Predicting iron absorption from an effervescent iron supplement in obese patients before and after Roux-en-Y gastric bypass: a preliminary study.


Journal

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)
ISSN: 1878-3252
Titre abrégé: J Trace Elem Med Biol
Pays: Germany
ID NLM: 9508274

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 14 01 2018
revised: 03 12 2018
accepted: 05 12 2018
entrez: 9 2 2019
pubmed: 9 2 2019
medline: 25 6 2019
Statut: ppublish

Résumé

Oral iron absorption is hampered in obese and bariatric patients, especially after Roux-en-Y gastric bypass (RYGB). As a result, iron deficiency, which is common in both patient groups, can be difficult to treat by oral supplements, often necessitating a switch to parenteral administration. The aim of this study was to find possible predictors of the extent of absorption of an effervescent iron gluconate oral supplement, which enables to pre-emptively identify those patients in which oral supplementation is likely to fail. The pharmacokinetic properties of 695 mg effervescent iron gluconate (80 mg Fe Low iron status persisted after surgery as there was no significant difference observed in TSAT (17.3 ± 5.2 vs. 20.2 ± 6.6%), ferritin (91.8 ± 68.6 vs. 136.2 ± 176.9 μg/L) and hepcidin concentration (32.0 ± 30.1 vs. 28.3 ± 21.3 ng/mL) after RYGB. The absorption of effervescent iron gluconate was similar pre- and post-RYGB [AUC The iron AUC

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
Oral iron absorption is hampered in obese and bariatric patients, especially after Roux-en-Y gastric bypass (RYGB). As a result, iron deficiency, which is common in both patient groups, can be difficult to treat by oral supplements, often necessitating a switch to parenteral administration. The aim of this study was to find possible predictors of the extent of absorption of an effervescent iron gluconate oral supplement, which enables to pre-emptively identify those patients in which oral supplementation is likely to fail.
METHODS METHODS
The pharmacokinetic properties of 695 mg effervescent iron gluconate (80 mg Fe
RESULTS RESULTS
Low iron status persisted after surgery as there was no significant difference observed in TSAT (17.3 ± 5.2 vs. 20.2 ± 6.6%), ferritin (91.8 ± 68.6 vs. 136.2 ± 176.9 μg/L) and hepcidin concentration (32.0 ± 30.1 vs. 28.3 ± 21.3 ng/mL) after RYGB. The absorption of effervescent iron gluconate was similar pre- and post-RYGB [AUC
CONCLUSIONS CONCLUSIONS
The iron AUC

Identifiants

pubmed: 30732902
pii: S0946-672X(18)30026-9
doi: 10.1016/j.jtemb.2018.12.002
pii:
doi:

Substances chimiques

Ferrous Compounds 0
Tablets 0
ferrous gluconate U1B11I423Z

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

68-73

Informations de copyright

Copyright © 2018 Elsevier GmbH. All rights reserved.

Auteurs

Ina Gesquiere (I)

KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Leuven, Belgium; KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium. Electronic address: ina.gesquiere@kuleuven.be.

Nele Steenackers (N)

KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium. Electronic address: nele.steenackers@kuleuven.be.

Matthias Lannoo (M)

KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium; University Hospitals Leuven/KU Leuven, Department of Abdominal Surgery, Campus Gasthuisberg, Leuven, Belgium. Electronic address: matthias.lannoo@uzleuven.be.

Veerle Foulon (V)

KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Leuven, Belgium. Electronic address: veerle.foulon@kuleuven.be.

Ann Mertens (A)

KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium. Electronic address: ann.mertens@uzleuven.be.

Ann Gils (A)

KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Leuven, Belgium. Electronic address: ann.gils@kuleuven.be.

Jan de Hoon (J)

University Hospitals Leuven/KU Leuven, Center for Clinical Pharmacology, Campus Gasthuisberg, Leuven, Belgium. Electronic address: jan.dehoon@uzleuven.be.

Patrick Augustijns (P)

KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Leuven, Belgium. Electronic address: patrick.augustijns@kuleuven.be.

Christophe Matthys (C)

KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium. Electronic address: christophe.matthys@uzleuven.be.

Bart Van der Schueren (B)

KU Leuven, Clinical and Experimental Endocrinology, and University Hospitals Leuven/KU Leuven, Campus Gasthuisberg, Leuven, Belgium. Electronic address: bart.vanderschueren@uzleuven.be.

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Classifications MeSH