PLoS ONE · 2009 · 117 citations · 9 references
MedicineEndocrinologyPhysiologyInflammationMetabolic RegulationPathophysiologyAdipose TissueBody Composition ChangesInflammatory BiomarkersInsulin ResistanceMetabolic InflammationMetabolic SyndromeInflammation-associated Insulin ResistanceLow-grade Chronic InflammationObesity-induced InflammationObesity-related Muscle DysfunctionSkeletal Muscle PhysiologySystemic Inflammation Markers
BACKGROUND: The two inflammatory molecules, S100A8 and S100A9, form a heterodimer, calprotectin. Plasma calprotectin levels are elevated in various inflammatory disorders. We hypothesized that plasma calprotectin levels would be increased in subjects with low-grade systemic inflammation i.e. either obese subjects or subjects with type 2 diabetes. METHODOLOGY/PRINCIPAL FINDINGS: Plasma calprotectin and skeletal muscle S100A8 mRNA levels were measured in a cohort consisting of 199 subjects divided into four groups depending on presence or absence of type 2 diabetes (T2D), and presence or absence of obesity. There was a significant interaction between obesity and T2D (p = 0.012). Plasma calprotectin was increased in obese relative to non-obese controls (p<0.0001), whereas it did not differ between obese and non-obese patients with T2D (p = 0.62). S100A8 mRNA levels in skeletal muscle were not influenced by obesity or T2D. Multivariate regression analysis (adjusting for age, sex, smoking and HOMA2-IR) showed plasma calprotectin to be strongly associated with BMI, even when further adjusted for fitness, CRP, TNF-alpha or neutrophil number. CONCLUSIONS/SIGNIFICANCE: Plasma calprotectin is a marker of obesity in individuals without type 2 diabetes.
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Brain-derived neurotrophic factor (BDNF) and type 2 diabetes
K. S. Krabbe, Anders R. Nielsen, Rikke Krogh‐Madsen et al. · Diabetologia · 2006 · 699 citations · Full text
Medicine, Neurobiology, Neuroscience +12