The added value of ferritin levels and genetic markers for the prediction of haemoglobin deferral

Author:

Vinkenoog Marieke12ORCID,Toivonen Jarkko3ORCID,van Leeuwen Matthijs2ORCID,Janssen Mart P.1ORCID,Arvas Mikko3ORCID

Affiliation:

1. Donor Medicine Research, Sanquin Research Amsterdam The Netherlands

2. Leiden Institute of Advanced Computer Science Leiden University Leiden The Netherlands

3. Research and Development, Finnish Red Cross Blood Service Helsinki Finland

Abstract

AbstractBackground and ObjectivesOn‐site haemoglobin deferral for blood donors is sometimes necessary for donor health but demotivating for donors and inefficient for the blood bank. Deferral rates could be reduced by accurately predicting donors' haemoglobin status before they visit the blood bank. Although such predictive models have been published, there is ample room for improvement in predictive performance. We aim to assess the added value of ferritin levels or genetic markers as predictor variables in haemoglobin deferral prediction models.Materials and MethodsSupport vector machines with and without this information (the full and reduced model, respectively) are compared in Finland and the Netherlands. Genetic markers are available in the Finnish data and ferritin levels in the Dutch data.ResultsAlthough there is a clear association between haemoglobin deferral and both ferritin levels and several genetic markers, predictive performance increases only marginally with their inclusion as predictors. The recall of deferrals increases from 68.6% to 69.9% with genetic markers and from 79.7% to 80.0% with ferritin levels included. Subgroup analyses show that the added value of these predictors is higher in specific subgroups, for example, for donors with minor alleles on single‐nucleotide polymorphism 17:58358769, recall of deferral increases from 73.3% to 93.3%.ConclusionIncluding ferritin levels or genetic markers in haemoglobin deferral prediction models improves predictive performance. The increase in overall performance is small but may be substantial for specific subgroups. We recommend including this information as predictor variables when available, but not to collect it for this purpose only.

Funder

Stichting Sanquin Bloedvoorziening

Publisher

Wiley

Subject

Hematology,General Medicine

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