Clinical and Echocardiographic Evaluation of Regional Systolic Function Detected by Tissue Doppler Imaging in Hypertrophic Cardiomyopathy

被引:0
作者
Kiavar, M. [1 ]
Behzadnia, N. [1 ]
Sadeghpour, A. [1 ]
Maddadi, Sh [1 ]
机构
[1] Shaheed Rajaie Cardiovasc Med & Res Ctr, Tehran, Iran
关键词
Hypertrophic cardiomyopathy; Echocardiography;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hypertrophic cardiomyopathy (HCM) is the most common type of the genetic cardiovascular diseases. Regarding to tremendous heterogeneity in the phenotypic expression of HCM, which is generally unrelated to genotype, we aimed to study, clinical and echocardiographic parameters such as Tissue Doppler Imaging (TDI) in various subtypes of HCM patients and evaluate the influence of race and gender in Iranian patients. Methods: Patients with HCM underwent a complete clinical and echocardiographic study including TDI to assess regional systolic contraction(in the 12 segments) and early diastolic annular velocity (Em) from the septal mitral annulus. Results: The study comprised 41 patients (20 women, mean age = 41 +/- 15 years) with mean LVEF 55%+/- 4.8% and mean maximal septal thickness 2.07cm. Considering LVOT gradient>30mmHg, hypertrophic obstructive cardiomyopathy (HOCM) was found in 18 (45%). Asymmetric septal hypertrophy (ASH) existed in 27 patients (67%), systolic anterior motion of anterior mitral leaflet (SAM) in 25 persons (64%). Nineteen patients (46.3%) were included in NYHA function class (FC) II and 6 (14.7%) in FC III or higher. We found syncope in 10 (24.4%), chest pain in 4 (9.8%), atrial fibrilation in 14.6 % and ventricular arrhythmias in (17.1%) of patients. History of ICD was seen in 7 (17.1%) and PPM in 9 cases. Mean E' velocity was 5.44 +/- 1.65 cm/sec and S velocity 5.70 +/- 1.49 cm/sec with significant lower S velocity and E' in syncope patients. Overall, HOCM patients had grade II diastolic dysfunction with E/E >15(17.54 +/- 7.46). Majority (25) of cases (61%) were categorized in type III of HCM. RV involvement was observed in 11 patients (28.2%). No significant differences existed between prevalence of syncope and dysrhythmia among HCM and HOCM patients. Conclusion: In our study, we found lower detection of latent HOCM, compared to other studies, suggestive of inadequate use of appropriate provocative maneuvers such as exercise stress echocardiography and amyl nitrate. We detected remarkably lower S velocity (5.70 +/- 1.49 cm/sec) and E' velocity (5.44 +/- 1.65 cm/sec) in HCM patients compared to normal subjects, with more significant reductions in patients with syncope.
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页码:137 / 145
页数:9
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共 19 条
  • [11] Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy
    Nagueh, SF
    Bachinski, LL
    Meyer, D
    Hill, R
    Zoghbi, WA
    Tam, JW
    Quiñones, MA
    Roberts, R
    Marian, AJ
    [J]. CIRCULATION, 2001, 104 (02) : 128 - 130
  • [12] HISTOPATHOLOGICAL FACTORS RELATED TO DIASTOLIC FUNCTION IN MYOCARDIAL HYPERTROPHY
    OHSATO, K
    SHIMIZU, M
    SUGIHARA, N
    KONISHI, K
    TAKEDA, R
    [J]. JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 1992, 56 (04): : 325 - 333
  • [13] Marked discordance between dynamic and passive diastolic pressure-volume relations in idiopathic hypertrophic cardiomyopathy
    Pak, PH
    Maughan, WL
    Baughman, KL
    Kass, DA
    [J]. CIRCULATION, 1996, 94 (01) : 52 - 60
  • [14] Differences in myocardial velocity gradient measured throughout the cardiac cycle in patients with hypertrophic cardiomyopathy, athletes and patients with left ventricular hypertrophy due to hypertension
    Palka, P
    Lange, A
    Fleming, AD
    Donnelly, JE
    Dutka, DP
    Starkey, IR
    Shaw, TRD
    Sutherland, GR
    Fox, KAA
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (03) : 760 - 768
  • [15] The effects of aging and physical activity on Doppler measures of diastolic function
    Prasad, Anand
    Popovic, Zoran B.
    Arbab-Zadeh, Armin
    Fu, Qi
    Palmer, Dean
    Dijk, Erika
    Greenberg, Neil L.
    Garcia, Mario J.
    Thomas, James D.
    Levine, Benjamin D.
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (12) : 1629 - 1636
  • [16] USE OF DOPPLER ECHOCARDIOGRAPHY AND AMYL NITRITE INHALATION TO CHARACTERIZE LEFT-VENTRICULAR OUTFLOW OBSTRUCTION IN HYPERTROPHIC CARDIOMYOPATHY
    SHEIKH, KH
    PEARCE, FB
    KISSLO, J
    [J]. CHEST, 1990, 97 (02) : 389 - 395
  • [17] Diastolic dysfunction and altered energetics in the αMHC403/+ mouse model of familial hypertrophic cardiomyopathy
    Spindler, M
    Saupe, KW
    Christe, ME
    Sweeney, HL
    Seidman, CE
    Seidman, JG
    Ingwall, JS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) : 1775 - 1783
  • [18] SPORADIC HYPERTROPHIC CARDIOMYOPATHY DUE TO DENOVO MYOSIN MUTATIONS
    WATKINS, H
    THIERFELDER, L
    HWANG, DS
    MCKENNA, W
    SEIDMAN, JG
    SEIDMAN, CE
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) : 1666 - 1671
  • [19] HYPERTROPHIC CARDIOMYOPATHY - CLINICAL SPECTRUM AND TREATMENT
    WIGLE, ED
    RAKOWSKI, H
    KIMBALL, BP
    WILLIAMS, WG
    [J]. CIRCULATION, 1995, 92 (07) : 1680 - 1692