Bahramali Ehsan, Rajabi Mona, Jamshidi Javad, Mousavi Seyyed Mohammad, Zarghami Mehrdad, Manafi Alireza, Firouzabadi Negar
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran Cardiology Departments, Fasa University of Medical Sciences, Fasa, Iran.
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
BMJ Open. 2016 Feb 9;6(2):e010282. doi: 10.1136/bmjopen-2015-010282.
To explore the association between ACE gene insertion/deletion (I/D) polymorphism with left ventricular hypertrophy (LVH) in patients with hypertension who have developed heart failure with preserved ejection fraction (HFpEF). Being a major contributor to the development of diastolic heart dysfunction, the renin angiotensin aldosterone system and its genetic variations are thought to induce LVH in hypertensive hearts apart from haemodynamic factors.
Case control study.
An Iranian referral university hospital.
176 patients with hypertension and a diagnosis of HFpEF on presence of symptoms of heart failure plus Doppler echocardiographic documentation of left ventricular (LV) diastolic dysfunction and/or elevated NT-proBNP levels. Those with significant coronary, valvular, pericardial and structural heart diseases were excluded as well as patients with atrial fibrillation, renal failure and pulmonary causes of dyspnoea. They were divided into two cohorts of 88 cases with and 88 controls without LVH, after determination of LV mass index, using two-dimensional and M-mode echocardiography. The I/D polymorphism of the ACE gene was determined using the PCR method.
The D allele was significantly more prevalent among cases with compared with controls without LVH (p=0.0007). Genotype distributions also differed significantly under additive (p=0.005, OR=0.53, 95% CI 0.34 to 0.84) and recessive (p=0.001, OR=0.29, 95% CI 0.13 to 0.66) models.
In patients with hypertension who develop HFpEF, the D allele of the ACE gene is probably associated with the development of LVH. With the detrimental effects of LVH on the heart's diastolic properties, this can signify the role of genetic contributors to the development of HFpEF in patients with hypertension and may serve as a future risk predictor for the disease.
探讨射血分数保留的心力衰竭(HFpEF)高血压患者中血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性与左心室肥厚(LVH)之间的关联。肾素血管紧张素醛固酮系统及其基因变异被认为是舒张性心功能不全发展的主要因素,除血流动力学因素外,其还可导致高血压性心脏病患者发生LVH。
病例对照研究。
伊朗一所转诊大学医院。
176例高血压患者,伴有心力衰竭症状且经多普勒超声心动图证实存在左心室(LV)舒张功能障碍和/或NT-proBNP水平升高,诊断为HFpEF。排除患有严重冠状动脉、瓣膜、心包和结构性心脏病的患者以及患有心房颤动、肾衰竭和肺部疾病导致呼吸困难的患者。使用二维和M型超声心动图测定LV质量指数后,将他们分为两组,88例有LVH的病例和88例无LVH的对照。采用聚合酶链反应(PCR)方法测定ACE基因的I/D多态性。
与无LVH的对照组相比,D等位基因在有LVH的病例中显著更常见(p=0.0007)。在加性模型(p=0.005,OR=0.53,95%CI 0.34至0.84)和隐性模型(p=0.001,OR=0.29,95%CI 0.13至0.66)下,基因型分布也有显著差异。
在发生HFpEF的高血压患者中,ACE基因的D等位基因可能与LVH的发生有关。鉴于LVH对心脏舒张特性的有害影响,这可能意味着遗传因素在高血压患者HFpEF发展中的作用,并可能作为该疾病未来的风险预测指标。