Evidence map›Paper›PMID 28236367›Full record

ArticleJournal of clinical laboratory analysis2018

Comparison of transferrin isoform analysis by capillary electrophoresis and HPLC for screening congenital disorders of glycosylation.

Mihika B Dave, Alpa J Dherai, Vrajesh P Udani, Anaita U Hegde, Neelu A Desai, Tester F Ashavaid

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Article in Journal of clinical laboratory analysis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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  6. Alcohol Biomarkers in Clinical and Forensic Contexts.Deutsches Arzteblatt international · 2018
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mihika B DaveResearch Department, P.D. Hinduja National Hospital & Medical Research Centre, Mumbai, Maharashtra, India.
Alpa J DheraiResearch Department, P.D. Hinduja National Hospital & Medical Research Centre, Mumbai, Maharashtra, India.ORCID http://orcid.org/0000-0002-5574-3798
Vrajesh P UdaniDepartment of Pediatric Neurology, P.D. Hinduja National Hospital & Medical Research Centre, Mumbai, Maharashtra, India.
Anaita U HegdeJaslok Hospital and Research Centre, Mumbai, Maharashtra, India.
Neelu A DesaiDepartment of Pediatric Neurology, P.D. Hinduja National Hospital & Medical Research Centre, Mumbai, Maharashtra, India.
Tester F AshavaidResearch Department, P.D. Hinduja National Hospital & Medical Research Centre, Mumbai, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransferrin, a major glycoprotein has different isoforms depending on the number of sialic acid residues present on its oligosaccharide chain. Genetic variants of transferrin as well as the primary (CDG) & secondary glycosylation defects lead to an altered transferrin pattern. Isoform analysis methods are based on charge/mass variations. We aimed to compare the performance of commercially available capillary electrophoresis CDT kit for diagnosing congenital disorders of glycosylation with our in-house optimized HPLC method for transferrin isoform analysis.

methodsThe isoform pattern of 30 healthy controls & 50 CDG-suspected patients was determined by CE using a Carbohydrate-Deficient Transferrin kit. The results were compared with in-house HPLC-based assay for transferrin isoforms.

resultsTransferrin isoform pattern for healthy individuals showed a predominant tetrasialo transferrin fraction followed by pentasialo, trisialo, and disialotransferrin. Two of 50 CDG-suspected patients showed the presence of asialylated isoforms. The results were comparable with isoform pattern obtained by HPLC. The commercial controls showed a <20% CV for each isoform. Bland Altman plot showed the difference plot to be within +1.96 with no systemic bias in the test results by HPLC & CE.

conclusionThe CE method is rapid, reproducible and comparable with HPLC and can be used for screening Glycosylation defects.

Indexed as

Chromatography, High Pressure LiquidCongenital Disorders of GlycosylationElectrophoresis, CapillaryFemaleHumansMaleProtein IsoformsTransferrinProtein IsoformsTransferrincapillary electrophoresisCDT kitcongenital disorders of glycosylationHPLCtransferrin isoforms

Identifiers

PMID28236367
PMCPMC6816929

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