Searchable abstracts of presentations at key conferences in endocrinology

ea0099rc13.1 | Rapid Communications 13: Late Breaking | ECE2024

MTHFR 677 TT and CT genotype related epigenetic changes and hyperhomocysteinemia in Hypothyroidism and its management, a family case report

Kvaratskhelia Tamar , Abzianidze Elene , Surmava Sandro , Kvaratskhelia Eka

Introduction: Hypothyroidism is a clinical syndrome resulting from a deficiency of thyroid hormones, which in turn results in a generalized slowing down of metabolic processes. There are consistent reports demonstrating that many diseases, including the thyroid gland dysfunction are associated with changes of serum homocysteine (tHcy) level, with its genetic and epigenetic causes.Case report: In 2018 we reported 51 and 52-year-old sisters diagnosed with ...

ea0070aep1105 | Hot topics (including COVID-19) | ECE2020

MTHFR C677T polymorphism frequency and DNA methylation status in Georgian population with non-autoimmune hypothyroidism

Kvaratskhelia Tamar , Abzianidze Elene , Kakulia Mzeona , Surmava Sandro , Asatiani Ketevan , Kvaratskhelia Eka

Introduction: Methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism results in thermolabile, reduced functioning enzyme and predicts hyperhomocisteinemia and altered DNA methylation. On the other hand, several studies indicated a higher plasma homocysteine (Hcy) levels in patients with primary hypothyroidism than in healthy, euthyroid individuals, including some experimental studies that indicated decreased MTHFR activity in hypothyroid patients. We cond...