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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Cakmak Genc G, Karakas Celik S, Arpaci D, Aktas T, Can M, Bayraktaroglu T, Dursun A
Granulysin Peptide and Gene Polymorphism in the Pathogenesis of Hashimoto Thyroiditis
Acta Endo (Buc) 2022, 18 (3): 288-293doi: 10.4183/aeb.2022/288
Background. Hashimoto thyroiditis (HT) is
an autoimmune disease and the most common cause of
hypothyroidism. The widespread lymphocyte infiltration in the
thyroid gland and intolerance of the body against its thyroid
antigens leads to the destruction of thyroid cells and impaired
thyroid function. Granulysin (GNLY) is a cytolytic antimicrobial
peptide that has been associated with a wide range of diseases
such as various infections, cancer, transplantation, and skin
problems. However, there are a few studies investigating the
relationship between HT and granulysin.
Aim. Our study aims to investigate whether
granulysin levels and GNLY gene polymorphism contribute
to the damaged immune response leading to HT.
Material and Methods. 100 unrelated patients
diagnosed with HT and 140 healthy individuals were included
in our study. Frequencies of GNLY rs10180391 and rs7908
gene polymorphisms were determined using PCR- RFLP
method and serum granulysin levels were determined using
ELISA.
Results. There is no statistical significance between
patient and control groups in terms of genotype and allele
frequencies of GNLY gene polymorphisms and serum levels
of granulysin.
Conclusion. In conclusion, granulysin and GNLY
gene polymorphisms do not appear to relate to HT disease.
Keywords: Hashimoto, thyroiditis, granulysin, GNLY, gene polymorphism.
Correspondence: Günes Çakmak Genç MD, Zonguldak Bülent Ecevit University, Training and Research Hospital, Department of
Medical Genetics, Kozlu, 67600 Zonguldak, Turkey, E-mail: gunes.cak@hotmail.com