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The HS-CRP is a laboratory equipment used for the measurement of high-sensitivity C-Reactive Protein (HS-CRP) levels. C-Reactive Protein is a biomarker that can be used to assess inflammation and cardiovascular risk.

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4 protocols using hs crp

1

Biomarker Profiles in Metabolic Health

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All blood samples were immediately obtained at 08:00 after overnight. Enzyme-linked immunosorbent assay was used to detect the high-sensitivity C-reactive protein (HS-CRP) (Lot 78034031, Bender Med Systems GmbH, Austria; minimum detection limit: 3 pg/ml; intra-assay CVs: 6.9%; inter-assay CVs: 13.1%), matrix metalloproteinase 2 (MMP2) (Lot 303216, R&D, USA; minimum detection limit: 0.047 ng/ml; intra-assay CVs: 5.6%; inter-assay CVs: 7.4%), soluble advanced glycation end products (sRAGE) (Lot 303510, R&D, USA; minimum detection limit: 4.12 pg/ml; intra-assay CVs: 5.7%; inter-assay CVs: 7.7%), and fractalkine (Lot 301156, R&D, USA; minimum detection limit: 0.018 ng/ml; intra-assay CVs: 2.6%; inter-assay CVs: 6.6%). The concentrations of serum AGE-peptides (AGE-P) were measured by flow injection assay (FIA) (24 (link)).
The subject was consumed a standardized breakfast (100 g steamed bread). Venous blood were sampled before and after breakfast, and fasting blood glucose (FBG), HbA1c, total cholesterol (TC), total triglyceride (TG), HDL, LDL, and postprandial blood glucose (PBG) were measured. The glomerular filtration rate (GFR) was estimated using the equation recommended by the National Kidney Foundation in the Modified Diet in Renal Disease (25 (link)).
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2

Cytokine and Biomarker Quantification

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Blood was collected and allowed to clot for 30 min. Sera were separated and frozen to -20°C within 1 hour of collection and then transferred for storage at -80°C until assayed. Samples were defrosted and IL-6, TNF-α, hsCRP and COMP levels were examined using cytokine-and protein-specific ELISA kits according to the manufacturers' instructions (IL-6: Bender Med-Systems, Austria; TNF-α: Biosource, USA; hsCRP: Biosource, USA; COMP: Anamar, Sweden). All samples of each participant were tested on the same plate to preclude the effect of inter-assay variability.
All samples were tested in duplicates, and the intra-assay and inter-assay coefficients of variation were ≤5%.
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3

Sleep Quality and Inflammation Markers

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Sleep quality was examined with the Pittsburgh Sleep Quality Index (PSQI), comprising 19 items that identify seven core elements of sleep: sleep quality, how long subjects take to fall asleep, percentage of time in bed, sleep duration, sleep disturbances, medications for sleep, and daytime dysfunction. Global scores of ≥5 indicate poorsleep and <5 good sleep with a sensitivity of 98.7 and specificity of 84.4 for the diagnosis of sleep quality. Total cholesterol (TC), triglycerides (TG), and high-density lipoprotein (HDL) were examined with a one-step enzymatic method (Erba Mannheim, London, UK) with a minimum detection limit of 0.1 mg/L. Low-density lipoprotein (LDL) was evaluated with the Friedewald equation. An Enzyme Linked Immunosorbent Assay (ELISA) was used to determine plasma levels of IL-6, IL-1β, TNF-α, and hsCRP(ThermoFisher Scientific, Waltham, MA, USA), on a microplate reader (Biotek Instruments Inc., Winooski, VT, USA). Diagnostic sensitivities of the kits were <1.0 pg/mL, 0.35 pg/mL, 1.75 pg/mL, and 9.38 pg/mL for IL-6, IL-1β, TNF-α, and hsCRP, respectively. The coefficients of variation for inter- and intra-assay analyses were less than 5% for all these assays.
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4

Clinical Laboratory Biomarker Analysis

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The following methods were used in the clinical laboratory: hs-CRP and fS-Fe (Thermo Fisher Scientific); S-β-carotene and fS-A-vitamin are in-house methods (diode array detection (DAD), reverse phase HPLC); fS-Q10 is an in-house method (electrochemical detection, reverse phase HPLC); B-Se, B-Zn are in-house methods (acid digestion, ICP-MS); fS-B12-vit has been analyzed by a subcontractor since 2002 (Yhtyneet Medix Laboratoriot, Microparticle Intrinsic Factor Immuno Assay (CMIA)).
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