Introduction: Patients with Hashimoto’s thyroiditis (HT) may report persistent emotional and cognitive symptoms even when thyroid hormone levels are within the reference range. This study characterized the symptom profile of HT patients with thyroid hormone levels within the reference ranges and examined whether peripheral inflammatory signaling was associated with emotional symptoms independent of thyroid-related factors. Methods: Clinical data were analyzed from 80 patients with HT whose free triiodothyronine and free thyroxine levels were within the reference ranges and who did not have suppressed thyroid-stimulating hormone (TSH). Thyroid-related quality of life was assessed using the Thyroid Patient-Reported Outcome-39 (ThyPRO-39). Serum interleukin-6 (IL-6) and interleukin-17 (IL-17) levels were measured by enzyme-linked immunosorbent assay. Associations between symptom domains, thyroid-related factors, and inflammatory markers were evaluated using multivariable linear regression models with log-transformed cytokine levels, adjusting for age, sex, elevated TSH, current levothyroxine sodium use, and thyroid autoantibodies. Results: The highest ThyPRO-39 scores were observed in tiredness and emotional domains, including emotional susceptibility, anxiety, and depressivity, whereas thyroid-related somatic and social functioning domains were relatively preserved. Neither elevated TSH, current levothyroxine sodium use, nor thyroid autoantibody levels showed significant independent associations with emotional symptom scores. Higher peripheral IL-6 levels were independently associated with increased emotional susceptibility, anxiety, and depressivity after adjustment for thyroid-related factors. No consistent independent associations were observed between IL-17 levels and emotional symptom domains. Conclusion: In HT patients with thyroid hormone levels within the reference ranges, emotional symptoms cannot be fully explained by TSH status, levothyroxine sodium use, or thyroid autoantibody levels. Peripheral IL-6 may be associated with emotional symptom burden beyond classical thyroid-related mechanisms.
Yao et al. (Thu,) studied this question.