Role of late gadolinium enhancement cardiovascular magnetic resonance in the risk stratification of hypertrophic cardiomyopathy

被引:137
作者
Ismail, Tevfik F. [1 ,2 ]
Jabbour, Andrew [1 ,2 ]
Gulati, Ankur [1 ]
Mallorie, Amy [1 ,2 ]
Raza, Sadaf [1 ,2 ]
Cowling, Thomas E. [1 ,2 ]
Das, Bibek [1 ,2 ]
Khwaja, Jahanzaib [1 ,2 ]
Alpendurada, Francisco D. [1 ]
Wage, Ricardo [1 ]
Roughton, Michael [3 ]
McKenna, William J. [4 ]
Moon, James C. [4 ]
Varnava, Amanda [5 ]
Shakespeare, Carl [1 ,6 ]
Cowie, Martin R. [1 ,2 ]
Cook, Stuart A. [1 ,2 ]
Elliott, Perry [4 ]
O'Hanlon, Rory [1 ]
Pennell, Dudley J. [1 ,2 ]
Prasad, Sanjay K. [1 ,2 ]
机构
[1] Royal Brompton Hosp, Cardiovasc Magnet Resonance Unit, London SW3 6NP, England
[2] Univ London Imperial Coll Sci Technol & Med, London, England
[3] R Squared Stat, London, England
[4] UCL, Inst Cardiovasc Sci, London, England
[5] West Hertfordshire Hosp NHS Trust, Hempstead, Herts, England
[6] South London Healthcare NHS Trust, Dept Cardiol, London, England
基金
英国医学研究理事会;
关键词
SUDDEN CARDIAC DEATH; IMPLANTABLE CARDIOVERTER-DEFIBRILLATORS; AMERICAN-COLLEGE; TASK-FORCE; CARDIOLOGY/EUROPEAN-SOCIETY; DELAYED ENHANCEMENT; PRACTICE GUIDELINES; CLINICAL PROFILE; MYOCARDIAL SCAR; PREVENTION;
D O I
10.1136/heartjnl-2013-305471
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Myocardial fibrosis identified by late gadolinium enhancement (LGE) cardiovascular magnetic resonance (CMR) in patients with hypertrophic cardiomyopathy (HCM) is associated with adverse cardiovascular events, but its value as an independent risk factor for sudden cardiac death (SCD) is unknown. We investigated the role of LGE-CMR in the risk stratification of HCM. Methods We conducted a prospective cohort study in a tertiary referral centre. Consecutive patients with HCM (n=711, median age 56.3 years, IQR 46.7-66.6; 70.0% male) underwent LGE-CMR and were followed for a median 3.5 years. The primary end point was SCD or aborted SCD. Results Overall, 471 patients (66.2%) had myocardial fibrosis (median 5.9% of left ventricular mass, IQR: 2.2-13.3). Twenty-two (3.1%) reached the primary end point. The extent but not the presence of fibrosis was a significant univariable predictor of the primary end point (HR per 5% LGE: 1.24, 95% CI 1.06 to 1.45; p=0.007 and HR for LGE: 2.69, 95% CI 0.91 to 7.97; p=0.073, respectively). However, on multivariable analysis, only LV-EF remained statistically significant (HR: 0.92, 95% CI 0.89 to 0.95; p<0.001). For the secondary outcome of cardiovascular mortality/aborted SCD, the presence and the amount of fibrosis were significant predictors on univariable but not multivariable analysis after adjusting for LV-EF and non-sustained ventricular tachycardia. Conclusions The amount of myocardial fibrosis was a strong univariable predictor of SCD risk. However, this effect was not maintained after adjusting for LV-EF. Further work is required to elucidate the interrelationship between fibrosis and traditional predictors of outcome in HCM.
引用
收藏
页码:1851 / 1858
页数:8
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