Biomarkers of erythropoiesis response to intravenous iron in a crossover pilot study in unexplained anemia of the elderly.


Journal

Hematology (Amsterdam, Netherlands)
ISSN: 1607-8454
Titre abrégé: Hematology
Pays: England
ID NLM: 9708388

Informations de publication

Date de publication:
Dec 2023
Historique:
pmc-release: 01 12 2024
medline: 1 5 2023
pubmed: 28 4 2023
entrez: 28 4 2023
Statut: ppublish

Résumé

Anemia is common in older adults, but often unexplained. Previously, we conducted a randomized, controlled trial of intravenous (IV) iron sucrose to study its impact on the 6-minute walk test and hemoglobin in older adults with unexplained anemia and ferritin levels of 20-200 ng/mL. In this report, we present for the first time the response of hemoglobin, as well as the dynamic response of biomarkers of erythropoiesis and iron indices, in a pooled analysis of the initially IV iron-treated group of 9 subjects and the subsequently IV iron treated 10 subjects from the delayed treatment group. We hypothesized that there would be a reproducible hemoglobin response from IV iron, and that iron indices and erythropoietic markers would reflect appropriate iron loading and reduced erythropoietic stress. To investigate the biochemical response of anemia to IV iron, we studied the dynamics of soluble transferrin receptor (STfR), hepcidin, erythropoietin (EPO), and iron indices over 12 weeks after treatment. In total, all 19 treated subjects were evaluable: 9 from initial treatment and 10 after cross-over. Hemoglobin rose from 11.0 to 11.7 g/dL, 12 weeks after initiating IV iron treatment of 1000 mg divided weekly over 5 weeks. We found early changes of iron loading after 1-2 IV iron dose: serum iron increased by 184 mcg/dL from a baseline of 66 mcg/dL, ferritin by 184 ng/mL from 68 ng/mL, and hepcidin by 7.49 ng/mL from 19.2 ng/mL, while STfR and serum EPO declined by 0.55 mg/L and 3.5 mU/mL from 19.2 ng/mL and 14 mU/mL, respectively. The erythroid response and evidence of enhanced iron trafficking are consistent with the hypothesis that IV iron overcomes iron deficient or iron-restricted erythropoiesis. These data provide new insight that iron-restricted erythropoiesis is a potential and targetable mechanism for patients diagnosed with unexplained anemia of the elderly and offers support for larger prospective trials of IV iron among anemic older adults of low to normal ferritin.

Identifiants

pubmed: 37114660
doi: 10.1080/16078454.2023.2204613
pmc: PMC10281558
mid: NIHMS1897279
doi:

Substances chimiques

Iron E1UOL152H7
Hepcidins 0
Ferritins 9007-73-2
Erythropoietin 11096-26-7
Receptors, Transferrin 0
Hemoglobins 0
Biomarkers 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-8

Subventions

Organisme : NIA NIH HHS
ID : U01 AG034661
Pays : United States

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Auteurs

Justin J Yoo (JJ)

Duke University School of Medicine, Durham, NC, USA.

Harvey J Cohen (HJ)

Center for the Study of Aging, Duke University School of Medicine, Durham, NC, USA.

Andrew S Artz (AS)

Department of Hematology, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.

Elizabeth Price (E)

Division of Hematology, Stanford University Medical Center, Palo Alto, NC, USA.

Jeffrey A Fill (JA)

Eli Lilly and Co, Indianapolis, IN, USA.

Josef Prchal (J)

University of Utah School of Medicine, Salt Lake City, UT, USA.

Shelly Sapp (S)

Duke University School of Medicine, Clinical Research Institute, Durham, NC, USA.

Huiman Barnhart (H)

Duke University School of Medicine, Clinical Research Institute, Durham, NC, USA.
Duke University School of Medicine, Durham, NC, USA.

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Classifications MeSH