Abstract
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Objectives To see if the first degree relatives of the children with autoimmune thyroid disease (AITD) may have clinical or sub-clinical thyroid abnormalities
Methods In this cross-sectional study, we studied 50 first-degree relatives of 50 children with proven AITD for the evidence of any abnormal thyroid function
Results Three study subjects (6%) were found to have overt hypothyroidism and 1 had asymptomatic goiter on examination. None was found to have features of hyperthyroidism. TPO-positive subjects had significantly low mean T3 levels (1.2 ±0.4 ng/mL; p=0.005) and high TSH (23.01±42.5 µIU/mL; p=0.0001) when compared with the corresponding levels (T3=1.63± 0.4ng/mL & TSH= 5.5 ±16.6 µIU/mL) in the TPO negative subjects. A significant proportion of the patients (67%) with TPO positivity were found to have raised TSH levels. TPO positivity was found to have 100% correlation with manifestation of hypothyroidism in mothers and sisters. TG antibodies were positive in 32 (64%) subjects predominantly in fathers (77%). TG positivity was found to have poor correlation with any clinical or biochemical thyroid abnormality. Both antibody positivity was found in 5 (10%) subjects (22% in fathers only) and these subjects were found to have low mean T3 (1.6± 0.4ng/mL; p=0.005) and high mean TSH levels (36.5± 5.6 µIU/mL; p=0.011) when compared with the anti-body negative individuals.
Conclusions Thyroid dysfunction can be detected in a significant proportion of first degree relatives of AITD children and may represent an initial phase of the disease which need to followed closely
- © 2009 by Society of Nuclear Medicine