2019
DOI: 10.1016/j.ajo.2019.04.011
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Changes in Retinal Microcirculation Precede the Clinical Onset of Diabetic Retinopathy in Children With Type 1 Diabetes Mellitus

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Cited by 71 publications
(74 citation statements)
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“… 25 The largest series in type 1 DM have been described in children, and they interestingly have shown controversial results. 26 30 Golebiewska et al reported that no differences were seen in the VD or FAZ area in any of the studied plexuses between patients with type 1 DM and controls ( n = 188 vs. 60); however, Niestrata-Ortiz et al described that FAZ area was different between diabetic and healthy children ( n = 112 vs. 30). 27 , 28 In this last paper, a greater FAZ area was also associated with a longer duration of the disease.…”
Section: Discussionmentioning
confidence: 93%
“… 25 The largest series in type 1 DM have been described in children, and they interestingly have shown controversial results. 26 30 Golebiewska et al reported that no differences were seen in the VD or FAZ area in any of the studied plexuses between patients with type 1 DM and controls ( n = 188 vs. 60); however, Niestrata-Ortiz et al described that FAZ area was different between diabetic and healthy children ( n = 112 vs. 30). 27 , 28 In this last paper, a greater FAZ area was also associated with a longer duration of the disease.…”
Section: Discussionmentioning
confidence: 93%
“…23 In studies conducted with changes in FAZ perimetry, AI, and FD, it has been shown that there may be differences in the early stages of the disease even in the preclinical stages. 24 In their study in diabetic children, it is shown that FAZ perimeter, AI, and FD change without retinopathy findings. Similarly, Lynch et al 25 performed a study in children with sickle cell anemia, in whom FAZ perimeter and AI showed a significant increase compared to the control group.…”
Section: Discussionmentioning
confidence: 94%
“…Zpomalení průtoku v MA způsobí jen 40% znázornitelnost na OCT-A vyšetření na rozdíl od FAG [40]. OCT-A ukazuje u pacientů bez DR snížení celkové denzity kapilár [41] a časné mikrovaskulární změny [38], a to bez rozdílu použitého přístroje [42], především v parafoveální oblasti DCP [43,44]. Tyto nálezy jsme také pozorovali.…”
Section: Metodikaunclassified