Geluk C A, Halkes C J M, De Jaegere P P Th, Plokker H W M, Cabezas M Castro
Neth Heart J. 2006 Apr;14(4):125-131.
Despite agreement on the need for screening for the presence of cardiovascular risk factors in first-degree family members of patients with premature coronary artery disease (CAD), this is not routinely carried out in relatives of normocholesterolaemic patients. We evaluated cardiovascular risk factors in family members of normocholesterolaemic patients with premature CAD.
Eligible index subjects were patients with premature CAD (<55 years in men and <65 years in women), who had undergone percutaneous transluminal coronary angioplasty. Patients with fasting total cholesterol levels >6.5 mmol/l were excluded. Sixteen index subjects were included with a mean age of 49±8 years and total cholesterol levels of 5.5±0.8 mmol/l. Sixty-four first-degree relatives from these 16 pedigrees were screened, namely 18 children, 42 siblings and four parents. National Cholesterol Education Program III guidelines were used to identify candidates for lipid-lowering treatment. Furthermore, the presence of four additional metabolic disorders was investigated: the metabolic syndrome, increased levels of lipoprotein(a) (Lp(a)), hyperhomocysteinaemia and postprandial hyperlipidaemia.
Of 64 relatives free of CAD, 34 subjects (53%) fulfilled the criteria to receive therapeutic advice, 20 of whom (31% of the relatives) were candidates for drug therapy. Sixty-one relatives were available for a full assessment of metabolic disorders and in 37 relatives (61%) at least one metabolic abnormality was present. Twelve subjects had hyper-Lp(a), seven subjects had postprandial hyperlipidaemia and two had the metabolic syndrome. Furthermore, 16 subjects had a combination of at least two out of four metabolic disorders.
Careful evaluation of coronary risk factors and metabolic variables in first-degree relatives of normocholesterolaemic CAD patients identifies a significant number of subjects at increased coronary risk in whom primary prevention measures should be initiated.
尽管对于筛查早发性冠状动脉疾病(CAD)患者的一级家庭成员中是否存在心血管危险因素已达成共识,但在血脂正常患者的亲属中,这一筛查并未常规开展。我们评估了血脂正常的早发性CAD患者家庭成员中的心血管危险因素。
符合条件的索引对象为早发性CAD患者(男性<55岁,女性<65岁),这些患者均接受了经皮腔内冠状动脉成形术。排除空腹总胆固醇水平>6.5 mmol/l的患者。纳入16名索引对象,平均年龄为49±8岁,总胆固醇水平为5.5±0.8 mmol/l。对这16个家系中的64名一级亲属进行了筛查,即18名子女、42名兄弟姐妹和4名父母。采用美国国家胆固醇教育计划第三次报告(NCEP III)指南来确定降脂治疗的候选对象。此外,还调查了另外四种代谢紊乱的存在情况:代谢综合征、脂蛋白(a) [Lp(a)]水平升高、高同型半胱氨酸血症和餐后高脂血症。
在64名无CAD的亲属中,34名受试者(53%)符合接受治疗建议的标准,其中20名(占亲属的31%)为药物治疗候选对象。61名亲属可进行代谢紊乱的全面评估,其中37名亲属(61%)存在至少一种代谢异常。12名受试者Lp(a)升高,7名受试者有餐后高脂血症,2名受试者患有代谢综合征。此外,16名受试者存在四种代谢紊乱中的至少两种组合情况。
对血脂正常的CAD患者一级亲属的冠状动脉危险因素和代谢变量进行仔细评估,可发现大量冠状动脉风险增加且应启动一级预防措施的受试者。