IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries
Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflam...
Gespeichert in:
Veröffentlicht in: | Circulation research 2022-02, Vol.130 (3), p.326-338 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 338 |
---|---|
container_issue | 3 |
container_start_page | 326 |
container_title | Circulation research |
container_volume | 130 |
creator | Corban, Michel T. Toya, Takumi Albers, Diana Sebaali, Faten Lewis, Bradley R. Bois, John Gulati, Rajiv Prasad, Abhiram Best, Patricia J.M. Bell, Malcolm R. Rihal, Charanjit S. Prasad, Megha Ahmad, Ali Lerman, Lilach O. Solseth, Mary L. Winters, Jeffrey L. Dietz, Allan B. Lerman, Amir |
description | Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflammatory effects. We evaluated safety and potential efficacy of intracoronary autologous CD34+ cell therapy for CED.
Twenty NOCAD patients with invasively diagnosed CED and persistent angina despite maximally tolerated medical therapy underwent baseline exercise stress test, GCSF (granulocyte colony stimulating factor)-mediated CD34+ cell mobilization, leukapheresis, and selective 1×10
CD34+ cells/kg infusion into left anterior descending. Invasive CED evaluation and exercise stress test were repeated 6 months after cell infusion. Primary end points were safety and effect of intracoronary autologous CD34+ cell therapy on CED at 6 months of follow-up. Secondary end points were change in Canadian Cardiovascular Society angina class, as-needed sublingual nitroglycerin use/day, Seattle Angina Questionnaire scores, and exercise time at 6 months. Change in CED was compared with that of 51 historic control NOCAD patients treated with maximally tolerated medical therapy alone.
Mean age was 52±13 years; 75% were women. No death, myocardial infarction, or stroke occurred. Intracoronary CD34+ cell infusion improved microvascular CED (%acetylcholine-mediated coronary blood flow increased from 7.2 [-18.0 to 32.4] to 57.6 [16.3-98.3]%;
=0.014), decreased Canadian Cardiovascular Society angina class (3.7±0.5 to 1.7±0.9, Wilcoxon signed-rank test,
=0.00018), and sublingual nitroglycerin use/day (1 [0.4-3.5] to 0 [0-1], Wilcoxon signed-rank test,
=0.00047), and improved all Seattle Angina Questionnaire scores with no significant change in exercise time at 6 months of follow-up. Historic control patients had no significant change in CED.
A single intracoronary autologous CD34+ cell infusion was safe and may potentially be an effective disease-modifying therapy for microvascular CED in humans. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03471611. |
doi_str_mv | 10.1161/CIRCRESAHA.121.319644 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2612037612</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2612037612</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4015-b9eabf37712b3db85fc8b7a453996057f70f0ce292e4c6c44daa29429c4f58d93</originalsourceid><addsrcrecordid>eNpFkd9u0zAUhy0EYmXwCCBfIqEU_01q7qI0sEqDTaWIS8tx7CWQ2sV2NvWheEc8dWOSZUvW9zvHxx8AbzFaYlzij81m22zb7_VFvcQELykWJWPPwAJzwgrGK_wcLBBCoqgoRWfgVYy_EMKMEvESnFEmCF1xugB_N1-vt1e3bdG0a7gLo5o-wY1LQWkfvFPhCOs5-cnf-DnCZk3ZB9iYaYK7wQR1OELrQ44ZlfbGJegtbB5zret9GsyUS8L1MdrZ6TR6B0cHr1UaMx7hzzENsHY3o1NQuR5-8853MYU5o7fmqVYdkgmjia_BC6umaN48nOfgx-d211wUl1dfNk19WWiGMC86YVRnaVVh0tG-W3GrV12lGKdClIhXtkIWaUMEMUyXmrFeKSIYEZpZvuoFPQfvT3UPwf-ZTUxyP0ad51bO5I-QpMQE0SrvGeUnVAcfYzBWHsK4z4-WGMl7U_LJlMym5MlUzr17aDF3e9P_Tz2qyQA7AXd-ytPH39N8Z4IcjJrSILNaRBEmBUEkL8RQcX_F6T-rc6Fz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2612037612</pqid></control><display><type>article</type><title>IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries</title><source>MEDLINE</source><source>American Heart Association Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Journals@Ovid Complete</source><creator>Corban, Michel T. ; Toya, Takumi ; Albers, Diana ; Sebaali, Faten ; Lewis, Bradley R. ; Bois, John ; Gulati, Rajiv ; Prasad, Abhiram ; Best, Patricia J.M. ; Bell, Malcolm R. ; Rihal, Charanjit S. ; Prasad, Megha ; Ahmad, Ali ; Lerman, Lilach O. ; Solseth, Mary L. ; Winters, Jeffrey L. ; Dietz, Allan B. ; Lerman, Amir</creator><creatorcontrib>Corban, Michel T. ; Toya, Takumi ; Albers, Diana ; Sebaali, Faten ; Lewis, Bradley R. ; Bois, John ; Gulati, Rajiv ; Prasad, Abhiram ; Best, Patricia J.M. ; Bell, Malcolm R. ; Rihal, Charanjit S. ; Prasad, Megha ; Ahmad, Ali ; Lerman, Lilach O. ; Solseth, Mary L. ; Winters, Jeffrey L. ; Dietz, Allan B. ; Lerman, Amir</creatorcontrib><description>Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflammatory effects. We evaluated safety and potential efficacy of intracoronary autologous CD34+ cell therapy for CED.
Twenty NOCAD patients with invasively diagnosed CED and persistent angina despite maximally tolerated medical therapy underwent baseline exercise stress test, GCSF (granulocyte colony stimulating factor)-mediated CD34+ cell mobilization, leukapheresis, and selective 1×10
CD34+ cells/kg infusion into left anterior descending. Invasive CED evaluation and exercise stress test were repeated 6 months after cell infusion. Primary end points were safety and effect of intracoronary autologous CD34+ cell therapy on CED at 6 months of follow-up. Secondary end points were change in Canadian Cardiovascular Society angina class, as-needed sublingual nitroglycerin use/day, Seattle Angina Questionnaire scores, and exercise time at 6 months. Change in CED was compared with that of 51 historic control NOCAD patients treated with maximally tolerated medical therapy alone.
Mean age was 52±13 years; 75% were women. No death, myocardial infarction, or stroke occurred. Intracoronary CD34+ cell infusion improved microvascular CED (%acetylcholine-mediated coronary blood flow increased from 7.2 [-18.0 to 32.4] to 57.6 [16.3-98.3]%;
=0.014), decreased Canadian Cardiovascular Society angina class (3.7±0.5 to 1.7±0.9, Wilcoxon signed-rank test,
=0.00018), and sublingual nitroglycerin use/day (1 [0.4-3.5] to 0 [0-1], Wilcoxon signed-rank test,
=0.00047), and improved all Seattle Angina Questionnaire scores with no significant change in exercise time at 6 months of follow-up. Historic control patients had no significant change in CED.
A single intracoronary autologous CD34+ cell infusion was safe and may potentially be an effective disease-modifying therapy for microvascular CED in humans. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03471611.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/CIRCRESAHA.121.319644</identifier><identifier>PMID: 34923853</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Adult ; Aged ; Angina Pectoris - etiology ; Angina Pectoris - therapy ; Antigens, CD34 - genetics ; Antigens, CD34 - metabolism ; Coronary Artery Disease - complications ; Coronary Artery Disease - therapy ; Endothelium, Vascular - pathology ; Female ; Humans ; Leukapheresis - methods ; Male ; Middle Aged ; T-Lymphocytes - metabolism ; T-Lymphocytes - transplantation ; Transplantation, Autologous</subject><ispartof>Circulation research, 2022-02, Vol.130 (3), p.326-338</ispartof><rights>Lippincott Williams & Wilkins</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4015-b9eabf37712b3db85fc8b7a453996057f70f0ce292e4c6c44daa29429c4f58d93</citedby><cites>FETCH-LOGICAL-c4015-b9eabf37712b3db85fc8b7a453996057f70f0ce292e4c6c44daa29429c4f58d93</cites><orcidid>0000-0002-3271-3887 ; 0000-0001-8654-3732 ; 0000-0002-9446-5313 ; 0000-0002-2713-0433 ; 0000-0002-4681-2798 ; 0000-0003-3410-9621 ; 0000-0001-9669-8009 ; 0000-0002-7934-8741 ; 0000-0003-2044-4664</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34923853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Corban, Michel T.</creatorcontrib><creatorcontrib>Toya, Takumi</creatorcontrib><creatorcontrib>Albers, Diana</creatorcontrib><creatorcontrib>Sebaali, Faten</creatorcontrib><creatorcontrib>Lewis, Bradley R.</creatorcontrib><creatorcontrib>Bois, John</creatorcontrib><creatorcontrib>Gulati, Rajiv</creatorcontrib><creatorcontrib>Prasad, Abhiram</creatorcontrib><creatorcontrib>Best, Patricia J.M.</creatorcontrib><creatorcontrib>Bell, Malcolm R.</creatorcontrib><creatorcontrib>Rihal, Charanjit S.</creatorcontrib><creatorcontrib>Prasad, Megha</creatorcontrib><creatorcontrib>Ahmad, Ali</creatorcontrib><creatorcontrib>Lerman, Lilach O.</creatorcontrib><creatorcontrib>Solseth, Mary L.</creatorcontrib><creatorcontrib>Winters, Jeffrey L.</creatorcontrib><creatorcontrib>Dietz, Allan B.</creatorcontrib><creatorcontrib>Lerman, Amir</creatorcontrib><title>IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflammatory effects. We evaluated safety and potential efficacy of intracoronary autologous CD34+ cell therapy for CED.
Twenty NOCAD patients with invasively diagnosed CED and persistent angina despite maximally tolerated medical therapy underwent baseline exercise stress test, GCSF (granulocyte colony stimulating factor)-mediated CD34+ cell mobilization, leukapheresis, and selective 1×10
CD34+ cells/kg infusion into left anterior descending. Invasive CED evaluation and exercise stress test were repeated 6 months after cell infusion. Primary end points were safety and effect of intracoronary autologous CD34+ cell therapy on CED at 6 months of follow-up. Secondary end points were change in Canadian Cardiovascular Society angina class, as-needed sublingual nitroglycerin use/day, Seattle Angina Questionnaire scores, and exercise time at 6 months. Change in CED was compared with that of 51 historic control NOCAD patients treated with maximally tolerated medical therapy alone.
Mean age was 52±13 years; 75% were women. No death, myocardial infarction, or stroke occurred. Intracoronary CD34+ cell infusion improved microvascular CED (%acetylcholine-mediated coronary blood flow increased from 7.2 [-18.0 to 32.4] to 57.6 [16.3-98.3]%;
=0.014), decreased Canadian Cardiovascular Society angina class (3.7±0.5 to 1.7±0.9, Wilcoxon signed-rank test,
=0.00018), and sublingual nitroglycerin use/day (1 [0.4-3.5] to 0 [0-1], Wilcoxon signed-rank test,
=0.00047), and improved all Seattle Angina Questionnaire scores with no significant change in exercise time at 6 months of follow-up. Historic control patients had no significant change in CED.
A single intracoronary autologous CD34+ cell infusion was safe and may potentially be an effective disease-modifying therapy for microvascular CED in humans. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03471611.</description><subject>Adult</subject><subject>Aged</subject><subject>Angina Pectoris - etiology</subject><subject>Angina Pectoris - therapy</subject><subject>Antigens, CD34 - genetics</subject><subject>Antigens, CD34 - metabolism</subject><subject>Coronary Artery Disease - complications</subject><subject>Coronary Artery Disease - therapy</subject><subject>Endothelium, Vascular - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Leukapheresis - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>T-Lymphocytes - metabolism</subject><subject>T-Lymphocytes - transplantation</subject><subject>Transplantation, Autologous</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkd9u0zAUhy0EYmXwCCBfIqEU_01q7qI0sEqDTaWIS8tx7CWQ2sV2NvWheEc8dWOSZUvW9zvHxx8AbzFaYlzij81m22zb7_VFvcQELykWJWPPwAJzwgrGK_wcLBBCoqgoRWfgVYy_EMKMEvESnFEmCF1xugB_N1-vt1e3bdG0a7gLo5o-wY1LQWkfvFPhCOs5-cnf-DnCZk3ZB9iYaYK7wQR1OELrQ44ZlfbGJegtbB5zret9GsyUS8L1MdrZ6TR6B0cHr1UaMx7hzzENsHY3o1NQuR5-8853MYU5o7fmqVYdkgmjia_BC6umaN48nOfgx-d211wUl1dfNk19WWiGMC86YVRnaVVh0tG-W3GrV12lGKdClIhXtkIWaUMEMUyXmrFeKSIYEZpZvuoFPQfvT3UPwf-ZTUxyP0ad51bO5I-QpMQE0SrvGeUnVAcfYzBWHsK4z4-WGMl7U_LJlMym5MlUzr17aDF3e9P_Tz2qyQA7AXd-ytPH39N8Z4IcjJrSILNaRBEmBUEkL8RQcX_F6T-rc6Fz</recordid><startdate>20220204</startdate><enddate>20220204</enddate><creator>Corban, Michel T.</creator><creator>Toya, Takumi</creator><creator>Albers, Diana</creator><creator>Sebaali, Faten</creator><creator>Lewis, Bradley R.</creator><creator>Bois, John</creator><creator>Gulati, Rajiv</creator><creator>Prasad, Abhiram</creator><creator>Best, Patricia J.M.</creator><creator>Bell, Malcolm R.</creator><creator>Rihal, Charanjit S.</creator><creator>Prasad, Megha</creator><creator>Ahmad, Ali</creator><creator>Lerman, Lilach O.</creator><creator>Solseth, Mary L.</creator><creator>Winters, Jeffrey L.</creator><creator>Dietz, Allan B.</creator><creator>Lerman, Amir</creator><general>Lippincott Williams & Wilkins</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>7X8</scope><orcidid>https://orcid.org/0000-0002-3271-3887</orcidid><orcidid>https://orcid.org/0000-0001-8654-3732</orcidid><orcidid>https://orcid.org/0000-0002-9446-5313</orcidid><orcidid>https://orcid.org/0000-0002-2713-0433</orcidid><orcidid>https://orcid.org/0000-0002-4681-2798</orcidid><orcidid>https://orcid.org/0000-0003-3410-9621</orcidid><orcidid>https://orcid.org/0000-0001-9669-8009</orcidid><orcidid>https://orcid.org/0000-0002-7934-8741</orcidid><orcidid>https://orcid.org/0000-0003-2044-4664</orcidid></search><sort><creationdate>20220204</creationdate><title>IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries</title><author>Corban, Michel T. ; Toya, Takumi ; Albers, Diana ; Sebaali, Faten ; Lewis, Bradley R. ; Bois, John ; Gulati, Rajiv ; Prasad, Abhiram ; Best, Patricia J.M. ; Bell, Malcolm R. ; Rihal, Charanjit S. ; Prasad, Megha ; Ahmad, Ali ; Lerman, Lilach O. ; Solseth, Mary L. ; Winters, Jeffrey L. ; Dietz, Allan B. ; Lerman, Amir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4015-b9eabf37712b3db85fc8b7a453996057f70f0ce292e4c6c44daa29429c4f58d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Angina Pectoris - etiology</topic><topic>Angina Pectoris - therapy</topic><topic>Antigens, CD34 - genetics</topic><topic>Antigens, CD34 - metabolism</topic><topic>Coronary Artery Disease - complications</topic><topic>Coronary Artery Disease - therapy</topic><topic>Endothelium, Vascular - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Leukapheresis - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>T-Lymphocytes - metabolism</topic><topic>T-Lymphocytes - transplantation</topic><topic>Transplantation, Autologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Corban, Michel T.</creatorcontrib><creatorcontrib>Toya, Takumi</creatorcontrib><creatorcontrib>Albers, Diana</creatorcontrib><creatorcontrib>Sebaali, Faten</creatorcontrib><creatorcontrib>Lewis, Bradley R.</creatorcontrib><creatorcontrib>Bois, John</creatorcontrib><creatorcontrib>Gulati, Rajiv</creatorcontrib><creatorcontrib>Prasad, Abhiram</creatorcontrib><creatorcontrib>Best, Patricia J.M.</creatorcontrib><creatorcontrib>Bell, Malcolm R.</creatorcontrib><creatorcontrib>Rihal, Charanjit S.</creatorcontrib><creatorcontrib>Prasad, Megha</creatorcontrib><creatorcontrib>Ahmad, Ali</creatorcontrib><creatorcontrib>Lerman, Lilach O.</creatorcontrib><creatorcontrib>Solseth, Mary L.</creatorcontrib><creatorcontrib>Winters, Jeffrey L.</creatorcontrib><creatorcontrib>Dietz, Allan B.</creatorcontrib><creatorcontrib>Lerman, Amir</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Corban, Michel T.</au><au>Toya, Takumi</au><au>Albers, Diana</au><au>Sebaali, Faten</au><au>Lewis, Bradley R.</au><au>Bois, John</au><au>Gulati, Rajiv</au><au>Prasad, Abhiram</au><au>Best, Patricia J.M.</au><au>Bell, Malcolm R.</au><au>Rihal, Charanjit S.</au><au>Prasad, Megha</au><au>Ahmad, Ali</au><au>Lerman, Lilach O.</au><au>Solseth, Mary L.</au><au>Winters, Jeffrey L.</au><au>Dietz, Allan B.</au><au>Lerman, Amir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2022-02-04</date><risdate>2022</risdate><volume>130</volume><issue>3</issue><spage>326</spage><epage>338</epage><pages>326-338</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><abstract>Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflammatory effects. We evaluated safety and potential efficacy of intracoronary autologous CD34+ cell therapy for CED.
Twenty NOCAD patients with invasively diagnosed CED and persistent angina despite maximally tolerated medical therapy underwent baseline exercise stress test, GCSF (granulocyte colony stimulating factor)-mediated CD34+ cell mobilization, leukapheresis, and selective 1×10
CD34+ cells/kg infusion into left anterior descending. Invasive CED evaluation and exercise stress test were repeated 6 months after cell infusion. Primary end points were safety and effect of intracoronary autologous CD34+ cell therapy on CED at 6 months of follow-up. Secondary end points were change in Canadian Cardiovascular Society angina class, as-needed sublingual nitroglycerin use/day, Seattle Angina Questionnaire scores, and exercise time at 6 months. Change in CED was compared with that of 51 historic control NOCAD patients treated with maximally tolerated medical therapy alone.
Mean age was 52±13 years; 75% were women. No death, myocardial infarction, or stroke occurred. Intracoronary CD34+ cell infusion improved microvascular CED (%acetylcholine-mediated coronary blood flow increased from 7.2 [-18.0 to 32.4] to 57.6 [16.3-98.3]%;
=0.014), decreased Canadian Cardiovascular Society angina class (3.7±0.5 to 1.7±0.9, Wilcoxon signed-rank test,
=0.00018), and sublingual nitroglycerin use/day (1 [0.4-3.5] to 0 [0-1], Wilcoxon signed-rank test,
=0.00047), and improved all Seattle Angina Questionnaire scores with no significant change in exercise time at 6 months of follow-up. Historic control patients had no significant change in CED.
A single intracoronary autologous CD34+ cell infusion was safe and may potentially be an effective disease-modifying therapy for microvascular CED in humans. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03471611.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>34923853</pmid><doi>10.1161/CIRCRESAHA.121.319644</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-3271-3887</orcidid><orcidid>https://orcid.org/0000-0001-8654-3732</orcidid><orcidid>https://orcid.org/0000-0002-9446-5313</orcidid><orcidid>https://orcid.org/0000-0002-2713-0433</orcidid><orcidid>https://orcid.org/0000-0002-4681-2798</orcidid><orcidid>https://orcid.org/0000-0003-3410-9621</orcidid><orcidid>https://orcid.org/0000-0001-9669-8009</orcidid><orcidid>https://orcid.org/0000-0002-7934-8741</orcidid><orcidid>https://orcid.org/0000-0003-2044-4664</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-7330 |
ispartof | Circulation research, 2022-02, Vol.130 (3), p.326-338 |
issn | 0009-7330 1524-4571 |
language | eng |
recordid | cdi_proquest_miscellaneous_2612037612 |
source | MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete |
subjects | Adult Aged Angina Pectoris - etiology Angina Pectoris - therapy Antigens, CD34 - genetics Antigens, CD34 - metabolism Coronary Artery Disease - complications Coronary Artery Disease - therapy Endothelium, Vascular - pathology Female Humans Leukapheresis - methods Male Middle Aged T-Lymphocytes - metabolism T-Lymphocytes - transplantation Transplantation, Autologous |
title | IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T02%3A02%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=IMPROvE-CED%20Trial:%20Intracoronary%20Autologous%20CD34+%20Cell%20Therapy%20for%20Treatment%20of%20Coronary%20Endothelial%20Dysfunction%20in%20Patients%20With%20Angina%20and%20Nonobstructive%20Coronary%20Arteries&rft.jtitle=Circulation%20research&rft.au=Corban,%20Michel%20T.&rft.date=2022-02-04&rft.volume=130&rft.issue=3&rft.spage=326&rft.epage=338&rft.pages=326-338&rft.issn=0009-7330&rft.eissn=1524-4571&rft_id=info:doi/10.1161/CIRCRESAHA.121.319644&rft_dat=%3Cproquest_cross%3E2612037612%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2612037612&rft_id=info:pmid/34923853&rfr_iscdi=true |