Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-06T05:04:45.172Z Has data issue: false hasContentIssue false

Dietary patterns and metabolic syndrome factors in a non-diabetic Italian population

Published online by Cambridge University Press:  01 September 2009

Maria Léa Corrêa Leite*
Affiliation:
Department of Epidemiology and Medical Informatics, Institute of Biomedical Technologies, National Research Council (CNR), Via Fratelli Cervi 93, 20090 Segrate, Milan, Italy
Alfredo Nicolosi
Affiliation:
Department of Epidemiology and Medical Informatics, Institute of Biomedical Technologies, National Research Council (CNR), Via Fratelli Cervi 93, 20090 Segrate, Milan, Italy Gertrude H. Sergievsky Center, School of Public Health, Columbia University, New York, NY, USA
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective

To examine the relationship between dietary patterns and metabolic syndrome.

Design

Population-based cross-sectional study. The K-means clustering method was used to identify dietary patterns and logistic regression models were used to compare the adjusted prevalence rates of metabolic syndrome factors, stratifying by obesity status.

Setting

The 1992–3 Italian Bollate Eye Study, a population-based survey carried out in the town of Bollate (Milan), Italy.

Subjects

A total of 1052 non-diabetic Italian subjects, 527 men and 525 women, aged 42–74 years.

Results

Five dietary clusters were identified: common, animal products, starch, vegetal/fat and vitamin/fibre. After adjusting for potential confounders, the starch group showed the highest prevalence of metabolic syndrome (36 %) followed by the animal products group (30 %); the vitamin/fibre (20 %) and vegetal/fat groups (19 %) showed the lowest prevalence. The starch group had more dyslipidaemia (higher TAG and lower HDL cholesterol levels) and the animal products group had a higher prevalence of impaired fasting glucose. The vitamin/fibre group had the lowest prevalence of abdominal obesity. The beneficial effect of the vegetal/fat and vitamin/fibre dietary patterns seemed stronger among the obese.

Conclusions

Our results confirm the deleterious effect of a very-low-fat, high-carbohydrate diet and also of high intakes of animal products. The consumption of a diet high in vegetal fats or rich in fruits and vegetables is associated with a healthier metabolic profile. Reducing obesity is essential to prevent metabolic syndrome, but even among the obese dietary habits are important for preserving healthy lipid and glycaemic profiles.

Type
Research Paper
Copyright
Copyright © The Authors 2009

Metabolic syndrome indicates a group of markers – abdominal obesity, atherogenic dyslipidaemia, increased blood pressure and high plasma glucose levels – whose presence points to a very high risk of developing diabetes or CVD. These outcomes can be effectively prevented by early syndrome management, particularly including lifestyle modifications(Reference Grundy1).

It is widely recognised that a healthy balanced diet is one of the principal elements in the prevention of diabetes and CVD, but it is still unclear which dietary pattern is the most beneficial for the successful management of metabolic syndrome and its complications, especially regarding the proportion and type of carbohydrates and fat(Reference Kelley2Reference Weinberg4). Furthermore, the possible influence of conditions such as overweight and obesity on the relationship between diet and the metabolic syndrome needs to be evaluated(Reference Baxter, Coyne and McClintock5).

We used the database of the Italian Bollate Eye Study(Reference Nicolosi6Reference Leite and Nicolosi8) to examine the relationships between dietary patterns and metabolic syndrome factors in an adult population.

Methods

We used data from the 1992–3 Italian Bollate Eye Study, which was designed to investigate the prevalence and risk factors of major eye diseases in a population consisting of a random sample of all individuals aged 40–74 years drawn from the residents’ list of the town of Bollate (Milan, Italy). A letter was sent to the sampled subjects (2882 individuals) to explain the study objectives and invite their participation, after which each one was contacted by phone in order to collect consent and schedule an appointment at the local hospital’s outpatient clinic. The project was approved by the National Research Council.

The hospital visit was attended by 1691 subjects (59 % of the original population sample), and included an interview concerning medical and family history, the past or current use of drugs, lifestyle habits, a 24 h diet recall and an FFQ, and anthropometric (height, weight, body circumferences and skinfold thicknesses) and blood pressure measurements (both arms). The FFQ was based on 166 items arranged into thirteen categories (number of items in parentheses): (i) bread/cereal products (n 23); (ii) eggs, meats, cured pork (n 28); (iii) fish (n 8); (iv) dairy products (n 8); (v) cheese (n 10); (vi) vegetables (n 26); (vii) oil/sauces/condiments (n 17); (viii) fruits (n 18); (ix) sweets (n 9); (x) beverages/coffee (n 6); (xi) alcohol (n 7); (xii) sugar (n 3); and (xiii) miscellaneous (n 3). The questionnaire was quantitative (a modification of Willett’s questionnaire for the Nurses’ Health Study(Reference Willett9)), with the quantities of food being assessed by means of photographs of food portions. A blood sample, drawn during fasting, was collected for laboratory tests (haematology, glycaemia, lipids).

The subjects were classified as non-smokers, ex-smokers or current smokers; and as teetotallers or consumers of ≤30 or >30 g alcohol/d. Education was classified at three levels: primary school or less; high school; further education. Physical activity was assessed on the basis of the time spent watching television, walking/cycling and practising sport.

Nutrient intake was calculated using the food composition database compiled for epidemiological studies in Italy(Reference Salvini, Parpinel, Gnagnarella, Maisonneuve and Turrini10), and cluster analysis was used to assess dietary patterns. In order to capture the qualitative aspects of the dietary habits of our subjects more accurately, we adjusted the measures of nutrient consumption by total energy intake using the residual method(Reference Willett and Stampfer11), and the energy-adjusted nutrient intakes were standardised in order to avoid any influence of different units of measurement. Inspection of the distributions of the energy-adjusted nutrients showed that no one among them was seriously skewed, so we standardised the variables without transformation. The partitioning clustering method (the K-means algorithm)(Reference Jobson12) was used to separate the subjects into non-overlapping subgroups based on similarities in their nutrient consumption profiles. The K-means algorithm is a simple, iterative procedure which is based on the definition of a point (centroid) in the space of records which represents an average location of the particular cluster. Thus, the coordinates of this point are averages of nutrient intakes of all subjects who belong to the cluster. This algorithm has as an input a predefined number k of clusters and the proper way to choose the right number of clusters is to try with different values for k. In principle, the best cluster solution will exhibit the smallest intra-cluster distances and largest inter-cluster distances. Distances between clusters increase as the number of clusters increases, but high values of k could result in non-workable small cluster size.

Metabolic syndrome was diagnosed on the basis of the National Cholesterol Education Program Adult Treatment Panel III criteria(13), which define it as the presence of three or more of the following risk determinants: (i) an increased waist circumference (>102 cm in men and >88 cm in women); (ii) high TAG level (≥150 mg/dl); (iii) low HDL cholesterol (HDL-C) level (<40 mg/dl in men and <50 mg/dl in women); (iv) increased blood pressure (≥130/≥85 mmHg); and (v) impaired fasting glucose level (≥100 mg/dl), as subsequently established in accordance with the American Diabetes Association’s revised definition of impaired fasting glucose(14).

Complete anthropometric, lifestyle, laboratory and dietary data were obtained relating to 1163 subjects. We excluded 111 subjects with diabetes (plasma glucose >125 mg/dl and/or self-referred diabetes) whose diet may have been modified after the onset of their disease.

Logistic regression models were used to compare the prevalence rates of the individual metabolic syndrome disorders across the different dietary pattern groups, adjusting for age, gender, education, smoking, alcohol consumption and the degree of physical activity as assessed on the basis of the frequency of practising sport and walking/cycling and the time spent watching television. These prevalence rates were calculated for all of the subjects as a whole and after stratifying by obesity status as defined by BMI values. Odds ratios were used to quantify and test the association between metabolic syndrome and the dietary patterns described by the clusters, accompanied by their 95 % confidence intervals(Reference Homer and Lemeshow15).

The data were analysed using the SPSS for Windows statistical software package version 10·0·7 (SPSS Inc. Chicago, IL, USA).

Results

The characteristics and metabolic profiles concerning the 1052 non-diabetic subjects (527 men and 525 women) are shown in Table 1.

Table 1 Characteristics and metabolic profile of the study population: individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3

Dietary patterns

Table 2 shows the results of the dietary data analysis. The last four columns show the overall daily mean intake of the twenty-seven nutrients entered into the cluster analysis for men and women. On the whole, the eating habits of our population combined some typical elements of the Mediterranean diet, such as a high intake of olive oil, fruit and vegetables, with those of a ‘wealthy’ diet, such as a high intake of processed meats and refined-grain products (food intake data not shown). These characteristics were reflected – at nutrient level – in a generally high intake of unsaturated fats, vitamins and minerals, as well as of cholesterol and Na. As a preliminary analysis of the men and women separately did not reveal any between-gender differences in the resulting clusters, we subsequently pooled the data, which also had the advantage of increasing statistical efficiency. The criteria chosen for determining the number of clusters resulted from a balance between the evaluation of the distances between final cluster centres (greater distances correspond to greater dissimilarities) and the cluster sizes. We started inputting k = 2 and proceeded by adding one cluster at the time. The solution chosen was a compromise between the increase in the distances between cluster centres and an acceptable reduction in cluster sizes. The most workable and interpretable solution was the five clusters result, which seemed to capture the nutrient intake patterns most appropriately.

Table 2 Nutrient intake patternsFootnote * and nutritional features of the five groups identified by cluster analysisFootnote among individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3

* Symbols +(−) describe the variation above (below) the mean expected intake: +(−), by <0·5 standard deviation units (sdu); ++ (− −), by 0·5−1·0 sdu; +++ (− − −), by 1·0−1·5 sdu; ++++ (− − − −), by >1·5 sdu.

The cluster analysis was based on the standardised residuals of the linear regression analysis of each nutrient v. total energy intake (except alcohol) within gender.

  1. 1. Common pattern: This was the largest group, and the final cluster centres were close to the overall mean expected intakes. Thus their characteristics are generally similar to those above described. This diet was moderately low in fat, which accounted for 26·9 % of energy (%E), but relatively high (12·1 %E) in MUFA. Its carbohydrate content was slightly high (57·7 %E). Men and women in this cluster had the lowest mean daily total energy intake, 11 792·6 and 9970·5 kJ, respectively.

  2. 2. Animal products pattern: The people in this group had the highest consumption of meat, eggs and dairy products. Their diet was high in protein (20·0 %E), particularly from animal sources (14·8 %E). They consumed relatively more fats (31·1 %E), particularly of the saturated type (11·9 %E). This diet was the richest in cholesterol, P, Zn, complex B vitamins and vitamin D; it was also low in carbohydrates (48·9 %E).

  3. 3. Starch pattern: The diet of the people in this, the smallest group was the richest in starch, vegetal proteins and Na, and the poorest in fats, vitamins and minerals. It was very high in carbohydrates (68·8 %E) and very low in fat (17·3 %E), and characterised by the highest intake of refined-grain products (bread, rice and pasta), thus containing more starch and substantially less dietary fibre. This group had the highest-energy diet: the mean daily energy intake was 18 542·2 kJ among men and 16 244·4 kJ among women.

  4. 4. Vegetal/fat pattern: This cluster consisted of the largest consumers of olive oil and, at the same time, fat sauces made with seed oil and/or butter. The people in this group also had the highest intake of dry fruits. Their diet was the highest in fat (38·4 %E) of all types, particularly unsaturated fat: 17·2 %E from MUFA and 6·1 %E from PUFA. It was also relatively poor in minerals and vitamins, except for vitamin E.

  5. 5. Vitamin/fibre pattern: The subjects in this cluster consumed the largest amounts of vegetables, legumes and especially fruit. Their diet was very rich in vitamins and minerals, and also contained the largest amount of fibre (4·5 g/1000 kJ). It had a moderately low fat content (25·2 %E) and a slightly high carbohydrate content (58·9 %E).

K-means clustering generated an ANOVA table showing F tests for each variable (nutrient intake), with the magnitude of the F values indicating how well the respective nutrients discriminated between clusters. Among the macronutrients, starch, animal protein, fibre and saturated fat were those most helpful in forming and differentiating the clusters; among the micronutrients, they were K, vitamins C and B6 and β-carotene (the highest values were found in the vitamin/fibre group and the lowest in the starch and vegetal/fat clusters; data not shown).

Prevalence of metabolic syndrome and associated factors

The subjects in the starch group showed the highest adjusted prevalence of metabolic syndrome: 35·9 % (Table 3). In comparison with the common group, the odds ratio for metabolic syndrome was 1·8 (95 % CI 1·0, 3·4): i.e. an 80 % greater likelihood of having the syndrome. The second highest prevalence rate was in the animal products group (29·5 %), followed by the common diet (23·6 %), vitamin/fibre (19·9 %) and vegetal/fat groups (18·9 %). These differences were probably because the greatest prevalence of high TAG levels (41·9 %) was in the starch group and the greatest prevalence of impaired fasting glucose levels (38·1 %) was in the animal products group. The starch group also showed the greatest prevalence of abdominal obesity (30·6 %), followed by the animal products groups (26·9 %); the lowest prevalence (17·5 %) was in the vitamin/fibre group.

Table 3 AdjustedFootnote * prevalence (%) of metabolic syndrome factors by dietary pattern, and odds ratios measuring the association between the dietary patterns and metabolic syndrome for all subjects and stratified by BMI categories: individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3

NCEP, National Cholesterol Education Program.

* The multiple logistic regression models include terms for age, gender, education, sports practice, walking/cycling, television watching, smoking, alcohol consumption and the cluster groups.

Prevalence of high blood pressure includes subjects on antihypertensive medication.

Among the normal-weight subjects, the prevalence of metabolic syndrome was about 3 % in all of the groups except for the vitamin/fibre group (0·8 %), which was due to the fact that they had the lowest prevalence of both abdominal obesity and high blood pressure. Although of normal weight, 9·8 % of the subjects in the starch group had a large waist circumference and 70·1 % of them had altered blood pressure. The animal products group had the highest prevalence of impaired fasting glucose levels (20·1 %).

Among the overweight subjects, the prevalence of the syndrome rose to about 20 % in the common, animal products and vitamin/fibre groups; in the vegetal/fat group, it was only 14·8 %, much lower than the 36·2 % in the starch group. This difference was due to the worse lipid profile in the starch group.

Among the subjects classified as obese on the basis of their BMI values, 85·2 % of the subjects in the vitamin/fibre group had a large waist circumference, but this was less than the 100·0 % in the starch group. The obese subjects in the starch and animal products groups had the greatest prevalence of dyslipidaemia (high TAG and low HDL-C levels), and about 50 % of the latter had impaired fasting glucose levels compared with 21·4 % in the vitamin/fibre cluster. The prevalence of metabolic syndrome among the obese was 73·2 % in the starch group and 72·6 % in the animal/products group, which contrasted with 46·0 % in the common group, 43·5 % in the vegetal/fat group and 36·3 % in the vitamin/fibre group.

In order to quantify the relationship between dietary patterns and obesity status and their reciprocal influence on the association with the prevalence of metabolic syndrome, we used a logistic regression model which included also a dichotomous variable (BMI ≥ 30·0 kg/m2) for obesity and a term for interaction between obesity and cluster groups. The estimated adjusted OR (95 % CI) for metabolic syndrome associated with obesity were 4·0 (2·4, 6·8) in the common pattern, 12·6 (5·8, 27·3) in the animal products group, 9·1 (2·0, 42·3) in the starch group, 5·9 (2·2, 15·6) in the vegetal/fat group and 3·3 (1·3, 8·1) in the vitamin/fibre cluster (data not shown).

Discussion

We found that the people in the starch group, who consumed a very-low-fat, high-carbohydrate diet, had the worst metabolic profile (particularly more dyslipidaemia and abdominal obesity) and the highest prevalence of metabolic syndrome (36 %). Their diet was rich in refined-grain products, which have been found to be positively associated with metabolic syndrome in other studies(Reference Sahyoun, Jacques, Zhang, Juan and McKeown16, Reference Esmaillzadeh, Mirmiran and Azizi17). Carbohydrate-induced atherogenic dyslipidaemia (higher TAG and lower HDL-C levels) is one of the most controversial and important issues in nutritional public health(Reference Parks and Hellerstein18), and the fact that low-fat diets are often rich in carbohydrates has raised questions concerning the wisdom of institutional recommendations advocating a reduction in dietary fat intake as a means of treating or preventing CVD(Reference Jeppesen, Schaaf, Jones, Zhou, Chen and Reaven19, Reference Abbasi, McLaughli, Lamendola, Kim, Tanaka, Wang, Nakajima and Reaven20).

With regard to dietary fat, there is growing consensus concerning the beneficial effects of MUFA and/or PUFA in terms of preventing diabetes and CVD(Reference Meyer, Kushi, Jacobs and Folson21Reference Kris-Etherton, Hecker and Binkoski24), but the detrimental effect of SFA is still controversial(Reference Feskens25, Reference Golomb26). In our study, the highest total fat intake was found in the vegetal/fat group, followed by the animal products group. SFA content was similarly high in these two groups, but the diet of the subjects in the vegetal/fat group had a higher proportion of unsaturated fats. These subjects had one of the best metabolic profiles and the lowest prevalence of metabolic syndrome (18·9 %), whereas the animal products group showed one of the worst metabolic profiles (at least among the obese), particularly in terms of plasma lipid and fasting glucose levels, and it had the second highest prevalence of metabolic syndrome (29·5 %). Two factors may help interpret this finding: (i) the different sources of SFA in the two diets, as it has been shown that different types of SFA have different functions and different metabolic effects(Reference German and Dillard27); and (ii) the protective effect of unsaturated fats against the deleterious effect of SFA, as suggested by the results of some in vitro studies(Reference Maedler, Oberholzer, Bucher, Spinas and Donath28, Reference Busch, Gurisik, Cordery, Sudlow, Denyer, Laybutt, Hughes and Biden29).

The prevalence of impaired fasting glucose was lowest in the starch group (21·4 %); this value was quite comparable to those in the other clusters, but fairly smaller than the highest value (38·1 %) in the animal products group. This result is in line with those obtained in metabolic studies, which have suggested that subjects with higher-fat diets containing a higher proportion of saturated fat are more prone to develop disturbances in glucose metabolism than subjects with lower intakes of fat(Reference Lichtenstein and Schwab30). A high-fat, low-carbohydrate diet has been found to induce insulin resistance in healthy men(Reference Bisschop, de Metz, Ackermans, Endert, Pijl, Kuipers, Meijer, Sauerwein and Romijn31) and to be associated with the onset of diabetes(Reference Marshall, Hamman and Baxter32), whereas a diet with a high ratio of polyunsaturated to saturated fatty acids (P/S) has been shown to improve cellular response to insulin compared with a low-P/S diet in normal and diabetic rats(Reference Field, Ryan, Thomson and Clandinin33). Moreover, a number of studies have shown that plasma glucose is not associated with carbohydrate intake in healthy adults(Reference Yang, Kerver, Park, Kayitsinga, Allison and Song34, Reference Coulston, Liu and Reaven35) nor in patients with mild diabetes(Reference Garg, Grundy and Unger36).

The inherent limitations of our study are related to the possible inaccuracy of the dietary information and the fact that its cross-sectional nature precludes causal inference. The method we used for the dietary survey (the FFQ) has been commonly adopted in epidemiological studies to assess usual intake of foods and nutrients, and it is well known that some degree of inaccuracy is inherent to this approach. However, results from validation studies(Reference Willett and Lenart37) have been generally accepted as indicative of the ability of the FFQ to rank individuals appropriately according to nutrient intake. Furthermore, advantages of the food frequency method include reasonable cost and direct assessment of usual intake, avoiding imprecision that results from day-to-day variation in food choices.

In relation to the effect of SFA, it is interesting to note that a preliminary exploratory analysis based on the individual nutrients (and made before we adopted the patterns approach) found that SFA was not related to metabolic syndrome factors. This observation underlines one of the advantages of the patterns approach: it provides a comprehensive picture of the dietary context in which a nutrient is consumed. Our results suggest that the effect of a high SFA intake in a ‘vegetal’ context may be different from its effect in an ‘animal protein’ context.

As a whole, the prevalence of central obesity was highest in the starch group (30·6 %) whose members had also the most energy-rich diet. However, in spite of the similar energy contents of their diets, subjects in the animal products group had a prevalence of abdominal obesity of about 27 % against the 17·5 % found in the vitamin/fibre cluster, suggesting that the type of diet is important to keep a healthy body shape. Another strong point of our study is that it was stratified by obesity status. Obesity is a key aetiological factor in the development of metabolic syndrome, and various studies suggest that it may mediate the effect of total and saturated fat intake on diabetes risk(Reference Mayer-Davis, Monaco, Hoen, Carmichael, Vitolins, Rewers, Haffner, Ayad, Bergman and Karter38, Reference van Dam, Willett, Rimm, Stampfer and Hu39). As obesity may mediate the deleterious effects of dietary factors, stratification is the most appropriate way to examine its role because adjusting for rather than stratifying by the factors that modify the role of independent variables underestimates the strength of the association(Reference Marchall and Bessesen40). In comparison with the animal products and starch groups, the prevalence of metabolic syndrome was lower in the vegetal/fat group and particularly in the vitamin/fibre group, and these differences were more marked among the obese subjects. These findings are in line with those of other studies which showed that the beneficial effects of PUFA on CVD risk(Reference Oh, Hu, Manson, Stampfer and Willett41) and of dietary fibre on insulin resistance(Reference McKeown, Meigs, Liu, Saltzman, Wilson and Jacques42) are greatest among the overweight and obese. The fact that these beneficial effects are greater in obese subjects is important because it suggests that, even in the case of failure to achieve weight loss, diet can reduce obesity-related risk factors for CVD.

Obesity status influenced variation in the frequency of the metabolic syndrome factors across dietary clusters in different ways. The prevalence of high TAG levels increased with obesity status in all groups, but was particularly high in the starch cluster and also in the animal products group. The prevalence of low HDL-C increased with obesity only among subjects reporting the starch or animal products diet, while it remained quite unchanged in the common, vegetal/fat and vitamin/fibre groups. The prevalence of high blood pressure levels seemed influenced by dietary habits particularly among the normal-weight subjects, with the lowest value in the vitamin/fibre group followed by the vegetal/fat cluster. Among overweight and obese subjects the prevalence of high blood pressure was similarly high in all dietary groups. From the analysis of the interaction between obesity and dietary pattern, our results show that dietary habits can modify the frequency of metabolic complications associated with obesity. The differences seem particularly due to the greater deterioration associated with obesity of both the lipid profile (in the starch and animal products groups) and the glycaemic profile (in the animal products group) when compared with the other clusters.

One characteristic of the animal products group is the high dietary content of animal protein. Some studies have found a direct relationship between the intake of red meat and the risk of CVD(Reference Gramenzi, Gentile, Fasoli, Negri, Parazzini and La Vecchia43, Reference Hu, Stampfer, Manson, Ascherio, Colditz, Speizer, Hennekens and Willett44), and others have shown that frequent consumption of processed meat increases the risk of diabetes(Reference Mayer-Davis, Monaco, Hoen, Carmichael, Vitolins, Rewers, Haffner, Ayad, Bergman and Karter38, Reference Schulze, Manson, Willett and Hu45). It is particularly interesting to consider the role of Fe as studies have shown that a higher intake of haem Fe (derived from animal products) is associated with an increased risk of both CVD and diabetes(Reference Ascherio, Willett, Rimm, Giovannucci and Stampfer46Reference Rajpathak, Ma, Manson, Willett and Hu48), whereas no association has been found in the case of non-haem Fe (which is rich in the vitamin/fibre pattern). Furthermore, it is well known that the intake of animal foods is the most important dietary determinant of the Fe status of a population, and serum ferritin has not only been found to be positively associated with metabolic syndrome(Reference Megan, Clark and Guallar49), but also proposed as a marker of insulin resistance syndrome(Reference Fernandez-Real, Ricart-Engel, Arroyo, Balanca, Casamitjana-Abella, Cabrero, Fernandez-Castaner and Soler50).

The characteristics of the diets in the vitamin/fibre group (rich in fruits and vegetables) and vegetal/fat group (rich in olive oil and nuts) combine the typical features of the Mediterranean diet: a high intake of unsaturated fats, vitamin E, fibre, minerals and other antioxidant vitamins. It is thought that oxidative stress plays a role in the pathophysiology of diabetes(Reference Maritim, Sanders and Watkins51) and CVD(Reference Molavi and Mehta52), and it has been found that adults with metabolic syndrome have suboptimal concentrations of a number of antioxidants, which may thus partially explain their increased risk of developing diabetes and CVD(Reference Ford, Mokdad, Giles and Brown53). Vitamins E, A and C and carotenoids are well-known antioxidants, and it has been found that virgin olive oil is beneficial in preventing oxidative processes(Reference Marrugat, Covas, Fito, Schroder, Miro-Casas, Gimeno, Lopez-Sabater, dela Torre and Farre54). Consequently, the beneficial effects of such dietary characteristics may be due to their role in preserving antioxidant status. One recent randomised trial has found that Mediterranean diets supplemented with olive oil or nuts have beneficial effects on cardiovascular risk factors in comparison with low-fat diets(Reference Estruch, Martinez-Gonzalez and Corella55). Furthermore, another nutrient common to the vitamin/fibre and vegetal/fat patterns is Mg, which has been consistently found to be inversely associated with the prevalence and incidence of metabolic syndrome(Reference Song, Ridker, Manson, Cook, Buring and Liu56Reference He, Liu, Daviglus, Morris, Loria, Van Horn, Jacobs and Savage58). Unfortunately, our data do not include Mg, but we know that nuts and vegetables are important sources of it.

In conclusion, the present results, showing the highest prevalence of metabolic syndrome in the starch group, support already compelling evidence about the deleterious effects of a very-low-fat diet rich in refined carbohydrates on lipid profile, particularly of overweight and obese subjects. Subjects in the animal products cluster, whose diet was rich in animal protein and fats, had the second highest prevalence of metabolic syndrome with the worst glycaemic profile. The results of our study also confirm the beneficial effects of diets rich in unsaturated fats, fruits and vegetables, probably due to their role in preserving antioxidant status, and suggest that rather than putting limits on the intake of total and saturated fat, greater attention should be paid to its sources – with the use of vegetable sources being recommended. The prevalence of metabolic syndrome was the lowest in the vegetal/fat group and vitamin/fibre group, markedly so among obese subjects. Since obesity is a key aetiological factor in the development of metabolic syndrome, the maintenance of normal body weight should be a primary goal in preventing it. However, even if this objective is not achieved, the adoption of beneficial dietary habits is important for preserving a healthy metabolic profile.

Acknowledgements

Conflict of interest declaration: There are no conflicts of interest. Sources of funding: The work was supported by research programme grant funding from the National Research Council (Italy) in the ambit of the Project Prevention and Control of Disease Factors (FATMA). Author contributions: A.N. designed the protocol, supervised the execution of the study and collaborated in writing the manuscript. M.L.C.L. did the statistical analysis and wrote the manuscript.

References

1.Grundy, SM (2006) Metabolic syndrome: connecting and reconciling cardiovascular and diabetes worlds. J Am Coll Cardiol 47, 10931100.CrossRefGoogle ScholarPubMed
2.Kelley, DE (2003) Sugars and starch in the nutritional management of diabetes mellitus. Am J Clin Nutr 78, Suppl., 858S864S.CrossRefGoogle ScholarPubMed
3.Schulze, MB & Hu, FB (2004) Dietary approaches to prevent the metabolic syndrome: quality versus quantity of carbohydrates. Diabetes Care 27, 613614.CrossRefGoogle ScholarPubMed
4.Weinberg, SL (2004) The diet–heart hypothesis: a critique. J Am Coll Cardiol 43, 731733.CrossRefGoogle Scholar
5.Baxter, AJ, Coyne, T & McClintock, C (2006) Dietary patterns and metabolic syndrome – a review of epidemiologic evidence. Asia Pac J Clin Nutr 15, 134142.Google ScholarPubMed
6.Nicolosi, A (1997) Le indagini di popolazione sulla prevalenza delle principali malattie oculari in Italia. In L’epidemiologia oftalmica in Italia, pp. 4370 [L Cerulli, M Miglior and F Ponte, editors]. Roma: INC.Google Scholar
7.Leite, MLC, Nicolosi, A, Firmo, JOA & Lima-Costa, MF (2007) Features of metabolic syndrome in non-diabetic Italians and Brazilians: a discriminant analysis. Int J Clin Pract 61, 3238.CrossRefGoogle ScholarPubMed
8.Leite, MLC & Nicolosi, A (2006) Lifestyle correlates of anthropometric estimates of body adiposity in an Italian middle-aged and elderly population: a covariance analysis. Int J Obes (Lond) 30, 926934.CrossRefGoogle Scholar
9.Willett, WC (editor) (1998) 1980 Nurses’ Health Study Dietary Questionnaire; Appendix 5-1. In Nutritional Epidemiology, 2nd ed., pp. 9597. New York: Oxford University Press.CrossRefGoogle Scholar
10.Salvini, S, Parpinel, M, Gnagnarella, P, Maisonneuve, P & Turrini, A (1998) Banca dati di composizione degli alimenti per studi epidemiologici in Italia. Milano: Istituto Europeo di Oncologia.Google Scholar
11.Willett, WC & Stampfer, MJ (1998) Implications of total energy intake for epidemiologic analysis. In Nutritional Epidemiology, 2nd ed., pp. 273301 [WC Willett, editor]. New York: Oxford University Press.CrossRefGoogle Scholar
12.Jobson, JD (1992) Applied Multivariate Data Analysis. vol. II: Categorical and Multivariate Methods. New York: Springer-Verlag.CrossRefGoogle Scholar
13.National Heart Lung and Blood Institute (2001) Third Report of the Expert Panel on Detection, Evaluation, and Treatment of the High Blood Cholesterol in Adults (Adult Treatment Panel III): Executive Summary. http://www.nhlbi.nih.gov/guidelines/cholesterol/atp_iii.htm (accessed December 2008).CrossRefGoogle Scholar
14.The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (2003) Follow-up report on the diagnosis of diabetes mellitus. Diabetes Care 26, 31603167.CrossRefGoogle Scholar
15.Homer, DW & Lemeshow, S (2000) Applied Logistic Regression, 2nd ed. New York: Wiley.CrossRefGoogle Scholar
16.Sahyoun, NR, Jacques, PF, Zhang, XL, Juan, W & McKeown, NM (2006) Whole-grain intake is inversely associated with the metabolic syndrome and mortality in older adults. Am J Clin Nutr 83, 124131.CrossRefGoogle ScholarPubMed
17.Esmaillzadeh, A, Mirmiran, P & Azizi, F (2005) Whole-grain consumption and the metabolic syndrome: a favorable association in Tehranian adults. Eur J Clin Nutr 59, 353362.CrossRefGoogle ScholarPubMed
18.Parks, EJ & Hellerstein, MK (2000) Carbohydrate-induced hypertriacylglycerolemia: historical perspective and review of biological mechanisms. Am J Clin Nutr 71, 412433.CrossRefGoogle ScholarPubMed
19.Jeppesen, J, Schaaf, P, Jones, C, Zhou, M-Y, Chen, Y-DI & Reaven, GM (1997) Effects of low-fat, high-carbohydrate diets on risk factors for ischemic heart disease in postmenopausal women. Am J Clin Nutr 65, 10271033.CrossRefGoogle ScholarPubMed
20.Abbasi, F, McLaughli, T, Lamendola, C, Kim, HS, Tanaka, A, Wang, T, Nakajima, K & Reaven, GM (2000) High carbohydrate diets, triglyceride-rich lipoproteins, and coronary heart disease risk. Am J Cardiol 85, 4548.CrossRefGoogle ScholarPubMed
21.Meyer, KA, Kushi, LH, Jacobs, DR & Folson, AR (2001) Dietary fat and incidence of type 2 diabetes in older Iowa women. Diabetes Care 24, 15281535.CrossRefGoogle ScholarPubMed
22.Ros, E (2003) Dietary cis-monounsaturated fatty acids and metabolic control in type 2 diabetes. Am J Clin Nutr 78, Suppl., 617S625S.CrossRefGoogle ScholarPubMed
23.Kris-Etherton, PM (1999) Monounsaturated fatty acids and risks of cardiovascular disease. Circulation 100, 12531258.CrossRefGoogle ScholarPubMed
24.Kris-Etherton, PM, Hecker, KD & Binkoski, AE (2004) Polyunsaturated fatty acids and cardiovascular health. Nutr Rev 62, 414426.CrossRefGoogle ScholarPubMed
25.Feskens, EJM (2001) Can diabetes be prevented by vegetable fat? Diabetes Care 24, 15171518.CrossRefGoogle ScholarPubMed
26.Golomb, BA (1998) Dietary fats and heart disease – dogma challenged? J Clin Epidemiol 51, 461464.Google ScholarPubMed
27.German, JB & Dillard, CJ (2004) Saturated fats: what dietary intake? Am J Clin Nutr 80, 550559.CrossRefGoogle ScholarPubMed
28.Maedler, K, Oberholzer, J, Bucher, P, Spinas, GA & Donath, MY (2003) Monounsaturated fatty acids prevent the deleterious effects of palmitate and high glucose on human pancreatic β-cell turnover and function. Diabetes 52, 726733.CrossRefGoogle ScholarPubMed
29.Busch, AK, Gurisik, E, Cordery, DV, Sudlow, M, Denyer, GS, Laybutt, DR, Hughes, WE & Biden, TJ (2005) Increased fatty acid desaturation and enhanced expression of stearoyl coenzyme A desaturase protects pancreatic β-cells from lipoapoptosis. Diabetes 54, 29172924.CrossRefGoogle ScholarPubMed
30.Lichtenstein, AH & Schwab, US (2000) Relationship of dietary fat to glucose metabolism. Atherosclerosis 150, 227243.CrossRefGoogle ScholarPubMed
31.Bisschop, PH, de Metz, J, Ackermans, MT, Endert, E, Pijl, H, Kuipers, F, Meijer, AJ, Sauerwein, HP & Romijn, JA (2001) Dietary fat content alters insulin-mediated glucose metabolism in healthy men. Am J Clin Nutr 73, 554559.CrossRefGoogle ScholarPubMed
32.Marshall, JA, Hamman, RF & Baxter, J (1991) High-fat, low-carbohydrate diet and the etiology of non-insulin-dependent diabetes mellitus: The San Luis Valley Diabetes Study. Am J Epidemiol 134, 590603.CrossRefGoogle ScholarPubMed
33.Field, CJ, Ryan, EA, Thomson, AB & Clandinin, MT (1990) Diet fat composition alters membrane phospholipid composition, insulin binding, and glucose metabolism in adipocytes from control and diabetic animals. J Biol Chem 265, 1114311150.CrossRefGoogle ScholarPubMed
34.Yang, EJ, Kerver, JM, Park, YK, Kayitsinga, J, Allison, DB & Song, WO (2003) Carbohydrate intake and biomarkers of glycemic control among US adults: the third National Health and Nutrition Examination Survey (NHANES III). Am J Clin Nutr 77, 14261433.CrossRefGoogle ScholarPubMed
35.Coulston, AM, Liu, GC & Reaven, GM (1983) Plasma glucose, insulin and lipid responses to high-carbohydrate low-fat diets in normal humans. Metabolism 32, 5256.CrossRefGoogle ScholarPubMed
36.Garg, A, Grundy, SM & Unger, RH (1992) Comparison of effects of high and low carbohydrate diets on plasma lipoproteins and insulin sensitivity in patients with mild NIDDM. Diabetes 41, 12781285.CrossRefGoogle ScholarPubMed
37.Willett, WC & Lenart, E (1998) Reproducibility and validity of food-frequency questionnaires. In Nutritional Epidemiology, 2nd ed., pp. 101147 [WC Willett, editor]. New York: Oxford University Press.CrossRefGoogle Scholar
38.Mayer-Davis, EJ, Monaco, JH, Hoen, HM, Carmichael, S, Vitolins, MZ, Rewers, MJ, Haffner, SM, Ayad, MF, Bergman, RN & Karter, AJ (1997) Dietary fat and insulin sensitivity in a triethnic population: the role of obesity. The Insulin Resistance Atherosclerosis Study (IRAS). Am J Clin Nutr 65, 7987.CrossRefGoogle Scholar
39.van Dam, RM, Willett, WC, Rimm, EB, Stampfer, MJ & Hu, FB (2002) Dietary fat and meat intake in relation to risk of type 2 diabetes in men. Diabetes Care 25, 417424.CrossRefGoogle ScholarPubMed
40.Marchall, JA & Bessesen, DH (2002) Dietary fat and the development of type 2 diabetes. Diabetes Care 25, 620622.CrossRefGoogle Scholar
41.Oh, K, Hu, FB, Manson, JE, Stampfer, MJ & Willett, WC (2005) Dietary fat intake and risk of coronary heart disease in women: 20 years of follow-up of the Nurses’ Health Study. Am J Epidemiol 161, 672679.CrossRefGoogle ScholarPubMed
42.McKeown, NM, Meigs, JB, Liu, S, Saltzman, E, Wilson, PW & Jacques, PF (2004) Carbohydrate nutrition, insulin resistance, and the prevalence of the metabolic syndrome in the Framingham Offspring Cohort. Diabetes Care 27, 438546.CrossRefGoogle ScholarPubMed
43.Gramenzi, A, Gentile, A, Fasoli, M, Negri, E, Parazzini, F & La Vecchia, C (1990) Association between certain foods and risk of acute myocardial infarction in women. BMJ 300, 771773.CrossRefGoogle ScholarPubMed
44.Hu, FB, Stampfer, MJ, Manson, JE, Ascherio, A, Colditz, GA, Speizer, FE, Hennekens, CH & Willett, WC (1999) Dietary saturated fats and their food sources in relation to the risk of coronary heart disease in women. Am J Clin Nutr 70, 10011008.CrossRefGoogle Scholar
45.Schulze, MB, Manson, JE, Willett, WC & Hu, FB (2003) Processed meat intake and incidence of type 2 diabetes in younger and middle-aged women. Diabetologia 46, 14651473.CrossRefGoogle ScholarPubMed
46.Ascherio, A, Willett, WC, Rimm, EB, Giovannucci, EL & Stampfer, MJ (1994) Dietary iron intake and risk of coronary disease among men. Circulation 89, 969974.CrossRefGoogle ScholarPubMed
47.van der A, DL, Peeters, PHM, Grobbee, DE, Marx, JJM & van der Schouw, YT (2004) Dietary haem iron and coronary heart disease in women. Eur Heart J 26, 257262.CrossRefGoogle ScholarPubMed
48.Rajpathak, S, Ma, J, Manson, J, Willett, WC & Hu, FB (2006) Iron intake and the risk of type 2 diabetes in women: a prospective cohort study. Diabetes Care 29, 13701376.CrossRefGoogle ScholarPubMed
49.Megan, J, Clark, JM & Guallar, E (2004) Serum ferritin and risk of the metabolic syndrome in US adults. Diabetes Care 27, 24222428.Google Scholar
50.Fernandez-Real, JM, Ricart-Engel, W, Arroyo, E, Balanca, R, Casamitjana-Abella, R, Cabrero, D, Fernandez-Castaner, M & Soler, J (1998) Serum ferritin as a component of the insulin resistance syndrome. Diabetes Care 21, 6268.CrossRefGoogle ScholarPubMed
51.Maritim, AC, Sanders, RA & Watkins, JB 3rd (2003) Diabetes, oxidative stress, and antioxidants: a review. J Biochem Mol Toxicol 17, 2438.CrossRefGoogle ScholarPubMed
52.Molavi, B & Mehta, JL (2004) Oxidative stress in cardiovascular disease: molecular basis of its deleterious effects, its detection, and therapeutic considerations. Curr Opin Cardiol 19, 488493.CrossRefGoogle ScholarPubMed
53.Ford, ES, Mokdad, AH, Giles, WH & Brown, DW (2003) The metabolic syndrome and antioxidant concentrations: findings from the third National Health and Nutrition Examination Survey. Diabetes 52, 23462352.CrossRefGoogle ScholarPubMed
54.Marrugat, J, Covas, MI, Fito, M, Schroder, H, Miro-Casas, E, Gimeno, E, Lopez-Sabater, MC, dela Torre, R & Farre, M (2004) Effects of differing phenolic content in dietary olive oils on lipids and LDL oxidation – a randomized controlled trial. Eur J Nutr 43, 140147.CrossRefGoogle ScholarPubMed
55.Estruch, R, Martinez-Gonzalez, MA, Corella, D et al. (2006) Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med 145, 111.CrossRefGoogle ScholarPubMed
56.Song, Y, Ridker, PM, Manson, JE, Cook, NR, Buring, JE & Liu, S (2005) Magnesium intake, C-reactive protein, and the prevalence of metabolic syndrome in middle-aged and older US women. Diabetes Care 28, 14381444.CrossRefGoogle Scholar
57.Guerrero-Romero, F & Rodriguez-Moran, M (2006) Hypomagnesemia, oxidative stress, inflammation, and metabolic syndrome. Diabetes Metab Res Rev 22, 471476.CrossRefGoogle ScholarPubMed
58.He, K, Liu, K, Daviglus, ML, Morris, SJ, Loria, CM, Van Horn, L, Jacobs, DR & Savage, PJ (2006) Magnesium intake and incidence of metabolic syndrome among young adults. Circulation 113, 16751682.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Characteristics and metabolic profile of the study population: individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3

Figure 1

Table 2 Nutrient intake patterns* and nutritional features of the five groups identified by cluster analysis† among individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3

Figure 2

Table 3 Adjusted* prevalence (%) of metabolic syndrome factors by dietary pattern, and odds ratios measuring the association between the dietary patterns and metabolic syndrome for all subjects and stratified by BMI categories: individuals aged 40–74 years, Bollate (Milan, Italy), 1992–3