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Clinical Trials/NCT00111267
NCT00111267CompletedNot Applicable

The Effect of Oral Vitamin B12 Supplementation on Cognitive Performance in Elderly People: the Brain12 Study

Wageningen University1 site in 1 country165 target enrollmentStarted: May 1, 2003Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
165
Locations
1
Primary Endpoint
Cognitive performance in the domains of attention, concentration, memory, executive function, speed

Study Overview

Brief Summary

The purpose of this trial is to study the effects of oral vitamin B12 supplementation and vitamin B12 combined with folic acid supplementation on cognitive performance for 24 weeks in elderly people with mild vitamin B12 deficiency.

Detailed Description

Mild vitamin B12 deficiency is highly prevalent in old age. Reasons for this high prevalence are not fully understood, but include atrophic gastritis and bacterial overgrowth which affect the absorption (active) of food-bound vitamin B12. In contrast, the ability to absorb crystalline vitamin B12 (e.g. the form found in fortified foods or vitamin pills) remains intact in old age. In both healthy and cognitively impaired elderly people, associations between vitamin B12 status and cognitive performance have been observed, and the follow-up of geriatric patients suggests effects of parenteral treatment in early cognitive impairment.

We investigated whether daily oral supplementation with 1,000 μg vitamin B12 or 1,000 μg vitamin B12 combined with 400 μg folate for 24 weeks improves cognitive performance in people over 70 years with vitamin B12 deficiency.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double

Eligibility Criteria

Ages
70 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Mild vitamin B12 deficiency:
  • •Low plasma vitamin B12 concentration (100 < B12 < 300 pmol/L)
  • •Elevated methylmalonic acid (MMA) concentration (> 0.32 umol/L)
  • •Creatinine concentration < 120 umol/L

Exclusion Criteria

  • •Severe cognitive impairment
  • •Gastrointestinal surgery or diseases
  • •Use of vitamin B12 injections or supplements containing > 25 ug vitamin B12 and/or 200 ug folic acid
  • •< 90% compliance during a 2 week placebo run in period
  • •No written informed consent
  • •Participation in other research studies

Outcomes

Primary Outcomes

Cognitive performance in the domains of attention, concentration, memory, executive function, speed

Secondary Outcomes

  • Blood biochemistry including vitamin B12, methylmalonic acid, holotranscobalamin, homocysteine, and red blood cell folate

Investigators

Sponsor Class
Other

Study Sites (1)

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