坂井 晶子
   Department   School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine
   Position   Assistant Professor
Language English
Title Cardiac Magnetic Resonance T1 Mapping and Late Gadolinium Enhancement Surrogate Major Cardiac Events in Systemic Sclerosis
Conference The 83rd Annual Scientific Meeting of the Japanese Circulation Society (JCS2019)
Promoters Japanese Circulation Society
Conference Type Nationwide Conferences
Presentation Type Poster notice
Lecture Type General
Publisher and common publisher◎SAKAI Akiko, NAGAO Michinobu, NAKAO Risako, WATANABE Eri, SAKAI Shuji, HAGIWARA Nobuhisa
Date 2019/03/30
Venue
(city and name of the country)
Yokohama, JAPAN
Summary *Poster Session (English) 37 CT MRI Myocardium
Introduction: Systemic sclerosis (SSC) is an autoimmune disease that progresses interstitial fibrosis in the systemic organs. In SSC, cardiac involvement causes myocardial fibrosis, leading to ventricular tachycardia (VT) and the worsening of heart failure. However, the prediction indicator is unknown. We investigate whether myocardial fibrosis by cardiac magnetic resonance (CMR) T1 mapping and late gadolinium enhancement (LGE) could be a surrogate marker for major adverse cardiac events (MACE) in patients with SSC. Methods: Thirty-two patients (mean age, 60 years; 29 women) with SSC underwent CMR for the assessment of cardiac function and myocardial fibrosis. The presence of LGE was evaluated in all patients. The extracellular volume fraction (ECV, %) for mid-left ventricular septum was derived from T1 mapping in sixteen patients. MACE was defined as cardiac death, VT or heart failure hospitalization. Results: MACE was observed in 8 (25%) patients for mean follow-up period of 36 months. The presence of LGE was seen in 6 patients with MACE (75%) and 4 patients without MACE (17%), and the frequency is significant higher in patients with MACE (p <0.05). ECV was significantly greater for patients with MACE than those without (40 ± 10% vs. 28 ± 5%, p< 0.05). Receiver operating curve analysis revealed that the area under the curves of the optimal ECV of 0.33 and the presence of LGE for prediction of MACE were 0.92 and 0.79, respectively. Conclusion: ECV and the presence of LGE can be used as surrogate markers for MACE in patients with SSC.