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dc.contributor.authorATICI, ADEM
dc.contributor.authorÇALIŞKAN, MUSTAFA
dc.contributor.authorBAYCAN, ÖMER FARUK
dc.contributor.authorBilgili, Ummuhan Zeynep
dc.contributor.authorTakir, Mumtaz
dc.contributor.authorKUL, ŞEREF
dc.contributor.authorTELCİ ÇAKLILI, Özge
dc.contributor.authorTutuncu, Yasemin
dc.contributor.authorOzcan, Fatma Betul
dc.contributor.authorAksu, Feyza
dc.date.accessioned2021-12-10T10:35:21Z
dc.date.available2021-12-10T10:35:21Z
dc.identifier.citationKUL Ş., TELCİ ÇAKLILI Ö., Tutuncu Y., Ozcan F. B. , Aksu F., BAYCAN Ö. F. , ATICI A., Bilgili U. Z. , Takir M., ÇALIŞKAN M., "Endothelial dysfunction in patients with acromegaly and It & rsquo;s association with Endocan", GROWTH HORMONE & IGF RESEARCH, cilt.56, 2021
dc.identifier.issn1096-6374
dc.identifier.othervv_1032021
dc.identifier.otherav_48a9573b-348e-4705-a7ec-c392c888c0a0
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170192
dc.identifier.urihttps://doi.org/10.1016/j.ghir.2020.101362
dc.description.abstractObjective: This study aims to assess endocan levels in patients with acromegaly who have active disease or disease in remission and to investigate a relation between endocan levels and endothelial dysfunction in these patients. Design: The study is a case-control study. Study was conducted at Istanbul Medeniyet University Goztepe Training and Research Hospital between 2013 and 2019. Patients who were older than 18 years with acromegaly diagnosis were recruited if they agreed to participate. Patients with uncontrolled diabetes (DM), hypertension (HT), hyperlipidemia, decompensated heart failure, immune or infectious diseases, moderate-severe valve disease and stage 3 or more advanced chronic kidney disease were excluded. There were 30 healthy control subjects who agreed to participate to the study. Patients with acromegaly were divided into two groups as: disease active patients and patients in remission. Serum endocan levels were measured with enzyme linked immunosorbent assay (ELISA) method endothelial function was assessed with flow mediated dilatation (FMD). Results: There were 85 patients included to the study. Twenty-three patients had active disease, 31 were in remission and 31 were healthy controls. FMD was higher in controls compared to patients in active disease and patients in remission (p < 0.001). There was no difference between patients with active disease for FMD and patients in remission (p = 0.088). There was statistically significant correlation between FMD and endocan and insulin like growth hormone-1 (IGF-1) levels of patients with acromegaly. As FMD increased endocan and IGF-1 decreased. A moderate negative relation between FMD and endocan was identified (p < 0.001, r:-0.409) as well as FMD and IGF-1 levels (p:0.011, r:-0.377). Along with endocan and IGF-1, DM, HT, sex, body mass index, age and uric acid were associated with changes in FMD. Conclusions: Endocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectHistoloji-Embriyoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectEndocrinology
dc.subjectCell Biology
dc.subjectMolecular Biology
dc.subjectEndocrine and Autonomic Systems
dc.subjectKlinik Tıp
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectHÜCRE BİYOLOJİSİ
dc.titleEndothelial dysfunction in patients with acromegaly and It & rsquo;s association with Endocan
dc.typeMakale
dc.relation.journalGROWTH HORMONE & IGF RESEARCH
dc.contributor.departmentİstanbul Medeniyet Üniversitesi , Tıp Fakültesi , Dahili Tıp Bilimleri
dc.identifier.volume56
dc.contributor.firstauthorID2629889


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