Bilaterally Asymmetric Corneal Ectasia Following SMILE With Asymmetrically Reduced Stromal Molecular Markers.

PURPOSE To evaluate extracellular matrix regulators and inflammatory factors in a patient who developed ectasia after small incision lenticule extraction (SMILE) despite normal preoperative tomographic and biomechanical evaluation. METHODS The SMILE lenticules from both eyes of the patient with ectasia and three control patients (5 eyes) matched for age, sex, and duration of follow-up were used for gene expression analysis of lysyl oxidase (LOX), matrix metalloproteinase 9 (MMP9), collagen types I alpha 1 (COLIA1) and IV alpha 1 chain (COLIVA1), transforming growth factor-beta (TGF-beta), bone morphogenetic protein 7 (BMP7), interleukin-6 (IL-6), cathepsin K, cluster of differentiation 68, integrin beta-1, and tissue inhibitor of metalloproteinase-1 (TIMP1). Furthermore, the functional role of LOX was assessed in vitro by studying the collagen gel contraction efficiency of LOX overexpressing in primary human corneal fibroblast cells. RESULTS Preoperatively, manifest refraction was -9.25 diopters (D) in the right eye and -10.00 D in the left eye. Corneal thickness, Pentacam (OCULUS Optikgeräte GmbH, Wetzlar, Germany) tomography, and Corvis biomechanical indices (OCULUS Optikgeräte GmbH) were normal. The ectatic eye lenticule (left) had reduced expression of LOX and COLIA1 compared to controls without ectasia. Increased mRNA fold change expression of TGF-beta, BMP7, IL-6, cathepsin K, and integrin beta-1 was noted in the ectatic left eye compared to controls; however, MMP9 and TIMP1 levels were not altered. Ectopic LOX expression in human corneal fibroblast induced significantly more collagen gel contraction, confirming the role of LOX in strengthening the corneal stroma. CONCLUSIONS Reduced preexisting LOX and collagen levels may predispose clinically healthy eyes undergoing refractive surgery to ectasia, presumably by corneal stromal weakening via inadequately cross-linked collagen. Preoperative molecular testing may reveal ectasia susceptibility in the absence of tomographic or biomechanical risk factors. [J Refract Surg. 2019;35(1):6-14.].

[1]  R. Atia,et al.  Unilateral corneal ectasia after small-incision lenticule extraction in a 43-year-old patient. , 2018, Journal of cataract and refractive surgery.

[2]  J. Alió,et al.  Small incision lenticule extraction (SMILE) in the correction of myopic astigmatism: outcomes and limitations - an update , 2017, Eye and Vision.

[3]  R. Shetty,et al.  In vivo confocal microscopy and tear cytokine analysis in post-LASIK ectasia , 2017, British Journal of Ophthalmology.

[4]  Priyanka Chevour,et al.  Lower Vitamin D Level and Distinct Tear Cytokine Profile Were Observed in Patients with Mild Dry Eye Signs but Exaggerated Symptoms , 2016, Translational vision science & technology.

[5]  R. Mohan,et al.  Differential Molecular Expression of Extracellular Matrix and Inflammatory Genes at the Corneal Cone Apex Drives Focal Weakening in Keratoconus. , 2016, Investigative ophthalmology & visual science.

[6]  R. Shetty,et al.  Correlation of Clinical and Biomechanical Outcomes of Accelerated Crosslinking (9 mW/cm2 in 10 minutes) in Keratoconus with Molecular Expression of Ectasia-Related Genes , 2016, Current eye research.

[7]  M. Blum,et al.  Five-year results of Small Incision Lenticule Extraction (ReLEx SMILE) , 2016, British Journal of Ophthalmology.

[8]  Jianjiang Xu,et al.  Association of Common Variants in LOX with Keratoconus: A Meta-Analysis , 2015, PloS one.

[9]  R. Sachdev,et al.  Unilateral corneal ectasia following small-incision lenticule extraction. , 2015, Journal of cataract and refractive surgery.

[10]  R. Shetty,et al.  Air-puff associated quantification of non-linear biomechanical properties of the human cornea in vivo. , 2015, Journal of the mechanical behavior of biomedical materials.

[11]  Xiang-chen Tao,et al.  Corneal ectasia 6.5 months after small-incision lenticule extraction. , 2015, Journal of cataract and refractive surgery.

[12]  M. El-Naggar Bilateral ectasia after femtosecond laser-assisted small-incision lenticule extraction. , 2015, Journal of cataract and refractive surgery.

[13]  R. Mohan,et al.  Attenuation of lysyl oxidase and collagen gene expression in keratoconus patient corneal epithelium corresponds to disease severity , 2015, Molecular vision.

[14]  William J Dupps,et al.  Biomechanics of corneal ectasia and biomechanical treatments. , 2014, Journal of cataract and refractive surgery.

[15]  J. Grauslund,et al.  Efficacy, safety, predictability, contrast sensitivity, and aberrations after femtosecond laser lenticule extraction , 2014, Journal of cataract and refractive surgery.

[16]  Qiang Zhou,et al.  Stat3 pathway correlates with the roles of leptin in mouse liver fibrosis and sterol regulatory element binding protein-1c expression of rat hepatic stellate cells. , 2013, The international journal of biochemistry & cell biology.

[17]  E. Liu,et al.  Telomerase directly regulates NF-κB-dependent transcription , 2012, Nature Cell Biology.

[18]  S. Parapuram,et al.  Integrin β1 is necessary for the maintenance of corneal structural integrity. , 2011, Investigative ophthalmology & visual science.

[19]  Michael J Lynn,et al.  Risk assessment for ectasia after corneal refractive surgery. , 2008, Ophthalmology.

[20]  H. Grossniklaus,et al.  Depth-dependent cohesive tensile strength in human donor corneas: implications for refractive surgery. , 2008, Journal of refractive surgery.

[21]  Y. Konttinen,et al.  Collagenolytic Proteinases in Keratoconus , 2006 .

[22]  A. Ljubimov,et al.  Identification of Cell Types in Human Diseased Corneas , 2001, Cornea.