Table 1.
Author | Year | Title | Subjects | Reasons of Exclusion |
---|---|---|---|---|
Amer et al. | 2017 | Consumption of whey in combination with dairy medium-chain fatty acids (MCFAs) may reduce lipid storage due to urinary loss of tricarboxylic acid cycle intermediates and increased rates of MCFAs oxidation | 52 abdominally overweight participants | The work analyses the metabolomics profile of patients subjected to different types of diet without distinguishing between patients with metabolic syndrome (or other traits of the latter) and healthy patients |
Boden et al. | 2015 | Excessive caloric intake acutely causes oxidative stress, GLUT4 carbonylation, and insulin resistance in healthy men | 3 subjects normal weight (BMI 23.0, 23.9, and 24.9) and 3 overweight (BMI 26.8, 28.7, and 28.1) | The study is not using a metabolomics approach to identify compounds |
Chen et al. | 2018 | Serum metabolomics model and its metabolic characteristics in patients with different syndromes of dyslipidemia based on nuclear magnetic resonance | 60 dyslipidemia patients (30 patients with SKYD and 30 patients with PDR) and 20 healthy subjects |
Despite the study using a metabolomics approach, exclusively analyses patients with secondary dyslipidemia in SKYD (Spleen and Kidney Yang Deficiency) and PDR (Phlegm-Dampness Retention) |
Chen et al. | 2019 | Trimethylamine N-Oxide Binds and Activates PERK to Promote Metabolic Dysfunction | Mouse model and cell culture | The study is not using a metabolomics approach to identify compounds; The study was not conducted on humans |
Grün et al. | 2018 | High-Density Lipoprotein Reduction Differentially Modulates to Classical and Nonclassical Monocyte Subpopulations in Metabolic Syndrome Patients and in LPS-Stimulated Primary Human Monocytes In Vitro | 86 women and men between 20 and 60 years old |
The study analyses the differences in monocyte subpopulations in patients with metabolic syndrome using flow cytometry (absence of a metabolomics approach) |
Heidenreich et al. | 2017 | Retinol saturase coordinates liver metabolism by regulating ChREBP activity | Mouse model and cell culture | The study was not conducted on humans |
Kempinska et al. | 2019 | The Association between SOCS11656G>A Polymorphism, Insulin Resistance and Obesity in Nonalcoholic Fatty Liver Disease (NAFLD) Patients | 138 patients with features of NAFLD 1000 controls |
The study analyses the presence of genetic polymorphisms associated with metabolic syndrome and insulin resistance without using a metabolomics approach for the identification of metabolites |
Kozyra et al. | 2018 | Human hepatic 3D spheroids as a model for steatosis and insulin resistance | Human hepatocyte 3D spheroid cultures | Study conducted on primary human hepatocyte 3D spheroid cultures |
Leboucher et al. | 2019 | The translational regulator FMRP controls lipid and glucose metabolism in mice and humans | 25 fragile X patients and 29 sex- and age-matched healthy subjects | The study analyses exclusively people with fragile X syndrome to assess how the absence of specific genes may influence the metabolic homeostasis; No metabolomics approaches were used |
Silvestri et al. | 2015 | Two non-psychoactive cannabinoids reduce intracellular lipid levels and inhibit hepatosteatosis | Mouse model and cell culture | The study was not conducted on humans |
Teslovich et al. | 2018 | Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study | 8545 non-diabetic men of mean age 57.3 ± 7.1 years | The study identifies genetic variants related to amino acid alterations in patients with metabolic syndrome |
Zimmermann et al. | 2010 | Alterations in lipid, carbohydrate, and iron metabolism in patients with non-alcoholic steatohepatitis (NASH) and metabolic syndrome | 37 patients with metabolic syndrome (25 NASH and 12 non-NASH) 37 controls |
The study is not using a metabolomics approach to identify compounds |