| Literature DB >> 32630022 |
Leonie Elizabeth1, Priscila Machado1,2, Marit Zinöcker3, Phillip Baker1,2, Mark Lawrence1,2.
Abstract
The nutrition literature and authoritative reports increasingly recognise the concept of ultra-processed foods (UPF), as a descriptor of unhealthy diets. UPFs are now prevalent in diets worldwide. This review aims to identify and appraise the studies on healthy participants that investigated associations between levels of UPF consumption and health outcomes. This involved a systematic search for extant literature; integration and interpretation of findings from diverse study types, populations, health outcomes and dietary assessments; and quality appraisal. Of 43 studies reviewed, 37 found dietary UPF exposure associated with at least one adverse health outcome. Among adults, these included overweight, obesity and cardio-metabolic risks; cancer, type-2 diabetes and cardiovascular diseases; irritable bowel syndrome, depression and frailty conditions; and all-cause mortality. Among children and adolescents, these included cardio-metabolic risks and asthma. No study reported an association between UPF and beneficial health outcomes. Most findings were derived from observational studies and evidence of plausible biological mechanisms to increase confidence in the veracity of these observed associations is steadily evolving. There is now a considerable body of evidence supporting the use of UPFs as a scientific concept to assess the 'healthiness' of foods within the context of dietary patterns and to help inform the development of dietary guidelines and nutrition policy actions.Entities:
Keywords: NOVA; dietary patterns; food processing; health outcomes; obesity; ultra-processed food
Mesh:
Year: 2020 PMID: 32630022 PMCID: PMC7399967 DOI: 10.3390/nu12071955
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
Inclusion and exclusion criteria used for screening studies.
| Description | |
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| Inclusion criteria |
Stated aim was to evaluate the relationship between UPF exposure and a given health outcome or outcomes. Healthy, free-living human subjects over two years of age (except when included in studies on all ages), any country/ethnicity. UPF category or sub-categories used in the study were defined and referenced to the NOVA food classification system, including the Dietary Guidelines for the Brazilian Population, based on NOVA. Original empirical research articles published in peer-reviewed journal, with full text available. Had clearly stated aim(s) and objectives, well defined and appropriate method, a clear statement of results, and conclusions consistent with the study findings. Published between 1 January 2009 and 21 May 2020. Available in the English language. |
| Exclusion criteria |
Study aim was to evaluate UPF exposure with non-health related outcome(s) or in non-human subjects or human populations with pre-existing health conditions or special needs (e.g., elite athletes, pregnant women); or UPF was the outcome not exposure. Studies using non-NOVA food classification systems or non-UPF exposure variables; UPF without definition and cited reference; studies on general food patterns. Conference proceedings, modelling studies, editorials, commentaries, opinions, study protocols, theses, articles where full text was unavailable. Published prior to 2009. Non-English language. |
Figure 1Flow Diagram of Database Search and Article Eligibility (modified from PRISMA flow diagram [43,44]).
Overweight, obesity and cardio-metabolic risks as outcomes in studies in adults *.
| Study Details | UPF Exposure | Outcomes | Results | |||||
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| Publication Author(s) Year | Study Type (Year) Setting | Population (Number) | Extraction Level | Relative exposure [UPF Reference Year] | Data Collection Method | Health Outcome(s) (Study Definition) | Data Collection Method | Key Findings |
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| Juul | Ecological | Adults | National + household sampling | BMI classified in prevalence overweight (BMI ≥ 25) and obesity (BMI ≥ 30) | National population statistics | From 1980 to 2008: rise in overweight prevalence for men from 35% to 54–56% and women from 26% to 39%; and obesity prevalence for men rose from 4.5% to 11% and for women from 5% to 10%. From 1960 to 2010 rise in UPF consumption of 142% tracks increase in overweight and obesity prevalence. | ||
| Monteiro | Ecological (1991–2008) Europe | Adults ≥ 18 years except Belgium ≥ 15 years ( | Household (National Sample) | UPF % total E purchases (continuous) [NOVA.2018] [ | Belgium, Sweden, Germany = one month food ** purchase record; | BMI classified in prevalence obesity (BMI ≥ 30) | National reports | UPF ranged 10.2–50.7% (median 26.4) of household total E in food purchases. Each 1% increase in UPF E availability was associated with 0.25% increase in obesity prevalence. |
| Vandevijvere 2019 | Ecological (Repeated cross-sectional) (2002–2014) | Adults | National | UPF total sales (volume/capita) | Volume sales of UPF (137 items from 212 food ** subgroups) | Mean population BMI | National reports | Increases in UPF volume sales/capita were directly associated with mean BMI trajectories. Every standard deviation increase in volume sales of UPF, mean BMI increased by 0.195 kg/m2 for men and 0.072 kg/m2 for women (drinks only), and 0.316 kg/m2 for men (foods only). |
| Canella | Cross-sectional | All ages ( | Household | UPF % total E purchases (quartiles) | 7-day food ** purchase record | BMI classified in excess weight (BMI > 25), obesity (BMI > 30) WHO BMI for age Z scores [children] | Trained personnel | UPF contributed 25.5% of total E purchased. Participants living in household strata belonging to the upper quartile of UPF consumption had higher mean BMI (Z score) (β = 0.19; 95% CI 0.14, 0.25) prevalence of obesity (β = 3.72; 95% CI 2.50, 4.94) and prevalence of excess weight (β = 6.27; 95% CI 4.15, 8.39), compared with those in the lowest quartile. As UPF consumption rose from Quartile 1 to Quartile 4, the prevalence of excess weight rose from 34.1% to 43.9%, and prevalence of obesity rose from 9.8% to 13.1%. |
| Adams | Cross-sectional | Adults | Individual | UPF % total E intake | 4-day food ** intake diary | BMI classified in overweight (BMI ≥ 25); obesity (BMI ≥ 30) | Trained personnel | UPF contributed 53% of total E intake. UPF consumption was not significantly associated with BMI, overweight and obesity, and obesity. |
| Louzada ‡ | Cross-sectional (2008–2009) | Adults | Individual (National Sample) | UPF % total E intake (quintiles) | 2 × 24-h food ** intake record | BMI classified in excess weight (BMI ≥ 25), obesity (BMI ≥ 30) [adults]; WHO BMI for age Z scores [children] | Trained personnel | UPF contributed to 29.6% of total E intake. Individuals in the upper quintile of UPF intake had significantly higher BMI (0.94 kg/m2; 95% CI = 0.42, 1.47) and higher odds of being obese (OR = 1.98; 95% CI = 1.26, 3.12) compared with the lowest quintile. No significant association with excess weight was found. |
| Nardocci | Cross-sectional | Adults > 18 years | Individual (National Sample) | UPF % total E intake (quintiles, and continuous) [NOVA2016.2018] [ | 1 × 24-h recall | BMI classified in overweight (25.0 ≤ BMI < 30.0); obesity (BMI ≥ 30) | Trained personnel | UPF contributed 45.1% of total E intake. Individuals in highest quintile UPF intake significantly had higher odds of being obese (OR = 1.32, 95% CI 1.05, 1.57, and overweight (OR = 1.03; 95% CI 1.01, 1.07), compared with individuals in lowest quintile. |
| Juul | Cross-sectional | Adults 20–64 years | Individual | UPF % total E intake | 2 available 24-h recall or 1 day otherwise | BMI classified in overweight and obesity (BMI ≥ 25), obesity (BMI ≥ 30); | Trained personnel | UPF contributed 56.1% of total E intake. Individuals in the highest quintile of UPF intake had significantly higher BMI (1.61 kg/m²; 95% CI 1.11, 2.10), and WC (4.07 cm, 95% CI 2.94, 5.19), and higher odds of having excess weight (OR = 1.48; 95% CI 1.25 to 1.76), obesity (OR = 1.53, 95% CI 1.29, 1.81), and abdominal obesity (OR = 1.62; 95% CI 1.39 to 1.89) compared with those in the lowest quintile. |
| Rauber 202 [ | Cross-sectional | Adults | Individual (National sample) | UPF % total E intake (quartiles) | 4-day food ** intake diary | BMI classified in obesity (BMI ≥ 30). WC classified in AO | Trained personnel | UPF contributed 54.3% of total E intake. Individuals in the highest quartile of UPF intake had higher BMI (1.66 kg/m2; 95%CI 0.96, 2.36) and WC (3.56cm, 95% CI 1.79, 5.33), and higher odds of obesity (OR = 1.90, 95% CI 1.39, 2.61) compared with the lowest quartile. |
| Julia | Cross-sectional | Adults Mean 43.8 years ( | Individual | UPF % total grams (quartiles) | 3 × 24 h records | BMI classified in overweight | Self-report # | UPF contributed 18.4% of total weight intake, and 35.9% of total E intake. Higher consumption of UPF by % E intake was independently associated with overweight (p < 0.0001); and higher intake by energy-weighted UPF was independently associated with overweight, and obesity (both |
| Silva | Cross-sectional (2008–2010) Brazil | Active and retired civil servants 35–64 years ( | Individual | UPF % total E intake | 114 item-FFQ | BMI classified in overweight (25.0-29.9); obesity (≥30); | Trained personnel | UPF contributed 22.7% of total E intake. Individuals in highest quartile UPF intake had significantly higher BMI (0.80 kg/m2; 95% CI 0.53, 1.07), WC (1.71 cm; 95% CI 1.02, 2.40), and higher odds of being overweight (OR = 1.31; 95% CI 1.13, 1.51), obese (OR = 1.41, 95% CI 1.18, 1.69), increased WC (OR = 1.31, 95% CI 0.96, 1.32), and significantly increased WC (OR = 1.41; 95% CI 1.20, 1.66), compared with individuals in the lowest quartile. |
| Da Silveira | Cross-sectional (2015) | Vegetarians > 16 years | Individual | UPF intake frequency | FFQ (number of items not specified) | BMI classified | Self-report # | Higher intake of UPF (≥3 times/day) was independently associated with overweight (OR = 2.33; 95% CI 1.36, 4.03). |
| Ali | Cross-sectional (2018) | Adults 18–59 years ( | Individual | UPF % total E intake (+continuous) | 2-day 24 h recall | BMI % Body fat | Trained | UPF contributed 23 % of total E intake. No significant findings between ultra-processed food consumption BMI, body fat percent ( |
| Mendonca 2016 | Prospective Cohort (1999–2012) | Adults Mean 37.6 years | Individual | UPF intake servings/day (quartiles) | 136-item FFQ | BMI classified in overweight/obesity | Self-report # | Participants in the highest quartile of UPF consumption were at a higher risk of developing overweight/obesity (HR = 1.26; 95% CI 1.10, 1.45) compared with those in the lowest quartile of consumption. |
| Canhada 2020 [ | Prospective Cohort (2008–2010) 3.8 years median | Adults | Individual | UPF % total E intake (quartiles) [NOVA 2016] [ | 114-item FFQ | Large weight gain (≥1·68 kg/year) | Trained personnel | UPF contributed 24.6% of total E intake. Participants in the highest quartile of UPF intake had greater risk of large weight (RR = 1.27; 95% CI 1.07, 1.50) and waist gains (RR = 1.33; 95% CI 1.12, 1.58), and of developing overweight/obesity (RR = 1.20; 95% CI 1.03, 1.40) compared with individuals in the lowest quartile. |
| Hall et al. | Randomised Controlled Trial (2018, 4 weeks) | Weight stable adults Mean 31.2 years | Individual | Whole diet UPF vs. MPF diet (ad libitum) [NOVA.2018] [ | Diets designed and analysed using ProNutra software | Energy Intake (kcal) | Trained personnel | Energy intake was greater during exposure to the UPF diet (508 ± 106 kcal/day; |
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| Lavigne- | Cross-sectional | Adults | Individual | UPF total E % intake (quintiles) [NOVA.2010] [ | 1 × 24-h food ** recall | Metabolic syndrome (MetS) (≥3 factor: high WC, HT TAG, BG; low HDL-C) | Trained personnel | UPF contributed 51.9% of total E intake. Those in highest quintile of UPF intake significantly associated with higher prevalence of MetS (OR = 1.90; 95% CI 1.14), higher prevalence of reduced HDL-C (OR = 2.05; 95% CI 1.25, 3.38), elevated fasting plasma glucose (OR = 1.76, 95% CI 1.04, 2.97) compared with those in the lowest quintile. |
| Nasreddine 2018 | Cross-sectional (2014) Lebanon | Adults | Individual | UPF ‘pattern’ vs. MPF and PF ‘pattern’ (quartiles) | 88-item FFQ | Metabolic syndrome | Trained personnel | UPF vs. MPF were 36.5% vs. 27.1% of total E intake. Those in highest quartile MPF/PF significantly lower odds MetS (OR = 0.18, 95% CI 0.04, 0.77); hyperglycaemia (OR = 0.25, 95% CI 0.07, 0.98), low HDL-C (OR = 0.17, 95% CI 0.05, 0.60) compared with those in the lowest quartile. No significant association between MetS and UPF. |
| Lopes | Cross-sectional (2008–2010) | Adults | Individual | UPF % total E intake | 114–item FFQ | C-reactive protein (CRP) level (mg/L) | Trained personnel | UPF contributed to 20% total E intake. Women in highest tercile UPF intake had higher levels of CRP (arithmetic mean = 1.14; 95% CI: 1.04–1.24) than lowest tercile of intake, no significance when controlling for BMI. No significant association was observed in men. |
| Martinez Steele | Cross-sectional | Adults ≥ 20 years | Individual | UPF Total E % intake (quintiles and continuous) | 2 available ×24-h recall, or 1 day otherwise. | Metabolic syndrome (≥3 factor of high WC, HT, TAG, BG; low HDL) | Trained personnel | UPF contributed 55.5% of total E intake. The highest quintile of UPF consumption was associated with higher MetS prevalence (PR = 1.28; 95% CI 1.09, 1.50) compared with the lowest quintile of UPF consumption. Each 10% increase in the consumption of UPF was associated with 4% increase in MetS prevalence (PR = 1.04; 95% CI 1.02, 1.07) |
| Mendonca 2017 | Prospective Cohort (1999–2013) | Adult graduates ( | Individual | UPF E intake servings per day (tertiles) | 136-item FFQ | Hypertension | Self-report ξ | Participants in the highest tertile of UPF intake had higher risk of developing hypertension (HR = 1.21; 95% CI 1.06–1.37) compared with those in the lowest tertile of intake. |
Results are presented for adjusted associations for potential confounders and statistically significant associations. NOVA refers to the food classification system [21] or earlier versions, as referenced; * Includes studies on all ages; ** includes beverages; # anthropometrics; ξ reported medical diagnosis, medication, or BP readings, ‡ results for adolescents are presented in Table 3; UPF: ultra-processed food (includes foods and beverages); BOA: Board of Agriculture; BMI: Body Mass Index [weight (kilograms)/height (metres)2]; E: energy in kilocalories or kilojoules; WHO: World Health Organisation; OR: odds ratio; CI: confidence interval; WC: waist circumference (cm); increased WC: (men ≥ 94; women ≥ 80; significantly increased WC (men ≥ 102; women ≥ 88); AO: abdominal obesity (men ≥ 102 cm; women ≥ 88 cm); FFQ: food frequency questionnaire; DGB: Dietary Guidelines for the Brazilian Population; HR: hazards ratio; RR: relative risk; MPF: unprocessed or minimally processed food; MetS: metabolic syndrome; HT: hypertension; TAG: triacylglycerol; BG: blood glucose; HDL-C: high density lipoprotein cholesterol; MPF and PF ‘pattern’: factor derived ‘pattern’ of mainly MPF and processed food (PF); CRP = C-reactive protein; BP = blood pressure.
Overweight, obesity and cardio-metabolic risks as outcome (children and adolescents).
| Study Details | UPF Exposure | Outcomes | Results | |||||
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| Publication Author(s) Year | Study Type (Year) Setting | Population (Number) | Extraction Level | Relative exposure | Data Collection Method | Health Outcome (Study Definition) | Data Collection Method | Key Findings |
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| Louzada * 2015 | Cross-sectional (2008-2009) Brazil | Children | Individua (National Sample) | UPF % total E intake (quintiles) | 2 × 24-h food ** intake record | WHO BMI-for-age Z-scores, in excess weight and obesity. | Trained personnel | UPF contribution ranged from ≤17% in lowest quintile to ≥52% in highest quintile. No significant association of UPF intake with mean BMI, excess weight or obesity was found. |
| Enes | Cross-sectional (2016) | Adolescents 10–18 years ( | Individual | UPF % total E intake | 58-items FFQ | Overweight Obesity BMI-for-age Z-scores | Trained personnel | UPF contributed 50.6% of total E intake. No association with UPF and anthropometric indicators. |
| Cunha et al. 2018 [ | Prospective Cohort (2010–2012), 3 years median follow-up Brazil | Adolescents 15.7 years baseline, 17.6 years follow-up ( | Individual | UPF intake (times/day) and daily E (kcal/day) [NOVA.2010] [ | 72-item FFQ | Trajectories of BMI (kg/m2)% body fat | Trained personnel | Baseline UPF intake was 9.7–12.5 times/day (boys) and 10.9–13.1 times/day (girls). There was no significant difference in BMI and % body fat trajectories during follow-up. |
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| Tavares 2012 [ | Cross-sectional (2006-2007) Brazil | Adolescents 12–19 years ( | Individual | UPF E intake (kJ) (quartiles)[NOVA.2009] [ | 90-item FFQ | Metabolic syndrome (MetS) (≥3 factor of high WC, HT, TAG, BG; low HDL) | Trained personnel (assumed) | Highest intake of UPF (>3rd quartile) was associated with higher MetS prevalence (PR = 2.49; |
| Melo 2017 [ | Cross-sectional (2012) Brazil | Adolescents 14–19 years ( | Individual | UPF intake frequency (<3 per week vs. ≥3 per week) | 84- item FFQ | Excess weight (BMI-for-age) | Trained personnel | UPF intake was ≥ 3 × week in 46.2% of adolescents. MPF intake inversely associated with excess weight. UPF intake was not significantly associated with excess weight, high WC and high blood pressure. |
| Rauber 2015 | Prospective cohort | Children 3–4 years at baseline; 7–8 years at follow-up ( | Individual | UPF % total E intake [NOVA.2014] [ | 2 × 24-h recall | Changes in lipid concentrations | Trained personnel | UPF contributed 42.6% at pre-school, 49.2% at school age of % E intake. For every 1% increase E intake from UPF, total cholesterol increased 0.43 mg/dL ( |
| Costa | Prospective Cohort | Children 4 years at baseline; 8 years at follow-up ( | Individual | UPF % total E intake | 2 × 24-h recalls | Changes in BMI (kg/m2), Waist circumference (cm) Glucose profile and insulin resistance | Trained personnel | UPF contributed 41.8% preschool, 47.8% at school age of % E intake. Consumption of UPF consumption at age 4 was associated with increased delta waist circumference (B = 0.07 cm; 95% CI 0.01, 0.013) from age 4 to 8 years. No significant associations were observed for BMI, glucose profile and insulin resistance. |
| Leffa 2020 [ | Prospective cohort (2011–2015) | Children | Individual | UPF % total E intake [NOVA.2018.2019] [ | 2 × 24-h recalls | Total cholesterol (TC) TAG | Trained personnel | UPF contributed 43.4% age 3 years, and 47.7% at age 6 years of % E intake. Those children in the highest tertile of consumption of UPF at age 3 had higher levels of TC (B = 0.22 mmol/L; 95 CI 0.04, 0.39) and TAG (B = 0.11 mmol/L; 95% CI 0.01, 0.20) at age 6 than those in the lowest tertile. |
Results are presented for adjusted associations for potential confounders and statistically significant associations. NOVA refers to the food classification system [21] or earlier versions, as referenced. * Also included in Table 2; ** food includes food and beverages; UPF: ultra-processed food (includes food and beverages); E: energy in kilocalories or kilojoules; WHO: World Health Organisation; BMI; Body Mass Index; FFQ; food frequency questionnaire; MetS; metabolic syndrome; WC: waist circumference; HT: hypertension; TAG: triacylglycerol; BG: blood glucose; HDL: high density lipoprotein; PR: prevalence; LDL: low-density lipoprotein; DGB: Dietary Guidelines for the Brazilian Population; TC: total cholesterol.
Diseases and mortality as outcomes.
| Study Details | UPF Exposure | Outcomes | Results | |||||
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| Publication Author(s) | Study Type (Year) Setting | Population | Extraction Level | Relative exposure | Data Collection Method | Health Outcome | Data Collection Method | Key Findings |
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| Queiroz 2018 | Case control study (2015) | Adult women Mean 53.1 years | Individual | UPF ≥ 5 day/week {NOVA.2010] [ | 98-item FFQ, 12-month recall | Breast cancer (BC) | Diagnosed BC | Regular consumption UPF (≥5 day/week) identified as risk factors for BC (OR = 2.35, 95% CI 1.08–5.12). |
| Fiolet 2018 | Prospective Cohort (2017), 5 years median follow-up | Adults | Individual | UPF % g (quartiles) | 3 × 24-h records | Overall, breast, prostate, and colorectal cancer | Self-report or/physician contact | UPF contribution in proportion of grams ranged from 18.7% lowest quartile to 32.3% in highest. A 10% increase in proportion of UPF consumption associated with a significant increase in overall (HR = 1.12; 95% CI 1.06; 1.18; |
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| Srour | Prospective cohort (2019), 5.2 years median follow-up France | Adults | Individual | UPF % grams (quartiles) [NOVA.2018] [ | 3 × 24 h records | Cardiovascular (CVD), coronary heart (CHD), cerebrovascular disease | Medical records, committee of doctors | UPF contribution averaged 17. 4% of total grams. A 10% increase in proportion of UPF consumption was associated with significant higher risk of overall CVD (HR = 1.12; 95% CI 1.05; −1.20, |
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| Srour 2019 | Prospective cohort (2017), 6.0 years median follow-up France | Adults ≥ 18 | Individual | UPF % g | 3 × 24 h records | Type 2 Diabetes (T2D) | ICD-10 code or T2D medication | Mean UPF contribution was 17.3% by weight, and 29.95% by % E intake. A 10% increase in the proportion of UPF consumption was associated with a significant higher risk of T2D (HR = 1.15; 95% CI 1.06; 1.25; |
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| Kim 2019 | Prospective cohort (2011), 19 years median follow-up | Adults | Individual | UPF frequency (times/day) (quartiles) [NOVA.2018] [ | 81-item FFQ, and 24-h recall | All-cause mortality (ACM) CVD mortality | National death index. CVD items 100–169 ICD-10 | Participants consumed UPF a mean 4 times/day. Individuals in the highest quartile of frequency of UPF consumption had significantly higher risk of ACM, (HR = 1.31; 95% CI 1.09; 1.58, |
| Schnabel 2019 | Prospective Cohort (2017), (median follow-up 7.1 years) | Adults ≥ 45 years ( | Individual | UPF % g | 3 × 24-h food record | ACM | National death registries. Causes by ICD-10 | UPF contributed 14.4% total weight, and 29.9% total E intake. A 10% increase in the proportion of UPF consumption was associated with a significant higher risk of ACM 1.14 (95% CI, 1.04–1.27; |
| Rico-Campà 2019 | Prospective Cohort (2014), (median follow-up 10.4 years) | Adults 20−91 years ( | Individual | UPF servings/day (quartiles) [NOVA.2016] [ | 136-item FFQ | ACM | Next of kin/Registries | UPF consumption ranged from 1.4 servings a day in lowest quintile to 5.3 servings a day in highest quintile. Individuals in the highest quartile of UPF consumption were at higher risk of ACM (HR = 1.62; 95% CI 1.13; 2.33) than those in the lowest quartile. No significant associations were found for cardiovascular and cancer mortality. |
| Blanco-Rojo 2019 | Prospective Cohort (2016), (mean follow-up 7.7 years) | Adults Mean 46.9 years | Individual | UPF % total E intake (quartiles) [NOVA.2018] [ | 880-item FFQ | ACM | National Death Index | UPF contributed 24.4% total E intake. Individuals in the highest quartile of UPF consumption were at higher risk of ACM (HR = 1.46; 95% CI 1.04-2.05; |
Results are presented for adjusted associations for potential confounders and statistically significant associations. NOVA refers to the food classification system [21] or earlier versions, as referenced; UPF: ultra-processed food (includes food and beverages); E:energy in calories or kilojoules; OR: odds ratio; FFQ: food frequency questionnaire; CI: confidence interval; HR: hazards ratio; food = food and beverages; BC = breast cancer; ICD-10:International Classification of Disease; CVDL cardiovascular disease, CHD: coronary heart disease; T2D:Type 2 diabetes; ACM: all-cause mortality.
Disorders and conditions as outcomes.
| Study Details | UPF Exposure | Outcomes | Results | |||||
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| Publication Author(s) | Study Type (Year) Setting | Population | Extraction Level | Relative exposure | Data Collection Method | Health Outcome (Study Definition) | Data Collection Method | Key Findings |
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| Schnabel 2018 | Cross-sectional | Age ≥ 18 years (mean 50.4) | Individual | UPF % total grams (quartiles) [NOVA.2018] [ | 3 × 24-h records | Functional gastrointestinal disorders (Rome III criteria) | Self-report * | UPF contributed to 16% of total food intake by weight; 33.0% by total E intake. Individuals in the highest quartile of UPF intake had significantly higher risk of IBS (OR = 1.25; 95% CI 1.12; 1.39) and FDy (OR = 1.25; CI 95% 1.05; 1.47) but not FDy alone, compared with those in the lowest quartile. |
| Vasseur 2020 [ | Prospective cohort (2016) 2.3 years mean follow-up France | Adults ≥ 18 years | Individual | UPF % total | 3 × 24 h records | Inflammatory bowel disease | Self-report ** | UPF contributed 17% food intake by weight in grams. No significant association was found with UPF consumption and IBD ( |
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| Adjibade 2019 [ | Prospective Cohort (2012), 5.4 years mean follow-up France | Adults age 18–86 years | Individual | UPF % total grams (quartiles) [NOVA.2018] [ | 3 × 24 h records | Depression (CES-D scale) | Self-report * | UPF contributed 5% by weight in grams and 32% E intake. Individuals in the highest quartile of UPF intake had significantly higher risk of developing depressive symptoms (HR = 1.30; 95% CI 1.15–1.47) than those in the lowest quartile. Each 10% increase in UPF consumption was HR of 1.21 (95% CI, 1.15–1.27). |
| Gomez-Donoso, 2019 [ | Prospective cohort (2016), 10.3 years median follow-up | Adults (mean 36.7 years) | Individual | UPF energy adjusted kcal/day (quartiles) [NOVA.2016] [ | 136–item FFQ | Depression | Self-report ** | Individuals in highest quartile UPF had significantly higher risk of depression (HR = 1.33; 95% CI 1.07–1.64); |
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| Sandoval-Insausti 2019 | Prospective Cohort | Adults ≥ 60 years ( | Individual | UPF intake % total E (quartiles) | Validated interview computerized diet history | Frailty (Fried’s criteria) | Trained personnel | UPF contributed mean of 19.3% total E intake. Individuals in the highest quartile of UPF intake had higher risk of frailty (OR = 3.67; 95% CI 2.00, 6.76) than those in the lowest quartile of intake. |
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| Melo et al. | Cross-sectional (2012) Brazil | Grade 9 students | Individual | UPF score, intake per week (quintiles) [NOVA 2018] [ | 6-UPF sub-categories FFQ | Asthma, wheezing in past 12 months | Self-report * | Individuals in the highest quintile of the UPF intake score had higher odds of having asthma (OR = 1.27; 95% CI 1.15, 1.41) or wheezing (OR = 1.42; 95% CI 1.35 to 1.50), than those in the lowest quintile. |
| Azeredo 2020 | Prospective Cohort (2004–2010) Brazil | Children mean age 6.8 years baseline; 11.0 years at follow-up ( | Individual | UPF % total E intake (quintiles) [NOVA.2018] [ | 55 (age 6) and 88 items (age 11) FFQ. | Wheezing, whistling or asthma in past 12 months | Self-report * | UPF contribution to total E intake was 42.3% at 6 years, and 33.7% at 11 years. Consumption of UPF at age 6 was not significantly associated with wheeze, asthma or severe asthma at age 11. |
Results are presented for adjusted associations for potential confounders and statistically significant associations. NOVA refers to the food classification system [21] or earlier versions, as referenced; food means foods and beverages; * self-report from questionnaire on condition, medical history, symptoms, medication use, and/or diagnosis by medical practitioner; ** questionnaire plus validation on sample laboratory test or interview; UPF: ultra-process food (includes food and beverages); E: energy in calories or kilojoules; OR: odds ratio; CI: confidence interval; IBS: irritable bowel syndrome; FDy: functional dyspepsia; IBD: inflammatory bowel disease; CES-D scale: Centre for Epidemiologic Studies Depression Scale; HR: hazards ratio; FFQ: food frequency questionnaire; HR: hazards ratio.