MiR-223-3p levels in the plasma and atherosclerotic plaques are increased in aged patients with carotid artery stenosis; association with HDL-related proteins
Background Cardiovascular diseases are still the main cause of death worldwide. Our aim was to analyse the link between miR-223-3p levels, dysfunctional HDL and the age of patients with carotid artery stenosis (CAS). Methods and results Thirty-two CAS patients enrolled for endarterectomy were divide...
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Veröffentlicht in: | Molecular biology reports 2022-07, Vol.49 (7), p.6779-6788 |
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creator | Barbalata, Teodora Moraru, Oriana E. Stancu, Camelia S. Sima, Anca V. Niculescu, Loredan S. |
description | Background
Cardiovascular diseases are still the main cause of death worldwide. Our aim was to analyse the link between miR-223-3p levels, dysfunctional HDL and the age of patients with carotid artery stenosis (CAS).
Methods and results
Thirty-two CAS patients enrolled for endarterectomy were divided in 2 groups: aged over 65 years (n = 19) and under 65 years (n = 13). Plasma samples and atherosclerotic plaques from the carotid artery were collected from all patients. Plaque levels of miR-223-3p and its primary transcript (pri-miR-223) were assessed, together with Drosha, Dicer, apolipoprotein (apo)A-I, apoE and myeloperoxidase (MPO) gene expression. In the plasma and plaques, miR-223-3p expression levels were significantly increased in CAS patients over 65 years. Positive correlations between plaque miR-223-3p and pri-miR-223 levels with Drosha, apoA-I and MPO expression were observed. Significantly increased miR-223-3p levels in the plasma of CAS patients over 65 years were measured. Significant correlations between plasma miR-223-3p levels and HDL-related proteins were determined. The variance of plasma miR-223-3p levels was predicted significantly by the multiple regression models using either age, clinical variables, blood lipids or oxidative and inflammatory parameters. Receiver operator characteristic analysis revealed that plasma miR-223-3p levels and HDL-related proteins (MPO activity/apoA-I ratio, MPO specific activity) were correlated with advanced age.
Conclusions
Taken together, these data suggest that plasma levels of miR-223-3p are independently associated with ageing in CAS patients and that, correlated with parameters associated with dysfunctional HDL, could predict the aggravation of CAS in elderly patients. |
doi_str_mv | 10.1007/s11033-021-06636-y |
format | Article |
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Cardiovascular diseases are still the main cause of death worldwide. Our aim was to analyse the link between miR-223-3p levels, dysfunctional HDL and the age of patients with carotid artery stenosis (CAS).
Methods and results
Thirty-two CAS patients enrolled for endarterectomy were divided in 2 groups: aged over 65 years (n = 19) and under 65 years (n = 13). Plasma samples and atherosclerotic plaques from the carotid artery were collected from all patients. Plaque levels of miR-223-3p and its primary transcript (pri-miR-223) were assessed, together with Drosha, Dicer, apolipoprotein (apo)A-I, apoE and myeloperoxidase (MPO) gene expression. In the plasma and plaques, miR-223-3p expression levels were significantly increased in CAS patients over 65 years. Positive correlations between plaque miR-223-3p and pri-miR-223 levels with Drosha, apoA-I and MPO expression were observed. Significantly increased miR-223-3p levels in the plasma of CAS patients over 65 years were measured. Significant correlations between plasma miR-223-3p levels and HDL-related proteins were determined. The variance of plasma miR-223-3p levels was predicted significantly by the multiple regression models using either age, clinical variables, blood lipids or oxidative and inflammatory parameters. Receiver operator characteristic analysis revealed that plasma miR-223-3p levels and HDL-related proteins (MPO activity/apoA-I ratio, MPO specific activity) were correlated with advanced age.
Conclusions
Taken together, these data suggest that plasma levels of miR-223-3p are independently associated with ageing in CAS patients and that, correlated with parameters associated with dysfunctional HDL, could predict the aggravation of CAS in elderly patients.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-021-06636-y</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Aging ; Animal Anatomy ; Animal Biochemistry ; Apolipoprotein E ; Apolipoproteins ; Arteriosclerosis ; Atherosclerosis ; Biomedical and Life Sciences ; blood ; Cardiovascular diseases ; Carotid arteries ; Carotid artery ; death ; elderly ; Gene expression ; Geriatrics ; High density lipoprotein ; Histology ; Inflammation ; Life Sciences ; Lipids ; Morphology ; myeloperoxidase ; Original Article ; Patients ; Peroxidase ; Plaques ; Plasma ; Plasma levels ; Proteins ; Regression analysis ; Stenosis ; variance ; Veins & arteries</subject><ispartof>Molecular biology reports, 2022-07, Vol.49 (7), p.6779-6788</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-cc96eb39f54b2dd39996f1b21d7e3c9e21c31160c828384c2f1bfb1ee140ff83</citedby><cites>FETCH-LOGICAL-c385t-cc96eb39f54b2dd39996f1b21d7e3c9e21c31160c828384c2f1bfb1ee140ff83</cites><orcidid>0000-0002-1394-9085</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-021-06636-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-021-06636-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Barbalata, Teodora</creatorcontrib><creatorcontrib>Moraru, Oriana E.</creatorcontrib><creatorcontrib>Stancu, Camelia S.</creatorcontrib><creatorcontrib>Sima, Anca V.</creatorcontrib><creatorcontrib>Niculescu, Loredan S.</creatorcontrib><title>MiR-223-3p levels in the plasma and atherosclerotic plaques are increased in aged patients with carotid artery stenosis; association with HDL-related proteins</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><description>Background
Cardiovascular diseases are still the main cause of death worldwide. Our aim was to analyse the link between miR-223-3p levels, dysfunctional HDL and the age of patients with carotid artery stenosis (CAS).
Methods and results
Thirty-two CAS patients enrolled for endarterectomy were divided in 2 groups: aged over 65 years (n = 19) and under 65 years (n = 13). Plasma samples and atherosclerotic plaques from the carotid artery were collected from all patients. Plaque levels of miR-223-3p and its primary transcript (pri-miR-223) were assessed, together with Drosha, Dicer, apolipoprotein (apo)A-I, apoE and myeloperoxidase (MPO) gene expression. In the plasma and plaques, miR-223-3p expression levels were significantly increased in CAS patients over 65 years. Positive correlations between plaque miR-223-3p and pri-miR-223 levels with Drosha, apoA-I and MPO expression were observed. Significantly increased miR-223-3p levels in the plasma of CAS patients over 65 years were measured. Significant correlations between plasma miR-223-3p levels and HDL-related proteins were determined. The variance of plasma miR-223-3p levels was predicted significantly by the multiple regression models using either age, clinical variables, blood lipids or oxidative and inflammatory parameters. Receiver operator characteristic analysis revealed that plasma miR-223-3p levels and HDL-related proteins (MPO activity/apoA-I ratio, MPO specific activity) were correlated with advanced age.
Conclusions
Taken together, these data suggest that plasma levels of miR-223-3p are independently associated with ageing in CAS patients and that, correlated with parameters associated with dysfunctional HDL, could predict the aggravation of CAS in elderly patients.</description><subject>Aging</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Apolipoprotein E</subject><subject>Apolipoproteins</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Biomedical and Life Sciences</subject><subject>blood</subject><subject>Cardiovascular diseases</subject><subject>Carotid arteries</subject><subject>Carotid artery</subject><subject>death</subject><subject>elderly</subject><subject>Gene expression</subject><subject>Geriatrics</subject><subject>High density lipoprotein</subject><subject>Histology</subject><subject>Inflammation</subject><subject>Life Sciences</subject><subject>Lipids</subject><subject>Morphology</subject><subject>myeloperoxidase</subject><subject>Original Article</subject><subject>Patients</subject><subject>Peroxidase</subject><subject>Plaques</subject><subject>Plasma</subject><subject>Plasma levels</subject><subject>Proteins</subject><subject>Regression analysis</subject><subject>Stenosis</subject><subject>variance</subject><subject>Veins & arteries</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqFkcGKFDEQhoMoOI6-gKeAFy9xU0k6ncaTrKu7MCLI3kMmXb2bpad7TGWUeRmf1bQtCB70kiLU9_9F1c_YS5BvQMr2ggCk1kIqENJabcX5EdtA02phutY9ZhupJQjjGnjKnhE9SCkNtM2G_fiUvgiltNBHPuI3HImniZd75Mcx0CHwMPU81H-eKY71LSkura8nJB4yVjpmDIT9ogt3tR5DSTgV4t9TuecxLJrqkQvmM6eC00yJ3vJANMdU2Xlayev3O5FxDGXxqCJMEz1nT4YwEr74Xbfs9sPV7eW12H3-eHP5bieidk0RMXYW97obGrNXfa-7rrMD7BX0LerYoYKoAayMTjntTFS1OewBEYwcBqe37PVqW-cumxV_SBRxHMOE84m8asGp1lgD_0cbq-oUW2-6Za_-Qh_mU57qHl5ZZ43qFCyUWqlYT0wZB3_M6RDy2YP0S7h-DdfXcP2vcP25ivQqogpPd5j_WP9D9RPp46l5</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Barbalata, Teodora</creator><creator>Moraru, Oriana E.</creator><creator>Stancu, Camelia S.</creator><creator>Sima, Anca V.</creator><creator>Niculescu, Loredan S.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-1394-9085</orcidid></search><sort><creationdate>20220701</creationdate><title>MiR-223-3p levels in the plasma and atherosclerotic plaques are increased in aged patients with carotid artery stenosis; association with HDL-related proteins</title><author>Barbalata, Teodora ; Moraru, Oriana E. ; Stancu, Camelia S. ; Sima, Anca V. ; Niculescu, Loredan S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-cc96eb39f54b2dd39996f1b21d7e3c9e21c31160c828384c2f1bfb1ee140ff83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aging</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Apolipoprotein E</topic><topic>Apolipoproteins</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Biomedical and Life Sciences</topic><topic>blood</topic><topic>Cardiovascular diseases</topic><topic>Carotid arteries</topic><topic>Carotid artery</topic><topic>death</topic><topic>elderly</topic><topic>Gene expression</topic><topic>Geriatrics</topic><topic>High density lipoprotein</topic><topic>Histology</topic><topic>Inflammation</topic><topic>Life Sciences</topic><topic>Lipids</topic><topic>Morphology</topic><topic>myeloperoxidase</topic><topic>Original Article</topic><topic>Patients</topic><topic>Peroxidase</topic><topic>Plaques</topic><topic>Plasma</topic><topic>Plasma levels</topic><topic>Proteins</topic><topic>Regression analysis</topic><topic>Stenosis</topic><topic>variance</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbalata, Teodora</creatorcontrib><creatorcontrib>Moraru, Oriana E.</creatorcontrib><creatorcontrib>Stancu, Camelia S.</creatorcontrib><creatorcontrib>Sima, Anca V.</creatorcontrib><creatorcontrib>Niculescu, Loredan S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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 Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbalata, Teodora</au><au>Moraru, Oriana E.</au><au>Stancu, Camelia S.</au><au>Sima, Anca V.</au><au>Niculescu, Loredan S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MiR-223-3p levels in the plasma and atherosclerotic plaques are increased in aged patients with carotid artery stenosis; association with HDL-related proteins</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><date>2022-07-01</date><risdate>2022</risdate><volume>49</volume><issue>7</issue><spage>6779</spage><epage>6788</epage><pages>6779-6788</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Cardiovascular diseases are still the main cause of death worldwide. Our aim was to analyse the link between miR-223-3p levels, dysfunctional HDL and the age of patients with carotid artery stenosis (CAS).
Methods and results
Thirty-two CAS patients enrolled for endarterectomy were divided in 2 groups: aged over 65 years (n = 19) and under 65 years (n = 13). Plasma samples and atherosclerotic plaques from the carotid artery were collected from all patients. Plaque levels of miR-223-3p and its primary transcript (pri-miR-223) were assessed, together with Drosha, Dicer, apolipoprotein (apo)A-I, apoE and myeloperoxidase (MPO) gene expression. In the plasma and plaques, miR-223-3p expression levels were significantly increased in CAS patients over 65 years. Positive correlations between plaque miR-223-3p and pri-miR-223 levels with Drosha, apoA-I and MPO expression were observed. Significantly increased miR-223-3p levels in the plasma of CAS patients over 65 years were measured. Significant correlations between plasma miR-223-3p levels and HDL-related proteins were determined. The variance of plasma miR-223-3p levels was predicted significantly by the multiple regression models using either age, clinical variables, blood lipids or oxidative and inflammatory parameters. Receiver operator characteristic analysis revealed that plasma miR-223-3p levels and HDL-related proteins (MPO activity/apoA-I ratio, MPO specific activity) were correlated with advanced age.
Conclusions
Taken together, these data suggest that plasma levels of miR-223-3p are independently associated with ageing in CAS patients and that, correlated with parameters associated with dysfunctional HDL, could predict the aggravation of CAS in elderly patients.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11033-021-06636-y</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1394-9085</orcidid></addata></record> |
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subjects | Aging Animal Anatomy Animal Biochemistry Apolipoprotein E Apolipoproteins Arteriosclerosis Atherosclerosis Biomedical and Life Sciences blood Cardiovascular diseases Carotid arteries Carotid artery death elderly Gene expression Geriatrics High density lipoprotein Histology Inflammation Life Sciences Lipids Morphology myeloperoxidase Original Article Patients Peroxidase Plaques Plasma Plasma levels Proteins Regression analysis Stenosis variance Veins & arteries |
title | MiR-223-3p levels in the plasma and atherosclerotic plaques are increased in aged patients with carotid artery stenosis; association with HDL-related proteins |
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