Shizukuda Yukitaka, Bolan Charles D, Tripodi Dorothy J, Yau Yu-Ying, Nguyen Tammy T, Botello Gilberto, Sachdev Vandana, Sidenko Stanislav, Ernst Inez, Waclawiw Myron A, Leitman Susan F, Rosing Douglas R
Cardiovascular Branch, Bethesda, Maryland, USA.
Am J Cardiol. 2006 Oct 1;98(7):954-9. doi: 10.1016/j.amjcard.2006.04.040. Epub 2006 Aug 15.
Patients with hereditary hemochromatosis (HH) have been reported to develop diastolic functional abnormalities detectable by echocardiography, but it is unknown whether these occur in asymptomatic subjects. Thus, this study tested whether echocardiographic left ventricular (LV) relaxation abnormalities are detectable in subjects with asymptomatic HH. Forty-three asymptomatic subjects with HH (C282Y homozygosity in the HFE gene) and 21 age- and gender-matched control subjects without known HFE mutations underwent echocardiography with comprehensive diastolic functional evaluations. Subjects with HH were in New York Heart Association functional class I and consisted of 22 newly diagnosed patients (group A) and 21 chronically phlebotomized subjects with stable iron levels (group B). Group A subjects showed significant iron overload compared with group B subjects and controls (group C) (ferritin 1,164 +/- 886 [p <0.05 vs groups B and C], 128 +/- 262, and 98 +/- 76 microg/L and transferrin saturation 79 +/- 19% [p <0.05 vs groups B and C], 42 +/- 21%, and 26 +/- 10% for groups A, B, and C, respectively). Echocardiographic evaluation revealed (1) no statistically significant abnormalities of Doppler LV relaxation in HH groups; (2) significant augmentation of atrial contractile function in subjects with HH compared with controls, which was not correlated with iron levels and treatment status; and (3) the preservation of overall LV systolic function in HH groups. In conclusion, the results of this study suggest that the augmentation of atrial contraction appears to be an early detectable echocardiographic cardiac manifestation of abnormal diastolic function in asymptomatic subjects with HH, which may reflect undetectable subclinical LV relaxation abnormalities.
据报道,遗传性血色素沉着症(HH)患者会出现可通过超声心动图检测到的舒张功能异常,但尚不清楚这些异常是否发生在无症状个体中。因此,本研究测试了无症状HH患者是否可检测到超声心动图左心室(LV)舒张异常。43名无症状HH患者(HFE基因C282Y纯合子)和21名年龄及性别匹配、无已知HFE突变的对照受试者接受了超声心动图检查及全面的舒张功能评估。HH患者处于纽约心脏协会心功能I级,包括22名新诊断患者(A组)和21名铁水平稳定的长期放血治疗患者(B组)。与B组受试者和对照组(C组)相比,A组受试者显示出明显的铁过载(铁蛋白分别为1,164±886 [与B组和C组相比,p<0.05]、128±262和98±76μg/L,转铁蛋白饱和度分别为79±19% [与B组和C组相比,p<0.05]、42±21%和26±10%,A、B、C组)。超声心动图评估显示:(1)HH组中多普勒LV舒张无统计学显著异常;(2)与对照组相比,HH患者心房收缩功能显著增强,这与铁水平和治疗状态无关;(3)HH组整体LV收缩功能得以保留。总之,本研究结果表明,心房收缩增强似乎是无症状HH患者舒张功能异常的一种早期可检测到的超声心动图心脏表现,这可能反映了难以检测到的亚临床LV舒张异常。