Mol. Cells

A Metabolomic Approach to Understanding the Metabolic Link between Obesity and Diabetes

Seokjae Park, Krishna Chaitanya Sadanala, and Eun-Kyoung Kim

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Obesity and diabetes arise from an intricate interplay between both genetic and environmental factors. It is well recognized that obesity plays an important role in the development of insulin resistance and diabetes. Yet, the exact mechanism of the connection between obesity and diabetes is still not completely understood. Metabolomics is an analytical approach that aims to detect and quantify small metabolites. Recently, there has been an increased interest in the application of metabolomics to the identification of disease biomarkers, with a number of well-known biomarkers identified. Metabolomics is a potent approach to unravel the intricate relationships between metabolism, obesity and progression to diabetes and, at the same time, has potential as a clinical tool for risk evaluation and monitoring of disease. Moreover, metabolomics applications have revealed alterations in the levels of metabolites related to obesity-associated diabetes. This review focuses on the part that metabolomics has played in elucidating the roles of metabolites in the regulation of systemic metabolism relevant to obesity and diabetes. It also explains the possible metabolic relation and association between the two diseases. The metabolites with altered profiles in individual disorders and those that are specifically and similarly altered in both disorders are classified, categorized and summarized.

Keywords: biomarkers, diabetes, metabolites, metabolomics, obesity


The term “metabolites” denotes all endogenous small molecules that are involved (as substrates, intermediates or products) in common metabolic reactions in biochemical pathways essential for growth, development, reproduction and stress response mechanisms (Goodacre et al., 2004). Metabolomics is defined as a technology aimed at measuring/profiling changes in the levels of metabolites present inside a cell, tissue, or organism in response to a genetic variation or pathophysiological stimuli (Oliver et al., 1998; Scarfe et al., 1998). Another aim of metabolomics is to evaluate the relative differences between biological samples on the basis of their metabolite profiles. It can deliver an immediate snapshot of the whole physiology of an organism. Current technological developments have allowed high-throughput profiling of a large number of metabolites in biological samples, with increasing applications in disease research (Shah et al., 2012). Metabolomics comprises qualitative and quantitative analysis of intracellular and intercellular metabolites using two distinct analytical approaches: (1) non-targeted metabolite profiling, i.e. identification and characterization of a large number of metabolites and their precursors; and (2) targeted metabolite profiling, with an emphasis on quantitative variations in metabolites of interest (e.g., amino acids, carbohydrates, lipids and nucleotides) based on a prior understanding of their biological roles in metabolic pathways (Sadanala et al., 2012).

In this review, we discuss the major metabolite changes observed in obesity and diabetes. The focus is on the altered metabolite profiles in each disorder and inter-related disease conditions. We also present a short list of metabolites commonly associated with both disorders. The concept of our review is based on metabolite classes such as amino acids, lipids, carbohydrates and nucleotides, in previous studies that proposed a cross-sectional relationship between obesity and diabetes.


Role of metabolomics in investigation of biomarkers in the diseases

Metabolomics studies allow identification of metabolites involved in disease mechanisms by observing metabolite level variations in diseased individuals in comparison with healthy ones (Cheng et al., 2012; Goek et al., 2012; Newgard et al., 2009; Pietiläinen et al., 2007; Rhee et al., 2011; Shaham et al., 2008; Wang et al., 2011; Zhao et al., 2010). Furthermore, the metabolic phenotypes of human populations will greatly facilitate evaluation of the metabolic response of each patient to treatment, making possible personalized clinical treatment. Sample-specific metabolomes can be studied, such as serum metabolome or liver tissue metabolome. Urine and blood (serum and plasma) are the biofluids that are most often used for metabolomics studies because both contain a multitude of detectable metabolites and can be obtained without or with minimal invasion. A number of other fluids such as saliva, bile, gut aspirate, cerebrospinal fluid, seminal fluid, amniotic fluid and synovial fluid have also been analyzed (Bala et al., 2006; Bollard et al., 2005; Gowda et al., 2006). More recently, metabolic profiling of complete tissues and their lipid and aqueous metabolites has received more attention for biomarker detection (Griffin and Kauppinen, 2007). These studies have identified potential biomarkers or revealed pathophysiology of diseases such as obesity, diabetes, cardiovascular diseases and cancers (Beger, 2013; Du et al., 2013).

Metabolomics has been used for biomarker discovery for a number of clinical conditions (Madsen et al., 2010; Vinayavekhin et al., 2010). Biomarkers are regularly used in clinical practice to measure disease severity and also to provide essential prognostic information related to survival. Biomarkers have also been used as alternatives to clinical endpoints both in clinical practice and in research settings, predominantly in novel drug development. By identifying the definite early biomarkers of disease, metabolomics provides better understanding of disease progression and metabolic pathways (Zhang et al., 2013).


Obesity is a medical condition, in which a large amount of fat accumulates in the body to the point that it may decrease the life span and result in such health problems as diabetes, cardiovascular disease, as well as bone and joint diseases (Haslam and James, 2005; Pataky et al., 2014). Obesity is responsible for about 5% of worldwide deaths, and the total economic losses from obesity are approximately $2 trillion, or 2.8% of global GDP, equivalent to the worldwide losses from smoking or armed violence, war and terrorism. Recently, several metabolites associated with obesity have been identified by metabolomics and confirmed to be disturbed extensively in both animal models and humans (Abu Bakar et al., 2015). Obesity affects the entire body and evidently involves metabolic variations, but the definite changes in metabolism during obesity and dysfunction of specific organs or cellular organelles related to obesity are not yet well understood (Kussmann et al., 2006). As metabolomics can swiftly detect subtle alterations in the metabolic network, it is exclusively poised to improve our knowledge of obesity and diseases related to obesity.


Diabetes mellitus (DM), usually called diabetes, is a collection of metabolic diseases characterized by elevated blood sugar levels over an extended period (Nyenwe et al., 2011). If untreated, diabetes can trigger many complications (Stolar, 1988). It is a chronic disease characterized by chronic hyperglycemia because of the absence or shortage of insulin, which may be due either to a gradual failure of pancreatic β-cell function and subsequently a lack of insulin production (type 1 diabetes, T1DM) or to the development of insulin resistance and consequently the loss of β-cell function (type 2 diabetes, T2DM). Using either animal models or oral glucose tolerance tests, metabolic studies have uncovered alterations in metabolites associated with pathways involved in the action of insulin, including lipolysis, ketogenesis, proteolysis and glucose metabolism (Friedrich, 2012). These results have revealed a switch from β-oxidation to glycolysis and fat storage in response to glucose intake. Moreover, metabolomics studies performed on diabetic patients and healthy subjects have revealed many significantly altered metabolic pathways and metabolic variations (Suhre et al., 2010).


Amino acid metabolism

Amino acids (AAs) are important biological compounds, which possess carboxylic and amine moieties as functional groups and serve as building blocks for proteins. They play key metabolic and physiological roles in all living organisms. It has been known that obesity is accompanied by an increase in circulating levels of several amino acids, including BCAAs (Chevalier et al., 2005; Felig et al., 1974; Krebs et al., 2007; Moore and Stein, 1954; Tremblay et al., 2007; Um et al., 2006). High fasting concentrations of BCAAs were found to be associated with obesity and low serum insulin levels.

The association between obesity and amino acid metabolism shows important physiological and clinical inferences. The concentrations of selected essential amino acids and their derivatives in blood, in specific BCAAs, tyrosine, phenylalanine and sulfur amino acids, are evidently changed with obesity (Adams, 2011). A distinctive metabolic picture related to BCAA catabolism was also found in obese subjects (Newgard et al., 2009). Reduced expression of mitochondrial branched chain amino transferase in adipose tissue is considered to be a reason for the increased levels of BCAAs in obesity (She et al., 2007). Decreased levels of glutamine and glycine are found in blood of obese individuals in comparison with lean controls (Xie et al., 2012), which was also observed in another previous study (Backman et al., 1975). Changes in the levels of a number of compounds involved in amino acid metabolism have been found in obese condition (Adams, 2011; Newgard et al., 2009). The levels of cysteine, glutamate, phenylalanine, threonine, tryptophan, tyrosine, pantothenic acid, α-hydroxyisovaleric acid, 3-methyl-2-oxobutyric acid, choline, glyceric acid, 2-ketoisocaproic acid, pipecolic acid, kynurenine, serotonin and isovaleryl carnitine are increased (Fiehn et al., 2010; Gogna et al., 2015; Moore et al., 2014; Zeng et al., 2010), whereas those of methionine, citrulline, 3-methylglutarylcarnitine and acylcarnitine are decreased (Kim et al., 2011; Mihalik et al., 2012; Oberbach et al., 2011; Wahl et al., 2012). Other metabolites such as, alanine, arginine, asparagine, glutamine, glycine, histidine, isoleucine, leucine, lysine, proline, valine, carnitines and hydroxycarnitines were increased in some studies (Fiehn et al., 2010; Kim et al., 2010; 2011; Moore et al., 2014; Oberbach et al., 2011; Wahl et al., 2012) and decreased in others (Mihalik et al., 2012).

Increased levels of amino acids can improve insulin secretion from primary islet cells and β-cell lines by diverse mechanisms (Brennan et al., 2002; Charles and Henquin, 1983; Dixon et al., 2003; Sener and Malaisse, 1980; Smith et al., 1997). The relationship between amino acids and insulin resistance has been known for decades (Felig et al., 1969; 1974; Gougeon et al., 2008), but with the arrival of comprehensive metabolomic profiling a more detailed picture emerges of how amino acids contribute to the progression of diabetes. The levels of cysteine, pantothenic acid, creatine, acetyl carnitine and butyryl carnitine are increased in diabetes patients (Bentley-Lewis et al., 2014; Fiehn et al., 2010; Guan et al., 2013; Suhre et al., 2010), whereas those of arginine, asparagine, glycine, methionine, citrulline, betaine, sarcosine, aspartic acid, benzoic acid, 4-hydroxyproline and 5-hydroxykynurenine are decreased (Bentley-Lewis et al., 2014; Diao et al., 2014; Fiehn et al., 2010; Floegel et al., 2013; Liu et al., 2013; Mihalik et al., 2012; Wang-Sattler et al., 2012). Other metabolites such as, alanine, glutamate, glutamine, histidine, isoleucine, leucine, lysine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, creatinine, 2-ketocaproic acid, pyroglutamic acid, choline, ornithine, carnitines and hydroxycarnitines were increased in some studies (Bentley-Lewis et al., 2014; Diao et al., 2014; Fiehn et al., 2010; Floegel et al., 2013; Liu et al., 2013; Mihalik et al., 2012; Palmer et al., 2015; Salek et al., 2007; Wang et al., 2011; Wang-Sattler et al., 2012; Zeng et al., 2010) and decreased in others (Bentley-Lewis et al., 2014; Diao et al., 2014; Fiehn et al., 2010; Liu et al., 2013; Mihalik et al., 2012; Palmer et al., 2015; Salek et al., 2007; Zeng et al., 2010). Glutamate and BCAAs are also found increased in T1DM (Oresic et al., 2008).

Lipid metabolism

Lipids are one of the main source of energy for metabolism. Blood lipids, obtained from food intake or from adipose tissue and liver, are mainly fatty acid derivatives and cholesterol. Obesity, which is characterized by fat deposits in tissues, is usually associated with elevated levels of plasma free fatty acids (FFAs) (Golay et al., 1986). Carnitine is an important metabolite linked to obesity, due to its involvement in fatty acid metabolism. It is well recognized that provision of FFAs can stimulate fatty acid oxidation (Randle, 1998). However, fatty acids can yield energy only via β-oxidation after esterification and transfer into the mitochondrion, which requires carnitine (Cha, 2008). Thus, higher levels of plasma FFAs in obesity may require more carnitine for effective β-oxidation. Consequently, the amount of carnitine in cells is the main factor regulating β-oxidation. Choline is a crucial dietary nutrient that is essential for the maintenance of cellular structure, methyl (one-carbon) metabolism, transport and metabolism of cholesterol (Blusztajn, 1998; Zeisel, 2000). Over 95% of the total choline present in most animal tissues is used for PC synthesis by the Kennedy pathway (Gibellini and Smith, 2010). The introduction of novel analytical and information technologies for management of large volumes of data has made it practical to characterize complex mixtures of lipids in body fluids and tissues (Lagarde et al., 2003; Wenk, 2005). Obesity and associated dyslipidemias may be caused by several factors (Despres et al., 1992). In obesity, the levels of non-essential fatty acids (oleic acid, palmitic acid, palmitoleic acid, stearic acid, stearoyl carnitine, 2-hydroxybutanoic acid and 3-hydroxybutanoic acid) are increased (Fiehn et al., 2010; Gogna et al., 2015; Kim et al., 2011; Moore et al., 2014), whereas those of ethanolamine and LysoPEs are decreased (Fiehn et al., 2010; Kim et al., 2011). LysoPCs, PCs, cholesteryl esters, ceramides, SMs and total fatty acids were increased in some studies (Kim et al., 2010; 2011; Moore et al., 2014; Pietiläinen et al., 2007; Samad et al., 2006; Wahl et al., 2012) and decreased in some others (Kim et al., 2010; 2011; Moore et al., 2014; Pietiläinen et al., 2007; Samad et al., 2006; Wahl et al., 2012)

Lipid abnormalities are common in diabetic patients, in particular in those with T2DM. Both the lipid profile and body fat mass have been reported to be the main predictors of metabolic disturbances and critical medical conditions, such as dyslipidemia, hypertension, diabetes and cardiovascular diseases (Du et al., 2013). Dyslipidemias make diabetic patients susceptible to heart disease and other problems related to atherosclerosis. A number of factors are likely to be responsible for diabetic dyslipidemia: the effects of insulin on apoprotein production in the liver, regulation of lipoprotein lipase, function of cholesteryl ester transfer protein and peripheral actions of insulin on adipose tissue and muscle (Mooradian et al., 2004; 2008). In diabetes, the levels of 1-monopalmitin, 1-monostearin, 1,2-distearoyl phosphatidylserine, ceramide, diacylglycerol, diacylphosphatidylcholines, fatty-acyl CoA, linoleic acid, myristic acid, oleic acid, palmitic acid, palmitoleic acid, stearic acid, tridecane, undecane, triacylglycerol, 2-hydroxybutanoic acid, and acetoacetic acid are increased (Fiehn et al., 2010; Liu et al., 2013; Salek et al., 2007; Villarreal-Pérez et al., 2014; Xu et al., 2013; Yan et al., 2014; Zeng et al., 2011), whereas those of acyl-alkyl-phosphatidylcholines and ethanolamine are decreased (Fiehn et al., 2010; Floegel et al., 2013; Suhre et al., 2010; Xu et al., 2013). Phosphatidylcholine, phosphatidylethanolamine, sphingomyelin and 3-hydroxybutanoic acid are increased in some studies (Drogan et al., 2015; Huang et al., 2011), and decreased in others (Floegel et al., 2013; Suhre et al., 2010; Xu et al., 2013). Phosphatidylcholine was also found decreased in T1DM (Oresic et al., 2008).

Carbohydrate metabolism

The progress of obesity is often explained by excessive consumption of high-fat and high-calorie diets (Saris, 2003; Siri-Tarino et al., 2010). Yet, the role of dietary carbohydrates in the development and maintenance of obesity is now also receiving increasing attention (Boling et al., 2009; Malik et al., 2010; Siri-Tarino et al., 2010; Wylie-Rosett and Davis, 2009). Obesity is associated with a decreased glucose disposal in adipose tissue. It has been reported that obesity leads to the development of hyperglycemia (Halaas et al., 1995), hyperlipidemia (Yamamoto et al., 2002), hyperinsulinemia (Berndt et al., 2005) and insulin resistance (Heilbronn et al., 2004). The pathways that metabolize carbohydrates include glycolysis, gluconeogenesis, the pentose phosphate pathway and the TCA cycle. Carbohydrate metabolism is vital to all metabolic processes. Glucose is catabolised via glycolysis to pyruvate, which under aerobic conditions is converted into acetyl coenzyme A, the entry point into the TCA cycle. Under anaerobic conditions, pyruvate is instead converted into lactate by lactate dehydrogenase. In obesity, the levels of glucose, lactic acid, fructose, glycerol, mannose, sorbitol, xylose, gluconic acid and glucuronic acid are increased (Fiehn et al., 2010; Gogna et al., 2015; Moore et al., 2014) whereas those of 1,5-anhydroglucitol and glycerol-3-phosphate are decreased (Fiehn et al., 2010; Moore et al., 2014).

Glucose concentration in blood reflects carbohydrate metabolism both in healthy people and in diabetics. In diabetes management, reduction in carbohydrate intake is the first and the most important step (Franz, 2008). Among compounds involved in carbohydrate metabolism, the levels of glucose, fructose, glycerol, inositol, mannose, sorbitol, xylose, 2,6-anhydrogalactose, 3,6-anhydrogalactose, gluconic acid, glucuronic acid, isopropanol, fumaric acid, malic acid and cis-aconitic acid are increased (Drogan et al., 2015; Fiehn et al., 2010; Gogna et al., 2015; Salek et al., 2007; Suhre et al., 2010; Xu et al., 2013; Zeng et al., 2010), whereas those of deoxygalactose, pyruvic acid, 1,5-anhydroglucitol and glycerol-3-phosphate are decreased in diabetes (Drogan et al., 2015; Fiehn et al., 2010; Suhre et al., 2010). Other metabolites such as acetic acid, deoxyglucose, lactic acid and citric acid were increased in some studies (Diao et al., 2014; Gogna et al., 2015; Salek et al., 2007; Suhre et al., 2010; Zeng et al., 2010) and decreased in others (Diao et al., 2014; Drogan et al., 2015). One metabolite, succinic acid is decreased in T1DM, though any significant changes are not observed in T2DM (Oresic et al., 2008).

Nucleotide metabolism

The study of nucleotide metabolism is vital for understanding of energy metabolism disorders, because nucleotides take part in most metabolic reactions and also act as coenzymes. Nucleotides are secreted from several body tissues and then build up in the blood circulation and other extracellular fluids. Release from cells and extracellular degradation both contribute to the nucleotide levels in the circulation. Persistently elevated blood nucleotide levels and constant purinergic signaling may play a pathophysiological role in metabolic disorders (Di Virgilio and Solini, 2002; Sellers et al., 2009; Sparks and Chatterjee, 2012). Nucleotide levels are extremely variable in obese subjects. High nucleotide levels observed in some morbidly obese subjects seem to be associated with the initial stage of insulin resistance (Sparks et al., 2014). Uric acid and uridine are strongly increased in obesity (Fiehn et al., 2010; Kim et al., 2011).

Analysis of the relationship between circulating nucleotide concentrations and clinical measures of T2DM demonstrated that changes in nucleotide metabolism are direct metabolic consequences of the disease and do not result from secondary complications (Dudzinska, 2014). In diabetes, compounds involved in nucleotide metabolism, including AMP, GMP, GTP, IMP, adenosine, guanosine and inosine are increased in both T1DM and T2DM (Dudzinska, 2014; Huang et al., 2011). Trimethylamine, glyoxylic acid and uridine are increased only in T2DM (Fiehn et al., 2010; Guan et al., 2013; Nikiforova et al., 2014; Padberg et al., 2014; Salek et al., 2007).

Besides the metabolites of major metabolic pathways, changes in the profiles of some other metabolites have been detected in obesity and diabetes. The levels of 3,6-anhydrogalactose, 7-ketodeoxycholic acid, heptadecanoic acid, inulobiose and myoinositol are increased, whereas those of, benzylalcohol, and a few glycerophospholipids are decreased in obesity (Fiehn et al., 2010; Gogna et al., 2015; Kim et al., 2011; Moore et al., 2014; Pietiläinen et al., 2007). The levels of cholesteryl-β- d-glucoside, dimethylamine, dimethylglucosamine, fructosamine and glycocholic acid are increased (Drogan et al., 2015; Fiehn et al., 2010; Huang et al., 2011; Liu et al., 2013; Padberg et al., 2014; Salek et al., 2007; Suhre et al., 2010).


Obesity and diabetes have many similar causes and are related. These disorders often occur together, and most patients with T2DM are obese or were previously obese (Bray, 2004; Stumvoll et al., 2005). Obesity is usually considered as to strongly increase the risk of the later development of diabetes. The question arises whether obesity is not only a risk factor but also a cause of T2DM. A strong increase in obesity initiates a parallel upward trend in the incidence of diabetes. According to Ford et al. (1997) for every kilogram of weight gain, the risk of diabetes increases by between 4.5% and 9%. The relationship between obesity and insulin resistance is probably a cause-and-effect relationship, since human and animal studies show that weight loss or gain is closely associated with an increase or decrease in insulin sensitivity, respectively (Bak et al., 1992; Freidenberg et al., 1988; Sims et al., 1973). Longitudinal studies have shown that people with a genetic predisposition to compromised insulin secretion develop diabetes when they have developed insulin resistance due to obesity. Hence, T2DM develops once insulin secretion deteriorates to a level at which it cannot further compensate for insulin resistance. Also, in a longitudinal study of normal glucose tolerance offspring of two diabetic parents, Warram et al. (1990), revealed that patients presenting insulin resistance and extreme body weight were at increased risk of developing T2DM.

Several investigations have linked the phenotype and metabolism and identified serum or plasma metabolic markers that are involved independently in developing obesity (He et al., 2012; Williams et al., 2006) and diabetes (Bao et al., 2009; Chen et al., 2009). The occurrence of diabetes is positively associated with increased BMI across several ethnic groups (Chan et al., 2009; Maskarinec et al., 2009). Thirty nine metabolites are associated with both diabetes and high BMI or obesity (Table 1). Among compounds involved in amino acid metabolism, the levels of BCAAs, cysteine, glutamine, phenylalanine, proline, tyrosine, threonine, tryptophan, choline and pantothenic acid are increased, whereas those of asparagine, glycine, methionine and citrulline are decreased in both obesity and diabetes. Among compounds involved in lipid metabolism, the levels of 2-hydroxybutanoic acid, 3-hydroxybutanoic acid, phosphatidylcholine, stearic acid, oleic acid, palmitic acid and palmitoleic acid are increased, whereas those of ethanolamine, lysophosphatidylcholine 18:2, lysophosphatidylethanolamine and sphingomyelin are decreased. Among compounds involved in carbohydrate metabolism, the levels of fructose, glycerol, mannose, xylose, sorbitol, lactate, glucose, gluconic acid and glucuronic acid are increased, whereas those of 1,5-anhydroglucitol and glycerol-3-phosphate are decreased. Among compounds involved in nucleotide metabolism, the level of uridine is increased. All these metabolites along with the references are categorized and summarized in Table 1.

Table 1.


This study summarizes the major metabolites, metabolite classes and pathways associated with obesity and diabetes with a focus on metabolites associated with both disorders. The study also discusses some aspects of the development of these disorders and transformation of obesity into a diabetic state. Overall, metabolomics research can provide comprehensive information about metabolite changes in the studied disease using various sample types in minimum quantities and in a very short time. The limitations of the reviewed studies were the differences in the analytical platforms used, gender, age, diet, ethnicity and the source species of the samples, which may have led to some misinterpretations in the assessment. Other unknown diseases may also affect the outcome of metabolomics studies.


Obesity and diabetes are well-known to be associated. This study provides information on all major metabolites associated with obesity and diabetes and also common metabolites associated with both disorders. The classification and changes in metabolites in each comparison have been represented in Fig. 1. These metabolites can be considered as biomarkers for metabolomics studies of obesity and diabetes and can be a focus area of future research. This study can also provide some therapeutic clues for treatment of obesity-related diabetes. Further studies are required to test whether the selected metabolites might be useful as diagnostic tools and to reveal the biological mechanisms that result in changes in the levels of certain metabolites in the pathogenesis of these metabolic diseases.

Figure F1
Summary of the metabolites changed in obesity and diabetes

Article information

Mol. Cells.Jul 31, 2015; 38(7): 587-596.
Published online 2015-06-15. doi:  10.14348/molcells.2015.0126
1Department of Brain & Cognitive Sciences, Daegu Gyeongbuk Institute of Science & Technology, Daegu 711-873, Korea
2Neurometabolomics Research Center, Daegu Gyeongbuk Institute of Science & Technology, Daegu 711-873, Korea
Received May 15, 2015; Accepted May 26, 2015.
Articles from Mol. Cells are provided here courtesy of Mol. Cells


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Figure 1

Summary of the metabolites changed in obesity and diabetes

Table 1.

List of the metabolites changed in both obesity and diabetes

Category Metabolites Origin Sample type Up/Down Platform References
Amino acid metabolism Asparagine human serum/plasma Bentley-Lewis et al., 2014; Moore et al., 2014
Citrulline human serum/plasma Mihalik et al., 2012; Oberbach et al., 2011
Glycine human serum/plasma Fiehn et al., 2010; Floegel et al., 2013; Mihalik et al., 2012; Palmer et al., 2015; Wang-Sattler et al., 2012
Methionine human serum/plasma Bentley-Lewis et al., 2014; Mihalik et al., 2012
Choline human serum Gogna et al., 2015
Cysteine human plasma Bentley-Lewis et al., 2014; Fiehn et al., 2010
Glutamine human serum/plasma/urine Gogna et al., 2015; Oberbach et al., 2011; Salek et al., 2007; Xu et al., 2013; Zeng et al., 2011
Isoleucine human serum/plasma Gogna et al., 2015; Moore et al., 2014; Suhre et al., 2010; Wang et al., 2011; Xu et al., 2013; Zeng et al., 2011
Leucine human serum/plasma Fiehn et al., 2010; Gogna et al., 2015; Kim et al., 2010; Moore et al., 2014; Oberbach et al., 2011; Palmer et al., 2015; Suhre et al., 2010; Villarreal-Pérez et al., 2014; Wang et al., 2011; Xu et al., 2013; Zeng et al., 2011
Pantothenic acid human serum Gogna et al., 2015, Suhre et al., 2010
rodent serum Kim et al., 2011
Phenylalanine human serum/plasma Floegel et al., 2013; Gogna et al., 2015; Moore et al., 2014; Oberbach et al., 2011, Palmer et al., 2015; Wang et al., 2011; Xu et al., 2013
Proline human serum Gogna et al., 2015; Oberbach et al., 2011; Xu et al., 2013
Threonine human serum Gogna et al., 2015
Tryptophan human serum/plasma Kim et al., 2010; Wang et al., 2011
Tyrosine human serum/plasma Kim et al., 2010; Moore et al., 2014; Oberbach et al., 2011; Villarreal-Pérez et al., 2014; Wang et al., 2011
rodent serum Kim et al., 2011
Valine human serum/plasma Gogna et al., 2015; Kim et al., 2010; Moore et al., 2014; Oberbach et al., 2011; Palmer et al., 2015; Suhre et al., 2010; Villarreal-Pérez et al., 2014; Wang et al., 2011; Xu et al., 2013
Lipid metabolism Ethanolamine human plasma Fiehn et al., 2010
Lysophosphatidylcholine C18:2 human serum Floegel et al., 2013; Wahl et al., 2012; Wang-Sattler et al., 2012
Lysophosphatidylethanolamine human plasma Liu et al., 2013
rodent serum Kim et al., 2011
Sphingomyelin human serum Floegel et al., 2013; Xu et al., 2013
rodent adipose tissue/plasma Samad et al., 2006
2-hydroxybutanoic acid human serum Fiehn et al., 2010; Moore et al., 2014
3-hydroxybutanoic acid human serum Fiehn et al., 2010; Gogna et al., 2015; Kim et al., 2010; Moore et al., 2014; Salek et al., 2007; Suhre et al., 2010; Zeng et al., 2011
Oleic acid human serum/plasma Fiehn et al., 2010; Liu et al., 2013; Xu et al., 2013; Yi et al., 2006; Zeng et al., 2011
Palmitic acid human serum/plasma Fiehn et al., 2010; Xu et al., 2013; Yi et al., 2006; Zeng et al., 2011
Palmitoleic acid human plasma Fiehn et al., 2010
Phosphatidylcholine human serum Drogan et al., 2015; Pietiläinen et al., 2007
rodent liver/serum Huang et al., 2011; Kim et al., 2011
Stearic acid human serum/plasma Fiehn et al., 2010; Xu et al., 2013; Yi et al., 2006; Zeng et al., 2011
Carbohydrate metabolism 1,5-anhydroglucitol human serum Drogan et al., 2015; Moore et al., 2014; Suhre et al., 2010
Glycerol-3-phosphate human plasma Fiehn et al., 2010
Fructose human serum/plasma Fiehn et al., 2010; Xu et al., 2013
Glucose human serum/plasma Drogan et al., 2015; Fiehn et al., 2010; Gogna et al., 2015
Glycerol human serum Gogna et al., 2015; Moore et al., 2014
rodent serum Diao et al., 2014
Gluconic acid human plasma Fiehn et al., 2010
Glucuronic acid human serum/plasma Fiehn et al., 2010; Suhre et al., 2010
Lactic acid human serum/plasma Gogna et al., 2015; Wang et al., 2011; Zeng et al., 2011
Mannose human serum Moore et al., 2014; Xu et al., 2013
Sorbitol human serum Gogna et al., 2015
Xylose human plasma Fiehn et al., 2010
Nucleotide metabolism Uridine human plasma Fiehn et al., 2010

, NMR; , LC/MS; , GC/MS