[Elsevier] Eur J Pediatr.

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Eur J Pediatr




. 2025 Jun 6;184(7):398.
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doi: 10.1007/s00431-025-06234-1.
Optical coherence tomography and angiography reveal early retinal alterations in pediatric-onset multiple sclerosis Selda Celik Dulger 1, Fatma Bagci 2, Ismail Solmaz 2, Deniz Yuksel 3, Bahadir Konuskan




Abstract
The purpose of this study is to investigate alterations in optical coherence tomography (OCT) and OCT angiography (OCT-A) parameters in patients with pediatric-onset multiple sclerosis (POMS). This prospective cross-sectional study included 37 POMS patients and 36 healthy controls (HCs). We performed OCT and OCT-A scans. POMS eyes were categorized into two subgroups: those with a history of optic neuritis (MS + ON) and those without (MS-ON). The mean ages of the POMS patients and HCs were 15.8 ㊣ 0.2 and 14.7 ㊣ 2.5 years, respectively (p = 0.266). Compared with that in HCs, the retinal nerve fiber layer (RNFL) thickness in MS + ON eyes was lower in three segments; it was significantly lower only in the temporal segment in MS-ON eyes. In all quadrants, except one, ganglion cell-inner plexiform layer (GC-IPL) thicknesses were significantly thinner in MS + ON and MS-ON eyes than in HCs. In multiple quadrants, vessel density (VD) in the radial peripapillary capillary (RPC) plexus was significantly lower in MS + ON eyes than in MS-ON and HCs. Compared with those of MS-ON and HCs, the whole and perifoveal VDs in the superficial capillary plexus (SCP) of MS + ON eyes were significantly lower. VD in the deep capillary plexus (DCP) and foveal avascular zone (FAZ) did not differ between groups.
Conclusion: The OCT-A findings in POMS patients include a reduction in vessel density in the macula and peripapillary area in the setting of optic neuritis. The thinning of the GC-IPL and RNFL was observed in POMS eyes irrespective of prior ON history, but ON was associated with more prominent thinning.
What is known: • On the basis of the reported clinical association between the MS course and retinal dysfunction, quantitative retinal vessel measurements may be potential markers for MS. • The literature shows that the majority of OCT and OCT-A studies were in adult MS patients, with a limited number of studies in children.
What is new: • In this study, we present 37 POMS patients, identify clinically silent retinal nerve fiber and ganglion cell loss independent of optic neuritis, and demonstrate a reduction in vessel density in the macula and peripapillary area in the setting of optic neuritis. • The inclusion of very early cases of MS, such as the pediatric group, may offer a unique opportunity to better understand the impact of retinal vascular changes on disease pathogenesis.



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