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Thyroid antibodies and depression: Is the relationship overstated?
Zhigang Tian1, Bo Wang2, Li Chen3
1Department of Interventional Therapy, Tianjin Cancer Hospital Airport Hospital, Tianjin, China.
Journal of Psychiatric Research
|August 12, 2025
Summary
Thyroid autoantibodies (TPOAb/TgAb) were not linked to depression symptoms in euthyroid adults. Lower normal FT3 levels showed a modest inverse association with depressive symptoms, warranting further study.
Area of Science:
- Endocrinology
- Psychiatry
- Immunology
Background:
- Depression is frequently linked to Hashimoto's thyroiditis (HT).
- Thyroid antibodies are increasingly implicated in the pathophysiology of depression.
- This study investigates the association between thyroid antibodies and depressive symptoms.
Purpose of the Study:
- To examine the relationship between thyroid autoantibodies and depressive symptoms in euthyroid adults.
- To determine if thyroid peroxidase antibodies (TPOAb) or thyroglobulin antibodies (TgAb) are associated with depression severity.
Main Methods:
- Utilized data from 2897 euthyroid adults in the U.S. National Health and Nutrition Examination Survey (NHANES) 2007-2012.
- Classified participants based on thyroid antibody status (TPOAb/TgAb).
- Employed survey-weighted linear regression and propensity score matching (PSM) to analyze associations with depressive symptoms (PHQ-9 scores).
Main Results:
- No significant differences in PHQ-9 depression scores were found between antibody-positive individuals and controls.
- Neither TPOAb nor TgAb positivity showed a significant association with depressive symptoms in unmatched or PSM analyses.
- Lower free T3 (FT3) levels within the normal range were inversely associated with PHQ-9 scores (β = -0.758, P = 0.01).
Conclusions:
- Thyroid autoantibody positivity (TPOAb, TgAb) is not significantly associated with depressive symptoms in euthyroid individuals.
- The observed inverse association between FT3 levels and depressive symptoms suggests a potential, albeit modest, relationship that requires further clinical investigation.
- Findings are limited by the cross-sectional design, representing single-time-point measurements.
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