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Chemiluminescent assay

Manufactured by DiaSorin
Sourced in Italy

Chemiluminescent assay is a laboratory technique used to detect and quantify specific analytes in a sample. It utilizes a chemical reaction that produces light, which is then measured and correlated to the concentration of the target analyte.

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Lab products found in correlation

2 protocols using chemiluminescent assay

1

Biochemical Evaluation of Metabolic Markers

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Biochemical evaluation was performed on an Architect-ci8200 automated analyzer (Abbott Diagnostics, Abbott Park, Illinois) and included serum glucose, albumin, total cholesterol, high-density lipoprotein- (HDL-) cholesterol, low-density lipoprotein- (LDL-) cholesterol, triglycerides, total calcium, magnesium, and phosphorus. We used a specific chemiluminescent assay to measure PTH intact molecule (DiaSorin Inc., Stillwater, Minesota) with a sensitivity of 1 pg/mL, inter- and intra-assay coefficients of variation (CV) of 5.3% and 3.5%, respectively, and a normal reference range of 15-65 pg/mL). Serum 25 (OH) D3 was measured by means of a chemiluminescent assay (DiaSorin Inc., Stillwater, Minnesota) with a sensitivity of 4 ng/ml and inter- and intra-assay CVs of 5.1% and 8.6%, respectively.
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2

Klotho and FGF-23 in CKD Patients

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A cross-sectional study was conducted in patients attending the Nephrology Department
of the Hospital das Clínicas of the São Paulo Medical School, FMUSP, from August
2016 to January 2017. Three groups of patients were included: 1) Control Group,
consisting of patients with hypertension, non-smokers and without CKD; 2) Patients
with CKD in stages III to IV (smokers and non-smokers); 3) Patients with CKD on
dialysis (smokers and non-smokers).
We included patients aged 18 to 70 years, in regular follow-up at the outpatient
clinic. Dialysis patients had been stable in the program for at least 6 months.
Patients with diabetes mellitus, neoplasia, lupus, serology positive for HIV virus,
as well as patients on immunosuppressants and corticosteroids were excluded. The
study was approved by the Research Ethics Committee of the Nove de Julho University
on June 4, 2016 (1,613,780).
We evaluated the patients' ages, genders, presence of comorbidities such as
hypertension and history of coronary and cerebrovascular disease, medications used
regularly and laboratory test results. Klotho dosages (IBL, Japan, sensitivity 6.15
pg/ml) were performed using enzyme-linked immunosorbent assay (ELISA), and those of
FGF-23 with chemiluminescent assay (Diasorin, Italy, sensitivity 5.0 pg/ml).
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