Patel Sanjay, Harmer Jason A, Loughnan Georgina, Skilton Michael R, Steinbeck Katharine, Celermajer David S
Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia.
Clin Endocrinol (Oxf). 2007 Jun;66(6):771-7. doi: 10.1111/j.1365-2265.2007.02808.x. Epub 2007 Apr 15.
Prader-Willi syndrome (PWS) is a genetic obesity syndrome characterized by hyperphagia, behavioural disturbance and intellectual disability. PWS appears to be associated with a high incidence of sudden death, suspected to be cardiopulmonary in origin. We therefore sought to provide an assessment of cardiac and vascular structure and function in patients with PWS.
Nine patients with genetically confirmed PWS, mean age 28 years, body mass index (BMI) 42 kg/m2, were compared with nine age- and gender-matched lean controls.
Lipid parameters, high-sensitivity C-reactive protein (hs-CRP) and fasting glucose and insulin were measured. To assess cardiac structure and function, a resting electrocardiogram (ECG), exercise stress test, 24-h continuous ECG monitoring, and echocardiogram were obtained. Patients and control subjects also underwent comprehensive noninvasive vascular assessment, including venous-occlusion forearm plethysmography, brachial artery flow-mediated dilatation (FMD), radial artery tonometry and carotid intima-media thickness (IMT) measurements.
All patients with PWS had significantly elevated hs-CRP (> 3.0 mg/l) (mean 11.5 mg/l, median 11.47, interquartile range: 4.48-15.8 mg/l), compared with controls (P < 0.001). Five of nine patients with PWS had subnormal exercise capacity (< 4 mets on exercise stress testing). Twenty-four-hour ECG monitoring revealed prolonged sinus pauses in one patient, up to 4.8 s, requiring pacemaker insertion. Microvascular function as assessed by peak hyperaemic flow response was decreased in PWS (6.1 +/- 1.0 times baseline flow vs. controls 13.5 +/- 1.6 times baseline flow, P = 0.01). Other measures were similar between PWS and controls.
This group of PWS patients had significantly raised levels of the inflammatory marker hs-CRP and evidence of microcirculatory dysfunction, both of which are associated with coronary artery disease and early sudden death. The sinus node dysfunction may in itself be a risk factor for sudden cardiac death.
普拉德-威利综合征(PWS)是一种遗传性肥胖综合征,其特征为食欲亢进、行为障碍和智力残疾。PWS似乎与猝死的高发生率相关,推测其起源于心肺系统。因此,我们试图对PWS患者的心脏和血管结构及功能进行评估。
9例经基因确诊的PWS患者,平均年龄28岁,体重指数(BMI)为42kg/m²,与9例年龄和性别匹配的瘦对照组进行比较。
测定血脂参数、高敏C反应蛋白(hs-CRP)、空腹血糖和胰岛素。为评估心脏结构和功能,进行静息心电图(ECG)、运动负荷试验、24小时连续心电图监测和超声心动图检查。患者和对照者还接受了全面的非侵入性血管评估,包括静脉阻塞性前臂体积描记法、肱动脉血流介导的扩张(FMD)、桡动脉张力测定和颈动脉内膜中层厚度(IMT)测量。
与对照组相比,所有PWS患者的hs-CRP均显著升高(>3.0mg/l)(平均11.5mg/l,中位数11.47,四分位间距:4.48 - 15.8mg/l)(P<0.001)。9例PWS患者中有5例运动能力低于正常水平(运动负荷试验中<4代谢当量)。24小时心电图监测显示1例患者窦性停搏延长,长达4.8秒,需要植入起搏器。PWS患者经峰值充血血流反应评估的微血管功能下降(6.1±1.0倍基线血流,而对照组为13.5±1.6倍基线血流,P = 0.01)。PWS组和对照组的其他测量结果相似。
这组PWS患者的炎症标志物hs-CRP水平显著升高,并有微循环功能障碍的证据,这两者均与冠状动脉疾病和早期猝死相关。窦房结功能障碍本身可能是心源性猝死的危险因素。