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Adivia1650

Manufactured by Siemens
Sourced in United States

The ADIVIA1650 is a laboratory equipment product offered by Siemens. It is a high-performance platform designed for clinical chemistry and immunoassay testing. The device utilizes advanced analytical technologies to provide accurate and reliable results. The core function of the ADIVIA1650 is to perform automated diagnostic testing on various biological samples.

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4 protocols using adivia1650

1

Fasting Glucose and Insulin Assessment

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Fasting glucose concentrations were determined according to standard procedures using an ADIVIA1650 (Siemens, Washington, DC, USA) in 2007, a Hitachi Automatic Analyzer 7600 (Hitachi, Tokyo, Japan) in 2008–2010, and Labospect 008AS (Hitachi, Tokyo, Japan) in 2019–2020. Insulin concentrations were measured using an immunoradiometric assay (INS-IRMA; Biosource, Nivelles, Belgium) with a 1470 WIZARD gamma-counter (PerkinElmer, Turku, Finland) in 2007–2010 and using an electrochemiluminescence immunoassay (ECLIA; Roche, Germany) with modular E801 (Roche, Germany) in 2019–2020. The assay detection limit was 1 μU/mL, and the intra- and inter-assay coefficients of variation were 2.2% and 6.5%, respectively. Insulin sensitivity was evaluated using the HOMA-IR index with the following equation: HOMA-IR=fasting insulin (μU/mL)×fasting glucose (mg/dL)/405.
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2

Comprehensive Clinical Measurements Protocol

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After 5 min of rest in a seated position, blood pressure was measured manually 3 times with 30 s intervals. Body mass index (BMI) was calculated by weight in kilograms divided by height in meters squared.
Blood samples were collected after fasting for at least 8 h and random spot urine samples were collected on the same visit. After being properly processed and refrigerated, they were transported in cold storage to the central laboratory within 24 h of collection. Glucose levels were measured using the hexokinase ultraviolet method with a Hitachi Automatic Analyzer 7600-210 (Hitachi, Marunouchi, Japan). Hemoglobin A1c (HbA1c) levels were measured with a high-performance liquid chromatography assay with a Tosoh G8 instrument (Tosoh, Shiba, Japan) [17 (link)]. Serum creatinine levels were measured by the colorimetric method using ADIVIA 1650 (Siemens, Malvern, PA, USA) in 2007 and the Jaffe rate-blanked and compensated method using the Hitachi Automatic Analyzer 7600 (Hitachi, Tokyo, Japan) in 2008–2018. Serum creatinine concentrations were calibrated to isotope-dilution mass spectrometry-traceable standard.
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3

Anthropometric and Metabolic Measurements

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Trained personnel measured the body weight and height using standard protocols to the nearest 0.1 kg and 0.1 cm, respectively. Blood pressure was manually measured using a mercury sphygmomanometer, and the values were corrected based on height of the arm during measurement, which was in accordance with the recommendation by the American Heart Association [22 (link)].
Blood samples were taken only if the participant had fasted for at least 8 h. Triglycerides (TG), HDL cholesterol, and fasting glucose were measured using ADIVIA1650 (Siemens/USA) from July 2007 to February 2008 and Hitachi Automatic Analyzer 7600 (Hitachi/Japan) from February 2008 to December 2012. Each measured HDL cholesterol value was corrected by the Lipid Standardization Program (LSP), as recommended by the Centers for Disease Control and Prevention. In each session, serum insulin was measured using the Gamma Counter (Hewlett Packard/USA) and 1470 WIZARD Gamma Counter (PerkinElmer/Finland).
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4

KNHANES Blood Sampling and Analysis Protocol

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Body mass index (BMI) was calculated as body weight (kg) divided by height squared (m2) [15 (link)]. Venous blood was collected after 8 h of fasting [17 ]. FBG levels were analyzed using the hexokinase method. The blood analytic instruments used in the KNHANES were ADIVIA 1650 (Siemens, Tarrytown, NY, USA) in 2008–2009, Hitachi Automatic Analyzer 7600 (Hitachi, Tokyo, Japan) in 2010–2012, Hitachi Automatic Analyzer 7600-210 (Hitachi, Tokyo, Japan) in 2013–2018, and Labospect 008AS (Hitachi, Tokyo, Japan) in and after 2019 [14 ]. The clinical test for HbA1c level was performed by high-performance liquid chromatography using HLC-723G7 (Tosoh, Tokyo, Japan) in 2008–2012 and Tosoh G8 (Tosoh, Tokyo, Japan) in and after 2013 along with appropriate reagents.
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