SAT0326 Efficacy and Safety of Autologous Platelet Lysate Eye Drops in Sjögren's Syndrome: A New Approach

Autor: Enrico Fusaro, Roberto Caporali, Vittoria Aragno, Clara Lisa Peroni, Simone Parisi, Federica Machetta, S. D'Antico, Carlomaurizio Montecucco, M. Scarati, V. Testa, Marta Priora
Rok vydání: 2016
Předmět:
Zdroj: Annals of the Rheumatic Diseases. 75:785.2-785
ISSN: 1468-2060
0003-4967
Popis: Background Sjogren9s Sydrome (SS) is a chronic multisystem autoimmune disease characterized by hypofunction of salivary and lacrimal glands. The result of the immune-mediate infiltration of the lacrimal gland is a severe dry eye disease. None of the commercially available artificial tear preparations and anti-inflammatory topical treatment has the properties of the human tears as Growth factors (GFs), that are necessary for maintenance of normal corneal epithelium. Platelet alfa granules are a major source of GFs and are rich in platelet derived growth factor (PDGF), which plays an important role in the maintenance of ocular surface and tear film stability (1). Objectives To determine the efficacy and safety of autologous platelet lysate (APL) eye drops in patients with primary SS dry eye, refractory to standard therapy, in comparison to patients treated with artificial tears. We focused on the effect of APL on cornea morphology with the in vivo confocal microscopy (IVCM). Methods We included patients with a diagnosis of SS according to the classification criteria of the American-European Consensus (2), a dry eye severity level ≥2 (Dry Eye Severity Grading Scheme, Workshop 2007). Patients were assigned in two groups, according to the randomization criteria 1:1 –Group A used autologous platelet lysate (BiomedDevice) QID for 90 days. –Group B used preservative-free artificial tears QID (Ialuronic Acid 0,2%) for 90 days. Ophthalmological assessments included: ocular surface disease index (OSDI), Schirmer test, fluoresceine score and break up time (BUT). Both Group A and Group B underwent IVCM; corneal basal epithelium, sub basal nerves, Langherans cells, anterior stroma activated keratocytes were evaluated. The study was conducted in accordance with the Declaration of Helsinki (1964) and approved by our Ethics Committee. Results 43 patients (female:male =42:43) with mean age of 59,75 years (SD±13,10) affected by primary SS from 7,48 years (SD±5,56) were enrolled. The two groups (A=22 pts; B=21 pts) did not have significant differences at baseline in terms of disease (duration, autoantibodies) and treatment (steroids, DMARDs) characteristics. In group A, the mean of improvement of OSDI, fluorescein score and BUT values (Δ38.82; Δ1.0; Δ1.5 respectively) were higher than group B (Δ7.07; Δ0.0; Δ0.0 respectively) with statistical significance (p Conclusions APL has proved to be effective and safety in the treatment of SS dry eye and IVCM seems to be a useful tool to visualize cornea morphologic modifications. Further studies are required to evaluate the long-term effects and the timing of retreatment. References Pezzotta S, Del Fante C, Scudeller L et al. Autologous platelet lysate for treatment of refractory ocular GVHD. Bone Marrow Transplantation 2012; 47, 1558–1563. Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjogren9s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002; 61:554–8. Disclosure of Interest None declared
Databáze: OpenAIRE
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