• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of springeropenLink to Publisher's site
Metabolomics
Metabolomics. Apr 2013; 9(2): 506–514.
Published online Oct 6, 2012. doi:  10.1007/s11306-012-0469-6
PMCID: PMC3608890

Targeted metabolomics profiles are strongly correlated with nutritional patterns in women

Abstract

Nutrition plays an important role in human metabolism and health. Metabolomics is a promising tool for clinical, genetic and nutritional studies. A key question is to what extent metabolomic profiles reflect nutritional patterns in an epidemiological setting. We assessed the relationship between metabolomic profiles and nutritional intake in women from a large cross-sectional community study. Food frequency questionnaires (FFQs) were applied to 1,003 women from the TwinsUK cohort with targeted metabolomic analyses of serum samples using the Biocrates Absolute-IDQ™ Kit p150 (163 metabolites). We analyzed seven nutritional parameters: coffee intake, garlic intake and nutritional scores derived from the FFQs summarizing fruit and vegetable intake, alcohol intake, meat intake, hypo-caloric dieting and a “traditional English” diet. We studied the correlation between metabolite levels and dietary intake patterns in the larger population and identified for each trait between 14 and 20 independent monozygotic twins pairs discordant for nutritional intake and replicated results in this set. Results from both analyses were then meta-analyzed. For the metabolites associated with nutritional patterns, we calculated heritability using structural equation modelling. 42 metabolite nutrient intake associations were statistically significant in the discovery samples (Bonferroni P < 4 × 10−5) and 11 metabolite nutrient intake associations remained significant after validation. We found the strongest associations for fruit and vegetables intake and a glycerophospholipid (Phosphatidylcholine diacyl C38:6, P = 1.39 × 10−9) and a sphingolipid (Sphingomyeline C26:1, P = 6.95 × 10−13). We also found significant associations for coffee (confirming a previous association with C10 reported in an independent study), garlic intake and hypo-caloric dieting. Using the twin study design we find that two thirds the metabolites associated with nutritional patterns have a significant genetic contribution, and the remaining third are solely environmentally determined. Our data confirm the value of metabolomic studies for nutritional epidemiologic research.

Electronic supplementary material

The online version of this article (doi:10.1007/s11306-012-0469-6) contains supplementary material, which is available to authorized users.

Keywords: Metabolomics, Twins, Dietary pattern, Nutrition habits, Food questionnaires

Introduction

Nutrition plays an important role in human metabolism and health. Metabolomics is considered a promising tool for nutritional studies (Oresic 2009). It aims to profile all low-molecular weight metabolites that are present in biological samples to enhance the understanding of the effect of a particular stimulus on metabolic pathways (Brennan 2008).

Combining the data obtained with multivariate data analysis tools allows the exploration of changes induced by a biological treatment or changes resulting from a particular phenotype. The interest in using metabolomics for nutritional research has increased recently given the intimate relationship between nutrients and metabolism (Brennan 2008). A key question that needs to be answered is to what extent do metabolomic profiles reflect nutritional patterns.

Some interventional studies have examined the role of specific foods or nutrients on metabolite patterns. For example, Llorach et al. (2010) assessed the role of a single dose of almond skin extract on the urine metabolome of 24 volunteers (12 who ingested a dietary supplement and 12 who ingested a placebo) over a 24 h period. The study identified 34 metabolites associated with the single dose of almond extract. Similar study designs have been applied to investigate the role of meat intake (Cross et al. 2011; Stella et al. 2006) and the role of three distinct dietary patterns (O’Sullivan et al. 2011) on a limited number of urinary biomarkers. Some observational studies have also been conducted. Altaimer et al. ran two observational studies in 284 male individuals to investigate the role of coffee consumption and different nutrients on serum metabolites. Coffee consumption was found to significantly correlate with metabolomic profilings (Altmaier et al. 2009) and dietary pattern highly associated with serum metabolite concentrations were identified (Altmaier et al. 2011) thus showing that metabolites are reliable candidates for risk assessment in prospective epidemiologic studies with blood sample collection at one time point and that it is highly relevant to explore the link between nutrient intake and metabolite patterns in an epidemiological (non interventional) setting.

The AbsoluteIDZ kit developed by Biocrates Life Science AG (Innsbruk, Austria) allows more than 160 targeted metabolites to be quantified in over four compound classes. The kit measures the targeted metabolites in an easy, reliable and robust way. Also, the 4 months reproducibility is good and a single measurement appears to be sufficient for risk assessment in epidemiologic studies with healthy subjects Floegel et al. (2011). In a previous study on 2,362 female twins, five distinct dietary patterns that best represent the sources of independent variation in dietary intake in the twins, were identified using food frequency questionnaires (FFQs): fruit and vegetables, high alcohol consumption, traditional English diet, dieting and low meat (Teucher et al. 2007). FFQ are particularly strong at detecting patterns consistently, and principal component analysis (PCA) derived pattern cores are widely used to assess association with health outcome, for example cardiovascular disease, stroke and the risk of cancer (Stricker et al. 2012; Schulze et al. 2001; Adebamowo et al. 2005; Ouderaa et al. 2006).

In the present study we assessed the role of dietary intake patterns on metabolomic parameters, also including foods (e.g. garlic) that are commonly perceived as related to an individual’s health in the context of complex chronic diseases such as metabolic syndrome or cardiovascular disease. Using a targeted metabolomics approach we analysed the correlation between metabolite serum levels using the Biocrates Absolute-IDQ™ Kit p150 and the above five dietary patterns in 892–965 individuals. These patterns essentially cover all relevant dietary intake information available in the FFQs and are broadly comparable to those reported in a number of large-scale population-based studies of nutrition (Stricker et al. 2012; Schulze et al. 2001; Adebamowo et al. 2005; Ouderaa et al. 2006). We also tested for coffee intake to be able to compare our data to previously published studies (Altmaier et al. 2009) and for garlic intake since, it has been highlighted as a beneficial dietary constituent (Baños et al. 2008). A recent study (Suhre et al. 2011) has shown the strong statistical power available even with relatively modest sample sizes to identify genes underlying metabolite circulating levels. However, not all metabolites are necessarily influenced by an individual’s genetic make-up. Having identified metabolites associated with dietary intake patterns or dietary components, we validated the results using identical twins discordant for that particular nutritional intake or dietary component. Moreover, we evaluated the heritability of these metabolites. The rationale of this study therefore is to provide investigators with some key information necessary to pursue the study of the molecular mechanisms that underlie the relationship between dietary patterns and health outcomes, including information on the genetic contribution to the metabolites that relate to dietary intake patterns.

Subjects and methods

Study population

Study subjects were twins enrolled in the TwinsUK registry, a national register of adult twins. Twins were recruited as volunteers by successive media campaigns without selecting for particular diseases or traits (Moayyeri et al. 2012). In this study we analysed data from 1,003 female twins who completed the FFQs and had metabolomic data available. The study was approved by St. Thomas’ Hospital Research Ethics Committee, and all twins provided informed written consent.

Dietary and other data

Twins were sent, by post, the 131-item FFQ which was developed for the EPIC (European Prospective Investigation into Cancer and Nutrition) Norfolk study (Bingham et al. 2001). Macro and micro nutrient intakes were calculated from an established nutrient database (Holland et al. 1991). For each food group, the frequency of intake (serving/wk) was adjusted for the total energy intake using the residual method. The energy-adjusted intakes were standardised and used in the PCA as previously described (Teucher et al. 2007). Dietary patterns were captured by five principal components of food consumption which accounted for 22 % of the total variance: fruit and vegetable, high alcohol, traditional English diet, hypo-caloric dieting and low meat. The five dietary patterns are PCA-generated scores. As such, they are independent variables standardized to have a mean of zero and a SD of one in the whole TwinsUK study population. Each dietary pattern should be considered as the representative of a particular food pattern intake. For instance, a positive fruit and vegetable score can be understood as an average high consumption of fruit, allium and cruciferous vegetable together with a low consumption of fried potatoes. Vice versa, a negative score may be taken to mean low consumption of fruit, allium and cruciferous vegetables together with high consumption of fried potatoes. Garlic and coffee are measured in terms of estimated weekly consumptions. Body mass index (BMI) was calculated as body weight in kilograms divided by the square of height in square meters.

Metabolomic measurements

The serum samples were collected after an overnight fast of all the study subjects. They were stored in −80º C freezers from which they were retrieved and sent to Germany for metabolite measurements. A targeted metabolomic assay was done in samples of fasting serum from participants in the British TwinsUK study (n = 1,003) using the Biocrates Absolute IDQ™-kit p150 (BIOCRATES Life Sciences AG, Innsbruck, Austria), as previously described (Illig et al. 2010; Mittelstrass et al. 2011; Römish-Margl et al. 2012). Briefly, the flow injection analysis (FIA) tandem mass spectrometry (MS/MS) method is used to quantify 163 known small molecule metabolites simultaneously by multiple reaction monitoring. Quantification of the metabolites is achieved by reference to appropriate internal standards. Reproducibility of the assay was performed in 23 serum samples. The mean of the coefficient of variation (CV) for the 163 metabolites was 0.07 and 90 % of the metabolites had a CV of <0.10.

Concentrations of all analysed metabolites are reported in μM.

Metabolites panel

The metabolomics dataset contains 41 acylcarnitines (Cx:y), hydroxylacylcarnitines [C(OH)x:y] and dicarboxylacylcarnitines (Cx:y-DC); 14 amino acids; one Sugar; 15 sphingomyelins (SMx:y) and sphingomyelin-derivatives [SM(OH)x:y]; and 92 glycerophospholipids (PC). Glycerophospholipids are differentiated with respect to the presence of ester (a) and ether (e) bonds in the glycerol moiety, where two letters (aa = diacyl, ae = acyl-alkyl) denote that two glycerol positions are bound to a fatty acid residue, while a single letter (a = acyl) indicates the presence of a single fatty acid residue. Lipid side chain composition is abbreviated as Cx:y, where x denotes the number of carbons in the side chain and y the number of double bonds. The full list of metabolites is presented in the supplementary material (Table S1).

Statistical analysis

Statistical analysis was carried out using Stata version 11. The metabolite serum concentrations were first log transformed as these were not normally distributed, but right-skewed. For each dietary variable, linear regression analysis (adjusting for age and BMI) was first undertaken by excluding MZ discordant twins (i.e. MZ twins with measures one SD apart).

Familial relatedness was accounted for using random intercept linear regression:

equation M1
1

where Yi and Xij are respectively the log-transformed metabolite (Y) and the dietary variable of twin j from pair i. ζj is the family-specific error component which represents the omitted family characteristics or unobserved heterogeneity. So the comparison between metabolite and dietary variables was performed between each twin pair.

We then ran for each significant metabolite-dietary variable (3 × 10−4 = 0.05/162) the same linear regression analysis on the discordant MZ twin pairs. Finally, we combined results using an inverse variance fixed effect meta-analysis. The fixed effect model provides a weighted average of the study estimates, the weights being the inverse of the variance of the study estimate. We used Bonferroni correction to account for multiple testing thus giving a significant threshold of 4 × 10−5 (0.05/7 nutrients × 163 metabolites).

For the metabolites associated with nutritional patterns, we first calculated the intra-class correlation coefficient (ICC) for MZ and DZ pairs. We then estimated heritability using structural equation modelling to separate the observed phenotypic variance into three latent sources of variation: additive genetic variance (A), shared/common environmental variance (C), and non-shared/unique environmental variance (E) (Neale and Cardon 1992). Additive genetic influences are indicated when MZ twins are more similar than DZ twins. The common environmental component estimates the contribution of family environment, which is assumed to be equal in both MZ and DZ twin pairs (Kyvic 2000), whereas the unique environmental component does not contribute to twin similarity, rather it estimates the effects that apply only to each individual including measurement error. Any greater similarity between MZ twins than DZ twins is attributed to greater sharing of genetic influences. Heritability is defined as the proportion of the phenotypic variation attributable to genetic factors, and is given by the equation, h2 = (A)/(A + C + E).

Results

1,003 females from TwinsUK with targeted metabolomic analyses of serum samples using the Biocrates Absolute-IDQ™ kit p150 (163 metabolites) were included in the analysis. Of these, 75 were MZ twin pairs, 228 were DZ twin pairs and 397 were singletons. The mean age of the study sample was 58.5 years (10.45 years SD) and the mean BMI was 25 kg/m2 (4.45 kg/m2 SD).

We first ran linear regression analysis, adjusting for age and BMI, in the larger population excluding MZ discordant twins.

We studied the correlation between metabolite levels and seven dietary intake patterns: coffee intake, garlic intake and nutritional scores derived from the FFQs summarizing fruit and vegetable intake, alcohol intake, meat intake, hypo-caloric dieting and a “traditional English” diet. These five dietary intake patterns derived from PCA (Teucher et al. 2007) are broadly comparable to those reported in a number of large-scale population-based studies of nutrition, such as the Nurses’ Health cohort in the U.S. (Adebamowo et al. 2005), and the EPIC Postdam study (Schulze et al. 2001). A description of the seven dietary intake patterns and the mean and SD values in the discovery and replication sets is presented in Table 1. We correlated these traits with 163 metabolite levels. 42 metabolite nutrient intake associations were statistically significant with Bonferroni P < 0.0003 (Supplementary Table 2), with many associations for both the fruit and vegetable and low meat scores. We then assessed whether these associations with dietary patterns were robust. In order to do so these 42 metabolite nutrient intake associations were tested in the identical twins discordant for the phenotype (i.e. MZ twins with the dietary measure or dietary pattern one SD apart or more). For each dietary variable, we identified between 14 and 20 independent monozygotic pairs discordant for the dietary variable. The regression (beta) coefficients were in the same direction in both analyses (discordant identical twins and the rest of the population) for 11 metabolites. We then combined results using inverse-variance fixed effects meta-analyses. Using a Bonferroni cut-off of 4 × 10−5 (0.05/7 nutrients × 163 metabolites), these are shown in Table 2. We find two significant associations with garlic intake, one with coffee intake, six with the dietary pattern for fruit and vegetable, and two with the “dieting” dietary pattern. The remaining 31 associations become not significant after this analysis and we find no validated metabolite associations with three of the five dietary intake patterns derived from FFQs (Table 2). The metabolites associated with nutrient intake and dietary patterns all fall within three broad categories: acylcarnitines, glycerophospholipids and sphingolipids. It is of interest therefore to understand what these metabolites represent and whether they are genetically determined or only environmentally determined. A brief description of pathways to which these metabolites belong are shown in Table 3. In addition, for each of these 11 metabolites, we also calculated the genetic contribution/heritability. The two metabolites negatively correlated with garlic intake are acylcarnitines C8:1 (Octenoylcarnitine, h2 = 44 %) and C5–DC(C6–OH)(Glutarylcarnitine, h2 = 0 %)—but only one of them shows evidence of a genetic component. Coffee intake was also negatively associated with a metabolite from the acylcarnitines pathway—C10:1(Decenoylcarnitine, h2 = 53 %). Finally, we could not compute the ACE model for PC aa C38:6 and PC ae C38:6 as, in both cases, the ICC for DZ was higher than the ICC for MZ, thus violating one of the ACE model assumption and indicating that circulating levels of these metabolites are not genetically determined.

Table 1
Food intake and dietary patterns scores in discovery and replication set
Table 2
Validated metabolite associations with dietary patterns
Table 3
Heritability of metabolites associated with dietary patterns

With regards to the PCA traits derived from the FFQs, we found the strongest associations with the fruit and vegetables score. Five of the six metabolites significantly and positively correlated with this variable were glycerophospholipids L PC aa C36:6 (Phosphatidylcholine diacyl C36:6, h2 = 54 %); PC aa C38:6 (Phosphatidylcholine diacyl C38:6, h2 = 0 %); PC aa C40:6 (Phosphatidylcholine diacyl C40:6, h2 = 57 %); PC ae C38:6 (Phosphatidylcholine acyl-alkyl C38:6, h2 = 0 %); and PC ae C40:6 (Phosphatidylcholine acyl-alkyl C40:6, h2 = 57 %). The sixth was a sphingolipid (SM C26:1: Sphingomyeline C26:1, h2 = 35 %). Finally, significant positive associations with an acylcarnitine—C9 (Nonacylcarnitine, h2 = 62 %) and a glycerophospholipid—PC ae C38:3 (Phosphatidylcholine acyl-alkyl C38:3, h2 = 38 %) were found for the hypo-caloric dieting score (Table 3).

Discussion

In this study we have investigated in a large cross-sectional population of women the role of dietary intake patterns on in metabolomic parameters. Our data support that garlic intake, coffee intake and dietary intake patterns from FFQs representing fruit and vegetables and low calorie intake are correlated with metabolite profiles. All of the associations found fall within three main pathways: acylcarnitines, glycerophospholipids and sphingolipids. However, no association between metabolite levels and meat intake, high alcohol consumption, or the “traditional English” diet were found.

The strongest association identified by our study is between a sphingolipid (Sphingomyeline C26:1 or SM C26:1) and fruit and vegetable intake. Diets rich in fruits and vegetables have been associated with a reduced risk of chronic disease, including cardiovascular disease (Esfahani et al. 2011). Current research indicates that fruit and vegetable concentrates significantly increase serum levels of antioxidant provitamins and vitamins (β-carotene, vitamins C and E) as well as folate, but reduce homocysteine and markers of oxidative stress (Esfahani et al. 2011). Interestingly, sphingolipid depletion has been shown to inhibit vitamin uptake (Stevens and Tang 1997). The other metabolites positively correlated with fruit and vegetable intake are phosphatidylcholines which are highly desaturated fatty acids and among most common constituents of biological membranes (Zhang et al. 2009). They are an essential biological component and widely used as a nutritional supplement for protecting cells from oxidation, increase fat burning and preventing cardiovascular disease (Ristic Medic et al. 2006). Lecithin contains fatty acids identified as the peroxisome proliferator-activated receptor (PPAR) agonists. Experimental data has shown that lecithin promotes adipocyte differentiation and differentiation-specific gene expression and increased triglycerides and free fatty acid levels in the adipocytes (Zhang et al. 2009). Phosphatidylcholine has also been shown to have an anti-inflammatory action (Eros et al. 2009). Therefore, there is a likely physiological link between the metabolites identified by us and the beneficial effects of fruit and vegetable intake which may also be reflected in cardiovascular and other health-related phenotypes.

Our study also confirms the association between coffee consumption with C10:1 which was previously reported by Atlmaier et al. (2009) in a study of German men only and this underlines the reliability and reproducibility of metabolomic data in nutritional research.

A glycerophospholipid is also associated with low-calorie dieting. The positive association between phosphatidylcholine acyl-alkyl C38:3 and “dieting” pattern suggests that increased glycerophospholipid levels may be one possible benefit of a low-calorie diet.

Both garlic and coffee intake were found to be negatively correlated with levels of three acylcarnitines whereas “dieting” was positively correlated with nonacylcarnitine (C9). Acylcarnitines are long-chain fatty acids. Comprehensive plasma acylcarnitine profiles in patients with type 2 diabetes have revealed elevated circulating markers of incomplete long-chain fatty acid catabolism and of acetylcarnitine, together with lower levels of propionylcarnitine. These metabolites appear to be sensitive indicators of biochemical pathways that are responsive to, or underlie, the severity of diabetes and long-term blood sugar control. (Adams et al. 2009). The increased levels of nonacylcarnitine (C9) with low-calorie dieting might thus be reflecting less efficient long fatty acid metabolism. On the other hand, the lower circulating levels of octenoylcarnitine (C8:1) and glutarylcarinitine (C5–DC/C6–0H) with garlic intake and of decenoylcarnitine (C10:1) with associated with coffee intake suggest a possible link between these foods and more efficient mitochondrial fat metabolism. Both garlic (Baños et al. 2008; Padiya et al. 2011) and coffee (Matsuura et al. 2012) have been implicated in decreased risk of metabolic syndrome and improved insulin sensitivity. It is therefore reasonable to hypothesize that the effect of garlic and coffee on acylcarnitines and mitochondrial fat metabolism may be part of the molecular link underlying such clinical observations. The results presented here illustrate the use of metabolomic profiling to gain insights on the role of nutrients on health. But in order to gain a reliable risk estimate with a single blood measurement the within-subject variance over time should be small compared with the between-subject variance. Otherwise the high sensitivity of the metabolome to internal or external stimuli (such as age, hormonal status, diet and lifestyle) may potentially limit their use for risk assessment in large-scale epidemiologic studies that are based on single blood measurement The reliability of the serum metabolite concentrations in the panel used in our study has been previously reported. Floegel et al. (2011) investigated the between- and within-person variation in the metabolite measurements of the 163 serum metabolites in Biocrates panel was analysed the in 100 subjects who had provided two fasting blood samples taken 4 months apart. The metabolite reliability expressed by the ICC (i.e. the ratio of between-person variance and total variance). All the metabolites that we identify as related to dietary intake patterns in our study showed fair to good reliability as defined by Floegel et al. (2011) (values ranging from 0.41 to 0.69) and hence should be reliable for risk assessment in prospective epidemiological studies and useful to researchers investigating the most reliable biomarkers to use in nutritional and healthy lifestyle studies.

Another interesting observation to come out of our study is that two thirds of the metabolites related to nutritional patterns have a significant genetic contribution, but one third have only an environmental contribution. For example, in the case of garlic one of the metabolites has an significant additive genetic component (e.g. octenoylcarnitine C8:1) yet the other metabolite associated appears to be due to environmental influences (e.g. glutarylcarinitine C5–DC/C6–OH).

The present study has several strengths. Firstly, we employed a two-stage analysis design—discovery and independent replication with stringent P values—thus minimizing the risk of false positive findings. Secondly, we used identical twins discordant for nutritional intake for the validation analysis. Metabolite levels may be influenced by many factors including genetics (Suhre et al. 2011). Since identical twins share 100 % of their genetic makeup and are matched perfectly for age, gender, social class, etc., we were able to validate the role of nutritional intake on metabolites; isolating the non-genetic contribution. Thus, these data help us understand the complex interplay between genetic and environmental influences that determine nutritional patterns.

The results presented here are consistent with data from the study carried out in men (Altmaier et al. 2011) in that we identify correlations between metabolomic measurements and the intake of certain nutrients and, in particular, nutritional patterns as summarized by principal component analyses. Given the strong results for individual metabolites found by the previous study, we have focused only on individual metabolites and not on metabolite ratios and we confirm that indeed there are very correlations with dietary patterns.

There are some limitations in the current study. Firstly, both our validation and replication samples consist of women only. Some of these metabolites may be influences by sex-hormone levels and results could be different in men. Secondly, we have used FFQs rather than other more reliable methods for assessing nutrient intake.

Over the past two decades, FFQs have become a well-accepted method for quantitative assessment of usual nutrient intake (Sempos et al. 1992) and their for assessing dietary composition has been documented objectively in prospective studies (Willett 1998). FFQ derived dietary intake patterns (using PCA) have been shown repeatedly in the literature to correlate with various health-outcomes such as cardiovascular risk, stroke, diabetes and cancer among others (Stricker et al. 2012; Schulze et al. 2001; Adebamowo et al. 2005; Ouderaa et al. 2006).

Although FFQs may not be perfect, they have been extensively validated for epidemiological studies needing large sample sizes. Notwithstanding, we have been able using FFQs and a targeted metabolomic approach to identify metabolites that are correlated with nutritional patterns and within these, to identify those that have a genetic component from those that are purely environmentally determined.

In conclusion, our results provide further support to the use of metabolomic analyses to identify the molecular mechanisms responsible for the links between nutrition and health. Whereas directly associating lifestyle habits with clinical endpoints provides only limited information about the underlying disease-causing mechanisms, the use of a metabolomic approach helps identify the molecular pathways underlying dietary patterns and these molecular mechanisms in turn can be more easily linked experimentally in smaller studies to relevant clinical outcomes (Jenab et al. 2009; Scalbert et al. 2009; Wishart 2008). Our study confirms that this technology has great potential in the area of nutritional assessment as metabolites reflects certain nutritional patterns and can help separate those metabolites related to nutrient that reflect inherited patterns of metabolism from those that are entirely due to environmental/lifestyle choices. In this context a metabolomic approach may provide useful biomarkers of disease prevention, early disease, or nutritional status, and eventually to identify potential molecular mechanisms in chronic disease processes that are modulated by dietary constituents and/or dietary patterns.

Electronic supplementary material

Acknowledgments

We thank Julia Scarpa, Tamara Halex and Arsin Sabunchi for metabolomic measurements performed at the Helmholtz Zentrum München, Genome Analysis Center, Metabolomics Core Facility. The study was funded by the Wellcome Trust by the EU FP7 small medium focused project 277849 EurHEALTHAgeing and by King’s Business Innovation Development Fund. The study also receives support from the Dept of Health via the National Institute for Health Research (NIHR) comprehensive Biomedical Research Centre award to Guy’s & St Thomas’ NHS Foundation Trust in partnership with King’s College London. W.R.-M. is funded by BMBF grant 03IS2061B (project Gani_Med). The KORA research platform study was initiated and financed by the Helmholtz Zentrum Muenchen—National Research Center for Environmental Health, which is funded by the German Federal Ministry of Education, Science, Research and Technology and by the State of Bavaria. KS is supported by ‘Biomedical Research Program’ funds at Weill Cornell Medical College in Qatar, a program funded by Qatar Foundation.

Open Access

This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Glossary

BMI
Body mass index
CV
Coefficient of variation
DZ
Dizygotic
EPIC
European prospective investigation into cancer and nutrition
FFQ
Food frequency questionnaire
MZ
Monozygotic
PCA
Principal components analysis
SD
Standard deviation

References

  • Adams SH, Hoppel CL, Lok KH, Zhao L, Wong SW, Minkler PE, Hwang DH, Newman JW, Garvey WT. Plasma acylcarnitine profiles suggest incomplete long-chain fatty acid beta-oxidation and altered tricarboxylic acid cycle activity in type 2 diabetic African-American women. Journal of Nutrition. 2009;139(6):1073–1081. doi: 10.3945/jn.108.103754. [PMC free article] [PubMed] [Cross Ref]
  • Adebamowo CA, Hu FB, Cho E, Spiegelman D, Holmes MD, Willett WC. Dietary patterns and the risk of breast cancer. Annals of Epidemiology. 2005;15(10):789–795. doi: 10.1016/j.annepidem.2005.01.008. [PubMed] [Cross Ref]
  • Altmaier E, Kastenmuller G, Romisch-Margl W, Thorand B, Weinberger KM, Adamski J, Illig T, Doring A, Suhre K. Variation in the human lipidome associated with coffee consumption as revealed by quantitative targeted metabolomics. Molecular Nutrition & Food Research. 2009;53:1357–1365. doi: 10.1002/mnfr.200900116. [PubMed] [Cross Ref]
  • Altmaier E, Kastenmuller G, Romisch-Margl W, Thorand B, Weinberger KM, Illig T, Adamski J, Doring A, Suhre K. Questionnaire-based self-reported nutrition habits associate with serum metabolism as revealed by quantitative targeted metabolomics. European Journal of Epidemiology. 2011;26:145–156. doi: 10.1007/s10654-010-9524-7. [PubMed] [Cross Ref]
  • Baños G, Pérez-Torres I, el Hafidi M. Medicinal agents in the metabolic syndrome. Cardiovascular & Hematological Agents in Medicinal Chemistry. 2008;6(4):237–252. doi: 10.2174/187152508785909465. [PubMed] [Cross Ref]
  • Bingham SA, Welch AA, McTaggart A, Mulligan AA, Runswick SA, Luben R, Oakes S, Khaw KT, Wareham N, Day NE. Nutritional methods in the European Prospective Investigation of Cancer in Norfolk. Public Health Nutrition. 2001;4:847–858. doi: 10.1079/PHN2000102. [PubMed] [Cross Ref]
  • Brennan L. Session 2: Personalised nutrition. Metabolomic applications in nutritional research. The Proceedings of the Nutrition Society. 2008;67:404–408. doi: 10.1017/S0029665108008719. [PubMed] [Cross Ref]
  • Cross AJ, Major JM, Sinha R. Urinary biomarkers of meat consumption. Cancer Epidemiology, Biomarkers & Prevention: A Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. 2011;20:1107–1111. doi: 10.1158/1055-9965.EPI-11-0048. [PMC free article] [PubMed] [Cross Ref]
  • Eros G, Varga G, Varadi R, Czobel M, Kaszaki J, Ghyczy M, Boros M. Anti-inflammatory action of a phosphatidylcholine, phosphatidylethanolamine and N-acylphosphatidylethanolamine-enriched diet in carrageenan-induced pleurisy. European Surgical Research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes. 2009;42:40–48. doi: 10.1159/000167856. [PubMed] [Cross Ref]
  • Esfahani A, Wong JM, Truan J, Villa CR, Mirrahimi A, Srichaikul K, Kendall CW. Health effects of mixed fruit and vegetable concentrates: a systematic review of the clinical interventions. Journal of the American College of Nutrition. 2011;30:285–294. [PubMed]
  • Floegel A, Drogan D, Wang-Sattler R, Prehn C, Illig T, Adamski J, Joost HG, Boeing H, Pischon T. Reliability of serum metabolite concentrations over a 4-month period using a targeted metabolomic approach. PLoS One. 2011;6:e21103. doi: 10.1371/journal.pone.0021103. [PMC free article] [PubMed] [Cross Ref]
  • Holland B, Welch AA, Unwin ID, Buss DH, Paul AA, Southgate DAT. The composition of foods. 5. London: HMSO Ministry of Agriculture, Fisheries and Food and Royal Chemistry; 1991.
  • Illig T, Gieger C, Zhai G, Romisch-Margl W, Wang-Sattler R, Prehn C, Altmaier E, Kastenmuller G, Kato BS, Mewes HW, Meitinger T, de Angelis MH, Kronenberg F, Soranzo N, Wichmann HE, Spector TD, Adamski J, Suhre K. A genome-wide perspective of genetic variation in human metabolism. Nature Genetics. 2010;42:137–141. doi: 10.1038/ng.507. [PMC free article] [PubMed] [Cross Ref]
  • Jenab M, Slimani N, Bictash M, Ferrari P, Bingham SA. Biomarkers in nutritional epidemiology: Applications, needs and new horizons. Human Genetics. 2009;125:507–525. doi: 10.1007/s00439-009-0662-5. [PubMed] [Cross Ref]
  • Kyvic K. Generalisability and assumptions of twin studies. In: Spector TD, Sneider H, MacGregor AJ, editors. Advances in twin and sib-pair analysis. London: Greenwich Medical Media; 2000. pp. 67–77.
  • Llorach R, Garrido I, Monagas M, Urpi-Sarda M, Tulipani S, Bartolome B, Andres-Lacueva C. Metabolomics study of human urinary metabolome modifications after intake of almond (Prunus dulcis (Mill.) D.A. Webb) skin polyphenols. Journal of Proteome Research. 2010;9:5859–5867. doi: 10.1021/pr100639v. [PubMed] [Cross Ref]
  • Matsuura H, Mure K, Nishio N, Kitano N, Nagai N, Takeshita. T. Relationship between coffee consumption and prevalence of metabolic syndrome among Japanese civil servants. Journal of Epidemiology. 2012;22(2):160–166. doi: 10.2188/jea.JE20110068. [PMC free article] [PubMed] [Cross Ref]
  • Mittelstrass K, Ried JS, Yu Z, Krumsiek J, Gieger C, Prehn C, Roemisch-Margl W, Polonikov A, Peters A, Theis FJ, Meitinger T, Kronenberg F, Weidinger S, Wichmann HE, Suhre K, Wang-Sattler R, Adamski J, Illig T. Discovery of sexual dimorphisms in metabolic and genetic biomarkers. PLoS Genetics. 2011;7:e1002215. doi: 10.1371/journal.pgen.1002215. [PMC free article] [PubMed] [Cross Ref]
  • Moayyeri, A., Hammond, C. J., Valdes, A. M., & Spector, T. D. (2012) Cohort profile: TwinsUK and healthy ageing twin study. International Journal of Epidemiology. doi: 10.1093/ije/dyr207. [PMC free article] [PubMed]
  • Neale M, Cardon L. Methodology for genetic studies of twins and families. Dordrecht: Kluwer Academic Publishers; 1992.
  • Oresic M. Metabolomics, a novel tool for studies of nutrition, metabolism and lipid dysfunction. Nutrition, Metabolism, and Cardiovascular Diseases: NMCD. 2009;19:816–824. doi: 10.1016/j.numecd.2009.04.018. [PubMed] [Cross Ref]
  • O’Sullivan A, Gibney MJ, Brennan L. Dietary intake patterns are reflected in metabolomic profiles: potential role in dietary assessment studies. The American Journal of Clinical Nutrition. 2011;93:314–321. doi: 10.3945/ajcn.110.000950. [PubMed] [Cross Ref]
  • Ouderaa F, Bingham S, Cross AJ, Nicholson JK. Susceptibility of human metabolic phenotypes to dietary modulation. Journal of Proteome Research. 2006;5:2780–2788. doi: 10.1021/pr060265y. [PubMed] [Cross Ref]
  • Padiya R, Khatua TN, Bagul PK, Kuncha M, Banerjee SK. Garlic improves insulin sensitivity and associated metabolic syndromes in fructose fed rats. Nutrition & Metabolism. 2011;8:53. doi: 10.1186/1743-7075-8-53. [PMC free article] [PubMed] [Cross Ref]
  • Ristić Medić D, Ristić V, Arsić A, Postić M, Ristić G, Blazencić Mladenović V, Tepsić J. Effects of soybean D-LeciVita product on serum lipids and fatty acid composition in type 2 diabetic patients with hyperlipidemia. Nutrition, Metabolism, and Cardiovascular Diseases. 2006;16(6):395–404. doi: 10.1016/j.numecd.2005.06.008. [PubMed] [Cross Ref]
  • Römish-Margl W, Prehn C, Bogumil R, Röhring C, Suhre K, Adamski J. Procedure for tissue sample preparation and metabolite extraction for high-throughput targeted metabolomics. Metabolomics. 2012;8:133–142. doi: 10.1007/s11306-011-0293-4. [Cross Ref]
  • Scalbert A, Brennan L, Fiehn O, Hankemeier T, Kristal BS, van Ommen B, Pujos-Guillot E, Verheij E, Wishart D, Wopereis S. Mass-spectrometry-based metabolomics: Limitations and recommendations for future progress with particular focus on nutrition research. Metabolomics. 2009;5:435–458. doi: 10.1007/s11306-009-0168-0. [PMC free article] [PubMed] [Cross Ref]
  • Schulze MB, Hoffmann K, Kroke A, Boeing H. Dietary patterns and their association with food and nutrient intake in the European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam study. British Journal of Nutrition. 2001;85(3):363–373. doi: 10.1079/BJN2000254. [PubMed] [Cross Ref]
  • Sempos, C. T., Briefel, R. R., Johnson, C. & Woteki, C. E. (1992). Process and rationale for selecting dietary methods for NHANES III. Vital and health statistics. Ser. 4: Documents and committee reports, pp. 85–90. [PubMed]
  • Stella C, Beckwith-Hall B, Cloarec O, Holmes E, Lindon JC, Powell J, van der Ouderaa F, Bingham S, Cross AJ, Nicholson JK. Susceptibility of human metabolic phenotypes to dietary modulation. Journal of Proteome Research. 2006;5:2780–2788. doi: 10.1021/pr060265y. [PubMed] [Cross Ref]
  • Stevens VL, Tang J. Fumonisin B1-induced sphingolipid depletion inhibits vitamin uptake via the glycosylphosphatidylinositol-anchored folate receptor. The Journal of Biological Chemistry. 1997;272:18020–18025. doi: 10.1074/jbc.272.29.18020. [PubMed] [Cross Ref]
  • Stricker, M. D., Onland-Moret, N. C., Boer, J. M., Van Der Schouw, Y. T., Verschuren, W. M., May, A. M., Peeters, P. H., & Beulens, J. W. (2012). Dietary patterns derived from principal component- and k-means cluster analysis: Long-term association with coronary heart disease and stroke. Nutrition Metabolism and Cardiovascular Diseases. doi: 10.1016/j.numecd.2012.02.006. [PubMed]
  • Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wagele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmuller G, Kottgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Romisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C. Human metabolic individuality in biomedical and pharmaceutical research. Nature. 2011;477:54–60. doi: 10.1038/nature10354. [PMC free article] [PubMed] [Cross Ref]
  • Teucher B, Skinner J, Skidmore PM, Cassidy A, Fairweather-Tait SJ, Hooper L, Roe MA, Foxall R, Oyston SL, Cherkas LF, Perks UC, Spector TD, Macgregor AJ. Dietary patterns and heritability of food choice in a UK female twin cohort. Twin Research and Human Genetics: The Official Journal of the International Society for Twin Studies. 2007;10:734–748. doi: 10.1375/twin.10.5.734. [PubMed] [Cross Ref]
  • Willett WC. Invited commentary: Comparison of food frequency questionnaires. American journal of epidemiology. 1998;148:1157–1159. doi: 10.1093/oxfordjournals.aje.a009600. [PubMed] [Cross Ref]
  • Wishart D. Metabolomics: Applications to food science and nutrition research. Food Science and Technology. 2008;19:482–493. doi: 10.1016/j.tifs.2008.03.003. [Cross Ref]
  • Zhang Y, Huang C, Sheng X, Gong Z, Zang YQ. Lecithin promotes adipocyte differentiation and hepatic lipid accumulation. International Journal of Molecular Medicine. 2009;23:449–454. doi: 10.3892/ijmm_00000155. [PubMed] [Cross Ref]

Articles from Springer Open Choice are provided here courtesy of Springer
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

  • MedGen
    MedGen
    Related information in MedGen
  • PubMed
    PubMed
    PubMed citations for these articles

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...