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Association between pan-immune-inflammation value and coronary slow flow phenomenon in patients with angiographically normal coronary arteries
Coronary slow flow phenomenon (CSFP) is characterized by the delayed contrast filling of terminal vessels of coronary arteries in the presence of normal or nearly normal epicardial coronary arteries. Given that inflammation plays a role in cardiovascular disorders, including CSFP, using peripheral b...
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Published in: | International journal of cardiology 2024-03, Vol.398, p.131631-131631, Article 131631 |
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description | Coronary slow flow phenomenon (CSFP) is characterized by the delayed contrast filling of terminal vessels of coronary arteries in the presence of normal or nearly normal epicardial coronary arteries. Given that inflammation plays a role in cardiovascular disorders, including CSFP, using peripheral blood-derived compound prognostic indexes could be a feasible way to predict the presence of CSFP. Therefore, in the present study, we evaluated the association between pan-immune-inflammation value (PIV) and the CSFP.
This single-center, retrospective study was composed of 612 patients aged over 18 years who underwent CAG for suspected stable ischemic heart disease. The association of clinical and laboratory parameters with the CSFP was evaluated with univariate and multivariate analyses.
The median age of the patients was 54 (IQR 46–63) and 61.3% of the patients were male. The 12.6% (84/612) of the patients had CSFP, while the coronary flow was normal in the remaining 87.4% of patients. The PIV levels had moderate success for the prediction of the CSFP (AUC: 0.675, 95% CI: 0.615–0.735, p |
doi_str_mv | 10.1016/j.ijcard.2023.131631 |
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This single-center, retrospective study was composed of 612 patients aged over 18 years who underwent CAG for suspected stable ischemic heart disease. The association of clinical and laboratory parameters with the CSFP was evaluated with univariate and multivariate analyses.
The median age of the patients was 54 (IQR 46–63) and 61.3% of the patients were male. The 12.6% (84/612) of the patients had CSFP, while the coronary flow was normal in the remaining 87.4% of patients. The PIV levels had moderate success for the prediction of the CSFP (AUC: 0.675, 95% CI: 0.615–0.735, p < 0.001). In multivariate analyses, male gender (OR: 4.858, 95% CI: 2.851–8.277, p < 0.001), presence of diabetes (OR: 2.672, 95% CI: 1.396–5.113, p = 0.003), lower HDL-C values (OR: 2.120, 95% CI: 1.286–3.496, p = 0.003), and higher PIV levels (OR: 2.527, 95% CI: 1.519–4.203, p < 0.001) were associated with a higher risk of CSFP.
We demonstrated that a higher risk of CSFP in patients with PIV levels. If supported by prospective evidence, PIV levels could be used as a minimally invasive reflector of CSFP.
•Peripheral blood-derived prognostic indexes could be feasible way to predict the presence of CSFP.•Patients with higher PIV levels were associated with a higher risk of CSFP.•PIV level could serve as a non-invasive, cost-effective, and easily accessible tool for predicting CSFP.</description><identifier>ISSN: 0167-5273</identifier><identifier>EISSN: 1874-1754</identifier><identifier>DOI: 10.1016/j.ijcard.2023.131631</identifier><identifier>PMID: 38048881</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Coronary angiography ; Coronary slow phenomenon ; Inflammation ; pan-immune-inflammation value</subject><ispartof>International journal of cardiology, 2024-03, Vol.398, p.131631-131631, Article 131631</ispartof><rights>2023 Elsevier B.V.</rights><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-f49196a39f55307f2bcd12478a62b7e18f77303516eb2dd4c1766d398d30a3e83</citedby><cites>FETCH-LOGICAL-c362t-f49196a39f55307f2bcd12478a62b7e18f77303516eb2dd4c1766d398d30a3e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38048881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akkaya, Suleyman</creatorcontrib><creatorcontrib>Cakmak, Umit</creatorcontrib><title>Association between pan-immune-inflammation value and coronary slow flow phenomenon in patients with angiographically normal coronary arteries</title><title>International journal of cardiology</title><addtitle>Int J Cardiol</addtitle><description>Coronary slow flow phenomenon (CSFP) is characterized by the delayed contrast filling of terminal vessels of coronary arteries in the presence of normal or nearly normal epicardial coronary arteries. Given that inflammation plays a role in cardiovascular disorders, including CSFP, using peripheral blood-derived compound prognostic indexes could be a feasible way to predict the presence of CSFP. Therefore, in the present study, we evaluated the association between pan-immune-inflammation value (PIV) and the CSFP.
This single-center, retrospective study was composed of 612 patients aged over 18 years who underwent CAG for suspected stable ischemic heart disease. The association of clinical and laboratory parameters with the CSFP was evaluated with univariate and multivariate analyses.
The median age of the patients was 54 (IQR 46–63) and 61.3% of the patients were male. The 12.6% (84/612) of the patients had CSFP, while the coronary flow was normal in the remaining 87.4% of patients. The PIV levels had moderate success for the prediction of the CSFP (AUC: 0.675, 95% CI: 0.615–0.735, p < 0.001). In multivariate analyses, male gender (OR: 4.858, 95% CI: 2.851–8.277, p < 0.001), presence of diabetes (OR: 2.672, 95% CI: 1.396–5.113, p = 0.003), lower HDL-C values (OR: 2.120, 95% CI: 1.286–3.496, p = 0.003), and higher PIV levels (OR: 2.527, 95% CI: 1.519–4.203, p < 0.001) were associated with a higher risk of CSFP.
We demonstrated that a higher risk of CSFP in patients with PIV levels. If supported by prospective evidence, PIV levels could be used as a minimally invasive reflector of CSFP.
•Peripheral blood-derived prognostic indexes could be feasible way to predict the presence of CSFP.•Patients with higher PIV levels were associated with a higher risk of CSFP.•PIV level could serve as a non-invasive, cost-effective, and easily accessible tool for predicting CSFP.</description><subject>Coronary angiography</subject><subject>Coronary slow phenomenon</subject><subject>Inflammation</subject><subject>pan-immune-inflammation value</subject><issn>0167-5273</issn><issn>1874-1754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u3SAQhVHVqrn5eYOqYtmNb8HYgDeVoihtKkXKJl0jDONcrvhxwc5VXqLPXFtO210XDAu-c4aZg9AHSvaUUP75uHdHo7Pd16Rme8ooZ_QN2lEpmoqKtnmLdgsmqrYW7Aydl3IkhDRdJ9-jMyZJI6WkO_TrupRknJ5ciriH6QQQ8ahj5UKYI1QuDl6HsL0_az8D1tFik3KKOr_g4tMJD2sZDxBTWE7EbrWYHMSp4JObDovkyaWnrMeDM9r7FxxTDtr_s9F5guygXKJ3g_YFrl7vC_Tj6-3jzV11__Dt-831fWUYr6dqaDracc26oW0ZEUPdG0vrRkjN614AlYMQjLCWcuhraxtDBeeWddIyohlIdoE-bb5jTj9nKJMKrhjwXkdIc1G17CSjDRcr2myoyamUDIMaswvLpxUlak1CHdWWhFqTUFsSi-zja4e5D2D_iv6sfgG-bAAscz47yKqYZWUGrMtgJmWT-3-H304_nyw</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Akkaya, Suleyman</creator><creator>Cakmak, Umit</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240301</creationdate><title>Association between pan-immune-inflammation value and coronary slow flow phenomenon in patients with angiographically normal coronary arteries</title><author>Akkaya, Suleyman ; Cakmak, Umit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-f49196a39f55307f2bcd12478a62b7e18f77303516eb2dd4c1766d398d30a3e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Coronary angiography</topic><topic>Coronary slow phenomenon</topic><topic>Inflammation</topic><topic>pan-immune-inflammation value</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akkaya, Suleyman</creatorcontrib><creatorcontrib>Cakmak, Umit</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akkaya, Suleyman</au><au>Cakmak, Umit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between pan-immune-inflammation value and coronary slow flow phenomenon in patients with angiographically normal coronary arteries</atitle><jtitle>International journal of cardiology</jtitle><addtitle>Int J Cardiol</addtitle><date>2024-03-01</date><risdate>2024</risdate><volume>398</volume><spage>131631</spage><epage>131631</epage><pages>131631-131631</pages><artnum>131631</artnum><issn>0167-5273</issn><eissn>1874-1754</eissn><abstract>Coronary slow flow phenomenon (CSFP) is characterized by the delayed contrast filling of terminal vessels of coronary arteries in the presence of normal or nearly normal epicardial coronary arteries. Given that inflammation plays a role in cardiovascular disorders, including CSFP, using peripheral blood-derived compound prognostic indexes could be a feasible way to predict the presence of CSFP. Therefore, in the present study, we evaluated the association between pan-immune-inflammation value (PIV) and the CSFP.
This single-center, retrospective study was composed of 612 patients aged over 18 years who underwent CAG for suspected stable ischemic heart disease. The association of clinical and laboratory parameters with the CSFP was evaluated with univariate and multivariate analyses.
The median age of the patients was 54 (IQR 46–63) and 61.3% of the patients were male. The 12.6% (84/612) of the patients had CSFP, while the coronary flow was normal in the remaining 87.4% of patients. The PIV levels had moderate success for the prediction of the CSFP (AUC: 0.675, 95% CI: 0.615–0.735, p < 0.001). In multivariate analyses, male gender (OR: 4.858, 95% CI: 2.851–8.277, p < 0.001), presence of diabetes (OR: 2.672, 95% CI: 1.396–5.113, p = 0.003), lower HDL-C values (OR: 2.120, 95% CI: 1.286–3.496, p = 0.003), and higher PIV levels (OR: 2.527, 95% CI: 1.519–4.203, p < 0.001) were associated with a higher risk of CSFP.
We demonstrated that a higher risk of CSFP in patients with PIV levels. If supported by prospective evidence, PIV levels could be used as a minimally invasive reflector of CSFP.
•Peripheral blood-derived prognostic indexes could be feasible way to predict the presence of CSFP.•Patients with higher PIV levels were associated with a higher risk of CSFP.•PIV level could serve as a non-invasive, cost-effective, and easily accessible tool for predicting CSFP.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38048881</pmid><doi>10.1016/j.ijcard.2023.131631</doi><tpages>1</tpages></addata></record> |
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subjects | Coronary angiography Coronary slow phenomenon Inflammation pan-immune-inflammation value |
title | Association between pan-immune-inflammation value and coronary slow flow phenomenon in patients with angiographically normal coronary arteries |
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