American Journal of Clinical Nutrition, Vol. 86, No. 6, 1633-1641,
December 2007
© 2007 American Society for Nutrition
ORIGINAL RESEARCH COMMUNICATION |
Sex-specific association of fatty acid binding protein 2 and microsomal triacylglycerol transfer protein variants with response to dietary lipid changes in the 3-mo Medi-RIVAGE primary intervention study1,2,3
Marguerite Gastaldi,
Sophie Dizière,
Catherine Defoort,
Henri Portugal,
Denis Lairon,
Michel Darmon and
Richard Planells
1 From the Institut National de la Santé et de la Recherche Medicale (INSERM), U476 "Nutrition Humaine et lipides," Marseille, F-13385 France; Institut national de la Recherche Agronomique (INRA), UMR 1260, Marseille, F-13385 France; and Univ Méditerranée Aix-Marseille 2, Faculté de Médecine, IPHM-IFR 125, Marseille, F-13385 France
2 Supported by the French Research Ministry (AQS grant), INSERM (IDS grant), the Provence-Alpes-Côte d'Azur Régional council, the Bouches du Rhône Général council, and the CRITT-PACA.
3 Reprints not available. Address correspondence to M Gastaldi, Univ Méditerranée Aix-Marseille 2, Faculté de Médecine, IPHM-IFR 125, Marseille, F-13385 France. E-mail: marguerite.gastaldi{at}medecine.univ-mrs.fr.
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ABSTRACT
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Background: The dietary guidelines targeted at reducing cardiovascular risk lead to largely heterogeneous responses in which genetic determinants are largely involved.
Objectives: We evaluated the effect of fatty acid binding protein 2 (FABP2) Ala54Thr and microsomal triacylglycerol transfer protein (MTTP) –493G/T allelic variations on plasma lipid markers, at baseline and on the response to the 3-mo Medi-RIVAGE primary prevention study.
Design: Subjects with moderate cardiovascular disease risk (n = 169) were advised to reduce total and saturated dietary fats and to increase intake of monounsaturated and polyunsaturated fats. They were genotyped for FABP2 Ala54Thr and MTTP –493G/T allelic variations, and plasma was processed for cardiovascular risk marker analyses.
Results: At baseline, men and women homozygous for Thr54 presented a significant opposite profile for plasma oleic acid (18:1), triacylglycerol-rich lipoprotein (TRL) cholesterol, and TRL phospholipids. In addition, all Thr/Thr men presented higher 18:1 values than did women. For the MTTP –493G/T polymorphism, although all TT subjects presented high apolipoprotein B-48, a genotype x sex interaction was present for palmitic acid, linolenic acid, eicosatrienoic acid, and insulin. The prudent diet clearly improved plasma lipid markers. FABP2 genotype did not interact much with the amplitude of the response. However, for MTTP polymorphism, men homozygous for the T allele displayed a significantly more pronounced response than did men carrying the G allele, which is particularly evident by their larger decrease in the Framingham score.
Conclusions: These 2 polymorphic loci are thus differently associated with the baseline lipid markers as well as with the response to nutritional recommendations, but both presented a marked sex-specific profile, with the response to diet being particularly efficient in men homozygous for the MTTP –493T allele.
Key Words: Serum lipids • dietary fats • fatty acid binding protein 2 • FABP2 polymorphism • microsomal triacylglycerol transfer protein • MTTP polymorphism • Mediterranean diet • risk assessment
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INTRODUCTION
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Cardiovascular diseases (CVDs) represent one of the main causes of death in developed countries and are thus one of the greatest concerns in public health. The various dietary guidelines that are provided by the nutrition research community are aimed at decreasing the incidence of such diseases (1). However, although nutritional recommendations are targeted to the whole population, responses to diet turned out to be largely heterogeneous, and a role for genetic determinants in the interindividual variation is now clearly admitted (2). One of the most widespread recommendations is to replace saturated fat with monounsaturated and polyunsaturated fats, and the variation of the response to such a dietary challenge may be due to the presence of allelic variants in the genes involved in fatty acid (FA) absorption and metabolism.
In the epithelial cells of the small intestine, the absorption of dietary long-chain FAs (LCFAs) represents a multistep process that involves 1) the uptake of LCFAs at the apical side of the cell, 2) the intracellular transport of LCFAs and their esterification, and 3) the formation and secretion of triacylglycerol-rich lipoproteins (TRLs) at the basal side of the cell. Among other processes, the assembly and secretion of TRLs involve the intracellular LCFA trafficking by FA binding proteins (FABPs) and the lipid transfer on the nascent apolipoprotein (apo) B polypeptide chain by the microsomal triacylglycerol transfer protein (MTP).
The human FA binding protein 2 (FABP2) gene encodes the intestinal FABP isoform (I-FABP) that is specifically expressed in enterocytes. In 1995, Baier et al (3) reported that a single nucleotide polymorphism (G to A) within the second exon at codon 54 predicted an amino acid substitution (Ala54Thr) that increases the in vitro binding affinity of the protein to LCFAs. Later, it was reported that, when challenged with an oral fat load, Thr54 homozygotes displayed a significantly greater increase in plasma chylomicron triacylglycerol and VLDL triacylglycerol (4). Another study found an association between Thr54 carriers and higher cholesterol concentration in chylomicron after ingesting olive oil (4, 5). All these modifications could be ascribed to an increased trafficking of FAs toward chylomicron assembly sites.
The role played by the MTP protein in the chylomicron or VLDL assembly was highlighted by studies showing that MTP activity was absent in abetalipoproteinemic subjects (6) and that a liver-specific deletion of the gene coding for MTP (MTTP) produced a dramatic reduction in plasma VLDL triacylglycerol and apo B-100 secretion. The most studied promoter polymorphism at the MTTP locus is located 493 bp (base pair) upstream from the transcriptional start site (–493G/T), but the association between this polymorphism and biological markers for risk of CVD is still controversial (7-12) and has never been addressed by intervention studies. The present study was undertaken to examine whether the FABP2 and MTTP gene variants were associated with different responses to a 3-mo dietary intervention targeted to reduce total fat intake concomitantly with a replacement of saturated FAs by monounsaturated and polyunsaturated FAs.
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SUBJECTS AND METHODS
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Subjects
The design and methods of the Medi-RIVAGE study have been previously reported (13), and a marked reduction of cardiovascular risk was shown (14). Briefly, 169 volunteers with moderate cardiovascular risks were provided with nutritional recommendations. They consumed a low-fat diet for 3 mo: either a Mediterranean-type diet adapted from the traditional model or an adaptation of the commonly prescribed low-fat American Heart Association–type diet. The compliance with dietary recommendations was followed by dietitians. Three-day food records (at entry and after 3 mo) and 24-h unscheduled dietary recalls (once a month) were realized. No differences were observed in the dietary compliance according to sex. The GENI program nutritional database (version 6.1; Micro6, Nancy, France) was used and is based on the French REGAL food database (14). At entry and at the end of the 3-mo period, biochemical analyses were performed as previously described (14). Informed consent was obtained for each subject, and the study was approved by the institution's ethics committee (ethics committee no. 98/25).
Polymorphism detection
Genomic DNA was prepared from white blood cells by a standard proteinase K-phenol method. The FABP2 Ala54Thr polymorphism and the MTTP –493G/T polymorphism were genotyped by a polymerase chain reaction restriction fragment length polymorphism assay (3, 7). For FABP2 genotyping the forward primer was 5'-CAGGTGTTAATATAGTGAAAAGG, and the reverse primer was 5'-TTACCCTGAGTTCAGTTCCG; the restriction cleavage was performed by Hha1 enzyme. For MTTP genotyping the forward primer was 5'-AGTTTCACACATAAGGACAATCATCTA and the reverse primer was 5'-GGATTTAAATTTAAACTGTTAATTCATATCAC. The restriction cleavage was performed by Hph1 enzyme.
Statistical analyses
Statistical analyses were performed with the SAS statistical software (SAS Institute, Cary, NC). A chi-square test was used to determine whether genotypes at each gene locus were in Hardy-Weinberg equilibrium. Logarithmic transformation was performed on individual values of apo B-48, linolenic acid (18:3), stearidonic acid (18:4), eicosapentaenoic acid (20:5), triacylglycerols, insulin, TRL cholesterol, TRL triacylglycerols, TRL phospholipids, and Framingham score to improve the normality of their distribution. Because the patients were assigned for 3 mo to 2 different diets, it was first checked whether those 2 populations could be merged for the present analysis. A repeated-measures (baseline and 3 mo) general linear model showed that the type of diet had no effect on the variables studied. In addition, it was checked by chi-square test that the distribution of the subjects as a function of their genotypes was not affected by the type of diet.
Before testing the effect of genotypes on the dependent variables, interfering covariables (adjustment factors) were identified. First, each dependent variable measured at baseline was tested in univariate general linear models with independent qualitative variables. Age was always included in the adjustment. Second, linear correlations between the dependent variables and the quantitative covariables were performed, and correlations significant at the 0.05 level were retained. Identified covariables were included as adjustment factors for testing the effect of genotypes at baseline and 3 mo. Professional activity (activity, retirement, inactivity), body mass index (in kg/m2), alcohol consumption, antihypertensive treatment (yes or no), smoking status (smoker, former smoker, never smoker), and menopausal status in women (yes, no or treated) were entered as covariables into the models. The effects of the genotypes at baseline were tested with general linear models. The effect of the genotypes on the response to the diet was tested in repeated-measures general linear models. Interactions of genotype by time and by sex were tested. Results were given for men and women separately when the interaction was significant.
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RESULTS
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The distribution of FABP2 genotypes was 0.51 for Ala54/Ala54, 0.40 for Ala54/Thr54, and 0.09 for Thr54/Thr54. The frequency of MTTP genotypes were 0.41 for –493GG, 0.49 for –493GT, and 0.10 for –493TT. The FABP2 Thr54-encoding allele had a frequency of 0.29, and the MTTP –493T variant had a frequency of 0.35. At both FABP2 and MTTP loci, the distribution of genotypes was not significantly different from that expected under the Hardy-Weinberg equilibrium (P = 0.920 and P = 0.593, respectively).
At entry, subjects homozygous for the Thr54-encoding allele had a significantly higher percentage of plasma stearic acid (16:0) (Table 1
). Interestingly, a significant interaction between genotype and sex was observed for the percentage of plasma oleic acid (18:1). This interaction points out that men and women exhibited a significant opposite profile with highest values for Thr/Thr men and lowest values for Thr/Thr women. In addition, men, but not women, homozygous for the Thr54-encoding allele had a significantly higher plasma percentage of oleic acid (18:1) than did men carrying the Ala-encoding allele. No significant differences could be found in any of the biochemical markers (Table 2), but, again, according to genotypes, men and women showed significantly opposite profiles for TRL cholesterol and TRL phospholipids. The lowest values for TRL cholesterol and TRL phospholipids were found in women homozygous for the Thr54-encoding allele, whereas highest values were found in men homozygous for the Thr54-encoding allele.
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TABLE 2. Fasting biochemical markers according to the Ala54Thr polymorphism of the fatty acid binding protein 2 gene1
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For the MTTP –493G/T polymorphism, Table 3 shows that all subjects homozygous for the T allele exhibited significant lower percentages for stearic acid (18:0) and higher percentages for 18:1. In addition, a significant genotype x sex interaction was observed when considering 16:0, 18:3, and eicosatrionioic acid (20:3). Interestingly, only TT men displayed higher 16:0 and lower 18:3 and 20:3 values. For the biochemical markers (Table 4), all TT subjects presented significant higher concentrations of apo B-48. Insulin values displayed a genotype x sex interaction with a different pattern in men and women.
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TABLE 3. Plasma fatty acid composition according to the –493 G/T polymorphism of the microsomal triglyceride transfer protein
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TABLE 4. Fasting biochemical markers according to the –493 G/T polymorphism of the microsomal triglyceride transfer protein1
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As expected, at the end of the 3-mo diet, all subjects reduced their fat intake with a sharp decrease in saturated FAs and a slight increase in monounsaturated and polyunsaturated FA consumption (14). Interestingly, when considering the FABP2 Ala54Thr polymorphism, the only difference observed in plasma FA composition concerned the 18:1 percentage: men and women exhibited a different profile of response linked to genotype. However, in all subjects homozygous for the Thr allele, the diet induced a significant higher decrease in fasting apo B than did the other 2 genotypes (Table 2
). As for the MTP –493G/T polymorphism, this work shows that there were genotype-specific differences in the response to diet. Indeed, TT subjects significantly reduced 16:0 and 18:1 and increased 18:2 (Table 3). In addition, a genotype x sex interaction was also observed: TT men significantly increased 18:0. For the biochemical markers (Table 4), subjects homozygous for MTP –493T also displayed a genotype-specific response in fasting apo B-48 values, total cholesterol, fasting triacylglycerols, and fasting TRL phospholipids. Moreover, this greater genotype-specific susceptibility appears also to be sex specific. Indeed, when we consider the Framingham score, which represents a "global" evaluation of risk, we observed in men a marked decrease of this score that is significantly more important than in women.
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DISCUSSION
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Our results show the interaction of sex with 2 gene polymorphisms and how the response to diet can be modulated by these polymorphisms. In this study, we did not find any relation between the Ala54Thr polymorphism at the FAB2 locus and fasting glucose or insulin concentrations, which is consistent with some previous data (15-19). An association between this polymorphism and insulin resistance was previously described in the Pima population, a group known to have a high prevalence of type 2 diabetes mellitus (3). Nevertheless, it was shown later that this association is likely to be linked to promoter variations, which are in complete genotypic concordance with the Ala54Thr substitution in Pima but not in white populations (20). Moreover, in young French-Canadians, among the components of the metabolic syndrome, only plasma triacylglycerol concentrations were shown to display an interaction with the FABP2 polymorphism (11). In our study, only men homozygous for the Thr allele showed a tendency to higher triacylglycerol concentrations (data not shown).
Previous experiments showed that in vitro, compared with the Ala isoform, the human I-FABP Thr protein presented a 2-fold higher affinity for 18:1 FAs (21). In addition, expression studies showed that Caco-2 cells transfected with the Thr-encoding allele exhibited a 2-fold increase in FA uptake and a 5-fold increase in triacylglycerol secretion than did Caco-2 cells transfected with the Ala-encoding allele (22). Finally, it was shown that human intestinal explants from carriers of the Thr allele displayed a marked increase in triacylglycerol secretion (23). In agreement with those studies, we showed here a significant association between the Thr54 variant and an altered fasting plasma FA profile (increase in 16:0 associated in men with an increase in 18:1). Our study also showed an interaction between the Ala/Thr polymorphism and sex because the Thr/Thr men showed high TRL-cholesterol and TRL-phospholipid concentrations. These latter alterations together with the increases in 16:0 and 18:1 might be associated with an increased risk of CVD. Such an interaction between this polymorphism and sex has already been described. Although not strictly comparable, data reported from the Framingham cohort showed that women but not men homozygous for the Ala54-encoding allele displayed lower total and LDL-cholesterol concentrations (24). Such a sex-specific difference, as observed in our study, can also be linked to recent data obtained from I-FABP knockout mice (25) in which females did not present any altered liver histology, whereas males showed centrolobular vacuolated hepatocytes.
Our study also highlighted a sex-specific link between allelic variation at the MTTP –493 locus and lipid metabolism at baseline. MTP is known to play a critical role in the assembly of triacylglycerol-rich particles in liver and intestine. However, some clues seem to indicate that the expression of the MTTP gene could be different for the tissue and could lead to compensatory effects. For example, an intestine-specific MTP deficiency in mice led to an increase in hepatic VLDL secretion (26). MTP inhibitors also may present different effects on intestine or liver (27).
The MTTP T allele was shown to be associated with an increase in gene expression (7) and with an increased production of small apo B-48–containing lipoproteins in the postprandial state (28). It is thus not surprising to observe in our study an increase in plasma apo B-48 concentration, the specific chylomicron apolipoprotein, in the subjects homozygous for the T allele. A longitudinal study in adult men has shown that T allele carriers presented a significantly increased risk of coronary heart disease (8). Paradoxically, however, this study also put forward that this increased risk was linked to a decrease in plasma total cholesterol in this subpopulation. Other works however did not show any modification in circulating cholesterol (10-12). In our study we can only observe a tendency to an increase in the T homozygous population. The increased risk observed by Ledmyr et al (8) might be associated to the modification of other lipid compounds that have long been linked to CVD risk. As a matter of fact, we observed in men homozygous for the T allele, an increase in the saturated FA 16:0 together with a decrease in polyunsaturated FAs (18:3 and 20:3). This pattern is known to be associated with CVD risk. Interestingly, this FA pattern appears to be sex specific because it is restricted to the male population.
Because several studies have cast light on the possible regulation of the MTTP gene expression by insulin (29, 30), we have searched for a possible link between fasting plasma insulin concentrations and the MTTP –493 polymorphism. Although no significant modification of this marker could be found according to genotype in the whole population, a significant genotype x sex interaction was observed.
The effect of the 3-mo diet resulted in a clear improvement of most biological markers (14). We must note that no differences in the dietary intakes of men and women were observed at baseline and at the end of the diet period. However, the response to diet differed according to the 2 loci. Indeed, the response did not seem to be greatly modulated by the Ala/Thr FABP2 polymorphism, except for the decrease in apo B in the Thr/Thr population and the different pattern of response in Thr/Thr men and women for 18:1. This lack of reactivity is not surprising because, to date, few studies reported the influence of the FABP2 Ala54Thr polymorphism on the efficiency of a diet in terms of modulation of the magnitude of the response. One study reported on a greatest high-fiber diet-induced response in plasma total and LDL cholesterol among dyslipidemic subjects homozygous for the Thr-encoding allele (31). A second study was performed in normolipidemic subjects who were submitted to a change from saturated fat to monounsaturated FAs. That study showed that carriers of the Thr-encoding allele presented an enhanced decrease in insulin sensitivity compared with Ala/Ala homozygous subjects. Although in that latter study and in ours, the type of diets was comparable, we did not detect any diet-induced difference in insulin sensitivity: all subjects had decreased fasting plasma insulin concentrations regardless of genotypes.
Finally, our study showed a clear interaction between the MTTP –493G/T variation and the magnitude in the response to the diet. Indeed, although biological markers for the risk of CVD clearly decreased after the 3-mo intervention, this improvement is particularly marked in men homozygous for the T allele than in the other subjects. The TT subjects, as a whole, showed a significantly higher response in reducing fasting cholesterol, apo B-48, TRL phospholipids, 16:0, and 18:1 and in increasing 18:2 values, but only TT men showed a major improvement of the Framingham score. This sex-related sensitivity to diet can be linked to the recent finding that, in men with familial hypercholesterolemia but not in women, this polymorphism modulated after-treatment plasma triacylglycerol values (32).
In conclusion, important new findings in this study show that FABP2 Ala54Thr and MTTP –493G/T polymorphisms are differently involved in the contribution to cardiovascular risk in men and women. These 2 polymorphisms interact with sex 1) at baseline on fasting biological markers showing an increased risk of CVD for FABP2 Thr/Thr and MTTP TT men and 2) after the 3-mo diet leading to a better response in MTTP TT men.
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ACKNOWLEDGMENTS
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We thank Chantal Bideau, Danielle Iniesta, and Nicole Peyrol for their technical help in SNP determination.
The author's responsibilities were as follows—MG: was involved in the interpretation of the data and wrote the manuscript; SD and MD: performed statistical analysis of data; HP and RP: were involved in blood analyses, CD: was involved in the collection of data; DL: coordinated the study, RP: designed the genetic study and contributed to the writing of the manuscript. None of the authors had a personal or financial conflict of interest.
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Received for publication May 3, 2007.
Accepted for publication July 31, 2007.
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ABSTRACT
INTRODUCTION
