FRI0246 Detection of left ventricular regional dysfunction and myocardial abnormalities using complementary cardiac magnetic resonance imaging in patients with systemic sclerosis without cardiac symptoms

Background In patients with systemic sclerosis (SSc), myocardial involvement is common, may have serious consequences, and may lead to a poor prognosis. Regional left ventricular (LV) dysfunction reflects myocardial involvement. The regional LV function in SSc has not been systematically studied usi...

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Veröffentlicht in:Annals of the rheumatic diseases 2013-06, Vol.71 (Suppl 3), p.397
Hauptverfasser: Kobayashi, H., Yokoe, I., Sato, H., Kobayashi, Y.
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container_issue Suppl 3
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container_title Annals of the rheumatic diseases
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creator Kobayashi, H.
Yokoe, I.
Sato, H.
Kobayashi, Y.
description Background In patients with systemic sclerosis (SSc), myocardial involvement is common, may have serious consequences, and may lead to a poor prognosis. Regional left ventricular (LV) dysfunction reflects myocardial involvement. The regional LV function in SSc has not been systematically studied using cardiac magnetic resonance (CMR) imaging. Combining perfusion and delayed enhancement MR imaging together may reveal important clues to the pathophysiologic mechanisms of myocardial involvements in SSc. Objectives We aimed to detect LV regional dysfunction and myocardial abnormalities in patients with SSc without cardiac symptoms using a CMR approach. Methods Consecutive patients with SSc who had no past history or current clinical findings of hypertension, coronary artery disease, valvular heart disease, atrial fibrillation, diabetes mellitus, dyslipidemia, or echocardiographic abnormalities and healthy controls underwent CMR on a 1.5 T scanner. Peak systolic regional radial strain (Err, %) was calculated from a feature tracking analysis on mid-left ventricular slices obtained with cine MRI in six segments. Furthermore, stress perfusion scan was performed to assess perfusion defects (PD) due to micro or macrovascular impairment, and delayed enhancement (DE) images were obtained d for the assessment of myocarditis and/or fibrosis. We compared the patients and controls in terms of prevalence of CMR abnormalities, and explored possible associations between CMR abnormalities and SSc disease characteristics. Group comparisons were made using the Wilcoxon Chi-square test, and the Tukey-Kramer’s test and Fisher’s exact test. Results We compared 19 patients with SSc (100%female; mean age, 58.8±8.7 years; 10 had limited cutaneous SSc and 9 diffuse cutaneous SSc) with 10 healthy controls (100% female; mean age, 55.7±4.52 years). No statistically significant differences were observed in baseline characteristics between the patients and healthy controls. The mean peak Err of all segments was significantly lower in the patients than the controls (0.49±0.04 vs.0.69±0.05; p=0.008).The mean peak Err of the patients with limited cutaneous SSc tended to be lower than those with diffuse cutaneous SSc (p=0.18). The mean peak Err of patients with digital ulcer tended to be lower than those without it (p=0.36). Other SSc characteristics were not associated with the mean peak Err. Five patients with DE (26.3%) and 11 patients with PD (57.9%) were observed. The mean peak Err in the
doi_str_mv 10.1136/annrheumdis-2012-eular.2703
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Regional left ventricular (LV) dysfunction reflects myocardial involvement. The regional LV function in SSc has not been systematically studied using cardiac magnetic resonance (CMR) imaging. Combining perfusion and delayed enhancement MR imaging together may reveal important clues to the pathophysiologic mechanisms of myocardial involvements in SSc. Objectives We aimed to detect LV regional dysfunction and myocardial abnormalities in patients with SSc without cardiac symptoms using a CMR approach. Methods Consecutive patients with SSc who had no past history or current clinical findings of hypertension, coronary artery disease, valvular heart disease, atrial fibrillation, diabetes mellitus, dyslipidemia, or echocardiographic abnormalities and healthy controls underwent CMR on a 1.5 T scanner. Peak systolic regional radial strain (Err, %) was calculated from a feature tracking analysis on mid-left ventricular slices obtained with cine MRI in six segments. Furthermore, stress perfusion scan was performed to assess perfusion defects (PD) due to micro or macrovascular impairment, and delayed enhancement (DE) images were obtained d for the assessment of myocarditis and/or fibrosis. We compared the patients and controls in terms of prevalence of CMR abnormalities, and explored possible associations between CMR abnormalities and SSc disease characteristics. Group comparisons were made using the Wilcoxon Chi-square test, and the Tukey-Kramer’s test and Fisher’s exact test. Results We compared 19 patients with SSc (100%female; mean age, 58.8±8.7 years; 10 had limited cutaneous SSc and 9 diffuse cutaneous SSc) with 10 healthy controls (100% female; mean age, 55.7±4.52 years). No statistically significant differences were observed in baseline characteristics between the patients and healthy controls. The mean peak Err of all segments was significantly lower in the patients than the controls (0.49±0.04 vs.0.69±0.05; p=0.008).The mean peak Err of the patients with limited cutaneous SSc tended to be lower than those with diffuse cutaneous SSc (p=0.18). The mean peak Err of patients with digital ulcer tended to be lower than those without it (p=0.36). Other SSc characteristics were not associated with the mean peak Err. Five patients with DE (26.3%) and 11 patients with PD (57.9%) were observed. The mean peak Err in the patients with PD and DE tended to be lower than in those without PD (p=0.18) and DE (p=0.17). PD was significantly associated with digital ulcer (p=0.0003). Conclusions Subclinical myocardial involvement, as detected by CMR, was prevalent in the SSc patients without cardiac symptoms. Evaluation with CMR appears to be useful in detecting subclinical myocardial involvement in SSc. Regional LV dysfunction and PD may associate with digital ulceration. Our findings could suggest a pathophysiological mechanism to explain the relationship between myocardial abnormalities and digital ischemia in SSc. Disclosure of Interest None Declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2012-eular.2703</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><ispartof>Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.397</ispartof><rights>2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2013 (c) 2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/71/Suppl_3/397.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/71/Suppl_3/397.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,777,781,3183,23552,27905,27906,77349,77380</link.rule.ids></links><search><creatorcontrib>Kobayashi, H.</creatorcontrib><creatorcontrib>Yokoe, I.</creatorcontrib><creatorcontrib>Sato, H.</creatorcontrib><creatorcontrib>Kobayashi, Y.</creatorcontrib><title>FRI0246 Detection of left ventricular regional dysfunction and myocardial abnormalities using complementary cardiac magnetic resonance imaging in patients with systemic sclerosis without cardiac symptoms</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Background In patients with systemic sclerosis (SSc), myocardial involvement is common, may have serious consequences, and may lead to a poor prognosis. Regional left ventricular (LV) dysfunction reflects myocardial involvement. The regional LV function in SSc has not been systematically studied using cardiac magnetic resonance (CMR) imaging. Combining perfusion and delayed enhancement MR imaging together may reveal important clues to the pathophysiologic mechanisms of myocardial involvements in SSc. Objectives We aimed to detect LV regional dysfunction and myocardial abnormalities in patients with SSc without cardiac symptoms using a CMR approach. Methods Consecutive patients with SSc who had no past history or current clinical findings of hypertension, coronary artery disease, valvular heart disease, atrial fibrillation, diabetes mellitus, dyslipidemia, or echocardiographic abnormalities and healthy controls underwent CMR on a 1.5 T scanner. Peak systolic regional radial strain (Err, %) was calculated from a feature tracking analysis on mid-left ventricular slices obtained with cine MRI in six segments. Furthermore, stress perfusion scan was performed to assess perfusion defects (PD) due to micro or macrovascular impairment, and delayed enhancement (DE) images were obtained d for the assessment of myocarditis and/or fibrosis. We compared the patients and controls in terms of prevalence of CMR abnormalities, and explored possible associations between CMR abnormalities and SSc disease characteristics. Group comparisons were made using the Wilcoxon Chi-square test, and the Tukey-Kramer’s test and Fisher’s exact test. Results We compared 19 patients with SSc (100%female; mean age, 58.8±8.7 years; 10 had limited cutaneous SSc and 9 diffuse cutaneous SSc) with 10 healthy controls (100% female; mean age, 55.7±4.52 years). No statistically significant differences were observed in baseline characteristics between the patients and healthy controls. The mean peak Err of all segments was significantly lower in the patients than the controls (0.49±0.04 vs.0.69±0.05; p=0.008).The mean peak Err of the patients with limited cutaneous SSc tended to be lower than those with diffuse cutaneous SSc (p=0.18). The mean peak Err of patients with digital ulcer tended to be lower than those without it (p=0.36). Other SSc characteristics were not associated with the mean peak Err. Five patients with DE (26.3%) and 11 patients with PD (57.9%) were observed. The mean peak Err in the patients with PD and DE tended to be lower than in those without PD (p=0.18) and DE (p=0.17). PD was significantly associated with digital ulcer (p=0.0003). Conclusions Subclinical myocardial involvement, as detected by CMR, was prevalent in the SSc patients without cardiac symptoms. Evaluation with CMR appears to be useful in detecting subclinical myocardial involvement in SSc. Regional LV dysfunction and PD may associate with digital ulceration. Our findings could suggest a pathophysiological mechanism to explain the relationship between myocardial abnormalities and digital ischemia in SSc. Disclosure of Interest None Declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVUcGOFCEUJEYTx9F_INlzr0DPAB1PZtZ1N9loYnTjjdA0PcvYQAu02jcvfp4_4Zf42jYbr54I9aoKXhVCZ5ScU1rz5zqEdGcn37lcMUJZZadBp3MmSP0AbeiOS4A5eYg2hJC62jVcPEZPcj7BlUgqN-jn5btrwnb81_cfF7ZYU1wMOPZ4sH3BX2woyZnFEyd7hJEecDfnfgorUYcO-zkanToHI92GmLweXHE24ym7cMQm-nGwHpx0mvHKNNjrY7DFGbDN4BqMxQ6wReACHjUYhJLxV1fucJ5zsR642Qw2xexWPE7l3i7PfizR56foUa-HbJ_9Pbfow-Wr94er6ubt6-vDy5uqpXxPIAcja9ZZLbRlmpkdkV3LGm00b1kHubCainYPjD1v-p42raGCSqulpF2jZb1FZ6vvmOLnyeaiTnFKkE5WVAjRCM4h7y16sbIM_Don26sxwZZpVpSopT_1T39q6U_96U8t_YG6WtUO1v92L9Xpk-KiFnv15vaganLFmovmo7oFPl_5rT_910O_AWL-veg</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Kobayashi, H.</creator><creator>Yokoe, I.</creator><creator>Sato, H.</creator><creator>Kobayashi, Y.</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>Elsevier Limited</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</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>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20130601</creationdate><title>FRI0246 Detection of left ventricular regional dysfunction and myocardial abnormalities using complementary cardiac magnetic resonance imaging in patients with systemic sclerosis without cardiac symptoms</title><author>Kobayashi, H. ; Yokoe, I. ; Sato, H. ; Kobayashi, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1650-49c832dea7ae2a2c408db29aca6b2d8182317b52de569ff19bc1718ea881d9a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, H.</creatorcontrib><creatorcontrib>Yokoe, I.</creatorcontrib><creatorcontrib>Sato, H.</creatorcontrib><creatorcontrib>Kobayashi, Y.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM 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 (ProQuest)</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, H.</au><au>Yokoe, I.</au><au>Sato, H.</au><au>Kobayashi, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FRI0246 Detection of left ventricular regional dysfunction and myocardial abnormalities using complementary cardiac magnetic resonance imaging in patients with systemic sclerosis without cardiac symptoms</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>71</volume><issue>Suppl 3</issue><spage>397</spage><pages>397-</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Background In patients with systemic sclerosis (SSc), myocardial involvement is common, may have serious consequences, and may lead to a poor prognosis. Regional left ventricular (LV) dysfunction reflects myocardial involvement. The regional LV function in SSc has not been systematically studied using cardiac magnetic resonance (CMR) imaging. Combining perfusion and delayed enhancement MR imaging together may reveal important clues to the pathophysiologic mechanisms of myocardial involvements in SSc. Objectives We aimed to detect LV regional dysfunction and myocardial abnormalities in patients with SSc without cardiac symptoms using a CMR approach. Methods Consecutive patients with SSc who had no past history or current clinical findings of hypertension, coronary artery disease, valvular heart disease, atrial fibrillation, diabetes mellitus, dyslipidemia, or echocardiographic abnormalities and healthy controls underwent CMR on a 1.5 T scanner. Peak systolic regional radial strain (Err, %) was calculated from a feature tracking analysis on mid-left ventricular slices obtained with cine MRI in six segments. Furthermore, stress perfusion scan was performed to assess perfusion defects (PD) due to micro or macrovascular impairment, and delayed enhancement (DE) images were obtained d for the assessment of myocarditis and/or fibrosis. We compared the patients and controls in terms of prevalence of CMR abnormalities, and explored possible associations between CMR abnormalities and SSc disease characteristics. Group comparisons were made using the Wilcoxon Chi-square test, and the Tukey-Kramer’s test and Fisher’s exact test. Results We compared 19 patients with SSc (100%female; mean age, 58.8±8.7 years; 10 had limited cutaneous SSc and 9 diffuse cutaneous SSc) with 10 healthy controls (100% female; mean age, 55.7±4.52 years). No statistically significant differences were observed in baseline characteristics between the patients and healthy controls. The mean peak Err of all segments was significantly lower in the patients than the controls (0.49±0.04 vs.0.69±0.05; p=0.008).The mean peak Err of the patients with limited cutaneous SSc tended to be lower than those with diffuse cutaneous SSc (p=0.18). The mean peak Err of patients with digital ulcer tended to be lower than those without it (p=0.36). Other SSc characteristics were not associated with the mean peak Err. Five patients with DE (26.3%) and 11 patients with PD (57.9%) were observed. The mean peak Err in the patients with PD and DE tended to be lower than in those without PD (p=0.18) and DE (p=0.17). PD was significantly associated with digital ulcer (p=0.0003). Conclusions Subclinical myocardial involvement, as detected by CMR, was prevalent in the SSc patients without cardiac symptoms. Evaluation with CMR appears to be useful in detecting subclinical myocardial involvement in SSc. Regional LV dysfunction and PD may associate with digital ulceration. Our findings could suggest a pathophysiological mechanism to explain the relationship between myocardial abnormalities and digital ischemia in SSc. Disclosure of Interest None Declared</abstract><cop>Kidlington</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><doi>10.1136/annrheumdis-2012-eular.2703</doi></addata></record>
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title FRI0246 Detection of left ventricular regional dysfunction and myocardial abnormalities using complementary cardiac magnetic resonance imaging in patients with systemic sclerosis without cardiac symptoms
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