Macular Microvasculature Is Different in Patients with Primary Sjögren's Disease Compared to Healthy Controls
- PMID: 40647699
- PMCID: PMC12248565
- DOI: 10.3390/diagnostics15131701
Macular Microvasculature Is Different in Patients with Primary Sjögren's Disease Compared to Healthy Controls
Abstract
Background/Objectives: This study investigates the macular microvasculature in a large cohort of primary Sjögren's disease (SjD) patients using optical coherence tomography angiography (OCTA), focusing on how disease duration, activity, and hydroxychloroquine (HCQ) treatment influence retinal microcirculation. Methods: A total of 106 eyes (53 SjD patients) and 70 eyes (35 age- and gender-matched healthy controls (HCs)) were examined. The vessel area density (VAD, %) and foveal avascular zone (FAZ, mm2) were measured in three retinal layers: Superficial Vascular Plexus (SVP), Intermediate Capillary Plexus (ICP), and Deep Capillary Plexus (DCP), respectively, in three peri-macular circular sectors (c1, c2, c3) each. Results: The VAD was significantly lower in c1 of the DCP in SjD compared to HCs (29.14 ± 7.07 vs. 31.78 ± 9.55, p = 0.038). The FAZ was significantly larger in SjD in both SVP (0.41 ± 0.13 vs. 0.34, 0.11, p < 0.001; Cohen's |d| = 0.55) and DCP (0.45 ± 0.15 vs. 0.4 ± 0.14, p = 0.014; Cohen's |d| ± 0.38). Significant correlations were observed between the FAZ size and reductions in the VAD in the SVP and DCP (p = 0.010, Cohen's |d| = 0.2; p < 0.001, Cohen's |d| ± 0.26) and across all layers combined (p = 0.019, Cohen's |d| = -0.18). Conclusions: There was a negative correlation between the VAD in the DCP and disease duration (ρ = -0.28, p = 0.040). No significant correlation was identified between the duration of HCQ intake and the VAD or FAZ. Our findings indicate microvascular alterations in the DCP of SjD, characterized by a reduced VAD and an enlarged FAZ, which may be attributable to inflammatory or arteriosclerotic factors. OCTA may prove to be a valuable tool for the stratification of vascular risk in SjD.
Keywords: OCTA imaging; Sjögren’s disease; macular microvasculature; retinal biomarker.
Conflict of interest statement
Potential conflicts of interest: The authors declare no relevant conflicts of interest to disclose. Outside the submitted work, the authors received honoraria for lectures, travel grants, or research grants. G.T.: no conflicts of interest. L.H.: nothing to declare. M.G.: nothing to declare. N.Z.: received a scholarship by Else Kröner Fresenius Foundation, research grants by Novartis, and financial support for conference attendance by Abbvie. B.H.: received honoraria from Abbvie; B.H. received funding from the DFG, BMBF, BMG, StMWK, LGL, and Gliead. C.M.: nothing to declare. T.W.: received honoraria for lectures by Abbvie, BMS, Chugai, Galapagos, Janssen, Lilly, Pfizer, UCB, and Roche. T.W. received funding from the DFG (German Research Foundation) under Germany’s Excellence Strategy—EXC 2155—project number 390874280. C.F.: nothing to declare. D.E.: received presentation honoraria from Abbvie, Amgen, BMS, Chugai, Cilag-Janssen, Galapagos, GSK, Medac, Lilly, Pfizer, Novartis, and Roche; participated in advisory boards for Abbvie, Galapagos, Amgen, and Novartis; and received research grants from Novartis and Abbvie. K.H.: no conflicts of interest.
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