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The potential impact of animal protein intake on global and abdominal obesity: evidence from the Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study

Published online by Cambridge University Press:  22 January 2015

Ala’a Alkerwi*
Affiliation:
Centre de Recherche Public Santé, Centre d’Etudes en Santé, 1 A rue Thomas Edison, L-1445 Strassen, Luxembourg
Nicolas Sauvageot
Affiliation:
Centre de Recherche Public Santé, Centre d’Etudes en Santé, 1 A rue Thomas Edison, L-1445 Strassen, Luxembourg
Jonathan D Buckley
Affiliation:
Nutritional Physiology Research Centre, University of South Australia, Adelaide, Australia
Anne-Françoise Donneau
Affiliation:
Département des Sciences de la Santé Publique, Université de Liège, Liège, Belgium
Adelin Albert
Affiliation:
Département des Sciences de la Santé Publique, Université de Liège, Liège, Belgium
Michèle Guillaume
Affiliation:
Département des Sciences de la Santé Publique, Université de Liège, Liège, Belgium
Georgina E Crichton
Affiliation:
Centre de Recherche Public Santé, Centre d’Etudes en Santé, 1 A rue Thomas Edison, L-1445 Strassen, Luxembourg Nutritional Physiology Research Centre, University of South Australia, Adelaide, Australia
*
* Corresponding author: Email [email protected]
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Abstract

Objective

To examine the association of total animal protein intake and protein derived from different dietary sources (meat; fish and shellfish; eggs; milk products) with global and abdominal obesity among adults in Luxembourg.

Design

Binary logistic regression analysis was used to assess the relationship between animal protein intake (as a percentage of total energy intake) and global obesity (BMI≥30·0 kg/m2) and abdominal obesity (waist circumference ≥102 cm for men and ≥88 cm for women), after controlling for potential confounders.

Setting

Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study.

Subjects

The study population was derived from a national cross-sectional stratified sample of 1152 individuals aged 18–69 years, recruited between November 2007 and January 2009.

Results

There was an independent positive association between total animal protein intake and both global (OR=1·18; 95 % CI 1·12, 1·25) and abdominal obesity (OR=1·14; 95 % CI 1·08, 1·20) after adjustment for age, gender, education, smoking, physical activity and intakes of total fat, carbohydrate, fibre, and fruit and vegetables. Protein intakes from meat, fish and shellfish were positively associated with global and abdominal obesity with further adjustment for vegetal protein and other sources of animal-derived protein (all P<0·01). Protein derived from eggs or milk products was unrelated to global or abdominal obesity.

Conclusions

Our findings suggest that protein derived from animal sources, in particular from meat, fish and shellfish, may be associated with increased risk of both global and abdominal obesity among presumably healthy adults in Luxembourg. These findings suggest that lower animal protein intakes may be important for maintenance of healthy body weight.

Type
Research Papers
Copyright
Copyright © The Authors 2015 

Obesity is a rapidly worsening public health problem associated with a variety of co-morbidities including type 2 diabetes, hypertension, stroke and CVD( 1 ). Obesity is impacting heavily upon health-care systems around the world, including Luxembourg, where 21 % of the population is obese( Reference Alkerwi, Sauvageot and Donneau 2 ). Obesity occurs in the context of a variety of interrelated demographic, socio-economic and lifestyle factors; nutrition is coming to the fore as a major modifiable determinant. Nutritional epidemiology has produced evidence that an energy-dense and high-fat diet, concomitant with physical inactivity, are independent risk factors for weight gain and obesity( Reference Astrup 3 Reference Mendoza, Drewnowski and Christakis 5 ).

The literature surrounding the effects of protein intake and particular sources of protein on body composition is unclear. Three recent meta-analyses have been conducted, comparing higher- v. lower-protein diets on health outcomes, including body composition( Reference Santesso, Akl and Bianchi 6 Reference Wycherley, Moran and Clifton 8 ), with conflicting conclusions. One indicates that a high protein intake in the context of an energy-restricted diet provides greater improvement in body composition compared with standard protein diets, matched for energy intake( Reference Wycherley, Moran and Clifton 8 ). Another systematic review concluded that higher-protein diets probably improve adiposity than lower-protein diets, but the effect is small( Reference Santesso, Akl and Bianchi 6 ). The most recent meta-analysis, which included studies using both energy-restricted and non-energy-restricted diets, reported no added benefit for body weight or body composition from a high-protein diet v. lower-protein diets( Reference Schwingshackl and Hoffmann 7 ). The reason for these different findings is not clear, but suggests that higher protein intakes may only benefit body composition when consumed as part of a weight-loss diet as there is no convincing evidence linking dietary protein intake and body weight under conditions of weight maintenance( Reference Hite, Feinman and Guzman 9 ). Nevertheless, protein-rich diets could have potential beneficial effects by increasing satiety and thermogenesis( Reference Paddon-Jones, Westman and Mattes 10 ), and other studies have suggested that replacing carbohydrate with protein from meat, poultry and dairy foods may have beneficial metabolic effects( Reference Farnsworth, Luscombe and Noakes 11 ) and help reduce abdominal obesity( Reference Merchant, Anand and Vuksan 12 ).

Evidence is emerging that the type of dietary protein consumed can elicit different health effects and play an important role in disease aetiology( Reference Velasquez and Bhathena 13 ). In general, plant proteins have been related to health benefits more than animal proteins( Reference Ashton, Dalais and Ball 14 Reference Lin, Bolca and Vandevijvere 17 ). While vegetable protein intakes have been found to be inversely associated with blood pressure( Reference Elliott, Stamler and Dyer 18 ), a high consumption of red and/or processed meat has been associated with a number of adverse cardiovascular health outcomes such as higher systolic blood pressure( Reference Tzoulaki, Brown and Chan 19 ), increased risk for type 2 diabetes( Reference Song, Manson and Buring 20 Reference Pan, Sun and Bernstein 22 ), ischaemic stroke( Reference Chen, Lv and Pang 23 ), global and central obesity( Reference Wagemakers, Prynne and Stephen 24 , Reference Wang and Beydoun 25 ) and weight gain( Reference Xu, Yin and Tong 26 , Reference Vergnaud, Norat and Romaguera 27 ).

Although the adverse effects of red and processed meat consumption are well documented, there is still lack of firm evidence regarding the effect of other sources of animal protein intake (fish, eggs and milk products) on health outcomes, including body weight status( Reference Hite, Feinman and Guzman 9 , Reference Clifton 28 ). The present study aimed to examine the association of animal protein intake and more specifically, intakes of animal protein derived from different sources, i.e. meats (red meat, poultry), fish and shellfish, eggs and milk products, with global and abdominal obesity in a nationally representative sample of adult participants in the Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) survey in Luxembourg. It was hypothesized that animal protein would be positively associated with obesity, but the association may vary according to protein source. The findings will contribute to current knowledge on the influence of animal protein intake on body weight status and help guide the development of future prevention/weight control intervention studies.

Methods

Study population

The study material consisted of individuals from the national ORISCAV-LUX study, a cross-sectional, population-based survey among adults aged 18–69 years. The data collection, sample design and representativeness have been reported in detail elsewhere( Reference Alkerwi, Sauvageot and Donneau 2 , Reference Alkerwi, Donneau and Sauvageot 29 , Reference Alkerwi, Sauvageot and Couffignal 30 ). Briefly, a stratified random sample of 1432 non-institutionalized individuals was enrolled between November 2007 and January 2009, with a participation rate (32·2 %) that corresponded to the theoretically expected rate upon which the sample size was calculated( Reference Alkerwi, Sauvageot and Couffignal 30 ). Participants with missing data (i.e. at least two pages of the FFQ were uncompleted) or implausible dietary data (i.e. with values of nutrient intakes outside the 1st and 99th percentiles of the distribution) were excluded (n 85). Those who reported currently being on diet for weight loss or for chronic CVD (diabetes, hypertension, dyslipidaemia) were also removed (n 195) from the analyses. Hence the final sample size used in the analysis was 1152 individuals.

The ORISCAV-LUX study received the approval of the Luxembourg national ethical committee and the national commission for private data protection. All participants provided written informed consent.

Data collection

Participant data were collected from three sources: (i) a self-administered questionnaire, including information on demographics, socio-economics, smoking history, diet and physical activity; (ii) anthropometric measurements; and (iii) blood sampling. Extensive quality control measures for the completeness and integrity of dietary and non-dietary information were applied with the help of trained research nurses.

Anthropometric measures and obesity assessment

Height, body weight and waist circumference (WC) were measured in light clothing without shoes, according to previously published methods( Reference Alkerwi, Sauvageot and Donneau 2 ). BMI was calculated as weight in kilograms divided by the square of height in metres (kg/m2). WC (centimetres) was measured at the level midway between the twelfth rib and the uppermost lateral border of the iliac crest at the end of normal expiration. Study participants were classified as normal weight (BMI<25·0 kg/m2), overweight (BMI≥25·0 to <30·0 kg/m2) or obese (BMI≥30·0 kg/m2)( Reference Chu, Rimm and Wang 31 ). Global obesity was defined as BMI≥30·0 kg/m2, while abdominal obesity was defined as WC≥102 cm for men and ≥88 cm for women( 32 ).

Dietary intakes

Dietary intake was assessed by means of a 134-item semi-quantitative FFQ, self-administered and then verified with the participant by trained staff. The overall validity of the FFQ examined against nutritional biomarkers( Reference Sauvageot, Alkerwi and Albert 33 ) and a 3 d dietary record( Reference Sauvageot, Alkerwi and Adelin 34 ) showed a satisfactory performance in detecting and ranking micro- and macronutrients. Participants were required to assign the frequency and quantity of foods and beverages habitually consumed during the preceding 3 months. Food intakes were calculated by multiplying the self-reported food portion by the frequency of consumption. Energy and nutrient intake data were compiled using a French food composition table( Reference Hercberg, Arnault and Astorg 35 ). To account for energy intake, macronutrients were adjusted for total daily energy intake and expressed as percentages of total energy intake (%E). Mathematically, a given intake was first divided by daily energy intake, then multiplied by 400 for protein and carbohydrate intake and by 900 for fat intake( Reference Willett, Howe and Kushi 36 ).

Animal protein sources

Consistent with the guidelines of the US Department of Agriculture( 37 ), protein derived from animal foods was divided into four broad categories: (i) meat; (ii) fish and shellfish; (iii) eggs; and (iv) milk products. The meat group was defined as the sum of the following types of meats: processed and unprocessed red meat including beef, pork, lamb, veal, game and poultry (chicken and turkey). Fish and shellfish included white fish, fatty fish such as salmon, canned fish such as tuna and seafood such as shrimp and squid. Milk products included milk, yoghurt and cheese (whole fat and reduced fat). The fraction of animal protein (8·59 %) derived from meat, fish and shellfish, eggs or dairy products mixed in prepared dishes (e.g. soup with pieces of meat, paella with meat or fish and shellfish, quiche with meat, eggs or cheese) was not included in the calculation of total animal protein.

Potential confounding factors

Based on an extensive literature review, several sociodemographic, lifestyle and dietary confounding factors were considered. Smoking status was dichotomized as ‘non-smoker’ and ‘smoker’. Physical activity was calculated as the total amount of time engaged in physical activity per week. Education status was classified into primary, secondary or tertiary level. The dietary factors were total fat (g/d), total carbohydrate (g/d), total fibre (g/d) and fruit and vegetable intake (g/d). These variables have been described in detail elsewhere( Reference Alkerwi, Donneau and Sauvageot 29 ).

Statistical analysis

Quantitative data were expressed as mean and standard deviation. Frequency tables were used for categorical findings. Participants’ demographic and dietary characteristics according to global obesity (normal weight, overweight, obese) and abdominal obesity (absent, present) were compared by ANOVA or the χ 2 test for contingency tables.

Total protein intake (animal and vegetal), total animal protein intake and protein intake from meats, fish and shellfish, eggs and milk products were used as the independent (explanatory) variables in the statistical analyses. All of these variables were expressed in g/d and in percentage of total daily energy intake (%E). Binary logistic regression was applied to assess the odds for global obesity (BMI≥30·0 kg/m2) and for abdominal obesity (WC≥102 cm for men and ≥88 cm for women), according to protein intakes. Three models were actually designed: model I adjusted for age and gender; model II further adjusted for education, smoking status, physical activity and intakes of total fat, carbohydrate, fibre, and fruit and vegetables; model III took also total vegetal protein into account. Finally, for each animal protein source, model III also made adjustment for protein intake from other animal sources. Results were expressed as odds ratios and 95 % confidence intervals. All main effect tests were two-sided at the 5 % critical level (P<0·05). Statistical calculations were done using the statistical software package IBM SPSS Statistics version 21.

Results

Participant characteristics according to animal protein intake

Animal protein intake varied considerably according to gender (P=0·039), with more men than women in each quartile of intake except the first. The intake of animal protein also varied significantly between normal-weight, overweight and obese participants (P<0·001); likewise in participants with abdominal obesity (Table 1).

Table 1 Participants’ characteristics according to animal protein intake, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

%E, percentage of total daily energy intake.

* P values are from ANOVA (continuous variables) or the χ 2 test (categorical variables).

Protein intakes

Participants with global or abdominal obesity exhibited higher total protein intake (%E) than those without the disorder (both P<0·001; Table 2). Total animal protein intake and protein intakes from meat and from fish and shellfish all increased significantly with body weight status (all P<0·0001; Table 3). Similarly, total animal protein intake, protein intake from meat and protein intake from fish and shellfish (all measured in g/d or as %E) were significantly higher in participants with abdominal obesity (all P<0·01). Protein derived from eggs or milk products did not differ according to body weight status.

Table 2 Participants’ total energy and macronutrient intakes according to global and abdominal obesity, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

%E, percentage of total daily energy intake.

* Total energy intake was positively correlated with waist circumference (as a continuous variable).

Table 3 Participants’ total vegetal and animal protein intakes and protein intakes from main animal sources, according to global and abdominal obesity status, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

%E, percentage of total daily energy intake.

Multivariate modelling of global and abdominal obesity

The major findings obtained from the multivariate modelling (models I–III) of global and abdominal obesity with respect to total protein, total animal protein and animal protein derived from each dietary source are displayed in Table 4. For model I (age- and gender-adjusted), total protein and total animal protein intakes (as %E) were found to be associated with increased odds for both disorders (all P<0·001). These associations remained significant when adjusting for education, smoking, physical activity and total fat, total carbohydrate, total fibre, fruit and vegetable intakes (model II).

Table 4 Multivariate modelling (models I–III) of global and abdominal obesity with respect to intakes of total protein, total animal protein and protein from main dietary sources based on 1152 participants from the Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study

%E, percentage of total daily energy intake.

Model I: adjusted for age and gender.

Model II: adjusted for age, gender, education, smoking, physical activity and intakes of total fat, total carbohydrates, total fibre, and fruit and vegetables.

Model IIIa: adjusted for covariates in model II and total vegetal protein (%E).

Model IIIb: adjusted for covariates in model II, total vegetal protein (%E) and protein from other animal sources (%E).

When examining the individual dietary sources of animal protein and controlling for other animal protein sources, protein derived from meat was independently related to global obesity (model III: OR=1·18; 95 % CI 1·11, 1·26) and abdominal obesity (OR=1·12; 95 % CI 1·05, 1·19). Likewise, a significant independent positive association was observed between protein derived from fish and shellfish and global obesity (model III: OR=1·18; 95 % CI 1·05, 1·33) and abdominal obesity (model III: OR=1·17; 95 % CI 1·04, 1·30). Protein consumption from eggs and milk products was unrelated to global and abdominal obesity.

Discussion

The present study has demonstrated a positive independent association between animal protein intake and both global and abdominal obesity in presumably healthy adults in Luxembourg. Higher animal protein intake was associated with higher odds of global and abdominal obesity, specifically from meat (red meat, poultry) and fish and shellfish consumption, but not eggs or milk products. The odds of global obesity increased by 18 % for every 1 % increase in total energy intake derived from meat products or from fish and shellfish (both P<0·01). Our results indicate that the four selected sources of animal protein may have a differential effect on obesity, independent of age, gender, education level, lifestyle behaviours and other dietary factors.

Although the literature on the animal protein intake–obesity relationship is not abundant, our data are consistent with a recent cross-sectional study conducted in a Belgian population( Reference Lin, Bolca and Vandevijvere 17 ), which showed positive associations between animal protein intake and BMI and WC in males, but not in females. To further investigate our data, a separate gender-specific sensitivity analyses showed similar positive significant relationships for both men and women with animal protein. These findings are also in line with a recently published prospective study, the Chicago Western Electric Study( Reference Bujnowski, Xun and Daviglus 15 ), which examined the association between protein intake and obesity in over 1000 American men over 7 years. Animal protein intake was positively associated with overweight and obesity, independent of energy, carbohydrate and fat intakes. Both abovementioned studies( Reference Bujnowski, Xun and Daviglus 15 , Reference Lin, Bolca and Vandevijvere 17 ) also found an inverse association between vegetable protein intake and obesity; no such associations were observed in the present study. We believe we have added to the current literature by evaluating the relationship between specific animal-protein food sources and obesity. The present findings concur with positive associations observed in other cross-sectional studies between red meat consumption and BMI( Reference Wang and Beydoun 25 , Reference Okubo, Sasaki and Murakami 38 , Reference Maskarinec, Novotny and Tasaki 39 ), WC( Reference Wang and Beydoun 25 , Reference Azadbakht and Esmaillzadeh 40 ) and the metabolic syndrome( Reference Azadbakht and Esmaillzadeh 40 , Reference Babio, Sorli and Bullo 41 ). Total meat consumption has also been positively associated with weight gain in both normal-weight and overweight adults over a 5-year follow-up period in a large European cohort( Reference Vergnaud, Norat and Romaguera 27 ).

Although a consensus exists that energy restriction promotes weight loss, the effect of varying the macronutrient composition of the diet (fat, protein, carbohydrates) on weight loss has been debated( Reference St Jeor, Howard and Prewitt 42 ). Several intervention trials indicate that low-carbohydrate diets promote a greater degree of weight loss in the short term than a conventional high-carbohydrate, low-fat diet( Reference Foster, Wyatt and Hill 43 Reference Stern, Iqbal and Seshadri 45 ), even when energy intake is matched( Reference Halyburton, Brinkworth and Wilson 46 ), but over the long term weight loss is similar to other that achieved with energy-restricted dietary patterns( Reference Brinkworth, Noakes and Buckley 47 ). Other studies have demonstrated that high-protein diets with concomitant decreases in energy intake may result in sustained weight loss or improved health( Reference Halton and Hu 48 , Reference Skov, Toubro and Ronn 49 ). In high-protein diets, weight loss is initially high due to fluid loss related to reduced carbohydrate intake, overall energy restriction and ketosis-induced appetite suppression( Reference St Jeor, Howard and Prewitt 42 ).

The biological mechanisms that might explain the adverse relationship between animal protein intake and the risk of obesity are still unclear. The high cholesterol, Fe and C-reactive protein levels in red meat may have detrimental effects on body weight and health outcomes( Reference Azadbakht and Esmaillzadeh 40 ). In addition, high-protein foods of animal sources (in particular red meats) are energy-dense, high-fat foods, particularly rich in SFA. This macronutrient composition may contribute to the adverse effect on body weight and energy regulation. Energy density may be a key element in body-weight regulation as it may alter appetite control signals (i.e. hunger and satiety)( Reference Vergnaud, Estaquio and Czernichow 50 ).

Most of the randomized controlled trials investigating protein consumption on health outcomes have focused on adjusting total protein in relation to other macronutrients in the diet, rather than on the types of protein or specific sources. As recognized by others( Reference Santesso, Akl and Bianchi 6 ), few randomized controlled trials examining protein intake and health outcomes have reported protein sources (animal v. vegetable). Including different food sources of protein within a high- or low-protein diet may contribute to the conflicting results among studies regarding the animal protein–obesity association. The present findings confirm our initial hypothesis regarding the varying effects according to animal dietary sources. The nutritional content of different protein sources included in the diet may have different influences on body weight and therefore help to explain some of the disparate findings. This will be an important distinction to make in future dietary trials. In addition, the diversity of study designs (cross-sectional, longitudinal, clinical trials) and differential control for confounders may explain the inconsistent findings.

Our contemporary nationwide database( Reference Alkerwi, Sauvageot and Donneau 2 , Reference Alkerwi, Sauvageot and Couffignal 30 ) constitutes an opportunity to examine associations between animal protein and anthropometric measures, with a focus on different animal protein sources, namely meat, fish, eggs and dairy products. As the ORISCAV-LUX measured a large set of potential dietary and non-dietary confounders, we trust that our ‘European’ findings contribute to a growing body of evidence indicating that high intakes of meat may not have a favourable effect on body composition. As in similar population-based studies, the ORISCAV-LUX survey has some limitations, related mainly to the current absence of a gold standard for dietary assessment. Food group and nutrient intakes were estimated by self-reported data. It is well known that overweight/obese people under-report their dietary intake to a greater extent than normal-weight people( Reference Macdiarmid and Blundell 51 ). Despite intensive efforts to minimize dietary reporting inaccuracies through extensive control procedures( Reference Alkerwi, Sauvageot and Donneau 2 ), diet is a complex exposure factor with measurement being subject to imprecision and a wide range of errors and biases. Two extensive validation studies( Reference Sauvageot, Alkerwi and Albert 33 , Reference Sauvageot, Alkerwi and Adelin 34 ) have been performed to examined the performance of the FFQ, showing that it performed well in assessing intakes of several foods and micronutrients and the observed correlations were within the range noted by other investigators. However, the complexity and expense to perform N analyses in 24 h urine collections (gold standard recovery biomarker to validate protein intake) may constitute a drawback in the present study.

The cross-sectional design of the study did not allow conclusions on causal relationships to be made. It precludes inferences about long-term dietary effects on obesity. However, it is less plausible that obese participants have altered their diet by consuming more meats and fish, since those who are currently on diet to reduce their weight or for a cardiovascular health problem (diabetes, hypertension, lipid disorders) were excluded from the analyses. The fact that there was no difference in physical activity between those who were normal weight and those who were obese (the same goes for abdominal obesity) suggests that the majority of those who were obese are trying to resist the state that they are in and perhaps may explain why they are eating more protein-rich foods and less carbohydrates. Unfortunately, we were not able to distinguish the individual associations between particular types of meat (red meat or poultry), as the FFQ was unable to capture this difference. The meat group included a wide range of meats, such as pork, beef, lamb and poultry, and cold processed meats, such as salami. Similarly, a variety of fish types were included within ‘fish and shellfish’ and distinctions between, for example, fatty fish and canned fish were unable to be made due to few cases.

Meat intake can be linked to adverse effects on adiposity through plausible mechanisms and the results from other previous prospective studies lend support to our findings. Along with the effect of meat consumption on the risk of other diseases, such as CVD, diabetes, metabolic syndrome and colorectal cancer, our findings build an added argument against adopting a high-animal-protein diet, specifically from meat, to maintain healthy weight. These findings may have practical implications for public health dietary recommendations. Notwithstanding, it should be kept in mind that protein is one of the three major macronutrients and an important source of energy, needed for both younger and elderly age groups( Reference Chernoff 52 ). In the present studied population, total protein intake contributed 15·8 % to total energy intake. Two-thirds of total protein intake (mean intake of 94·5 g/d) was derived from animal protein (mean intake of 62·6 g/d) and one-third was from vegetable protein (mean intake of 29·3 g/d; data not shown).

Conclusion

Consumption of animal protein, particularly that derived from meat products, showed a positive association with adiposity measures among presumably healthy adults in Luxembourg, independently of gender, age, educational level, smoking status, physical activity and intakes of fibre, fat and carbohydrates. The consumption of meat, a major source of animal protein, plays a vital role in providing a diversified and nutritious diet. Animal products are major sources of a wide range of essential micronutrients; in particular, vitamin A and minerals such as Fe and Zn. Any emphasis placed on the need to reduce animal protein intake in the diet of apparently healthy people should be seen in the sense of opting for other sources of animal protein, such as eggs or dairy products, rather than increasing carbohydrate or fat consumption. In the scarcity of robust evidence from long-term, high-cost prospective and interventional trials, our findings may constitute a relevant contribution to the prevention and control of obesity.

Acknowledgements

Financial support: This research work was supported by a research grant from the National Fund of Research (Fond National de Recherche (FNR)); project DIQUA-LUX, 58 70 404. The FNR had no role in the design, analysis or writing of this article. Conflict of interest: None. Author contributions: Both M.G. and G.E.C. contributed equally to the supervision. A. Alkerwi was involved in the conception and design of the ORISCAV-LUX survey, coordinated the field data collection, conceived the present research, contributed to data analyses and drafted the manuscript. N.S. conducted the statistical analyses and contributed to data interpretation. A.-F.D. participated in the statistical analyses. J.D.B. and A. Albert contributed to the critical revision of the manuscript and intellectual content. G.E.C. and M.G. provided expertise and oversight throughout the process. All of the authors reviewed drafts and approved the final version of the manuscript. Ethics of human subject participation: The ORISCAV-LUX study received the approval of the Luxembourg national ethical committee and the national commission for private data protection. All participants provided written informed consent.

References

1. World Health Organization (2003) Diet, Nutrition and the Prevention of Chronic Diseases. WHO Technical Report Series no. 916. Geneva: WHO.Google Scholar
2. Alkerwi, A, Sauvageot, N, Donneau, AF et al. (2010) First nationwide survey on cardiovascular risk factors in Grand-Duchy of Luxembourg (ORISCAV-LUX). BMC Public Health 10, 468.CrossRefGoogle ScholarPubMed
3. Astrup, A (2001) Healthy lifestyles in Europe: prevention of obesity and type II diabetes by diet and physical activity. Public Health Nutr 4, 499515.CrossRefGoogle ScholarPubMed
4. Ledikwe, JH, Blanck, HM, Kettel Khan, L et al. (2006) Dietary energy density is associated with energy intake and weight status in US adults. Am J Clin Nutr 83, 13621368.Google Scholar
5. Mendoza, JA, Drewnowski, A & Christakis, DA (2007) Dietary energy density is associated with obesity and the metabolic syndrome in US adults. Diabetes Care 30, 974979.Google Scholar
6. Santesso, N, Akl, EA, Bianchi, M et al. (2012) Effects of higher- versus lower-protein diets on health outcomes: a systematic review and meta-analysis. Eur J Clin Nutr 66, 780788.Google Scholar
7. Schwingshackl, L & Hoffmann, G (2013) Long-term effects of low-fat diets either low or high in protein on cardiovascular and metabolic risk factors: a systematic review and meta-analysis. Nutr J 12, 48.Google Scholar
8. Wycherley, TP, Moran, LJ, Clifton, PM et al. (2012) Effects of energy-restricted high-protein, low-fat compared with standard-protein, low-fat diets: a meta-analysis of randomized controlled trials. Am J Clin Nutr 96, 12811298.Google Scholar
9. Hite, AH, Feinman, RD, Guzman, GE et al. (2010) In the face of contradictory evidence: report of the Dietary Guidelines for Americans Committee. Nutrition 26, 915924.CrossRefGoogle ScholarPubMed
10. Paddon-Jones, D, Westman, E, Mattes, RD et al. (2008) Protein, weight management, and satiety. Am J Clin Nutr 87, issue 5, 1558S1561S.Google Scholar
11. Farnsworth, E, Luscombe, ND, Noakes, M et al. (2003) Effect of a high-protein, energy-restricted diet on body composition, glycemic control, and lipid concentrations in overweight and obese hyperinsulinemic men and women. Am J Clin Nutr 78, 3139.Google Scholar
12. Merchant, AT, Anand, SS, Vuksan, V et al. (2005) Protein intake is inversely associated with abdominal obesity in a multi-ethnic population. J Nutr 135, 11961201.CrossRefGoogle Scholar
13. Velasquez, MT & Bhathena, SJ (2007) Role of dietary soy protein in obesity. Int J Med Sci 4, 7282.CrossRefGoogle ScholarPubMed
14. Ashton, EL, Dalais, FS & Ball, MJ (2000) Effect of meat replacement by tofu on CHD risk factors including copper induced LDL oxidation. J Am Coll Nutr 19, 761767.Google Scholar
15. Bujnowski, D, Xun, P, Daviglus, ML et al. (2011) Longitudinal association between animal and vegetable protein intake and obesity among men in the United States: the Chicago Western Electric Study. J Am Diet Assoc 111, 11501155.e1.Google Scholar
16. Kelemen, LE, Kushi, LH, Jacobs, DR Jr et al. (2005) Associations of dietary protein with disease and mortality in a prospective study of postmenopausal women. Am J Epidemiol 161, 239249.Google Scholar
17. Lin, Y, Bolca, S, Vandevijvere, S et al. (2011) Plant and animal protein intake and its association with overweight and obesity among the Belgian population. Br J Nutr 105, 11061116.Google Scholar
18. Elliott, P, Stamler, J, Dyer, AR et al. (2006) Association between protein intake and blood pressure: the INTERMAP Study. Arch Intern Med 166, 7987.Google Scholar
19. Tzoulaki, I, Brown, IJ, Chan, Q et al. (2008) Relation of iron and red meat intake to blood pressure: cross sectional epidemiological study. BMJ 337, a258.Google Scholar
20. Song, Y, Manson, JE, Buring, JE et al. (2004) A prospective study of red meat consumption and type 2 diabetes in middle-aged and elderly women: the Women’s Health Study. Diabetes Care 27, 21082115.Google Scholar
21. Djousse, L, Gaziano, JM, Buring, JE et al. (2009) Egg consumption and risk of type 2 diabetes in men and women. Diabetes Care 32, 295300.Google Scholar
22. Pan, A, Sun, Q, Bernstein, AM et al. (2013) Changes in red meat consumption and subsequent risk of type 2 diabetes mellitus three cohorts of US men and women. JAMA Intern Med 173, 13281335.CrossRefGoogle ScholarPubMed
23. Chen, GC, Lv, DB, Pang, Z et al. (2013) Red and processed meat consumption and risk of stroke: a meta-analysis of prospective cohort studies. Eur J Clin Nutr 67, 9195.Google Scholar
24. Wagemakers, JJ, Prynne, CJ, Stephen, AM et al. (2009) Consumption of red or processed meat does not predict risk factors for coronary heart disease; results from a cohort of British adults in 1989 and 1999. Eur J Clin Nutr 63, 303311.CrossRefGoogle Scholar
25. Wang, Y & Beydoun, MA (2009) Meat consumption is associated with obesity and central obesity among US adults. Int J Obes (Lond) 33, 621628.CrossRefGoogle ScholarPubMed
26. Xu, F, Yin, XM & Tong, SL (2007) Association between excess bodyweight and intake of red meat and vegetables among urban and rural adult Chinese in Nanjing, China. Asia Pac J Public Health 19, 39.Google Scholar
27. Vergnaud, AC, Norat, T, Romaguera, D et al. (2010) Meat consumption and prospective weight change in participants of the EPIC-PANACEA study. Am J Clin Nutr 92, 398407.Google Scholar
28. Clifton, P (2012) Effects of a high protein diet on body weight and comorbidities associated with obesity. Br J Nutr 108, Suppl. 2, S122S129.CrossRefGoogle ScholarPubMed
29. Alkerwi, A, Donneau, AF, Sauvageot, N et al. (2012) Dietary, behavioural and socio-economic determinants of the metabolic syndrome among adults in Luxembourg: findings from the ORISCAV-LUX study. Public Health Nutr 15, 849859.Google Scholar
30. Alkerwi, A, Sauvageot, N, Couffignal, S et al. (2010) Comparison of participants and non-participants to the ORISCAV-LUX population-based study on cardiovascular risk factors in Luxembourg. BMC Med Res Methodol 10, 80.Google Scholar
31. Chu, NF, Rimm, EB, Wang, DJ et al. (1998) Clustering of cardiovascular disease risk factors among obese schoolchildren: the Taipei Children Heart Study. Am J Clin Nutr 67, 11411146.Google Scholar
32. National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) (2002) Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation 106, 31433421.Google Scholar
33. Sauvageot, N, Alkerwi, A, Albert, A et al. (2013) Use of food frequency questionnaire to assess relationships between dietary habits and cardiovascular risk factors in NESCAV study: validation with biomarkers. Nutr J 12, 143.Google Scholar
34. Sauvageot, N, Alkerwi, Aa, Adelin, A et al. (2013) Validation of the food frequency questionnaire used to assess the association between dietary habits and cardiovascular risk factors in the NESCAV Study. J Nutr Food Sci 3, 208.Google Scholar
35. Hercberg, S, Arnault, N, Astorg, P et al. (2006) Tables de composition des aliments/SU.VI.MAX . Paris: Economica.Google Scholar
36. Willett, WC, Howe, GR & Kushi, LH (1997) Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr 65, 4 Suppl, 1220S1228S.Google Scholar
37. US Department of Agriculture, Agricultural Research Service (2010) Report of the Dietary Guidelines Advisory Committee on the Dietary Guidelines for Americans. Washington, DC: USDA/ARS.Google Scholar
38. Okubo, H, Sasaki, S, Murakami, K et al.; Freshmen in Dietetic Courses Study II group (2008) Three major dietary patterns are all independently related to the risk of obesity among 3760 Japanese women aged 18–20 years. Int J Obes (Lond) 32, 541549.Google Scholar
39. Maskarinec, G, Novotny, R & Tasaki, K (2000) Dietary patterns are associated with body mass index in multiethnic women. J Nutr 130, 30683072.Google Scholar
40. Azadbakht, L & Esmaillzadeh, A (2009) Red meat intake is associated with metabolic syndrome and the plasma C-reactive protein concentration in women. J Nutr 139, 335339.Google Scholar
41. Babio, N, Sorli, M, Bullo, M et al. (2012) Association between red meat consumption and metabolic syndrome in a Mediterranean population at high cardiovascular risk: cross-sectional and 1-year follow-up assessment. Nutr Metab Cardiovasc Dis 22, 200207.Google Scholar
42. St Jeor, ST, Howard, BV, Prewitt, TE et al.; Nutrition Committee of the Council on Nutrition Physical Activity, and Metabolism of the American Heart Association (2001) Dietary protein and weight reduction: a statement for healthcare professionals from the Nutrition Committee of the Council on Nutrition, Physical Activity, and Metabolism of the American Heart Association. Circulation 104, 18691874.Google Scholar
43. Foster, GD, Wyatt, HR, Hill, JO et al. (2003) A randomized trial of a low-carbohydrate diet for obesity. N Engl J Med 348, 20822090.Google Scholar
44. Samaha, FF, Iqbal, N, Seshadri, P et al. (2003) A low-carbohydrate as compared with a low-fat diet in severe obesity. N Engl J Med 348, 20742081.CrossRefGoogle ScholarPubMed
45. Stern, L, Iqbal, N, Seshadri, P et al. (2004) The effects of low-carbohydrate versus conventional weight loss diets in severely obese adults: one-year follow-up of a randomized trial. Ann Intern Med 140, 778785.CrossRefGoogle ScholarPubMed
46. Halyburton, AK, Brinkworth, GD, Wilson, CJ et al. (2007) Low- and high-carbohydrate weight-loss diets have similar effects on mood but not cognitive performance. Am J Clin Nutr 86, 580587.CrossRefGoogle Scholar
47. Brinkworth, GD, Noakes, M, Buckley, JD et al. (2009) Long-term effects of a very-low-carbohydrate weight loss diet compared with an isocaloric low-fat diet after 12 mo. Am J Clin Nutr 90, 2332.Google Scholar
48. Halton, TL & Hu, FB (2004) The effects of high protein diets on thermogenesis, satiety and weight loss: a critical review. J Am Coll Nutr 23, 373385.CrossRefGoogle ScholarPubMed
49. Skov, AR, Toubro, S, Ronn, B et al. (1999) Randomized trial on protein vs carbohydrate in ad libitum fat reduced diet for the treatment of obesity. Int J Obes Relat Metab Disord 23, 528536.Google Scholar
50. Vergnaud, AC, Estaquio, C, Czernichow, S et al. (2009) Energy density and 6-year anthropometric changes in a middle-aged adult cohort. Br J Nutr 102, 302309.CrossRefGoogle Scholar
51. Macdiarmid, J & Blundell, J (1998) Assessing dietary intake: who, what and why of under-reporting. Nutr Res Rev 11, 231253.Google Scholar
52. Chernoff, R (2004) Protein and older adults. J Am Coll Nutr 23, 6 Suppl. 627S630S.Google Scholar
Figure 0

Table 1 Participants’ characteristics according to animal protein intake, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

Figure 1

Table 2 Participants’ total energy and macronutrient intakes according to global and abdominal obesity, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

Figure 2

Table 3 Participants’ total vegetal and animal protein intakes and protein intakes from main animal sources, according to global and abdominal obesity status, Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study (n 1152)

Figure 3

Table 4 Multivariate modelling (models I–III) of global and abdominal obesity with respect to intakes of total protein, total animal protein and protein from main dietary sources based on 1152 participants from the Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study