Elimination of lipaemic interference by high-speed centrifugation.


Journal

Biochemia medica
ISSN: 1846-7482
Titre abrégé: Biochem Med (Zagreb)
Pays: Croatia
ID NLM: 9610305

Informations de publication

Date de publication:
15 Feb 2023
Historique:
received: 11 07 2022
accepted: 02 10 2022
entrez: 11 1 2023
pubmed: 12 1 2023
medline: 13 1 2023
Statut: ppublish

Résumé

In order to deliver high quality results, detection and elimination of possible analytical interferences, such as lipaemia, is crucial. The aim of this study is to evaluate the efficacy of high-speed centrifugation in eliminating lipaemic interference and to define own lipaemic index (LI) for the studied biochemical analytes. Evaluated analytes were: albumin, alkaline phosphatase, alanine-aminotransferase (ALT), aspartate-aminotransferase (AST), calcium, creatinine, gamma-glutamyltransferase (GGT), glucose, phosphates, total proteins, urea and total bilirubin. Those analytes and LIs have been analysed in duplicate in the Roche Diagnostics-c8000 analyser in samples centrifuged at 3000 rpm/10 minutes in the SL16 (Thermo Scientific, Waltham, USA) centrifuge and according to an own high-speed centrifugation protocol (12,900 rpm/15 minutes) in the MicroCL17R (Thermo Scientific, Waltham, USA) centrifuge. Lipaemia has been measured in each sample. The efficiency of high-speed centrifugation is verified by the Wilcoxon test (P < 0.05). In cases where significant differences are observed, our own LI is calculated. For ALT and AST, it is verified by McNemar test (P < 0.05 There were statistically significant differences in analyte concentration before and after high-speed centrifugation for: albumin, creatinine, GGT, glucose, phosphates, urea and total bilirrubin. Own LI is calculated. McNemar test shows statistically significant diferences in the proportion of delivered results before and after high-speed centrifugation in ALT, AST and creatinine. This study confirms the efficacy of high-speed centrifugation protocol for all the considered analytes, excepting calcium, alkaline phosphatase and total proteins.

Identifiants

pubmed: 36627977
doi: 10.11613/BM.2023.010703
pii: bm-33-1-010703
pmc: PMC9807237
doi:

Substances chimiques

Calcium SY7Q814VUP
Creatinine AYI8EX34EU
Alkaline Phosphatase EC 3.1.3.1
Glucose IY9XDZ35W2
Alanine Transaminase EC 2.6.1.2
Albumins 0
Phosphates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

010703

Informations de copyright

Croatian Society of Medical Biochemistry and Laboratory Medicine.

Déclaration de conflit d'intérêts

Potential conflict of interest None declared.

Références

Ann Lab Med. 2018 Nov;38(6):518-523
pubmed: 30027694
Clin Chim Acta. 2013 Nov 15;426:33-40
pubmed: 23981842
Clin Biochem. 2014 Mar;47(4-5):309-14
pubmed: 24434304
Biochem Med (Zagreb). 2011;21(1):86-92
pubmed: 22141212
Biochem Med (Zagreb). 2014 Feb 15;24(1):57-67
pubmed: 24627715

Auteurs

Gemma Solé-Enrech (G)

Clinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.

Ruth Cano-Corres (R)

Clinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.

Maria Isabel Aparicio-Calvente (MI)

Clinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.

Nino Spataro (N)

Clinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.

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Classifications MeSH