Takemura G, Takatsu Y, Fujiwara H
Department of Internal Medicine, Hyogo Prefectural Amagasaki Hospital, Japan.
Heart. 1998 Jan;79(1):78-85. doi: 10.1136/hrt.79.1.78.
Abnormal microcirculation has been suggested in hearts with pathological conditions, particularly in hypertrophic hearts, even in the presence of normal epicardial coronary arteries. However, the morphology of coronary capillaries has not been well investigated in those hearts.
Ultrastructural morphometry of the capillaries in 47 endomyocardial biopsy specimens taken from 30 patients was performed.
Six patients had hypertrophic cardiomyopathy with dilated cardiomyopathy-like features (DCM-like HCM), six had HCM, six had DCM, five had postmyocarditis, and seven were normal subjects.
The short axial diameters of capillaries were similar among the groups. Abnormal stenosis of more than 90% luminal narrowing was found in 31% of capillaries of the DCM-like HCM group, 16% of the HCM group, 13% of the DCM group, 11% of the postmyocarditis group, and 2% of the normal subjects. Mean (SD) stenosis of the lumen was most severe in DCM-like HCM (78(8)%), and more severe in HCM (67(9)%), DCM (66(8)%), and postmyocarditis (68(4)%) than normal subjects (56(8)%). The mean cross sectional areas of capillaries were similar among the groups; however, the endothelial cellular area was significantly (p < 0.05) greater in DCM-like HCM (24.2 (8.2) microns2) than in normal subjects (14.7 (1.8) microns2), indicating that capillary narrowing was due to the increased volume of capillary endothelial cells. The endothelial cells of the stenosed capillaries showed severely oedematous changes of the cytoplasm wholely or partially, but the cytoplasmic organelles and nuclei appeared intact.
Narrowing of the coronary capillaries may be of pathophysiological significance in microcirculatory abnormality in hypertrophic hearts, particularly in patients with DCM-like HCM.
已有研究表明,在患有病理状况的心脏中,尤其是肥厚型心脏,即使心外膜冠状动脉正常,其微循环也会出现异常。然而,这些心脏中冠状动脉毛细血管的形态尚未得到充分研究。
对30例患者的47份心内膜活检标本中的毛细血管进行了超微结构形态测定。
6例患有类似扩张型心肌病特征的肥厚型心肌病(DCM样HCM),6例患有肥厚型心肌病(HCM),6例患有扩张型心肌病(DCM),5例患有心肌炎后心肌病,7例为正常受试者。
各组间毛细血管的短轴直径相似。在DCM样HCM组的31%的毛细血管、HCM组的16%、DCM组的13%、心肌炎后心肌病组的11%以及正常受试者的2%中发现了超过90%管腔狭窄的异常狭窄。管腔的平均(标准差)狭窄在DCM样HCM中最为严重(78(8)%),在HCM(67(9)%)、DCM(66(8)%)和心肌炎后心肌病(68(4)%)中比正常受试者(56(8)%)更严重。各组间毛细血管的平均横截面积相似;然而,DCM样HCM(24.2(8.2)平方微米)中的内皮细胞面积显著(p<0.05)大于正常受试者(14.7(1.8)平方微米),表明毛细血管狭窄是由于毛细血管内皮细胞体积增加所致。狭窄毛细血管的内皮细胞整体或部分显示出细胞质的严重水肿变化,但细胞质细胞器和细胞核看起来完好无损。
冠状动脉毛细血管狭窄可能在肥厚型心脏的微循环异常中具有病理生理学意义,尤其是在患有DCM样HCM的患者中。