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Endocrine Abstracts (2015) 37 GP26.01 | DOI: 10.1530/endoabs.37.GP.26.01

1Clinic for Endocrinology, Diabetes and Diseases of Metabolism, Clinical Centre of Serbia, University of Belgrade, Belgrade, Serbia; 2Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, Leiden, The Netherlands; 3Institute for Gerontology and Palliative Care, Belgrade, Serbia; 4Faculty of Philosophy, University of Belgrade, Belgrade, Serbia; 5Institute of Neurology, Clinical Centre of Serbia, University of Belgrade, Belgrade, Serbia.


Introduction: There is an increasing awareness for intrinsic imperfections of endocrine replacement therapy affecting general well-being in the long-term. For thyroid hormone, many factors affect the variable responses to hormone replacement, like common genetic variations in deiodinase and thyroid hormone transport proteins, and the inability to provide adequate individual combined T4 and T3 therapy. Despite levothyroxine (L-T4) replacement in primary hypothyroidism and restoration of biochemical euthyroidism, many patients have persistent complaints that have anecdotally been associated to high levels of antibodies against TPO (anti-TPO).

Aim of the study: i) To assess quality of life (QoL) in patients with Hashimoto’s thyroiditis (HT) on adequate L-T4 replacement and ii) to explore potential associations with serum TSH and anti-TPO.

Design: Cross-sectional, case–control study.

Patients and controls: One hundred and twenty patients on long-term L-T4 replacement for HT (mean age 54.0±14.0 years, range 21–75 years) and 60 euthyroid control subjects (aged 53.1±12.4), matched for age, gender, and educational level.

Methods: Evaluation of FT4, TSH, and anti-TPO concentrations, and of QoL as measured with the Short Form-36 Health Survey (SF-36) for mental health and vitality in both patients and controls. Patients and controls were subdivided into two age groups: 20–49 years (GR1) and 50–75 years (GR2), with a mean duration of L-T4 replacement of 3.95 and 9.27 years respectively.

Results: FT4 and FT3 levels were not different between patients and controls, but TSH was slightly higher in Hashimoto patients (GR1 3.64±2.74 vs 1.93±1.10, P<0.05 and GR2 3.93±2.84 vs 1.91±0.90, P<0.05). SF-36 scores in the patients were significantly lower for both age groups compared with controls (patients vs controls): dimension A–physical health; GR1: 70.18±15.74 vs 76.54±13.71, P<0.05; GR2: 55.84±20.2 vs 75.1±121.0, P<0.01; SF-36 score GR1: 69.8±16.4 vs 76.4±14.1, P<0.05; GR2: 57.6±21.1 vs 73.7±14.2, P<0.05. In addition, in both groups anti-TPO levels, but not TSH, were associated with SF-36 scores subscale2 r=−0.208, P=0.029; subcale3 (body pain) r=−0.268, P=0.005; subcale4 (general health) r=−0.198, P=0.038; dimension A r=−0.224, P=0.019; and SF-36 score r=−0.191, P=0.046.

Conclusion: Patients on long-term L-T4 replacement for HT have impaired QoL that is associated with higher anti-TPO levels.

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