Format

Send to

Choose Destination
See comment in PubMed Commons below
Eur J Clin Invest. 2016 May;46(5):434-9. doi: 10.1111/eci.12617. Epub 2016 Apr 15.

Association of a transcobalamin II genetic variant with falsely low results for the holotranscobalamin immunoassay.

Author information

1
Nutristasis Unit (St. Thomas' Hospital), Viapath, London, UK.
2
Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
3
Medical Eye Unit, Guy's and St. Thomas' NHS Foundation Trust, Moorfields Eye Hospital, The National Hospital for Neurology and Neurosurgery, London, UK.
4
School of Medicine, Trinity College Dublin, Dublin, Ireland.

Abstract

BACKGROUND:

The clinical use of holotranscobalamin (holoTC) testing to evaluate vitamin B12 status has increased in recent years. We present two patients (African Caribbean and Indian heritage), in which the holoTC assay indicated severe B12 deficiency (< 5 pmol/L). Additional clinical tests revealed that these patients had normal levels of total vitamin B12 in blood and unremarkable levels of two other markers of vitamin B12 status, homocysteine and methylmalonic acid. We hypothesized that these patients carry a variant in the transcobalamin gene (TCN2) that influences the most widely commercially available holoTC test - Active-B12 (Axis-Shield Diagnostics Ltd).

DESIGN:

Exon sequencing of the TCN2 gene was carried out. Protein characterization included total transcobalamin (TCN2) detection by Western blot, and holoTC by (57) Co-labelled B12 binding followed by size fractionation.

RESULTS:

Exon sequencing of TCN2 revealed both patients were homozygous for the minor allele of rs35838082 (p.R215W). Western blot and chromatographic analyses revealed that the serum of these patients contains intact transcobalamin and that this variant-containing protein binds vitamin B12 . The variant is rare in Caucasians (minor allele frequency (MAF) < 0·01) but more common in South Asians (MAF ~ 0·02) and those of African origin (MAF ~ 0·25).

CONCLUSIONS:

The impeded ability to detect normal levels of holoTC in these two patients may be due to this variant interfering with the detection of holoTC by one or both of the monoclonal antibodies currently employed in the Active-B12 test. Laboratories should be aware of this variant and use confirmatory tests when applicable.

KEYWORDS:

Holotranscobalamin; cobalamin; monoclonal antibody; single nucleotide polymorphism; transcobalamin; vitamin B12

PMID:
26951924
DOI:
10.1111/eci.12617
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Wiley
    Loading ...
    Support Center