TY - JOUR
T1 - Left ventricular concentric geometry is associated with impaired relaxation in hypertension
T2 - The HyperGEN study
AU - De Simone, Giovanni
AU - Kitzman, Dalane W.
AU - Chinali, Marcello
AU - Oberman, Albert
AU - Hopkins, Paul N.
AU - Rao, Dabeeru C.
AU - Arnett, Donna K.
AU - Devereux, Richard B.
N1 - Funding Information:
Supported in part by grants HL55673, HL54471, HL54472, HL54473, HL54495, HL54496, HL54509, HL54515 from the National Heart, Lung and Blood Institute, and grant M10RR0047-34 (GCRC) from the National Institutes of Health, Bethesda, MD, USA.
PY - 2005/5
Y1 - 2005/5
N2 - Aims: We tested the hypothesis that abnormal left ventricular (LV) relaxation is associated with concentric LV geometry. Methods and results: Doppler LV filling properties were studied in 1384 hypertensive participants without cardiovascular disease, from the HyperGEN population (731 women, 784 obese, 236 diabetic) and compared in four LV geometry groups; normal, concentric remodelling (3.5%), eccentric (23%), and concentric LV hypertrophy (4%), based on echocardiographic LV mass index (in g/m2.7). Abnormal LV relaxation was identified by European Society of Cardiology criteria in 275 subjects (20%). After accounting for significant confounders, E/A ratio and isovolumic relaxation time were not related to the presence of LV hypertrophy, but indicated abnormal relaxation when LV geometry was concentric (both P < 0.0001). Deceleration time of E velocity was prolonged with LV hypertrophy (P < 0.03), but the behaviour in relation to concentric LV geometry differed in the presence (prolonged) or absence (reduced) of LV hypertrophy (P = 0.05), a difference independently related to the magnitude of both transmitral gradients and stroke volume (all P < 0.05). Logistic regression showed that, compared with normal LV geometry, the odds of abnormal LV relaxation was 2.3-fold greater when LV geometry was concentric and that LV hypertrophy conferred a borderline higher risk than normal LV mass. Conclusions: In hypertensive individuals without prevalent cardiovascular disease from a multi-ethnic population-based sample, delayed LV relaxation is independently associated with concentric LV geometry.
AB - Aims: We tested the hypothesis that abnormal left ventricular (LV) relaxation is associated with concentric LV geometry. Methods and results: Doppler LV filling properties were studied in 1384 hypertensive participants without cardiovascular disease, from the HyperGEN population (731 women, 784 obese, 236 diabetic) and compared in four LV geometry groups; normal, concentric remodelling (3.5%), eccentric (23%), and concentric LV hypertrophy (4%), based on echocardiographic LV mass index (in g/m2.7). Abnormal LV relaxation was identified by European Society of Cardiology criteria in 275 subjects (20%). After accounting for significant confounders, E/A ratio and isovolumic relaxation time were not related to the presence of LV hypertrophy, but indicated abnormal relaxation when LV geometry was concentric (both P < 0.0001). Deceleration time of E velocity was prolonged with LV hypertrophy (P < 0.03), but the behaviour in relation to concentric LV geometry differed in the presence (prolonged) or absence (reduced) of LV hypertrophy (P = 0.05), a difference independently related to the magnitude of both transmitral gradients and stroke volume (all P < 0.05). Logistic regression showed that, compared with normal LV geometry, the odds of abnormal LV relaxation was 2.3-fold greater when LV geometry was concentric and that LV hypertrophy conferred a borderline higher risk than normal LV mass. Conclusions: In hypertensive individuals without prevalent cardiovascular disease from a multi-ethnic population-based sample, delayed LV relaxation is independently associated with concentric LV geometry.
KW - Arterial hypertension
KW - Cardiac function
KW - Diastolic function
KW - Gardiovascular risk
KW - Hypertrophy
UR - http://www.scopus.com/inward/record.url?scp=18844373365&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehi019
DO - 10.1093/eurheartj/ehi019
M3 - Article
C2 - 15618056
AN - SCOPUS:18844373365
SN - 0195-668X
VL - 26
SP - 1039
EP - 1045
JO - European heart journal
JF - European heart journal
IS - 10
ER -