Endothelial dysfunction in patients with acromegaly and It's association with Endocan
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. The study is a case-control study. Study was conducted at Istanbul Medeniyet Univer...
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| Published in | Growth hormone & IGF research Vol. 56; p. 101362 |
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| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Scotland
Elsevier Ltd
01.02.2021
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1096-6374 1532-2238 1532-2238 |
| DOI | 10.1016/j.ghir.2020.101362 |
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| Abstract | 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.
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).
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.
Endocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly.
•Acromegaly causes atherosclerosis that can reveal itself as endothelial dysfunction.•Endocan is a marker of inflammation and it's associated with cardiovascular diseases.•There is an association between endocan and endothelial dysfunction.•Endocan can be useful to detect early signs of atherosclerosis. |
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| AbstractList | 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.
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).
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.
Endocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly.
•Acromegaly causes atherosclerosis that can reveal itself as endothelial dysfunction.•Endocan is a marker of inflammation and it's associated with cardiovascular diseases.•There is an association between endocan and endothelial dysfunction.•Endocan can be useful to detect early signs of atherosclerosis. 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.OBJECTIVEThis 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.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).DESIGNThe 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).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.RESULTSThere 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.Endocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly.CONCLUSIONSEndocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly. 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. 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). 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. Endocan levels and endothelial function measured with FMD have an inverse relationship. Endocan may prove to be a marker for endothelial dysfunction in acromegaly. |
| ArticleNumber | 101362 |
| Author | Caliskan, Mustafa Takir, Mumtaz Kul, Seref Aksu, Feyza Baycan, Omer Faruk Caklili, Ozge Telci Tutuncu, Yasemin Bilgili, Ummuhan Zeynep Ozcan, Fatma Betul Atici, Adem |
| Author_xml | – sequence: 1 givenname: Seref surname: Kul fullname: Kul, Seref organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey – sequence: 2 givenname: Ozge Telci surname: Caklili fullname: Caklili, Ozge Telci email: wattersonx@gmail.com organization: Istanbul University, Istanbul Faculty of Medicine, Department of Endocrinology, Istanbul, Turkey – sequence: 3 givenname: Yasemin surname: Tutuncu fullname: Tutuncu, Yasemin organization: Endocrinology and Metabolism Clinic, Haydarpaşa Education and Training Hospital, Istanbul, Turkey – sequence: 4 givenname: Fatma Betul surname: Ozcan fullname: Ozcan, Fatma Betul organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey – sequence: 5 givenname: Feyza surname: Aksu fullname: Aksu, Feyza organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey – sequence: 6 givenname: Omer Faruk surname: Baycan fullname: Baycan, Omer Faruk organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey – sequence: 7 givenname: Adem surname: Atici fullname: Atici, Adem organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey – sequence: 8 givenname: Ummuhan Zeynep surname: Bilgili fullname: Bilgili, Ummuhan Zeynep organization: Bezmi Alem University Medical School, Istanbul, Turkey – sequence: 9 givenname: Mumtaz surname: Takir fullname: Takir, Mumtaz organization: Istanbul Medeniyet University Faculty of Medicine, Department of Endocrinology and Metabolism, Istanbul, Turkey – sequence: 10 givenname: Mustafa surname: Caliskan fullname: Caliskan, Mustafa organization: Istanbul Medeniyet University Faculty of Medicine, Department of Cardiology, Istanbul, Turkey |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33221710$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1016/j.atherosclerosis.2017.12.019 10.1530/EJE-16-1064 10.1002/jcp.24485 10.1016/j.ghir.2006.03.006 10.1111/jch.12440 10.1161/01.HYP.34.1.89 10.1111/j.1742-1241.2008.01750.x 10.1046/j.1365-2265.2001.01256.x 10.1210/endo.137.5.8612517 10.1530/EJE-16-0117 10.1210/jc.2003-030967 10.3748/wjg.v22.i23.5422 10.1152/ajpheart.1999.276.3.H815 10.1161/01.ATV.0000105902.89459.09 10.1016/j.atherosclerosis.2011.05.034 10.1111/j.1750-3639.2012.00578.x 10.1210/jcem.87.7.8573 10.1007/s10439-013-0957-5 10.1507/endocrj.K07E-125 10.1111/j.1582-4934.2010.01161.x 10.1158/1078-0432.CCR-06-0185 10.1210/jc.2010-2225 10.1007/s12020-018-1797-8 10.1042/CS20100400 10.1161/01.RES.0000021127.83364.7D 10.1038/s41574-018-0058-5 10.1007/s11060-014-1377-6 10.1016/S0735-1097(01)01746-6 10.1159/000204355 10.1007/s11102-015-0698-6 10.1046/j.1365-2265.1998.00620.x 10.1111/crj.12487 10.1530/ERC-17-0253 10.1210/jcem.87.7.8643 10.1161/ATVBAHA.107.156257 10.1038/ki.2014.227 10.1210/jc.2007-1213 10.1152/ajpendo.2000.279.1.E176 10.1007/s10549-016-4057-8 10.7150/jca.7691 10.1111/j.1540-8175.2006.00342.x 10.1530/EJE-08-0452 10.1210/jc.2005-0597 10.1210/er.2002-0022 |
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| Keywords | Acromegaly Endothelial dysfunction Endocan Flow mediated dilatation |
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| SubjectTerms | Acromegaly Acromegaly - complications Acromegaly - pathology Aged Cardiovascular Diseases - complications Case-Control Studies Endocan Endothelial dysfunction Endothelium, Vascular - pathology Female Flow mediated dilatation Glucose Tolerance Test Humans Inflammation - complications Insulin-Like Growth Factor I - biosynthesis Linear Models Male Middle Aged Neoplasm Proteins - blood Proteoglycans - blood ROC Curve |
| Title | Endothelial dysfunction in patients with acromegaly and It's association with Endocan |
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