martes, 19 de noviembre de 2013

Elevated Plasma Vitamin B12 Levels as a Marker for Cancer: A Population-Based Cohort Study

Elevated Plasma Vitamin B12 Levels as a Marker for Cancer: A Population-Based Cohort Study

Elevated Plasma Vitamin B12 Levels as a Marker for Cancer: A Population-Based Cohort Study

  1. Henrik Toft Sørensen
+ Author Affiliations
  1. Affiliations of authors: Department of Clinical Epidemiology (JFBA, LP, HTS) and Department of Clinical Biochemistry (JFBA, EN), Aarhus University Hospital, Aarhus, Denmark.
  1. Correspondence to: JFB Arendt, BSc, Department of Clinical Epidemiology, Aarhus University Hospital, Olof Palmes Allé 43–45, DK-8200 Aarhus, Denmark (e-mail: johan.frederik.berg.arendt@sun.au.dk).
  • Received February 6, 2013.
  • Revision received September 22, 2013.
  • Accepted September 30, 2013.

Abstract

Background A substantial proportion of patients referred for plasma vitamin B12 (cobalamin [Cbl]) measurement present with high Cbl levels, which have been reported in patients with different cancer types. However, the cancer risk among patients with newly diagnosed high Cbl levels has not been adequately examined.
Methods We conducted this cohort study using population-based Danish medical registries. Patients referred for Cbl measurement with levels greater than the lower reference limit (≥200 pmol/L) were identified from the population of Northern Denmark during the period of 1998 to 2009 using a database of laboratory test results covering the entire population. Data on cancer incidence (follow-up 1998–2010), Cbl treatment, and prior diagnoses were obtained from medical registries. Patients receiving Cbl treatment were excluded. Cancer risks were calculated as standardized incidence ratios (SIRs) with 95% confidence intervals (CIs), stratified by plasma Cbl levels. All statistical tests were two-sided.
Results We identified 333 667 persons without prevalent cancer and not receiving Cbl treatment. Six percent had Cbl levels greater than the upper reference limit (≥601 pmol/L). Cancer risk increased with higher Cbl levels and was highest during the first year of follow-up (Cbl 601–800 pmol/L: SIR = 3.44, 95% CI = 3.14 to 3.76; Cbl >800 pmol/L: SIR = 6.27, 95% CI = 5.70 to 6.88; both P < .001). The risks were particularly elevated for hematological and smoking- and alcohol-related cancers for persons with high Cbl levels.
Conclusions High Cbl levels were associated with the risk of subsequently diagnosed cancer, mostly within the first year of follow-up. This may have clinical implications for the interpretation of high Cbl levels.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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