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The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)The International Journal of Romanian Society of Endocrinology / Registered in 1938
in ISI Thomson Master Journal List
Acta Endocrinologica (Buc)
Diri H, Sener EF, Bayram F, Dundar M, Simsek Y, Baspinar O, Zararsiz G
Genetic Disorders of Pituitary Development in Patients with Sheehan'S Syndrome
Acta Endo (Buc) 2016, 12 (4): 413-417doi: 10.4183/aeb.2016.413
Introduction. Genetic disorders associated with the development of the pituitary gland and cranial bones may cause a genetic tendency toward Sheehan’s syndrome (SS). Our aim in this study was to investigate expression disorders in the genes responsible for the development of the pituitary gland and cranial bones in patients with SS. Materials and Methods. Forty-four patients who were previously diagnosed with SS and 43 healthy women were compared in terms of the mean expression values of genes including the prophet of PIT-1 (PROP1), HESX homeobox 1 (HESX1), POU class 1 homeobox 1 (POU1F1), LIM homeobox 3 (LHX3), LHX4, glioma-associated oncogene homolog 2 (GLI2), orthodenticle homeobox 2 (OTX2), SIX homeobox 3 (SIX3), SIX6, T-box transcription factor 19 (TBX19), transducin-like enhancer protein 1 (TLE1), TLE3, distal-less homeobox 2 (DLX2), DLX5, MSH homeobox 2 (MSX2), and paired box 3 (PAX3). Results. The mean expression values of the HESX1, TLE1, TLE3, and MSX2 genes were significantly different in the SS group from the healthy control group, while the mean expression values of the remaining genes were similar. Conclusion. The present study concludes that abnormal expressions of HESX1, TLE1, TLE3, and MSX2 genes may cause a genetic predisposition to the development of SS.
Keywords: Sheehan’s syndrome, etiopathogenesis, genetic, pituitary development.
Correspondence: Halit Diri MD, Erciyes University Medical School, Dept. of Endocrinology, Kayseri, 38039, Turkey, E-mail: firstname.lastname@example.org