TY - JOUR
T1 - Intrinsic biventricular dysfunction in Marfan syndrome
AU - de Witte, Piet
AU - Aalberts, Jan J. J.
AU - Radonic, Teodora
AU - Timmermans, Janneke
AU - Scholte, Arthur J.
AU - Zwinderman, Aeilko H.
AU - Mulder, Barbara J. M.
AU - Groenink, Maarten
AU - van den Berg, Maarten P.
PY - 2011/12
Y1 - 2011/12
N2 - Background Marfan syndrome (MFS) is an autosomal, dominantly inherited, connective tissue disorder usually caused by a mutation in the fibrillin-1 gene (FBN1). As fibrillin-1 is a component of the extracellular matrix of the myocardium, mutations in FBN1 may cause impairment of ventricular function. Furthermore, aortic elasticity is decreased in patients with MFS, which might also impair ventricular function. We assessed biventricular function and the influence of aortic elasticity in patients with MFS by means of cardiac MRI.Methods and results Cardiac magnetic resonance was performed in 144 patients with MFS without significant valvular dysfunction, previous cardiac surgery or previous aortic surgery. Biventricular diastolic and systolic volumes were measured, and ejection fractions were calculated. Flow wave velocity, a measurable derivative of aortic elasticity, was measured between the ascending aorta and the bifurcation. When compared to healthy controls (n = 19), left ventricular ejection fraction (LVEF) was impaired in patients with MFS (53% +/- 7% vs 57% +/- 4%, pConclusions Biventricular ejection fraction was impaired in patients with MFS, and the impairment was independent of aortic elasticity and b-blocker usage. There was also a strong correlation between LVEF and RVEF. Our findings suggest intrinsic myocardial dysfunction in patients with MFS.
AB - Background Marfan syndrome (MFS) is an autosomal, dominantly inherited, connective tissue disorder usually caused by a mutation in the fibrillin-1 gene (FBN1). As fibrillin-1 is a component of the extracellular matrix of the myocardium, mutations in FBN1 may cause impairment of ventricular function. Furthermore, aortic elasticity is decreased in patients with MFS, which might also impair ventricular function. We assessed biventricular function and the influence of aortic elasticity in patients with MFS by means of cardiac MRI.Methods and results Cardiac magnetic resonance was performed in 144 patients with MFS without significant valvular dysfunction, previous cardiac surgery or previous aortic surgery. Biventricular diastolic and systolic volumes were measured, and ejection fractions were calculated. Flow wave velocity, a measurable derivative of aortic elasticity, was measured between the ascending aorta and the bifurcation. When compared to healthy controls (n = 19), left ventricular ejection fraction (LVEF) was impaired in patients with MFS (53% +/- 7% vs 57% +/- 4%, pConclusions Biventricular ejection fraction was impaired in patients with MFS, and the impairment was independent of aortic elasticity and b-blocker usage. There was also a strong correlation between LVEF and RVEF. Our findings suggest intrinsic myocardial dysfunction in patients with MFS.
KW - LEFT-VENTRICULAR FUNCTION
KW - PULSE-WAVE VELOCITY
KW - SIGNIFICANT VALVULAR REGURGITATION
KW - AXIS SYSTOLIC FUNCTION
KW - BETA-BLOCKER THERAPY
KW - NORMAL-SIZED AORTA
KW - CARDIAC-FUNCTION
KW - ADULTS
KW - DISTENSIBILITY
KW - DIMENSIONS
U2 - 10.1136/heartjnl-2011-300169
DO - 10.1136/heartjnl-2011-300169
M3 - Article
SN - 1355-6037
VL - 97
SP - 2063
EP - 2068
JO - Heart
JF - Heart
IS - 24
ER -