ORIGINAL ARTICLE
Emmalee Gisslevik1*, Love Svanqvist2, Ingmar Skoog2, Lauren Lissner3 and Elisabet Rothenberg1
1Faculty of Health Sciences, Kristianstad University, Kristianstad, Sweden; 2Neuropsychiatric Epidemiology Unit, Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Centre for Ageing and Health (AgeCap) at the University of Gothenburg, Gothenburg, Sweden; 3Department of Community Medicine and Public Health, at the University of Gothenburg, Gothenburg, Sweden
Background: Dietary habits throughout life significantly influence health in old age; yet, little is known about the relationship between meal pattern and mortality among older adults.
Objective: This study aimed to prospectively investigate the association between meal pattern variables and 15-year all-cause mortality in a cohort of 70-year-olds from the Gothenburg H70 study, considering relevant covariates.
Design: A total of 551 individuals (321 women and 230 men) were included. Dietary intake was assessed using the diet history method, reflecting intake over the preceding 3 months. Meal patterns were described by the usual daily frequency of main meals, light meals, snacks, beverages, and total intake occasions (IO). Statistical analyses included Cox proportional hazards regression, Student’s t-test, and Chi-square test.
Results: Subjects who were deceased at follow-up had a higher prevalence of undernutrition risk indicators (based on low body mass index [BMI], weight/appetite change, and eating difficulties) at baseline compared to those living 15 years later (P = 0.02). In the fully adjusted Cox model, individuals with high total intake frequencies (>5 per day) showed a significantly increased hazard ratio (1.51) for mortality compared to those with medium frequencies. Additionally, medium-high snack frequency (>2–3 snacks/day) was associated with an elevated mortality risk, independent of total energy intake and other covariates.
Discussion: These findings suggest a potential association between frequent daily IO, particularly snacks, and increased mortality risk, which is not fully explained by total energy consumption or other covariates.
Conclusions: The 15-year follow-up provides a long-term view of meal patterns’ impact on longevity, indicating that higher daily consumption frequencies may be associated with increased mortality risk between ages 70 and 85. Further research should examine the nutritional composition of various meal patterns to clarify these associations.
Keywords: meal patterns; all-cause mortality; eating frequency; dietary habits; geriatric health; ageing population; survival analysis; longitudinal study; Cox regression
Citation: Food & Nutrition Research 2025, 69: 11445 - http://dx.doi.org/10.29219/fnr.v69.11445
Copyright: © 2025 Emmalee Gisslevik et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
Received: 29 October 2024; Revised: 13 March 2025; Accepted: 17 March 2025; Published: 8 May 2025
*Emmalee Gisslevik, Faculty of Health Science, Kristianstad University, SE-291 88 Kristianstad, Sweden.
Email: emmalee.gisslevik@gmail.com
Competing interests and funding: The study was financed by grants from the Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement (ALF965812, ALF716681, ALF722441, ALF965812), Stena Foundation, Swedish Research Council (11267, 2005-8460, 2007-7462, 2012-5041, 2015-02830, 2019-01096, 2022-00882, 2013-8717, NEAR 2017-00639), Swedish Research Council for Health, Working Life and Wellfare (2004-0145, 2006-0596, 2008-1111, 2010-0870, 2013-1202, 2018-00471, 2001-2646, 2003-0234, 2004-0150, 2006-0020, 2008-1229, 2012-1138, AGECAP 2013-2300, 2013-2496), Konung Gustaf V:s och Drottning Victorias Frimurarestiftelse, Hjärnfonden (FO2014-0207, FO2016-0214, FO2018-0214, FO2019-0163, FO2020-0235,), Alzheimerfonden (AF-554461, AF-647651, AF-743701, AF-844671, AF-930868, AF-940139, AF-968441, AF-980935), Eivind och Elsa K:son Sylvans stiftelse, The Alzheimer's Association Zenith Award (ZEN-01-3151), The Alzheimer's Association Stephanie B. Overstreet Scholars (IIRG-00-2159), The Bank of Sweden Tercentenary Foundation, Stiftelsen Söderström-Königska Sjukhemmet, Stiftelsen för Gamla Tjänarinnor, Handlanden Hjalmar Svenssons Forskningsfond, and by Agneta Prytz-Folke och Gösta Folkes stiftelse. The authors declare no potential conflicts of interest.
Life expectancy has increased in Europe as well as globally, with older adults living longer due to lifestyle changes, improved living conditions, and better health (1–4). In the Gothenburg H70 Birth Cohort Studies, positive health trends have been demonstrated in five birth cohorts examined at the same age over the past 50 years, with later-born cohorts generally at better health (5–9). As one example, today’s 70 year-olds show healthier dietary patterns compared to earlier cohorts (10–12).
However, the older population is characterized by significant heterogeneity in terms of health and vigour. Health trajectories evolve differently between individuals, being influenced by factors such as lifestyle, socioeconomic factors, and genetics (13). Non-communicable diseases (NCDs) – chronic conditions such as cardiovascular diseases, cancers, and diabetes – are prevalent among older adults and are often associated with lifestyle factors such as suboptimal diet and physical inactivity (14).
Suboptimal diets increase the risk of malnutrition, encompassing an associated shift from overnutrition (i.e. a risk of overweight and obesity) to undernutrition (risk of insufficient energy/nutrients) with advancing age (15, 16). In later life, undernutrition becomes particularly concerning due to its associations with higher infection risk, prolonged recovery, increased mortality, and reduced quality of life. Even though multiple physiological, social, and behavioural factors contribute to these challenges, diet remains a common denominator that can either alleviate or exacerbate malnutrition in all its forms, underscoring the importance of addressing dietary patterns for healthy ageing (16).
Traditionally, research on diet-disease relationships has focused on specific nutrients and their imbalances, overlooking the interactive nature of nutrients within whole foods. Additionally, people consume a wide range of food items, making it crucial to examine the role of overall diet and food patterns in preventing diet-related morbidity and mortality (17), an area that has been the focus of recent nutrition research (18, 19).
Moreover, dietary intake is commonly grouped into different combinations of foods according to the time of the day consumed – a so-called ‘meal pattern’ (17, 18, 20). Recent studies suggest that certain meal patterns – such as skipping meals, longer overnight fasts, and fewer daily eating occasions – may negatively affect health outcomes in older adults. Specifically, skipping breakfast and fasting for over 11 h overnight have been associated with adverse effects on longevity (21, 22).
While research within this area has attracted increased attention (17, 23), the predictive value of meal patterns in relation to all-cause mortality has been explored less often in population-based samples of older adults, leaving a limited understanding of how meal patterns influence mortality risk (23, 24).
Therefore, the aim of this prospective study is to investigate the association between meal pattern variables and 15-year all-cause mortality while also considering relevant covariates in a cohort of 70-year-olds from the Gothenburg H70 birth cohort studies.
Data are derived from the Gothenburg H70 Birth Cohort Studies (H70 studies) in cooperation with the Population Study of Women (PPSW) in Gothenburg (9, 25–28). The H70 studies are multidisciplinary population studies examining birth cohorts of older populations in Gothenburg, Sweden. Participants are systematically recruited using a systematic sampling method, where samples are selected from the Swedish Population Register based on birth dates to yield a representative sample of community-dwelling 70-year-olds. These studies include comprehensive health examinations, focusing on various age-related risk and protective factors, extensively described previously (25–27, 29).
The present study cohort includes individuals born in 1930 who were examined between 2000 and 2002. Initially, 896 individuals were systematically selected and invited to participate. After excluding those who were ineligible (e.g. deceased or emigrated) or unreachable, the effective sample consisted of 852 eligible subjects. Of these, 604 (71%) took part in the main health examinations, which included somatic, neuropsychological, psychiatric, anthropometric, physiological, and genetic tests (Fig. 1). Of the participants in the main examinations, 554 (233 men, 321 women) also completed a diet history (DH) interview. However, 50 participants did not complete the dietary assessment due to various reasons, including impaired cognitive function, difficulties with the Swedish language, early departure during the study day, or the unavailability of a dietician (11). Three individuals were excluded from the final analysis: one due to missing/incomplete dietary data and two due to death within the first year. This resulted in a final sample size of n = 551, consisting of 230 men and 321 women. Among the women, 255 were originally recruited to the PPSW (12) and had been followed longitudinally since 1968. The remaining women were recruited in 2000 at age 70 by the H70 study.
Divergence between participants and non-participants has previously been investigated by re-contacting subjects who did not attend the 2000 health examinations (30). The results showed no statistical divergences between participants and non-participants in terms of self-rated health, history of myocardial infarction, diabetes, or smoking status. However, differences were observed in marital status, with a higher proportion of married men among participants (75%) compared to non-responders (56%, P < 0.0001), while no substantial differences were noted among women. The most common reasons for non-participation were undefined refusal and illness or ongoing medical care (30).
Mortality status was checked using the Swedish population register on 21 May 2016. The median follow-up time was 15 years (q1–q3 = 12.0–15.2 years). The birth cohort and characteristics of participants and non-participants have been described in detail previously (9, 11, 31). All subjects provided written informed consent, and the Regional Ethical Review Board in Gothenburg approved the studies with reference numbers S227-00 and S377-99. The study was conducted in accordance with the principles of the Declaration of Helsinki.
Dietary intake was assessed using the DH method, which is a semi-structured interview including questions about the usual frequencies and portion sizes of food intake over the preceding 3 months (25, 26). The interviews lasted for about an hour, during which participants were asked to report what they usually eat and drink for each meal and, as far as possible, to specify the food items and amounts consumed. The protocol involved open-ended questions with the aim to illustrate participants’ total intake of food and drinks in an ordinary day. The interviews were conducted face-to-face by trained dieticians. The DH has undergone validation and demonstrated comparable energy intakes (EI) to those predicted by the heart rate method, with some underreporting (12%) observed among overweight participants using double-labelled water (10, 28). Detailed descriptions of the dietary examination procedures have been published previously (12).
To calculate nutrient intake, the Swedish food composition database ‘PC-kost’ (maintained by the Swedish National Food Administration) was utilized. The energy and nutrient variables examined in this study included total daily EI in kcal/day, percentage of energy (E%) from macronutrients and alcohol, and protein intake in grams per day.
Meal pattern classifications and coding were applied to data derived from the DH interviews. A modified version of Berteus Forslund et al.’s (32) meal classification scheme was used to categorize food intake occasions (IO) into four meal types: light meal/breakfast, main meal, snack meal, and drink-only. The term ‘IO’ is used to describe all types of consumption, including occasions when only beverages are consumed, and ‘eating occasions’ refer solely to instances where solid food is consumed (Table 1). As part of the modifications, for example, ‘breakfast’ was defined as the first eating occasion of the day and consistently coded as ‘light meal/breakfast’, as opposed to the original method wherein the meals were defined by their composition regardless of time of the day.
Additional coding instructions were implemented, such as classifying meals involving fewer than two sandwiches as ‘snack meals’ and those involving two or more sandwiches as ‘light meals’. Drinks other than water were coded as individual IO, and overnight fast was defined as the time between the participant’s last eating occasion of the evening and their first eating occasion the next morning, excluding drink-only occasions.
When meals were recorded in a time interval (e.g. 10:00–12:00), the mean time was calculated (e.g. 11:00). Common phrases such as ‘sometimes a bun’ were recorded as 0.5 snack meals. When the frequency of a meal was specified as less than once per day (e.g. 2 times per week), the average intake was calculated per day (0.3 times/day) in order to maximize the coding agreement to allow for future comparison with other cohorts. A logbook was created to gather any uncertain meal descriptions from the DH data, which were audited for agreement.
Several continuous meal pattern variables were categorized to simplify the data representation. Each variable was grouped into specific intervals using cut-off points to define interval groups. For ‘total number of IO’, it was divided into four interval groups: low, medium, medium high, and high frequency. The cut-off points were set as follows: low frequency (≤3), medium frequency (>3–4), medium high frequency (>4–5), and high frequency (>5). Similarly, ‘snack meal’ was binned into four interval groups: low, medium, medium high, and high frequency. The cut-off points for this variable were low frequency (≤1), medium frequency (>1–2), medium high frequency (>2–3), and high frequency (>3). The cut-off points were selected based on variable distribution and the goal of creating balanced groups. For drinks, the cut-off points were <1 and ≥1, while for the main meal variable, the categories were <1, 1, and >1. Regarding overnight fast duration, the first grouping category followed the recommended duration of ≤11 h (33). This group included 25% of the subjects and was further divided into exact quarter groups using the Statistical Package for the Social Sciences (SPSS) binning function. The resulting interval groups were ≤11h referred to as ‘recommended duration’, >11–12.3 h as ‘medium-high duration’, >12.3–13.3 h as ‘high duration’, and >13.3 h as ‘very high duration’.
Participants provided information regarding health variables during a general health examination, (31) including measured body mass index (BMI), self-assessed health situation, nutritional risk indicators, and number of medications. Additionally, socioeconomic variables such as educational level, marital status, and self-assessed economic situation, as well as lifestyle characteristics like cigarette smoking and physical activity level (PAL), were reported at baseline.
BMI (based on measured height and weight values, kg/m2) was categorized into three groups: underweight <22, normal weight 22–27, and overweight/obesity >27 according to age-related values presented in the European Society for Clinical Nutrition and Metabolism (ESPEN) guidelines (34). Marital status was dichotomised to married and not married (unmarried/divorced/widowed). Self-rated health was assessed using the general question, ‘How would you rate your health?’ with response options ranging from very good to very poor. Smoking habits were categorized as never smoked, former smoker, and current smoker. ‘Leisure-time physical activity’ and ‘activity level during labour/household work’ were classified on four levels, respectively. The two physical activity variables were, in a second step, quantified into an estimated PAL-value (PAL-value) in accordance with the PAL-estimate template developed and described by Johansson and Westerterp (35). Education was dichotomised into ≤lower than mandatory school and higher than mandatory school.
Risk indicators for undernutrition were defined based on the three assessment points outlined by the National Board of Health and Welfare for assessing nutritional risk, which balances three assessment items: 1) recent weight loss, 2) eating difficulties, and 3) underweight status (36). In this paper, these three assessment points were captured through questions about 1) recent weight/appetite changes, 2) eating/chewing difficulties, and 3) BMI <22. Individuals meeting any of the three criteria were classified as ‘at risk of undernutrition’.
Descriptive statistics are presented as means ± standard deviations (SD) for continuous variables and as counts and percentages for categorical variables. Baseline differences by mortality status were evaluated using independent t-tests for normally distributed continuous variables and Mann–Whitney U tests for non-normally distributed variables. Categorical variables were analysed using chi-square and Fisher’s exact tests as appropriate.
To examine the association between meal pattern variables and 15-year mortality, Cox proportional hazards regression was used as the primary analytical method. Initially, crude models were applied, followed by two progressively adjusted models (Model 1 and Model 2). Model 1 included adjustments for smoking habits, gender, and self-assessed health status, while Model 2 further incorporated education, EI, economic situation, and marital status. Each categorical variable was compared against a reference group, designated as ‘medium frequency’ for meal pattern variables and ‘recommended duration’ for overnight fasts. Results are expressed as hazard ratios (HR) with corresponding 95% confidence intervals (CI).
As a supplementary analysis, logistic regression models were also conducted, using the same covariates as the Cox regression models, to provide additional insights. These results are discussed briefly in the text but are primarily presented in the supplementary material for reference.
All statistical analyses were conducted using SPSS version 25, with a significance level set at P ≤ 0.05.
Out of the total 551 participants included, 59% were alive at 15-year follow-up and 41% were deceased. For meal pattern frequencies, the total average number of IO was 4.9 per day, of which 1.0 was main meal, 1.9 were snack meals, 1.7 were light meals/breakfast, 0.25 were drink-only occasions, and there were 12 h of overnight fasting.
Baseline demographic and nutritional characteristics, stratified by mortality status at 15-year follow-up, are presented in Table 2. At baseline, significant differences were observed between those who were deceased at follow-up and those who were living across several characteristics (Table 2). Among those who were deceased at follow-up, a higher proportion were male, current or past smokers, had an education level below mandatory schooling, reported poor self-rated health, and indicated a poor economic situation. Additionally, a greater proportion of those deceased at follow-up had at least one undernutrition risk indicator. This group also showed a significantly lower estimated PAL and used a higher number of medications.
| 15-year mortality status | |||||
| Living | Deceased | ||||
| n Mean |
% (SD) |
n Mean |
% (SD) |
P1 | |
| Gender | <0.001* | ||||
| Female | 213a | 65% | 108b | 48% | |
| Male | 113a | 35% | 117b | 52% | |
| Body mass index | 26.87a | (4.06) | 27.22a | (4.54) | 0.349 |
| Body mass index categories | 0.286 | ||||
| Underweight | 24a | 7% | 19a | 9% | |
| Normal weight | 167a | 51% | 98a | 44% | |
| Overweight | 135a | 41% | 104a | 47% | |
| Physical activity level | 1.64a | (0.08) | 1.62b | (0.11) | 0.003* |
| Smoking | <0.001* | ||||
| Never smoked | 185a | 57% | 74b | 33% | |
| Smoker | 35a | 11% | 46b | 21% | |
| Former smoker | 106a | 33% | 103b | 46% | |
| No. of medications | 2.93a | (2.63) | 3.42b | (2.96) | 0.048* |
| Health | 0.005* | ||||
| Excellent | 88a | 28% | 38b | 18% | |
| Good | 177a | 55% | 119a | 56% | |
| Poor | 55a | 17% | 57b | 27% | |
| Marital status | 0.138 | ||||
| Married | 224a | 69% | 139a | 63% | |
| Not Married | 102a | 31% | 83a | 37% | |
| Economic situation | 0.063 | ||||
| Excellent | 89a | 28% | 52a | 24% | |
| Good | 207a | 64% | 133a | 62% | |
| Poor | 25a | 8% | 30b | 14% | |
| Education | 0.025* | ||||
| Above mandatory school | 140a | 43% | 74b | 34% | |
| Below mandatory school | 184a | 57% | 146b | 66% | |
| Energy intake (kcal) | 2155.17a | (605.36) | 2248.98a | (671.20) | 0.089 |
| Energy (kcal/kg body weight) | 29.40a | (8.81) | 29.51a | (9.74) | 0.889 |
| Protein (g/day) | 84.54a | (22,18) | 86.92a | (26,21) | 0.267 |
| Alcohol (E%) | 2.38a | (2.78) | 3.18a | (4.01) | 0.082 |
| Undernutrition risk indicators | 0.022* | ||||
| No | 245a | 75% | 149b | 66% | |
| Yes | 81a | 25% | 76b | 34% | |
| Note: Values in the same row and subtable not sharing the same subscript are significantly different at P < 0.05 in the two-sided test of equality for column proportions. Cells with no subscript are not included in the test. [1] Based on independent sample t-tests and chi-square test. [*] Significant at P ≤ 0.05. |
|||||
No difference in mean BMI or the distribution of BMI categories was shown between the groups. Similarly, no differences were found for total EI (kcal), EI per kilogram of body weight, and protein intake (g/day). However, when stratified by sex (data not shown), a significant difference in average protein intake (g/day) was observed between living and deceased women (M = 78.4, SD = 18.8; M = 73.2, SD = 19.0; P < 0.021).
Student’s t-test (data shown in the supplementary file) revealed that the daily number of IO had a similar average of approximately 5 in both groups, regardless of mortality status. Similarly, the average number of snack meals per day was about 2 in both groups. The total number of eating occasions and light meals/breakfast was slightly lower among deceased subjects compared to those alive. However, Student’s t-test indicated no significant differences in the continuous meal pattern variables, except for drink-only occasions, where the deceased group demonstrated a higher average intake (0.21 vs. 0.31; P = 0.04).
Regarding categorical meal pattern intervals (Table 3), a somewhat lower proportion of deceased subjects were categorized in the medium (>3–4) IO interval and a somewhat lower proportion of alive subject was in the ‘≥1’ drink-only interval compared to those deceased at follow up. Chi-square tests showed that the drink categories were the only variable that showed significant relations between deceased and alive X2(1, N = 551) = 4.2, P = 0.04.
| 15-year mortality status | |||||
| Living | Deceased | ||||
| n | % | n | % | P1 | |
| Intake occasions grouped | 0.188 | ||||
| Low ≤3 | 13a | 4 | 13a | 6 | |
| Medium >3–4 | 100a | 31 | 51b | 23 | |
| Medium high >4–5 | 121a | 37 | 92a | 41 | |
| High >5 | 92a | 28 | 69a | 31 | |
| Main meals grouped | 0.773 | ||||
| <1 | 298a | 91 | 203a | 91 | |
| =1 | 9a | 3 | 5a | 2 | |
| >1 | 19a | 6 | 16a | 7 | |
| Snack meals grouped | 0.277 | ||||
| Low ≤1 | 98a | 30 | 74a | 33 | |
| Medium >1–2 | 128a | 39 | 71a | 32 | |
| Medium high >2–3 | 75a | 23 | 63a | 28 | |
| High >3 | 25a | 8 | 17a | 8 | |
| Drink-only grouped | 0.041* | ||||
| <1 | 272a | 83 | 172b | 76 | |
| ≥1 | 54a | 17 | 53b | 24 | |
| Overnight fast grouped | 0.943 | ||||
| Medium ≤11.00 | 99a | 30 | 64a | 28 | |
| Medium high >11–12.00 | 71a | 22 | 51a | 23 | |
| High >12.15–13.00 | 80a | 25 | 59a | 26 | |
| Very high >13.00 | 76a | 23 | 51a | 23 | |
| Note: Values in the same row and subtable not sharing the same subscript are significantly different at P < 0.05 in the two-sided test of equality for column proportions. Cells with no subscript are not included in the test. [1] based on chi-square test. [*] significant at P ≤ 0.05, not adjusted for covariates. |
|||||
Cox proportional hazards regression analyses revealed that higher intake frequencies were associated with an increased risk of mortality compared to the reference category. In the fully adjusted model, individuals with 4–5 and more than 5 IO per day had a significantly higher hazard of 15-year mortality (HR = 1.51, P = 0.02 and HR = 1.56, P = 0.02, respectively) compared to those in the reference group with 3–4 IO per day (Table 4).
| Crude | Model 1a | Model 2b | ||||||||||
| B | HR | (95% CI) | P | B | HR | (95% CI) | P | B | HR | (95% CI) | P | |
| Intake occasion groups | ||||||||||||
| References: 3–4 | ||||||||||||
| <3 Low | 0.61 | 1.85 | (0.98–3.47) | 0.06 | 0.60 | 1.82 | (0.97–3.42) | 0.06 | 0.52 | 1.68 | (0.87–3.24) | 0.12 |
| >4–5 Medium high | 0.37 | 1.45 | (1.03–2.04) | 0.04* | 0.40 | 1.49 | (1.04–2.14) | 0.03* | 0.41 | 1.51 | (1.05–2.16) | 0.03* |
| >5 High | 0.30 | 1.35 | (0.93–1.94) | 0.11 | 0.41 | 1.51 | (1.04–2.20) | 0.03* | 0.44 | 1.56 | (1.07–2.27) | 0.02* |
| Snack meal groups | ||||||||||||
| References: 1–2 | ||||||||||||
| <1 Low | 0.28 | 1.32 | (0.95–1.84) | 0.10 | 0.40 | 1.49 | (1.06–2.10) | 0.02* | 0.40 | 1.49 | (1.06–2.11) | 0.02* |
| >2–3 Medium high | 0.31 | 1.37 | (0.97–1.93) | 0.07 | 0.42 | 1.51 | (1.06–2.16) | 0.02* | 0.41 | 1.51 | (1.05–2.17) | 0.03* |
| >3 High | 0.16 | 1.17 | (0.69–2.00) | 0.56 | 0.43 | 1.54 | (0.89–2.68) | 0.13 | 0.47 | 1.59 | (0.91–2.78) | 0.10 |
| ≥1 Drink meal | 0.35 | 1.41 | (1.04–1.93) | 0.03* | 0.32 | 1.38 | (1.00–1.90) | 0.05* | 0.30 | 1.35 | (0.98–1.86) | 0.68 |
| CI, confidence interval. a Model 1, the included variables are health situation, smoking habits, and gender. b Model 2, the variables of Model 1 as well as education, EI, economic situation, and marital status are included as covariates. [*] Significant at P ≤ 0.05. |
||||||||||||
Regarding snack meals, the Cox regression analyses showed significant associations for both the ≤1 and 2–3 snack meals per day groups, with HR of 1.49 (P = 0.022) and 1.51 (P = 0.025), respectively, compared to the reference group of more than 1–2 snack meals per day.
In contrast, no significant associations were observed between drink-only occasions and 15-year mortality in the fully adjusted Cox model.
Overall, these analyses indicate a higher HR associated with more frequent intake intervals, particularly for those beyond 4–5 occasions per day, even after adjusting for EI and other covariates. Figures 2 and 3 illustrate the cumulative survival functions for different IO groups and snack meal groups, respectively, across the Cox regression models, highlighting the impact of meal frequency on survival over a follow-up period of up to 6,000 days.
Fig. 2. The cumulative survival functions for different IO Groups in the fully adjusted model, including covariates such as health status, smoking habits, gender, total EI, marital status, and education level (Model 2). Each plot compares the survival distributions against a reference group with medium IO frequency (3–4 times per day), illustrating the impact of these variables on survival over a follow-up period of up to 6,000 days.
Fig. 3. The cumulative survival functions for different ‘Snack Meal Groups’ in the fully adjusted model, including covariates such as health status, smoking habits, gender, total EI, marital status, and education level (Model 2). Each plot compares the survival distributions against a reference group with medium snack meal frequency (>1–2 times per day), illustrating the impact of these variables on survival over a follow-up period of up to 6,000 days.
We examined the meal pattern in relation to 15-year all-cause mortality in a population-based sample of community-dwelling 70-year-olds, first examined 2000–2002 and followed up in 2015. The study is part of the Gothenburg H70 birth cohort studies. We found significant relationships between meal pattern variables and increased risk of mortality. At follow-up, 59% of the participants remained alive. In line with official health statistics of Sweden (37), deceased subjects were to a greater extent male, current/past smokers, had lower education levels, reported worse self-assessed health, and indicated a poorer economic situation compared to those who remained alive. Additionally, there was a higher proportion of subjects with risk indicators for undernutrition among those deceased at follow-up compared to those alive (Table 2). No significant differences in meal pattern variables were observed in relation to mortality status based on bivariate analyses, except for drink-only intakes, which were more frequent among those deceased at follow-up (Table 3). However, Cox regression analyses using categorical meal pattern variables revealed significant associations between higher total IO and increased mortality risk, as well as between snack meal frequencies and mortality (Table 4). These associations remained significant even after adjusting for EI and other covariates.
The World Health Organization (WHO) recommends 5–6 small non-fatty meals for older adults (2). A meal pattern associated with greater food variety and lower body fat, blood glucose, and lipid levels, especially if larger meals are eaten early in the day. The Swedish Food Agency recommends three main meals and at least three snack meals per day and an overnight fast not exceeding 11 h within the care of frail older adults to counteract undernutrition (36). Several smaller meals distributed over more hours make it easier to cover energy and nutrient needs, particularly for those with poor appetites (38). These recommendations target older adults, but from different perspectives. The aim of the WHO recommendations is metabolic control, while the Swedish recommendations focus on the risk of undernutrition. The new Nordic Nutrition Recommendations (NNR) 2023 (39) state that there is not enough evidence to set dietary guidelines on meal patterns and underscore the variability of meal patterns within the context of an energy-balanced and nutritionally adequate diet (39). This perspective aligns with our interpretation of the findings, suggesting that while meal patterns may influence mortality risk, they should not be viewed in isolation from the nutritional quality of the diet.
As stated in the section titled ‘Introduction’, older adults as a group are characterized by large heterogeneity in terms of health and vigour. Therefore, recommendations to decrease the risk for metabolic conditions such as cardiovascular disease are relevant for some part of the ageing population at the same time as recommendations to decrease the risk of undernutrition are relevant for another part. The current sample was derived from the general population of 70-year-olds in Gothenburg and consisted of older adult participants generally in quite good health and not comparable to frail seniors, to whom the dietary advice above from the Swedish authorities applies. However, despite the generally good health status, risk indicators for undernutrition were present in both groups but significantly more prevalent among the deceased compared to individuals alive at follow-up at age 85.
Putting our results in the context of the present science with regard to meal frequency, a narrative literature review in various populations showed that the most common temporal meal patterns, irrespective of dietary intake method, were a ‘3 meals/day pattern’, a ‘skipping breakfast pattern’, and a ‘nibbling’ pattern consisting of smaller but more frequent meals (40). Initial research largely suggested that higher meal frequency might offer protective effects against metabolic risk factors such as weight gain and diabetes (41–47). Conversely, more recent longitudinal studies indicate that frequent meals and snacks may increase the risk of adverse health outcomes, including coronary heart disease (CHD), weight gain, and type 2 diabetes (48–51). For instance, Cahill et al. (50) conducted a prospective cohort study examining meal frequency and CHD risk in older men. Although their results were not statistically significant, they identified a trend: men consuming 1–2 meals daily had a relative risk (RR) of CHD of 1.10, those eating 4–5 meals had an RR of 1.05, and men eating six or more meals daily had an RR of 1.26, compared to a baseline of 3 meals per day, after adjusting for total EI, diet composition, and other risk factors.
Our findings contribute to this complex picture. In the crude analysis, we found no significant association between total daily IO and 15-year mortality. However, when controlling for factors such as subjective health, smoking habits, and gender, our adjusted models revealed that individuals consuming more than five meals daily faced an increased hazard of mortality over the 15-year period. This consistent trend across models suggests a potential risk associated with higher meal frequencies, aligning with Cahill et al.’s observation of elevated CHD risk in men eating six or more meals per day (50).
Contrastingly, our analysis also found that certain intake frequencies – specifically, the consumption of 2–3 snack meals per day – were consistently associated with a higher hazard of mortality, regardless of the model adjustments. While our study focused primarily on meal frequency and type, these findings highlight the need for future research to incorporate meal composition alongside meal patterns to gain a more comprehensive understanding of their relationship with health outcomes.
Moreover, the interplay between meal frequency and nutritional quality cannot be overlooked. For example, the relations between meal frequencies and weight gain have shown a positive association with higher sugar intake (23, 48, 49), and it is suggested that increased food stimuli by several meals per day may increase the desire to overeat. According to Paoli et al. (23), the contrasting results on meal frequency and health can be explained by the fact that a reduced number of meals often reflects a disadvantageous distribution, such as skipping breakfast, having a light lunch, and a calorie-dense dinner, which can lead to poor metabolic control (52). This highlights the importance of distinguishing between individuals who follow a healthy eating pattern despite fewer meals and those whose reduced meal frequency is due to disadvantageous habits.
Our study aligns with current research, which presents conflicting results on the relationship between meal patterns and health outcomes. These discrepancies likely arise from variations in populations and differing methods of classifying meal patterns. While meal frequency is influential, it is not the sole determinant of health impacts. The nutritional content of meals, particularly the quality and balance of macronutrients, plays a critical role in shaping long-term health trajectories. For example, replacing protein with simple carbohydrates like sugars alters metabolic response, affecting both short- and long-term health (48, 53). Shang (54) demonstrated that higher protein and fat intake at breakfast, combined with lower carbohydrate intake, was associated with a lower rate of cognitive decline over 9 years in older adults. Their study also found that high-frequency diets substituting carbohydrates with protein may help delay or prevent cognitive decline, likely due to better glycaemic control and reduced postprandial insulin responses (48). Additionally, the quality of fat is important for both dementia and cardiovascular disease risks (55). Thus, our research emphasizes the need for a nuanced approach in public health strategies that extends beyond meal frequency to include a holistic consideration of dietary composition.
Strengths in the present study include its population-based study design, the use of an age-standardized sample, and a prospective approach spanning 15 years. These features are particularly valuable in a research field where data on the long-term health effect of meal frequency in older adults remains limited. The method for meal type classifications used was a modified version of Berteus Forslund et al. (32), using a predetermined meal definition which increases the standardization of the coding. Inter-observer variations were minimized as one person coded all data. However, meal patterns could be classified by different methods, meaning that comparison with other studies may involve uncertainty (17).
A further strength is adjustment for relevant covariates. In the first model, gender, self-assessed health, and smoking were included, all of which were significant across the analysed meal pattern variables. The second model additionally included total EI, education, economic situation, and marital status (Table 4). While not all of the variables in the final model, they are well established as important covariates in previous studies examining dietary habits and health.
However, predicting mortality by analysing meal frequency does not stand alone. Additional information on food and nutrient composition is important to understand the complete health effect of meal patterns. Therefore, it is a limitation that we only could report protein intake and alcohol expressed as energy %.
Another limitation regarding generalizability is the participation rate at baseline, which was 61%. Population-based studies often face challenges related to positive self-selection bias, as individuals who choose to participate may be healthier or more motivated than non-participants. This may result in an under-representation of individuals with poorer health or lower socioeconomic status. A positive association between dietary quality and socioeconomic status at age 70 has previously been demonstrated in this cohort (56), highlighting the potential influence of socioeconomic factors on both meal patterns and mortality outcomes. However, baseline differences between those deceased and alive at follow-up were consistent with official health statistics of Sweden (14, 57), suggesting that the cohort reflects broader population trends. It is also worth noting that gender distribution was skewed, with women being over-represented – an expected outcome given their longer life expectancy compared to men (57). While this reflects demographic realities, it may limit the generalizability of findings to men. It is also important to consider that individuals with impaired cognitive function or language difficulties were more likely to be excluded from dietary assessments, which could introduce selection bias related to meal patterns and mortality risk.
Based on the present results and existing evidence for the association between meal frequency and health in older adults, future studies might include nutritional and food composition of different types of meals, which might add deeper understanding of the effect of meal pattern on health (58).
The 15-year follow-up in this study offers a comprehensive and long-term perspective on the relationship between meal patterns and longevity among older adults. Our results indicate that frequent daily consumption of snacks or total intake episodes is associated with increased risk of mortality between 70 and 85 years, independently of the amount of energy consumed. Specifically, individuals with high total intake frequencies (more than five IO per day) and those with snack frequencies of two to three snacks per day exhibited a significantly elevated risk of 15-year mortality.
Given the implications of these findings, further research is warranted to explore the underlying mechanisms linking meal frequency and mortality. Detailed investigations into the nutritional composition of different meal patterns, as well as their metabolic and physiological impacts, could provide deeper insights into how meal frequency affects health. Therefore, future studies should consider the potential influence of meal timing, quality of food consumed, and individual metabolic responses.
The authors would like to thank all participants of the Gothenburg H70 birth cohort study for their invaluable contribution to this research.
We would be grateful if you could update these sections in the final version. Please don’t hesitate to let us know if anything needs to be adjusted to better fit the journal’s format, or if further clarification is needed.
| 1. | Eurostat. Population structure and ageing. Available from: https://ec.europa.eu/eurostat/statistics-explained/index.php/Population_structure_and_ageing [cited 27 Oct 2024]. |
| 2. | World Health Organization. Keep fit for life: meeting the nutritional needs of older persons. Geneva: World Health Organization; 2003. |
| 3. | Shlisky J, Bloom DE, Beaudreault AR, Tucker KL, Keller HH, Freund-Levi Y, et al. Nutritional considerations for healthy aging and reduction in age-related chronic disease. Adv Nutr 2017; 8(1): 17–26. doi: 10.3945/an.116.013474 |
| 4. | Benziger CP, Roth GA, Moran AE. The global burden of disease study and the preventable burden of NCD. Glob Heart 2016; 11(4): 393–7. doi: 10.1016/j.gheart.2016.10.024 |
| 5. | Skoog I, Börjesson-Hanson A, Kern S, Johansson L, Falk H, Sigström R, et al. Decreasing prevalence of dementia in 85-year olds examined 22 years apart: the influence of education and stroke. Sci Rep 2017; 7(1): 6136. doi: 10.1038/s41598-017-05022-8 |
| 6. | Xinyue Z, Joas E, Waern M, Östling S, Börjesson-Hanson A, Skoog I. Prevalence of cardiovascular disorders and risk factors in two 75-year-old birth cohorts examined in 1976–1977 and 2005–2006. Aging Clin Exp Res 2013; 25(4): 377–83. doi: 10.1007/s40520-013-0058-1 |
| 7. | Wilhelmson K, Allebeck P, Steen B. Improved health among 70-year olds: comparison of health indicators in three different birth cohorts. Aging Clin Exp Res 2002; 14(5): 361–70. doi: 10.1007/bf03324463 |
| 8. | Hörder H, Skoog I, Johansson L, Falk H, Frändin K. Secular trends in frailty: a comparative study of 75-year olds born in 1911–12 and 1930. Age Ageing 2015; 44(5): 817–22. doi: 10.1093/ageing/afv084 |
| 9. | Falk H, Johansson L, Ostling S, Thøgersen Agerholm K, Staun M, Høst Dørfinger L, et al. Functional disability and ability 75-year-olds: a comparison of two Swedish cohorts born 30 years apart. Age Ageing 2014; 43(5): 636–41. doi: 10.1093/ageing/afu018 |
| 10. | Rothenberg E, Bosaeus I, Steen B. Evaluation of energy intake estimated by a diet history in three free-living 70 year old populations in Gothenburg, Sweden. Eur J Clin Nutr 1997; 51(1): 60–6. doi: 10.1038/sj.ejcn.1600363 |
| 11. | Eiben G, Andersson CS, Rothenberg E, Sundh V, Steen B, Lissner L. Secular trends in diet among elderly Swedes – cohort comparisons over three decades. Public Health Nutr 2004; 7: 637–44. doi: 10.1079/PHN2003576 |
| 12. | Samuelsson J, Rothenberg E, Lissner L, Eiben G, Zettergren A, Skoog I. Time trends in nutrient intake and dietary patterns among five birth cohorts of 70-year-olds examined 1971–2016: results from the Gothenburg H70 birth cohort studies, Sweden. Nutr J 2019; 18(1): 66. doi: 10.1186/s12937-019-0493-8 |
| 13. | National Board of Health and Welfare (Socialstyrelsen). Statistics on causes of death 2020. Stockholm: Socialstyrelsen; 2021. Available from: https://www.socialstyrelsen.se/globalassets/sharepoint-dokument/artikelkatalog/statistik/2021-6-7453.pdf [cited 27 Oct 2024] |
| 14. | National Board of Health and Welfare (Socialstyrelsen). Dödsorsaksregistret [Cause of Death Register]. Stockholm: Socialstyrelsen; 2022. Available from: https://www.statistikdatabasen.scb.se/pxweb/sv/ssd/START__LE__LE0201__LE0201H%c3%a4lsa/Tema525/ [cited 27 Oct 2024] |
| 15. | Kaiser MJ, Bauer JM, Rämsch C, Uter W, Guigoz Y, Cederholm T, et al. Frequency of malnutrition in older adults: a multinational perspective using the mini nutritional assessment. J Am Geriatr Soc 2010; 58(9): 1734–8. doi: 10.1111/j.1532-5415.2010.03016.x |
| 16. | Agarwal E, Miller M, Yaxley A, Isenring E. Malnutrition in the elderly: a narrative review. Maturitas 2013; 76(4): 296–302. doi: 10.1016/j.maturitas.2013.07.013 |
| 17. | Leech RM, Worsley A, Timperio A, McNaughton SA. Understanding meal patterns: definitions, methodology and impact on nutrient intake and diet quality. Nutr Res Rev 2015; 28(1): 1–21. doi: 10.1017/S0954422414000262 |
| 18. | Nordic Council of Ministers. Nordic Nutrition Recommendations 2012: integrating nutrition and physical activity. Copenhagen: Nordic Council of Ministers; 2014. |
| 19. | Asher G, Sassone-Corsi P. Time for food: the intimate interplay between nutrition, metabolism, and the circadian clock. Cell 2015; 161(1): 84–92. doi: 10.1016/j.cell.2015.03.015 |
| 20. | Huseinovic E, Winkvist A, Freisling H, Slimani N, Boeing H, Buckland G, et al. Timing of eating across ten European countries – results from the European Prospective Investigation into Cancer and Nutrition (EPIC) calibration study. Public Health Nutr 2019; 22(2): 324–35. doi: 10.1017/s1368980018002288 |
| 21. | Söderström L, Rosenblad A, Thors Adolfsson E, Bergkvist L. Malnutrition is associated with increased mortality in older adults regardless of the cause of death. Br J Nutr 2017; 117(4): 532–40. doi: 10.1017/s0007114517000435 |
| 22. | Chen H, Zhang B, Ge Y, Shi H, Song S, Xue W, et al. Association between skipping breakfast and risk of cardiovascular disease and all cause mortality: a meta-analysis. Clin Nutr 2020; 39(10): 2982–8. doi: 10.1016/j.clnu.2020.02.004 |
| 23. | Paoli A, Tinsley G, Bianco A, Moro T. The influence of meal frequency and timing on health in humans: the role of fasting. Nutrients 2019; 11(4): 719. doi: 10.3390/nu11040719 |
| 24. | Soderstrom L, Thors Adolfsson E, Rosenblad A, Frid H, Saletti A, Bergkvist L. Mealtime habits and meal provision are associated with malnutrition among elderly patients admitted to hospital. Clin Nutr 2013; 32(2): 281–8. doi: 10.1016/j.clnu.2012.07.013 |
| 25. | Rothenberg E, Bosaeus I, Steen B. Food habits in three 70-year-old free-living populations in Gothenburg, Sweden. A 22-year cohort study. Scand J Nutr 1996; 40(3): 104–10. |
| 26. | Steen B. Nutrition in 70-year-olds. Dietary habits and body composition. A report from the population study of 70-year-old people in Gothenburg, Sweden. Naringsforskning 1977; 21(3): 201–23. Available from: http://hdl.handle.net/2077/14253 [cited 15 Feb 2025]. |
| 27. | Steen B, Isaksson B, Svanborg A. Intake of energy and nutrients and meal habits in 70-year-old males and females in Gothenburg, Sweden. A population study. Acta Med Scand Suppl 1977; 611: 39–86. doi: 10.1111/j.0954-6820.1977.tb18069.x |
| 28. | Rothenberg E, Bosaeus I, Lernfelt B, Landahl S, Steen B. Energy intake and expenditure: validation of a diet history by heart rate monitoring, activity diary and doubly labeled water. Eur J Clin Nutr 1998; 52(11): 832–8. doi: 10.1038/sj.ejcn.1600655 |
| 29. | Bengtsson C, Ahlqwist M, Andersson K, Björkelund C, Lissner L, Söderström M. The prospective population study of women in Gothenburg, Sweden, 1968–69 to 1992–93. A 24-year follow-up study with special reference to participation, representativeness, and mortality. Scand J Prim Health Care 1997; 15(4): 214–9. doi: 10.3109/02813439709035031 |
| 30. | Bergh I, Steen G, Waern M, Johansson B, Odén A, Sjöström B, et al. Pain and its relation to cognitive function and depressive symptoms: a Swedish population study of 70-year-old men and women. J Pain Sympt Manage 2003; 26(4): 903–12. doi: 10.1016/S0885-3924(03)00329-4 |
| 31. | Wetterberg H, Rydén L, Ahlner F, Erhag FH, Gudmundsson P, Guo X, et al. Representativeness in population-based studies of older adults: five waves of cross-sectional examinations in the Gothenburg H70 Birth Cohort Study. BMJ Open 2022; 12(12): e068165. doi: 10.1136/bmjopen-2022-068165 |
| 32. | Berteus Forslund H, Lindroos AK, Sjostrom L, Lissner L. Meal patterns and obesity in Swedish women-a simple instrument describing usual meal types, frequency and temporal distribution. Eur J Clin Nutr 2002; 56(8): 740–7. doi: 10.1038/sj.ejcn.1601387 |
| 33. | Swedish Food Agency. Bra måltider i äldreomsorgen: råd för ordinära och särskilda boenden – hemtjänst och äldreboenden. Uppsala: Livsmedelsverket; 2019. |
| 34. | Cederholm T, Jensen GL, Correia M, Gonzalez MC, Fukushima R, Higashiguchi T, et al. GLIM criteria for the diagnosis of malnutrition – a consensus report from the global clinical nutrition community. Clin Nutr 2019; 38(1): 1–9. doi: 10.1016/j.clnu.2018.08.002 |
| 35. | Johansson G, Westerterp KR. Assessment of the physical activity level with two questions: validation with doubly labeled water. Int J Obes (Lond) 2008; 32(6): 1031–3. doi: 10.1038/ijo.2008.42 |
| 36. | National Board of Health and Welfare (Socialstyrelsen). Näring för god vård och omsorg – En vägledning för att förebygga och behandla undernäring [Nutrition for good care and services – A guide to prevent and treat malnutrition] Stockholm: Socialstyrelsen; 2011. Available from: http://hkr.diva-portal.org/smash/get/diva2:639755/FULLTEXT01.pdf [cited 15 Feb 2025]. |
| 37. | Public Health Agency of Sweden [Folkhälsomyndigheten]. Folkhälsans utveckling – årsrapport Folkhälsomyndigheten; 2022. Available from: https://www.folkhalsomyndigheten.se/publikationer-och-material/ [cited 15 Feb 2025]. |
| 38. | Swedish Food Agency [Livsmedelsverket]. Mat och måltider i äldreomsorgen – vetenskapliga underlag om måltidsmiljö och verksamhetsstruktur, fysiologiska och sensoriska aspekter av åldrandet samt särskilda näringsbehov hos sköra äldre. Uppsala: Livsmedelsverket; 2017. |
| 39. | Nordic Council of Ministers. Nordic nutrition recommendations 2023: integrating environmental aspects. Copenhagen: Nordic Council of Ministers; 2023. |
| 40. | O’Hara C, Gibney ER. Meal pattern analysis in nutritional science: recent methods and findings. Adv Nutr 2021; 12(4): 1365–78. doi: 10.1093/advances/nmaa175 |
| 41. | Fábry P, Fodor J, Hejl Z, Geizerová H, Balcarová O. Meal frequency and ischaemic heart-disease. Lancet 1968; 2(7561): 190–1. doi: 10.1016/s0140-6736(68)92622-6 |
| 42. | Fábry P, Hejl Z, Fodor J, Braun T, Zvolankova K. The frequency of meals. Its relation to overweight, hypercholesterolaemia, and decreased glucose-tolerance. Lancet 1964; 2(7360): 614–5. doi: 10.1016/s0140-6736(64)90510-0 |
| 43. | Jenkins DJ, Wolever TM, Vuksan V, Brighenti F, Cunnane SC, Rao AV, et al. Nibbling versus gorging: metabolic advantages of increased meal frequency. N Engl J Med 1989; 321(14): 929–34. doi: 10.1056/nejm198910053211403 |
| 44. | Jones PJ, Leitch CA, Pederson RA. Meal-frequency effects on plasma hormone concentrations and cholesterol synthesis in humans. Am J Clin Nutr 1993; 57(6): 868–74. doi: 10.1093/ajcn/57.6.868 |
| 45. | McGrath SA, Gibney MJ. The effects of altered frequency of eating on plasma lipids in free-living healthy males on normal self-selected diets. Eur J Clin Nutr 1994; 48(6): 402–7. |
| 46. | Schoenfeld BJ, Aragon AA, Krieger JW. Effects of meal frequency on weight loss and body composition: a meta-analysis. Nutr Rev 2015; 73(2): 69–82. doi: 10.1093/nutrit/nuu017 |
| 47. | Keast DR, Nicklas TA, O’Neil CE. Snacking is associated with reduced risk of overweight and reduced abdominal obesity in adolescents: National Health and Nutrition Examination Survey (NHANES) 1999–2004. Am J Clin Nutr 2010; 92(2): 428–35. doi: 10.3945/ajcn.2009.28421 |
| 48. | Kanaley JA, Heden TD, Liu Y, Fairchild TJ. Alteration of postprandial glucose and insulin concentrations with meal frequency and composition. Br J Nutr 2014; 112(9): 1484–93. doi: 10.1017/s0007114514002128 |
| 49. | Ohkawara K, Cornier MA, Kohrt WM, Melanson EL. Effects of increased meal frequency on fat oxidation and perceived hunger. Obesity (Silver Spring) 2013; 21(2): 336–43. doi: 10.1002/oby.20032 |
| 50. | Cahill LE, Chiuve SE, Mekary RA, Jensen MK, Flint AJ, Hu FB, et al. Prospective study of breakfast eating and incident coronary heart disease in a cohort of male US health professionals. Circulation 2013; 128(4): 337–43. doi: 10.1161/circulationaha.113.001474 |
| 51. | Van der Heijden AA, Hu FB, Rimm EB, Van Dam RM. A prospective study of breakfast consumption and weight gain among U.S. men. Obesity (Silver Spring) 2007; 15(10): 2463–9. doi: 10.1038/oby.2007.292 |
| 52. | Mekary RA, Giovannucci E, Willett WC, Van Dam RM, Hu FB. Eating patterns and type 2 diabetes risk in men: breakfast omission, eating frequency, and snacking. Am J Clin Nutr 2012; 95(5): 1182–9. doi: 10.3945/ajcn.111.028209 |
| 53. | Kempf K, Röhling M, Banzer W, Braumann KM, Halle M, McCarthy D, et al. High-protein, low-glycaemic meal replacement decreases fasting insulin and inflammation markers – a 12-month subanalysis of the ACOORH trial. Nutrients 2021; 13(5): 1433. doi: 10.3390/nu13051433 |
| 54. | Shang X, Hill E, Li Y, He M. Energy and macronutrient intakes at breakfast and cognitive declines in community-dwelling older adults: a 9-year follow-up cohort study. Am J Clin Nutr 2021; 113(5): 1093–103. doi: 10.1093/ajcn/nqaa403 |
| 55. | Marx W, Veronese N, Kelly JT, Smith L, Hockey M, Collins S, et al. The dietary inflammatory index and human health: an umbrella review of meta-analyses of observational studies. Adv Nutr 2021; 12(5): 1681–90. doi: 10.1093/advances/nmab037 |
| 56. | Cabrera C, Rothenberg E, Eriksson BG, Wedel H, Eiben G, Steen B, Lissner L. Socio-economic gradient in food selection and diet quality among 70-year olds. J Nutr Health Aging 2007; 11(6): 466–73. |
| 57. | Statistics Sweden (SCB). Befolkning 2022. Stockholm: Statistics Sweden; 2022. Available from: https://www.scb.se/hitta-statistik/statistik-efter-amne/befolkning/ [cited 27 Oct 2024]. |
| 58. | Potter M, Vlassopoulos A, Lehmann U. Snacking recommendations worldwide: a scoping review. Adv Nutr 2018; 9(2): 86–98. doi: 10.1093/advances/nmx003 |