Maeda Katsuhide, Yamaki Shigeo, Kado Hideaki, Asou Toshihide, Murakami Arata, Takamoto Shinichi
Department of Cardiothoracic Surgery, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Circulation. 2004 Sep 14;110(11 Suppl 1):II139-46. doi: 10.1161/01.CIR.0000138223.74524.4e.
Restrictive atrial septal defect (ASD) (including intact atrial septum [IAS]) has been reported to be a risk factor that negatively impacts survival in hypoplastic left heart syndrome (HLHS). Although lymphangiectasia and "arterialization" of the veins of the lung in HLHS with restrictive ASD have been reported, they cannot fully explain the high mortality. We have introduced a new method of evaluating the development of the pulmonary vasculature in histological sections and used it to assess patients' lungs. We tested the hypothesis that the small pulmonary arteries (SPA), which are pulmonary arteries in a histological section whose radii are approximately 25 microm to 250 microm, in HLHS with restrictive ASD are hypoplastic, but that the alveoli are not, to elucidate the mechanism underlying the poor outcome of these patients.
Fourteen HLHS patients between 1 day and 40 days of age were studied. In 8 cases, the ASD was restrictive [R(+) group], and in the other 6 cases it was not [R(-) group]. Specimens from 12 autopsies of cases with no congenital heart or pulmonary disease were examined as a control group (C group). As a novel histological parameter, we assessed the size of SPA in relation to the size of accompanying bronchioles to identify SPA underdevelopment. To evaluate the development of alveoli and interstitial tissue, radial alveolar counts (RAC), which reflect alveolar maturity and complexity, were also performed. Statistical comparisons between groups were made by analysis of covariance with age as a covariant factor. When the radius of the accompanying bronchiole was 100 microm, the radius of the SPA was 34.0+/-10.8 microm in the R(+) group, and significantly lower than the 46.6+/-8.5 microm in R(-) group (P=0.0022) and 70.5+/-8.4 microm in the C group (P<0.0001). The RAC was in 3.5+/-0.9 in the R(+) group, 3.4+/-0.6 in the R(-) group, and 3.7+/-0.9 in the C group (no significant differences between groups).
The SPA in HLHS with restrictive ASD were underdeveloped compared with the SPA in HLHS with nonrestrictive ASD and the controls, but their alveoli were not hypoplastic. Based on these results, it is speculated that SPA hypoplasia may be responsible for the poor outcome of HLHS with restrictive ASD.
据报道,限制性房间隔缺损(ASD)(包括完整房间隔[IAS])是影响左心发育不全综合征(HLHS)患者生存的一个危险因素。尽管已有报道称,HLHS合并限制性ASD患者存在淋巴管扩张和肺静脉“动脉化”,但这些现象无法完全解释其高死亡率。我们引入了一种在组织学切片中评估肺血管发育的新方法,并用于评估患者的肺部情况。我们验证了以下假设:在HLHS合并限制性ASD患者中,组织学切片中半径约为25微米至250微米的小肺动脉(SPA)发育不全,但肺泡发育正常,以以此以阐明这些患者预后不良的机制。
对14例年龄在1天至40天之间的HLHS患者进行了研究。其中8例患者的ASD为限制性[R(+)组],另外6例患者的ASD为非限制性[R(-)组]。选取12例无先天性心脏病或肺部疾病患者的尸检标本作为对照组(C组)。作为一种新的组织学参数,我们通过评估SPA与伴行细支气管大小的关系来确定SPA发育不全。为了评估肺泡和间质组织的发育情况,还进行了反映肺泡成熟度和复杂性的径向肺泡计数(RAC)。以年龄作为协变量,通过协方差分析对各组进行统计学比较。当伴行细支气管半径为100微米时,R(+)组中SPA的半径为34.0±10.8微米,显著低于R(-)组的46.6±8.5微米(P = 0.0022)和C组的70.5±8.4微米(P < 0.0001)。RAC在R(+)组为3.5±0.9,在R(-)组为3.4±0.6,在C组为3.7±0.9(各组间无显著差异)。
与HLHS合并非限制性ASD患者及对照组相比,HLHS合并限制性ASD患者的SPA发育不全,但其肺泡未发育不全。基于这些结果,推测SPA发育不全可能是HLHS合并限制性ASD患者预后不良的原因。