Influence of consanguinity on the pattern of familial aggregation of congenital cardiovascular anomalies in an outpatient population: studies from the eastern province of Saudi Arabia.

Mohamed A Seliem, Issam H Bou-Holaigah, Nouriya Al-Sannaa
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引用次数: 14

Abstract

Background: Familial aggregation of congenital heart disease (CHD) has been well described in different populations, in particular those with a high consanguinity rate. Extensive genetic study of affected families has improved the understanding of basic genetics of different cardiac lesions.

Objective: To identify the role of consanguinity as a risk factor among familial cases of CHD in a stable outpatient population of a tertiary care center in the Eastern Province of Saudi Arabia.

Methods: All familial cases of CHD seen over 5 years (1996-2000) in the Division of Pediatric Cardiology were identified. The presence or absence of parental consanguinity (first cousin marriage) was defined in each of these families.

Results: Ninety-three cases were identified in 37 families. Twenty-three (62%) families resulted from consanguineous marriages. In 4 families where there were 2 marriages, the affected children came from the consanguineous marriage in 3 of these families. Discordant lesions occur only among non-consanguineous cases, while all consanguineous cases were concordant. Five sets of twins of the same sex (one set are monozygotic by DNA analysis) occurred among consanguineous marriages, in 3 of these both twins were affected with the same disease. Affected parents were seen in 2 families with consanguineous marriage and none in the non-consanguineous marriages. The prevalence of dilated cardiomyopathy was much higher among consanguineous cases (26 vs. 2).

Conclusions: Familial aggregation of congenital heart disease is common in our population. Consanguinity is common in these families, and the distribution of congenital heart disease differs in this subgroup compared to the rest of the familial cases. Further genetic studies of these families may help to shed more light on basic genetics and the specific pathogenetic mechanisms involved.

亲属关系对门诊人群先天性心血管异常家族聚集模式的影响:来自沙特阿拉伯东部省份的研究
背景:先天性心脏病(CHD)的家族聚集性已在不同人群中得到很好的描述,特别是那些具有高血缘率的人群。对受影响家庭的广泛遗传研究提高了对不同心脏病变的基本遗传学的理解。目的:在沙特阿拉伯东部省的一个三级保健中心的稳定门诊人群中,确定血缘关系作为家族性冠心病病例的危险因素的作用。方法:收集小儿心脏科1996-2000年间所有家族性冠心病病例。在这些家庭中,存在或不存在父母的血缘关系(第一表兄弟婚姻)是明确的。结果:37个家庭共93例。23个(62%)家庭是由近亲婚姻形成的。在4个有2次婚姻的家庭中,受影响的儿童来自其中3个家庭的近亲婚姻。不一致病变仅发生在非近亲病例中,而所有近亲病例均一致。同血缘婚姻中出现5对同性双胞胎(其中1对DNA分析为同卵双胞胎),其中3对双胞胎同时患同一疾病。近亲婚姻家庭中有2例,非近亲婚姻家庭中无一例。扩张性心肌病的患病率在近亲亲属病例中要高得多(26比2)。结论:先天性心脏病的家族聚集性在我们的人群中很常见。血缘关系在这些家庭中很常见,与其他家族病例相比,该亚组先天性心脏病的分布有所不同。对这些家族的进一步遗传研究可能有助于揭示更多的基本遗传学和所涉及的具体发病机制。
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