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Cobas modular platform

Manufactured by Roche
Sourced in Switzerland

The Cobas Modular Platform is a comprehensive, automated laboratory system designed for clinical diagnostics. It provides an integrated solution for performing a wide range of in vitro diagnostic tests, including immunoassays, clinical chemistry, and specialized analyses. The platform is engineered to deliver reliable results, optimize workflow, and enhance laboratory productivity.

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4 protocols using cobas modular platform

1

Comprehensive Community Health Assessment

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A team of community health workers was trained to enroll participants and to conduct household questionnaires assessing sociodemographic and behavioral variables. Participants were invited to a clinic visit where standing and sitting height, weight, and waist circumference where measured in triplicate using standardized techniques. Systolic and diastolic blood pressure were also measured in triplicate using an automatic monitor (OMRON HEM-780, Omron Healthcare, Hoffman Estates, IL, USA) previously validated for an adult population [39] (link). In this study, we used the mean of the second and third measurements. Fasting blood samples were obtained using standardized methods and calibrated tools [38] . Total cholesterol, triglycerides, high-density lipoprotein cholesterol (HDL-C), and insulin were measured in serum, whereas fasting glucose was assessed in plasma using an enzymatic colorimetric method (GOD-PAP, Modular P-E/Roche-Cobas, Germany). Triglycerides and HDL-C were measured using a Cobas Modular Platform automated analyzer and reagents supplied by Roche Diagnostics (Basel, Switzerland). All samples were analyzed in a single facility, and, for quality assurance, the quality of assays was checked with regular external standards and internal duplicate assays and monitored by BioRad (Hercules, CA, USA).
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2

CRONICAS Cohort Study Fieldwork Protocol

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Fieldwork activities and procedures of the CRONICAS Cohort Study have been described in detail elsewhere.15 Trained community health workers applied face-to-face questionnaires. After completing the questionnaire, an appointment for a clinical assessment was arranged to ensure an adequate fasting period, between 8 and 12 hours, where a total of 13.5 mL of blood was drawn. Standing height was measured using standardized techniques. After a 5-minute resting period, blood pressure was measured using an automatic monitor OMRON HEM-780 (OMRON, Tokyo, Japan) validated for adult population.
For laboratory procedures, Cobas Modular Platform automated analyzer and reagents from Roche Diagnostics were used to measure triglycerides, total cholesterol, and HDL-c. Also, LDL-c was measured using this method in participants with triglycerides ≥400 mg/dL. However, if participants had triglycerides below 400 mg/dL, the Friedewald equation was used to calculate LDL-c in mg/dL. Non-HDL-c was also estimated by subtracting HDL-c from total cholesterol. Serum glucose was measured using an enzymatic colorimetric method (GOD-PAP; Modular P-E/Roche-Cobas, Grenzach-Wyhlen, Germany).
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3

Oral Glucose Tolerance Test Protocol

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Each potential participant was visited in their respective household and checked to ensure that they were the selected person and that they met the selection criteria. Then, they were invited to participate in the study using the informed consent form. After this initial visit, an appointment was scheduled to guarantee an appropriate fasting period (between 8 and 12 hours) to obtain the blood samples for the study.
The sample was obtained by trained personnel, and the fasting time was confirmed before the oral glucose tolerance test. A 7.5-mL blood sample was obtained at the time of the first evaluation; then, 75 g of anhydrous glucose in 300 mL of water was administered orally and, after two hours, the second blood sample was taken. These samples were analyzed in a certified private laboratory in Lima. For the glucose measurement, a Cobas Modular Platform (Roche Diagnostics, Basel, Switzerland) automatic analyzer was used with reagents provided by Roche Diagnostics. During the two-hour waiting period, the participant answered the questionnaire, and blood pressure and anthropometric measurements (weight and height) were taken.
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4

Steroid Measurement Techniques Comparison

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In our laboratory, steroids are currently routinely measured only by commercial immunological methods. Analytes CORT, DHEAS, E2, PROG, and TES are currently routinely measured by electrochemiluminescence (ECLIA) IA “Elecsys” on the Cobas modular platform from Roche Diagnostics GmbH (Mannheim, Germany). ANDRO is measured by solid-phase, competitive chemiluminescent enzyme IA Immulite 2000 from Siemens Healthineers AG (Erlangen, Germany), and 17P by chemiluminescence IA IDS-iSYS from Immunodiagnostic Systems Ltd. (Bolton, UK); DHEA samples are routinely forwarded to external laboratory MVZ Labor Ravensburg (Ravensburg, Germany), where they are measured by an ELISA from Demeditec (Kiel, Germany). Details such as working principle and main performance data of all IAs are summarized in Table S18.
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