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青紫型先天性心脏病与冠状动脉粥样硬化形成

Cyanotic congenital heart disease and coronary artery atherogenesis.

作者信息

Fyfe Alistair, Perloff Joseph K, Niwa Koichiro, Child John S, Miner Pamela D

机构信息

Dallas Heart Group, Dallas, TX, USA.

出版信息

Am J Cardiol. 2005 Jul 15;96(2):283-90. doi: 10.1016/j.amjcard.2005.03.060.

Abstract

Hypoxemic erythrocytotic residents of high altitudes lack coronary atherosclerosis and have low cholesterol levels. It was postulated that hypoxemic erythrocytotic adults with cyanotic congenital heart disease (CCHD) might be analogous. The incidence of coronary atherosclerosis in this patient population has not been established, and hypocholesterolemia has not previously been recognized. Accordingly, 279 patients were divided into 4 groups: group A: 143 cyanotic patients not operated on (54 men and 89 women, aged 18 to 69 years); group B: 47 cyanotic patients (28 men and 19 women rendered acyanotic by operation at age 22 to 69 years); group C: 41 acyanotic patients not operated on (22 men and 19 women, aged 22 to 75 years); and group D: 48 patients acyanotic before and after operation (24 men and 24 women, aged 21 to 70 years). Coronary arteries were studied angiographically in 59 patients and at necropsy in 5 subjects aged 37 to 56 years. Total cholesterol was <160 mg/dl in 58% of group A, 52% of group B, 10% of group C, and 12% of group D (p <0.000001, chi-square analysis). Angiograms disclosed dilated coronary arteries without obstruction. Necropsy disclosed ectatic coronary arteries with structural abnormalities of the media. In conclusion, this study provides the first quantitative and qualitative data on antiatherogenic changes in lipoproteins in adults with CCHD. The coronary arteries are atheroma free because hypocholesterolemia acts in concert with the antiatherogenic properties of upregulated nitric oxide, hyperbilirubinemia, hypoxemia, and low platelet counts. The persistence of hypocholesterolemia after the surgical elimination of cyanosis suggests a genetic determinant.

摘要

高海拔地区低氧性红细胞增多的居民没有冠状动脉粥样硬化,且胆固醇水平较低。据推测,患有青紫型先天性心脏病(CCHD)的低氧性红细胞增多的成年人可能类似。该患者群体中冠状动脉粥样硬化的发病率尚未确定,且此前未认识到低胆固醇血症。因此,将279例患者分为4组:A组:143例未接受手术的青紫患者(54例男性和89例女性,年龄18至69岁);B组:47例青紫患者(28例男性和19例女性,在22至69岁时通过手术变为非青紫);C组:41例未接受手术的非青紫患者(22例男性和19例女性,年龄22至75岁);D组:48例手术前后均为非青紫的患者(24例男性和24例女性,年龄21至70岁)。对59例患者进行了冠状动脉造影研究,并对5例年龄在37至56岁的患者进行了尸检。A组58%、B组52%、C组10%和D组12%的总胆固醇<160 mg/dl(卡方分析,p<0.000001)。血管造影显示冠状动脉扩张无阻塞。尸检发现冠状动脉扩张伴中膜结构异常。总之,本研究提供了关于CCHD成年患者脂蛋白抗动脉粥样硬化变化的首批定量和定性数据。冠状动脉无动脉粥样硬化,因为低胆固醇血症与上调的一氧化氮、高胆红素血症、低氧血症和低血小板计数的抗动脉粥样硬化特性协同作用。青紫症手术消除后低胆固醇血症的持续存在提示有遗传决定因素。

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