Persistent elevation of plasma vitamin B12 is strongly associated with solid cancer.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
25 06 2021
Historique:
received: 09 02 2021
accepted: 15 06 2021
entrez: 26 6 2021
pubmed: 27 6 2021
medline: 4 11 2021
Statut: epublish

Résumé

Elevated plasma vitamin B12 has been associated with solid cancers, based on a single B12 measurement. We evaluated the incidence of solid cancers following B12 measurement in patients with persistent elevated B12, compared to patients without elevated B12 and to patients with non-persistent elevated B12. The study population included patients with at least two plasma B12 measurements without already known elevated-B12-related causes. Patients with elevated plasma B12 (≥ 1000 ng/L) at first measurement (n = 344) were matched for age and sex with patients having 2 normal B12 measurements (< 1000 ng/L) (NN group, n = 344). The patients with elevated plasma B12 at first measurement were split into 2 groups, according to the presence (EE group, n = 144) or the absence (EN group, n = 200) of persistent elevated plasma B12 at second measurement. We compared the cancer-free survival during 60 months between the groups after adjustment for the other elevated-B12-related causes in a survival competing risk model. Compared to the NN group, a persistent elevated plasma B12 ≥ 1000 ng/mL was strongly associated with the occurrence of solid cancer (HR 5.90 [95% CI 2.79-12.45], p < 0.001), contrary to non-persistent plasma B12 elevation (p = 0.29). These results could help to select patients in whom the screening for solid cancers would be of interest.

Identifiants

pubmed: 34172805
doi: 10.1038/s41598-021-92945-y
pii: 10.1038/s41598-021-92945-y
pmc: PMC8233305
doi:

Substances chimiques

Vitamin B 12 P6YC3EG204

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

13361

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Auteurs

Valentin Lacombe (V)

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

Floris Chabrun (F)

Department of Biochemistry and Genetics, Angers University Hospital, Angers, France.

Carole Lacout (C)

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

Alaa Ghali (A)

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

Olivier Capitain (O)

Ouest Institute of Cancerology, Angers, France.

Anne Patsouris (A)

Ouest Institute of Cancerology, Angers, France.

Christian Lavigne (C)

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

Geoffrey Urbanski (G)

Department of Internal Medicine and Clinical Immunology, Angers University Hospital, Angers, France. urbanskigeoffrey@gmail.com.
Department of Internal Medicine and Clinical Immunology, Angers University Hospital, 4 rue Larrey, 49000, Angers, France. urbanskigeoffrey@gmail.com.

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Classifications MeSH