Oral vitamin B12 supplementation in pernicious anemia: a prospective cohort study.

Anemia Atrophic gastritis Pernicious anemia Vitamin B12 Vitamin B12 deficiency

Journal

The American journal of clinical nutrition
ISSN: 1938-3207
Titre abrégé: Am J Clin Nutr
Pays: United States
ID NLM: 0376027

Informations de publication

Date de publication:
24 May 2024
Historique:
received: 10 01 2024
revised: 17 04 2024
accepted: 22 05 2024
medline: 27 5 2024
pubmed: 27 5 2024
entrez: 26 5 2024
Statut: aheadofprint

Résumé

The absorption of vitamin B12 (B12) is hindered in pernicious anemia (PA) due to intrinsic factor deficiency. Traditionally, intramuscular B12 injections were the standard treatment, bypassing the impaired absorption. Although there is potential for oral B12 supplementation through passive enteral absorption, it is not commonly prescribed in PA due to limited studies assessing its efficacy. We aimed to assess the efficacy of oral B12 supplementation in PA. We enrolled participants diagnosed with incident B12 deficiency related to PA. The diagnosis of PA was based on the presence of classical immune gastritis and of anti-intrinsic factor and/or anti-parietal cell antibodies. To evaluate the B12 status, we measured total plasma B12, plasma homocysteine, plasma methylmalonic acid (pMMA), and urinary methylmalonic acid/creatinine ratio. Participants were treated with oral cyanocobalamin at a dosage of 1000 μg/day throughout the study duration. Clinical and biological B12 deficiency-related features were prospectively and systematically assessed over the one-year study duration. We included 26 patients with B12 deficiency revealing PA. Following one month of oral B12 supplementation, 88.5% of patients were no longer deficient in B12, with significant improvement of plasma B12 (407 [297-485] vs 148 [116-213] pmol/L, p<0.0001), plasma homocysteine (13.5 [10.9-29.8] vs 18.6 [13.7-46.8] μmol/L, p<0.0001), and pMMA (0.24 [0.16-0.38] vs 0.56 [0.28-1.09] pmol/L, p<0.0001) levels compared to baseline. The enhancement of these biological parameters persisted throughout the 12-month follow-up, with no patients showing B12 deficiency by the end of the follow-up period. The median time to reverse initial B12 deficiency abnormalities ranged from 1 month for hemolysis to 4 months for mucosal symptoms. Oral supplementation with 1000 μg/day of cyanocobalamin improved B12 deficiency in PA.

Sections du résumé

BACKGROUND BACKGROUND
The absorption of vitamin B12 (B12) is hindered in pernicious anemia (PA) due to intrinsic factor deficiency. Traditionally, intramuscular B12 injections were the standard treatment, bypassing the impaired absorption. Although there is potential for oral B12 supplementation through passive enteral absorption, it is not commonly prescribed in PA due to limited studies assessing its efficacy.
OBJECTIVE OBJECTIVE
We aimed to assess the efficacy of oral B12 supplementation in PA.
METHODS METHODS
We enrolled participants diagnosed with incident B12 deficiency related to PA. The diagnosis of PA was based on the presence of classical immune gastritis and of anti-intrinsic factor and/or anti-parietal cell antibodies. To evaluate the B12 status, we measured total plasma B12, plasma homocysteine, plasma methylmalonic acid (pMMA), and urinary methylmalonic acid/creatinine ratio. Participants were treated with oral cyanocobalamin at a dosage of 1000 μg/day throughout the study duration. Clinical and biological B12 deficiency-related features were prospectively and systematically assessed over the one-year study duration.
RESULTS RESULTS
We included 26 patients with B12 deficiency revealing PA. Following one month of oral B12 supplementation, 88.5% of patients were no longer deficient in B12, with significant improvement of plasma B12 (407 [297-485] vs 148 [116-213] pmol/L, p<0.0001), plasma homocysteine (13.5 [10.9-29.8] vs 18.6 [13.7-46.8] μmol/L, p<0.0001), and pMMA (0.24 [0.16-0.38] vs 0.56 [0.28-1.09] pmol/L, p<0.0001) levels compared to baseline. The enhancement of these biological parameters persisted throughout the 12-month follow-up, with no patients showing B12 deficiency by the end of the follow-up period. The median time to reverse initial B12 deficiency abnormalities ranged from 1 month for hemolysis to 4 months for mucosal symptoms.
CONCLUSIONS CONCLUSIONS
Oral supplementation with 1000 μg/day of cyanocobalamin improved B12 deficiency in PA.

Identifiants

pubmed: 38797248
pii: S0002-9165(24)00484-2
doi: 10.1016/j.ajcnut.2024.05.019
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest ☒ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. None.

Auteurs

Valentin Lacombe (V)

Department of Internal Medicine and Clinical Immunology, University Hospital, Angers, France; MitoVasc unit, Inserm U1083, CNRS UMR6015, Angers University, France.

Emeline Vinatier (E)

Laboratory of Immunology, University Hospital, Angers, France.

Guillaume Roquin (G)

Department of Gastroenterology, University Hospital, Angers, France.

Marie-Christine Copin (MC)

Department of Pathology, University Hospital, Angers, France.

Estelle Delattre (E)

Department of Internal Medicine and Clinical Immunology, University Hospital, Angers, France.

Sami Hammi (S)

Department of Internal Medicine and Clinical Immunology, University Hospital, Angers, France.

Christian Lavigne (C)

Department of Internal Medicine and Clinical Immunology, University Hospital, Angers, France.

Cédric Annweiler (C)

Department of Geriatric Medicine and Memory Clinic, University Hospital, Angers, France.

Odile Blanchet (O)

Centre de Ressources Biologiques, BB-0033-00038, University Hospital, Angers, France.

Juan Manuel Chao de la Barca (JM)

MitoVasc unit, Inserm U1083, CNRS UMR6015, Angers University, France; Laboratory of Biochemistry and Molecular Biology, University Hospital, Angers, France.

Pascal Reynier (P)

MitoVasc unit, Inserm U1083, CNRS UMR6015, Angers University, France; Laboratory of Biochemistry and Molecular Biology, University Hospital, Angers, France.

Geoffrey Urbanski (G)

Department of Internal Medicine and Clinical Immunology, University Hospital, Angers, France; MitoVasc unit, Inserm U1083, CNRS UMR6015, Angers University, France; Department of Orofacial Sciences, University of California, San Francisco, USA; Department of Immunology and Allergology, University Hospital, Geneva, Switzerland. Electronic address: urbanskigeoffrey@gmail.com.

Classifications MeSH