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Homocysteine and Dementia: An International Consensus Statement

Authors :
Andrew McCaddon
Michael Fenech
Rima Obeid
Irwin H. Rosenberg
A. David Smith
Teodoro Bottiglieri
Babak Hooshmand
Joshua W. Miller
Helga Refsum
Source :
Journal of Alzheimer's Disease
Publication Year :
2018

Abstract

Identification of modifiable risk factors provides a crucial approach to the prevention of dementia. Nutritional or nutrient-dependent risk factors are especially important because dietary modifications or use of dietary supplements may lower the risk factor level. One such risk factor is a raised concentration of the biomarker plasma total homocysteine, which reflects the functional status of three B vitamins (folate, vitamins B12, B6). A group of experts reviewed literature evidence from the last 20 years. We here present a Consensus Statement, based on the Bradford Hill criteria, and conclude that elevated plasma total homocysteine is a modifiable risk factor for development of cognitive decline, dementia, and Alzheimer’s disease in older persons. In a variety of clinical studies, the relative risk of dementia in elderly people for moderately raised homocysteine (within the normal range) ranges from 1.15 to 2.5, and the Population Attributable risk ranges from 4.3 to 31%. Intervention trials in elderly with cognitive impairment show that homocysteine-lowering treatment with B vitamins markedly slows the rate of whole and regional brain atrophy and also slows cognitive decline. The findings are consistent with moderately raised plasma total homocysteine (>11 μmol/L), which is common in the elderly, being one of the causes of age-related cognitive decline and dementia. Thus, the public health significance of raised tHcy in the elderly should not be underestimated, since it is easy, inexpensive, and safe to treat with B vitamins. Further trials are needed to see whether B vitamin treatment will slow, or prevent, conversion to dementia in people at risk of cognitive decline or dementia.

Details

ISSN :
18758908 and 13872877
Volume :
62
Issue :
2
Database :
OpenAIRE
Journal :
Journal of Alzheimer's disease : JAD
Accession number :
edsair.doi.dedup.....a6a97fe49536662e2317443a06ea1456