Wilcken D E, Wang X L, Greenwood J, Lynch J
Department of Cardiovascular Medicine, University of New South Wales, Sydney, Australia.
J Pediatr. 1993 Oct;123(4):519-26. doi: 10.1016/s0022-3476(05)80944-8.
Because premature coronary vascular disease in a first-degree relative increases risk of the disease and the mechanisms may include genetically determined abnormal levels of circulating apolipoproteins, we explored the relationships between schoolchildren's apolipoprotein levels and coronary events in their parents and grandparents. We measured capillary blood concentrations of lipoprotein(a) (Lp(a) and apolipoproteins (apo B and apo A-1) in dried blood spot samples obtained by finger prick from 2010 schoolchildren aged 8 to 12 years, and questioned parents about coronary vascular events in the children's parents and grandparents. Of the 2010 questionnaires sent, 1030 (51%) were returned fully completed. Twenty-three fathers, one mother, and 645 grandparents had had coronary vascular events. There were significant associations between increased Lp(a) levels in children and the numbers of grandparents with coronary vascular events and with increasing grandparent coronary history scores (p < 0.01). There were also positive associations for apo B (p < 0.01) but none for apo A-1. Discriminate analysis showed that the log-transformed Lp(a) level was the variable most predictive of event numbers and of history scores in grandparents (Wilks lambda value = 0.984; p = 0.026); the apo B level was also predictive (Wilks lambda value = 0.988; p = 0.041), but neither the apo A-1 level nor the apo B/A-1 ratio was. We conclude that high Lp(a) and apo B levels in children aged 8 to 12 years are associated with increased risk of coronary vascular disease in older family members, even with a generation gap. These apolipoproteins may largely account for the independent contribution of family history to disease risk. Measurements of Lp(a) and apo B in schoolchildren may help to identify children and their families at increased risk and may facilitate targeting of prevention.
由于一级亲属中过早发生冠状动脉疾病会增加患病风险,其机制可能包括基因决定的循环载脂蛋白水平异常,因此我们探讨了学童的载脂蛋白水平与他们父母及祖父母冠状动脉事件之间的关系。我们通过手指针刺采集了2010名8至12岁学童的干血斑样本,测量其中脂蛋白(a) [Lp(a)]、载脂蛋白(载脂蛋白B和载脂蛋白A-1)的毛细血管血浓度,并向家长询问学童父母及祖父母的冠状动脉事件情况。在发出的2010份问卷中,1030份(51%)被完整填答返回。23名父亲、1名母亲和645名祖父母曾发生冠状动脉事件。儿童Lp(a)水平升高与有冠状动脉事件的祖父母数量以及祖父母冠状动脉病史评分增加之间存在显著关联(p < 0.01)。载脂蛋白B也存在正相关(p < 0.01),而载脂蛋白A-1则无相关性。判别分析显示,对数转换后的Lp(a)水平是预测祖父母事件数量和病史评分的最有效变量(威尔克斯λ值 = 0.984;p = 0.026);载脂蛋白B水平也具有预测性(威尔克斯λ值 = 0.988;p = 0.041),但载脂蛋白A-1水平和载脂蛋白B/载脂蛋白A-1比值均无此作用。我们得出结论,8至12岁儿童的高Lp(a)和载脂蛋白B水平与老年家庭成员冠状动脉疾病风险增加相关,即使存在代际差异。这些载脂蛋白可能在很大程度上解释了家族史对疾病风险的独立影响。检测学童的Lp(a)和载脂蛋白B可能有助于识别患病风险增加的儿童及其家庭,并有助于实施针对性预防措施。