Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis
RATIONALE:Cardiac involvement and hypotension dominate the prognosis of light-chain amyloidosis (AL). Evidence suggests that there is also peripheral vascular involvement in AL but its prognostic significance is unknown. OBJECTIVE:To evaluate vascular dysfunction in patients with AL as a potential f...
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Veröffentlicht in: | Circulation research 2019-09, Vol.125 (8), p.744-758 |
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creator | Stamatelopoulos, Kimon Georgiopoulos, Georgios Athanasouli, Fani Nikolaou, Panagiota-Efstathia Lyka, Marita Roussou, Maria Gavriatopoulou, Maria Laina, Aggeliki Trakada, Georgia Charakida, Marietta Delialis, Dimitris Petropoulos, Ioannis Pamboukas, Constantinos Manios, Efstathios Karakitsou, Marina Papamichael, Christos Gatsiou, Aikaterini Lambrinoudaki, Irene Terpos, Evangelos Stellos, Konstantinos Andreadou, Ioanna Dimopoulos, Meletios A Kastritis, Efstathios |
description | RATIONALE:Cardiac involvement and hypotension dominate the prognosis of light-chain amyloidosis (AL). Evidence suggests that there is also peripheral vascular involvement in AL but its prognostic significance is unknown.
OBJECTIVE:To evaluate vascular dysfunction in patients with AL as a potential future area of intervention, we assessed the prognostic utility of flow-mediated dilatation (FMD), a marker of vascular reactivity, which is augmented under conditions of hypotension and autonomic dysfunction.
METHODS AND RESULTS:We prospectively evaluated 115 newly diagnosed untreated AL patients in whom FMD was measured. FMD in AL patients was significantly higher than age-, sex- and risk factors–matched controls (4.0% versus 2.32%; P=0.006) and comparable with control groups at lower cardiovascular risk (P>0.1). Amyloidosis patients presented increased plasma and exhaled markers of the NO pathway while their FMD significantly correlated with augmented sustained vasodilatation after sympathetic stimulation. Increased FMD (≥4.5%) was associated with early mortality (hazard ratio, 4.36; 95% CI, 1.41–13.5; P=0.010) and worse survival (hazard ratio, 2.11; 95% CI, 1.17–3.82; P=0.013), even after adjustment for Mayo stage, nerve involvement and low systolic blood pressure. This finding was confirmed in a temporal validation AL cohort (n=55; hazard ratio, 4.2; 95% CI, 1.45–12.3; P=0.008). FMD provided significant reclassification value over the best prognostic model (continuous Net Reclassification Index, 0.61; P=0.001). Finally, better hematologic response was associated with lower posttreatment FMD.
CONCLUSIONS:FMD is relatively increased in AL and independently associated with inferior survival with substantial reclassification value. Reactive vasodilation merits further investigation as a novel risk biomarker in AL.Visual OverviewAn online visual overview is available for this article. |
doi_str_mv | 10.1161/CIRCRESAHA.119.314862 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6784773</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2272219975</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4564-e59f8b53433815208f7b5a6086439361052507ecb361d7c875afd480a938cdab3</originalsourceid><addsrcrecordid>eNpVkV1PFDEUhhsjkXXxJ2jm0pvBfk7bG5PNBIRkiWRBb5tOp8NUO1tsu5D993YzCHJ1vp5z-qYvAB8RPEWoQV_ay027ObtZXaxKLU8JoqLBb8ACMUxryjh6CxYQQllzQuAxeJ_SLwgRJVi-A8eFhkhSuQC3G6tNdg-2-qlT6J3X2YVtdR1t70xO1VWIWXuX95U7dN2k47662adsJ2eqtbsbc92OugxX094H14fk0gk4GrRP9sNTXIIf52e37UW9_v7tsl2ta0NZQ2vL5CA6RighosiGYuAd0w0UDSWSNAgyzCC3pit5z43gTA89FVBLIkyvO7IEX-e797tusr2x2xy1V_ezTBW0U68nWzequ_CgGi4oLx-zBJ-fDsTwZ2dTVpNLxnqvtzbsksKYY4yk5KygbEZNDClFOzw_g6A6OKJeHCm1VLMjZe_T_xqft_5ZUAA6A4_BZxvTb797tFGNVvs8qmIhJBDhGhcaSsxhfWhR8hejrphl</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2272219975</pqid></control><display><type>article</type><title>Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis</title><source>American Heart Association</source><source>Journals@Ovid Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Stamatelopoulos, Kimon ; Georgiopoulos, Georgios ; Athanasouli, Fani ; Nikolaou, Panagiota-Efstathia ; Lyka, Marita ; Roussou, Maria ; Gavriatopoulou, Maria ; Laina, Aggeliki ; Trakada, Georgia ; Charakida, Marietta ; Delialis, Dimitris ; Petropoulos, Ioannis ; Pamboukas, Constantinos ; Manios, Efstathios ; Karakitsou, Marina ; Papamichael, Christos ; Gatsiou, Aikaterini ; Lambrinoudaki, Irene ; Terpos, Evangelos ; Stellos, Konstantinos ; Andreadou, Ioanna ; Dimopoulos, Meletios A ; Kastritis, Efstathios</creator><creatorcontrib>Stamatelopoulos, Kimon ; Georgiopoulos, Georgios ; Athanasouli, Fani ; Nikolaou, Panagiota-Efstathia ; Lyka, Marita ; Roussou, Maria ; Gavriatopoulou, Maria ; Laina, Aggeliki ; Trakada, Georgia ; Charakida, Marietta ; Delialis, Dimitris ; Petropoulos, Ioannis ; Pamboukas, Constantinos ; Manios, Efstathios ; Karakitsou, Marina ; Papamichael, Christos ; Gatsiou, Aikaterini ; Lambrinoudaki, Irene ; Terpos, Evangelos ; Stellos, Konstantinos ; Andreadou, Ioanna ; Dimopoulos, Meletios A ; Kastritis, Efstathios</creatorcontrib><description>RATIONALE:Cardiac involvement and hypotension dominate the prognosis of light-chain amyloidosis (AL). Evidence suggests that there is also peripheral vascular involvement in AL but its prognostic significance is unknown.
OBJECTIVE:To evaluate vascular dysfunction in patients with AL as a potential future area of intervention, we assessed the prognostic utility of flow-mediated dilatation (FMD), a marker of vascular reactivity, which is augmented under conditions of hypotension and autonomic dysfunction.
METHODS AND RESULTS:We prospectively evaluated 115 newly diagnosed untreated AL patients in whom FMD was measured. FMD in AL patients was significantly higher than age-, sex- and risk factors–matched controls (4.0% versus 2.32%; P=0.006) and comparable with control groups at lower cardiovascular risk (P>0.1). Amyloidosis patients presented increased plasma and exhaled markers of the NO pathway while their FMD significantly correlated with augmented sustained vasodilatation after sympathetic stimulation. Increased FMD (≥4.5%) was associated with early mortality (hazard ratio, 4.36; 95% CI, 1.41–13.5; P=0.010) and worse survival (hazard ratio, 2.11; 95% CI, 1.17–3.82; P=0.013), even after adjustment for Mayo stage, nerve involvement and low systolic blood pressure. This finding was confirmed in a temporal validation AL cohort (n=55; hazard ratio, 4.2; 95% CI, 1.45–12.3; P=0.008). FMD provided significant reclassification value over the best prognostic model (continuous Net Reclassification Index, 0.61; P=0.001). Finally, better hematologic response was associated with lower posttreatment FMD.
CONCLUSIONS:FMD is relatively increased in AL and independently associated with inferior survival with substantial reclassification value. Reactive vasodilation merits further investigation as a novel risk biomarker in AL.Visual OverviewAn online visual overview is available for this article.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/CIRCRESAHA.119.314862</identifier><identifier>PMID: 31401949</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Original Research</subject><ispartof>Circulation research, 2019-09, Vol.125 (8), p.744-758</ispartof><rights>2019 American Heart Association, Inc.</rights><rights>2019 The Authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4564-e59f8b53433815208f7b5a6086439361052507ecb361d7c875afd480a938cdab3</citedby><cites>FETCH-LOGICAL-c4564-e59f8b53433815208f7b5a6086439361052507ecb361d7c875afd480a938cdab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3687,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31401949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stamatelopoulos, Kimon</creatorcontrib><creatorcontrib>Georgiopoulos, Georgios</creatorcontrib><creatorcontrib>Athanasouli, Fani</creatorcontrib><creatorcontrib>Nikolaou, Panagiota-Efstathia</creatorcontrib><creatorcontrib>Lyka, Marita</creatorcontrib><creatorcontrib>Roussou, Maria</creatorcontrib><creatorcontrib>Gavriatopoulou, Maria</creatorcontrib><creatorcontrib>Laina, Aggeliki</creatorcontrib><creatorcontrib>Trakada, Georgia</creatorcontrib><creatorcontrib>Charakida, Marietta</creatorcontrib><creatorcontrib>Delialis, Dimitris</creatorcontrib><creatorcontrib>Petropoulos, Ioannis</creatorcontrib><creatorcontrib>Pamboukas, Constantinos</creatorcontrib><creatorcontrib>Manios, Efstathios</creatorcontrib><creatorcontrib>Karakitsou, Marina</creatorcontrib><creatorcontrib>Papamichael, Christos</creatorcontrib><creatorcontrib>Gatsiou, Aikaterini</creatorcontrib><creatorcontrib>Lambrinoudaki, Irene</creatorcontrib><creatorcontrib>Terpos, Evangelos</creatorcontrib><creatorcontrib>Stellos, Konstantinos</creatorcontrib><creatorcontrib>Andreadou, Ioanna</creatorcontrib><creatorcontrib>Dimopoulos, Meletios A</creatorcontrib><creatorcontrib>Kastritis, Efstathios</creatorcontrib><title>Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>RATIONALE:Cardiac involvement and hypotension dominate the prognosis of light-chain amyloidosis (AL). Evidence suggests that there is also peripheral vascular involvement in AL but its prognostic significance is unknown.
OBJECTIVE:To evaluate vascular dysfunction in patients with AL as a potential future area of intervention, we assessed the prognostic utility of flow-mediated dilatation (FMD), a marker of vascular reactivity, which is augmented under conditions of hypotension and autonomic dysfunction.
METHODS AND RESULTS:We prospectively evaluated 115 newly diagnosed untreated AL patients in whom FMD was measured. FMD in AL patients was significantly higher than age-, sex- and risk factors–matched controls (4.0% versus 2.32%; P=0.006) and comparable with control groups at lower cardiovascular risk (P>0.1). Amyloidosis patients presented increased plasma and exhaled markers of the NO pathway while their FMD significantly correlated with augmented sustained vasodilatation after sympathetic stimulation. Increased FMD (≥4.5%) was associated with early mortality (hazard ratio, 4.36; 95% CI, 1.41–13.5; P=0.010) and worse survival (hazard ratio, 2.11; 95% CI, 1.17–3.82; P=0.013), even after adjustment for Mayo stage, nerve involvement and low systolic blood pressure. This finding was confirmed in a temporal validation AL cohort (n=55; hazard ratio, 4.2; 95% CI, 1.45–12.3; P=0.008). FMD provided significant reclassification value over the best prognostic model (continuous Net Reclassification Index, 0.61; P=0.001). Finally, better hematologic response was associated with lower posttreatment FMD.
CONCLUSIONS:FMD is relatively increased in AL and independently associated with inferior survival with substantial reclassification value. Reactive vasodilation merits further investigation as a novel risk biomarker in AL.Visual OverviewAn online visual overview is available for this article.</description><subject>Original Research</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkV1PFDEUhhsjkXXxJ2jm0pvBfk7bG5PNBIRkiWRBb5tOp8NUO1tsu5D993YzCHJ1vp5z-qYvAB8RPEWoQV_ay027ObtZXaxKLU8JoqLBb8ACMUxryjh6CxYQQllzQuAxeJ_SLwgRJVi-A8eFhkhSuQC3G6tNdg-2-qlT6J3X2YVtdR1t70xO1VWIWXuX95U7dN2k47662adsJ2eqtbsbc92OugxX094H14fk0gk4GrRP9sNTXIIf52e37UW9_v7tsl2ta0NZQ2vL5CA6RighosiGYuAd0w0UDSWSNAgyzCC3pit5z43gTA89FVBLIkyvO7IEX-e797tusr2x2xy1V_ezTBW0U68nWzequ_CgGi4oLx-zBJ-fDsTwZ2dTVpNLxnqvtzbsksKYY4yk5KygbEZNDClFOzw_g6A6OKJeHCm1VLMjZe_T_xqft_5ZUAA6A4_BZxvTb797tFGNVvs8qmIhJBDhGhcaSsxhfWhR8hejrphl</recordid><startdate>20190927</startdate><enddate>20190927</enddate><creator>Stamatelopoulos, Kimon</creator><creator>Georgiopoulos, Georgios</creator><creator>Athanasouli, Fani</creator><creator>Nikolaou, Panagiota-Efstathia</creator><creator>Lyka, Marita</creator><creator>Roussou, Maria</creator><creator>Gavriatopoulou, Maria</creator><creator>Laina, Aggeliki</creator><creator>Trakada, Georgia</creator><creator>Charakida, Marietta</creator><creator>Delialis, Dimitris</creator><creator>Petropoulos, Ioannis</creator><creator>Pamboukas, Constantinos</creator><creator>Manios, Efstathios</creator><creator>Karakitsou, Marina</creator><creator>Papamichael, Christos</creator><creator>Gatsiou, Aikaterini</creator><creator>Lambrinoudaki, Irene</creator><creator>Terpos, Evangelos</creator><creator>Stellos, Konstantinos</creator><creator>Andreadou, Ioanna</creator><creator>Dimopoulos, Meletios A</creator><creator>Kastritis, Efstathios</creator><general>American Heart Association, Inc</general><general>Lippincott Williams & Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190927</creationdate><title>Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis</title><author>Stamatelopoulos, Kimon ; Georgiopoulos, Georgios ; Athanasouli, Fani ; Nikolaou, Panagiota-Efstathia ; Lyka, Marita ; Roussou, Maria ; Gavriatopoulou, Maria ; Laina, Aggeliki ; Trakada, Georgia ; Charakida, Marietta ; Delialis, Dimitris ; Petropoulos, Ioannis ; Pamboukas, Constantinos ; Manios, Efstathios ; Karakitsou, Marina ; Papamichael, Christos ; Gatsiou, Aikaterini ; Lambrinoudaki, Irene ; Terpos, Evangelos ; Stellos, Konstantinos ; Andreadou, Ioanna ; Dimopoulos, Meletios A ; Kastritis, Efstathios</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4564-e59f8b53433815208f7b5a6086439361052507ecb361d7c875afd480a938cdab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Original Research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stamatelopoulos, Kimon</creatorcontrib><creatorcontrib>Georgiopoulos, Georgios</creatorcontrib><creatorcontrib>Athanasouli, Fani</creatorcontrib><creatorcontrib>Nikolaou, Panagiota-Efstathia</creatorcontrib><creatorcontrib>Lyka, Marita</creatorcontrib><creatorcontrib>Roussou, Maria</creatorcontrib><creatorcontrib>Gavriatopoulou, Maria</creatorcontrib><creatorcontrib>Laina, Aggeliki</creatorcontrib><creatorcontrib>Trakada, Georgia</creatorcontrib><creatorcontrib>Charakida, Marietta</creatorcontrib><creatorcontrib>Delialis, Dimitris</creatorcontrib><creatorcontrib>Petropoulos, Ioannis</creatorcontrib><creatorcontrib>Pamboukas, Constantinos</creatorcontrib><creatorcontrib>Manios, Efstathios</creatorcontrib><creatorcontrib>Karakitsou, Marina</creatorcontrib><creatorcontrib>Papamichael, Christos</creatorcontrib><creatorcontrib>Gatsiou, Aikaterini</creatorcontrib><creatorcontrib>Lambrinoudaki, Irene</creatorcontrib><creatorcontrib>Terpos, Evangelos</creatorcontrib><creatorcontrib>Stellos, Konstantinos</creatorcontrib><creatorcontrib>Andreadou, Ioanna</creatorcontrib><creatorcontrib>Dimopoulos, Meletios A</creatorcontrib><creatorcontrib>Kastritis, Efstathios</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stamatelopoulos, Kimon</au><au>Georgiopoulos, Georgios</au><au>Athanasouli, Fani</au><au>Nikolaou, Panagiota-Efstathia</au><au>Lyka, Marita</au><au>Roussou, Maria</au><au>Gavriatopoulou, Maria</au><au>Laina, Aggeliki</au><au>Trakada, Georgia</au><au>Charakida, Marietta</au><au>Delialis, Dimitris</au><au>Petropoulos, Ioannis</au><au>Pamboukas, Constantinos</au><au>Manios, Efstathios</au><au>Karakitsou, Marina</au><au>Papamichael, Christos</au><au>Gatsiou, Aikaterini</au><au>Lambrinoudaki, Irene</au><au>Terpos, Evangelos</au><au>Stellos, Konstantinos</au><au>Andreadou, Ioanna</au><au>Dimopoulos, Meletios A</au><au>Kastritis, Efstathios</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2019-09-27</date><risdate>2019</risdate><volume>125</volume><issue>8</issue><spage>744</spage><epage>758</epage><pages>744-758</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><abstract>RATIONALE:Cardiac involvement and hypotension dominate the prognosis of light-chain amyloidosis (AL). Evidence suggests that there is also peripheral vascular involvement in AL but its prognostic significance is unknown.
OBJECTIVE:To evaluate vascular dysfunction in patients with AL as a potential future area of intervention, we assessed the prognostic utility of flow-mediated dilatation (FMD), a marker of vascular reactivity, which is augmented under conditions of hypotension and autonomic dysfunction.
METHODS AND RESULTS:We prospectively evaluated 115 newly diagnosed untreated AL patients in whom FMD was measured. FMD in AL patients was significantly higher than age-, sex- and risk factors–matched controls (4.0% versus 2.32%; P=0.006) and comparable with control groups at lower cardiovascular risk (P>0.1). Amyloidosis patients presented increased plasma and exhaled markers of the NO pathway while their FMD significantly correlated with augmented sustained vasodilatation after sympathetic stimulation. Increased FMD (≥4.5%) was associated with early mortality (hazard ratio, 4.36; 95% CI, 1.41–13.5; P=0.010) and worse survival (hazard ratio, 2.11; 95% CI, 1.17–3.82; P=0.013), even after adjustment for Mayo stage, nerve involvement and low systolic blood pressure. This finding was confirmed in a temporal validation AL cohort (n=55; hazard ratio, 4.2; 95% CI, 1.45–12.3; P=0.008). FMD provided significant reclassification value over the best prognostic model (continuous Net Reclassification Index, 0.61; P=0.001). Finally, better hematologic response was associated with lower posttreatment FMD.
CONCLUSIONS:FMD is relatively increased in AL and independently associated with inferior survival with substantial reclassification value. Reactive vasodilation merits further investigation as a novel risk biomarker in AL.Visual OverviewAn online visual overview is available for this article.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>31401949</pmid><doi>10.1161/CIRCRESAHA.119.314862</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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title | Reactive Vasodilation Predicts Mortality in Primary Systemic Light-Chain Amyloidosis |
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