Press Release
Reply to ADA President's statement
``There is no sound scientific evidence supporting a link
between amalgam fillings and systemic diseases or chronic illness"
From: Murray J. Vimy DMD
Sent: Thursday, July 05, 2001 10:03 AM
Subject: For Immediate Release
CALGARY, CANADA, July 4, 2001 FOR IMMEDIATE RELEASE
The news release by the American Dental Association (ADA) dated June 13,
2001 contains a very significant error. The ADA President Dr. Robert M.
Anderton is reported as saying, ``There is no sound scientific evidence supporting a link
between amalgam fillings and systemic diseases or chronic illness''. Yet, it is
well known in the published, peer-reviewed dental journals
that mercury leaks directly from amalgam into adjacent oral tissues causing
periodontal disease (gum disease).
Critical Fact #1:
In 1957, Zander (JADA, 55:11-15) reported "materials used in restorative
dentistry may be a contributing factor in gingival disease."
Critical Fact #2:
In 1961, App (J Prosth Dent 11:522-532) suggested that there was greater
chronic inflammation around amalgam sites than non-amalgam areas.
Critical fact #3:
In 1964, Trott and Sherkat (J CDA, 30:766-770) showed that the presence of
amalgam correlates with gingival disease. Such disease was not present at
contralateral amalgam-free sites.
Critical fact #4:
In 1969, Sanches Sotres et al (J. Periodo. l40: 543-546) confirmed Trott and
Sherkat findings.
Critical fact #5:
In 1972, Turgeon et al. (J CDA 37:255-256) reported the presence of very
significant erythema around amalgam restorations that was not present at
control non-amalgam sites.
Critical fact #6:
In 1973, Trivedi and Talim (J. Prosth. Dentistry, 29:73-81) demonstrated
that 62.5% of amalgam sites have inflammatory periodontal tissue reaction.
Thus, as early as 1973, a case can be made that the presence of dental
mercury-amalgam results in chronic inflammation and bleeding in the gingival
tissue adjacent to it; in other words, in situ amalgam produced chronic
Gingivitis.
Critical fact #7:
In 1974, Freden et al. (Odontol. Revy, 25: 207-210) showed that gingival
biopsy material from sites not adjacent to amalgam had 1-10 �g mercury/gram
of tissue (mean=3); whereas, gingival biopsy sites near amalgams contained
19-380 �g mercury/gram of tissue (mean=147).
Critical fact #8:
In 1976, Goldschmidt et al (J. Perio. Res., 11:108-115) demonstrated that
amalgam corrosion products were cytotoxic to gingival cells at
concentrations of 10-6; that is, micrograms/gram of tissue.
Critical fact #9:
In 1984, the year of the NIDR/ADA Workshop, Fisher et al (J Oral Rehab,
11:399-405) reported that at amalgam sites alveolar bone loss was very
pronounced and statistically significant as compared to control non-amalgam
sites! In other words, in situ amalgam produces chronic Periodontitis.
This suggests that placing mercury fillings leads to a dentist-induced
disease, periodontal disease, which the same dentists then treat.
This is iatrogenesis.
Thus, for the ADA to conclude ``There is no sound scientific evidence
supporting a link between amalgam fillings and systemic diseases or
chronic illness'' is incorrect. Periodontal disease is one of the most prevalent
chronic diseases in Man, and mercury fillings contribute significantly!
Such statements by ADA spokespersons suggest that the ADA
and its advisors may be knowingly disinforming the public
through the media or they lack an understanding of the scientific research
about mercury release from amalgam published in their own journals.
Murray J. Vimy DMD,
Clinical Associate Professor,
Faculty of Medicine,
University of Calgary.
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