It was hypothesized that supplementation of omega-3 fatty acids could increase physical activity (PA) levels, where traditional interventions often fail. The aim of this double-blind, randomized, placebo-controlled trail was to evaluate the effects of 15-week administration of omega-3 fatty acids on objectively measured PA and relative body weight in 8–9 year-old children. The children were randomly assigned to supplementation of omega-3 fatty acids or placebo. Primary outcome was change in PA counts per minute (cpm), and secondly change in body mass index standard deviation score (BMI SDS). Covariance models were applied adjusting for age, gender, weight status, PA and intervention season. Compliance was controlled for by analyzing fatty acid composition in plasma. The intention to treat population consisted of 362 children (omega-3 n = 177, placebo n = 185). No significant effects of omega-3 fatty acids on PA or relative body weight were observed. In covariance models no effects were observed by gender, weight status or change in PA (all p > 0.05), but inactive children increased their PA more than children classified as active at baseline (p < 0.05).
Obesity in childhood has immediate consequences on health, including hyperlipidemia, hypertension, abnormal glucose tolerance, and psychosocial health effects1,2. Since treatment of obesity is difficult3, prevention has been pronounced as a public health priority. It is well known that dietary intake affects body weight4. The importance of physical activity (PA) for obesity prevention is under debate but it is possible that PA during childhood can be protective against obesity5. More importantly, PA prevents and reduces obesity-related comorbidities such as diabetes and cardiovascular diseases6,7. Several attempts have been made to increase PA in school-aged children but this has proven difficult to affect using traditional interventions8.
There is considerable evidence that a high intake of omega-3 fatty acids has beneficial effects on health by, for example, favorably improving triglyceride levels, affecting blood clotting and vasoconstriction, having inflammatory properties and reducing body fat9. The mechanisms by which omega-3 fatty acids reduce body fat are not well understood, but altered gene expression, favoring increased fat oxidation in adipose, liver, cardiac, intestinal and skeletal muscle tissue and reduced fat deposition in adipose tissue have been suggested10. In rodents and in humans, omega-3 fatty acids stimulate β-oxidation, and inhibit fatty acid synthesis and very-low density lipoprotein secretion11. Also, an enhancement of post-prandial satiety may lead to reduced food intake and contribute to a reduction in body fat10. In this context, omega-3 supplementation may have potential anti-obesity properties. The mechanisms by which omega-3 could influence PA is unclear but improvement of bodily capacity may influence the experience of PA in a more positive direction and by that affecting PA behaviors. Omega-3 fatty acids affect muscle mass and strength12 and it has been found to increase performance in cancer patients13. Only one study has explored the associations between omega-3 fatty acids and PA in humans14. In that study, it was found that adult patients with pancreatic cancer increased their total energy expenditure and physical activity level after eight weeks of omega-3 supplementation.
In 2008, a pilot study was carried out in Stockholm, Sweden. The aim was to evaluate if motivational interviewing (MI) could increase PA in children aged 6–10 years with low initial PA levels. Children were randomly assigned to one of four treatments, comprising: supplementation of omega-3 and MI; placebo and MI; supplementation of omega-3 only; or placebo only. No effect of MI was found on PA, but children in the omega-3-group did increase their PA levels (unpublished data). In this study, we aimed to confirm or reject these results on a larger sample of children.
The objective of this study was to evaluate the effect of 15 weeks’ administration of 732 mg/day of omega-3 fatty acids (556 mg EPA, 176 mg DHA) on PA and relative body weight in children aged 7–9 years.
Material and Methods
Study design and participants
This double-blind, randomized, placebo-controlled trail examined 7–9 year-old children during autumn 2011 and spring 2012, recruited from public elementary schools in Stockholm, Sweden. After inviting a broad range of elementary schools from all over Stockholm, 18 agreed to participate. Children without diseases or syndromes that affect hormonal levels other than well-controlled hypothyroidism were included. A total of 423 children (boys, n = 209; girls, n = 214) were eligible and enrolled in this study. Of the 423 children, 204 were allocated to the omega-3 fatty acids group and 219 to the placebo group. Written informed consent was obtained from each child and their parents or guardians. The study was approved by the Regional Ethical Review Board in Stockholm, Sweden, and the methods were carried out in accordance with this approval (Dnr. 2011/1176-31/2). The study has also been registered in Clinical Trials Registry (clinicaltrials.gov Date: 25/03/2011, ID: NCT01087411).
Children were randomly assigned to 15 weeks of omega-3 fatty acid supplementation or placebo (rapeseed oil) via a double-blind procedure. Information about the allocation was concealed until the follow up data were collected. Once participants were randomized, baseline measures (anthropometrics, background data and PA) were taken and repeated after the intervention period (at week 15). All the measures took place during normal school hours in a quiet room within the school, and were performed by two trained researchers, blinded to the randomization. At the beginning of the trial school staff and parents were given instructions for dispensing capsules and a diary to record capsule consumption. A set of standard written materials was provided to the parents along with nutritional counseling about healthy eating. To determine compliance, levels of omega-3 fatty acids EPA and DHA (fractions (%) of total fatty acids) were measured through blood samples before and after the intervention in a subgroup (33 and 39 children in the intervention and placebo groups, respectively). The blood samples were collected after an overnight fast by a research nurse with extensive experience of blood sampling in children. The EPA and DHA levels in the lipid fractions in plasma were analyzed using the gas-liquid chromatography (GLC) technique.
Height and weight were measured using standard clinical procedures with a transportable Harpenden stadiometer and a digital scale (Tanita BWB 800S, Tanita, Tokyo, Japan). Height was measured to the nearest 0.01 m and weight to the nearest 0.1 kg. All children were measured in the morning wearing underwear only. Body mass index (BMI) was calculated as weight in kilograms divided by height in meters squared and was expressed in kg/m2. Body mass index standard deviation score (BMI SDS), a measure of relative weight in children that accounts for difference in BMI by age and gender, was calculated using a reference standard15. Children were categorized as having normal weight, overweight, or obesity, as defined by the International Obesity Task Force (IOTF)16.
Measurements of PA
The Actigraph GT3X+ accelerometer (Actigraph, Pensacola, Florida, USA) was used to monitor PA during seven consecutive days. Children were asked to wear the accelerometer on the non-dominant wrist without removing it except for during swimming and bathing. Data were collected at 30 Hz and summarized over 10-second epochs. To exclude sleep time, the hours between 9 pm and 8 am were removed prior to data analysis, based on a previous study exploring sleep patterns among Swedish 6–10 year olds17. Ten consecutive minutes with zero counts were considered as non-wear time and was removed from the analysis. Children with at least 4 days of accelerometer data, with at least 10 hours of registration per day were included18.
The intervention season was divided into fall-winter or winter-spring. The children had repeated PA measurements within either fall-winter (n = 144), or winter-spring (n = 218), and difference in mean PA level between intervention seasons was assessed. Outcome measures were average PA counts per minute (cpm) for the vertical axis. Quartiles of PA level at baseline and follow-up were also calculated. PA level at baseline was categorized into; physically inactive (Q1) or physically active (Q2–4). PA change from baseline was categorized into; PA decreased (quartile of PA follow up - quartile of PA baseline <0), PA unchanged (quartile PA follow up – quartile PA baseline = 0) or PA increased (quartile of PA follow up - quartile of PA baseline >0).
The omega-3 fatty acids were administered in soft gel fruit-flavored capsules, provided by Midsona AB. The capsules were chewable and did not need to be swallowed whole. As in the previous pilot study, the daily dose consisted of four capsules, in total 732 mg of omega-3 fatty acids (556 mg EPA, 176 mg DHA), 60 mg of omega-6 (fatty acid GLA) and 9.6 mg of vitamin E in natural form, i.e. alpha-tocopherol (antioxidant). The placebo group received capsules, containing rapeseed oil, identical in appearance to omega-3 fatty acids tablets. The content of a full day’s dose was equivalent to about 10 kcal, which was deemed not to affect a child’s energy balance significantly.
Intent-to-treat (ITT) analyses were carried out, including all participants who took at least one dose of omega-3 supplement or placebo and had baseline data on weight, height and PA. The last observation carried forward (LOCF) method was applied for missing PA and BMI SDS at follow-up, after controlling to ensure that missing data did not differ significantly between groups. Comparisons between the omega-3 and the placebo groups were examined using multivariate analysis of covariance (ANCOVA). Analyses of subgroups were conducted by gender, intervention season, baseline weight status, baseline PA level, and change in PA. Differences in EPA and DHA levels between baseline and follow-up were assessed with paired t-test. Sample size (with 80% power and alfa 0.05) was calculated based upon previous findings in the absence of references for expected variance. With data at hand today the sample size needed to detect a 10% change in PA between groups varied from 52 (26 per group) to 102 (51 per group).
The primary outcome variable was change in PA level from baseline to follow up, calculated by subtracting baseline PA cpm from PA cpm at follow-up. The fixed effects model was used for the main analysis and tested for potential intervention effects on PA level from: intervention group; sex; intervention season (fall-winter/winter-spring); and weight status at baseline. Age and PA cpm at baseline were included as covariates. Differences in PA change were also assessed by PA quartile at baseline (physically inactive (Q1) vs. physically active (Q2–4)).
The second outcome was change in BMI SDS from baseline to follow-up, calculated by subtracting baseline from follow-up BMI SDS. The fixed effects analysis tested for potential intervention effects on BMI SDS from: intervention group; intervention season; sex; baseline weight status; and change in PA (decreased, unchanged, increased). Baseline age and BMI SDS were included as covariates. Differences between the two groups in PA cpm and anthropometric measures at baseline were assessed with the independent samples t-test. PA differences in intervention seasons between the two groups were tested with univariate ANOVA. The categorical variables were analyzed using chi-square tests. A p-value < 0.05 was defined as the level of significance. Statistical analyses were performed using the software SPSS statistics (Version 17.0, 2008, SPSS Inc., Chicago, IL, USA).
A total of 423 children were randomized to omega-3 and placebo. Sixty-one children were excluded from the ITT population, due to lack of baseline anthropometric measures (n = 10) or PA data (n = 51). The ITT population consisted of 362 children (omega-3 supplement n = 177, placebo n = 185). The mean age was 8.5 (SD 0.3) years and the proportion of boys was 50% (n = 181). Average BMI SDS was 0.3 (SD 1.2) and 81% had a normal weight, 14% had overweight and 5% had obesity. The children accumulated on average 2492 (SD 413) PA cpm. Baseline demographics, anthropometric measures, PA levels, and percentage sedentary time in the ITT population are shown in Table 1. The two groups did not differ according to any other demographic or PA variable, except for a significantly lower BMI SDS at baseline in the omega-3 group, compared with the placebo group (0.2 (SD 1.2) vs. 0.5 (SD 1.2), p = 0.035). In both groups, PA level in winter-spring was significantly higher than that in fall-winter. In the subgroup analysis, no differences between the groups were found in fractions of EPA and DHA (EPA 0.2 (SD 0.4)%, DHA 4.0 (SD 0.7)%) at baseline. The group receiving omega-3 increased their levels of EPA to 3.5 (SD 1.3) and DHA to 5.5 (SD 1.0), while levels in the placebo group remained the same (p < 0.001).
Change in PA
In both groups, PA levels increased significantly over the intervention period (145 (SD 383) cpm, p < 0.001). No significant effect of the intervention on PA cpm was observed in adjusted analysis (p = 0.43; Table 2). Furthermore, no significant effect of the intervention on PA cpm was found in any of the subgroups (all p > 0.05, Table 2). Change in PA did not differ by gender or between normal weight and overweight/obese children. Children who were classified as inactive at baseline increased their PA levels significantly more than children who were classified as active at baseline (change in mean cpm 224 vs. 119; p < 0.05). The increase in PA was also significantly higher during the winter-spring period compared with the fall-winter period (change in mean cpm 229 vs 143; p < 0.01).
Change in BMI SDS
BMI SDS did not change significantly over the intervention period (p = 0.91). No significant differences in change in BMI SDS were observed according to sex, BMI SDS (normal weight or overweight/obesity), intervention season or activity level at baseline or follow-up. There was no significant effect of the intervention on change in BMI SDS in adjusted analyses (p = 0.97, Table 3). In subgroup analyses, no significant effects of the intervention on BMI SDS change were observed (all p > 0.05, Table 3).
The aim of this study was to explore whether omega-3 fatty acid supplementation affects PA or BMI SDS in healthy 7–9 year-old children. No significant effect on either PA or BMI SDS was identified. The study was based upon results from a previous pilot study performed by our group where we found effects of omega-3 supplementation on PA. The possible mechanisms linking omega-3 with PA can only be speculated upon. It is possible that the favorable effects of omega-3 on bodily function increases the appreciation of PA and by that affect the behavior12,13. In this study, children in both the intervention and control group increased their activity levels over the intervention period. This effect is likely due to seasonal variation. Swedish children are more active during summer time, when daylight and outdoor temperature facilitates outdoor play19. One important finding was, however, that children with the lowest initial levels of PA increased their PA significantly more that those with higher levels. This result is commensurate with results from a previous pilot study where children with low initial PA levels increased their PA irrespective of omega-3 supplementation. It could also be an effect of regression to the mean20. To our knowledge, only one other previous study has examined the effect of omega-3 on PA in humans14. In that study, where energy expenditure and physical activity level were assessed using doubly-labeled water, it was found that omega-3 supplementation increased PA in a small sample of patients with advanced pancreatic cancer.
Accumulating evidence from epidemiological and clinical studies suggests that an increased intake of omega-3 fatty acids can decrease the degree of obesity, enhance weight loss21, and decrease body fat mass22. Also, in children, lower levels of omega-3 fatty acids have been associated with increased body weight23,24. Contrary to these studies, omega-3 supplementation had no effect on BMI SDS in this study. The effect of omega-3 supplementation can vary by dosage, duration, sex and age25. The dose of omega-3 that was used in the present study is comparable to those used in most other trials of omega-3 fatty acids for child behavior26,27. It was also the exact same dose as had been used in the previous pilot study where we found an impact on PA. According to the Nordic Nutrition Recommendations (NNR), the recommended intake of omega-3 fatty acids for children and adults is ≥1 E%. For eight-year-old children that corresponds to at least 2 grams per day28. The dosage in this study (732 mg/day) is considerably lower than these recommendations and it is possible that the dose was too low to achieve an intervention effect. However, in addition to the supplementation provided, children are expected to ingest a substantial amount from food. A national survey found the average intake of omega-3 Swedish children 8–9 years to be 1,3 g/day29. Together with the supplementary dose of omega-3 given in this study, children were assumed to reach the recommendations of intake in this age group. Also, when this study was conducted, a higher dosage had not been sufficiently studied in children <12 years of age. Another possible reason for the lack of intervention effect is that the duration of the intervention was too short. In a meta-analysis, where most included studies had an intervention length of 2–3 months, a favorable effect on body weight was observed in adults21. In children, 12 weeks of omega-3 supplementation had a small but significant effect on BMI26. In accordance with this study, some previous studies have failed to find any effect of omega-3 supplementation on body composition in children30,31,32, indicating a need for further studies on this population. In comparison, our intervention was longer.
Strengths of the study are that the included participants were representative of the normal Swedish population regarding the proportion of with normal weight, overweight and obesity. They were also recruited from schools across a variety of socioeconomic areas in Stockholm County. To ensure compliance, blood levels of DHA and EPA were analyzed and found to differ significantly between the omega-3- and the placebo group throughout the intervention period. This indicates that the soft gel fruit-flavored capsule suits a pediatric population well as an omega-3 substitute. PA was measured objectively with accelerometry and anthropometric measurements were taken by trained researchers, blinded to the randomization.
Some limitations should be acknowledged. First, the participating children may have been particularly interested in the study, potentially causing a selection bias. It is possible that the study results are not generalizable to other populations. Secondly, higher BMI has been associated with lower blood levels of DHA after omega-3 supplementation33. Therefore, it is possible that higher baseline BMI SDS in the placebo group led to lower levels of DHA in plasma and moderated the impact on PA. Third, during the intervention period, children did not have energy restricted or controlled diets, which may have confounded the outcome34. Most studies in animals and humans, which have shown effects of omega-3 fatty acids on body weight and/or body composition, indicate that these effects are independent of energy intake. One study showed, however, that weight loss achieved through caloric restriction was enhanced when fish oil was included in the diet10. Last, as mentioned, the dosage of omega-3 may not have been enough to affect PA or relative weight. Instead of using standard doses, it is possible that the results would have been different if the dose was based on the body weight of each child. However, the dose was exactly the same as in the pilot study where an effect on PA was found. There is a need to further explore the interaction of PA and omega-3 fatty acids on different populations.
Omega-3 supplementation was not found to affect PA or BMI SDS in healthy children. Children with lower initial levels of PA increased their PA more than children with higher initial levels. Thus, supplementation of omega-3 fatty acids could have the potential to increase PA in individuals with low levels of PA.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
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The invaluable and excellent assistance of the research nurses Kerstin Ekbom and Michaela Forssén is greatly appreciated. This study was supported by Midsona AB; Swedish Council for Working Life and Social Research; The Swedish Heart-Lung Foundation and Stockholm Free Masons’ Foundation for Children’s Welfare.
The authors declare no competing interests.
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Svensson, V., Johansson, E., Fischer, M. et al. Omega-3 fatty acids does not affect physical activity and body weight in primary school children – a double-blind randomized placebo-controlled trial. Sci Rep 8, 12725 (2018) doi:10.1038/s41598-018-31229-4
International Journal of Molecular Sciences (2019)