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Ldl cholesterol plus 2nd generation

Manufactured by Roche
Sourced in Switzerland

The LDL-Cholesterol plus 2nd generation is a laboratory instrument used for the quantitative determination of low-density lipoprotein (LDL) cholesterol levels in human serum or plasma. It utilizes a homogeneous enzymatic method to directly measure LDL cholesterol without the need for sample pretreatment or ultracentrifugation.

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3 protocols using ldl cholesterol plus 2nd generation

1

Standardized Lipid Measurement Protocols

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Serum concentrations of TC, TG, HDL, and LDL were measured using enzymatic methods with an automatic analyzer (Cobas 8000 c702, Roche, Mannheim, Germany). LDL was measured using LDL-cholesterol plus 2nd generation reagent on samples between July 4, 2017, and February 4, 2018, and LDL-cholesterol Gen.3 (Roche, Mannheim, Germany) between February 5 and November 30, 2018. TC, TG, and HDL were measured using Cholesterol Gen.2, TRIGL, and HDL-Cholesterol plus 3rd generation, respectively. The accuracy of lipid measurements was assured through the Accuracy Based Lipid Survey proficiency testing program by the College of American Pathologists and by the Lipids Standardization Program by the Centers for Disease Control, USA [25 (link)].
For population 3 (validation cohort 2, KNHANES 2017), serum TC, TG, HDL, and LDL were measured using enzymatic methods with an automatic analyzer Hitachi 7600–210 (Hitachi, Tokyo, Japan) using PureautoS CHO-N, Pureauto S TG-N, Cholestest N HDL, and Cholestest LDL reagents (Sekisui Medical, Tokyo, Japan), respectively [24 (link)].
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2

Cardiometabolic Risk Biomarkers in Fasting Plasma

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Fasted (8–10 h) blood samples were collected from all participants, enzymatic colorimetric assay was used to measure fasting plasma glucose (FPG) (Hexokinase activity assay, Abcam), total cholesterol (Cholesterol Gen.2, Roche), high density lipoproteins (HDLC) cholesterol (LDL-Cholesterol plus 2nd generation, Roche), triglycerides (Triglycerides/Glycerol Blanked, Roche) concentrations using Dimension Autoanalyzer (Cobas501, Roche, Switzerland). Low-density lipoprotein (LDLC) cholesterol serum concentration was calculated with Friedewald’s formula. Basal Insulin was analyzed by an immunoradiometric assay (BioSource International, Camarillo, CA, USA) in a Beckman Coulter (Fullerton, CA, USA). The homeostatic model assessment for insulin resistance index was calculated using the formula: HOMA-IR = fasting serum insulin (Fins, mU/L) *fasting plasma glucose (FPG, mmol/L) /22.5.
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3

Serum Irisin and Metabolic Markers

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Participants underwent blood sampling for the assessment of blood chemistry and hormonal parameters. The quantitative measurement of irisin in human serum samples was performed using a commercial enzyme linked immunosorbent assay (ELISA) kit (Irisin ELISA Kit EK-067-52; Phoenix Pharmaceuticals Inc., CA) according to the manufacturer’s instructions. Basal insulin was analyzed by an immunoradiometric assay (BioSource International, Camarillo, CA, USA) in a Beckman Coulter (Fullerton, CA, USA). Enzymatic colorimetric assay was used to measure fasting plasma glucose (FPG) (Hexokinase activity assay, Abcam), total cholesterol (Cholesterol Gen.2, Roche), high-density lipoproteins (HDL) cholesterol (LDL-Cholesterol plus 2nd generation, Roche), triglycerides (Triglycerides/Glycerol Blanked, Roche) concentrations using a Dimension Autoanalyzer (Cobas501, Roche, Switzerland). The homeostatic model assessment index was calculated following the formulas: HOMA-IR = fasting serum insulin (FINS, mU/L) × fasting plasma glucose (FPG, mmol/L)/22.5; HOMA-IS = 1/(FPG (mmol/L) × FINS (mIU/L)). Low-density lipoprotein (LDL) cholesterol serum concentration was calculated with Friedewald’s formula.
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