Iron homeostasis during anemia of inflammation: a prospective study of patients with tuberculosis.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
14 10 2021
Historique:
received: 02 01 2021
accepted: 02 04 2021
pubmed: 21 4 2021
medline: 15 12 2021
entrez: 20 4 2021
Statut: ppublish

Résumé

Anemia of inflammation is a hallmark of tuberculosis. Factors controlling iron metabolism during anemia of inflammation and its resolution are uncertain. Whether iron supplements should be given during antituberculosis treatment to support hemoglobin (Hb) recovery is unclear. Before and during treatment of tuberculosis, we assessed iron kinetics, as well as changes in inflammation and iron metabolism indices. In a 26-week prospective study, Tanzanian adults with tuberculosis (N = 18) were studied before treatment and then every 2 weeks during treatment; oral and intravenous iron tracers were administered before treatment and after intensive phase (8/12 weeks) and complete treatment (24 weeks). No iron supplements were given. Before treatment, hepcidin and erythroferrone (ERFE) were greatly elevated, erythrocyte iron utilization was high (∼80%), and iron absorption was negligible (<1%). During treatment, hepcidin and interleukin-6 levels decreased ∼70% after only 2 weeks (P< .001); in contrast, ERFE did not significantly decrease until 8 weeks (P< .05). ERFE and interleukin-6 were the main opposing determinants of hepcidin (P< .05), and greater ERFE was associated with reticulocytosis and Hb repletion (P< .01). Dilution of baseline tracer concentration was 2.6-fold higher during intensive phase treatment (P< .01), indicating enhanced erythropoiesis. After treatment completion, iron absorption increased ∼20-fold (P< .001), and Hb increased ∼25% (P< .001). In tuberculosis-associated anemia of inflammation, our findings suggest that elevated ERFE is unable to suppress hepcidin, and iron absorption is negligible. During treatment, as inflammation resolves, ERFE may remain elevated, contributing to hepcidin suppression and Hb repletion. Iron is well absorbed only after tuberculosis treatment, and supplementation should be reserved for patients remaining anemic after treatment. This trial was registered at www.clinicaltrials.gov as #NCT02176772.

Identifiants

pubmed: 33876222
pii: S0006-4971(21)00881-8
doi: 10.1182/blood.2020010562
doi:

Substances chimiques

Erfe protein, human 0
Hepcidins 0
Peptide Hormones 0
Iron E1UOL152H7

Banques de données

ClinicalTrials.gov
['NCT02176772']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1293-1303

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 by The American Society of Hematology.

Auteurs

Colin I Cercamondi (CI)

Laboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.

Nicole U Stoffel (NU)

Laboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.

Diego Moretti (D)

Laboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.
Fernfachhochschule Schweiz, Brig, Switzerland.

Thomas Zoller (T)

Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin-Berlin Institute of Health, Berlin, Germany.
Department of Infectious Diseases, Respiratory and Critical Care Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Dorine W Swinkels (DW)

Department of Laboratory Medicine, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
Hepcidinanalysis.com, Nijmegen, The Netherlands.

Christophe Zeder (C)

Laboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.

Francis Mhimibra (F)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Jerry Hella (J)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Lukas Fenner (L)

Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland; and.

Michael B Zimmermann (MB)

Laboratory of Human Nutrition, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.
MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.

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Classifications MeSH