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肺动脉高压的遗传学:一个大型日本同源人群研究。

Genetics in pulmonary arterial hypertension in a large homogeneous Japanese population.

机构信息

Kyorin University Center for Comprehensive Regional Collaboration, Tokyo, Japan.

Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Clin Genet. 2018 Jul;94(1):70-80. doi: 10.1111/cge.13154. Epub 2018 Jan 25.

DOI:10.1111/cge.13154
PMID:29023671
Abstract

Pulmonary arterial hypertension (PAH) is a rare but serious disease with a grave prognosis. Bone morphogenetic protein type 2 receptor (BMPR2) gene is a strong pathogenic factor for PAH. As a collaborative team from Kyorin University and Keio University in Japan, we have analyzed the BMPR2 gene in 356 probands and more than 50 family members, including secondary patients. Importantly, the study population is a racially, ethnically, and socially homogeneous population. In PAH patients, there is a high incidence of unique mutations in BMPR2, and several mutations are frequently observed in the Japanese population, suggesting that these common and recurring mutations may be highly pathogenic or have high penetrance, explaining why they are found frequently throughout the world. We have also mapped each breakpoint of exonic deletions/duplications and found that most break and rejoining points are in the Alu elements. Reviewing the distribution of the reported mutations on each exon of BMPR2 revealed that the number and frequency of mutations are imbalanced among exons. The penetrance of BMPR2 gene mutations was 3-fold higher in females than males. Full elucidation of BMPR2-mediated pathogenic mechanisms in PAH requires persistent efforts to achieve precision or individualized medicine as a therapeutic strategy for PAH.

摘要

肺动脉高压(PAH)是一种罕见但严重的疾病,预后不良。骨形态发生蛋白 2 型受体(BMPR2)基因是 PAH 的一个重要致病因素。作为来自日本庆应义塾大学和桐荫横滨大学的合作团队,我们对 356 名先证者和 50 多名包括二级亲属在内的家系成员的 BMPR2 基因进行了分析。重要的是,该研究人群是一个种族、民族和社会高度同质的群体。在 PAH 患者中,BMPR2 存在高发生率的独特突变,其中一些突变在日本人群中频繁出现,这表明这些常见且反复出现的突变可能具有高度致病性或高外显率,这解释了为什么它们在世界各地频繁出现。我们还对每个外显子缺失/重复的断点进行了定位,发现大多数断裂和重新连接点位于 Alu 元件中。回顾 BMPR2 每个外显子上报道的突变分布,发现突变的数量和频率在外显子之间不平衡。BMPR2 基因突变的外显率在女性中是男性的 3 倍。要充分阐明 BMPR2 介导的 PAH 发病机制,需要持续努力实现精准医学或个体化医学作为 PAH 的治疗策略。

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