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In systemic sclerosis macrovascular damage of hands digital arteries correlates with microvascular damage
Institution:1. Institute for Space Astrophysics and Planetology, INAF, Via del Fosso del cavaliere 100, 00133 Rome, Italy;2. Institute of Atmospheric Sciences and Climate, CNR, Via del Fosso del cavaliere 100, 00133 Rome, Italy;1. Department of Neonatology, The Townsville Hospital, Queensland 4814, Australia;2. Mothers and Babies Research Centre, Hunter Medical Research Institute, HMRI, The University of Newcastle, NSW 2310, Australia;3. College of Public Health, Medical and Veterinary Sciences, James Cook University, QLD 4814, Australia;4. Department of Optometry and Vision Science, University of Melbourne, Victoria, Australia;5. Centre for Environmental Sciences, Hasselt University, Hasselt, Belgium;6. Health Unit, Flemish Institute for Technological Research (VITO), Mol, Belgium
Abstract:ObjectiveTo 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.MethodsCDUS, NVC, Laser Doppler Perfusion Imaging (LDPI) and photoplethysmography (PPG) were performed in 36 systemic sclerosis (SSc) patients and 20 healthy controls.ResultsCDUS 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 microvasculare 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.ConclusionPPDA blood flow dysfunction is already present in early disease. Structural macrovascular damage progresses with worsening of SSc microangiopathy.
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