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Endocrine Abstracts (2015) 37 EP927 | DOI: 10.1530/endoabs.37.EP927

University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.


Introduction: Despite adequate treatment with LT4 monotherapy, many patients with primary hypothyroidism still report complaints, as this treatment can not exactly imitate the endogenous homeostasis. We examined whether the different domains of HR-QOL were affected by the existence of a thyroid disorder and use of LT4 substitution, and whether a lower ratio of free triiodothyronine (fT3)–free thyroxine (fT4) could predict lower HR-QOL.

Methods: A total of 16 631 participants from the population-based LifeLines Cohort Study, of Western European descent and with normal TSH values (0.4–4.5 mU/l), were evaluated; 368 of them used LT4 monotherapy. TSH, fT4 and fT3) were measured with electrochemiluminescent immunoassay on the Roche Modular E170 Analyzer. HR-QOL was assessed using the Short Form-36 questionnaire.

Results: Mean (±S.D.) age was 51±13 years and BMI 26.9±4.7 kg/m2 in the LT4 users, vs 43±13 years and 25.5±3.8 kg/m2 in the non-users; 90% of LT4 users were females. We observed considerably higher fT4 and lower fT3 levels in LT4 users, with the fT3/fT4-ratio being 25% lower in LT4 users, despite similar TSH levels in both groups. 50% of LT4 users had a fT3/fT4-ratio which was below the 2.5th percentile of euthyroid individuals. LT4 users reported poorer HR-QOL, the largest reduction was observed in physical functioning, bodily pain, general health and vitality. In the non-users, those in the lowest tertile of the fT3/fT4-ratio reported a significantly lower HR-QOL in the domains physical functioning, bodily pain, and general health compared to participants in the middle and highest tertile.

Conclusion: Patients treated with LT4 monotherapy for primary hypothyroidism report low HR-QOL. In subjects not using LT4, a lower fT3/fT4-ratio was associated with more impairments in HR-QOL.

Disclosure: This work was supported by NCHA, Netherlands Consortium for Healthy Ageing, Bio-SHaRE-EU, Biobank Standardisation and Harmonisation for research excellence in the European Union. Bioresource research impact factor BRIF4568.

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