Computational Cardiovascular Science Group, Department of Computer Science, University of Oxford, Oxford, OX1 3QD, UK.
Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, OX3 9DU, UK.
Cardiovasc Diabetol. 2024 Oct 19;23(1):371. doi: 10.1186/s12933-024-02465-y.
Type 2 diabetes mellitus (T2DM) is a major risk factor for heart failure with preserved ejection fraction and cardiac arrhythmias. Precursors of these complications, such as diabetic cardiomyopathy, remain incompletely understood and underdiagnosed. Detection of early signs of cardiac deterioration in T2DM patients is critical for prevention. Our goal is to quantify T2DM-driven abnormalities in ECG and cardiac imaging biomarkers leading to cardiovascular disease.
We quantified ECG and cardiac magnetic resonance imaging biomarkers in two matched cohorts of 1781 UK Biobank participants, with and without T2DM, and no diagnosed cardiovascular disease at the time of assessment. We performed a pair-matched cross-sectional study to compare cardiac biomarkers in both cohorts, and examined the association between T2DM and these biomarkers. We built multivariate multiple linear regression models sequentially adjusted for socio-demographic, lifestyle, and clinical covariates.
Participants with T2DM had a higher resting heart rate (66 vs. 61 beats per minute, p < 0.001), longer QTc interval (424 vs. 420ms, p < 0.001), reduced T wave amplitude (0.33 vs. 0.37mV, p < 0.001), lower stroke volume (72 vs. 78ml, p < 0.001) and thicker left ventricular wall (6.1 vs. 5.9mm, p < 0.001) despite a decreased Sokolow-Lyon index (19.1 vs. 20.2mm, p < 0.001). T2DM was independently associated with higher heart rate (beta = 3.11, 95% CI = [2.11,4.10], p < 0.001), lower stroke volume (beta = -4.11, 95% CI = [-6.03, -2.19], p < 0.001) and higher left ventricular wall thickness (beta = 0.133, 95% CI = [0.081,0.186], p < 0.001). Trends were consistent in subgroups of different sex, age and body mass index. Fewer significant differences were observed in participants of non-white ethnic background. QRS duration and Sokolow-Lyon index showed a positive association with the development of cardiovascular disease in cohorts with and without T2DM, respectively. A higher left ventricular mass and wall thickness were associated with cardiovascular outcomes in both groups.
T2DM prior to cardiovascular disease was linked with a higher heart rate, QTc prolongation, T wave amplitude reduction, as well as lower stroke volume and increased left ventricular wall thickness. Increased QRS duration and left ventricular wall thickness and mass were most strongly associated with future cardiovascular disease. Although subclinical, these changes may indicate the presence of autonomic dysfunction and diabetic cardiomyopathy.
2 型糖尿病(T2DM)是射血分数保留型心力衰竭和心律失常的主要危险因素。这些并发症的前兆,如糖尿病心肌病,仍不完全了解和诊断不足。在 T2DM 患者中检测心脏恶化的早期迹象对于预防至关重要。我们的目标是量化导致心血管疾病的 T2DM 驱动的心电图和心脏成像生物标志物异常。
我们在两个匹配的队列中量化了 1781 名英国生物库参与者的心电图和心脏磁共振成像生物标志物,这些参与者有无 T2DM,并且在评估时没有诊断出心血管疾病。我们进行了一项配对的横断面研究,比较了两个队列中的心脏生物标志物,并检查了 T2DM 与这些生物标志物之间的关联。我们建立了多元多线性回归模型,依次调整了社会人口统计学、生活方式和临床协变量。
与无 T2DM 组相比,有 T2DM 组的静息心率更高(66 次/分钟比 61 次/分钟,p<0.001),QTc 间期更长(424 毫秒比 420 毫秒,p<0.001),T 波振幅更低(0.33 毫伏比 0.37 毫伏,p<0.001),心排量更低(72 毫升比 78 毫升,p<0.001),左心室壁更厚(6.1 毫米比 5.9 毫米,p<0.001),尽管 Sokolow-Lyon 指数降低(19.1 毫米比 20.2 毫米,p<0.001)。T2DM 与心率升高(β=3.11,95%CI=[2.11,4.10],p<0.001)、心排量降低(β=-4.11,95%CI=[-6.03,-2.19],p<0.001)和左心室壁增厚(β=0.133,95%CI=[0.081,0.186],p<0.001)独立相关。在不同性别、年龄和体重指数的亚组中,趋势一致。在非白人背景的参与者中,观察到的差异较少。在有和没有 T2DM 的队列中,QRS 持续时间和 Sokolow-Lyon 指数与心血管疾病的发展呈正相关。较高的左心室质量和壁厚度与两组的心血管结局相关。
心血管疾病之前的 T2DM 与更高的心率、QTc 延长、T 波振幅降低以及更低的心排量和增加的左心室壁厚度有关。较长的 QRS 持续时间和左心室壁厚度和质量与未来的心血管疾病最密切相关。尽管是亚临床的,但这些变化可能表明存在自主神经功能障碍和糖尿病心肌病。