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37 protocols using i2000

1

Predialysis Blood Tests and FGF23

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Predialysis blood tests were collected, which include prealbumin, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, total protein, albumin, blood urea nitrogen, serum creatinine, uric acid, parathyroid hormone (PTH), 25-hydroxy vitamin D (25(OH)D), triglyceride, cholesterol, high density lipoprotein, low density lipoprotein, serum phosphate, and calcium. PTH was measured using an intact assay by a chemiluminescent method (Abbott i2000); serum 25(OH)D was measured by electrochemiluminescence immunoassay (Roche Cobas e601). The samples for measuring FGF23 were ethylenediaminetetraacetic acid plasma. We collected all the samples with other blood test samples on the same day in July 2011 before dialysis. After centrifugation for 10 min at 2000 rpm, all plasmas were stored at −80°C as soon as possible. Plasma FGF23 level was measured using a C-terminal assay (FGF23 [C-Term] ELISA, Immutopics Inc., San Clamente, CA, USA). Body mass index was calculated as weight in kilograms divided by height in meters squared.
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2

Serum AFP Concentration Measurement

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The measurement of serum AFP concentration was done using the enzyme immunoassay method (Abbott Immunization i2000).
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3

Umbilical Cord Blood Serum Biomarker Assay

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After birth, umbilical cord blood collected from patients was immediately centrifuged at 1500× g for 10 minutes and serum samples were separated. Serum samples were stored at −80°C before performing assays and were thawed only once prior to use. Serum glucose and insulin levels were measured by a clinical chemistry analyzer (Abbott ARCHITECT C8000 and i2000, respectively). Serum levels of leptin, SDC1, GPC3, GPC1, and WISP1/CCN4 were measured by a commercial enzyme-linked immunosorbent assay kit according to the manufacturer’s instructions (FineTest, Wuhan). Samples were measured with a micropla te reader at 450 nm wavelength (Epoch, Biotek). All assays coefficient of variation were determined with inter-assay cv: <10% and intra-assay cv: <8%, respectively.
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4

Validation of SARS-CoV-2 Antibody Assay

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Detection of SARS-CoV-2 antibodies was performed by the Abbott Diagnostics SARS-CoV-2 IgG assay on an Abbott Architect i2000 according to the manufacturer’s instructions. This qualitative assay detects IgG binding to an undisclosed epitope of the SARS-CoV-2 nucleocapsid protein. The amount of IgG antibodies to SARS-CoV-2 in each sample is determined by comparing its chemiluminescent relative light unit (RLU) to the calibrator RLU (index S/C). Using an index S/C threshold of 1.4, the manufacturer reported a sensitivity of 86.4% 7 days after symptom onset and 100% after 14 days, and a specificity of 99.6%, using RT-PCR as the gold standard. These figures were corroborated by a validation study using a set of samples from patients who tested positive for SARS-CoV-2 by RT-PCR and in samples obtained in 2018–2019, thus before the epidemic (sensitivity of 100% 17 days after symptom onset and a specificity of 99.9%) (Bryan et al., 2020 (link)). A further verification study by the National Centre for Microbiology (Spain) used samples obtained before 8 December 2019 and showed a sensitivity of 89.7% in serum samples from RT-PCR-positive patients 14 days after symptom onset and a specificity of 100% (Pollán et al., 2020 (link)).
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5

Serum SCCAg Analysis for Surgery

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Serum samples were taken routinely at the patient’s initial visit before surgery for SCCAg analysis. Serum SCCAg levels were analyzed using an automated chemiluminescence immunoassay (CLIA) system (i2000, Abbott, USA) according to the manufacturer’s instructions. The recommended cutoff level of 1.5 ng/ml was applied. Ten patients had no serum SCCAg data.
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6

Comprehensive Thyroid Function Assessment

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Blood samples were collected, and thyroid function was tested, by evaluating the levels of thyroid stimulating hormone (TSH), total triiodothyronine (TT3), serum total thyroxine (TT4), total triiodothyronine (TT3), free triiodothyronine (FT3) and free T4(FT4). Serum levels of TSH, TT3, TT4, FT3 and FT4 were determined by automated chemiluminescent immunoassays (Abbott i2000, Wiesbaden, Germany). Laboratory reference ranges were as follows: TSH, 0.56–5.91 μIU/ml; TT3, 1.01–2.48 nmol/l; TT4, 69.97–152.52 nmol/l; FT3, 3.28–6.47 pmol/l; FT4, 7.64–16.03 pmol/l. Thyroid dysfunction was defined as a decrease in TSH, FT3 or FT4.
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7

Comprehensive Health Assessment Protocol

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All participants in the initial cohort underwent a general health questionnaire and anthropometric and laboratory testing in Shandong Provincial Qianfoshan Hospital. Body weight and height were measured by standardized procedures when the participants wore light clothes and without shoes. Body mass index (BMI) was calculated as weight (kg) divided by height squared (m2). Blood pressure was measured on the right arm by an automated sphygmomanometer after a 5-min rest.
The related biomarkers, including fasting plasma glucose (FPG), total cholesterol (TC), triglyceride (TG), low-density lipoprotein-cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transpeptidase (GGT), blood urea nitrogen (BUN), serum creatinine (CREA), blood uric acid (BUA), haemoglobin (HB), white blood cell count (WBC) and CEA, were measured by the laboratory specialists using standard clinical and laboratory protocols. CEA was measured by two automatic immunoassay analysers in the hospital: Abbott i2000 (Chicago, USA; the reference of CEA is (0–5) ng/ml) and Johnson Vitros 3600 (Rochester, New York, USA; the reference is (0–3) ng/ml). All the biomarkers were measured in the Center for Health Management of the hospital.
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8

Thyroid Dysfunction in Kidney Transplant

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A prospective single center study in 12 months period included 40 stabile a sample of 80 patients divided into two groups, test and control. In the study group is 40 stable patients with transplanted kidney of which 26 respondents forms a subgroup with duration of hemodialysis to 72 months and 14 patients forms a subgroup with duration of dialysis over 72 months before transplantation. In the control group are 40 patients with normal renal function.
Exclusion criteria were previous thyroid disorders, systemic illnesses, critically ill patients, acute inflammatory diseases.
The values of T3, T4, TSH were measured on the device Abbott Architect i2000. Reference values for TSH are 0.35 to 4.94 mIU/mL. Reference values for T4 are from 63.06 to 150.58 nmol/L, and for T3 are from 0.44 to 0.89 nmol/L. FT4 and FT3 were determined by radioimmunoassay RIA using commercial kits available. The reference values are: FT3 from 2.5 to 5.8 nmol/L, FT4 from 11.5 to 23 pmol/L. Subclinical hypothyroidism is defined by the finding of elevated TSH> 4.4 mmol/L and normal values of T3 and T4 (29 (link)). Clinical hypothyroidism is defined by the finding of TSH >10 mmol/L and a decreased level of T3 and T4 (29 (link)). Low T3 syndrome is defined by finding T3 <0.89 nmol/L, a low T4 syndrome by finding T4 <63.06 nmol/L and high T4 syndrome by findings T4 >150 nmol/L (30 (link)).
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9

Ascites Tumor Marker Assay

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Ascites samples obtained by paracentesis were collected in tubes, and then sent for tumor marker assay. Carcinoembryonic antigen (CEA), cancer antigen CA15-3 and CA19-9 were tested on Abbott i2000 by the chemiluminescence method using manufacture’s chemiluminescent immunoassay reagents (Abbott, Chicago, IL).
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10

Comprehensive Metabolite Analysis in Dried Blood and Urine

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Amino acids, free carnitine, and acyl-carnitines in dried blood spots were analyzed by liquid chromatography-tandem mass spectrometry (API 3200, Triple Quad 4500; Applied Biosystems, CA, USA). The concentrations of the metabolites were calculated automatically using the Chemoview software [2 (link), 28 (link)].
Gas chromatography and mass spectrometry (GC/MS) was performed with GCMS-QP 2010 (Shimadzu Corporation, Kyoto, Japan) to analyze urine organic acids, according to a previously established protocol [28 (link)–30 (link)]. Data were collected using the GC/MS solution software. Plasma tHCY was detected by chemiluminescence immunoassay (Abbott I2000, USA).
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