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Liaison test

Manufactured by DiaSorin
Sourced in United States

The LIAISON test is a diagnostic laboratory equipment product manufactured by DiaSorin. It is designed to perform immunoassay testing, a technique used for the detection and quantification of specific analytes in a sample. The core function of the LIAISON test is to provide accurate and reliable results for clinical laboratory testing, enabling healthcare professionals to make informed decisions about patient care.

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4 protocols using liaison test

1

Standardized Biomarker Assessment of Calcium-Phosphate Metabolism

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Blood specimens were obtained in a standardized fashion in the morning, after at least 12 h of fasting and 30 min of resting in a supine position in a quiet, environmentally controlled room. Fasting morning urinary samples and 24-h urinary samples were collected. The serum PTH levels were determined using Elecsys PTH (1–84) test (Cobas®, Roche Diagnostics GmbH, Germany). Vitamin D (25(OH)D3) levels were measured using the LIAISON test (DiaSorin Inc., USA). To calculate [Ca]alb and [Ca2+]pH, we used the standard formulas [14 (link), 15 (link)].
The laboratory calibration references for Ca-P metabolism parameters were as follows: [Ca]alb. (serum), 2.19–2.54 mmol/L; [Ca2+]pH (serum), 1.13–1.32 mmol/L; daily urinary Ca secretion, 2.5–6.25 mmol/24 h (females) and 3.75–7.5 mmol/24 h (males); phosphates (serum), 0.9–1.5 mmol/L; phosphates (urine), 40–136 mg/dL; daily urinary phosphate secretion, 0.4–1.3 g/24 h; PTH (serum), 10–65 pg/mL; and 25(OH)D3, 30–80 ng/mL.
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2

Denosumab's Effects on Bone Metabolism

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This was a prospective study in patients never previously treated with denosumab. Patients were clinically and biochemically evaluated at baseline and 4 and 12 weeks after the first subcutaneously administrated 60 mg dose of denosumab: anthropometric measures (body weight, height) were recorded; bone metabolism was investigated by measurement of serum calcium, albumin, phosphate, total alkaline phosphatase (ALP), PTH, and 25-hydroxyvitamin D (25OHD) on blood samples collected after an overnight fasting. serum calcium, phosphate, and albumin were measured according to routinely used laboratory kits. Serum PTH was assayed by electrochemiluminescence on an Elecsys 2010 (Roche Diagnostics, Mannheim, Germany), while serum 25OHD was assayed by a chemiluminescent assay (LIAISON test, DiaSorin Inc., Stillwater, MN, USA). Albumin-corrected calcium was calculated according the following formula: serum calcium (mg/dL) −  0.8 ∗ [4.0 – albumin (g/dL)].
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3

Venous Blood Sampling and Biochemical Analysis

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Venous blood sampling was collected the day before the diagnostic procedure after an overnight fasting, and biochemical and hormonal markers were measured in all patients. Serum calcium, phosphate, magnesium, and creatinine were measured by routine assays. Serum calcium levels were corrected for the serum albumin concentrations according to the formula: serum total calcium (mg/dL) − 0.8 × [serum albumin (g/dL) − 4.0]. Serum albumin concentrations were within the normal range in all patients indicating the absence of malnutrition. Ionized calcium concentrations were assayed by Liquichek Blood Gas (IL Synthesis Series, Bio-Rad Laboratories, Segrate, MI, Italy). Serum 25OHD concentrations were measured by a chemiluminescent assay (LIAISON test, DiaSorin Inc., Stillwater, MN, USA) with mean intra- and interassay coefficients of variation (CV) of 4.5% and 7.5%, respectively. Serum NT-proBNP and PTH were measured by Electrochemiluminescence on an Elecsys 2010 (Roche Diagnostics, Mannheim, Germany).
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4

Bone Mineral Density and Bone Metabolism Markers in Primary Hyperparathyroidism

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PHPT patients were investigated by dual-energy X-ray absorptiometry (DEXA) scanner for the measurement of segmental bone mineral density (BMD) using a Hologic densitometer. Participants were scanned in light clothing, while lying flat on their backs with arms at their sides.
Venous blood samples were collected after an overnight fasting in all patients. Serum calcium, ionized calcium, phosphate, creatinine, and total alkaline phosphatase were measured according to the routinely used laboratory kits. Serum PTH levels were determined by electrochemiluminescence on an Elecsys 2010 (Roche Diagnostics, Mannheim, Germany), and serum 25-hydroxyvitamin D (25OHD) was measured by a chemiluminescent assay (LIAISON® test, DiaSorin Inc., Stillwater, MN, USA). Plasma IL-17A levels were assayed by Human IL-17 Quantikine ELISA kit (R&D System, Cat. D1700; intra-assay CV 4.7%, interassay CV 8.4%, sensitivity <3.0 pg/ml, by considering an additional point to the low range of the standard curve); plasma OPG was determined by the Human Osteoprotegerin ELISA kit (BioVendor, Cat. RD194003200; intra-assay CV 4.9%, interassay CV 9.0%, sensitivity 0.03 pmol/l) and plasma soluble RANKL by the sRANKL (total) human ELISA kit (BioVendor, Cat. RD193004200R; intra-assay CV 11.5%, inter-assay CV 12.7%, sensitivity 0.4 pmol/l).
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