Journal Pre-proof Associations of appetitive behaviors in 7 year old children with their cardiometabolic health at 10 years of age Sarah Warkentin, Ana C. Santos, Andreia Oliveira PII:
S0939-4753(20)30023-5
DOI:
https://doi.org/10.1016/j.numecd.2020.01.007
Reference:
NUMECD 2212
To appear in:
Nutrition, Metabolism and Cardiovascular Diseases
Received Date: 30 September 2019 Revised Date:
6 January 2020
Accepted Date: 7 January 2020
Please cite this article as: Warkentin S, Santos AC, Oliveira A, Associations of appetitive behaviors in 7 year old children with their cardiometabolic health at 10 years of age, Nutrition, Metabolism and Cardiovascular Diseases, https://doi.org/10.1016/j.numecd.2020.01.007. This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. © 2020 Published by Elsevier B.V. on behalf of The Italian Society of Diabetology, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition, and the Department of Clinical Medicine and Surgery, Federico II University.
Associations of appetitive behaviors in 7 year old children with their cardiometabolic health at 10 years of age Sarah Warkentina; Ana C. Santos a,b; Andreia Oliveiraa,b
a
EPIUnit - Instituto de Saúde Pública, Universidade do Porto, Porto, Portugal; Departamento de Ciências da Saúde Pública e Forenses e Educação Médica, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
b
Corresponding Author Sarah Warkentin, EPIUnit – Instituto de Saúde Pública, Universidade do Porto [Institute of Public Health of the University of Porto] Address: Rua das Taipas, 135-139, 4050-600 - Porto, Portugal. Tel.: +351 222 061 820. Email:
[email protected]
Declarations of interest None
Word counts: Abstract: 245 Text: 3893 Number of references: 52 Number of Figures: 2 Number of Tables: 4
List of abbreviations CVD: Cardiovascular diseases BMI: Body Mass Index CEBQ: Children`s Eating Behavior Questionnaire CEBQ-EF: Enjoyment of food CEBQ-FR: Food responsiveness CEBQ-EOE: Emotional overeating CEBQ-DD: Desire to drink CEBQ-SR: Satiety responsiveness CEBQ-SE: Slowness in eating CEBQ-FF: Food fussiness CEBQ-EUE: Emotional undereating TG: Triglycerides HDL-c: High-density lipoprotein-cholesterol WC: Waist circumference SBP: Systolic blood pressure HOMA-IR: Homeostatic model assessment-insulin resistance M: Means SD: Standard deviation Md: Median IQR: Interquartile range
1 2
Introduction Cardiovascular diseases (CVDs) are end-points of gradual progression of atherosclerosis and this
3
process begins early in life, with clinical manifestations occurring decades later [1]. It is nowadays
4
believed that, by promoting optimal cardiovascular health in adolescents, long-term beneficial effects can
5
be seen in adulthood [2]. Cardiovascular health, as proposed by the American Heart Association (AHA),
6
includes health behaviors (such as being physically active, eating a healthy diet, being in the normal Body
7
Mass Index (BMI) range and not smoking) and risk factors (i.e. having normal blood pressure, glucose
8
and cholesterol levels) [3]. In light of this, weight alone does not seem to be a good measure of CVD risk;
9
children with normal weight but already showing metabolical alterations may not be correctly targeted
10
and still have a higher risk of future CVDs [4]. In addition, cohort studies worldwide have described
11
strong and significant tracking, between childhood and adulthood, of different cardiovascular risk factors,
12
such as having high serum lipids, BMI, and blood pressure [5,6], besides the tracking of health behaviors,
13
such as being physically active [7] and eating a healthy diet [8]. Thus, identifying those children at greater
14
risk, by using a cluster of preclinical CVD markers besides actual weight, may help in the development of
15
targeted interventions that could decrease morbidity and mortality and also be cost-effective [9,10].
16
The AHA and the World Health Organization (WHO) link chronic diseases, which are the leading
17
cause of death and disabilities worldwide, to social determinants and behavioral risk factors [3,10], such
18
as eating habits. Aiming to measure eating behaviors, a number of psychometric tools have been
19
developed in the past three decades. The Children`s Eating Behavior Questionnaire (CEBQ), designed to
20
assess a range of appetitive traits [11], previously described as important predictors of child eating and
21
weight status [12–17]. Positive responses to food, or ´food approach` behaviors, such as showing
22
enjoyment in food intake or eating in response to external food cues, are hypothesized to contribute to
23
energy intake [12] and weight gain [13–17] among children. ‘Food avoidant’ behaviors, such as child`s
24
fussy eating, child`s sensitivity to feelings of fullness and slowness in eating, are likely to reduce food
25
intake [18]. Since nowadays most children dwell within obesogenic environments with great availability
26
of various energy-dense, palatable, cheap, and nutrient-poor foods [19,20], these appetitive traits are
27
likely to enhance the risk of future CVDs.
28
Studies of obesity-related behaviors have been published in the past years, linking these appetitive
29
behaviors to weight status and body composition[14–17,21–25], but there is a lack of studies that
30
associate these appetitive traits to important cardiometabolic risk factors. The aim of this study was to
31
investigate whether appetitive behaviors among 7-year-olds are associated with their cardiometabolic
32
health three years later. We predicted that CEBQ subdomains measuring ‘food approach` behaviors, i.e.
33
Enjoyment of food, Food responsiveness, Emotional overeating and Desire to drink would be positively
34
associated with cardiometabolic risk, while the ´food avoidant` subdomains Satiety responsiveness,
35
Slowness in eating, Food fussiness and Emotional undereating would be higher scored in those children
36
with lower risk.
37 38
Methods
39
Study population
1
40
This study included singleton children from Generation XXI, an ongoing prospective population-
41
based birth cohort from northern Portugal, described elsewhere [26,27]. Children were recruited at birth
42
in 2005/2006 at public Maternity hospitals of Porto. Of all eligible mothers, 91% agreed to participate (8
43
495 mothers and 8 647 children at baseline).
44
All families were invited for the follow-ups at ages 4 years (y) (2009-2011), 7y (2012-2014) and 10y
45
(2015-2017). The present study included data from the baseline, and the 7y and 10y follow-ups. From the
46
6 115 children that attended at both 7y and 10y follow-ups, and after exclusion of children without data of
47
interest the present investigation included 2 951 children (please see the inclusion and exclusion
48
flowchart in Figure 1).
49 50 51
Measures Since our sample is composed of children, we examined variables that are associated with known
52
cardiometabolic risk [10] rather than hard end-points of cardiovascular events. These variables included
53
triglycerides (TG), high-density lipoprotein-cholesterol (HDL-c), waist circumference (WC), systolic
54
blood pressure (SBP) and homeostatic model assessment-insulin resistance (HOMA-IR).
55
Venous blood samples were collected in a fasting condition. TG and HDL-c were measured using an
56
enzymatic colorimetric assay and HOMA-IR was computed as follows: glucose (mg/dL) x insulin
57
(µU/mL)/405 [28]. Blood pressure was measured from the brachial artery of the right arm, with a random
58
zero sphygmomanometer (Medel® ELITE, S. Polo de Torrile, Italy), being recorded as the mean of two
59
measurements, with a 5-minute interval. Height, weight and WC were measured according to standard
60
procedures [29]. BMI was computed for each child, and age- and sex- specific BMI reference z-scores
61
[30] were calculated. The measurement of cardiometabolic parameters and anthropometric data were
62
collected in the 7y follow-up.
63
Cardiometabolic risk z-scores, adjusted for child´s sex and age, were created. Z-scores of TG, HDL-
64
c, WC and HOMA-IR were calculated as follows: Z= ([value of continuous variable - mean]/SD). For
65
blood pressure, in order to avoid misclassification of children who are very tall or short, z-scores were
66
adjusted for age, sex and height, according to the American Academy of Pediatrics [31]. Next, we
67
categorized cardiometabolic risk, in which the higher risk group was composed by individuals in the
68
upper quartile of TG, HOMA-IR, WC and SBP z-scores and in the first quartile of HDL-c z-score [32]
69
and the remaining children were categorized as having “lower risk”. We chose to estimate adverse
70
glucose homeostasis using the HOMA-IR score rather that fasting glucose, as defined by the International
71
Diabetes Federation (IDF) definition [33], since HOMA-IR is a frequently used parameter in clinical and
72
epidemiological research and provides a reliable estimate of insulin resistence among chidren and
73
adolescents [34]. The inclusion of risk factors other than the traditional IDF factors in the calculation of
74
metabolic risk may strengthen the ability of tracking children in higher risk of cardiovascular diseases, by
75
improving sensitivity and specificity [32].
76
Eating behaviors were measured at 7y using a translated and previously validated version of the
77
original CEBQ to Portuguese school-aged children [13]. Parents or main caregivers were asked to
78
respond to the questionnaire, which is divided into eight subdomains: Enjoyment of food (CEBQ-EF, e.g.
79
My child enjoys eating), Food responsiveness (CEBQ-FR, e.g. My child's always asking for food), Desire
2
80
to drink (CEBQ-DD, e.g. If given the chance, my child would drink continuously throughout the day),
81
Emotional overeating (CEBQ-EOE, e.g. My child eats more when worried), Food fussiness (CEBQ-FF,
82
e.g. My child refuses new foods at first), Satiety responsiveness (CEBQ-SR, e.g. My child gets full up
83
easily), Slowness in eating (CEBQ-SE, e.g. My child takes more than 30 minutes to finish a meal) and
84
Emotional undereating (CEBQ-EUE, e.g. My child eats less when s/he is angry). The response format is a
85
5-point Likert scale, ranging from ´Never` to ´Always`. In accordance with the original scale, five of the
86
items were reverse-scored due to opposite phrasing. In questionnaires that had <50% of missing data
87
items (~3%), data were recovered by replacement for the average of the remaining questions within each
88
subdomain of the participant. Albuquerque and colleagues (2017) showed a good internal consistency of
89
the validated CEBQ (Cronbach´s α ranged from 0.74 to 0.85 [13]).
90
Child`s dietary intake was evaluated through a food frequency questionnaire that determined
91
frequency of intake at 7y. It was previously validated in a sub-sample from Generation XXI, by
92
comparing data with 3-day food records and nutrient biomarkers [35]. Parents or the main caregiver were
93
asked how many times, on average, the child had consumed that specific food during the previous six
94
months. Response options ranged from ´4 times or more per day` to ´Never`, and answers were converted
95
into daily frequency. The mean daily intake of fruit and vegetables was calculated by including data from
96
four food groups: fruits, vegetable soups, cooked and raw vegetables. Vegetable soups were asked
97
separately to vegetables, as it is a common preparation in Portugal. This variable was then dichotomized
98
into greater or equal to 5 a day vs. lower consumption of fruit and vegetables per day, according to the
99
WHO recommendations.
100
Physical activity at 7y was accessed by the questions: ´How long does the child spend, on average
101
per day, in active leisure-time activities (e.g. running, playing ball, cycling)? during the week (Monday to
102
Friday)` and ´How long does the child spend, on average per day, in active leisure-time activities (e.g.
103
running, playing ball, cycling)? during the weekend (Saturday to Sunday)`, and answers were given in
104
average time, per week/weekend, in hours. Time of physical activity was summed and a continuous
105
variable with the daily average time spend in physical activities during the whole week, in hours, was
106
created.
107
Maternal characteristics at baseline were assessed by interviews with trained professionals, using
108
standardized questionnaires. The current study used maternal educational level, recorded by completed
109
years of schooling, and BMI before pregnancy, calculated using weight and height (Kg/m2), as control
110
variables in the analyses.
111 112 113
Statistical Analysis Continuous variables were described as means (M) and standard deviations (SD) or as median (Md)
114
and interquartile range (IQR) and binary variables as counts and percentages. For continuous variables,
115
independent sample t-tests or Mann-Whitney U-tests were performed to analyze differences on boys and
116
girls; for categorical variables, chi-square tests were performed.
117
In order to investigate the associations between appetitive behaviors and cardiometabolic parameters,
118
linear regressions were conducted with each of the five parameters that composed the cardiometabolic
119
risk, stratified by child´s sex. A set of variables were entered in the model (maternal BMI and educational
3
120
level, mean daily time of physical activity, and mean daily consumption of fruit and vegetables) to
121
investigate if associations remained unchanged. A second adjustment was performed, with the inclusion
122
of the first set of confounders plus the remaining cardiometabolic parameters (e.g. HDL-c model adjusted
123
for Model 1 plus TG, SBP, HOMA-IR and WC z-scores). To estimate the association of each CEBQ
124
subdomain at 7y with the cardiometabolic risk group at 10y, logistic regressions were performed. The
125
same covariates included in the linear regressions were used for adjustment in the logistic regression
126
models and these were chosen based on previous literature and tested in the current sample. In addition to
127
the first adjustment, we further adjusted the models for child’s BMI at 7y of age.
128
Statistical analyses were carried out using SPSS (Statistical Package for Social Sciences) v. 25.0
129
(SPSS Inc., Chicago, IL). Statistical significance and 95% Confidence intervals were described using
130
Bonferroni`s correction.
131 132 133 134
Ethics Generation XXI was approved by the University of Porto Medical School/ S. João Hospital Centre Ethics Committee and by the Portuguese Data Protection Authority.
135
All the phases of the study complied with the Ethical Principles for Medical Research Involving
136
Human Subjects expressed in the Declaration of Helsinki. Accordingly, a written informed consent from
137
the parents (or legal substitute) and an oral consent from the children were obtained in each evaluation.
138 139 140
Results Mothers had, on average, 12 years of schooling, with a median age at baseline of 30 years. Girls
141
scored, on average, higher in CEBQ-SE compared to boys. At the age of 10, one in every four children
142
was classified as overweight (BMIz +1 to +2 SD) and 18% of boys and nearly 16% of girls were obese
143
(BMIz >+2 SD). Regarding cardiometabolic parameters at 10 years of age, girls showed significantly
144
lower values of glucose (Girls M±SD: 86.30 mg/dL±6.10 vs. Boys: 87.82 mg/dL ±9.71), HDL-c (Girls
145
M±SD: 53.84 mg/dL±10.52 vs. Boys: 56.60 mg/dL±10.34) and higher values of TG (Girls Md±IQR:
146
64.00 mg/dL±34.00 vs. Boys: 56.00 mg/dL±31.00), HOMA-IR (Girls Md±IQR: 2.02±1.66 vs. Boys:
147
1.52±1.15) and WC (Girls Md±IQR: 66.50 cm±14.42 vs. Boys 64.90 cm±13.00).
148
For both sexes, five subdomains had significant differences, when comparing the group with a
149
higher cardiometabolic risk to the reference group (i.e. lower risk). The ´food avoidant` measures, CEBQ-
150
SR, CEBQ-SE and CEBQ-FF were lower among children in the risk group. On the other hand, children
151
with more ´food approach` behaviors, such as CEBQ-FR and CEBQ-EF had significantly higher values in
152
the higher risk group. Additionally, girls with higher scores in Emotional overeating were also more
153
frequently classified in the higher cardiometabolic risk group (Figure 2).
154
Linear regressions were performed in order to investigate the associations of the CEBQ appetitive
155
behaviors at 7y and the later individual cardiometabolic parameters z-scores in both sexes (Table 2a and
156
Table 2b). Regarding ´food avoidant` behaviors, greater responsiveness to satiety cues (CEBQ-SR)
157
showed a protective effect in cardiometabolic health, especially among girls (HDL-c: adj. model 1
158
β=0.21, 95%CI 0.10; 0.32; HOMA-IR: adj. model 1 β=-0.19, 95%CI -0.30; -0.09; WC: adj. model 1 β=-
159
0.46, 95%CI -0.55; -0.36; SBP: adj. β=-0.12, 95%CI -0.20; -0.04). The association of food avoidant
4
160
subdomains and WC was the only one that remained significantly associated in boys and girls after
161
further adjusting for the remaining cardiometabolic parameters, although it was greatly weakened.
162
Children with slower eating rate (CEBQ-SE) showed a positive association with HDL-c and a negative
163
association (i.e. a protective effect) with TG, HOMA-IR, WC and SBP z-scores, but almost all of these
164
associations (with exception to WCz) were no longer significant after further adjustment for the
165
remaining cardiometabolic parameters. Food fussiness showed a negative association with WCz, with
166
significant effects only among girls (adj. model 2 β=-0.11, 95%CI -0.19;-0.03), independently of the other
167
cardiometabolic parameters. Eating less in response to emotional stimuli was positively associated with
168
HDL-c levels only among girls, and negatively associated with WC among boys, after adjustment for the
169
remaining cardiometabolic parameters.
170
´Food approach` behaviors, such as Enjoyment of food, Food responsiveness and Emotional
171
overeating, showed strong positive effects, in both sexes, in TG, HOMA-IR, WC and SBP z-scores. The
172
positive associations of the ´food approach` behaviors CEBQ-EF, CEBQ-FR and CEBQ-EOE and WC
173
remained after further adjustments (i.e. adjusting for Model 1 plus the remaining cardiometabolic
174
parameters – TG, HDL-c, SBP and HOMA-IR z-scores), in both boys and girls. Desire to drink only
175
showed a significant positive association, in the first adjusted model (Model 1), with SBP among girls.
176
However, this effect was not maintained after further adjustments (Model 2).
177
The associations between appetitive behaviors at 7y and the cardiometabolic risk score at 10y are
178
described in Table 3. Overall, children with higher scores in ‘food avoidant` subdomains, namely CEBQ-
179
SR and CEBQ-SE showed lower cardiometabolic risk, whereas children with higher scores in CEBQ-EF,
180
CEBQ-FR and CEBQ- EOE showed higher odds of being in the higher cardiometabolic risk group. In
181
multivariate analyses, less appetitive children (with higher scores in CEBQ-SR) and who eat slowly had
182
lower odds of high cardiometabolic risk; the associations were consistent in both sexes, with similar odds
183
in CEBQ-SR and CEBQ-SE. After initial adjustment for potential confounders, children with higher
184
Enjoyment of food, Food responsiveness, and Emotional overeating, showed the greatest cardiometabolic
185
risks; boys had between 2.50 and 3.66 times greater cardiometabolic risk, and girls had a risk greater than
186
2 in all appetitive behaviors. Eating more in response to emotional stimuli was significantly associated
187
with greater cardiometabolic risk only among girls (CEBQ-EOE: OR=2.18, 95CI% 1.23; 3.87). In the
188
additional adjustment for child’s BMIz at 7 years of age, the associations did not remain statistically
189
significant (adjusted Model 2).
190 191 192
Discussion Appetitive behaviors of 7-years-old children were associated with cardiometabolic risk factors three
193
years later, however these associations were influenced by child`s weight status. First, a higher metabolic
194
risk among children with greater scores in ´food approach` behaviors, such as CEBQ-EF, CEBQ-FR and
195
CEBQ-EOE was observed. Studies related these behaviors to child`s excessive body weight in developed
196
[12,13] and developing countries [23,36]. The majority used BMI as the only indicator of child`s
197
nutritional status, however this does not provide sufficient information on body composition and does not
198
solely reflect the complexity of obesity [37–39]. Visceral fat accumulation is a major contributor to
199
cardiometabolic risk [37] and the inclusion of direct measures of adiposity, such as WC and other
5
200
cardiometabolic markers, is warranted. A small number of cross-sectional studies have linked subjective
201
eating behaviors with adiposity markers. Studies among Finish [24], English [40] and Malaysian [25]
202
school-aged children showed a positive association between ´food approach` behaviors and the same
203
body fat indicator used in this study (i.e. WC) and an inverse relation with ´food avoidant` measures
204
(CEBQ-SE and CEBQ-SR). To our knowledge, this is the first study, with a longitudinal design, that
205
investigated the relationship between eating behaviors and well-known cardiometabolic risk factors years
206
later.
207
The current study shows associations of appetitive traits and cardiometabolic parameters, however,
208
most of these effects disappeared when adjusting for other cardiometabolic parameters. Notwithstanding,
209
it is important to highlight that the greatest effects of appetitive traits were related to WC, showing that
210
metabolic traits in childhood are mainly driven by adiposity. Besides using the traditional indicator of
211
BMI, other health markers, such as WC and HOMA-IR, may be used in the identification of children with
212
higher cardiometabolic risk. In the current study, WC remained as the outcome more consistently and
213
strongly related with appetite behaviors. Furthermore, a recent study that explored the accuracy of body
214
fat patterns and single measures, using the same Portuguese birth cohort study as shown here, evidenced
215
that, in children, waist-to-height ratio is a proxy of DXA-fat mass, rather than DXA-central fat [41].
216
Nonetheless, in the current study, BMI was shown to be a key parameter in the relationship between
217
appetitive traits and the cardiometabolic risk.
218
Food fussiness showed a strong protective effect in WC among girls and HOMA-IR among boys.
219
Studies among school-aged children and adolescents reported an inverse relation between fussy/picky
220
eating and BMI [42,43]. Therefore, even though Food fussiness was associated with decreased
221
cardiometabolic parameters, this does not mean that a fussier child is a healthier child, since this behavior
222
is associated with other risks, such as the consumption of a low variety of foods [44,45], disliking of
223
fruits and vegetables [18] and micronutrient deficiencies [45].
224
Greater Satiety responsiveness, Slowness in eating and Emotional undereating have been negatively
225
associated with child adiposity [21,23,25,46], which are reflected in the current results. Children who eat
226
faster are less sensitive to internal satiety cues and children who overeat depending on their emotional
227
state, tend to have higher adiposity and, consequently, a higher cardiometabolic risk. Furthermore, a
228
lower consumption of food groups, such as fruit and vegetables, bread, protein foods, snacks and total
229
energy intake was seen among preschoolers with higher scores in CEBQ-SR [12]. In adults, eating
230
quickly has been associated with an adverse lipid profile, higher blood pressure and glucose levels and
231
obesity, suggesting that a slower eating rate has an effect in satiety control [47]. Finally, hyperphagic
232
response to stress and distress increases the risk of weight gain, since stress conditions tend to favour the
233
consumption of sweet foods in the absence of hunger [48]. The greater effect of eating in response to
234
emotions in the cardiometabolic risk score was observed among girls in the current sample, showing that
235
this group is probably the most affected by this behavior.
236
A child`s interest in food consumption (CEBQ-EF), and eating in response to external food cues
237
(CEBQ-FR) [11], showed the greatest odds in the cardiometabolic risk group. This effect remained
238
significant when investigating the cardiometabolic risk score without the inclusion of the direct measure
239
of adiposity (WC), showing its effect in the increase of cardiometabolic risk, independently of child´s fat
6
240
quantity and distribution (data not shown). However, when further adjusting the logistic regression
241
models for child’s BMI at 7 years, the effects were no longer observed, suggesting that child’s BMI at 7
242
years may underpin the relationship between food approach and food avoidant behaviors at 7 years and
243
cardiometabolic risk 3 years later. We hypothesized that appetitive traits would be associated with
244
cardiometabolic health in school-age children and our findings show that the associations were in the
245
predicted direction of associations – however largely dependent on child’s weight status. As described,
246
today`s obesogenic food environment may lead to a food consumption beyond energy requirements,
247
driven by pleasure and not by physical hunger. CEBQ-EF and CEBQ-FR have been linked to a reward-
248
related approach motivation, leading to overconsumption among preschoolers [49]. Children with higher
249
scores in appetitive behaviors such as CEBQ-FR showed a weaker satiety regulation and a higher risk of
250
having an unhealthy diet, with preference for noncore foods [18]. Moreover, it is important to highlight
251
that only 40% of the children met WHO`s recommendation in the consumption of fruit and vegetables.
252
Previous analyses in the Generation XXI cohort have shown that adherence at 7y to a dietary pattern rich
253
in energy-dense foods, processed meat and low in vegetables increased several cardiometabolic
254
parameters at 10y [50]. So, to maintain an adequate weight and prevent the occurrence of CVD, a healthy
255
dietary pattern, with increased amounts of fruits, vegetables, whole grains, legumes and seafoods, with
256
age-appropriate portion sizes and foods, is encouraged [20].
257
Since cardiometabolic risk factors tend to occur simultaneously and not alone, we clustered these
258
cardiometabolic risks in childhood by creating a risk score. A study of pooled birth cohorts evidenced that
259
the IDF diagnostic criteria included less children at risk, when compared to the clustering of different
260
factors, such as HOMA-IR, cardiorespiratory fitness and leptin [32]. The use of continuous, age-adjusted,
261
standardized variables have been described and seems to be a more accurate method to track
262
cardiometabolic risk in children and adolescents [51,52], as was done in the current study. However, we
263
should be aware that higher levels of cardiometabolic parameters are not indicative of existing disease, as
264
most children in our sample are apparently healthy. Nonetheless, our study suggests that at early ages,
265
such as 7y, having certain appetitive behaviors could have an association with metabolic parameters,
266
leading in the long-term to diseases.
267
Regarding study`s limitations, since the sample is composed of school-aged children, we currently
268
were not able to study associations between eating behaviors and clinical outcomes of cardiometabolic
269
events. Instead, we used well-known cardiometabolic markers that could predict future CVDs. We also
270
did not adjust for puberty, but stratified analysis by sex were conducted and, at 10y, pubertal development
271
is just beginning (only 3% of girls had already had menarche). The strengths of the current study include
272
the large sample size and the prospective design of the study. Moreover, the current study had available
273
standardized measures of weight, height and WC instead of reported values, and a standardized method in
274
the assessment of cardiometabolic parameters and eating behaviors was followed.
275
This is the first study to investigate appetitive behaviors in school-aged children and their relation to
276
cardiometabolic risk factors three years later. The majority of studies in child’s eating behaviors link
277
appetitive behaviors to adiposity (through BMI or weight), but lack in associating them to a wider range
278
of metabolic markers. Clustering additional important CVD risk factors along with the child’s adiposity in
7
279
the tracking of altered eating behavior might strengthen the ability of tracking children at higher risk of
280
CVDs.
281
Our study adds important findings in the investigation of eating behaviors and cardiometabolic health
282
in children. Appetitive behaviors of 7-year-old children were associated with cardiometabolic risk factors
283
three years later, but this association is largely dependent of child´s body fat (WC) and weight (BMI),
284
strong predictors of cardiometabolic health. When investigating cardiometabolic parameters in isolation,
285
appetitive traits such as Food responsiveness, Enjoyment of food and Emotional overeating increased
286
cardiometabolic risk, but again this is highly dependent on a child`s level of body fat. In general, ´food
287
avoidant’ behaviors protect against cardiometabolic risk and ‘food approach’ behaviors increase
288
cardiometabolic risk.
289 290
Acknowledgements
291
Generation XXI was funded by Programa Operacional de Saúde – Saúde XXI, Quadro Comunitário de
292
Apoio III and Administração Regional de Saúde Norte (Regional Department of Ministry of Health). It
293
has support from the Portuguese Foundation for Science and Technology and from the Calouste
294
Gulbenkian Foundation. This study was supported through FEDER from the Operational Programme
295
Factors of Competitiveness – COMPETE and through national funding from the Foundation for Science
296
and Technology – FCT (Portuguese Ministry of Education and Science) under the projects “Appetite
297
regulation and obesity in childhood: a comprehensive approach towards understanding genetic and
298
behavioural influences” (PTDC/SAU-EPI/30334/2017; POCI-01-0145-FEDER-030334);
299
“Appetite and adiposity - evidence for gene-environment interplay in children” (IF/01350/2015); “HIneC:
300
When do health inequalities start? Understanding the impact of childhood social adversity on health
301
trajectories from birth to early adolescence” (POCI-01-0145-FEDER-029567; Reference: PTDC/SAU-
302
PUB/29567/2017), and through Investigator Contracts (IF/01350/2015 – AO ; IF/01060/2015 - ACS).
303
The authors gratefully acknowledge the families enrolled in Generation XXI for their kindness, all
304
members of the research team for their enthusiasm and perseverance and the participating hospitals and
305
their staff for their help and support.
306 307 308 309 310 311 312 313 314 315 316 317 318
8
319
References
320
[1]
Laitinen TT, Pahkala K, Magnussen CG, Viikari JSA, Oikonen M, Taittonen L, et al. Ideal
321
cardiovascular health in childhood and cardiometabolic outcomes in adulthood: The
322
Cardiovascular Risk in Young Finns Study. Circulation 2012;125:1971–8.
323
doi:10.1161/CIRCULATIONAHA.111.073585.
324
[2]
Pahkala K, Hietalampi H, Laitinen TT, Viikari JSA, Rönnemaa T, Niinikoski H, et al. Ideal
325
Cardiovascular Health in Adolescence: Effect of Lifestyle Intervention and Association With
326
Vascular Intima-Media Thickness and Elasticity (The Special Turku Coronary Risk Factor
327
Intervention Project for Children [STRIP] Study). Circulation 2013;127:2088–96.
328
doi:10.1161/CIRCULATIONAHA.112.000761.
329
[3]
Lloyd-Jones DM, Hong Y, Labarthe D, Mozaffarian D, Appel LJ, Van Horn L, et al. Defining
330
and setting national goals for cardiovascular health promotion and disease reduction: The
331
american heart association’s strategic impact goal through 2020 and beyond. Circulation
332
2010;121:586–613. doi:10.1161/CIRCULATIONAHA.109.192703.
333
[4]
334 335
Bridger TL, Wareham A. Beyond BMI: The Next Chapter in Childhood Obesity Management. Curr Obes Rep 2014;3:321–9. doi:10.1007/s13679-014-0114-y.
[5]
Juhola J, Magnussen CG, Viikari JSA, Kähönen M, Hutri-Kähönen N, Jula A, et al. Tracking of
336
Serum Lipid Levels, Blood Pressure, and Body Mass Index from Childhood to Adulthood: The
337
Cardiovascular Risk in Young Finns Study. J Pediatr 2011;159:584–90.
338
doi:10.1016/j.jpeds.2011.03.021.
339
[6]
Joshi SM, Katre PA, Kumaran K, Joglekar C, Osmond C, Bhat DS, et al. Tracking of
340
cardiovascular risk factors from childhood to young adulthood - The Pune Children’s Study. Int J
341
Cardiol 2014;175:176–8. doi:10.1016/j.ijcard.2014.04.105.
342
[7]
Telama R, Yang X, Leskinen E, Kankaanpää A, Hirvensalo M, Tammelin T, et al. Tracking of
343
physical activity from early childhood through youth into adulthood. Med Sci Sports Exerc
344
2014;46:955–62. doi:10.1249/MSS.0000000000000181.
345
[8]
Movassagh EZ, Baxter-Jones ADG, Kontulainen S, Whiting SJ, Vatanparast H. Tracking dietary
346
patterns over 20 years from childhood through adolescence into young adulthood: The
347
saskatchewan pediatric bone mineral accrual study. Nutrients 2017;9:1–14.
348
doi:10.3390/nu9090990.
349
[9]
350 351
Children and Young Adults. N Engl J Med 2015;373:1307–17. doi:10.1056/NEJMoa1502821. [10]
352 353
Skinner AC, Perrin EM, Moss LA, Skelton JA. Cardiometabolic Risks and Severity of Obesity in
World Health Organization (WHO). Technical package for cardiovascular disease management in primary health care. 2016. doi:10.1016/j.cortex.2008.06.011.
[11]
Wardle J, Guthrie CA, Sanderson S, Rapoport L. Development of the Children’s Eating
354
Behaviour Questionnaire. J Child Psychol Psychiatry 2001;42:963–70. doi:10.1111/1469-
355
7610.00792.
356
[12]
Carnell S, Pryor K, Mais LA, Warkentin S, Benson L, Cheng R. Lunch-time food choices in
357
preschoolers: Relationships between absolute and relative intakes of different food categories, and
358
appetitive characteristics and weight. Physiol Behav 2016;162:151–60.
9
359 360
doi:10.1016/j.physbeh.2016.03.028. [13]
Albuquerque G, Severo M, Oliveira A. Early Life Characteristics Associated with Appetite-
361
Related Eating Behaviors in 7-Year-Old Children. J Pediatr 2017;180:38-46.e2.
362
doi:10.1016/j.jpeds.2016.09.011.
363
[14]
Jaarsveld CHM Van, Llewellyn CH, Johnson L, Wardle J. Prospective associations between
364
appetitive traits and weight gain in infancy. Am J Clin Nutr 2011;94:1562–7.
365
doi:10.3945/ajcn.111.015818.Individual.
366
[15]
de Barse LM, Tiemeier H, Leermakers ETM, Voortman T, Jaddoe VWV, Edelson LR, et al.
367
Longitudinal association between preschool fussy eating and body composition at 6 years of age:
368
The Generation R Study. Int J Behav Nutr Phys Act 2015;12:2–9. doi:10.1186/s12966-015-0313-
369
2.
370
[16]
Quah PL, Chan YH, Aris IM, Pang WW, Toh JY, Tint MT, et al. Prospective associations of
371
appetitive traits at 3 and 12 months of age with body mass index and weight gain in the first 2
372
years of life. BMC Pediatr 2015;15:1–10. doi:10.1186/s12887-015-0467-8.
373
[17]
Derks IPM, Sijbrands EJG, Wake M, Qureshi F, van der Ende J, Hillegers MHJ, et al. Eating
374
behavior and body composition across childhood: a prospective cohort study. Int J Behav Nutr
375
Phys Act 2018;15:1–9. doi:10.1186/s12966-018-0725-x.
376
[18]
Fildes A, Mallan KM, Cooke L, van Jaarsveld CHM, Llewellyn CH, Fisher A, et al. The
377
relationship between appetite and food preferences in British and Australian children. Int J Behav
378
Nutr Phys Act 2015;12:1–10. doi:10.1186/s12966-015-0275-4.
379
[19]
380 381
Chan RSM, Woo J. Prevention of Overweight and Obesity: How Effective is the Current Public Health Approach. Int J Res Public Heal 2010;73390:765–83. doi:10.3390/ijerph7030765.
[20]
Van Horn L, Carson JAS, Appel LJ, Burke LE, Economos C, Karmally W, et al. Recommended
382
Dietary Pattern to Achieve Adherence to the American Heart Association/American College of
383
Cardiology (AHA/ACC) Guidelines: A Scientific Statement from the American Heart
384
Association. Circulation 2016;134:e505–29. doi:10.1161/CIR.0000000000000462.
385
[21]
386 387
Webber L, Hill C, Saxton J, Van Jaarsveld CHM, Wardle J. Eating behaviour and weight in children. Int J Obes 2009;33:21–8. doi:10.1038/ijo.2008.219.
[22]
Warkentin S, Mais LA, Latorre M do RD de O, Carnell S, Taddei JA de AC. Parents Matter:
388
Associations of Parental BMI and Feeding Behaviors With Child BMI in Brazilian Preschool and
389
School-Aged Children. Front Nutr 2018;5. doi:10.3389/fnut.2018.00069.
390
[23]
Santos JL, Ho-Urriola JA, González A, Smalley S V., Domínguez-Vásquez P, Cataldo R, et al.
391
Association between eating behavior scores and obesity in Chilean children. Nutr J 2011;10:1–8.
392
doi:10.1186/1475-2891-10-108.
393
[24]
Eloranta AM, Lindi V, Schwab U, Tompuri T, Kiiskinen S, Lakka HM, et al. Dietary factors
394
associated with overweight and body adiposity in Finnish children aged 6-8 years: The PANIC
395
Study. Int J Obes 2012;36:950–5. doi:10.1038/ijo.2012.89.
396
[25]
Tay CW, Chin YS, Lee ST, Khouw I, Poh BK. Association of Eating Behavior with Nutritional
397
Status and Body Composition in Primary School-Aged Children. Asia-Pacific J Public Heal
398
2016;28:47S-58S. doi:10.1177/1010539516651475.
10
399
[26]
Larsen PS, Kamper-Jørgensen M, Adamson A, Barros H, Bonde JP, Brescianini S, et al.
400
Pregnancy and birth cohort resources in Europe: A large opportunity for aetiological child health
401
research. Paediatr Perinat Epidemiol 2013;27:393–414. doi:10.1111/ppe.12060.
402
[27]
Alves E, Correia S, Barros H, Azevedo A. Prevalence of self-reported cardiovascular risk factors
403
in Portuguese women: A survey after delivery. Int J Public Health 2012;57:837–47.
404
doi:10.1007/s00038-012-0340-6.
405
[28]
Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis
406
model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin
407
concentrations in man. Diabetologia 1985;28:412–9. doi:10.1007/BF00280883.
408
[29]
Gibson RS. Principles of Nutritional Assessment. 2nd ed. Oxford University Press; 2005.
409
[30]
World Health Organization. WHO | The WHO Child Growth Standards. Geneva: World Health
410 411
Organization; 2006. [31]
National High Blood Pressure Education Program Working Group on High Blood Pressure in
412
Children and Adolescents. Fourth Report On The Diagnosis, Evaluation, And Treatment Of High
413
Blood Pressure In Children And Adolescents. Washington, DC: 2005.
414
[32]
Andersen LB, Lauersen JB, Brønd JC, Anderssen SA, Sardinha LB, Steene-Johannessen J, et al.
415
A New Approach to Define and Diagnose Cardiometabolic Disorder in Children. J Diabetes Res
416
2015;2015:1–10. doi:10.1155/2015/539835.
417
[33]
Zimmet P, Alberti KGM, Kaufman F, Tajima N, Silink M, Arslanian S, et al. The metabolic
418
syndrome in children and adolescents ? an IDF consensus report. Pediatr Diabetes 2007;8:299–
419
306. doi:10.1111/j.1399-5448.2007.00271.x.
420
[34]
Yin J, Li M, Xu L, Wang Y, Cheng H, Zhao X, et al. Insulin resistance determined by
421
Homeostasis Model Assessment (HOMA) and associations with metabolic syndrome among
422
Chinese children and teenagers. Diabetol Metab Syndr 2013;5:1–9. doi:10.1186/1758-5996-5-71.
423
[35]
Vilela S, Severo M, Moreira T, Ramos E, Lopes C. Evaluation of a short food frequency
424
questionnaire for dietary intake assessment among children. Eur J Clin Nutr 2018;73:679–91.
425
doi:10.1038/s41430-018-0200-4.
426
[36]
Passos DR dos, Gigante DP, Maciel FV, Matijasevich A. Children’s eating behavior: comparison
427
between normal and overweight children from a school in Pelotas, Rio Grande do Sul, Brazil.
428
Rev Paul Pediatr (English Ed 2015;33:42–9. doi:10.1016/S2359-3482(15)30029-4.
429
[37]
Frühbeck G, Busetto L, Dicker D, Yumuk V, Goossens GH, Hebebrand J, et al. The ABCD of
430
Obesity: An EASO Position Statement on a Diagnostic Term with Clinical and Scientific
431
Implications. Obes Facts 2019:131–6. doi:10.1159/000497124.
432
[38]
433 434
Freedman DS, Sherry B. The Validity of BMI as an Indicator of Body Fatness and Risk Among Children. Pediatrics 2009;124:S23–34. doi:10.1542/peds.2008-3586e.
[39]
Freedman DS, Butte NF, Taveras EM, Lundeen EA, Blanck HM, Goodman AB, et al. BMI z-
435
Scores are a poor indicator of adiposity among 2- to 19-year-olds with very high BMIs, NHANES
436
1999-2000 to 2013-2014. Obesity 2017;25:739–46. doi:10.1002/oby.21782.
437 438
[40]
Carnell S, Wardle J. Appetite and adiposity in children: Evidence for a behavioral susceptibility theory of obesity. Am J Clin Nutr 2008;88:22–9. doi:10.1093/ajcn/88.1.22.
11
439
[41]
440 441
Santos S, Severo M, Lopes C, Oliveira A. Anthropometric Indices Based on Waist Circumference as Measures of Adiposity in Children. Obesity 2018;26:810–3. doi:10.1002/oby.22170.
[42]
Rahill S, Kennedy A, Walton J, McNulty BA, Kearney J. The factors associated with food
442
fussiness in Irish school-aged children. Public Health Nutr 2019;22:164–74.
443
doi:10.1017/S1368980018002835.
444
[43]
Berger PK, Hohman EE, Marini ME, Savage JS, Birch LL. Girls’ picky eating in childhood is
445
associated with normal weight status from ages 5 to 15 y. Am J Clin Nutr 2016;104:1577–82.
446
doi:10.3945/ajcn.116.142430.
447
[44]
Vilela S, Hetherington MM, Oliveira A, Lopes C. Tracking diet variety in childhood and its
448
association with eating behaviours related to appetite: The generation XXI birth cohort. Appetite
449
2018;123:241–8. doi:10.1016/j.appet.2017.12.030.
450
[45]
451 452
picky eaters: A cause for concern?1-3. Am J Clin Nutr 2016. doi:10.3945/ajcn.116.137356. [46]
453 454
Taylor CM, Northstone K, Wernimont SM, Emmett PM. Macro-and micronutrient intakes in
Viana V, Sinde S, Saxton JC. Children’s Eating Behaviour Questionnaire: Associations with BMI in Portuguese children. Br J Nutr 2008;100:445–50. doi:10.1017/S0007114508894391.
[47]
Shin YN, Kim DH, Bok AR, Jang JS, Nam GE, Lee KS, et al. Eating rate is associated with
455
cardiometabolic risk factors in Korean adults. Nutr Metab Cardiovasc Dis 2012.
456
doi:10.1016/j.numecd.2012.02.003.
457
[48]
458 459
Blissett J, Haycraft E, Farrow C. Inducing preschool children’s emotional eating: Relations with parental feeding practices. Am J Clin Nutr 2010;17:359–65. doi:10.3945/ajcn.2010.29375.
[49]
Vandeweghe L, Vervoort L, Verbeken S, Moens E, Braet C. Food approach and food avoidance
460
in young children: Relation with reward sensitivity and punishment sensitivity. Front Psychol
461
2016;7:1–10. doi:10.3389/fpsyg.2016.00928.
462
[50]
463 464
Pinto A, Santos AC, Lopes C, Oliveira A. Dietary patterns at 7 year-old and their association with cardiometabolic health at 10 year-old. Clin Nutr 2019. doi:10.1016/j.clnu.2019.05.007.
[51]
Sardinha LB, Santos DA, Silva AM, Grøntved A, Andersen LB, Ekelund U. A comparison
465
between BMI, waist circumference, and waist-to-height ratio for identifying cardio-metabolic risk
466
in children and adolescents. PLoS One 2016;11:e0149351. doi:10.1371/journal.pone.0149351.
467
[52]
Reuter CP, Andersen LB, de Moura Valim AR, Reuter ÉM, Borfe L, Renner JDP, et al. Cutoff
468
points for continuous metabolic risk score in adolescents from southern Brazil. Am J Hum Biol
469
2019:e23211. doi:10.1002/ajhb.23211.
470 471 472 473 474 475 476 477 478
12
479 480 481 482 483 484 485
Figure legends Figure 2: SE: Standard error; TG: Triglycerides; HOMA-IR: Homeostatic model assessment-insulin resistance; WC: Waist circumference; SBP: Systolic blood pressure; HDL-c: High-density lipoprotein cholesterol. CEBQ: Children’s Eating Behavior Questionnaire; CEBQ-SR: Satiety responsiveness; CEBQ-SE: Slowness in eating; CEBQ-FF: Food fussiness; CEBQ-EUE: Emotional undereating; CEBQDD: Desire to drink; CEBQ-FR: Food responsiveness; CEBQ-EF: Enjoyment of food; CEBQ-EOE: Emotional overeating. *p<0.05; **p≤0.001 according to Mann-Whitney U-test.
13
Boys
Girls Mean±SD
p-value
Mother`s characteristics Age at baseline (y)* Education at baseline (y)* BMI before pregnancy (Kg/m2)*
30.00±6.00 12.00±7.00 23.08±4.82
30.00±6.00 12.00±8.00 23.13±4.76
0.519 0.957 0.854
912(59.60) 618(40.40) 1.29±1.14
829(58.30) 593(41.70) 1.14±1.00²
0.0012
2.68±0.68 2.85±0.88 2.95±0.78 2.46±0.76 2.25±0.82 2.04±0.74 3.04±0.78 1.82±0.61
2.71±0.68 3.01±0.86¹ 2.95±0.75 2.44±0.75 2.18±0.79¹ 2.05±0.81 3.03±0.82 1.83±0.67
0.279 <0.0011 0.985 0.454 0.010 0.561 0.641 0.632
140.93±6.27 37.19±8.27 18.58±3.17
141.41±6.70 38.30±9.24 18.98±3.58
0.044 0.0011 0.0011
880 (57.50) 375 (24.50) 275 (18.00)
826 (58.10) 370 (26.00) 226 (15.90)
0.274
87.82±9.71 56.60±10.34 56.00±31.00 1.52±1.15 64.90±13.00 108.50±12.00 68.87±6.96
86.30±6.10 53.84±10.52 64.00±34.00 2.02±1.66 66.50±14.42 108.00±13.00 68.36±7.02¹
<0.0011 <0.0011 <0.0012 <0.0012 <0.0012 0.495 0.023
1501 (98.20) 28 (1.80)
1390 (97.70) 32 (2.30)
0.436
Child`s eating and physical activity habits at 7y Fruit and vegetables intake (portions/day) (n(%)) <5 ≥5 Average time spent in physical activity (hours/day)*
0.477
Child`s eating behaviors at 7y (CEBQ) CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE Child`s characteristics at 10y Height (cm) Weight (Kg) BMI (Kg/m2) Weight status (n(%)) Normal weight (-2 to +1SD) Overweight (+1 to +2SD) Obesity (>+2SD) Child`s cardiometabolic characteristics at 10y Glucose (mg/dL) HDL-c (mg/dL) TG (mg/dL)* HOMA – IR* WC (cm)* SBP (mmHg)* DBP (mmHg) Cardiometabolic risk score (n(%)) Lower risk Higher risk
Table 1. Mothers` and child`s characteristics at baseline and follow-ups at 7y and 10y of age (n=2 951). ¹statistical significance using Bonferroni correction, in independent sample t-test; ²statistical significance using Bonferroni correction, in Mann-Whitney U-test; SD: Standard deviation; *Median and interquartile range (Md(IQR)); CEBQ: Children’s Eating Behavior Questionnaire; CEBQ-SR: Satiety responsiveness; CEBQ-SE: Slowness in eating; CEBQ-EF: Enjoyment of food; CEBQFR: Food responsiveness; CEBQ-DD: Desire to drink; CEBQ-FF: Food fussiness; CEBQ-EUE: Emotional undereating; CEBQEOE: Emotional overeating. Child’s eating behaviors could range from 1 - ´Never` to 5 - ´Always`. BMI: Body Mass index; HDL-c: High-density lipoprotein cholesterol; TG: Triglycerides; HOMA-IR: Homeostatic model assessment-insulin resistance; WC: Waist circumference; SBP: Systolic blood pressure; DBP: Diastolic blood pressure; Higher risk: children in the 4th quartile of TG, HOMAIR, WC and SBP z-scores and in the 1st quartile of HDL-c z-score.
Table 2a. Linear regression models showing associations between appetitive behaviors at 7y and lipids profile and insulin resistance at 10y, stratified by child´s sex. Appetitive behaviors at 7y CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE
CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE
Crude model
HDL-c z-score Adj. model 1
Adj. model 2
Crude model
0.13 (0.03; 0.23) 0.11 (0.03; 0.19) 0.06 (-0.03; 0.15) 0.03 (-0.06; 0.12) -0.06 (-0.14; 0.03) -0.15 (-0.25; -0.06) -0.15 (-0.24; -0.06) -0.05 (-0.16; 0.07)
0.12 (0.02; 0.23) 0.11 (0.03; 0.19) 0.06 (-0.03; 0.16) 0.02 (-0.07; 0.11) -0.05 (-0.14; 0.03) -0.15 (-0.24; -0.05) -0.14 (-0.23; -0.05) -0.04 (-0.15; 0.08)
0.05 (-0.06; 0.15) 0.04 (-0.04; 0.12) 0.03 (-0.06; 0.12) 0.02 (-0.07; 0.10) -0.03 (-0.11; 0.06) -0.02 (-0.12; 0.08) -0.05 (-0.14; 0.05) 0.03 (-0.08; 0.15)
-0.07 (-0.17; 0.04) -0.10 (-0.18; -0.02) -0.06 (-0.15; 0.04) 0.02 (-0.08; 0.11) 0.07 (-0.01; 0.16) 0.21 (0.12; 0.31) 0.13 (0.04; 0.22) 0.09 (-0.03; 0.21)
0.22 (0.11; 0.33) 0.16 (0.08; 0.24) 0.10 (0.00; 0.19) 0.11 (0.01; 0.20) -0.02 (-0.11; 0.07) -0.17 (-0.26; -0.08) -0.18 (-0.27; -0.09) -0.09 (-0.20; 0.02)
0.21 (0.10; 0.32) 0.15 (0.07; 0.24) 0.10 (0.00; 0.20) 0.10 (0.00; 0.20) -0.01 (-0.10; 0.09) -0.16 (-0.25; -0.07) -0.17 (-0.26; -0.08) -0.08 (-0.19; 0.03)
0.08 (-0.03; 0.18) 0.04 (-0.04; 0.12) 0.04 (-0.05; 0.13) 0.07 (-0.02; 0.16) 0.02 (-0.07; 0.10) 0.00 (-0.09; 0.09) -0.02 (-0.11; 0.07) 0.03 (-0.07; 0.13)
-0.10 (-0.21; 0.00) -0.10 (-0.18; -0.01) -0.03 (-0.13; 0.06) -0.03 (-0.13; 0.07) 0.04 (-0.06; 0.13) 0.18 (0.09; 0.27) 0.15 (0.06; 0.24) 0.13 (0.02; 0.24)
TG z-score Adj. model 1 Adj. model 2 Boys β (95% CI)* -0.07 0.06 (-0.17; 0.04) (-0.04; 0.16) -0.01 -0.10 (-0.08; 0.07) (-0.18; -0.02) -0.06 0.00 (-0.15; 0.03) (-0.09; 0.08) 0.02 0.03 (-0.07; 0.11) (-0.05; 0.11) 0.07 0.04 (-0.01; 0.16) (-0.04; 0.12) 0.08 0.21 (-0.01; 0.18) (0.12; 0.30) -0.01 0.13 (-0.10; 0.08) (0.03; 0.22) 0.09 0.01 (-0.03; 0.20) (-0.10; 0.12) Girls β (95% CI)* -0.10 0.07 (-0.21; 0.01) (-0.04; 0.17) 0.05 -0.10 (-0.04; 0.13) (-0.18; -0.01) -0.05 0.02 (-0.15; 0.05) (-0.07; 0.11) -0.03 0.02 (-0.13; 0.07) (-0.07; 0.11) 0.04 0.01 (-0.06; 0.13) (-0.07; 0.10) 0.02 0.17 (-0.07; 0.11) (0.08; 0.26) -0.02 0.14 (-0.10; 0.07) (0.05; 0.23) 0.02 0.12 (-0.08; 0.13) (0.01; 0.23)
Crude model
HOMA-IR z-score Adj. model 1
Adj. Model 2
-0.21 (-0.31; -0.10) -0.15 (-0.23; -0.07) -0.10 (-0.19; -0.01) -0.02 (-0.11; 0.08) 0.05 (-0.04; 0.13) 0.24 (0.15; 0.34) 0.22 (0.13; 0.31) 0.17 (0.05; 0.28)
-0.20 (-0.30; -0.10) -0.15 (-0.23; -0.07) -0.12 (-0.21; -0.03) -0.01 (-0.10; 0.08) 0.05 (-0.04; 0.13) 0.23 (0.14; 0.32) 0.21 (0.12; 0.30) 0.15 (0.04; 0.27)
0.00 (-0.09; 0.09) 0.03 (-0.04; 0.10) -0.07 (-0.15; 0.01) 0.02 (-0.06; 0.10) -0.01 (-0.08; 0.06) -0.06 (-0.15; 0.03) -0.03 (-0.11; 0.05) 0.00 (-0.10; 0.09)
-0.20 (-0.31; -0.09) -0.22 (-0.30; -0.13) -0.05 (-0.14; 0.05) -0.08 (-0.17; 0.02) 0.08 (-0.01; 0.17) 0.26 (0.17; 0.35) 0.24 (0.15; 0.32) 0.19 (0.08; 0.30)
-0.19 (-0.30; -0.09) -0.21 (-0.29; -0.13) -0.08 (-0.18; 0.02) -0.06 (-0.16; 0.03) 0.06 (-0.04; 0.15) 0.23 (0.15; 0.32) 0.22 (0.14; 0.31) 0.15 (0.05; 0.26)
0.04 (-0.06; 0.13) -0.03 (-0.10; 0.05) 0.01 (-0.08; 0.09) -0.03 (-0.11; 0.05) 0.02 (-0.06; 0.10) -0.02 (-0.10; 0.07) -0.01 (-0.10; 0.07) -0.01 (-0.11; 0.08)
HDL-c: High-density lipoprotein cholesterol; TG: Triglycerides; HOMA-IR: Homeostatic model assessment-insulin resistance. CEBQ-SR: Satiety responsiveness; CEBQ-SE: Slowness in eating; CEBQ-FF: Food fussiness; CEBQ-EUE: Emotional undereating; CEBQ-DD: Desire to drink; CEBQ-FR: Food responsiveness; CEBQ-EF: Enjoyment of food; CEBQ-EOE: Emotional overeating.*95% Confidence interval with Bonferroni correction. Model 1 adjusted for maternal BMI and education, child mean daily time of physical activity, and mean daily consumption of fruits and vegetables at 7y. Model 2 adjusted for Model 1 plus remaining cardiometabolic parameters. Bold values are significant.
Table 2b. Linear regression models showing associations between appetitive behaviors at 7y and waist circumference and systolic blood pressure at 10y, stratified by child´s sex. Appetitive behaviors at 7y CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE
CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE
Crude model
WC z-score Adj. model 1
-0.47 (-0.57; -0.37) -0.37 (-0.44; -0.29) -0.08 (-0.17; 0.01) -0.11 (-0.20; -0.02) 0.08 (-0.01; 0.16) 0.56 (0.47; 0.65) 0.51 (0.42; 0.59) 0.36 (0.24; 0.47)
-0.45 (-0.54; -0.36) -0.35 (-0.43; -0.28) -0.09 (-0.17; 0.00) -0.08 (-0.17; 0.01) 0.07 (-0.01; 0.16) 0.53 (0.45; 0.61) 0.48 (0.40; 0.56) 0.32 (0.21; 0.43)
-0.48 (-0.58; -0.38) -0.40 (-0.48; -0.32) -0.14 (-0.24; -0.04 -0.09 (-0.19; 0.01) 0.10 (0.01; 0.19) 0.52 (0.43; 0.60) 0.49 (0.40; 0.57) 0.38 (0.27; 0.48)
-0.46 (-0.55; -0.36) -0.38 (-0.45; -0.30) -0.17 (-0.26; -0.08) -0.07 (-0.16; 0.02) 0.06 (-0.03; 0.15) 0.48 (0.40; 0.56) 0.46 (0.38; 0.54) 0.31 (0.21; 0.42)
Adj. model 2 Crude model Boys β (95% CI)* -0.05 -0.36 (-0.12; 0.03) (-0.44; -0.27) -0.28 -0.08 (-0.34; -0.21) (-0.14; -0.02) -0.03 0.00 (-0.11; 0.05) (-0.06; 0.07) -0.02 -0.08 (-0.09; 0.05) (-0.15; 0.00) 0.04 0.05 (-0.03; 0.11) (-0.02; 0.11) 0.42 0.12 (0.34; 0.49) (0.05; 0.19) 0.38 0.11 (0.31; 0.45) (0.04; 0.17) 0.06 0.25 (-0.03; 0.14) (0.15; 0.34) Girls β (95% CI)* -0.33 -0.13 (-0.41; -0.24) (-0.21; -0.05) -0.26 -0.11 (-0.32; -0.19) (-0.17; -0.05) -0.04 -0.11 (-0.12; 0.03) (-0.19; -0.03) -0.03 -0.01 (-0.10; 0.05) (-0.08; 0.07) 0.03 0.10 (-0.05; 0.10) (0.03; 0.17) 0.34 0.17 (0.27; 0.40) (0.11; 0.24) 0.32 0.18 (0.25; 0.39) (0.11; 0.24) 0.22 0.16 (0.13; 0.30) (0.07; 0.24)
SBP z-score Adj. model 1
Adj. Model 2
-0.04 (-0.11; 0.03) -0.07 (-0.13; -0.02) 0.00 (-0.06; 0.07) -0.01 (-0.08; 0.05) 0.03 (-0.03; 0.10) 0.11 (0.04; 0.18) 0.10 (0.03; 0.16) 0.04 (-0.04; 0.13)
0.03 (-0.06; 0.11) -0.02 (-0.09; 0.04) 0.03 (-0.05; 0.10) 0.01 (-0.07; 0.08) 0.03 (-0.04; 0.10) 0.05 (-0.04; 0.13) 0.04 (-0.04; 0.12) 0.01 (-0.08; 0.11)
-0.12 (-0.20; -0.04) -0.10 (-0.17; -0.04) -0.04 (-0.12; 0.03) 0.00 (-0.07; 0.07) 0.08 (0.01; 0.15) 0.16 (0.09; 0.23) 0.17 (0.10; 0.23) 0.14 (0.05; 0.22)
-0.04 (-0.13; 0.06) 0.00 (-0.08; 0.07) -0.02 (-0.10; 0.06) 0.02 (-0.06; 0.11) 0.03 (-0.05; 0.11) 0.05 (-0.04; 0.13) 0.06 (-0.03; 0.14) 0.04 (-0.06; 0.13)
WC: Waist circumference; SBP: Systolic blood pressure. CEBQ-SR: Satiety responsiveness; CEBQ-SE: Slowness in eating; CEBQFF: Food fussiness; CEBQ-EUE: Emotional undereating; CEBQ-DD: Desire to drink; CEBQ-FR: Food responsiveness; CEBQ-EF: Enjoyment of food; CEBQ-EOE: Emotional overeating. *95% Confidence interval with Bonferroni correction. Model 1 adjusted for maternal BMI and education, child mean daily time of physical activity and mean daily consumption of fruit and vegetables at 7y. Model 2 adjusted for Model 1 plus remaining cardiometabolic parameters. Bold values are significant.
Table 3. Logistic regression models showing associations between appetitive behaviors at 7y and the cardiometabolic risk score at 10y, stratified by child´s sex (n=2 951). Girls
Boys Appetitive behaviors at 7y CEBQ-SR CEBQ-SE CEBQ-FF CEBQ-EUE CEBQ-DD CEBQ-FR CEBQ-EF CEBQ-EOE
Participants no.
Lower risk: 1501 Higher risk: 28
Crude model 0.37 (0.16; 0.89) 0.47 (0.24; 0.92) 0.57 (0.29; 1.12) 0.68 (0.34; 1.38) 1.16 (0.63; 2.14) 2.53 (1.48; 4.32) 3.72 (1.87; 7.40) 1.87 (0.86; 4.07)
Adjusted model 1 OR (95% CI)* 0.39 (0.16; 0.93) 0.49 (0.25; 0.95) 0.54 (0.27; 1.09) 0.71 (0.35; 1.44) 1.14 (0.61; 2.12) 2.50 (1.45; 4.32) 3.66 (1.81; 7.40) 1.75 (0.80; 3.82)
Adjusted model 2 0.95 (0.37; 2.46) 1.00 (0.48; 2.07) 0.64 (0.31; 1.32) 0.79 (0.37; 1.69) 0.96 (0.50; 1.83) 1.03 (0.53; 2.00) 1.50 (0.68; 3.31) 0.93 (0.43; 2.05)
Participants no.
Crude model
Lower risk: 1390 Higher risk: 32
0.35 (0.16; 0.79) 0.48 (0.26; 0.88) 0.65 (0.34; 1.25) 0.78 (0.40; 1.51) 1.12 (0.61; 2.04) 2.47 (1.56; 3.91) 2.36 (1.29; 4.30) 2.39 (1.38; 4.15)
Adjusted model 1 OR (95% CI)* 0.37 (0.17; 0.82) 0.49 (0.27; 0.91) 0.60 (0.31; 1.17) 0.80 (0.41; 1.56) 1.02 (0.55; 1.89) 2.33 (1.46; 3.71) 2.22 (1.22; 4.04) 2.18 (1.23; 3.87)
Adjusted model 2 0.78 (0.30; 2.01) 1.03 (0.54; 2.00) 0.83 (0.41; 1.68) 0.83 (0.40; 1.72) 0.82 (0.42; 1.63) 1.19 (0.69; 2.06) 0.98 (0.49; 1.97) 1.31 (0.71; 2.41)
Cardiometabolic risk: higher risk category was classified as being in the 4th quartile of waist circumference, systolic blood pressure, triglycerides and homeostatic model assessment-insulin resistance zscores and 1st quartile of high-density lipoprotein-cholesterol z-score. CEBQ-SR: Satiety responsiveness; CEBQ-SE: Slowness in eating; CEBQ-FF: Food fussiness; CEBQ-EUE: Emotional undereating; CEBQ-DD: Desire to drink; CEBQ-FR: Food responsiveness; CEBQ-EF: Enjoyment of food; CEBQ-EOE: Emotional overeating. OR: Odds ratio; *95% Confidence interval with Bonferroni correction. Bold values are significant. Model 1 adjusted for maternal BMI and education, child mean daily time of physical activity and mean daily consumption of fruit and vegetables at 7y. Model 2 adjusted for Model 1 plus child’s BMIz at 7y.
Figure 1. Study flowchart of participants.
Figure 2. Mean (+SE) of child’s appetitive behaviors at 7y of age, according to higher risk (4th quartile of TG, HOMA-IR, WC and SBP z-scores and 1st quartile of HDL-c z-score) and lower risk group of the cardiometabolic risk at 10y of age, stratified by sex.
Highlights of the manuscript “Associations of appetitive behaviors at 7 years old with cardiometabolic health in 10- year-old children” • • • •
Child appetitive traits are associated with cardiometabolic risk 3 years later; Food approach behaviors are associated with increased cardiometabolic risk; Food avoidant behaviors are associated with lower cardiometabolic risk; Associations with cardiometabolic health are highly dependent on child`s adiposity.