Abstract | OBJECTIVES: SUBJECTS: DESIGN AND INTERVENTION: In a 2 x 2 x 2 factorial design trial, 149 people at high-risk of dementia were randomized to receive either low-dose aspirin (81 mg) or placebo; and folic acid (2 mg) plus vitamin B12 (1 mg) or placebo; and vitamins E (500 mg) plus C (200 mg) or placebo. Participants were seen twice before and once after 12 weeks of treatment. MAIN OUTCOME MEASURES: At each visit, participants had their cognitive function assessed and had blood collected for homocysteine, folate and vitamin B12 determination and urine collected for markers of platelet activation (11-dehydro-thromboxane B2) and reactive oxygen species (8-epi-PGF2 alpha). RESULTS: CONCLUSIONS:
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Authors | Robert Clarke, Georgina Harrison, Sue Richards, Vital Trial Collaborative Group |
Journal | Journal of internal medicine
(J Intern Med)
Vol. 254
Issue 1
Pg. 67-75
(Jul 2003)
ISSN: 0954-6820 [Print] England |
PMID | 12823643
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Isoprostanes
- Platelet Aggregation Inhibitors
- Thromboxanes
- Vitamins
- Homocysteine
- Folic Acid
- Vitamin B 12
- Aspirin
- Riboflavin
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Topics |
- Aged
- Aged, 80 and over
- Aspirin
(therapeutic use)
- Cognition Disorders
(prevention & control)
- Dementia
(prevention & control)
- Female
- Folic Acid
(blood)
- Follow-Up Studies
- Homocysteine
(blood)
- Humans
- Isoprostanes
(blood)
- Male
- Middle Aged
- Oxidative Stress
- Platelet Activation
(drug effects)
- Platelet Aggregation Inhibitors
(therapeutic use)
- Riboflavin
(therapeutic use)
- Thromboxanes
(blood)
- Vitamin B 12
(therapeutic use)
- Vitamins
(therapeutic use)
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