Searchable abstracts of presentations at key conferences in endocrinology

ea0063p1024 | Interdisciplinary Endocrinology 2 | ECE2019

Association of the Period3 clock gene polymorphism with adrenocorticotropin-stimulated cortisol levels among patients with autoimmune thyroid disease

Helvaci Nafiye , Oguz Seda , Kabacam Serkan , Karabulut Erdem , Akbiyik Filiz , Alikasifoglu Mehmet , Gurlek Alper

Background: Immune function and responses are tightly regulated by the circadian clock system and hypothalamic-pituitary-adrenal (HPA) axis. Accumulating evidence supports that there is a strong mutual relationship between these two regulatory systems at multiple levels. Recent publications suggest that the clock system may also regulate glucocorticoid release from adrenal glands by altering the sensitivity of the adrenal cortex to adrenocorticotropic hormone (ACTH).<p cla...

ea0049gp212 | Thyroid 2 | ECE2017

Association of the Period3 clock gene polymorphism with autoimmune thyroid diseases

Helvaci Nafiye , Oguz Seda , Kabacam Serkan , Karabulut Erdem , Akbiyik Filiz , Alikasifoglu Mehmet , Gurlek Alper

Background: Circadian rhythmicity is generated by a set of genes including Period3. Changes in the expression of Period3 and other clock genes have been linked with regulation of the immune system. Period3 polymorphisms have been associated with circadian disruption and so immune system dysregulation and altered secretion of several cytokines, which can lead to inflammatory and autoimmune disorders.Aim: To investigate the influence of a polymorphism in P...

ea0041ep646 | Endocrine tumours and neoplasia | ECE2016

A novel mutation of the menin gene in a family with multiple endocrine neoplasia type 1

Nahit Sendur Suleyman , Dogrul Ahmet , Kabacam Serkan , Abbasoglu Osman , Onder Sevgen , Sokmensuer Cenk , Erbas Belkis , Dagdelen Selcuk , Alikasifoglu Mehmet , Erbas Tomris

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant genetic disorder characterized by parathyroid adenomas, enteropancreatic endocrine tumors and anterior pituitary adenomas. It is caused by inactivating mutations of the MEN1 tumor suppressor gene, encoding menin (chromosome 11q13). A large family with several members affected were evaluated for clinical and genetic characteristic of MEN1.The index male patient (42 yr) presented ...