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Observational Study
. 2018 Jun;256(6):1159-1163.
doi: 10.1007/s00417-018-3946-4. Epub 2018 Mar 10.

Ocular manifestation in Marfan syndrome: corneal biomechanical properties relate to increased systemic score points

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Observational Study

Ocular manifestation in Marfan syndrome: corneal biomechanical properties relate to increased systemic score points

Dido Scheibenberger et al. Graefes Arch Clin Exp Ophthalmol. 2018 Jun.

Abstract

Purpose: To evaluate corneal deformation to an air puff as a new noninvasive tool to document disease status in Marfan syndrome (MFS) METHODS: Prospective observational cohort study. We included patients diagnosed with MFS who had their routine cardiovascular follow-up and applied the revised Ghent nosology to define two subgroups according to a high (≥ 7) and a low (< 7 points) systemic score. Dynamic Scheimpflug-based biomechanical analyses (CorvisST® [CST; Oculus GmbH]) were performed. The main outcome measure was the displacement of the corneal apex as given by the parameters highest concavity (HC; in ms), peak distance (PD; in mm), and highest concavity deformation amplitude (DA; mm).

Results: Forty-three eyes of 43 individuals (19 female, 24 male; mean age 42.0 ± 12.0 years, range 18-67 years) diagnosed with MFS were included. Applying the Ghent criteria, 21 patients had an advanced systemic score of ≥ 7, and 22 had score points < 7. There were no differences in age or sex between both groups. In contrast, HC was faster (P = 0.004), and PD (P < 0.001) was longer in those individuals with systemic score ≥ 7; maximum DA did not result in a statistically significant difference between the groups (P = 0.250).

Conclusions: In vivo noninvasive biomechanical analyses with CST offer a new, non-invasive method to identify pathologic corneal deformation responses in adults with MFS. In the future, corneal deformation to an air puff could thus assist early identification of patients with high Ghent score as an adjunct to existing diagnostic tests.

Keywords: Corneal biomechanics; Corvis ST; Ghent criteria; Marfan syndrome.

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