Abstract
Background. Mercury, or Hg, is a neurotoxin that has been speculated to play a role in the pathogenesis of Alzheimer's disease, or AD. Dental amalgam releases low levels of Hg vapor and is a potential source of Hg for a large segment of the adult population. Methods. The authors studied 68 subjects with AD and 33 control subjects without AD to determine Hg levels in multiple brain regions at autopsy and to ascertain the subjects' dental amalgam status and history. The subjects were from central Kentucky and Elm Grove, Wis. The authors conducted dental amalgam assessments during the lives of the majority of subjects and in some subjects at the time of autopsy only. The authors also determined three dental amalgam index scores - Event (placement, repair or removal of amalgam), Location and Time In Mouth - in addition to the numbers of and surface area of occlusal amalgam restorations. The authors determined Hg levels in multiple brain regions and performed full neuropathologic evaluations to confirm the normal status of the brain or the presence of AD. Results. The authors found no significant association of AD with the number, surface area or history of having dental amalgam restorations. They also found no statistically significant differences in brain Hg level between subjects with AD and control subjects. Conclusions. Hg in dental amalgam restorations does not appear to be a neurotoxic factor in the pathogenesis of AD. The authors found that brain Hg levels are not associated with dental amalgam, either from existing amalgam restorations or according to subjects' dental amalgam restoration history. Clinical Implications. Dental amalgam restorations, regardless of number, occlusal surface area or time, do not relate to brain Hg levels.
Original language | English |
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Pages (from-to) | 191-199 |
Number of pages | 9 |
Journal | Journal of the American Dental Association |
Volume | 130 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1999 |
Bibliographical note
Funding Information:This work was supported by National Institute of Health grants RO1 AG 10664, 1-P01-AG 05119, 5-P50-AG 05144 and RO1 AG 09862.
Funding
This work was supported by National Institute of Health grants RO1 AG 10664, 1-P01-AG 05119, 5-P50-AG 05144 and RO1 AG 09862.
Funders | Funder number |
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National Institutes of Health/National Institute of Environmental Health Sciences | 1-P01-AG 05119, RO1 AG 10664, 5-P50-AG 05144, RO1 AG 09862 |
National Institute on Aging | P01AG005119 |
National Institute on Aging |
ASJC Scopus subject areas
- General Dentistry