Skip to main content
The American Journal of Clinical Nutrition logoLink to The American Journal of Clinical Nutrition
. 2019 Dec 18;111(2):266–279. doi: 10.1093/ajcn/nqz276

Whole milk compared with reduced-fat milk and childhood overweight: a systematic review and meta-analysis

Shelley M Vanderhout 1,3,4, Mary Aglipay 3, Nazi Torabi 5, Peter Jüni 2,4, Bruno R da Costa 2,4, Catherine S Birken 6,7,8, Deborah L O'Connor 1,8, Kevin E Thorpe 2,4, Jonathon L Maguire 1,2,3,4,6,7,8,
PMCID: PMC6997094  PMID: 31851302

ABSTRACT

Background

The majority of children in North America consume cow-milk daily. Children aged >2 y are recommended to consume reduced-fat (0.1–2%) cow-milk to lower the risk of obesity.

Objectives

To evaluate the relation between cow-milk fat consumption and adiposity in children aged 1–18 y.

Methods

Embase (Excerpta Medica Database), CINAHL (Cumulative Index to Nursing and Allied Health Literature), MEDLINE, Scopus, and Cochrane Library databases from inception to August 2019 were used. The search included observational and interventional studies of healthy children aged 1–18 y that described the association between cow-milk fat consumption and adiposity. Two reviewers extracted data, using the Newcastle–Ottawa Scale to assess risk of bias. Meta-analysis was conducted using random effects to evaluate the relation between cow-milk fat and risk of overweight or obesity. Adiposity was assessed using BMI z-score (zBMI).

Results

Of 5862 reports identified by the search, 28 met the inclusion criteria: 20 were cross-sectional and 8 were prospective cohort. No clinical trials were identified. In 18 studies, higher cow-milk fat consumption was associated with lower child adiposity, and 10 studies did not identify an association. Meta-analysis included 14 of the 28 studies (n = 20,897) that measured the proportion of children who consumed whole milk compared with reduced-fat milk and direct measures of overweight or obesity. Among children who consumed whole (3.25% fat) compared with reduced-fat (0.1–2%) milk, the OR of overweight or obesity was 0.61 (95% CI: 0.52, 0.72; P < 0.0001), but heterogeneity between studies was high (I2 = 73.8%).

Conclusions

Observational research suggests that higher cow-milk fat intake is associated with lower childhood adiposity. International guidelines that recommend reduced-fat milk for children might not lower the risk of childhood obesity. Randomized trials are needed to determine which cow-milk fat minimizes risk of excess adiposity. This systematic review and meta-analysis was registered with PROSPERO (registration number: CRD42018085075).

Keywords: cow-milk fat, children, overweight, obesity, meta-analysis

Introduction

Childhood obesity has tripled in the past 40 y, with nearly 1 in 3 North American children now overweight or obese (1–3). Over the same period, consumption of whole-fat cow-milk has halved (4). The American Academy of Pediatrics and the Canadian Paediatric Society recommend that children switch from whole-fat cow-milk (3.25%) to reduced-fat cow-milk (0.1 to 2%) at 2 y of age to limit fat intake and minimize the risk of childhood obesity (5, 6). European (7), British (8), and Australian (9) health authorities have provided similar recommendations. Healthcare providers (10) and families (11) frequently follow this guideline, and school and child-care nutrition policies (12–14) often reflect them. Since 1970 whole–cow-milk availability has dropped by 80% in North America, whereas reduced-fat milk purchases have tripled (15, 16).

Given that cow-milk is consumed daily by 88% of children aged 1 to 3 y and by 76% of children aged 4 to 8 y in Canada (17) and is a major dietary source of energy, protein, and fat for children in North America (17, 18), understanding the relation between cow-milk fat and risk of overweight or obesity is important. Systematic reviews and meta-analyses on the relation between total dairy consumption and child adiposity have had conflicting findings (Supplemental Table 1). According to these studies, higher cow-milk intake in children is associated with taller height and better bone and dental health (19–21). Although these studies evaluated total dairy consumption, they did not consider cow-milk fat specifically. The objectives of this study were to systematically review and meta-analyze the relation between whole-fat (3.25%) relative to reduced-fat (0.1 to 2%) cow-milk and adiposity in children.

Methods

A systematic review and meta-analysis of the literature was conducted. The study was designed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines (PRISMA-P) (22) and registered as a PROSPERO systematic review and meta-analysis (registration number: CRD42018085075).

Inclusion criteria

Types of studies

Studies included in the search were original works published in English in a peer-reviewed journal. Cross-sectional, cohort, case-control, and longitudinal studies, as well as intervention trials, both controlled and not controlled, were included in the search strategy. There were no restrictions on date or length of follow-up.

Population

Studies that included healthy children aged 1–18 y with ≥10 human subjects were considered. Studies that examined undernourished or disease populations (other than asthma) were excluded.

Exposures

The primary exposure was cow-milk fat, categorized as skim (0.1% fat), 1% fat, 2% fat, or whole or homogenized (3.25% fat). Measures of exposure included FFQ, multiday food record, 24-h food recall, or any other validated or nonvalidated dietary measurement tool. Dietary pattern analyses were not included.

Outcomes

The primary outcome was childhood adiposity. These measures included BMI z-score (zBMI), BMI, weight for age, body fat mass, lean body mass, waist circumference, waist-to-hip ratio, body fat percentage, skinfold thickness, and prevalence of overweight or obesity as defined by the WHO (23), CDC (24), or International Obesity Task Force (IOTF) (25) cutoffs. When sufficient information was not available in the full text publication, study authors were contacted by email to obtain additional data.

Meta-analysis

Meta-analysis included studies that reported the number of children who consumed whole (3.25%), 2%, 1%, or skim (0.1%) milk regularly (a priori defined as typically, daily, or ≥4 times per week), as well as the number of children from each of these groups who were classified as either healthy weight, or overweight or obese (overweight and obese were included as 1 category) assessed using BMI standardized according to the WHO (23), CDC (24), or IOTF (25) criteria.

Search methods

A comprehensive search strategy was developed by a research librarian (NT) with expertise in systematic reviews. From inception to August 2019, Embase, CINAHL (Cumulative Index to Nursing and Allied Health Literature), MEDLINE, Scopus, and the Cochrane Library were searched on March 23, 2018 and updated on August 2, 2019 using Medical Subject Headings (MeSH) and keywords (see Supplemental Methods for search strategies).

Data extraction, management, and analysis

Study selection

To evaluate study eligibility 2 reviewers (MA and SMV) independently reviewed study titles, abstracts, and full texts if needed. Both reviewers applied inclusion and exclusion criteria and differences were examined and resolved by consensus, which was achieved 100% of the time. Full-text articles were retrieved for potentially eligible studies and reviewed. Characteristics of included full-text studies were summarized.

Data extraction

Two reviewers (MA and SMV) extracted data from eligible studies using standardized data extraction tables adapted from the Cochrane Data Extraction Template (26). Differences were resolved by consensus 100% of the time.

Data management

Covidence (27) software was used to select studies, review results, and resolve discrepancies between reviewers. All included study records were kept in spreadsheet format.

Data synthesis

Studies included in the analysis were described according to a standardized coding system that captured key elements of each study including descriptors of the study setting, population size and age (mean and range), exposure or intervention, comparator group, method of data collection, outcome measures, type of analysis, and results.

Risk of bias and study quality assessment

Risk of bias was assessed using the Newcastle–Ottawa Scale (NOS) (28) for nonrandomized analyses, which expresses the risk of bias on a numerical scale ranging from 0 to 9; scores <7 are considered low risk (28). (NOS criteria can be found in Table 2.) The NOS-guided review included an examination of participant selection, comparability of children consuming whole or reduced-fat milk, and exposure and outcome measure ascertainment (28). To allow sufficient follow-up time for a meaningful change in adiposity to occur, the minimum acceptable follow-up time was prespecified as 1 y. Study comparability, defined as whether studies adjusted for similar confounding variables, was specified a priori as studies that adjusted for important characteristics including: birth weight or baseline weight (for prospective cohort studies), milk volume consumed, and parent BMI. Studies that adjusted for each of these factors were awarded 2 points, whereas 1 point was allocated if adjustment was performed using ≥4 other covariates. Reports were assigned 1 point for ascertainment of exposure only when structured interviews or medical records were used for data collection (28). Risk of bias was assessed by 2 reviewers (MA and SMV) and consensus was achieved 100% of the time.

TABLE 2.

Risk of bias according to the Newcastle–Ottawa Scale (28) for nonrandomized studies1

Representativeness of the exposed cohort Selection of the nonexposed cohort Ascertainment of exposure Outcome of interest not present at start Comparability of cohorts on the basis of the design or analysis Assessment of outcome Duration sufficient for outcomes to occur (>1 y) Adequacy of follow-up of cohorts Total Overall risk of bias
Cross-sectional studies (n = 20)
Acharya et al., 2011 (41) X X X X 4 High
Barba et al., 2005 (42) X X X X 4 High
Barbiero et al., 2008 (43) X  — 1 High
Beck et al., 2017 (44) X X X X X 5 High
Charvet and Huffman, 2019 (39) X X X X 4 High
Dodd et al., 2010 (37) X X X X 4 High
Eriksson et al., 2010 (45) X X X 2 High
Gaylis et al., 2017 (46) X X 2 High
Kim and Mallo, 2019 (47) X X X 3 High
LaRowe et al., 2007 (48) X X X X X 5 High
Mazahery et al., 2018 (49) X X X 3 High
Milla Tobarra et al., 2014 (50)  — X X 2 High
Nelson et al., 2004 (51) X X X X X 5 High
Nilsen et al., 2017 (52) X X X X 4 High
O'Connor et al., 2006 (53) X X X X 4 High
Papandreou et al., 2013 (54) X X X X X 5 High
Ruxton et al., 1996 (55) X X X 3 High
Schroeder et al., 2014 (56) X X X X 4 High
Tovar et al., 2012 (57) X X X X 4 High
Vanderhout et al., 2016 (58) X X X X 4 High
Total low risk (out of 20) 0
Prospective cohort studies (n = 8)
Berkey et al., 2005 (59) X X XX X X 6 High
Bigornia et al., 2014 (60) X X X X X X 6 High
DeBoer et al., 2015 (36) X X X X X 5 High
Dubois et al., 2016 (61) X X X X X 5 High
Huh et al., 2010 (62) X X X XX X X 7 Low
Noel et al., 2011 (63) X X X X X X 6 High
Scharf et al., 2013 (38) X X X X X X 6 High
Wosje et al., 2001 (40) X X X X X 5 High
Total low risk (out of 8) 1

1Each study can be awarded a maximum of 1 X for each numbered item within the Selection and Exposure categories. A maximum of 2 Xs can be given for Comparability. Two Xs were awarded if studies accounted for volume of milk consumed, prior weight status (birth weight for cross-sectional studies), and parent BMI. One X was awarded for adjusting for ≥4 other covariates. By design, cross-sectional studies were considered unable to achieve comparable cohorts; a maximum of 1 X could only be awarded. The original NOS uses stars, which were replaced with Xs for ease of visual interpretation. We specified follow-up time to be adequate if study duration was >1 y. If participants who were missing/lost to follow-up were not reported, no X was allocated. As per NOS guidelines, studies were considered low risk of bias if they received ≥7 Xs (28). NOS, Newcastle–Ottawa Scale.

Statistical analysis

For each study, participant information, design, and results were summarized. We derived crude ORs and extracted adjusted ORs, whenever available, for overweight or obesity among children who consumed whole (3.25%) milk, compared with children who consumed reduced-fat (0.1–2%) milk regularly. A random effects model based on the restricted maximum likelihood estimator was decided a priori and used to separately pool crude and adjusted ORs of overweight or obesity. Each study was included as a random effect to account for between-study variation in this model. Sensitivity analyses were performed using the Knapp–Hartung method (29) and inverse-variance weights. Because prospective cohort studies can reveal different relations than cross-sectional studies, we performed a subgroup analysis according to study design. Additionally, we analyzed studies in subgroups according to risk of bias (high compared with low) and age (1–5 y, 6–11 y, and 12–18 y). Subgroup analyses were accompanied by tests for interaction between each subgroup and the main effect from the random-effects meta-regression, by using an interaction term in metaregression models for study design (cross-sectional compared with prospective cohort), risk of bias (high compared with low), and age group (1–5 y, 6–11 y, and 12–18 y). Heterogeneity across included studies was estimated using the I2 statistic (30). Heterogeneity was considered low (<40%), moderate (40–60%), or high (>60%) (31). Publication bias was assessed using a funnel plot and Egger test (32).

Finally, we conducted a dose–response metaregression to quantify the association between percentage of fat in cow-milk consumed and the odds of overweight or obesity. Only studies that reported group-specific odds for ≥3 types of cow-milk fat were included in this analysis. For the dose–response analysis, we first used a fixed-effect approach to estimate the dose–response relations within each study. Then, we used a random-effects approach to combine across studies the dose–response estimates that were generated in the first step for each study (33) to obtain regression coefficients, and their respective standard errors. R software version 3.2.2 (34) was used for all analyses, using the “metafor” package (35).

Results

The database search identified 5862 potentially eligible studies. After exclusion of duplicates (n = 1861), 4001 reports underwent title and abstract review. Studies that did not meet inclusion criteria (n = 3915) were removed resulting in 86 published studies that underwent full text review (Figure 1). Reasons for exclusion included wrong exposure, wrong outcome, wrong patient population, dietary pattern analysis only, or wrong study design such as case reports or editorials. Twenty-eight studies met all inclusion criteria. Of these, 20 were cross-sectional and 8 were prospective cohort studies (see Table 1 for study characteristics). No interventional studies were identified. Most studies (n = 23) compared consumption of whole milk (3.25% fat) with reduced-fat milk (0.1%, 1%, or 2% fat). Four studies (36–39) compared whole and 2% milk with 1% and skim milk. One study compared whole milk with 2% milk (40).

FIGURE 1.

FIGURE 1

Systematic review study selection process.

TABLE 1.

Data summary1

Cross-sectional studies
Author, year No. of children; age range; location Exposure; method Outcome Variables adjusted for Adjusted result P value
Acharya et al., 2011 (41) 770; 3–5 y; USA Frequency of low- or high-fat milk intake; 24-h recall and FFQ with trained interviewers zBMI (CDC) Energy intake Reduced-fat milk was positively associated with 0.52 (95% CI: 0.29, 0.75) higher zBMI. Children who consumed reduced-fat milk were more likely to be OB (OR = 2.98; 95% CI: 1.46, 6.05) 0.03
Barba et al., 2005* (42) 884; 3–11 y; Italy Frequency of milk consumption by milk fat content; parent-completed questionnaire zBMI (IOTF) Age, birth weight, parental OW/OB, parental education level, physical activity, frequency of consumption of the other groups of foods (dairy foods, fish, cereals, meat, fruit, vegetables, sweet beverages, snacks) Whole milk was associated with 0.112 lower zBMI (95% CI: −0.19, −0.33). Children who consumed whole milk least often were more likely to be OW than those who consumed it most often (OR = 2.18; 95% CI: 1.30, 3.66) 0.005
Barbiero et al., 2008* (43) 405; 10–18 y; Brazil OW/OB (WHO) Dietary habits, food intake by parent-completed questionnaire None Reduced-fat milk greater among children with OB Whole milk: normal-weight 91.7%, OW 89.7%, OB 61.1% Skimmed milk: normal-weight 8.3%, OW 10.3%, OB 38.9% 0.08
Beck et al., 2017* (44) 135; 3 y; USA Milk fat; 24-h recall by trained research assistant OW/OB (CDC) Gender, maternal BMI, maternal education, maternal marital status, mother's preferred language, and mother's total years in the USA Children with severe OB had a lower intake of cow-milk fat and were more likely to consume skim (0.1%) milk (OR = 0.89; 95% CI: 0.81, 0.97) 0.01
Charvet and Huffman, 2019* (39) 197; 3–4 y; USA Beverage intake, measured using a nutrition and sociodemographic characteristics questionnaire BMI percentile (CDC), measured by trained Women, Infants, and Children staff None A higher proportion of children with OW or OB consumed reduced-fat cow-milk than children with underweight or normal weight 0.014
Dodd et al., 2013* (37) 2314; 6–18 y; USA Weight status (OW/OB), measured by field interviewers using standardized procedures (CDC) Beverage consumption, child- and parent-completed 24-h recall interviews NR No significant differences in cow-milk fat and weight status. Normal-weight elementary and middle-school children were more likely to consume 2%/whole milk. Among high-school children, OW/OB children were more likely to consume reduced-fat milk (effect sizes NR) NR
Eriksson and Strandvik, 2010 (45) 114; 8 y; Sweden Food intake, parent- and child-completed 24-h recall with registered dietitian BMI (IOTF) None Children who never/seldom consumed whole milk had a mean BMI of 17.7, whereas children who consumed 1 serving/d of whole milk had a mean BMI = 16.2, >1 serving/d mean BMI = 15.4. Overall difference of 2.3 BMI BMI, <0.001
Gaylis et al., 2017* (46) 598; 13–19 y; USA Self-reported BMI, categorized into healthy, OW, OB (CDC) Frequency of whole and low-fat milk consumption, child-completed FFQ None No difference in cow-milk fat intake between weight categories (effect size NR) NR
Kim and Mallo, 2019 (47) 529; 3–4 y; USA BMI percentile (CDC), measured by trained Women, Infants, and Children staff Cow-milk fat consumed, assessed during telephone interview None A higher proportion of children with OW or OB consumed reduced-fat cow-milk than children with normal weight <0.01
LaRowe et al., 2007 (48) 1334; 2–11 y; USA Beverage intake patterns, interview by caregiver BMI (CDC) Age, sex, ethnicity, household income, Healthy Eating Index score, physical activity, birth weight Among children aged 6–11 y, those who consumed whole milk had lowest BMI and higher healthy eating scores. BMI was significantly higher in the water, sweetened drinks, and soda patterns (adjusted mean BMI = 19.9, 18.7, and 18.7, respectively) compared with the mix/light and whole-milk patterns (adjusted mean BMI = 18.2 and 17.8, respectively) (P < 0.05) BMI, <0.05; >85th percentile (both age groups), <0 0.0001
Proportion of children aged 6–11 y with OW/OB: whole milk 22.1%, soda 35.2%, mix/light drinker 28%, water 42.6%, sweetened drinks 35.4%
Proportion of children aged 2–5 y with OW/OB: whole milk 26.9%, mix/light drinker 15.0%, water 25.8%, fruit juice 19.6%
In children aged 2–5 y, no significant association between milk fat content and BMI (effect size NR)
Mazahery et al., 2018* (49) 1155; 2–4 y; New Zealand Frequency and fat content of milk consumption (questionnaire) BMI, measured by trained testers (IOTF) NR Higher odds of consuming reduced-fat milk among OW/OB (OR = 1.74; 95% CI: 1.20, 2.54 for OW; OR = 1.48; 95% CI: 0.73, 3.01 for OB), compared with normal-weight children OW, <0.05; OB, >0.05
Milla Tobarra et al., 2014 (50) 373; 9–11 y; Spain Beverage intake, child-completed 24-h recall BMI (IOTF) Age, cardiovascular fitness OW/OB children were less likely to drink whole milk than thin or normal weight children Girls, 0.002; boys, 0.043
Thin girls consumed a mean 2.9 mL/kg/d more whole milk than OW/OB girls; thin boys 2.8 mL/kg/d more whole milk than OW/OB boys
Nelson et al., 2004* (51) 451; 2–4 y; USA BMI, measured by a medical provider (CDC) Nutrition and sociodemographic characteristics Race/ethnicity, age, sex, birthplace of the parent, fat content of milk consumed by children in family, fruit/vegetable consumption, exercise Children who consumed whole milk were less likely (OR = 0.50; 95% CI: 0.31, 0.80) to be OW/OB <0.01
Nilsen et al., 2017* (52) 2104; 7–9 y; Sweden Food and beverage intake frequency, parent-completed questionnaire OW/OB (WHO) Gender, parental weight status, parents’ education level and area of living Odds of being OW/OB were higher among those who consumed reduced-fat milk (OR = 1.90; 95% CI: 1.40, 2.48) compared with those who consumed whole milk. Inverse association between odds of OW/OB and whole milk consumption (OR = 0.60; 95% CI: 0.39, 0.78) 0.001
O'Connor et al., 2006 (53) 1160; 2–5 y; USA Beverage consumption, parent-completed 24-h recall interview BMI percentile Age, ethnicity, gender, income, energy consumed, physical activity No significant association between cow-milk fat and weight status (effect size NR) NR
Papandreou et al., 2013 (54) 607; 7–15 y; Greece Beverage intake 24-h recall × 3 d by registered dietitian BMI, OW/OB (IOTF) Age, gender, income, energy intake, physical activity Cow-milk fat was not significantly associated with weight status (effect size NR) NR
Ruxton et al., 1996 (55) 136; 7–8 y; Scotland Milk intake, 7-d food record by parents zBMI NR No significant relation between fat content or volume of milk and anthropometry or growth (effect size NR) NR
Schroeder et al., 2014 (56) 1149; 10–18 y; Spain Beverage consumption, 24-h recall by child zBMI Age, energy underreporting, mother's educational level, physical activity, television viewing, energy intake Comparison between reduced-fat and whole milk on zBMI not significant. For boys, OR = 1.21; 95% CI: 0.95, 1.56; for girls, OR = 10.4; 95% CI: 0.79, 1.37 for higher zBMI Boys, 0.199; girls, 0.792
Tovar et al., 2012* (57) 217; 6–11 y; USA OW and OB prevalence (CDC) Diet quality, parent completed questionnaire Age, gender, race/ethnicity, state of residence, number of members in the household, family government assistance OW (OR = 0.90; 95% CI: 0.40, 1.80) and OB children less likely (OR = 0.40; 95% CI: 0.20, 0.70) to consume whole milk than normal-weight children OW, 0.80; OB, 0.001
Vanderhout et al., 2016* (58) 2738; 1–5 y; Canada Milk fat content consumed, parent-completed FFQ zBMI (WHO) Age, sex, vitamin D supplementation, minutes per day of both outdoor free play and screen time, milk and SSB volume consumed daily, maternal BMI, skin pigmentation, family income, maternal ethnicity, date Participants who consumed whole milk had 0.72 (95% CI: 0.68, 0.76) lower zBMI score than children who consumed reduced-fat milk <0.0001
Prospective cohort studies
Author, year No. of children; age range; location Duration Exposure Outcome Variables adjusted for Adjusted result P value
Berkey et al., 2005 (59) 12,829; 9–14 y; USA 3 y Dietary intake, self-administered FFQ BMI (CDC) Prior-year BMI z-score, physical activity and inactivity, race or ethnicity, sex, age and maturational stage, height growth Among boys, 0.027 higher BMI (95% CI: 0.002, 0.053) with every daily serving of 1% milk, and girls 0.021 higher BMI per daily serving of reduced-fat milk (95% CI: 0.001, 0.04). BMI gains among children who consumed whole milk were nonsignificant. Dairy fat (cheese, butter, etc.) was nonsignificantly associated with BMI (effect NR) <0.05, dairy fat NR
Bigornia et al., 2014* (60) 2282; 10–13 y; UK 3 y Dairy fat, parent-assisted 3-d food records Body fat %, BMI (IOTF) Sex, volume of dairy intake, age, height, maternal education, maternal OW status, physical activity, pubertal stage, dieting at follow-up, baseline intakes of cereal, total fat, total protein, fiber, 100% fruit juice, fruit and vegetables, SSBs, dietary reporting errors at follow-up Children who consumed the most whole-fat dairy compared with the least whole-fat dairy at age 10 and 13 had the lowest risk of excess fat mass (OR = 0.64; 95% CI: 0.41, 1.00), and a lower risk of OW (OR = 0.65; 95% CI: 0.40, 1.06) at age 13 Fat mass, 0.03; OW, 0.24; BMI gains, <0 0.01. Reduced fat NR
High vs. low whole-fat dairy consumption also had the smallest gains in BMI: 2.5 kg/m2 (95% CI: 2.2, 2.7) vs. 2.8 kg/m2 (95% CI: 2.5, 3.0). Reduced-fat dairy associations with adiposity were nonsignificant
DeBoer et al., 2015 (36) 8950; 4–5 y; USA 1 y Volume and fat content of milk, parent online interview zBMI (CDC) Sex, race/ethnicity, SES Every 1% increase in milk fat was associated with 0.176 (95% CI: −0.197, −0.155) lower zBMI among 4-y-olds and 0.139 lower zBMI (95% CI: −0.173, −0.105) among 5-y-olds <0.001
DuBois et al., 2016 (61) 304; 9–14 y; Canada 5 y Dietary intake, 2 × 24-h recalls by parent and child with registered dietitian BMI (IOTF) Each twin served to balance characteristics of other twin Heavier boy twins consumed more whole milk and alternatives than their leaner twin; heavier girl twins consumed less whole milk than their leaner twin. Reduced-fat milk consumption among girls was associated with a 0.32 higher BMI from age 9 to 14 y; whole milk did not have a significant relation with BMI <0.05
Huh et al., 2010* (62) 852; 2–3 y; USA 1 y Volume and fat content of milk consumed, parent-completed FFQ zBMI (CDC) Age, sex, race/ethnicity, energy intake, nondairy beverage intake, TV viewing, maternal BMI and education; paternal BMI, 2-y zBMI Higher intake of whole milk at age 2 y associated with −0.09 unit per daily serving, (95% CI: −0.16, −0.01) lower zBMI at age 3 y zBMI, 0.02 OR for OW: whole milk, 0.84; 1%/skim, 0.83
Cow-milk fat intake not related to OW, ORs for OW at age 3 were 1.04 (95% CI: 0.74, 1.44) for whole milk, 0.91 (95% CI: 0.20, 1.34) for 2% milk, and 0.95 (95% CI: 0.58, 1.55) for 1%/skim milk
Noel et al., 2011 (63) 2245; 10–13 y; UK 3 y Milk fat, parent- and child- completed 3-d food records Body fat % Age, sex, height, physical activity, pubertal status, maternal BMI, maternal education, dietary intakes of total fat, ready-to-eat breakfast cereal, 100% fruit juice, and SSB intake, calcium, total energy intake, metabolic rate At age 13, per daily serving of whole milk, a 1.32% lower body fat (95% CI: −2.36, −0.27) was seen. Longitudinal relations were nonsignificant 0.01
Scharf et al., 2013 (38) 8350; 2–4 y; USA 2 y Milk fat, parent-completed online questionnaire zBMI (CDC) Sex, race, SES, juice and SSB intake, number of glasses of milk daily, maternal BMI Children who consumed reduced-fat (skim/1%) milk had higher odds of OW (age 2 OR = 1.64; 95% CI: 1.32, 2.03; age 4 OR = 1.63; 95% CI: 1.23, 1.86) or OB (age 2 OR = 1.57; 95% CI: 1.03, 2.42; age 4 OR = 1.64; 95% CI: 1.04, 2.60) than those consuming whole/2% milk. Children who were normal weight at age 2 who consumed skim/1% milk more likely to become OW/OB at age 4 (OR = 1.57; 95% CI: 1.03, 2.42) OW age 2, 4, OB age 4: <0 0.0001; OW age 4: 0.002; becoming OW/OB age 4: 0.04
Wosje et al., 2001 (40) 51; 1–2 y; USA 1 y Milk fat consumption at 12, 18, and 24 mo, 3-d food record, parent completed Weight, body fat change NR No difference in weight or body fat at 12, 18, or 24 mo, or changes in anthropometry between children consuming reduced-fat or whole milk (effect sizes NR) NR

1Adiposity outcomes, where reported, were standardized according to WHO, CDC, or IOTF (International Obesity Task Force). *Studies included in the meta-analysis. NR, not reported, OB, obesity, defined as >95th percentile for BMI and >2 for zBMI (64); OW, overweight, defined by >85th percentile for BMI or >1 for zBMI; SES, socioeconomic status; SSB, sugar-sweetened beverage; zBMI, BMI z-score.

Nineteen studies used zBMI, 4 prospective cohort studies used percentage body fat change, and 5 studies used overweight or obesity categories as the primary adiposity outcome. Three studies used 2008 WHO (23) growth standards, 14 studies used 2000 CDC (24) growth standards, 7 used 2000 IOTF (25) growth standards, and 4 studies either did not specify or used other standards for zBMI measurement.

Eighteen (36, 38, 39, 41–45, 47–49, 51, 52, 57, 58, 60, 63, 65) studies reported that higher cow-milk fat was associated with lower child adiposity. Ten studies (37, 40, 46, 50, 53–56, 59, 61) reported no association between cow-milk fat and child adiposity.

Risk-of-bias assessment

Risk of bias assessed using the NOS suggested that 1 of 8 prospective cohort studies and 0 of 20 cross-sectional studies were low risk of bias (Table 2). Common limitations that increased risk of bias included cross-sectional study design, nonstandardized dietary assessments that were either study specific or not validated, lack of adjustment for clinically important covariates (including volume of milk consumed, parent BMI, and child adiposity assessed prior to the outcome), and study duration too short to detect a meaningful change in adiposity (defined a priori as 1 y) (66).

Association between cow-milk fat and child overweight or obesity

Fourteen (38,42–44,46,47,49, 51,52, 57,58, 60, 62, 65) studies met the meta-analysis inclusion criteria; 11 were cross-sectional and 3 were prospective cohort studies. All studies included in the meta-analysis compared whole (3.25% fat) milk with reduced-fat (0.1–2%) milk consumption, allowing an OR to be calculated. A total of 20,897 healthy children aged 1–18 y were included in the meta-analysis. Children were from 7 countries (United States, United Kingdom, Canada, Brazil, Sweden, New Zealand, and Italy). Anthropometric standards used to determine overweight or obesity categories included the WHO (23), CDC (24), or IOTF (25) growth standards in 6, 5, and 3 studies respectively.

Crude analysis of all 14 studies revealed that among children who consumed whole milk compared with reduced-fat milk, the pooled OR for overweight or obesity was 0.61 (95% CI: 0.52, 0.72; P < 0.0001) (Figure 2). Heterogeneity measured by the I2 statistic was 73.8% (P < 0.0001). A sensitivity analysis using inverse-variance weights did not reveal different results. Subgroup analysis by study design revealed no significant interaction between cross-sectional and prospective cohort studies (P = 0.07; Supplemental Table 2). For the 11 cross-sectional studies (n = 9413), the pooled OR of overweight or obesity was 0.56 (95% CI: 0.46, 0.69; P = 0.0001), and for the 3 prospective cohort studies (n = 11,484) it was 0.76 (95% CI: 0.63, 0.92; P = 0.006). Risk of bias (high compared with low) and age group were also not significant modifiers of the relation between cow-milk fat and child adiposity (Supplemental Table 2 and Supplemental Figures 1–5). Analyses of 5 studies (49, 51, 52, 57, 58) that reported adjusted ORs did not show differences between crude and adjusted estimates (adjusted OR: 0.53; 95% CI: 0.44, 0.63; crude OR: 0.55; 95% CI: 0.46, 0.66); see Supplemental Figure 6. Results of the sensitivity analysis using the Knapp–Hartung method (29) to pool the 14 studies (crude OR: 0.62; 95% CI: 0.52, 0.73) were similar to the main results (crude OR: 0.61; 95% CI: 0.52, 0.72)). Publication bias, visualized using a funnel plot (Supplemental Figure 7), was difficult to ascertain given the high heterogeneity (I2 = 73.8%) and relatively low number of included studies.

FIGURE 2.

FIGURE 2

Crude OR of overweight/obesity comparing children consuming whole milk with children consuming reduced-fat milk. (A) Cross-sectional studies only; (B) prospective cohort studies only. Pooled effects were determined using random effects models; I2 = 73.8%. P values for pooled ORs: cross-sectional studies P < 0.0001; prospective cohort studies P = 0.006.

The dose–response meta-analysis results are shown in Figure 3. Data were available from 7 studies (38, 39, 44,52, 57, 58, 65) which included 14,582 children aged 2 to 11 y, and demonstrated a linear association between higher cow-milk fat and lower child adiposity. For each 1% higher cow-milk fat consumed, the overall crude OR for overweight or obesity was 0.75 (95% CI: 0.65, 0.87; P = 0.004; τ2 = 0.01; I2 = 64%).

FIGURE 3.

FIGURE 3

Dose–response relation between cow-milk fat and odds of overweight or obesity. Seven studies provided data on 14,582 participants and were included in this analysis. Each circle represents a group of participants in each study consuming different concentrations of cow-milk fat. The size of the circles represents the inverse of the variance of the group-specific log odds. P value is derived from a dose–response metaregression with an OR of 0.75 (95% CI: 0.65, 0.87; τ2 = 0.010; I2 = 64%).

Discussion

This systematic review and meta-analysis has identified that relative to reduced-fat cow-milk, whole-fat cow-milk consumption was associated with lower odds of childhood overweight or obesity. The direction of the association was consistent across a range of study designs, settings, and age groups and demonstrated a dose effect. Although no clinical trials were identified, existing observational research suggests that consumption of whole milk compared with reduced-fat milk does not adversely affect body weight or body composition among children and adolescents. To the contrary, higher milk fat consumption appears to be associated with lower odds of childhood overweight or obesity.

Findings from the present study suggest that cow-milk fat, which has not been examined in previous meta-analyses, could play a role in the development of childhood overweight or obesity. Several mechanisms have been proposed that might explain why higher cow-milk fat consumption could result in lower childhood adiposity. One theory involves the replacement of calories from less healthy foods, such as sugar-sweetened beverages, with cow-milk fat (67). Consumption of beverages high in added sugar has been associated with increased risk of overweight and obesity during childhood (68). Other theories involve satiety mechanisms such that higher milk fat consumption might induce satiety through the release of cholecystokinin and glucagon-like peptide 1 (69, 70) thereby reducing desire for other calorically dense foods. Another possibility is that lower satiety from reduced-fat milk could result in increased milk consumption causing higher weight gain relative to children who consume whole milk, as observed in the study by Berkey et al. (59).

Cow-milk fat might offer cardiometabolic benefits. The types of fat found in cow-milk, including trans-palmitoleic acid, could be metabolically protective. Higher circulating trans-palmitoleic acid has been associated with lower adiposity, serum LDL cholesterol and triglyceride concentrations, and insulin resistance, and higher HDL cholesterol in several large adult cohort studies (71–73). However, diets that replace dairy fat with unsaturated fatty acids might also offer cardiometabolic protection (74, 75)

Confounding by indication and reverse causality (76) are plausible alternate explanations. Parents of children who have lower adiposity might choose higher-fat milk to increase weight gain. Similarly, parents of children who have higher adiposity might choose lower-fat milk to reduce the risk of overweight or obesity (44, 48). The majority of children included in this systematic review were involved in prospective cohort studies, in which the potential for reverse causality is lower than in cross-sectional studies. Results from these 11,484 children were consistent with the overall findings. Two of the included prospective cohort studies (59, 62) attempted to address confounding by indication by adjusting for baseline BMI; 1 of these repeated the statistical analysis only among participants with normal-weight BMI values, with similar findings (62). Clinical trial data would have provided better evidence for the directionality of this relation; however, none were available.

This study had a number of strengths. The meta-analysis included a large, diverse sample of children from around the world. The number of potentially eligible studies was maximized by the comprehensive search strategy and contact with authors to obtain missing data. Also, study selection, data collection, and risk of bias assessment were performed by 2 independent reviewers, which improved accuracy and consistency. All studies included in the meta-analysis used trained individuals to obtain anthropometric measurements, and weight status was standardized using growth reference standards (WHO, CDC, and IOTF). Using metaregression techniques, differences in study design, risk of bias, and age group were taken into account. Finally, a dose–response meta-analysis was conducted, which demonstrated a linear relation between higher cow-milk fat and lower child adiposity (Figure 3).

This study had a number of limitations. First, included studies were all observational. Only 1 study in this analysis was considered to have low risk of bias, and all studies in the meta-analysis had high risk of bias. Risk of bias included cross-sectional designs and lack of adjustment for clinically important covariates. For example, cow-milk volume was accounted for in only 11 of 28 studies in the systematic review, and in 5 of 14 studies in the meta-analysis. Adjustment for volume in future studies would allow for a clearer understanding of whether higher cow-milk fat protects against higher adiposity, or reduced-fat cow-milk increases adiposity. However, among these studies, comparison of adjusted compared with crude odds demonstrated consistent findings. Residual confounding by variables not accounted for in the individual analyses is also possible; this is a common limitation for meta-analyses of observational studies. Heterogeneity was relatively high (I2 = 73.8%), which might have been attributable to a variety of factors including varied methods of ascertainment of exposure and outcome, and differences in study design and follow-up duration. Although subgroup analyses of prospective cohort studies revealed results comparable to the overall metaregression, these comparisons might not have had sufficient power to detect clinically meaningful differences. However, 11,484 children were involved in prospective cohort studies making large differences in effect size unlikely. Although only studies with standardized dietary measurements were included, measurement error was possible due to recall bias or lack of validation of dietary assessment tool. Error in adiposity measurement could also have introduced bias, although weights and heights were measured by trained individuals and standardized protocols were used in all studies included in the meta-analysis. Differences in adiposity measurement (i.e., body fat percentage, zBMI, BMI), and different growth standards could have contributed to heterogeneity. For example, use of the WHO rather than IOTF or CDC standards could have resulted in a greater proportion of overweight or obese children being reported (77). Future studies using WHO growth standards, which are believed to represent optimal child growth (23), would help to minimize heterogeneity and overcome these limitations. Consideration for relevant outcomes such as cardiovascular risk should be included in future analyses to understand other effects of cow-milk fat. Publication bias was also possible as demonstrated by a funnel plot and Egger test.

In conclusion, observational evidence supports that children who consume whole milk compared with reduced-fat milk have lower odds of overweight or obesity. Given that the majority of children in North America consume cow-milk on a daily basis, clinical trial data and well-designed prospective cohort studies involving large, diverse samples, using standardized exposure and outcome measurements, and with long study duration would help determine whether the observed association between higher milk fat consumption and lower childhood adiposity is causal.

Supplementary Material

nqz276_Supplemental_File

ACKNOWLEDGEMENTS

The authors’ responsibilities were as follows—SMV, JLM: conceptualized and designed the research study, performed initial statistical analyses, drafted the manuscript, approved the final manuscript as submitted, had full access to all the data in the study, and took responsibility for the integrity of the data and the accuracy of the data analysis; NT: developed and implemented the systematic review search strategy, generating the initial search results; MA, SMV: independently reviewed study titles, abstracts, and full texts to determine included studies, performed data extraction, and evaluated each study for risk of bias; CB, DO: assisted in refining the study design, reviewed and revised the manuscript, and approved the final manuscript as submitted; KT, BD, PJ: reviewed and revised statistical analysis as well as the manuscript, and approved the final manuscript as submitted; and all authors: read and approved the final manuscript. Author Disclosures: JLM received an unrestricted research grant for a completed investigator-initiated study from the Dairy Farmers of Canada (2011–2012), and Ddrops provided nonfinancial support (vitamin D supplements) for an investigator-initiated study on vitamin D and respiratory tract infections (2011–2015). All other authors report no conflicts of interest.

Notes

Funding was provided by the Canadian Institutes of Health Research (CIHR) Institute of Human Development, Child and Youth Health (grant number MOP-333560). The funding agency had no role in study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.

Abbreviations used: IOTF, International Obesity Task Force; NOS, Newcastle–Ottawa Scale; zBMI, body mass index z-score.

Supplemental Methods, Supplemental Tables 1 and 2, and Supplemental Figures 1–7 are available from the “Supplementary data” link in the online posting of the article and from the same link in the online table of contents at https://academic.oup.com/ajcn/.

References

  • 1. Ogden C, Carroll M. Prevalence of obesity among children and adolescents: United States, trends 1963–1965 through 2007–2008. Atlanta, GA: Centers for Disease Control and Prevention; 2010. [Google Scholar]
  • 2. NCD Risk Factor Collaboration. Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults. Lancet. 2017;390(10113):2627–42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Childhood obesity facts [Internet]. Atlanta, GA: Centers for Disease Control and Prevention; 2015; [date cited: 2019]. Available from: http://www.cdc.gov/healthyschools/obesity/facts.htm. [Google Scholar]
  • 4. Stewart H, Dong D, Carlson A. Why are Americans consuming less fluid milk? A look at generational differences in intake frequency. Washington, DC: United States Department of Agriculture; 2013. Contract No. 149. [Google Scholar]
  • 5. Gidding SS, Dennison BA, Birch LL, Daniels SR, Gillman MW, Lichtenstein AH, Rattay KT, Steinberger J, Stettler N, Van Horn L et al.. Dietary recommendations for children and adolescents: a guide for practitioners. Pediatrics. 2006;117(2):544–59. [DOI] [PubMed] [Google Scholar]
  • 6. Caring for Kids. Feeding your baby in the first year [Internet]. Ottawa: Canadian Pediatric Society; 2014; [updated 2019]. Available from: http://www.caringforkids.cps.ca/handouts/feeding_your_baby_in_the_first_year. [Google Scholar]
  • 7. Food-based dietary guidelines in the WHO European region [Internet]. Copenhagen: WHO; 2003; [cited 2019]. Available from: http://www.euro.who.int/en/health-topics/disease-prevention/nutrition/publications/technical-documents/dietary-recommendations-and-nutritional-requirements/food-based-dietary-guidelines-in-the-who-european-region. [Google Scholar]
  • 8. What to feed young children [Internet]. United Kingdom: National Health Service; 2016; [cited 2019]. Available from: https://www.nhs.uk/conditions/pregnancy-and-baby/understanding-food-groups/#milk-and-dairy-products. [Google Scholar]
  • 9. Department of Health and Aging. Infant feeding guidelines. Canberra; Government of Australia; 2013. [Google Scholar]
  • 10. Rourke L, Godwin M, Rourke J, Pearce S, Bean J. The Rourke Baby Record Infant/Child Maintenance Guide: do doctors use it, do they find it useful, and does using it improve their well-baby visit records?. BMC Fam Pract. 2009;10:28. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Danyliw AD, Vatanparast H, Nikpartow N, Whiting SJ. Beverage patterns among Canadian children and relationship to overweight and obesity. Appl Physiol Nutr Metab. 2012;37(5):900–6. [DOI] [PubMed] [Google Scholar]
  • 12. Ministry of Child and Youth Services. Student nutrition program nutrition guidelines. Ontario; Government of Ontario; 2016. [Google Scholar]
  • 13. Policy position statement on school nutrition [Internet]. Washington, DC; American Heart Association; 2013; [cited 2019] Available from: https://www.yourethecure.org. [Google Scholar]
  • 14. Lucas PJ, Patterson E, Sacks G, Billich N, Evans CEL. Preschool and school meal policies: an overview of what we know about regulation, implementation, and impact on diet in the UK, Sweden, and Australia. Nutrients. 2017;9(7):E736. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Bentley J. Trends in U.S. per capita consumption of dairy products, 1970–2012. Washington, DC: United States Department of Agriculture Economic Research Service; 2014; [cited 2019] Available from: https://www.ers.usda.gov/amber-waves/2014/june/trends-in-us-per-capita-consumption-of-dairy-products-1970-2012/. [Google Scholar]
  • 16. St. Pierre M. Changes in Canadians’ preferences for milk and dairy products. Ottawa: Statistics Canada; 2017; [cited 2019] Available from: https://www.statcan.gc.ca. [Google Scholar]
  • 17. Garriguet D. Beverage consumption of children and teens. Ottawa: Statistics Canada; 2008. Contract No. 4. [PubMed] [Google Scholar]
  • 18. Grimes CA, Szymlek-Gay EA, Nicklas TA. Beverage consumption among U.S. children aged 0–24 months: National Health and Nutrition Examination Survey (NHANES). Nutrients. 2017;9(3):E264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Kouvelioti R, Josse AR, Klentrou P. Effects of dairy consumption on body composition and bone properties in youth: a systematic review. Curr Dev Nutr. 2017;1(8):e001214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. de Beer H. Dairy products and physical stature: a systematic review and meta-analysis of controlled trials. Econ Hum Biol. 2012;10(3):299–309. [DOI] [PubMed] [Google Scholar]
  • 21. Dror DK, Allen LH. Dairy product intake in children and adolescents in developed countries: trends, nutritional contribution, and a review of association with health outcomes. Nutr Rev. 2014;72(2):68–81. [DOI] [PubMed] [Google Scholar]
  • 22. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group . Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336–41. [DOI] [PubMed] [Google Scholar]
  • 23. WHO. WHO child growth standards: methods and development. Geneva: WHO; 2006. [Google Scholar]
  • 24. National Center for Chronic Disease Prevention and Health Promotion. Body mass index-for-age percentiles. Hyattsville, MD: National Center for Health Statistics; 2000. [Google Scholar]
  • 25. Cole TJ, Bellizzi MC, Flegal KM, Dietz WH. Establishing a standard definition for child overweight and obesity worldwide: international survey. Br Med J. 2000;320(7244):1240–3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Sambunjak D, Cumpston M, Watts C. Module 4: selecting studies and collecting data [Internet]. Cochrane Interactive Learning. The Cochrane Collaboration; 2017; [cited 2019]. Available from: https://training.cochrane.org/interactivelearning/module-4-selecting-studies-and-collecting-data. [Google Scholar]
  • 27. Covidence Software Platform. Melbourne: Veritas Health Innovation; Available from: https://www.covidence.org. [Google Scholar]
  • 28. Wells GA, Shea B, O'Connell D, Peterson J, Welch V. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. Ottawa: The Ottawa Hospital; 2011 [cited 2019]. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. [Google Scholar]
  • 29. Hartung J, Knapp G. A refined method for the meta-analysis of controlled clinical trials with binary outcome. Stat Med. 2001;20(24):3875–89. [DOI] [PubMed] [Google Scholar]
  • 30. Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58. [DOI] [PubMed] [Google Scholar]
  • 31. Cochrane Handbook for Systematic Reviews of Interventions, version 5.1.0.Higgins JG Green S.(eds). The Cochrane Collaboration;2011. [Google Scholar]
  • 32. Cochrane Handbook for Systematic Reviews of Interventions, 10.4.3.1 Recommendations on testing for funnel plot asymmetry.Higgins JG Green S.(eds). The Cochrane Collaboration; 2011. [Google Scholar]
  • 33. Thompson SG, Higgins JP. How should meta-regression analyses be undertaken and interpreted?. Stat Med. 2002;21(11):1559–73. [DOI] [PubMed] [Google Scholar]
  • 34.R Core Team. R: A Language and Environment for Statistical Computing. Vienna: R foundation for Statistical Computing; 2018. [Google Scholar]
  • 35. Viechtbauer W. The metafor package. A meta-analysis package for R [Internet]. Available from: http://www.metafor-project.org/doku.php. [Google Scholar]
  • 36. DeBoer MD, Agard HE, Scharf RJ. Milk intake, height and body mass index in preschool children. Arch Dis Child. 2015;100(5):460–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Dodd AH, Briefel R, Cabili C, Wilson A, Crepinsek MK. Disparities in consumption of sugar-sweetened and other beverages by race/ethnicity and obesity status among United States schoolchildren. J Nutr Educ Behav. 2013;45(3):240–9. [DOI] [PubMed] [Google Scholar]
  • 38. Scharf RJ, Demmer RT, DeBoer MD. Longitudinal evaluation of milk type consumed and weight status in preschoolers. Arch Dis Child. 2013;98:335–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Charvet A, Huffman FG. Beverage intake and its effect on body weight status among WIC preschool-age children. J Obes. 2019;2019:3032457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Wosje KS, Specker BL, Giddens J. No differences in growth or body composition from age 12 to 24 months between toddlers consuming 2% milk and toddlers consuming whole milk. J Am Diet Assoc. 2001;101(1):53–6. [DOI] [PubMed] [Google Scholar]
  • 41. Acharya K, Feese M, Franklin F, Kabagambe EK. Body mass index and dietary intake among Head Start children and caregivers. J Am Diet Assoc. 2011;111(9):1314–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42. Barba G, Troiano E, Russo P, Venezia A, Siani A. Inverse association between body mass and frequency of milk consumption in children. Br J Nutr. 2005;93(1):15–19. [DOI] [PubMed] [Google Scholar]
  • 43. Barbiero SM, Pellanda LC, Cesa CC, Campagnolo P, Beltrami F, Abrantes CC. Overweight, obesity and other risk factors for IHD in Brazilian schoolchildren. Public Health Nutr. 2008;12(5):710–15. [DOI] [PubMed] [Google Scholar]
  • 44. Beck AL, Heyman M, Chao C, Wojcicki J. Full fat milk consumption protects against severe childhood obesity in Latinos. Prev Med Rep. 2017;8:1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Eriksson S, Strandvik B. Food choice is reflected in serum markers and anthropometric measures in healthy 8-yr-olds. Eur J Clin Nutr Met. 2010;5:e117–e24. [Google Scholar]
  • 46. Gaylis JB, Levy SS, Kviatkovsky S, DeHamer R, Young Hong M. Relationships between physical activity, food choices, gender and BMI in Southern Californian teenagers. Int J Adolesc Med Health [Internet]. 2017. doi:10.1515/ijamh-2017-0067. [DOI] [PubMed] [Google Scholar]
  • 47. Kim LP, Mallo N. Maternal perceptions of self-weight and child weight may influence milk choice of participants in the special supplemental nutrition program for women, infants, and children (WIC). J Obes. 2019;2019:3654728. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48. LaRowe TL, Moeller SM, Adams AK. Beverage patterns, diet quality, and body mass index of US preschool and school-aged children. J Am Diet Assoc. 2007;107(7):1124–33. [DOI] [PubMed] [Google Scholar]
  • 49. Mazahery H, Camargo CA Jr, Cairncross C, Houghton LA, Grant CC, Coad J, Conlon CA, von Hurst PR. Type of cows' milk consumption and relationship to health predictors in New Zealand preschool children. N Z Med J. 2018;131(1468):54–68. [PubMed] [Google Scholar]
  • 50. Milla Tobarra M, Martínez-Vizcaíno V, Garcia N, Garcia-Prieto J, Arias-Palencia N, Garcia-Hermoso A. The relationship between beverage intake and weight status in children: the Cuenca study. Nutr Hosp. 2014;30(4):818–24. [DOI] [PubMed] [Google Scholar]
  • 51. Nelson JA, Chiasson MA, Ford V. Childhood overweight in a New York City WIC population. Am J Public Health. 2004;94(3):458–62. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Nilsen BB, Yngve A, Monteagudo C, Tellstrom R, Scander H, Werner B. Reported habitual intake of breakfast and selected foods in relation to overweight status among seven- to nine-year-old Swedish children. Scand J Public Health. 2017;45(8):886–94. [DOI] [PubMed] [Google Scholar]
  • 53. O'Connor TM, Yang SJ, Nicklas TA. Beverage intake among preschool children and its effect on weight status. Pediatrics. 2006;118(4):e1010–8. [DOI] [PubMed] [Google Scholar]
  • 54. Papandreou D, Andreou E, Heraclides A, Rousso I. Is beverage intake related to overweight and obesity in school children?. Hippokratia. 2013;17(1):42–6. [PMC free article] [PubMed] [Google Scholar]
  • 55. Ruxton CH, O'Sullivan KR, Kirk TR, Belton NR, Holmes MA. The contribution of breakfast to the diets of a sample of 136 primary-schoolchildren in Edinburgh. Br J Nutr. 1996;75(3):419–31. [DOI] [PubMed] [Google Scholar]
  • 56. Schroeder H, Mendez MA, Ribas L, Funtikova A, Gomez S, Fito M, Aranceta J, Serra-Majem L. Caloric beverage drinking patterns are differentially associated with diet quality and adiposity among Spanish girls and boys. Eur J Pediatr. 2014;173:1169–77. [DOI] [PubMed] [Google Scholar]
  • 57. Tovar A, Chui K, Hyatt RR, Kuder J, Kraak VI, Choumenkovitch SF, Hastings A, Bloom J, Economos CD. Healthy-lifestyle behaviors associated with overweight and obesity in US rural children. BMC Pediatr. 2012;12:102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58. Vanderhout SM, Birken CS, Parkin PC, Lebovic G, Chen Y, O'Connor DL, Maguire JL. Collaboration TAK. Relation between milk-fat percentage, vitamin D, and BMI z score in early childhood. Am J Clin Nutr. 2016;104(6):1657–64. [DOI] [PubMed] [Google Scholar]
  • 59. Berkey CS, Rockett HR, Willett WC, Colditz GA. Milk, dairy fat, dietary calcium, and weight gain: a longitudinal study of adolescents. Arch Pediatr Adolesc Med. 2005;159(6):543–50. [DOI] [PubMed] [Google Scholar]
  • 60. Bigornia SJ, LaValley MP, Moore LL, Northstone K, Emmett P, Ness AR, Newby PK. Dairy intakes at age 10 years do not adversely affect risk of excess adiposity at 13 years. J Nutr. 2014;144(7):1081–90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61. Dubois L, Diasparra M, Bogl LH, Fontaine-Bisson B, Bedard B, Tremblay RE, Kaprio J, Boivin M. Dietary intake at 9 years and subsequent body mass index in adolescent boys and girls: a study of monozygotic twin Pairs. Twin Res Hum Genet. 2016;19(1):47–59. [DOI] [PubMed] [Google Scholar]
  • 62. Huh SY, Rifas-Shiman SL, Rich-Edwards JW, Taveras EM, Gillman MW. Prospective association between milk intake and adiposity in preschool age children. J Am Diet Assoc. 2010;110(4):563–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63. Noel SE, Ness AR, Northstone K, Emmett P, Newby PK. Cross-sectional and prospective associations between milk and adiposity in children. FASEB J [Internet] 2011;25(1Suppl). Available from: https://www.fasebj.org/doi/abs/10.1096/fasebj.25.1_supplement.781.19. [Google Scholar]
  • 64. The WHO Child Growth Standards. BMI-for-age [Internet]. Geneva: WHO; 2006; [cited 2019] Available from: https://who.int/childgrowth/en. [Google Scholar]
  • 65. Huh SY, Rifas-Shiman SL, Rich-Edwards JW, Taveras EM, Gillman MW. Prospective association between milk intake and adiposity in preschool-aged children. J Am Diet Assoc. 2010;110(4):563–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66. Mead E, Brown T, Rees K, Azevedo LB, Whittaker V, Jones D, Olajide J, Mainardi GM, Corpeleijn E, O'Malley C et al.. Diet, physical activity and behavioural interventions for the treatment of overweight or obese children from the age of 6 to 11 years. Cochrane Database Syst Rev. 2017;6:CD012651 doi:10.1002/14651858.CD012651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67. Lanou AJ, Barnard ND. Dairy and weight loss hypothesis: an evaluation of the clinical trials. Nutr Rev. 2008;66(5):272–9. [DOI] [PubMed] [Google Scholar]
  • 68. Keller A, Heitmann BL, Olsen N. Sugar-sweetened beverages, vascular risk factors and events: a systematic literature review. Public Health Nutr. 2015;18(7):1145–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69. Aziz AA, Anderson GH. Functional dairy products. Cambridge, UK: Woodhead Publishing; 2002. [Google Scholar]
  • 70. Anini Y, Brubaker PL. Role of leptin in the regulation of glucagon-like peptide-1 secretion. Diabetes. 2003;52(2):252–9. [DOI] [PubMed] [Google Scholar]
  • 71. Mozaffarian D, Cao H, King IB, Lemaitre RN, Song X, Siscovick DS, Hotamisligil GS. Trans-palmitoleic acid, metabolic risk factors, and new-onset diabetes in U.S. adults: a cohort study. Ann Intern Med. 2010;153(12):790–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72. Mozaffarian D, de Oliveira Otto MC, Lemaitre RN, Fretts AM, Hotamisligil G, Tsai MY, Siscovick DS, Nettleton JA. trans-Palmitoleic acid, other dairy fat biomarkers, and incident diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA). Am J Clin Nutr. 2013;97(4):854–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73. Liu XR, Deng ZY, Hu JN, Fan YW, Liu R, Li J, Peng JT, Su H, Peng Q, Li WF. Erythrocyte membrane trans-fatty acid index is positively associated with a 10-year CHD risk probability. Br J Nutr. 2013;109(9):1695–703. [DOI] [PubMed] [Google Scholar]
  • 74. Brassard D, Tessier-Grenier M, Allaire J, Rajendiran E, She Y, Ramprasath V, Gigleux I, Talbot D, Levy E, Tremblay A et al.. Comparison of the impact of SFAs from cheese and butter on cardiometabolic risk factors: a randomized controlled trial. Am J Clin Nutr. 2017;105(4):800–9. [DOI] [PubMed] [Google Scholar]
  • 75. Chen M, Li Y, Sun Q, Pan A, Manson JE, Rexrode KM, Willett WC, Rimm EB, Hu FB. Dairy fat and risk of cardiovascular disease in 3 cohorts of US adults. Am J Clin Nutr. 2016;104(5):1209–17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76. Psaty BM, Koepsell TD, Lin D, Weiss NS, Siscovick DS, Rosendaal FR, Pahor M, Furberg CD. Assessment and control for confounding by indication in observational studies. J Am Geriatr Soc. 1999;47(6):749–54. [DOI] [PubMed] [Google Scholar]
  • 77. Shields M, Tremblay MS. Canadian childhood obesity estimates based on WHO, IOTF and CDC cut-points. Int J Pediatr Obes. 2010;5(3):265–73. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

nqz276_Supplemental_File

Articles from The American Journal of Clinical Nutrition are provided here courtesy of American Society for Nutrition

RESOURCES