Sapienza University of Rome, Department of Clinical Medicine, Clinical Immunology Unit-Scleroderma Center, Italy.
Microvasc Res. 2011 Nov;82(3):410-5. doi: 10.1016/j.mvr.2011.07.009. Epub 2011 Jul 24.
To assess morphology and blood flow of the proper palmar digital arteries (PPDA) by color Doppler ultrasonography (CDUS) and its relationship with nailfold videocapillaroscopy (NVC), skin blood perfusion and digital arteries pulsatility of hands in SSc patients and healthy controls.
CDUS, NVC, laser Doppler perfusion imaging (LDPI) and photoplethysmography (PPG) were performed in 36 systemic sclerosis (SSc) patients and 20 healthy controls.
CDUS was pathologic in 69% of patients with SSc and in none of healthy controls (p<0.0001). SSc patients with low vascular damage (early capillaroscopic pattern) have a normal morphology of PPDA, but the blood flow, evaluated by peak systolic velocity (PSV) and end diastolic velocity (EDV), is reduced and vascular resistance, measured by resistive index (RI) and pulsatility index (PI), increased. At this stage the LDPI mean perfusion and digital artery pulsatility, evaluated by PPG, were reduced. The US changes appear with microvascular damage progression (active and late capillaroscopic patterns), while the PPDA blood flow progressively decreases (PSV and EDV decreased, RI and PI increased). The macrovascular damage correlates with disease duration. Anti-topoisomerase I represents an independent predictive factor for macrovascular damage. We not observed any association between digital ulcer history, pulmonary fibrosis and US findings.
PPDA blood flow dysfunction is already present in early disease. Structural macrovascular damage progresses with worsening of SSc microangiopathy.
通过彩色多普勒超声(CDUS)评估原发性掌侧指动脉(PPDA)的形态和血流,并研究其与系统性硬化症(SSc)患者和健康对照者的甲襞微循环血管(NVC)、皮肤血流灌注和手部动脉搏动性的关系。
对 36 例 SSc 患者和 20 例健康对照者进行了 CDUS、NVC、激光多普勒灌注成像(LDPI)和光体积描记法(PPG)检查。
CDUS 在 69%的 SSc 患者中存在病理改变,而在健康对照者中无一例存在(p<0.0001)。低血管损伤(早期毛细血管镜模式)的 SSc 患者 PPDA 形态正常,但血流峰值收缩速度(PSV)和舒张末期速度(EDV)降低,血管阻力(RI 和 PI)增加。在这个阶段,LDPI 平均灌注和通过 PPG 评估的数字动脉搏动性降低。当微血管损伤进展(活动期和晚期毛细血管镜模式)时,US 改变出现,而 PPDA 血流逐渐减少(PSV 和 EDV 降低,RI 和 PI 增加)。大血管损伤与疾病持续时间相关。抗拓扑异构酶 I 是大血管损伤的独立预测因素。我们未观察到手指溃疡史、肺纤维化与 US 发现之间存在任何关联。
PPDA 血流功能障碍在疾病早期就已经存在。结构性大血管损伤随着 SSc 微血管病变的恶化而进展。