TY - JOUR
T1 - A randomized-controlled, double-blind study of the impact of selenium supplementation on thyroid autoimmunity and inflammation with focus on the GPx1 genotypes
AU - De Farias, C. R.
AU - Cardoso, B. R.
AU - De Oliveira, G. M.B.
AU - De Mello Guazzelli, I. C.
AU - Catarino, R. M.
AU - Chammas, M. C.
AU - Cozzolino, S. M.F.
AU - Knobel, M.
PY - 2015/10/23
Y1 - 2015/10/23
N2 - Purpose: To analyze the impact of selenium supplementation on serum antiTPO levels and thyroid echogenicity in patients with CAT, evaluating the response in subgroups with different GPx1 genotypes. Methods: CAT patients (n = 55) with positive antiTPO were randomized to selenomethionine (SeMet) 200 μg daily (n = 28) or placebo (n = 27) for 3 months. Assessments included GPx1 genotyping at baseline and serum levels of plasma selenium, erythrocyte GPx1 activity, antiTPO and thyroid echogenicity at baseline, and 3 and 6 months. Results: In the SeMet group, the increase in plasma levels of selenium and erythrocyte GPx1 activity was similar among patients with different GPx1 genotypes. In the overall cohort, patients randomized to SeMet showed a 5 % decrease in antiTPO levels at 3 months (p = non-significant) and 20 % at 6 months (p < 0.001 versus 3 months). In contrast, patients in the placebo group did not show significant changes in antiTPO levels at any time point. Subgroup analysis showed that patients with different GPx1 genotypes presented comparable responses in antiTPO levels and echogenicity index to SeMet. Conclusions: Selenium supplementation decreased serum antiTPO levels in CAT patients, with similar response among patients with different GPx1 genotypes.
AB - Purpose: To analyze the impact of selenium supplementation on serum antiTPO levels and thyroid echogenicity in patients with CAT, evaluating the response in subgroups with different GPx1 genotypes. Methods: CAT patients (n = 55) with positive antiTPO were randomized to selenomethionine (SeMet) 200 μg daily (n = 28) or placebo (n = 27) for 3 months. Assessments included GPx1 genotyping at baseline and serum levels of plasma selenium, erythrocyte GPx1 activity, antiTPO and thyroid echogenicity at baseline, and 3 and 6 months. Results: In the SeMet group, the increase in plasma levels of selenium and erythrocyte GPx1 activity was similar among patients with different GPx1 genotypes. In the overall cohort, patients randomized to SeMet showed a 5 % decrease in antiTPO levels at 3 months (p = non-significant) and 20 % at 6 months (p < 0.001 versus 3 months). In contrast, patients in the placebo group did not show significant changes in antiTPO levels at any time point. Subgroup analysis showed that patients with different GPx1 genotypes presented comparable responses in antiTPO levels and echogenicity index to SeMet. Conclusions: Selenium supplementation decreased serum antiTPO levels in CAT patients, with similar response among patients with different GPx1 genotypes.
KW - Autoimmunity
KW - Genetic
KW - Glutathione peroxidase GPx1
KW - Polymorphism
KW - Selenium
KW - Thyroid gland
UR - http://www.scopus.com/inward/record.url?scp=84942090752&partnerID=8YFLogxK
U2 - 10.1007/s40618-015-0285-8
DO - 10.1007/s40618-015-0285-8
M3 - Article
C2 - 25894865
AN - SCOPUS:84942090752
SN - 0391-4097
VL - 38
SP - 1065
EP - 1074
JO - Journal of Endocrinological Investigation
JF - Journal of Endocrinological Investigation
IS - 10
ER -
