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Advia 1650 chemistry analyzer

Manufactured by Siemens
Sourced in United States

The ADVIA 1650 chemistry analyzer is a diagnostic instrument used in clinical laboratories for the analysis of various chemical components in biological samples, such as blood and urine. It is designed to provide accurate and reliable results for a wide range of analytes, including enzymes, electrolytes, and metabolites. The ADVIA 1650 utilizes advanced automation and analytical technologies to streamline the testing process and enhance the efficiency of the laboratory workflow.

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2 protocols using advia 1650 chemistry analyzer

1

Metabolic Markers and Insulin Resistance

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Blood samples were obtained after at least an 8-hour overnight fast. The venous blood sample was then delivered to the central laboratory. Levels of fasting blood glucose, triglycerides, total cholesterol, and high-density lipoprotein cholesterol (HDL-C) were measured using an ADVIA 1650 chemistry analyzer (Siemens, Washington, DC, USA) in 2007, and a Hitachi 7600 automatic analyzer (Hitachi, Tokyo, Japan) from 2008 to 2010. For HDL-C, corrected values using the conversion equations recommended by the KCDC were used [22 (link)]. LDL-C was calculated using the Friedewald equation. Serum insulin was measured by 1470 Wizard gamma counter (Perkin-Elmer, Turku, Finland).
For quantification of IR, HOMA-IR was calculated as follows: HOMA-IR = fasting insulin (μU/dL) × fasting glucose (mg/dL) / 22.5. TyG index, TyG-WC, TyG-BMI were calculated using the formula published previously. The TyG index [17 (link),18 (link)]: Ln[TG (mg/ dL) × fasting glucose (mg/dL)/2]. TyG-BMI, TyG-WC and TyG-WHtR indicate TyG index x BMI [20 (link)], TyG index x WC [20 (link)] and TyG index x WHtR, respectively.
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2

Measuring Serum Testosterone and SHBG in Twins

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Blood samples were drawn in the morning (around 10 a.m.) after overnight fasting. Serum was immediately separated and stored at −70°C. We measured TT and SHBG immediately after thawing the frozen serum by electrochemiluminescence immunoassay using commercial ADVIA Centaur XP (Siemens, Erlange, Germany) for TT and a MODULAR ANALYTICS E170 analyzer (Roche, Basel, Switzerland) for SHBG. The minimum concentration measurable at the laboratory was 0.35 nmol L−1 for TT and SHBG. Inter-assay coefficients of variation were <7.6% for TT and <2% for SHBG. Albumin levels in fresh sera were measured by colorimetry using an ADVIA 1650 chemistry analyzer (Siemens). Free testosterone (cFT) and bioavailable testosterone (cBAT) levels were calculated using Vermeulen's method.18 (link)
Body mass index (BMI) was calculated using measured weight and height (kg m−2). Information on health habits was obtained using a self-administered questionnaire.
We ascertained the zygosity of twin pairs using 16 short tandem repeat markers including one sex-determining marker for 67% of twin pairs and a self-administered zygosity questionnaire for the remaining 33%. Ascertainment of zygosity using the questionnaire was 94.3% accurate compared to ascertainment by the short tandem repeat marker.19 (link)
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