Harbaum Lars, Hennigs Jan K, Pott Julian, Ostermann Jonna, Sinning Christoph R, Sau Arunashis, Sieliwonczyk Ewa, Ng Fu Siong, Rhodes Christopher J, Tello Khodr, Klose Hans, Gräf Stefan, Wilkins Martin R
Imperial College London, London, United Kingdom of Great Britain and Northern Ireland.
Hamburg, Germany;
Am J Respir Crit Care Med. 2024 Oct 7;211(1):113-23. doi: 10.1164/rccm.202404-0721OC.
While sex differences in right heart phenotypes have been observed, the molecular drivers remain unknown.
To provide biological insights into sex differences in the structure and function of the right ventricle (RV) using common genetic variation.
RV phenotypes were obtained from cardiac magnetic resonance imaging in 18,156 women and 16,171 men from the UK Biobank. Observational analyses and sex-stratified genome-wide association studies were performed. Candidate female-specific loci were evaluated against invasively measured cardiac performance in 479 female patients with idiopathic or heritable pulmonary arterial hypertension (PAH), recruited to the UK NIHR BioResource Rare Diseases study.
Sex was associated with differences in RV volumes and ejection fraction in models adjusting for left heart counterparts, blood pressure, lung function and sex hormone levels. Six genome-wide significant loci (13%) revealed heterogeneity of allelic effects between women and men, and significant sex-by-genotype interaction. These included two sex-specific candidate loci present in women only: a locus for RV ejection fraction in and a locus for RV end-systolic volume near . Epigenetic data in RV tissue indicate that variation at the locus likely alters transcriptional regulation. In female patients with PAH, a variant located in the promoter of was significantly associated with cardiac index (effect size 0.16 l/min/m), despite similar RV afterload.
has emerged as a biologically plausible candidate gene for female-specific genetic determination of RV function, showing associations with cardiac performance under chronically increased afterload in female patients with PAH.
虽然已观察到右心表型存在性别差异,但其分子驱动因素仍不清楚。
利用常见基因变异,深入了解右心室(RV)结构和功能的性别差异。
从英国生物银行的18156名女性和16171名男性中获取心脏磁共振成像的RV表型。进行了观察性分析和按性别分层的全基因组关联研究。针对英国国家卫生研究院生物资源罕见病研究招募的479名特发性或遗传性肺动脉高压(PAH)女性患者,根据侵入性测量的心脏功能评估候选女性特异性基因座。
在调整了左心对应指标、血压、肺功能和性激素水平的模型中,性别与RV容积和射血分数的差异相关。6个全基因组显著基因座(13%)显示了女性和男性之间等位基因效应的异质性,以及显著的性别与基因型相互作用。其中包括仅在女性中存在的两个性别特异性候选基因座:一个位于[具体位置1]的RV射血分数基因座和一个位于[具体位置2]附近的RV收缩末期容积基因座。RV组织中的表观遗传数据表明,[具体基因座]处的变异可能会改变转录调控。在PAH女性患者中,尽管RV后负荷相似,但位于[具体基因]启动子区域的一个变异与心脏指数显著相关(效应大小为0.16 l/min/m)。
[具体基因]已成为女性特异性RV功能遗传决定的一个生物学上合理的候选基因,在PAH女性患者慢性后负荷增加的情况下,显示出与心脏功能的关联。