Active transforming growth factor-β2 in the aqueous humor of posterior polymorphous corneal dystrophy patients.

PLoS One

Laboratory of the Biology and Pathology of the Eye, Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Czech Republic.

Published: April 2017

AI Article Synopsis

  • The study investigates the levels of TGF-β2 protein in the aqueous humor of patients with posterior polymorphous corneal dystrophy (PPCD), a condition marked by irregular growth of corneal endothelial cells.
  • Active TGF-β2 was found to be significantly higher in PPCD patients compared to control samples, indicating a potential link between elevated TGF-β2 and the disease phenotype.
  • The research suggests that these increased levels of TGF-β2 may serve as an additional characteristic of PPCD, though they do not appear to be influenced by factors like age, gender, or treatment history.

Article Abstract

Purpose: Posterior polymorphous corneal dystrophy (PPCD) is characterized by abnormal proliferation of corneal endothelial cells. It was shown that TGF-β2 present in aqueous humor (AH) could help maintaining the corneal endothelium in a G1-phase-arrest state. We wanted to determine whether the levels of this protein are changed in AH of PPCD patients.

Methods: We determined the concentrations of active TGF-β2 in the AH of 29 PPCD patients (42 samples) and 40 cadaver controls (44 samples) by ELISA. For data analysis the PPCD patients were divided based on either the molecular genetic cause of their disease as PPCD1 (37 samples), PPCD3 (1 sample) and PPCDx (not linked to a known PPCD loci, 4 samples) or on the presence (17 samples) or absence (25 samples) of secondary glaucoma or on whether they had undergone penetrating keratoplasty (PK, 32 samples) or repeated PK (rePK, 7 samples).

Results: The level of active TGF-β2 in the AH of all PPCD patients (mean ± SD; 386.98 ± 114.88 pg/ml) in comparison to the control group (260.95 ± 112.43 pg/ml) was significantly higher (P = 0.0001). Compared to the control group, a significantly higher level of active TGF-β2 was found in the PPCD1 (P = 0.0005) and PPCDx (P = 0.0022) groups. Among patients the levels of active TGF-β2 were not significantly affected by gender, age, secondary glaucoma or by the progression of dystrophy when one or repeated PK were performed.

Conclusion: The levels of active TGF-β2 in the AH of PPCD patients are significantly higher than control values, and thus the increased levels of TGF-β2 could be a consequence of the PPCD phenotype and can be considered as another feature characterizing this disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393593PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0175509PLOS

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