Right Ventricular Abnormalities on Cardiovascular Magnetic Resonance Imaging in Patients With Sarcoidosis.
Right Ventricular Abnormalities on Cardiovascular Magnetic Resonance Imaging in Patients With Sarcoidosis.
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DOI:
10.1016/j.jcmg.2019.12.011
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发表时间:
2020-06
影响因子:
14
通讯作者:
Shenoy, Chetan
中科院分区:
文献类型:
--
作者:
Velangi, Pratik S.;Chen, Ko-Hsuan Amy;Kazmirczak, Felipe;Okasha, Osama;von Wald, Lisa;Roukoz, Henri;Farzaneh-Far, Afshin;Markowitz, Jeremy;Nijjar, Prabhjot S.;Bhargava, Maneesh;Perlman, David;Akcakaya, Mehmet;Shenoy, Chetan
关键词:
In patients with sarcoidosis, right ventricular (RV) abnormalities have been described on many imaging modalities. On cardiovascular magnetic resonance (CMR), RV abnormalities include RV systolic dysfunction quantified as an abnormal RV ejection fraction (RVEF), and RV late gadolinium enhancement (LGE). We aimed to determine the prevalence on CMR of RV systolic dysfunction and RV LGE, their determinants, and their impact on long-term adverse outcomes in patients with sarcoidosis. We studied consecutive patients with biopsy-proven sarcoidosis who underwent CMR for suspected cardiac involvement. They were followed for two endpoints: all-cause death, and a composite arrhythmic endpoint of sudden cardiac death or significant ventricular arrhythmia. Among 290 patients, RV systolic dysfunction (RVEF <40% in men and <45% in women) and RV LGE were present in 35 (12.1%) and 16 (5.5%) respectively. The median follow-up time was 3.2 years (interquartile range 1.6 to 5.7 years) for all-cause death and 3.0 years (interquartile range 1.4 to 5.5 years) for the arrhythmic endpoint. On Cox proportional hazards regression multivariable analyses, only RVEF was independently associated with all-cause death (HR 1.05 for every 1% decrease; 95% CI 1.01–1.09; p=0.022) after adjustment for LVEF, LV LGE extent, and the presence of RV LGE. RVEF was not associated with the arrhythmic endpoint (HR 1.01; 95% CI 0.96–1.06; p=0.67). Conversely, RV LGE was not associated with all-cause death (HR 2.78; 95% CI 0.36–21.66; p=0.33), while it was independently associated with the arrhythmic endpoint (HR 5.43; 95% CI 1.25–23.47; p=0.024). In our study of patients with sarcoidosis, RV systolic dysfunction and RV LGE had distinct prognostic associations; RV systolic dysfunction but not RV LGE was independently associated with all-cause death, while RV LGE but not RV systolic dysfunction was independently associated with sudden cardiac death or significant ventricular arrhythmia. Our findings may indicate distinct implications for the management of RV abnormalities in sarcoidosis.
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