Sclerostin and Bone Metabolism Markers in Hyperthyroidism before Treatment and Interrelations between Them

  • İlker Sarıtekin Bülent Ecevit University faculty of Medicine department of Biochemistry
  • Şerefden Acikgoz Bülent Ecevit University Faculty of Medicine Department of Biochemistry
  • Taner Bayraktaroğlu Bülent Ecevit University Faculty of Medicine Department of Endocrine and Metabolism
  • Fatih Kuzu Bülent Ecevit University Faculty of Medicine Department of Endocrine and Metabolism
  • Murat Can Bülent Ecevit University Faculty of Medicine Department of Biochemistry
  • Berrak Güven Bülent Ecevit University Faculty of Medicine Department of Biochemistry
  • Görkem Mungan Bülent Ecevit University Faculty of Medicine Department of Biochemistry
  • Çağatay Büyükuysal Bülent Ecevit University Faculty of Medicine Department of Biostatistics
  • Selda Sarıkaya Bülent Ecevit University Faculty of Medicine Department of Physical Medicine and Rehabilitation
Keywords: hyperthyroidism, sclerostin, bone metabolism markers


       Sclerostin is a glycoprotein that is produced by osteocytes and reduces the formation of bones by inhibiting Wnt signal pathway. Thyroid hormones are related with Wnt signal pathway and it has been reported that the increasing thyroid hormones in hyperthyroidism fasten the epiphysis maturation in childhood, increase the risk of bone fractures by stimulating the bone loss in adults.

       The aim of this study is examining the sclerostin serum levels, the relation between sclerostin and thyroid hormones and the biochemical markers of bone metabolism  in patients with hyperthyroidism whose treatments have not started yet.

       No difference was found in the serum sclerostin levels between the hyperthyroidism group and the control group (p=0.452). The serum osteocalcin levels and 24-hour urinary phosphorus excretion were found to be higher in the hyperthyroid group than the control group (p<0.001, p=0.009). A positive correlation (p<0.001) was determined between the sclerostin and bone Alkaline phosphatase levels; a negative correlation (p<0.05) between the osteocalcin and thyroid stimulating hormone (TSH); a positive correlation (p<0.001, p<0.001) between the osteocalcin and  thyroid hormones (FT3 , FT4); and a positive correlation (p<0.001) between the deoxypyridinoline and hydroxyproline. No correlation was determined between sclerostin and TSH, FT3, FT4 (p>0.05). We are considering that a long-term study that covers the pre-treatment and post-treatment periods in hyperthyroidism patients, and the search during destruction and construction periods of the skeleton mineralization would be more enlightening; and the assessment of the synthesis of the sclerostin in bone tissue and in the serum level might show differences. 


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