Public Defence: Ingrid Marie Hardang

Cand.med. Ingrid Marie Hardang at Institute of Clinical Medicine will be defending the thesis “Iron deficiency biomarkers and hepcidin isoforms in COPD” for the degree of PhD (Philosophiae Doctor).

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Due to copyright issues, an electronic copy of the thesis must be ordered from the faculty. For the faculty to have time to process the order, the order must be received by the faculty at the latest 2 days before the public defence. Orders received later than 2 days before the defence will not be processed. After the public defence, please address any inquiries regarding the thesis to the candidate.

Trial Lecture – time and place

See Trial Lecture.

Adjudication committee

  • First opponent: Professor Anders Blomberg, Umeå University, Sweden
  • Second opponent: Research leader Kjersti Oppen, Vestre Viken Hospital Trust, Norway
  • Third member and chair of the evaluation committee: Associate professor Olav Inge Klingenberg, University of Oslo

Chair of the Defence

Associate Professor Lise Sofie Nissen-Meyer, University of Oslo

Principal Supervisor

Professor II Gunnar Einvik, University of Oslo

Summary

The conclusion from this thesis is that iron deficiency was more prevalent in patients with chronic obstructive pulmonary disease (COPD) than in individuals without COPD, and its prevalence increased with disease severity.

The primary aim of this PhD project was to improve understanding of biomarker-defined iron deficiency in individuals with COPD across different phenotypes. A further aim was to investigate whether isoforms of the iron-regulatory peptide hepcidin could help explain the iron deficiency observed in COPD. In the absence of bone marrow assessment, which is the gold standard for diagnosing iron deficiency, we relied on blood-based iron-related biomarkers.

Three biomarker-based criteria for iron deficiency were applied: a) ferritin below a predefined cutoff (<30 µg/L without inflammation, <100 µg/L with inflammation) b) transferrin saturation <20% c) the combination of a) and b) These criteria were applied in two study populations: 1) 84 stable, hospital-referred COPD patients and 59 elderly individuals randomly drawn from the population registry 2) 1002 ever-smokers invited to a lung cancer screening programme, of whom 233 had COPD

In both populations, the iron deficiency criteria overlapped only partially. Among COPD patients with severe respiratory failure, the estimated prevalence of iron deficiency ranged from about 25% to 70%, depending on the criterion used. However, regardless of definition, the highest prevalence was consistently seen in those with the most severe COPD.

We found no evidence that levels of any hepcidin isoform explained iron deficiency in COPD.

Apart from low ferritin levels having a high positive predictive value for iron deficiency, existing biomarkers of iron deficiency demonstrated unknown diagnostic value in COPD patients.

Additional information

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Published Mar. 3, 2026 9:31 AM - Last modified Mar. 16, 2026 10:38 AM