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Ysi 2300 glucose analyzer

Manufactured by Yellow Springs Instruments

The YSI 2300 glucose analyzer is a laboratory instrument designed for the rapid and accurate measurement of glucose concentrations in a variety of samples. It utilizes a glucose-specific enzyme electrode to provide precise glucose readings.

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2 protocols using ysi 2300 glucose analyzer

1

Metabolic Syndrome Diagnosis Criteria

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The National Cholesterol Education Program/Adult Treatment Panel III (NCEP ATP III) [26 (link), 27 (link)] definition was used to classify participants having MetS in the Health ABC cohort at the baseline and 6-year follow-up visit. Three of the five components are required for diagnosis: (1) waist circumference ≥102 cm (men) and ≥88 cm (women), (2) hypertension ≥130 mm Hg systolic or ≥85 mm Hg diastolic or antihypertensive medications, (3) fasting blood glucose ≥100 mg/dl or treatment for impaired fasting glucose, (4) triglycerides ≥150 mg/dl or specific treatment, and (5) HDL-C ≤40 mg/dl in men and ≤50 mg/dl in women. Waist circumference was measured using a flexible measuring tape on bare skin at the level of maximal circumference, midway between the lower ribs and anterior superior iliac spine at the level of the umbilicus by trained technicians. Seated systolic and diastolic blood pressures were measured by a manual mercury sphygmomanometer using a standardized protocol. Fasting plasma glucose levels were measured by an automated glucose oxidase reaction (YSI 2300 glucose analyzer, Yellow Springs Instruments, Yellow Springs, Ohio). Triglyceride and high-density lipoprotein (HDL) cholesterol concentrations were measured by a colorimetric technique (Johnson and Johnson Vitros 950 analyzer, Rochester, New York).
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2

Lipid and Glucose Biomarker Assessment

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Lipid parameters were assessed using standard laboratory procedures. Plasma glucose was measured in duplicate by the glucose oxidase method using an automated YSI 2300 glucose analyzer (Yellow Springs Instruments, Yellow Springs, OH). Plasma insulin and C-peptide were measured in duplicate by double-antibody radioimmunoassays (Millipore, Billerica, MA). Samples from matched case subjects and normal control subjects were assayed simultaneously.
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