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Iron status determination in individuals with Helicobacter pylori infection: conventional vs. new laboratory biomarkers

  • Dietmar Enko EMAIL logo , Helga Wagner , Gernot Kriegshäuser , Julia Wögerer , Gabriele Halwachs-Baumann , Wolfgang J. Schnedl , Sieglinde Zelzer , Günter Fauler , Harald Mangge , Herrmann Markus and Andreas Meinitzer
Published/Copyright: January 7, 2019

Abstract

Background

Helicobacter pylori has been associated with iron deficiency (ID). This study is aimed at investigating ID with conventional (ferritin, transferrin saturation [TSAT]) and new biomarkers (soluble transferrin receptor [sTfR], sTfR/log ferritin, reticulocyte hemoglobin content [CHr], hepcidin-25) in patients sub-grouped by the presence or absence of H. pylori infection.

Methods

In total, 200 consecutive outpatients, who were referred for the H. pylori13C-urea breath test (13C-UBT), underwent blood testing for ID. Additionally, Thomas-plot (TP)-analyses (sTfR/log ferritin, CHr) were calculated.

Results

Fifty-three and 147 individuals were found with and without H. pylori infection, respectively. Patients with H. pylori infection showed a higher sTfR concentration (p<0.02) and a higher sTfR/log ferritin ratio (p<0.05). Based on a ferritin <30 μg/L and/or a TSAT <20%, 25/53 (47.2%) patients with H. pylori infection and 63/147 (42.9%) without H. pylori infection showed ID. Based on TP-analyses, 10/53 (18.9%) patients with and 17/147 (11.6%) without H. pylori infection were identified with ID. Completed eradication therapy tended to be associated with functional ID.

Conclusions

Helicobacter pylori infection was associated with significantly higher plasma sTfR concentrations and sTfR/log ferritin ratios. Patients with H. pylori eradication therapy were more often detected with functional ID compared to patients without eradication therapy, when using the new biomarkers.


Corresponding author: Dietmar Enko, MD, Institute of Clinical Chemistry and Laboratory Medicine, General Hospital Steyr, Sierningerstr. 170, 4400 Steyr, Austria; and Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria, Phone: +43 50554 66 25307, Fax: +43 50554 66 25304

  1. Author contributions: DE wrote the manuscript. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2018-1182).


Received: 2018-11-03
Accepted: 2018-12-05
Published Online: 2019-01-07
Published in Print: 2019-06-26

©2019 Walter de Gruyter GmbH, Berlin/Boston

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