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Endothelial dysfunction in Graves' disease
Graves' disease (GD) is an organ-specific autoimmune thyroid disease, characterized by hyperthyroidism due to excessive production of thyroid hormone induced by thyrotropin receptor-specific stimulatory autoantibodies. In this study, we determined serum levels of the soluble forms of ICAM-1, VC...
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Published in: | Advances in medical sciences 2013, Vol.58 (1), p.31-37 |
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description | Graves' disease (GD) is an organ-specific autoimmune thyroid disease, characterized by hyperthyroidism due to excessive production of thyroid hormone induced by thyrotropin receptor-specific stimulatory autoantibodies. In this study, we determined serum levels of the soluble forms of ICAM-1, VCAM-1, vWF, IL-6, IL-12, IL-18, fibrinogen and CRP in patients with subclinical (SH) and overt hyperthyroidism (OH) caused by GD to elucidate a possible role of those parameters as markers of endothelium dysfunction (ED).
The study included 96 patients: 52 with GD and 44 euthyroid controls, divided into 3 groups according to their thyroid function tests: SH, OH and controls (CG).
The values of IL-6, IL-12 and IL-18 were significantly higher in GD than in CG patients (p < 0.0001, p < 0.0001; p < 0.00001, respectively). Significant difference of sVCAM-1 values were found in the patients with GD compared to CG (p < 0.0001). Patients with GD had significantly higher levels of PAI-1 (p < 0.00001), vWF (p < 0.0001), fibrinogen (p < 0.0001) in comparison to CG. In patients with OH, we observed statistically higher values of fibrinogen compared to SH group (p < 0.05). There were no significant differences in serum concentration of other study parameters in patients with SH compared to the OH.
ED occurs during subclinical and overt hyperthyroidism causing decreased fibrinolytic activity, hypercoagulability and increased levels of IL-6, Il-12 and IL-18. These results support the notion that serum cytokines could be used as a marker of GD activity. Results of this study support the opinion that GD might require treatment as early as in the phase of SH. |
doi_str_mv | 10.2478/v10039-012-0047-1 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1399933307</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1896112614601681</els_id><sourcerecordid>3369101961</sourcerecordid><originalsourceid>FETCH-LOGICAL-c381t-3dd668b4ecb1dfb603399ea96e11271ad9047df187b7511e531c66913c8e823c3</originalsourceid><addsrcrecordid>eNp9kM9LwzAUx4Mobk7_AC8y8KAI0bykTRs8yZg_YOBFz6FNXjGja2fSDvbfm9npwYOnPMLnfd-XDyHnwG55kuV3G2BMKMqAU8aSjMIBGUOucpowxg-_Z0kBuByRkxCWjEkuGTsmIy5k_M3SMbmZN7btPrB2RT2121D1jelc20xdM33yxQbD1dS6gEXAU3JUFXXAs_07Ie-P87fZM128Pr3MHhbUiBw6KqyVMi8TNCXYqpRMCKWwUBJjkwwKq2JVW0GelVkKgKkAI6UCYXLMuTBiQq6H3LVvP3sMnV65YLCuiwbbPmiIeUoIwbKIXv5Bl23vm9hOQ5okCXAleaRgoIxvQ_BY6bV3q8JvNTC9E6kHkTqK1DuR8cSEXOyT-3KF9nfjx1wE7gcAo4qNQ6-DcdgYtM6j6bRt3T_xX2qgfnk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1544412962</pqid></control><display><type>article</type><title>Endothelial dysfunction in Graves' disease</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Popławska-Kita, A ; Szelachowska, M ; Modzelewska, A ; Siewko, K ; Dzięcioł, J ; Klimiuk, PA ; Górska, M</creator><creatorcontrib>Popławska-Kita, A ; Szelachowska, M ; Modzelewska, A ; Siewko, K ; Dzięcioł, J ; Klimiuk, PA ; Górska, M</creatorcontrib><description><![CDATA[Graves' disease (GD) is an organ-specific autoimmune thyroid disease, characterized by hyperthyroidism due to excessive production of thyroid hormone induced by thyrotropin receptor-specific stimulatory autoantibodies. In this study, we determined serum levels of the soluble forms of ICAM-1, VCAM-1, vWF, IL-6, IL-12, IL-18, fibrinogen and CRP in patients with subclinical (SH) and overt hyperthyroidism (OH) caused by GD to elucidate a possible role of those parameters as markers of endothelium dysfunction (ED).
The study included 96 patients: 52 with GD and 44 euthyroid controls, divided into 3 groups according to their thyroid function tests: SH, OH and controls (CG).
The values of IL-6, IL-12 and IL-18 were significantly higher in GD than in CG patients (p < 0.0001, p < 0.0001; p < 0.00001, respectively). Significant difference of sVCAM-1 values were found in the patients with GD compared to CG (p < 0.0001). Patients with GD had significantly higher levels of PAI-1 (p < 0.00001), vWF (p < 0.0001), fibrinogen (p < 0.0001) in comparison to CG. In patients with OH, we observed statistically higher values of fibrinogen compared to SH group (p < 0.05). There were no significant differences in serum concentration of other study parameters in patients with SH compared to the OH.
ED occurs during subclinical and overt hyperthyroidism causing decreased fibrinolytic activity, hypercoagulability and increased levels of IL-6, Il-12 and IL-18. These results support the notion that serum cytokines could be used as a marker of GD activity. Results of this study support the opinion that GD might require treatment as early as in the phase of SH.]]></description><identifier>ISSN: 1896-1126</identifier><identifier>EISSN: 1898-4002</identifier><identifier>DOI: 10.2478/v10039-012-0047-1</identifier><identifier>PMID: 23612675</identifier><language>eng</language><publisher>Netherlands: Elsevier Urban & Partner Sp. z o.o</publisher><subject>Adult ; Biomarkers - blood ; Blood Coagulation ; C-Reactive Protein - metabolism ; endothelium ; Endothelium, Vascular - metabolism ; Endothelium, Vascular - physiopathology ; Female ; Fibrinogen - metabolism ; Fibrinolysis ; Graves Disease - blood ; Graves Disease - complications ; Graves' disease ; Humans ; hyperthyroidism ; Hyperthyroidism - blood ; Hyperthyroidism - etiology ; Intercellular Adhesion Molecule-1 - blood ; Interleukin-12 - blood ; Interleukin-18 - blood ; Interleukin-6 - blood ; Male ; Middle Aged ; Thyroid Function Tests ; Vascular Cell Adhesion Molecule-1 - blood ; von Willebrand Factor - metabolism</subject><ispartof>Advances in medical sciences, 2013, Vol.58 (1), p.31-37</ispartof><rights>2013 Medical University of Bialystok</rights><rights>Copyright De Gruyter Open Sp. z o.o. 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-3dd668b4ecb1dfb603399ea96e11271ad9047df187b7511e531c66913c8e823c3</citedby><cites>FETCH-LOGICAL-c381t-3dd668b4ecb1dfb603399ea96e11271ad9047df187b7511e531c66913c8e823c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23612675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Popławska-Kita, A</creatorcontrib><creatorcontrib>Szelachowska, M</creatorcontrib><creatorcontrib>Modzelewska, A</creatorcontrib><creatorcontrib>Siewko, K</creatorcontrib><creatorcontrib>Dzięcioł, J</creatorcontrib><creatorcontrib>Klimiuk, PA</creatorcontrib><creatorcontrib>Górska, M</creatorcontrib><title>Endothelial dysfunction in Graves' disease</title><title>Advances in medical sciences</title><addtitle>Adv Med Sci</addtitle><description><![CDATA[Graves' disease (GD) is an organ-specific autoimmune thyroid disease, characterized by hyperthyroidism due to excessive production of thyroid hormone induced by thyrotropin receptor-specific stimulatory autoantibodies. In this study, we determined serum levels of the soluble forms of ICAM-1, VCAM-1, vWF, IL-6, IL-12, IL-18, fibrinogen and CRP in patients with subclinical (SH) and overt hyperthyroidism (OH) caused by GD to elucidate a possible role of those parameters as markers of endothelium dysfunction (ED).
The study included 96 patients: 52 with GD and 44 euthyroid controls, divided into 3 groups according to their thyroid function tests: SH, OH and controls (CG).
The values of IL-6, IL-12 and IL-18 were significantly higher in GD than in CG patients (p < 0.0001, p < 0.0001; p < 0.00001, respectively). Significant difference of sVCAM-1 values were found in the patients with GD compared to CG (p < 0.0001). Patients with GD had significantly higher levels of PAI-1 (p < 0.00001), vWF (p < 0.0001), fibrinogen (p < 0.0001) in comparison to CG. In patients with OH, we observed statistically higher values of fibrinogen compared to SH group (p < 0.05). There were no significant differences in serum concentration of other study parameters in patients with SH compared to the OH.
ED occurs during subclinical and overt hyperthyroidism causing decreased fibrinolytic activity, hypercoagulability and increased levels of IL-6, Il-12 and IL-18. These results support the notion that serum cytokines could be used as a marker of GD activity. Results of this study support the opinion that GD might require treatment as early as in the phase of SH.]]></description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Blood Coagulation</subject><subject>C-Reactive Protein - metabolism</subject><subject>endothelium</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Fibrinogen - metabolism</subject><subject>Fibrinolysis</subject><subject>Graves Disease - blood</subject><subject>Graves Disease - complications</subject><subject>Graves' disease</subject><subject>Humans</subject><subject>hyperthyroidism</subject><subject>Hyperthyroidism - blood</subject><subject>Hyperthyroidism - etiology</subject><subject>Intercellular Adhesion Molecule-1 - blood</subject><subject>Interleukin-12 - blood</subject><subject>Interleukin-18 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Thyroid Function Tests</subject><subject>Vascular Cell Adhesion Molecule-1 - blood</subject><subject>von Willebrand Factor - metabolism</subject><issn>1896-1126</issn><issn>1898-4002</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kM9LwzAUx4Mobk7_AC8y8KAI0bykTRs8yZg_YOBFz6FNXjGja2fSDvbfm9npwYOnPMLnfd-XDyHnwG55kuV3G2BMKMqAU8aSjMIBGUOucpowxg-_Z0kBuByRkxCWjEkuGTsmIy5k_M3SMbmZN7btPrB2RT2121D1jelc20xdM33yxQbD1dS6gEXAU3JUFXXAs_07Ie-P87fZM128Pr3MHhbUiBw6KqyVMi8TNCXYqpRMCKWwUBJjkwwKq2JVW0GelVkKgKkAI6UCYXLMuTBiQq6H3LVvP3sMnV65YLCuiwbbPmiIeUoIwbKIXv5Bl23vm9hOQ5okCXAleaRgoIxvQ_BY6bV3q8JvNTC9E6kHkTqK1DuR8cSEXOyT-3KF9nfjx1wE7gcAo4qNQ6-DcdgYtM6j6bRt3T_xX2qgfnk</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Popławska-Kita, A</creator><creator>Szelachowska, M</creator><creator>Modzelewska, A</creator><creator>Siewko, K</creator><creator>Dzięcioł, J</creator><creator>Klimiuk, PA</creator><creator>Górska, M</creator><general>Elsevier Urban & Partner Sp. z o.o</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>2013</creationdate><title>Endothelial dysfunction in Graves' disease</title><author>Popławska-Kita, A ; Szelachowska, M ; Modzelewska, A ; Siewko, K ; Dzięcioł, J ; Klimiuk, PA ; Górska, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-3dd668b4ecb1dfb603399ea96e11271ad9047df187b7511e531c66913c8e823c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Blood Coagulation</topic><topic>C-Reactive Protein - metabolism</topic><topic>endothelium</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Female</topic><topic>Fibrinogen - metabolism</topic><topic>Fibrinolysis</topic><topic>Graves Disease - blood</topic><topic>Graves Disease - complications</topic><topic>Graves' disease</topic><topic>Humans</topic><topic>hyperthyroidism</topic><topic>Hyperthyroidism - blood</topic><topic>Hyperthyroidism - etiology</topic><topic>Intercellular Adhesion Molecule-1 - blood</topic><topic>Interleukin-12 - blood</topic><topic>Interleukin-18 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Thyroid Function Tests</topic><topic>Vascular Cell Adhesion Molecule-1 - blood</topic><topic>von Willebrand Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Popławska-Kita, A</creatorcontrib><creatorcontrib>Szelachowska, M</creatorcontrib><creatorcontrib>Modzelewska, A</creatorcontrib><creatorcontrib>Siewko, K</creatorcontrib><creatorcontrib>Dzięcioł, J</creatorcontrib><creatorcontrib>Klimiuk, PA</creatorcontrib><creatorcontrib>Górska, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>East Europe, Central Europe Database</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Advances in medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Popławska-Kita, A</au><au>Szelachowska, M</au><au>Modzelewska, A</au><au>Siewko, K</au><au>Dzięcioł, J</au><au>Klimiuk, PA</au><au>Górska, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelial dysfunction in Graves' disease</atitle><jtitle>Advances in medical sciences</jtitle><addtitle>Adv Med Sci</addtitle><date>2013</date><risdate>2013</risdate><volume>58</volume><issue>1</issue><spage>31</spage><epage>37</epage><pages>31-37</pages><issn>1896-1126</issn><eissn>1898-4002</eissn><abstract><![CDATA[Graves' disease (GD) is an organ-specific autoimmune thyroid disease, characterized by hyperthyroidism due to excessive production of thyroid hormone induced by thyrotropin receptor-specific stimulatory autoantibodies. In this study, we determined serum levels of the soluble forms of ICAM-1, VCAM-1, vWF, IL-6, IL-12, IL-18, fibrinogen and CRP in patients with subclinical (SH) and overt hyperthyroidism (OH) caused by GD to elucidate a possible role of those parameters as markers of endothelium dysfunction (ED).
The study included 96 patients: 52 with GD and 44 euthyroid controls, divided into 3 groups according to their thyroid function tests: SH, OH and controls (CG).
The values of IL-6, IL-12 and IL-18 were significantly higher in GD than in CG patients (p < 0.0001, p < 0.0001; p < 0.00001, respectively). Significant difference of sVCAM-1 values were found in the patients with GD compared to CG (p < 0.0001). Patients with GD had significantly higher levels of PAI-1 (p < 0.00001), vWF (p < 0.0001), fibrinogen (p < 0.0001) in comparison to CG. In patients with OH, we observed statistically higher values of fibrinogen compared to SH group (p < 0.05). There were no significant differences in serum concentration of other study parameters in patients with SH compared to the OH.
ED occurs during subclinical and overt hyperthyroidism causing decreased fibrinolytic activity, hypercoagulability and increased levels of IL-6, Il-12 and IL-18. These results support the notion that serum cytokines could be used as a marker of GD activity. Results of this study support the opinion that GD might require treatment as early as in the phase of SH.]]></abstract><cop>Netherlands</cop><pub>Elsevier Urban & Partner Sp. z o.o</pub><pmid>23612675</pmid><doi>10.2478/v10039-012-0047-1</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Biomarkers - blood Blood Coagulation C-Reactive Protein - metabolism endothelium Endothelium, Vascular - metabolism Endothelium, Vascular - physiopathology Female Fibrinogen - metabolism Fibrinolysis Graves Disease - blood Graves Disease - complications Graves' disease Humans hyperthyroidism Hyperthyroidism - blood Hyperthyroidism - etiology Intercellular Adhesion Molecule-1 - blood Interleukin-12 - blood Interleukin-18 - blood Interleukin-6 - blood Male Middle Aged Thyroid Function Tests Vascular Cell Adhesion Molecule-1 - blood von Willebrand Factor - metabolism |
title | Endothelial dysfunction in Graves' disease |
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