Intravenous Iron Replacement Improves Exercise Tolerance in COPD: A Single-Blind Randomized Trial.
Anemia, Iron-Deficiency
/ drug therapy
Exercise Tolerance
Ferric Compounds
Ferritins
/ therapeutic use
Humans
Iron
/ therapeutic use
Iron Deficiencies
Maltose
/ analogs & derivatives
Pulmonary Disease, Chronic Obstructive
/ complications
Quality of Life
Single-Blind Method
Transferrins
/ therapeutic use
Treatment Outcome
Aerobic capacity
Chronic obstructive pulmonary disease
Exercise limitation
Intravenous iron
Non-anaemic iron deficiency
Quality of life
Journal
Archivos de bronconeumologia
ISSN: 1579-2129
Titre abrégé: Arch Bronconeumol
Pays: Spain
ID NLM: 0354720
Informations de publication
Date de publication:
Oct 2022
Oct 2022
Historique:
received:
11
03
2021
revised:
25
07
2021
accepted:
08
08
2021
pubmed:
22
3
2022
medline:
7
10
2022
entrez:
21
3
2022
Statut:
ppublish
Résumé
Iron deficiency affects exercise capacity because of the critical role iron plays in the optimal functioning of skeletal muscle metabolism. We hypothesized that intravenous iron may improve exercise tolerance, quality of life (QoL), and daily physical activity (DPA) in patients with chronic obstructive pulmonary disease (COPD). This was a placebo-controlled, single-blind, parallel-group, randomized clinical trial. Iron deficiency was defined as a ferritin level<100ng/mL or a ferritin level between 100 and 299ng/mL with a transferrin saturation<20%, with or without mild anaemia. Patients were randomized at a 2:1 ratio to receive intravenous ferric carboxymaltose or placebo. The primary objective was to investigate whether intravenous iron replacement improved endurance time from baseline by at least 33%. The secondary objectives were to evaluate impact on QoL using the COPD Assessment Test (CAT) and on DPA by accelerometry. We included 66 patients, 44 (66.7%) in the intervention group and 22 (33.3%) in the placebo group. Among patients receiving ferric carboxymaltose, 23 (52.3%) achieved the primary endpoint compared to 4 (18.2%) in the placebo group [p=0.009; relative risk 3.12, (95% CI, 1.19-8.12)]. CAT score decreased -3 (-6.0-1.3) points from baseline in the intervention group (p=0.007), in contrast to placebo group [-1 (-4.0-2.3) points, p=0.236] with no differences in DPA and adverse events in both groups. Iron replacement improved exercise capacity and QoL in stable COPD patients with iron deficiency. The treatment was well tolerated. EudraCT 2016-001238-89.
Identifiants
pubmed: 35312562
pii: S0300-2896(21)00229-5
doi: 10.1016/j.arbres.2021.08.011
pii:
doi:
Substances chimiques
Ferric Compounds
0
Transferrins
0
ferric carboxymaltose
6897GXD6OE
Maltose
69-79-4
Ferritins
9007-73-2
Iron
E1UOL152H7
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
spa
Sous-ensembles de citation
IM
Pagination
689-698Informations de copyright
Copyright © 2021 SEPAR. Published by Elsevier España, S.L.U. All rights reserved.