Effects of lipemia on capillary serum protein electrophoresis in native ultra-lipemic material and intravenous lipid emulsion added sera.

Autor:	Şeneş M; Medical Biochemistry, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye., Alpdemir M; Medical Biochemistry, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye., Kırtıl G; Medical Biochemistry, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye., Öğüş E; Medical Biochemistry, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye., Çolak Samsum E; Medical Biochemistry, Ministry of Health Pursaklar State Hospital, Ankara, Türkiye., Alpdemir MF; Medical Biochemistry, Ankara Bilkent City Hospital, Ankara, Türkiye.
Jazyk:	angličtina
Zdroj:	Clinical chemistry and laboratory medicine [Clin Chem Lab Med] 2022 Dec 30; Vol. 61 (6), pp. 1054-1064. Date of Electronic Publication: 2022 Dec 30 (Print Publication: 2023).
DOI:	10.1515/cclm-2022-0955
Abstrakt:	Objectives: This study aims to investigate the effect of natural ultralipemic material (NULM) and intravenous lipid emulsion (IVLE) on capillary serum protein electrophoresis (SPEP). Methods: NULM material was prepared from leftover patients' lipemic serum sample (triglyceride concentration >2,000 mg/dL) pool by a refrigerated high-speed centrifuge, and IVLE Omegaven lipid emulsion (30%) was used. Serum pools for interference study were prepared from patient samples for which serum protein electrophoresis was studied as Normal SPEP and M Peak SPEP. For both types of lipemia (DULM and IVLE), five pools with triglyceride concentrations of ∼4.52 mmol/L, ∼7.91 mmol/L, ∼14.69 mmol/L, ∼21.47 mmol/L, and ∼28.25 mmol/L were prepared. SPEP was studied in each pool with Sebia Capillarys Minicap. A repeated measure ANOVA test was used to determine the difference between the pools, and interferograms were used to evaluate the interference effect. Results: Interference was not detected in IVLE added Normal SPEP and M Peak SPEP pools, either % or concentrations of fractions. In NULM-added Normal SPEP and M Peak SPEP pools, significant positive interference in albumin % (p=0.002 and p<0.001 respectively) and significant negative interference in gamma% (p<0.001 and p=0.005 respectively) and M protein peak (p=0.002) fractions were detected. However, significant positive interference was seen only for albumin concentration fractions (p<0.001 for both pools). Conclusions: It is vital to use NULM instead of IVLE solutions in lipemia interference studies for all laboratory tests, including CZE SPEP. The fractions concentration values calculated with the total protein concentration should be used for evaluating SPEP results. (© 2022 Walter de Gruyter GmbH, Berlin/Boston.)
Databáze:	MEDLINE
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