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首页> 外文期刊>Trends in Cardiovascular Medicine >Molecular insight into heart development and congenital heart disease: An update review from the Arab countries
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Molecular insight into heart development and congenital heart disease: An update review from the Arab countries

机译:心脏发育和先天性心脏病的分子洞察力:阿拉伯国家的最新评论

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Congenital heart defect (CHD) has a major influence on affected individuals as well as on the supportive and associated environment such as the immediate family. Unfortunately, CHD is common worldwide with an incidence of approximately 1% and consequently is a major health concern. The Arab population has a high rate of consanguinity, fertility, birth, and annual population growth, in addition to a high incidence of diabetes mellitus and obesity. All these factors may lead to a higher incidence and prevalence of CHD within the Arab population than in the rest of the world, making CHD of even greater concern. Sadly, most Arab countries lack appropriate public health measures directed toward the control and prevention of congenital malformations and so the importance of CHD within the population remains unknown but is thought to be high. In approximately 85% of CHD patients, the multifactorial theory is considered as the pathologic basis. The genetic risk factors for CHD can be attributed to large chromosomal aberrations, copy number variations (CNV) of particular regions in the chromosome, and gene mutations in specific nuclear transcription pathways and in the genes that are involved in cardiac structure and development. The application of modern molecular biology techniques such as high-throughput nucleotide sequencing and chromosomal array and methylation array all have the potential to reveal more genetic defects linked to CHD. Exploring the genetic defects in CHD pathology will improve our knowledge and understanding about the diverse pathways involved and also about the progression of this disease. Ultimately, this will link to more efficient genetic diagnosis and development of novel preventive therapeutic strategies, as well as gene-targeted clinical management. This review summarizes our current understanding of the molecular basis of normal heart development and the pathophysiology of a wide range of CHD. The risk factors that might account for the high prevalence of CHD within the Arab population and the measures required to be undertaken for conducting research into CHD in Arab countries will also be discussed. (C) 2015 Elsevier Inc. All rights reserved.
机译:先天性心脏缺陷(CHD)对受影响的个体以及支持性和相关环境(例如直系亲属)具有重大影响。不幸的是,冠心病在全世界很普遍,其发病率约为1%,因此是主要的健康问题。除了糖尿病和肥胖症的高发率外,阿拉伯人口的血缘,生育力,出生率和年均人口增长率很高。所有这些因素可能导致阿拉伯人群中冠心病的发病率和患病率高于世界其他地区,这使人们更加关注冠心病。令人遗憾的是,大多数阿拉伯国家缺乏针对控制和预防先天性畸形的适当公共卫生措施,因此冠心病在人口中的重要性仍然未知,但被认为很高。在大约85%的CHD患者中,多因素理论被认为是病理基础。冠心病的遗传危险因素可归因于较大的染色体畸变,染色体上特定区域的拷贝数变异(CNV),特定核转录途径以及涉及心脏结构和发育的基因中的基因突变。现代分子生物学技术的应用,例如高通量核苷酸测序,染色体阵列和甲基化阵列,都有可能揭示更多与冠心病有关的遗传缺陷。探索CHD病理学中的遗传缺陷将提高我们对所涉及的各种途径以及该病进展的认识和了解。最终,这将与更有效的遗传诊断和新型预防性治疗策略的开发以及以基因为目标的临床管理联系在一起。这篇综述总结了我们目前对正常心脏发育的分子基础和多种冠心病的病理生理学的理解。还将讨论可能导致阿拉伯人口中冠心病普遍流行的风险因素,以及在阿拉伯国家进行冠心病研究所需采取的措施。 (C)2015 Elsevier Inc.保留所有权利。

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