TY - JOUR
T1 - Comparison of Clinical Features in Blacks Versus Whites with Hypertrophic Cardiomyopathy
AU - Sorensen, Lars L.
AU - Pinheiro, Aurelio
AU - Dimaano, Veronica Lea
AU - Pozios, Iraklis
AU - Nowbar, Alexandra
AU - Liu, Hongyun
AU - Luo, Hong Chang
AU - Lin, Xiaoping
AU - Olsen, Niels T.
AU - Hansen, Thomas F.
AU - Sogaard, Peter
AU - Abraham, Maria R.
AU - Abraham, Theodore P.
N1 - Funding Information:
The authors would like to express our gratitude to the sonographers and nurses of the Johns Hopkins Echocardiography Laboratories for their technical expertise and contributions to data collection and thank Glenn Lie and Gunnar Hansen (GE Ultrasound, Horten, Norway) for providing us analysis software. The authors appreciate the support received from the Dr. Lawrence and Sheila Pakula Foundation , Baltimore, MD, Friends in Red, Baltimore and the Hypertrophic Cardiomyopathy Association (HCMA), Morristown, NJ.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - To date, there has not been a large systematic examination of the hypertrophic cardiomyopathy (HC) phenotype in blacks versus whites. In this study, we investigate differences in presentation of HC between blacks and whites. We included 441 consecutive patients with HC seen at the Johns Hopkins HC clinic in the period from February 2005 to June 2012. We compared 76 blacks for clinical presentation, electrocardiogram, exercise capacity, left ventricular morphology, and hemodynamics by echocardiography to 365 whites. Black patients with HC more often presented with abnormal electrocardiogram (93% vs 80%, p = 0.009), driven by a significant difference in repolarization abnormalities (79% vs 56%, p <0.001). Apical hypertrophy was more common in blacks (26% vs 9%, p <0.001); however, blacks had less severe systolic anterior movement of the mitral valve and had significantly lower left ventricular outflow tract gradients at rest (9 mm Hg; interquartile range [IQR] 7 to 19 vs 16 mm Hg; IQR 8 to 40, p <0.001) and during provocation (36 mm Hg; IQR 16 to 77 vs 59 mm Hg; IQR 26 to 110, p = 0.002). Despite the nonobstructive pathophysiology, blacks had lower exercise capacity (adjusted difference 1.45 metabolic equivalents [0.45 to 2.45], p = 0.005). In conclusion, blacks have an HC phenotype characterized by lower prevalence of the well-recognized echocardiographic features of HC such as systolic anterior movement of the mitral valve and left ventricular outflow tract obstruction and display worse exercise capacity.
AB - To date, there has not been a large systematic examination of the hypertrophic cardiomyopathy (HC) phenotype in blacks versus whites. In this study, we investigate differences in presentation of HC between blacks and whites. We included 441 consecutive patients with HC seen at the Johns Hopkins HC clinic in the period from February 2005 to June 2012. We compared 76 blacks for clinical presentation, electrocardiogram, exercise capacity, left ventricular morphology, and hemodynamics by echocardiography to 365 whites. Black patients with HC more often presented with abnormal electrocardiogram (93% vs 80%, p = 0.009), driven by a significant difference in repolarization abnormalities (79% vs 56%, p <0.001). Apical hypertrophy was more common in blacks (26% vs 9%, p <0.001); however, blacks had less severe systolic anterior movement of the mitral valve and had significantly lower left ventricular outflow tract gradients at rest (9 mm Hg; interquartile range [IQR] 7 to 19 vs 16 mm Hg; IQR 8 to 40, p <0.001) and during provocation (36 mm Hg; IQR 16 to 77 vs 59 mm Hg; IQR 26 to 110, p = 0.002). Despite the nonobstructive pathophysiology, blacks had lower exercise capacity (adjusted difference 1.45 metabolic equivalents [0.45 to 2.45], p = 0.005). In conclusion, blacks have an HC phenotype characterized by lower prevalence of the well-recognized echocardiographic features of HC such as systolic anterior movement of the mitral valve and left ventricular outflow tract obstruction and display worse exercise capacity.
UR - http://www.scopus.com/inward/record.url?scp=84964331059&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2016.03.017
DO - 10.1016/j.amjcard.2016.03.017
M3 - Journal article
C2 - 27084053
AN - SCOPUS:84964331059
SN - 0002-9149
VL - 117
SP - 1815
EP - 1820
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 11
ER -