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Removal of dental amalgam decreases anti-TPO and anti-Tg autoantibodies inautoimmune thyroiditis

 

 

 

Neuro Endocrinol Lett. 2006 Jun 28;27(Suppl1) [Epub ahead of print]

 

Removal of dental amalgam decreases anti-TPO and anti-Tg autoantibodies in patients with autoimmune thyroiditis.

 

Sterzl I, Prochazkova J, Hrda P, Matucha P, Bartova J, Stejskal VD.

 

The Institute of Immunology and Microbiology, 1st Medical Faculty, Charles University, and General Faculty Hospital, Prague, Czech Republic. This email address is being protected from spambots. You need JavaScript enabled to view it..

 

OBJECTIVES: The impact of dental amalgam removal on the levels of anti- thyroid peroxidase (anti-TPO) and anti-thyroglobulin (anti-Tg) antibodies was studied in patients with autoimmune thyroiditis (AT) with and without mercury allergy. METHODS: Thirty-nine patients with AT were tested by an optimized lymphocyte proliferation test, MELISA(R) for allergy (hypersensitivity) to inorganic mercury. Patients were divided into two groups: Group I (n = 12) with no hypersensitivity to mercury and Group II (n = 27) with hypersensitivity to mercury. Amalgam fillings were removed from the oral cavities of 15 patients with hyperensitivity to mercury (Group IIA) and left in place in the remaining 12 patients (Group IIB). The laboratory markers of AT, anti-TPO and anti-Tg autoantibodies were determined in all groups at the beginning of the study and six months later. RESULTS: Compared to levels at the beginning of the study, only patients with mercury hypersensitivity who underwent amalgam replacement (Group IIA) showed a significant decrease in the levels of both anti-Tg (p=0.001) and anti-TPO (p=0.0007) autoantibodies. The levels of autoantibodies in patients with or without mercury hypersensitivity (Group I and Group IIB) who did not replace amalgam did not change. CONCLUSION: Removal of mercury-containing dental amalgam in patients with mercury hypersensitivity may contribute to successful treatment of autoimmune thyroiditis.

 

PMID: 16804512 [PubMed - as supplied by publisher]

 


 

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