Horizontal box plots are shown in which the middle line represents the median er-MedDiet score (range, 0-17; higher score indicates higher adherence), boxes represent the interquartile range (IQR), whiskers extend to the most extreme observed values with 1.5 × IQR of the nearer quartile, and the dots represent observed values outside that range.
Participants in the intervention group were encouraged to follow an energy-reduced Mediterranean diet, accompanied by physical activity promotion and behavioral support, while participants in the control group were encouraged to follow the traditional Mediterranean diet with ad libitum caloric intake. Horizontal box plots are shown in which the middle line represents the within-group median change in observed risk factors, boxes represent the interquartile range (IQR), and whiskers extend to the most extreme observed values with 1.5 × IQR of the nearer quartile. All differences are expressed in common units of baseline SD of each factor for comparability. HDL indicates high-density lipoprotein; LDL, low-density lipoprotein.
Horizontal box plots are shown in which the middle line represents the median change in observed risk factors, boxes represent the interquartile range (IQR), whiskers extend to the most extreme observed values with 1.5 × IQR of the nearer quartile, and the dots represent observed values outside that range. HDL indicates high-density lipoprotein; LDL, low-density lipoprotein.
Statistical analysis plan
eTable 1. Definitions of scores capturing the four dietary patterns.
eTable 2. Baseline dietary variables and their changes by randomized treatment group: Foods and foods groups.
eTable 3. Sensitivity analysis. Baseline, 6-month and 12-month changes in quality dietary scores by randomized treatment group: completers only.
eTable 4. Sensitivity analysis. Baseline, 6-month and 12-month changes in food items by randomized treatment group: completers only.
eTable 5. Sensitivity analysis. Baseline values, 6-month and 12-month changes in nutrient intake by randomized treatment group: completers only
eTable 6. Sensitivity analysis. Baseline and 6- and 12- month changes in quality dietary scores by randomized treatment group: All randomized participants. Replacing all missing values with baseline value.
eTable 7. Sensitivity analysis. Baseline values, 6-month and 12- month changes in food items by randomized treatment group: all randomized participants. Replacing all missing values with baseline value
eTable 8. Sensitivity analysis. Baseline values, 6-month and 12-month changes in nutrient intake by randomized treatment group: all randomized participants. Replacing all missing values with baseline value.
eTable 9. Baseline and 12- month change (95% confidence intervals) in risk factors, by treatment group: all randomized 245 participants (multiple imputation [MI]) and completers only.
eFigure 1. Mean values (95% CI) of scores capturing the 4 quality dietary patterns at baseline, at 6 months and at 12 months according to the randomized treatment group.
eFigure 2. Percentage of participants complying with the intended dietary changes by randomized treatment group
eFigure 3 Changes in nutritional variables (expressed in common units of baseline standard deviations) after 6 and 12 months in the control and in the intervention group.
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Sayón-Orea C, Razquin C, Bulló M, et al. Effect of a Nutritional and Behavioral Intervention on Energy-Reduced Mediterranean Diet Adherence Among Patients With Metabolic Syndrome: Interim Analysis of the PREDIMED-Plus Randomized Clinical Trial. JAMA. 2019;322(15):1486–1499. doi:10.1001/jama.2019.14630
What is the effect of a nutritional and behavioral intervention focused on encouraging an energy-reduced Mediterranean diet and physical activity on the dietary pattern of participants after 12 months?
In this preliminary analysis of an ongoing randomized clinical trial involving 6874 participants, an intervention focused on encouraging an energy-reduced Mediterranean diet and promoting physical activity, compared with advice to follow an energy-unrestricted Mediterranean diet, resulted in a significant increase in a measure of diet adherence, the 17-item energy-reduced Mediterranean diet score, at 12 months (4.7 points vs 2.5 points; score range, 0-17; minimal clinically important difference, 1 point).
A nutritional and behavioral intervention focused on encouraging an energy-reduced Mediterranean diet and physical activity led to a significant improvement in a measure of diet adherence at 12 months. Further evaluation of the effects on long-term cardiovascular and other health outcomes is needed.
High-quality dietary patterns may help prevent chronic disease, but limited data exist from randomized trials about the effects of nutritional and behavioral interventions on dietary changes.
To assess the effect of a nutritional and physical activity education program on dietary quality.
Design, Setting, and Participants
Preliminary exploratory interim analysis of an ongoing randomized trial. In 23 research centers in Spain, 6874 men and women aged 55 to 75 years with metabolic syndrome and no cardiovascular disease were enrolled in the trial between September 2013 and December 2016, with final data collection in March 2019.
Participants were randomized to an intervention group that encouraged an energy-reduced Mediterranean diet, promoted physical activity, and provided behavioral support (n = 3406) or to a control group that encouraged an energy-unrestricted Mediterranean diet (n = 3468). All participants received allotments of extra-virgin olive oil (1 L/mo) and nuts (125 g/mo) for free.
Main Outcomes and Measures
The primary outcome was 12-month change in adherence based on the energy-reduced Mediterranean diet (er-MedDiet) score (range, 0-17; higher scores indicate greater adherence; minimal clinically important difference, 1 point).
Among 6874 randomized participants (mean [SD] age, 65.0 [4.9] years; 3406 [52%] men), 6583 (96%) completed the 12-month follow-up and were included in the main analysis. The mean (SD) er-MedDiet score was 8.5 (2.6) at baseline and 13.2 (2.7) at 12 months in the intervention group (increase, 4.7 [95% CI, 4.6-4.8]) and 8.6 (2.7) at baseline and 11.1 (2.8) at 12 months in the control group (increase, 2.5 [95% CI, 2.3-2.6]) (between-group difference, 2.2 [95% CI, 2.1-2.4]; P < .001).
Conclusions and Relevance
In this preliminary analysis of an ongoing trial, an intervention that encouraged an energy-reduced Mediterranean diet and physical activity, compared with advice to follow an energy-unrestricted Mediterranean diet, resulted in a significantly greater increase in diet adherence after 12 months. Further evaluation of long-term cardiovascular effects is needed.
isrctn.com Identifier: ISRCTN89898870
The disease burden of elevated body mass index (BMI) has increased rapidly during the past 3 decades1,2 in close association with excess caloric intake and poor nutritional quality. Evaluations of lifestyle interventions to mitigate overweight and obesity are among the top priorities in public health. High adherence to high-quality dietary patterns coupled with reduced calorie intake may represent a sound solution for confronting adiposity-associated chronic diseases that can compromise the sustainability of most health systems.3
Quiz Ref IDGood adherence to the traditional Mediterranean diet presents an optimal nutrient profile4-6; has been associated with reduced all-cause mortality,3 nonfatal cardiovascular disease,4,7-9 type 2 diabetes and its long-term complications,10,11 and overweight/obesity12; and has demonstrated long-term sustainability and nutritional quality.13 An energy-reduced Mediterranean diet may represent an optimal model for participants with overweight or obesity to be evaluated in large long-term randomized clinical trials (RCTs). This was the rationale behind the PREDIMED-Plus trial.14 However, the main challenge for feasibility of large RCTs examining nutritional interventions using a whole dietary pattern is the expected adherence with the intended goals. Because randomly allocating thousands of healthy, free-living participants to follow a diet that was not their choice for several years may not be an easy endeavor, the selected dietary goals should have sufficient appeal. In this context, the traditional Mediterranean diet seems sufficiently attractive and realistic for individuals to adhere to. Initial results of the pilot study of 626 participants of this trial were previously reported.15
The aim of this study was to examine adherence and changes in risk factors after the 12-month intervention of an energy-reduced Mediterranean diet vs a control Mediterranean diet. This study reports interim 1-year results focused on exploratory end points of a larger ongoing RCT.
The methods have been published14,15 and are described in detail in Supplement 1 and Supplement 2. Briefly, this multicenter, parallel-group, randomized, single-blind clinical trial is evaluating the long-term effects of a lifestyle intervention including an energy-reduced Mediterranean diet, promotion of physical activity, and behavioral support for weight loss (intervention group) vs a control group following a traditional Mediterranean diet without any caloric restriction on cardiovascular events. This trial was approved by the institutional review board of all participating institutions. All participants provided written informed consent.
Eligible participants were community-dwelling men aged 55 to 75 years and women aged 60 to 75 years without cardiovascular disease at baseline who had an initial BMI of 27 to 40 and met at least 3 criteria for metabolic syndrome.16 Between September 2013 and December 2016, participants were recruited in 23 Spanish National Health System research centers in Spain. Participants were randomized in a 1:1 ratio to the intervention group or to the control group using a computer-generated random number internet-based system with stratification by center, sex, and age (<65 years, 65-70 years, and >70 years) in blocks of 6 participants. The randomization procedure was blinded to all staff members and principal investigators and was audited for all centers. For participant couples sharing the same household, randomization was done by cluster, with the couple as the unit of randomization.
Participants randomized to the intervention group were instructed to follow an energy-reduced Mediterranean diet, accompanied by physical activity promotion and behavioral support, with the purpose of accomplishing specific weight loss objectives.14,15 Trained dietitians conducted a group session, an individual motivational interview, and a phone call each month during the first year. Considering basal metabolic rate and level of physical activity of each participant in the intervention group, a reduction of approximately 30% of estimated energy requirements, which represents a reduction of approximately 600 kcal/d, was recommended. However, actual energy intake reduction was expected to be modest because the trial was conducted among free-living participants and levels of physical activity were expected to increase.
Participants in the control group attended 2 educational sessions per year on the traditional Mediterranean diet with ad libitum caloric intake, all contents previously used in PREDIMED trial8 and general lifestyle recommendations according to usual care practices in the Spanish National Health System. This group received an individual visit, telephone call, and group session every 6 months during the first year.
The energy-reduced Mediterranean diet differed from the diet recommended to the control group in that there were more restrictive limits for red and processed meats, butter, margarine or cream, and carbonated sweetened beverages. Also, for participants following the energy-reduced Mediterranean diet, it was recommended to not add sugar to beverages and to limit white bread and refined cereal consumption, while promoting the consumption of whole grains. Participants in both groups were provided with an allotment of extra-virgin olive oil (1 L/mo) and almonds (125 g/mo) for free. However, we recommended that all participants consume a total of 500 g/mo of mixed nuts.
Baseline and follow-up examinations were conducted by trained dietitians and included the assisted completion of different questionnaires by the participant. Results of a validated 143-item semiquantitative food frequency questionnaire were collected at baseline and at 6 and 12 months17 during face-to-face visits to assess food habits during the preceding 6 months. Food composition tables were used to derive energy and nutrient intake.18
Changes in 4 dietary scores19-21 (eTable 1 in Supplement 3) that reflected adherence to dietary patterns were assessed. Three of the scores measured adherence to the Mediterranean diet and a 17-item questionnaire was used to assess adherence to the energy-reduced Mediterranean diet (er-MedDiet score). This 17-item questionnaire is a modified version of the previously validated 14-item Mediterranean Diet Adherence Screener (MEDAS) questionnaire, which was also used in this trial.20 In the 17-item version,14 more restrictive cutoffs for some caloric-dense items were used and a few additional items aimed to reduce caloric intake were added. The third measure was the Mediterranean Diet Score (MDS),19 a well-known measure that has repeatedly shown to be inversely associated with all-cause mortality and the risk of clinical cardiovascular events in large prospective cohort studies. The fourth measure was the Prime Diet Quality Score (PDQS), which is based on the Prime Screen questionnaire and tries to meet both simplicity in assessing dietary habits and high discriminative ability to identify associations with the risk of noncommunicable diseases.21
At baseline and the 6- and 12-month follow-up visits, information was collected on physical activity,22,23 lifestyle, medication use, and other variables. At each visit, nurses measured waist circumference (midway between the lowest rib and the iliac crest, using an anthropometric tape), weight (using high-quality electronic calibrated scales), and height (using a wall-mounted stadiometer) twice. Blood pressure was measured 3 times using a validated semiautomatic oscillometer (Omron HEM-705CP). At baseline, 6 months, and 12 months, plasma total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides concentrations were measured in blood samples collected after an overnight fast and using standard enzymatic methods.
Quiz Ref IDThe primary end point for this interim analysis was change from baseline to 12 months in adherence to the energy-reduced Mediterranean diet, measured with the er-Med Diet score (range, 0-17; higher scores indicate greater adherence; minimally clinically important difference, 1 point). Secondary end points included the MEDAS score (range, 0-14), the MDS (range, 0-9), and the PDQS (range, 0-42) (eTable 1 in Supplement 3). For all secondary end point measures, higher scores indicate better dietary quality. Other secondary outcomes were changes in nutrients (measured via total energy intake; percentage of energy from macronutrients and alcohol; and the intake of fiber, long-chain Ω-3 fatty acids, dietary cholesterol, and sodium); consumption of key food items, including refined and extra-virgin olive oil, nuts, fruits, vegetables, cereals (whole grain and refined), legumes, fish, meat (red and processed), pastries, dairy (yogurt and fermented, low-fat, and whole-fat dairy), and alcohol (red wine); and cardiovascular risk factors, including body weight, waist circumference, body mass index (BMI), total serum cholesterol, HDL cholesterol, LDL cholesterol, non–HDL cholesterol, total cholesterol:HDL cholesterol ratio, triglycerides, and systolic and diastolic blood pressure.
We compared the percentage of participants in each group who achieved any favorable dietary changes (ie, any change in the desirable direction) and also the percentage of participants with clinically meaningful changes in classic risk factors. We considered reductions of at least 5% in BMI,24 body weight,25 waist circumference,25 total cholesterol, LDL cholesterol,26 non–HDL cholesterol, and cholesterol:HDL cholesterol ratio; reductions of at least 5 mm Hg in systolic or at least 2.5 mm Hg in diastolic blood pressure27; and an increase of at least 5% in HDL cholesterol as minimal clinically important differences.28 For triglycerides, we considered a 10% reduction as the minimal clinically important difference.29
Calculation of sample size was done for the primary end point of the overall trial (composite of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death).14 We used the database from the overall trial, which was dated on March 12, 2019. Principal analyses included all randomized participants with baseline nutritional data, regardless of whether they had incomplete information at follow-up visits, with multiple imputation procedures for missing data. Secondary analyses included only participants with complete information available at each follow-up visit.
For the principal analysis, we excluded participants who did not complete food frequency questionnaires at baseline and who had total energy intake beyond prespecified limits (500-3500 kcal/d for women and 800-4000 kcal/d for men).30 For the post hoc sensitivity analyses (completers only), we further excluded participants without nutritional information at follow-up (Figure 1).
In the main analyses, multiple imputation methods used an iterative Markov chain Monte Carlo method (STATA “mi” command). We generated 8 imputations for each missing measurement. Imputed missing values were used for follow-up data but not for baseline data. The imputation models included sex, age, smoking status, education level, BMI, physical activity, study group, total energy intake, and the baseline value of the variable that was imputed as predictors.
Mixed-effects linear models were used to assess changes in nutritional variables from baseline to 6- and 12-month follow-up in all randomized participants and completer-only analyses. We fitted a 3-level mixed linear model with random intercepts at site, participant, and cluster family level. All secondary analyses were exploratory; therefore, no additional adjustment was conducted to adjust for type I error.
Post hoc sensitivity analyses were conducted by (1) including only participants with complete information available at 6- or 12-month follow-up (completers only; eTables 3, 4, and 5 in Supplement 3) and (2) repeating all analyses after replacing all missing values with baseline values (eTables 6, 7, and 8 in Supplement 3). All analyses were conducted with Stata, version 15.0 (Stata Corp). All statistical tests were 2-sided and P < .05 was deemed statistically significant.
Of 6874 patients who were recruited and randomized, 53 who did not complete the food frequency questionnaire at baseline (28 from the intervention group and 25 from the control group) and 238 with total energy intake beyond prespecified limits (106 from the intervention and 132 from the control group) were excluded. A total of 6583 participants (3406 men and 3177 women; 3272 in the intervention group and 3311 in the control group) were analyzed (Figure 1). Imputed missing values for nutritional variables were 12.7% at 6 months and 12.2% at 12 months. Baseline characteristics of participants in the intervention and control groups were similar (Table 1).
The mean (SD) er-MedDiet score was 8.5 (2.6) at baseline and 13.2 (2.7) at 12 months in the intervention group (increase, 4.7 [95% CI, 4.6-4.8]) and 8.6 (2.7) at baseline and 11.1 (2.8) at 12 months in the control group (increase, 2.5 [95% CI, 2.3-2.6]) (between-group difference, 2.2 [95% CI, 2.1-2.4]; P < .001; eFigure 1 in Supplement 3). The improvements in the er-MedDiet score in the intervention group represented a significant 55% ([95% CI, 55%-56%]; P < .001) relative increase over 12 months (Table 2). Figure 2 shows the distribution of er-MedDiet scores at baseline and at the 12-month follow-up in each group. The intervention group exhibited greater improvements in the overall distribution of this score.
The mean (SD) baseline PDQS value was 21.1 (3.7) in both groups. Within-group changes in PDQS scores were significant at 12 months in the control group (difference, 4.4 [95% CI, 4.2-4.7]; P < .001) and in the intervention group (difference, 6.9 [95% CI, 6.6-7.1]; P < .001). There was a statistically significant difference in the PDQS score at 12 months between the groups (difference, 2.4 [95% CI, 2.1-2.8]; P <.001). These differences were maintained in post hoc sensitivity analyses (eFigure 1, eTable 3, and eTable 6 in Supplement 3). Results for the other dietary scores can be seen in Table 2.
Significant reductions in the consumption of specific foods or food groups after 12 months were observed (eTable 2 in Supplement 3). Baseline consumption of refined grains was 779 g/wk in both groups and reductions after 12 months were −535 g/wk (95% CI, −559 to −510) in the intervention group compared with −226 g/wk (95% CI, −249 to −203) in the control group, with a significant between-group difference of −309 g/wk ([95% CI, −340 to −277]; P <.001). For pastries, mean baseline consumption was 114 g/wk in the control group and 121 g/wk in the intervention group, with significant within-group differences after 12 months of −60 g/wk ([95% CI, −67 to −53]; P < .001) in the control group and −109 g/wk ([95% CI, −116 to −102]; P < .001) in the intervention group. The between-group difference of −49 g/wk in pastry consumption was also statistically significant ([95% CI, −59 to −39]; P <.001). Significant reductions in red meat consumption were also observed; the between-group difference after 12 months was −39 g/wk ([95% CI, −51 to −28]; P<.001). Some of the greatest increases were observed for vegetables, with mean baseline consumption of 2130 g/wk in the control group and 2168 g/wk in the intervention group and within-group differences after 12 months of 137 g/wk (95% CI, 100-175) in the control group and 347 g/wk (95% CI, 306-389) in intervention group; the between-group difference of 210 g/wk was significant ([95% CI, 157-263]; P <.001). The 12-month between-group difference was also significant for fruits (difference, 197 g/wk [95% CI, 118-276]; P <.001) and for nuts (baseline consumption in both groups, 60 g/wk; 12-month between-group difference, 35 g/wk [95% CI, 27-43]; P <.001) (eTable 2 in Supplement 3). Post hoc sensitivity analyses showed similar results (eTable 4 and eTable 7 in Supplement 3).
Mean (SD) total energy intake at baseline was 2369 (555) kcal/d in the control group and 2355 (555) kcal/d in the intervention group; the 12-month between-group difference in energy intake was statistically significant (difference, −102 kcal/d [95% CI, −129 to −75]; P <.001) (Table 3; eTable 5 and eTable 8 in Supplement 3). The mean percentage of energy from carbohydrates decreased in both groups, with a statistically significant 12-month between-group difference of −1.4% ([95% CI, −1.8 to −1.0]; P <.001). Increases in energy from monounsaturated fatty acids were observed from the mean (SD) baseline intake of 20.6% (4.6) of total energy intake in the control group and 20.5% (4.7) in the intervention group; within-group significant increases after 12 months were observed in the control group (difference, 3.0% [95% CI, 2.8%-3.2%]; P <.001) and the intervention group (difference, 3.9% [95% CI, 3.7%-4.1%]; P <.001), with a significant between-group difference of 0.9% ([95% CI, 0.6%-1.2%]; P < .001). The proportion of participants achieving any favorable dietary changes was significantly higher in the intervention than in the control group for most comparisons (eFigure 2 in Supplement 3).
eFigure 3 in Supplement 3 shows differences in total energy and nutrient intake between both groups, comparing changes at the 6-month and 12-month follow-up with all differences expressed in common units of baseline SD of each nutritional variable for the sake of comparability.
The mean changes after 6 and 12 months in cardiovascular risk factors and the percentage of participants who attained a clinically meaningful change in risk factors after 12 months are presented in Figure 3 and Figure 4.
With few exceptions, such as LDL cholesterol, significant and clinically meaningful favorable changes for the intervention vs the control group in body weight, waist circumference, BMI, HDL cholesterol, non–HDL cholesterol, total cholesterol:HDL cholesterol ratio, serum triglycerides, and systolic and diastolic blood pressure after 12 months were observed (Figure 3; eTable 9 in Supplement 3). For example, mean waist circumference was 108 cm at baseline in both the control and intervention groups, and the between-group difference at 12 months was −3.3 cm ([95% CI, −3.6 to −2.9]; P <.001). Mean systolic blood pressure was 139 mm Hg at baseline in the control group and 140 mm Hg in the intervention group, with a between-group difference at 12 months of −1.9 ([95% CI, −2.7 to −1.1]; P <.001).
Quiz Ref IDIn this preliminary analysis of an ongoing clinical trial, an intervention that encouraged an energy-reduced Mediterranean diet and physical activity, compared with advice to follow an energy-unrestricted Mediterranean diet, resulted in a significantly greater increase in diet adherence to an energy-reduced Mediterranean diet at 12 months. Improvements in diet quality, energy intake, and cardiovascular risk factors also were observed in the energy-reduced Mediterranean diet group. These findings are consistent with the previously reported preliminary findings from the pilot study of 626 participants of this trial.14
Quiz Ref IDThe intervention program included individual interviews and group motivational sessions with counseling to follow the traditional Mediterranean diet and reduce caloric intake and showed meaningful and sustainable short- and long-term changes in overall dietary quality and risk factors. The control group only received a low-intensity intervention promoting a traditional Mediterranean diet, without any special effort in energy reduction, physical activity, or weight loss beyond the usual care received in the Spanish National Health System. Because of this, the level of participant interaction was 6-fold higher in the intervention than in the control group, with 18 interactions in the intervention group vs 3 in the control group in 6 months. Participants in both groups received free extra-virgin olive oil and nuts.
Change at 12 months in the 17-item MedDiet score, which measured adherence to an energy-reduced Mediterranean diet, was the primary end point. In the intervention group, the MedDiet score increased significantly more in the intervention group than in the control group. These results showing sufficient contrast support the effectiveness of this study intervention to overcome the most difficult challenge in dietary intervention trials, namely the adherence of participants to the intervention. Furthermore, these dietary changes were paralleled by successful changes in most classic risk factors.
Quiz Ref IDBoth randomized groups were educated in following a Mediterranean diet. Therefore, it is of no surprise that olive oil consumption, the hallmark of a Mediterranean diet, increased in both groups. Many beneficial effects attributed to the Mediterranean diet were due to the consumption of extra-virgin olive oil, which contains high amounts of dietary bioactive phenolic compounds with antioxidant and anti-inflammatory properties.31 These compounds are not present in common, refined varieties of olive oil. Participants in both groups reduced their consumption of this suboptimal refined variety of olive oil. The energy reduction applied only to the intervention group may in part explain why no meaningful between-group differences in extra-virgin olive oil consumption were observed.
The effectiveness of the intervention, reflected by significant changes in dietary habits and reduced cardiovascular risk factors, support that nutritional interventions and behavioral therapies in patients at high cardiovascular risk, including patients with diabetes and metabolic syndrome, are likely to facilitate modifications of targeted dietary habits, reductions in body weight, and improvements in risk factors.32,33 A 2019 systematic review34 concluded that the most effective dietary interventions should avoid low participation rates and promote high retention rates, have long study duration, intervene at multiple levels, and include multiple face-to-face interactions. This trial, with 36 interactions during the first year, represents one of the largest RCTs in which all these characteristics were present. These continuous interactions between trained personnel and the participants of the PREDIMED-Plus trial partially explain the attained results. However, because this is an interim exploratory analysis of an ongoing trial, these results should be considered preliminary. Also, further analyses are needed to assess whether the effect size and adherence are maintained after a longer follow-up.
The principal strengths of the present study are its randomized design and its large sample size. Repeated data collection and main analyses based on inclusion of all randomized participants are additional strengths.
This study has several limitations. First, the use of self-reported data to evaluate nutritional changes could be a source of information bias. Second, recall bias, social desirability bias, and other potential reporting biases may have affected the results. However, the tools used to repeatedly evaluate food and nutrient intake were previously validated,17,20 and it seems reasonable to assume that these biases, if they existed, would be similar in both groups because both groups received advice encouraging a Mediterranean diet. Importantly, dietary results were paralleled by changes in objectively measured risk factors that are free from these potential issues. Third, the strategy of donating food items was used as an incentive for attendance to educational sessions and to foster adherence. However, this strategy can also represent a limitation regarding the generalizability of these results to populations in which access to or affordability of high-quality olive oil and tree nuts might be a barrier. Fourth, these findings are based on interim and preliminary analyses within the context of the overall main outcomes of an ongoing RCT, and whether and how these results may be related to long-term cardiovascular and other health outcomes are unknown. Fifth, the dietary intervention was multifaceted and it is not possible to determine which aspects of the intervention may be influencing the outcomes.
In this preliminary analysis of an ongoing trial, an intervention that encouraged an energy-reduced Mediterranean diet and physical activity, compared with advice to follow an energy-unrestricted Mediterranean diet, resulted in a significantly greater increase in diet adherence after 12 months. Further evaluation of long-term cardiovascular effects is needed.
Corresponding Authors: Miguel A. Martínez-González, MD, Department of Preventive Medicine and Public Health, University of Navarra, C/Irunlarrea, 1, 31080 Pamplona, Navarra, Spain (email@example.com); Jordi Salas-Salvadó, MD, Human Nutrition Unit, Faculty of Medicine and Health Sciences, Universitat Rovira i Virgili, C/ Sant Llorenç, 21, 43201 Reus, Tarragona, Spain (firstname.lastname@example.org).
Accepted for Publication: August 23, 2019.
Correction: This article was corrected on November 1, 2021, to correct an error in eTable 1 in Supplement 2 in which it was not indicated that the outcome "Bone density and body composition measured with DXA" was measured at 1- and 3-year follow-up.
Author Contributions: Drs Martínez-González and Salas-Salvadó had full access to all of the data in the study, take responsibility for the integrity of the data and the accuracy of the data analysis. Drs Martínez-González and Salas-Salvadó equally contributed as co–senior authors.
Concept and design: Corella, Fitó, Wärnberg, Martínez, Serra-Majem, Estruch, Pintó, Bueno-Cavanillas, Delgado-Rodriguez, Daimiel, Vidal, Sorlí, Gómez-Gracia, Basora, Toledo, Díaz-López, Salas-Salvadó, Martínez-González.
Acquisition, analysis, or interpretation of data: Sayon-Orea, Razquin, Bulló, Corella, Fitó, Romaguera, Vioque, Alonso-Gomez, Wärnberg, Martínez, Serra-Majem, Estruch, Tinahones, Lapetra, Pintó, Tur, López-Miranda, Bueno-Cavanillas, Delgado-Rodriguez, Matía-Martín, Daimiel, Martín-Sánchez, Vidal, Vázquez, Ros, Ruiz-Canela, Sorlí, Castañer, Fiol, Navarrete-Muñoz, Arós, Gómez-Gracia, Zulet, Sánchez-Villegas, Casas, Bernal-López, Santos-Lozano, Corbella, Bouzas, García-Arellano, Asensio, Schröder, Moñino, García de la Hera, Tojal-Sierra, Toledo, Díaz-López, Goday, Salas-Salvadó, Martínez-González.
Drafting of the manuscript: Sayon-Orea, Fitó, Alonso-Gomez, Martínez, Tinahones, Pintó, Vidal, Bernal-López, Salas-Salvadó, Martínez-González.
Critical revision of the manuscript for important intellectual content: Razquin, Bulló, Corella, Fitó, Romaguera, Vioque, Wärnberg, Martínez, Serra-Majem, Estruch, Tinahones, Lapetra, Pintó, Tur, López-Miranda, Bueno-Cavanillas, Delgado-Rodriguez, Matía-Martín, Daimiel, Martín-Sánchez, Vidal, Vázquez, Ros, Ruiz-Canela, Sorlí, Castañer, Fiol, Navarrete-Muñoz, Arós, Gómez-Gracia, Zulet, Sánchez-Villegas, Casas, Bernal-López, Santos-Lozano, Corbella, Bouzas, García-Arellano, Basora, Asensio, Schröder, Moñino, García de la Hera, Tojal-Sierra, Toledo, Díaz-López, Goday, Salas-Salvadó.
Statistical analysis: Sayon-Orea, Razquin, Martínez, Pintó, Bueno-Cavanillas, Gómez-Gracia, Corbella, Toledo, Díaz-López, Martínez-González.
Obtained funding: Corella, Romaguera, Vioque, Wärnberg, Martínez, Serra-Majem, Estruch, Tinahones, Pintó, Tur, López-Miranda, Bueno-Cavanillas, Delgado-Rodriguez, Daimiel, Martín-Sánchez, Vidal, Ros, Sorlí, Fiol, Arós, Bernal-López, Corbella, Basora, Toledo, Díaz-López, Salas-Salvadó, Martínez-González.
Administrative, technical, or material support: Corella, Romaguera, Serra-Majem, Estruch, Pintó, Tur, López-Miranda, Delgado-Rodriguez, Fiol, Navarrete-Muñoz, Casas, Corbella, Bouzas, García-Arellano, Basora, Moñino, Díaz-López, Salas-Salvadó, Martínez-González.
Supervision: Bulló, Corella, Fitó, Vioque, Martínez, Serra-Majem, Tinahones, Pintó, Tur, López-Miranda, Bueno-Cavanillas, Matía-Martín, Daimiel, Vidal, Sorlí, Gómez-Gracia, Zulet, Sánchez-Villegas, Basora, Goday, Salas-Salvadó, Martínez-González.
Conflict of Interest Disclosures: Dr Ros reported receiving grants, personal fees, and nonfinancial support from the California Walnut Commission during the conduct of the study and grants, personal fees, nonfinancial support from Alexion; grants from Amgen and Pfizer; grants and personal fees from Sanofi Aventis; personal fees and nonfinancial support from Ferrer International, Danone, and Merck Sharp & Dohme; and personal fees from Amarin outside the submitted work. Dr Corella reported receiving grants from Instituto de Salud Carlos III during the conduct of the study. Dr Romaguera reported receiving grants from Instituto de Salud Carlos III, Spanish government during the conduct of the study and grants from Fundación AstraZeneca outside the submitted work. Dr Estruch reported receiving grants from Instituto de Salud Carlos III and olive oil for the trial from Fundacion Patrimonio Comunal Olivarero \during the conduct of the study and personal fees from Brewers of Europe, Fundación Cerveza y Salud, Interprofesional del Aceite de Oliva, Instituto Cervantes, Instituto Cervantes, Pernaud Richar, Fundación Dieta Mediterránea, Wine and Culinary International Forum; nonfinancial support from Sociedad Española de Nutrición and Fundación Bosch y Gimpera; and grants from Uriach Laboratories outside the submitted work. Dr López-Miranda reported receiving grants from Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III during the conduct of the study. Dr Matía-Martín reported receiving grants from Instituto de Salud Carlos III during the conduct of the study and personal fees from Organización Interprofesional Láctea outside the submitted work. Dr Vidal reported receiving grants from Instituto de Salud Carlos III during the conduct of the study. Dr Fiol reported receiving grants from Instituto de Salud Carlos III, Spanish government during the conduct of the study. Dr Arós reported receiving grants from Instituto de Salud Carlos III, Fondo de Investigaciones Sanitarias (Spain) and from CIBEROBN, Instituto de Salud Carlos III (Spain) during the conduct of the study. Dr Moñino reported receiving grants from Instituto de Salud Carlos III, Spanish government during the conduct of the study. Dr Bouzas reported received a Fernando Tarongí Bauzà grant. Dr Salas-Salvado reported receiving research support from the Instituto de Salud Carlos III, Ministerio de Educación y Ciencia, Departament de Salut Pública de la Generalitat de Catalunya, the European Commission, the California Walnut Commission, Patrimonio Comunal Olivarero, La Morella Nuts, and Borges S.A; receiving consulting fees or travel expenses from Danone, California Walnut Commission, Eroski Foundation, Instituto Danone, Nestle, and Abbott Laboratories, receiving nonfinancial support from Hojiblanca, Patrimonio Comunal Olivarero, and Almond Board of California; serving on the board of and receiving grant support through his institution from the International Nut and Dried Foundation and the Eroski Foundation; and grants and personal fees from Instituto Danone. No other disclosures were reported.
Funding/Support: This work was supported by the European Research Council (Advanced Research grant 2014-2019; agreement #340918; granted to Dr Martínez-González); the official Spanish institutions for funding scientific biomedical research, CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn) and Instituto de Salud Carlos III (ISCIII) through the Fondo de Investigación para la Salud (FIS), which is cofunded by the European Regional Development Fund (coordinated FIS projects led by Drs Salas-Salvadó and Vidal, including the following projects: PI13/00673, PI13/00492, PI13/00272, PI13/01123, PI13/00462, PI13/00233, PI13/02184, PI13/00728, PI13/01090, PI13/01056, PI14/01722, PI14/00636, PI14/00618, PI14/00696, PI14/01206, PI14/01919, PI14/00853, PI14/01374, PI14/00972, PI14/00728, PI14/01471, PI16/00473, PI16/00662, PI16/01873, PI16/01094, PI16/00501, PI16/00533, PI16/00381, PI16/00366, PI16/01522, PI16/01120, PI17/00764, PI17/01183, PI17/00855, PI17/01347, PI17/00525, PI17/01827, PI17/00532, PI17/00215, PI17/01441, PI17/00508, PI17/01732, PI17/00926, PI19/00957, PI19/00386, PI19/00309, PI19/01032, PI19/00576, PI19/00017, PI19/01226, PI19/00781, PI19/01560, PI19/01332) and the Especial Action Project “Implementación y evaluación de una intervención intensivasobre la actividad física Cohorte PREDIMED-Plus” (Dr Salas-Salvadó); the Recercaixa (grant number 2013ACUP00194) (Dr Salas-Salvadó); the SEMERGEN grant; International Nut and Dried Fruit Council–FESNAD (Long-term effects of an energy-restricted Mediterranean diet on mortality and cardiovascular disease 2014 –2015; No. 201302) (Dr Martinez-Gonzalez); the AstraZeneca Young Investigators Award in Category of Obesity and T2D 2017 (Dr Romaguera); grants from the Consejería de Salud de la Junta de Andalucía (PI0458/2013; PS0358/2016; PI0137/2018), the PROMETEO/2017/017 grant from the Generalitat Valenciana, the SEMERGEN grant; grant of support to research groups 35/2011 (Balearic Islands Gov; FEDER funds) (Drs Tur and Bouzas).
Role of the Funder/Sponsor: The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Group Information: Nonauthor collaborators who contributed to data collection and assistance: P. Buil-Cosiales, Z. Vázquez, A. Sanchez Tainta, B. SanJulian Aranguren, E. Goñi, I. Barrientos, M. Canales, M. Arias, E. Lorenzo, M.J. Cobo, A. Rico, F.J. Basterra Gortari, I. Zazpe, M. Bes-Rastrollo, J. Diez-Espino, O. Lecea-Juarez, J. Carlos Cenoz-Osinaga, J. Bartolome-Resano, E. Lozano-Oloriz, B. Cano-Valles, S. Eguaras, E. Pascual Roquet-Jalmar, I. Galilea-Zabalza, H. Lancova, R. Ramallal, M.L. Garcia-Perez, V. Estremera-Urabayen, M.J. Ariz-Arnedo, C. Hijos-Larraz, C. Fernandez Alfaro, B. Iñigo-Martinez, R. Villanueva Moreno, S. Martin-Almendros, L. Barandiaran-Bengoetxea, C. Fuertes-Goñi, A. Lezaun-Indurain, M.J. Guruchaga-Arcelus, O. Olmedo-Cruz, B. Iñigo-Martínez, L. Escriche-Erviti, R. Ansorena-Ros, R. Sanmatin-Zabaleta, J. Apalategi-Lasa, J. Villanueva-Telleria, M.M. Hernández-Espinosa, I. Arroyo-Bergera, L. Herrera-Valdez, L. Dorronsoro-Dorronsoro (Department of Preventive Medicine and Public Health, University of Navarra-Navarra Institute for Health Research (IdiSNA), Osasunbidea-SNS, Pamplona, Spain); R. Pedret Llaberia, R. Gonzalez, R. Sagarra Álamo, F. París Palleja, J. Balsells, J.M. Roca, T. Basora Gallisa, J. Vizcaino, P. Llobet Alpizarte, C. Anguera Perpiñá, M. Llauradó Vernet, C. Caballero, M. Garcia Barco, M.D. Morán Martínez, J. García Rosselló, A. Del Pozo, C. Poblet Calaf, P. Arcelin Zabal, X. Floresví, M. Ciutat Benet, A. Palau Galindo, J.J. Cabré Vila, F. Dolz Andrés, M. Soler, M. Gracia Vidal, J. Vilalta J. Boj Casajuana, M. Ricard, F. Saiz, A. Isach, M. Sanchez Marin Martinez, E. Granado Font, C, Lucena Luque, C. Mestres Sola, M. Bulló, N. Babio, N. Becerra-Tomás, G. Mestres, J. Basora, G. Mena-Sánchez, L. Barrubés Piñol, M. Gil Segura, C. Papandreou, N. Rosique-Esteban, S. Chig, I. Abellán Cano, V. Ruiz García, A. Salas-Huetos, I. Paz-Graniel, L. Sánchez Niembro, P. Hernandez-Alonso, S. Canudas, L. Camacho-Barcia, J. García-Gavilán, A. Díaz-López(Rovira i Virgili University, Department of Biochemistry and Biotechnology, Human Nutrition Unit, University Hospital of Sant Joan de Reus, Pere Virgili Institute for Health Research, Reus, Spain); J.I. González, O. Portolés, R. Fernández-Carrión, C. Ortega-Azorín, R. Barragán, E.M. Asensio, O. Coltell, C. Sáiz, R. Osma, E. Férriz, I. González-Monje, F. Giménez-Fernández, L. Quiles, P. Carrasco, P. Guillem Saiz, A. Carratalá-Calvo, C. Valero-Barceló, F. Antón, C. Mir, S. Sánchez-Navarro, J. Navas, I. González-Gallego, L. Bort-Llorca, L. Pérez-Ollero, M. Giner-Valero, R. Monfort-Sáez, J. Nadal-Sayol, V. Pascual-Fuster, M. Martínez-Pérez, C. Riera, M.V. Belda, A. Medina, E. Miralles, M.J. Ramírez-Esplugues, M. Rojo-Furió, G. Mattingley, M.A. Delgado, M.A. Pages, Y. Riofrío, L. Abuomar, N. Blasco-Lafarga, R. Tosca, L. Lizán, A.M. Valcarce, M.D. Medina, R. Martínez-Lacruz, S. de Valcárcel, N. Tormo, O. Felipe-Román, S. Lafuente, E.I. Navío, G. Aldana, J.V. Crespo, J.L. Llosa, L. González-García, R. Raga-Marí (Department of Preventive Medicine, University of Valencia, University Jaume I, Conselleria de Sanitat de la Generalitat Valenciana, Valencia, Spain); M.A. Muñoz; M.D. Zomeño, A. Hernaéz, L. Torres, M. Quifer, R. Llimona, G Freixer, A. Pérez, M. Farràs, R. Elosua, J. Vila, I. Subirana, S. Pérez, J.J. Chillaron Jordan, J.A. Flores Lerroux, D. Benaiges Boix, Llauradó G, M. Farré, E. Menoyo, D. Muñoz-Aguayo, S. Gaixas, G. Blanchart, A. Sanllorente, M. Soria, J. Valussi, A. Cuenca, L. Forcano, A. Pastor, A. Boronat, S. Tello, M. Cabañero, L. Franco, H. Schröder, R. De la Torre, C. Medrano, J. Bayó, M.T. García, V. Robledo, P. Babi, E. Canals, N. Soldevila, L. Carrés, C. Roca, M.S. Comas, G. Gasulla, X. Herraiz, A. Martínez, E. Vinyoles, J.M. Verdú, M. Masague Aguade, E. Baltasar Massip, M. Lopez Grau, M. Mengual, V. Moldon, M. Vila Vergaz, R. Cabanes Gómez, R. Ciurana, M. Gili Riu, A. Palomeras Vidal, F Peñas A. Raya, M.A. Sebastian, M. Valls (Cardiovascular Risk and Nutrition Research Group, Hospital del Mar Medical Research Institute, Barcelona. Department of Medicine, Autonomous University of Barcelona, Barcelona, Spain); S. González Palacios, L. Torres Collado, L. Compañ Gabucio, A. Oncina Canovas, L. Notario-Barandiaran, D. Orozco Beltran, S. Pertusa Martínez, A. Asensio, I. Candela García, J. Manuel Zazo, C. Gisbert Sellés, N. Fernández Brufal, J. Román Maciá, C. Sánchez Botella, M. García Muñoz, C. Barceló, M.C. Altozano Rodado, N. Iranzo García, M.C. Martínez Vergara, M.A. Sempere Pascual, S.J. Miralles Gisbert, A. González Botella, C.M. López García, R. Valls Enguix, N. Gómez Bellvert, I. López Aguilera, R. Lloret Macián, A. Pastor Morell, E. Alonso Bartolomé, J.J. Ballester Baixauli, M.T. Cano Sánchez, B.E. Ayús Rojo, E.P. Cases Pérez, C. Tercero Maciá, L.A. Mira Castejón, I.A. García García, M. Jordá Ballesta, C. Pastor Polo, E. Puig Agulló, M. Damaj Hamieh, V. Martínez Avilés, M.A. Belmar Bueno, M.V. Hernándis Marsán (Nutritional Epidemiology Unit, Miguel Hernandez University, ISABIAL-FISABIO, Alicante, Spain); A. Colom, J. Konieczna, M. Morey, R. Zamanillo, A.M. Galmés, V. Pereira, M.A. Martín, A. Yáñez, J. Llobera, J. Ripoll, R. Prieto, F. Grases, A. Costa, C. Fernández-Palomeque, E. Fortuny, M. Noris, S. Munuera, F. Tomás, F. Fiol, A. Jover, J.M. Janer, C. Vallespir, I. Mattei, N. Feuerbach, M. del Mar Sureda, S. Vega, L. Quintana, A. Fiol, M. Amador, S. González, J. Coll, A. Moyá (Hospital Son Espases and Institute for Health Research Illes Balears, Palma de Mallorca, Spain); I. Abete, I. Cantero, C. Cristobo, I. Ibero-Baraibar, J. Ágreda Martínez, M.D. Lezáun Burgui, N. Goñi Ruiz, R. Bartolomé Resano, E. Cano Cáceres, T. Elcarte López, E. Echarte Osacain, B. Pérez Sanz, I. Blanco Platero, S.A. Andueza Azcárate, A. Gimeno Aznar, E. Ursúa Sesma, B. Ojeda Bilbao, J. Martinez Jarauta, L. Ugalde Sarasa, B. Rípodas Echarte, M.V. Güeto Rubio (Department of Nutrition, Food Sciences, and Physiology, Center for Nutrition Research, University of Navarra, Osasunbidea-SNS, Pamplona, Spain); F.J. Barón-López, J.C. Fernández García, N. Pérez-Farinós, N. Moreno-Morales, M. del C. Rodríguez-Martínez, J. Pérez-López, J.C. Benavente-Marín, E. Crespo Oliva, E. Contreras Fernández, F.J. Carmona González, R. Carabaño Moral, S. Torres Moreno, M.V. Martín Ruíz, M. Alcalá Cornide, V. Fuentes Gómez (Department of Nursing, School of Health Sciences, Málaga, Spain); A. Garcia-Rios, J. Criado García, A.I. Jiménez Morales, N. Delgado Casado, A. Ortiz Morales, J.D. Torres Peña, F.J. Gómez Delgado, F. Rodríguez Cantalejo, J. Caballero Villaraso, J.F. Alcalá, P.J. Peña Orihuela, G. Quintana Navarro (Lipids and Atherosclerosis Unit, Department of Internal Medicine, Maimonides Biomedical Research Institute of Cordoba, Reina Sofia University Hospital, University of Cordoba, Cordoba, Spain); M. Domenech, C. Viñas, S. Castro-Barquero, A.M. Ruiz-León, M. Sadurní, G. Frontana, P. Villanueva, M. Gual, R. Soriano, M. Camafort, C. Sierra, E. Sacanella, A. Sala-Vila, J. M. Cots, I. Sarroca, M. García, N. Bermúdez, A. Pérez, I. Duaso, A. de la Arada, R. Hernández, C. Simón, M.A. de la Poza, I. Gil, M. Vila, C. Iglesias, N. Assens, M. Amatller, LL. Rams, T. Benet, G. Fernández, J. Teruel, A. Azorin, M. Cubells, D. López, J.M. Llovet, M.L. Gómez, P. Climente, L. de Paula, J. Soto, C. Carbonell, C. Llor, X. Abat, A. Cama, M. Fortuny, C. Domingo, A. I. Liberal, T. Martínez, E. Yañez, M. J. Nieto, A. Pérez, E. Lloret, C. Carrazoni, A. M. Belles, C. Olmos, M. Ramentol, M. J. Capell, I. Giner, A. Muñoz, R. Martín, E. Moron, A. Bonillo, G. Sánchez, C. Calbó, J. Pous, M. Massip, Y. García, M.C. Massagué, R. Ibañez, J. Llaona, T. Vidal, N. Vizcay, E. Segura, C. Galindo, M. Moreno, M. Caubet, J. Altirriba, G. Fluxà, P. Toribio, E. Torrent, J. J. Anton, A. Viaplana, G. Vieytes, N. Duch, A. Pereira, M. A. Moreno, A. Pérez, E. Sant, J. Gené, H. Calvillo, F. Pont, M. Puig, M. Casasayas, A. Garrich, E. Senar, A. Martínez, I. Boix, E. Sequeira, V. Aragunde, S. Riera, M. Salgado, M. Fuentes, E. Martín, A. Ubieto, F. Pallarés, C. Sala, A. Abilla, S. Moreno, E. Mayor, T. Colom, A. Gaspar, A. Gómez, L. Palacios, R. Garrigosa (Department of Internal Medicine, IDIBAPS, Hospital Clínic, University of Barcelona, Barcelona, Spain); L. García Molina, B. Riquelme Gallego, N. Cano Ibañez, A. Maldonado Calvo, A. López Maldonado, E.M. Garrido, A. Baena Dominguez, F. García Jiménez, E. Thomas Carazo, A. Jesús Turnes González, F. González Jiménez, F. Padilla Ruiz, J. Machado Santiago, M.D. Martínez Bellón, A. Pueyos Sánchez, L. Arribas Mir, R. Rodríguez Tapioles, F. Dorador Atienza, L. Baena Camus, C. Osorio Martos, D. Rueda Lozano, M. López Alcázar, F. Ramos Díaz, M. Cruz Rosales Sierra, P. Alguacil Cubero, A. López Rodriguez, F. Guerrero García, J. Tormo Molina, F. Ruiz Rodríguez (Department of Preventive Medicine and Public Health, University of Granada, Granada, Spain); J. Rekondo, I. Salaverria, M.C. Belló, A. Loma-Osorio, P. Bruyel, L. Goicolea, C. Sorto, A. Casi Casanellas, M.L. Arnal Otero, J. Ortueta Martínez De Arbulo, J. Vinagre Morgado, J. Romeo Ollora, J. Urraca, M.I. Sarriegui Carrera, F.J. Toribio, E. Magán, A. Rodríguez, S. Castro Madrid, M.T. Gómez Merino, M. Rodríguez Jiménez, M. Gutiérrez Jodra, B. López Alonso, J. Iturralde Iriso, C. Pascual Romero, A. Izquierdo De La Guerra (University Hospital Araba, Vitoria, Spain); M. Abbate, E. Angullo, E. Argelich, M.M. Bibiloni, X. Capó, S. Carreres, L. Gallardo, J.M. Gámez, B. García, C. García, A. Julibert, C. Gómez, I. Llompart, A. Martorell, C.M. Mascaró, D. Mateos, M, Monserrat, S. Montemayor, A. Pons, A. Pouso, J. Ramos, V. Ramos, T. Ripoll, T. Rodríguez, L. Sanz, A. Sureda, S. Tejada, L. Ugarriza (Research Group on Community Nutrition & Oxidative Stress, University of Balearic Islands, Palma de Mallorca, Spain); M.R. Bernal López, M. Macías González, J. Ruiz Nava, J.C. Fernández García, A. Muñoz Garach, A. Vilches Pérez, A. González Banderas, J. Alcaide Torres, A. Vargas Candela, M. León Fernández, R. Hernández Robles, S. Santamaría Fernández, J.M. Marín, S. Valdés Hernández, J.C. Villalobos, A. Ortiz (Virgen de la Victoria Hospital, University of Málaga, Málaga, Spain); J. Álvarez-Pérez, E.M. Díaz Benítez, F. Díaz-Collado, J. Pérez-Cabrera, L.T. Casañas-Quintana, R.B. García-Guerra, I. Bautista-Castaño, C. Ruano-Rodríguez, F. Sarmiento de la Fe, J.A. García-Pastor, B. Macías-Gutiérrez, I. Falcón-Sanabria, C. Simón-García, A.J. Santana-Santana, J.B. Álvarez-Álvarez, B.V. Díaz-González, J.M. Castillo Anzalas, R.E. Sosa-Also, J. Medina-Ponce (University of Las Palmas de Gran Canaria, Las Palmas, Spain); S. Abajo Olea, A. Adlbi Sibai, A. Aguado Arconada, L. Álvarez, E. Carriedo Ule, M. Escobar Fernández, J.I. Ferradal García, J.P. Fernández Vázquez, M. García González, C. González Donquiles, C. González Quintana, F. González Rivero, M. Lavinia Popescu, J.I. López Gil, J. López de la Iglesia, A. Marcos Delgado, C. Merino Acevedo, S. Reguero Celada, M. Rodríguez Bul, L. Vilorio-Marqués (Biomedicine Institute (IBIOMED); University of León, and Primary Health Care Management of León (Sacyl), León, Spain); L. Miró-Moriano, C. Domínguez-Espinaco, S. Vaquero-Díaz, F.J. García-Corte, A. Santos-Calonge, C. Toro-Cortés, N. Pelegrina-López, V. Urbano-Fernández, M. Ortega-Calvo, J. Lozano-Rodríguez, I. Rivera-Benítez, M. Caballero-Valderrama, P. Iglesias-Bonilla, P. Román-Torres, Y. Corchado-Albalat, L. Mellado-Martín (Department of Family Medicine, Primary Care District of Sevilla, Sevilla, Spain); A.I. de Cos, S. Gutierrez, S. Artola, A. Galdon, I. Gonzalo (Department of Endocrinology, Foundation Jiménez-Díaz, Madrid, Spain); A. Galera, M. Gimenez-Gracia, R. Figueras, M. Poch, R. Freixedas, F. Trias, I. Sarasa, M. Fanlo, H. Lafuente, M. Liceran, A. Rodriguez-Sanchez, C. Pallarols, J. Monedero, X. Corbella, E. Corbella (Lipids and Vascular Risk Unit, Internal Medicine, University Hospital of Bellvitge, Hospitalet de Llobregat, Barcelona, Spain); A. Altés, I. Vinagre, C. Mestre, J. Viaplana, M. Serra, J. Vera, T. Freitas, E. Ortega, I. Pla (Department of Endocrinology, IDIBAPS, Hospital Clinic, University of Barcelona, Barcelona, Spain); J.M. Ordovás, V. Micó, L. Berninches, M.J. Concejo, J. Muñoz, M. Adrián, Y. de la Fuente, C. Albertos, E. Villahoz, M.L. Cornejo, C. Cuesta. Montero A., Valdés, MC (Nutritional Genomics and Epigenomics Group, Institute IMDEA-Food, CEI UAM+CSIC, Madrid, Spain); J.J. Gaforio, S. Moraleda, N. Liétor, J.I. Peis, T. Ureña, M. Rueda, M.I. Ballesta (Division of Preventive Medicine, University of Jaén, Jaén, Spain); C. Moreno Lopera, C. Aragoneses Isabel, M.A. Sirur Flores, M. Ceballos de Diego, T. Bescos Cáceres, Y. Peña Cereceda, M. Martínez Abad, R. Cabrera Vélez, M. González Cerrajero, M.A. Rubio Herrera, M. Torrego Ellacuría, A. Barabash Bustelo, M. Ortiz Ramos, A. Larrad Sainz (Department of Endocrinology and Nutrition, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Madrid, Spain); J. Fernández-Crehuet Navajas, M. Gutiérrez Bedmar, A. García Rodriguez, A. Mariscal Larrubia, M. Carnero Varo, C. Muñoz Bravo (Department of Preventive Medicine, University of Malaga, Malaga, Spain). Additional support groups: C. Botella, F. Fernandez-Aranda, R. Lamuela, A. Marcos, M. del Puy Portillo, G. Sáez.
Data Sharing Statement: See Supplement 4.
Additional Contributions: We thank all the volunteers for their participation and personnel for the contribution in the PREDIMED-Plus trial. We also thank all the investigators of the PREDIMED-Plus study. The support provided by Dr Borge Nordestgaard, MD (Department of Clinical Medicine, Copenhagen University, Denmark), who did not receive compensation, to help us set minimal important differences in lipid levels is acknowledged.