | 56 | 57 | 57 | 58 |
≥ 2 times /day | 48 | 44 | 43 | 43 | 42 |
Milk | |||||
< 2 times /day | 73 | 63 | 56 | 65 | 64 |
≥ 2 times /day | 40 | 37 | 44 | 35 | 36 |
Food insecurity | |||||
Secure (0 to 1) | 81 | 73 | 70 | 75 | 67 |
Insecure (2 to 6) | 32 | 27 | 30 | 25 | 33 |
Moderate physical activity | |||||
< 5 days/week | 68 | 50 | 69§ | 57 | 64 |
≥ 5 days/week | 45 | 50 | 31 | 43 | 36 |
Physical function | |||||
Poor to moderate (0–9) | 67 | 62 | 57 | 57 | 62 |
Good (10–12) | 46 | 38 | 43 | 43 | 38 |
Self-reported health | |||||
Poor to fair (0–1) | 41 | 29 | 43 | 29 | 47‡ |
Good to excellent (2–5) | 72 | 71 | 57 | 71 | 53 |
Diabetes | |||||
No | 69 | 71 | 52§ | 72 | 44‖ |
Yes | 44 | 29 | 48 | 28 | 56 |
Heart disease | |||||
No | 81 | 77 | 67 | 76 | 64 |
Yes | 32 | 23 | 33 | 24 | 36 |
High blood pressure | |||||
No | 29 | 35 | 18§ | 28 | 22 |
Yes | 84 | 65 | 82 | 72 | 78 |
Arthritis | |||||
No | 42 | 42 | 33 | 40 | 33 |
Yes | 71 | 58 | 67 | 60 | 67 |
For demographic variables (age, gender, sex, education) the rows within an obesity category add up to 100; for all other variables the columns within a variable add up to 100.
Health conditions: diabetes; heart disease; high blood pressure; and arthritis were self-reported.
Significance level:
trend at p ≤ 0.10;
significant at p ≤ 0.05;
significant at p ≤ 0.01;
significant at p ≤ 0.001.
A series of multivariate logistical regression models analyses were used to assess the independent associations of the dichotomized variables with obesity (OB-BMI and OB-WC): model 1 included eating behaviors only; model 2 included all model 1 variables plus the mental health variables; model 3 included all model 2 variables plus the food group variables sweets, salty snacks, and fruit; model 4 included all model 3 variables plus physical activity, physical function, food insecurity; model 5 included all model 4 variables plus self-reported health and health conditions (diabetes, high blood pressure, heart disease, arthritis); and model 6 included all model 5 variables plus the demographic variables (age, race, sex, education). Odds ratios are reported for the independent variables of interest, which were eating behaviors (CR, UE, and EE), food group intake (sweets, salty snacks, and fruit), and mental health (depression, anxiety, and stress).
RESULTS
The sample was composed of 113 congregate meal participants, the mean age was 74, 74% were female, and 45% were black. Mean BMI was 31 kg/m2 and 54% had a BMI ≥ 30. Mean WC for men was 45 inches, and WC for women was 39 inches; 40% were classified as obese using WC cut off measure reflecting BMI class I obesity.(19) Chronic health conditions were prevalent: 39% reported diabetes, 74% high blood pressure, 28% heart disease, and 63% arthritis.
The bivariate association of characteristics of eating behaviors, mental health, and food intake with obesity (OB-BMI and OB-WC) showed that obese participants defined by both measures of obesity were more likely to report CR (p ≤ 0.01 – p ≤ 0.001) and UE (p ≤ 0.05 – p ≤ 0.01) compared to non-obese, but only obese participants defined by OB-BMI were more likely to engage in EE behaviors (p ≤ 0.0001) (Table 1). Additionally, compared to the non-obese participants, obese participants were more likely to be anxious, whether obesity was defined by OB-BMI (p ≤ 0.10) or OB-WC (p ≤ 0.01). However, no relationship was seen between obesity and depression or stress. Finally, compared to the non-obese participants, obese participants defined by OB-WC were more likely to consume sweets two or more times a day (p ≤ 0.05) and less likely to consume 3 or more servings of fruit per day (p ≤ 0.07).
Six multivariate logistical regression models were used to assess the independent associations of the eating behaviors, food group servings, and mental health with both measures of obesity, when controlled for potential confounders. The models for each obesity variable are shown in Tables 2 and 3. For both measures of obesity, CR was robustly associated with an increased risk of adiposity (Tables 2 and 3), while reporting symptoms of anxiety was associated with increased risk of obesity defined by OB-WCB (Table 3) by at least 4-fold in the final fully adjusted model (model 6).
TABLE 2.
Variables | C statistic |
Cognitive Restraint OR (95% CI) |
Uncontrolled Eating OR (95% CI) |
Emotional Eating OR (95% CI) |
Sweets OR (95% CI) |
Salty Snacks OR (95% CI) |
Fruits OR (95% CI) |
Depression OR (95% CI) |
Anxiety OR (95% CI) |
Stress OR (95% CI) |
|
---|---|---|---|---|---|---|---|---|---|---|---|
Model 1 | Eating behaviors | 0.73 | 3.3 (1.4, 7.5)§ |
1.3 (0.5, 3.1) |
2.8 (1.2, 6.7)‡ |
||||||
Model 2 | + Sweets, salty snacks, and fruit | 0.74 | 3.3 (1.4, 7.6)§ |
1.3 (0.6, 3.2) |
2.9 (1.2, 7.3)‡ |
0.8 (0.3, 2.0) |
1.0 (0.4, 2.4) |
0.9 (0.4, 2.2) |
|||
Model 3 | + Depression, anxiety, stress | 0.76 | 3.3 (1.4, 7.7)§ |
1.4 (0.5, 3.5) |
3.0 (1.2, 7.8)‡ |
0.7 (0.3, 2.0) |
0.9 (0.3, 2.3) |
0.8 (0.3, 2.0) |
0.8 (0.2, 3.0) |
2.4 (0.8, 7.7) |
0.5 (0.1, 3.9) |
Model 4 | + Food insecurity, moderate physical activity, and physical function | 0.78 | 4.1 (1.6, 10.3)§ |
1.3 (0.5, 3.5) |
3.0 (1.1, 7.9)‡ |
0.6 (0.2, 1.6) |
0.9 (0.4, 2.4) |
0.9 (0.3, 2.3) |
0.6 (0.2, 2.4) |
2.6 (0.8, 8.4) |
0.8 (0.1, 6.0) |
Model 5 | + Self reported health, diabetes, hypertension, heart disease, and diabetes | 0.78 | 4.0 (1.5, 10.4)§ |
1.2 (0.4, 3.5) |
2.8 (1.0, 7.8)‡ |
0.6 (0.2, 1.9) |
0.9 (0.3, 2.6) |
1.0 (0.4, 2.6) |
0.6 (0.1, 2.3) |
2.3 (0.6, 8.0) |
0.8 (0.1, 6.6) |
Model 6 | + Demographics | 0.84 | 4.8 (1.7, 13.7)§ |
0.9 (0.3, 2.8) |
3.1 (1.0, 9.9)‡ |
0.7 (0.2, 2.3) |
1.0 (0.3, 3.0) |
1.1 (0.3, 3.2) |
0.4 (0.1, 1.9) |
2.2 (0.6, 8.8) |
1.2 (0.1, 11.3) |
Dependent variable is non-obese (BMI < 30 kg/m2, n = 52) vs. obese (BMI ≥ 30 kg/m2, n = 61).
Each eating behavior coded as the median split; sweets, salty snacks, and fruit as the upper tertile vs. lower two tertiles; depression, anxiety, and stress coded as normal versus mild, moderate or severe. As indicated, models controlled for these potential cofounders: food insecurity, physical activity, physical function, self-reported health, health conditions, and demographics.
Significance level:
significant at p ≤ 0.05;
significant at p ≤ 0.01;
significant at p ≤ 0.001;
significant at p ≤ 0.0001.
TABLE 3.
Variables | C statistic | Cognitive Restraint OR (95% CI) |
Uncontrolled Eating OR (95% CI) |
Emotional Eating OR (95% CI) |
Sweets OR (95% CI) |
Salty Snacks OR (95% CI) |
Fruits OR (95% CI) |
Depression OR (95% CI) |
Anxiety OR (95% CI) |
Stress OR (95% CI) |
|
---|---|---|---|---|---|---|---|---|---|---|---|
Model 1 | Eating behaviors | 0.70 | 2.7 (0.7, 4.8)‡ |
2.0 (0.9, 4.8) |
1.2 (0.5, 2.8) |
||||||
Model 2 | + Sweets, salty snacks, and fruit | 0.77 | 3.3 (1.3, 8.2)§ |
2.1 (0.8, 5.4) |
0.9 (0.4, 2.5) |
3.1 (1.2, 8.1)‡ |
1.6 (0.6, 4.0) |
0.3 (0.1, 0.8)‡ |
|||
Model 3 | + Depression, anxiety, stress | 0.81 | 3.1 (1.2, 8.1)‡ |
2.2 (0.8, 5.9) |
1.0 (0.3, 2.7) |
3.0 (1.1, 8.2)‡ |
1.5 (0.6, 4.0) |
0.2 (0.1, 0.7)§ |
0.4 (0.1, 2.2) |
6.1 (1.8, 20.2)§ |
1.2 (0.3, 5.7) |
Model 4 | + Food insecurity, moderate physical activity, and physical function | 0.81 | 3.1 (1.1, 8.1)‡ |
2.2 (0.8, 6.0) |
1.0 (0.3, 2.8) |
3.1 (1.1, 8.7)‡ |
1.5 (0.6, 4.0) |
0.2 (0.7, 0.6)§ |
0.5 (0.1, 2.3) |
6.0 (1.8, 20.0)§ |
1.1 (0.2, 5.6) |
Model 5 | + Self reported health, diabetes, hypertension, heart disease, and diabetes | 0.84 | 4.1 (1.3, 12.7)§ |
1.2 (0.4, 3.9) |
1.1 (0.3, 3.9) |
6.6 (1.9, 23.2)§ |
1.2 (0.4, 3.5) |
0.3 (0.1, 0.8)‡ |
0.2 (0.0, 1.6) |
5.3 (1.4, 20.8)‡ |
2.0 (0.3, 14.1) |
Model 6 | + Demographics | 0.89 | 4.3 (1.2, 15.2)‡ |
1.1 (0.3, 4.3) |
1.9 (0.5, 8.1) |
16.8 (3.2, 87.3)‖ |
1.1 (0.3, 3.9) |
0.6 (0.2, 2.0) |
0.1 (0.0, 0.9)‡ |
8.9 (1.9, 42.7)§ |
2.9 (0.3, 27.7) |
Dependent variable is non-obese (WC Class I Obesity, < 43 inches for men, < 42 inches for women, n = 68) vs. obese (WC ≥ 43 inches for men, ≥ 42 inches for women, n = 45).
Each eating behavior coded as the median split; sweets, salty snacks, and fruit as the upper tertile vs. lower two tertiles; depression, anxiety, and stress coded as normal versus mild, moderate or severe. As indicated, models controlled for these potential cofounders: food insecurity, physical activity, physical function, self-reported health, health conditions, and demographics.
Significance level:
significant at p ≤ 0.05;
significant at p ≤ 0.01;
significant at p ≤ 0.001;
significant at p ≤ 0.0001.
Similar to our previous findings (8), in the final model (model 6) of Table 2, when controlling for all confounding variables, reporting CR increased the risk of obesity by 4-fold (p ≤ 0.01), while a 3-fold increase in risk of obesity was seen when reporting EE behavior (p ≤ 0.05).
In model 5 of Table 3, CR (OR = 4.1, CI 1.3 – 12.7, p ≤ 0.01), sweets (OR = 6.6, CI 1.9 – 23.2, p ≤ 0.01), fruit intake (OR = 0.3, CI 0.1 – 0.8, p ≤ 0.05), and anxiety (OR = 5.3, CI 1.4 – 20.8, p ≤ 0.05) were consistently and significantly associated with an increased risk of obesity defined by OB-WC. When controlled for demographics in the final model (model 6) the negative relationship with fruit intake was attenuated (OR = 0.6, CI 0.2 – 2.0, p ≤ 0.10); however, reporting depression remained negatively associated with obesity in this final model (OR = 0.1, CI 0.0 – 0.9, p ≤ 0.05).
DISCUSSION
This paper expands our previous findings on the associations of obesity with eating behaviors, dietary patterns, and mental health, confirming previous conclusions (9) that CR and EE are robustly associated with OB-BMI (Table 2), even when controlled for confounding factors such as food group intake. The following discussion of our findings will focus primarily on the models exploring the relationship of these factors with OB-WC, because waist circumference has been associated to a greater extent than BMI with obesity-related co-morbidities (2, 27) including diabetes (28), dyslipidemia (29), coronary heart disease (30), inflammation (31), and mortality in older adults (32).
As seen in the fully adjusted model of Table 3, CR was associated with obesity, which confirms and extends our previous observation in this sample.(9) Similar to other findings (33), we discovered that obesity assessed by BMI, but not WC, was associated with EE. The positive association of EE with BMI and not WC may be due to our small sample size. Further longitudinal research is needed to identify the relationship between eating behaviors and various measures of adiposity in older adults.
In the fully adjusted model, similar to the prior findings in this sample, frequency of eating sweets (17) remained positively associated with OB-WC, and in most models fruit consumption was negatively associated with obesity (Table 3). The association of sweet intake with abdominal adiposity is likely due to the frequency of consumption, high-energy content, and possibly increased consumption of fructose.(34, 35) The availability of sweets (e.g. cinnamon rolls, candy bars, soft drinks) rather than healthy snacks (fresh fruit, 100% fruit juice, low-fat granola bars) may increase the frequency of sweets consumption in this sample as previously discussed.(17)
Anxiety was robustly associated with OB-WC even in the fully adjusted model (Table 3). However, as we considered this association, we suspected that several questions in the anxiety subscale might be symptoms of obesity-related health problems rather than of anxiety. We felt this was the case for two questions found to be significantly associated with OB-WC. There was a relatively high affirmative response among obese participants for the questions, “Were you aware of the action of your heart (e.g., sense of heart rate increase, heart missing a beat) in the absence of physical exertion?” and “Did you experience difficulty breathing (e.g. excessively rapid breathing, breathlessness) in the absence of physical exertion?” Our observation is similar to others in that obesity is known to be linked to increased heart rate and difficulty breathing.(36) These changes such as elevated heart rate may however be due to changes in fundamental physiological mechanisms causing increased sympathetic activity (37) and sympathovagal balance (38) with resultant hypertension, insulin resistance, hyperlipidemia, and renal dysfunction (39, 40). This has particular relevance for obese older adults because an elevated heart rate is an independent predictor for mortality (41), and Carnethon et al (42) found that a higher heart rate at baseline was associated with diabetes and mortality. Difficulty breathing is one of many common respiratory symptoms in obese individuals and it is postulated that the causes are due to reduced functional residual capacity of the lungs reduction in lung volume due to abdominal distribution of fat, decreased lung compliance (e.g. closure of airways, increased alveolar surface area, increased blood volume), increased oxygen cost due to increased breathing frequency, and disproportional distribution of VO2 caused by increased adiposity.(43) Therefore, even though breathing difficulties and increased heart rate are symptoms of anxiety, the lack of association of obesity with psychological symptoms found in the other anxiety subscale questions suggest that the anxiety subscale is identifying serious symptoms of obesity and obesity related disorders instead of symptoms of anxiety. Further research is needed to disentangle the physical and psychological associations between obesity and anxiety in this population.
Depression was associated with only one measure of obesity, OB-WC, and only in the fully adjusted model, but as can be seen in Table 3 this was a negative relationship such that those with symptoms of depression were less likely to be obese. The association of obesity and depression is complex and this negative association has also been observed by others.(44, 45) Our cross-sectional study design does not permit us to fully examine the potentially multi-directional relationships of depression and obesity in this population.
The findings that the odds of being obese were increased with anxiety, decreased with depression, and were not associated with stress suggest a complex relationship between mental health and obesity in this sample. Also of concern is that two of the anxiety-related questions may be capturing the physical symptoms of obesity and not anxiety per se. Thus it may be important to continue to explore the relationship of obesity with both eating behaviors and mental health and to refine the measures of mental health, especially anxiety. More in-depth research and collaborations with psychologists are needed to further explain the relationship between anxiety and obesity in this group.
Practical implications
Additional research and interventions are needed to address the potential problem of high intake of sweets as a causal contributor to obesity and creating a healthy food environment for these congregate meal participants.(17) By including in the dialog the seniors being served, senior center directors, AAA directors, vendor and congregate meal dietitians, and nutritionists in the State Unit on Aging, progress could be made toward goals such as exchanging unhealthy foods for healthy snacks in the senior center, exploring new ways to create healthy and palatable congregate meals that seniors enjoy and eat, and establishing guidelines that regulate unhealthy outside food being taken into the senior centers. Current education programs focus mainly on the health benefits of fruits, vegetables, whole grains, and low fat meats and milk products. In the future, nutrition education programs could provide more information on the potential health risks of high intakes of processed foods that contain large amounts of energy, sugar (high fructose corn syrup, sucrose, and related ingredients), saturated fat, and trans fats, as well as how to decrease the intakes of energy and foods with these ingredients. Previous nutrition education interventions (8, 21, 46, 47) have successfully increased the intake of fruit and vegetables, increased physical activity and physical function, and improved hemoglobin A1C, therefore, well-designed education programs focused on foods and healthy weight management are likely to meet with success.
Abnormal eating behaviors (e.g., CR, UE, and EE) need to be addressed in this aging cohort. In younger populations, some successful weight loss programs have specifically targeted these three inappropriate eating behaviors. For example, Keranen et al (48) utilized intensive counseling in individual and group settings to identify eating behaviors, recognize the situations in which they emerge, learn about the consequences of participating in these behaviors, and monitor their improvements in their food choices. However, there is little research specifically addressing how to target these eating behaviors in weight loss programs for older adults.
This study is not without limitations. Eating behaviors and mental health were self-reported in questionnaires and not clinically diagnosed. Food group intake was assessed subjectively, but the questions were adapted from the validated Block food frequency questionnaire (49) and BRFSS (50). This study was cross-sectional and therefore doesn’t lend itself to a causal inference of obesity with eating behaviors, food intake, or mental health symptoms; however, the robust associations of obesity with CR and intake of sweets warrants further investigation.
TAKE AWAY POINTS.
Obesity is, and will continue to be, a major health issue facing the aging population. Through the identification of modifiable behaviors, changes can be made to reduce the detrimental impact of obesity on health care costs, chronic health conditions, disability and mortality.(51–54)
This study presents information regarding the association of obesity with abnormal eating behaviors, food intake, and mental health symptoms that may be useful for the development of future weight management strategies in a congregate meal setting.
Strategies to consider include (1) creating a healthy food environment focused on reducing the availability of unhealthy food choices and replacing them with healthier, nutrient dense options; (2) developing an educational program that explains the impact foods, ingredients, and excess energy have on the aging body; and (3) collaboration with dietitians for one-on-one and group counseling.
We have reported previously that congregate meal participants can improve many aspects of their nutrition, physical activity and chronic disease self-management.(15) Thus, the results of this study can be used as part of the process to develop multidisciplinary interventions that target eating behaviors, food intake, and mental health to improve healthy weight management.
Acknowledgement
Partial support for this research was provided by ARCS Foundation, Atlanta, GA; Northeast Georgia Area Agency on Aging; USDA NIFA GEO-00708; and NIH grant 5T32 AG00029-35.
References
- 1.Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the united states, 2011–2012. JAMA. 2014;311(8):806–814. doi: 10.1001/jama.2014.732. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Guh DP, Zhang W, Bansback N, Amarsi Z, Birmingham CL, Anis AH. The incidence of co-morbidities related to obesity and overweight: a systematic review and meta-analysis. BMC Public Health. 2009;9:88. doi: 10.1186/1471-2458-9-88. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Luppino FS, de Wit LM, Bouvy PF, Stijnen T, Cuijpers P, Penninx BW, et al. Overweight, obesity, and depression: a systematic review and meta-analysis of longitudinal studies. Arch Gen Psychiatry. 2010;67(3):220–229. doi: 10.1001/archgenpsychiatry.2010.2. [DOI] [PubMed] [Google Scholar]
- 4.Soczynska JK, Kennedy SH, Woldeyohannes HO, Liauw SS, Alsuwaidan M, Yim CY, et al. Mood disorders and obesity: understanding inflammation as a pathophysiological nexus. Neuromolecular Med. 2011;13(2):93–116. doi: 10.1007/s12017-010-8140-8. [DOI] [PubMed] [Google Scholar]
- 5.Simon GE, Von Korff M, Saunders K, Miglioretti DL, Crane PK, van Belle G, et al. Association between obesity and psychiatric disorders in the US adult population. Arch Gen Psychiatry. 2006;63(7):824–830. doi: 10.1001/archpsyc.63.7.824. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Hsiao PY, Jensen GL, Hartman TJ, Mitchell DC, Nickols-Richardson SM, Coffman DL. Food intake patterns and body mass index in older adults: a review of the epidemiological evidence. J Nutr Gerontol Geriatr. 2011;30(3):204–224. doi: 10.1080/21551197.2011.591266. [DOI] [PubMed] [Google Scholar]
- 7.de Lauzon B, Romon M, Deschamps V, Lafay L, Borys JM, Karlsson J, et al. The Three-Factor Eating Questionnaire-R18 is able to distinguish among different eating patterns in a general population. J Nutr. 2004;134(9):2372–2380. doi: 10.1093/jn/134.9.2372. [DOI] [PubMed] [Google Scholar]
- 8.Porter KN, Fischer JG, Johnson MA. Improved physical function and physical activity in older adults following a community-based intervention: Relationships with a history of depression. Maturitas. 2011;70(3):290–294. doi: 10.1016/j.maturitas.2011.07.024. [DOI] [PubMed] [Google Scholar]
- 9.Porter KN, Johnson MA. Obesity is more strongly associated with inappropriate eating behaviors than with mental health in older adults receiving congregate meals. J Nutr Gerontol Geriatr. 2011;30(4):403–415. doi: 10.1080/21551197.2011.623960. [DOI] [PubMed] [Google Scholar]
- 10.CV OS. In: The Aging Services Network: Serving a vunerable and growing elderly population in tough economic times. Forum NHP, editor. Washington, D.C.: 2011. [Google Scholar]
- 11.Administration on Aging HaHS, editor. 2011 Annual Report. Washington, DC: 2012. [Google Scholar]
- 12.Brewer DP, Catlett CS, Porter KN, Lee JS, Hausman DB, Reddy S, et al. Physical limitations contribute to food insecurity and the food insecurity-obesity paradox in older adults at senior centers in Georgia. J Nutr Elder. 2010;29(2):150–169. doi: 10.1080/01639361003772343. [DOI] [PubMed] [Google Scholar]
- 13.Penn DM, Fischer JG, Sun Lee J, Hausman DB, Johnson MA. High BMI and waist circumference are associated with a high prevalence of comorbidities in older Americans Act programs in Georgia senior centers. J Nutr Health Aging. 2009;13(9):827–832. doi: 10.1007/s12603-009-0220-9. [DOI] [PubMed] [Google Scholar]
- 14.Johnson MA, Hawthorne NA, Brackett WR, Fischer JG, Gunter EW, Allen RH, et al. Hyperhomocysteinemia and vitamin B-12 deficiency in elderly using Title IIIc nutrition services. Am J Clin Nutr. 2003;77(1):211–220. doi: 10.1093/ajcn/77.1.211. [DOI] [PubMed] [Google Scholar]
- 15.Johnson MA, Fischer JG, Park S. Vitamin D deficiency and insufficiency in the Georgia Older Americans Nutrition Program. J Nutr Elder. 2008;27(1–2):29–46. doi: 10.1080/01639360802059704. [DOI] [PubMed] [Google Scholar]
- 16.Lee JS, Fischer JG, Johnson MA. Food insecurity, food and nutrition programs, and aging: experiences from Georgia. J Nutr Elder. 2010;29(2):116–149. doi: 10.1080/01639366.2010.480895. [DOI] [PubMed] [Google Scholar]
- 17.Porter KN. Obesity and its relationship with eating behaviors, mental health, and food intake in congregate meal participants. University of Georgia; 2012. [Google Scholar]
- 18.Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults--The Evidence Report. National Institutes of Health. Obes Res. 1998;6(Suppl 2):51S–209S. [PubMed] [Google Scholar]
- 19.Ardern CI, Janssen I, Ross R, Katzmarzyk PT. Development of health-related waist circumference thresholds within BMI categories. Obes Res. 2004;12(7):1094–1103. doi: 10.1038/oby.2004.137. [DOI] [PubMed] [Google Scholar]
- 20.Angle S, Engblom J, Eriksson T, Kautiainen S, Saha MT, Lindfors P, et al. Three factor eating questionnaire-R18 as a measure of cognitive restraint, uncontrolled eating and emotional eating in a sample of young Finnish females. Int J Behav Nutr Phys Act. 2009;6:41. doi: 10.1186/1479-5868-6-41. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Hendrix SJ, Fischer JG, Reddy RD, Lommel TS, Speer EM, Stephens H, et al. Fruit and vegetable intake and knowledge increased following a community-based intervention in older adults in Georgia senior centers. J Nutr Elder. 2008;27(1–2):155–178. doi: 10.1080/01639360802060249. [DOI] [PubMed] [Google Scholar]
- 22.Ellis J, Johnson MA, Fischer JG, Hargrove JL. Nutrition and health education intervention for whole grain foods in the Georgia older Americans nutrition programs. J Nutr Elder. 2005;24(3):67–83. doi: 10.1300/J052v24n03_06. [DOI] [PubMed] [Google Scholar]
- 23.Cheong JMK JM, Lewis RD, Fischer JG, Johnson JT. Reduction in modifiable osteoporosis-related risk factors among older adults in the Older Americans Nutrition Program. Family Econ. Nutrition Rev. 2003;15(1):83–91. [Google Scholar]
- 24.Antony MM, Bieling PJ, Cox BJ, Enns MW, Swinson RP. Psychometric properties of the 42-item and 21-item versions of the Depression Anxiety Stress Scales in clinical groups and a community sample. Psychological Assessment. 1998;10(2):176–181. [Google Scholar]
- 25.Wolfe WS, Frongillo EA, Valois P. Understanding the experience of food insecurity by elders suggests ways to improve its measurement. J Nutr. 2003;133(9):2762–2769. doi: 10.1093/jn/133.9.2762. [DOI] [PubMed] [Google Scholar]
- 26.National Center for Chronic Disease Prevention adn Health Promotion CfDCaP, editor. Behavioral Risk Factor Surveillance System: Arthritis Question. Atlanta, GA: 2007. [Google Scholar]
- 27.Janssen I, Katzmarzyk PT, Ross R. Waist circumference and not body mass index explains obesity-related health risk. Am J Clin Nutr. 2004;79(3):379–384. doi: 10.1093/ajcn/79.3.379. [DOI] [PubMed] [Google Scholar]
- 28.Wang Y, Rimm EB, Stampfer MJ, Willett WC, Hu FB. Comparison of abdominal adiposity and overall obesity in predicting risk of type 2 diabetes among men. Am J Clin Nutr. 2005;81(3):555–563. doi: 10.1093/ajcn/81.3.555. [DOI] [PubMed] [Google Scholar]
- 29.Snider RL, Pai RK, Kusumoto FM. The importance of the evolution of ST-T wave changes for differentiating acute pericarditis from myocardial ischemia. Cardiol Rev. 2004;12(3):138–140. doi: 10.1097/01.crd.0000110745.25012.ba. [DOI] [PubMed] [Google Scholar]
- 30.Canoy D. Distribution of body fat and risk of coronary heart disease in men and women. Curr Opin Cardiol. 2008;23(6):591–598. doi: 10.1097/HCO.0b013e328313133a. [DOI] [PubMed] [Google Scholar]
- 31.Panagiotakos DB, Pitsavos C, Yannakoulia M, Chrysohoou C, Stefanadis C. The implication of obesity and central fat on markers of chronic inflammation: The ATTICA study. Atherosclerosis. 2005;183(2):308–315. doi: 10.1016/j.atherosclerosis.2005.03.010. [DOI] [PubMed] [Google Scholar]
- 32.Jacobs EJ, Newton CC, Wang Y, Patel AV, McCullough ML, Campbell PT, et al. Waist circumference and all-cause mortality in a large US cohort. Arch Intern Med. 2010;170(15):1293–1301. doi: 10.1001/archinternmed.2010.201. [DOI] [PubMed] [Google Scholar]
- 33.de Lauzon-Guillain B, Basdevant A, Romon M, Karlsson J, Borys JM, Charles MA. Is restrained eating a risk factor for weight gain in a general population? Am J Clin Nutr. 2006;83(1):132–138. doi: 10.1093/ajcn/83.1.132. [DOI] [PubMed] [Google Scholar]
- 34.Pollock NK, Bundy V, Kanto W, Davis CL, Bernard PJ, Zhu H, et al. Greater fructose consumption is associated with cardiometabolic risk markers and visceral adiposity in adolescents. J Nutr. 2012;142(2):251–257. doi: 10.3945/jn.111.150219. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Stanhope KL, Schwarz JM, Havel PJ. Adverse metabolic effects of dietary fructose: results from the recent epidemiological, clinical, and mechanistic studies. Curr Opin Lipidol. 2013;24(3):198–206. doi: 10.1097/MOL.0b013e3283613bca. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Kurukulasuriya LR, Stas S, Lastra G, Manrique C, Sowers JR. Hypertension in obesity. Med Clin North Am. 2011;95(5):903–917. doi: 10.1016/j.mcna.2011.06.004. [DOI] [PubMed] [Google Scholar]
- 37.Lambert EA, Rice T, Eikelis N, Straznicky NE, Lambert GW, Head GA, et al. Sympathetic Activity and Markers of Cardiovascular Risk in Nondiabetic Severely Obese Patients: The Effect of the Initial 10% Weight Loss. Am J Hypertens. 2014 doi: 10.1093/ajh/hpu050. [DOI] [PubMed] [Google Scholar]
- 38.Pal GK, Chandrasekaran A, Hariharan AP, Dutta TK, Pal P, Nanda N, et al. Body mass index contributes to sympathovagal imbalance in prehypertensives. BMC Cardiovasc Disord. 2012;12:54. doi: 10.1186/1471-2261-12-54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Kuo JJ, Jones OB, Hall JE. Chronic cardiovascular and renal actions of leptin during hyperinsulinemia. Am J Physiol Regul Integr Comp Physiol. 2003;284(4):R1037–R1042. doi: 10.1152/ajpregu.00480.2002. [DOI] [PubMed] [Google Scholar]
- 40.Sartor DM. Sympathoinhibitory signals from the gut and obesity-related hypertension. Clin Auton Res. 2013;23(1):33–39. doi: 10.1007/s10286-012-0171-9. [DOI] [PubMed] [Google Scholar]
- 41.Jensen MT, Suadicani P, Hein HO, Gyntelberg F. Elevated resting heart rate, physical fitness and all-cause mortality: a 16-year follow-up in the Copenhagen Male Study. Heart. 2013;99(12):882–887. doi: 10.1136/heartjnl-2012-303375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Carnethon MR, Yan L, Greenland P, Garside DB, Dyer AR, Metzger B, et al. Resting heart rate in middle age and diabetes development in older age. Diabetes Care. 2008;31(2):335–339. doi: 10.2337/dc07-0874. [DOI] [PubMed] [Google Scholar]
- 43.Littleton SW. Impact of obesity on respiratory function. Respirology. 2012;17(1):43–49. doi: 10.1111/j.1440-1843.2011.02096.x. [DOI] [PubMed] [Google Scholar]
- 44.Aziz R, Steffens DC. What are the causes of late-life depression? Psychiatr Clin North Am. 2013;36(4):497–516. doi: 10.1016/j.psc.2013.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Blazer DG. Depression in late life: review and commentary. J Gerontol A Biol Sci Med Sci. 2003;58(3):249–265. doi: 10.1093/gerona/58.3.m249. [DOI] [PubMed] [Google Scholar]
- 46.Fitzpatrick SE, Reddy S, Lommel TS, Fischer JG, Speer EM, Stephens H, et al. Physical activity and physical function improved following a community-based intervention in older adults in Georgia senior centers. J Nutr Elder. 2008;27(1–2):135–154. doi: 10.1080/01639360802060223. [DOI] [PubMed] [Google Scholar]
- 47.Speer EM, Reddy S, Lommel TS, Fischer JG, Heather S, Park S, et al. Diabetes self-management behaviors and A1c improved following a community-based intervention in older adults in Georgia senior centers. J Nutr Elder. 2008;27(1–2):179–200. doi: 10.1080/01639360802060298. [DOI] [PubMed] [Google Scholar]
- 48.Keranen AM, Savolainen MJ, Reponen AH, Kujari ML, Lindeman SM, Bloigu RS, et al. The effect of eating behavior on weight loss and maintenance during a lifestyle intervention. Prev Med. 2009;49(1):32–38. doi: 10.1016/j.ypmed.2009.04.011. [DOI] [PubMed] [Google Scholar]
- 49.Block G, Hartman AM, Naughton D. A reduced dietary questionnaire: development and validation. Epidemiology. 1990;1(1):58–64. doi: 10.1097/00001648-199001000-00013. [DOI] [PubMed] [Google Scholar]
- 50.Prevention USDoHaHSCfDCa, editor. Behavioral Risk Factor Surveillance System Survey Data. Atlanta, Georgia: 2005. [Google Scholar]
- 51.Finkelstein EA, Trogdon JG, Cohen JW, Dietz W. Annual medical spending attributable to obesity: payer-and service-specific estimates. Health Aff (Millwood) 2009;28(5):w822–w831. doi: 10.1377/hlthaff.28.5.w822. [DOI] [PubMed] [Google Scholar]
- 52.Mathus-Vliegen EM. Prevalence, pathophysiology, health consequences and treatment options of obesity in the elderly: a guideline. Obes Facts. 2012;5(3):460–483. doi: 10.1159/000341193. [DOI] [PubMed] [Google Scholar]
- 53.Porter Starr KN, McDonald SR, Bales CW. Obesity and Physical Frailty in Older Adults: A Scoping Review of Lifestyle Intervention Trials. J Am Med Dir Assoc. 2014 doi: 10.1016/j.jamda.2013.11.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Poggiogalle E, Migliaccio S, Lenzi A, Donini LM. Treatment of body composition changes in obese and overweight older adults: insight into the phenotype of sarcopenic obesity. Endocrine. 2014 doi: 10.1007/s12020-014-0315-x. [DOI] [PubMed] [Google Scholar]