Retinitis Pigmentosa Clinical Trial
Official title:
Management of Retinitis Pigmentosa Via Repetitive Electromagnetic Stimulation and Autologous Platelet Rich Plasma
The aim of this study is to investigate whether natural progression rate can be slowed down with subtenon PRP or PRP application combined with rEMS in retinitis pigmentosa cases.
Retinitis pigmentosa (RP) is a progressive external retinal degeneration resulting from
mutation in any of the 260 genes found in the retinal pigment epithelium (RPE). The
progression rate and findings of the disease are heterogeneous according to genetic mutation
and heredity type. The initial symptom of the disease is usually night blindness (nyctalopia)
beginning in childhood or adolescent period. Narrowing in the visual field and legal
blindness develops as the disease progresses. If low grade inflammation is added, the disease
is complicated by cataracts, epiretinal membrane and macular edema. In the fundus
examination, the appearance of midperiferal bone spicule pigmentation is usually sufficient
to diagnosis. Developments in optical coherence tomography (OCT) technology enable detailed
imaging of the sensorial retina and the ellipsoid zone. The ellipsoid zone (EZ) is an image
of the inner and outer segments of photoreceptor cells. Loss of EZ is considered the gold
standard in the diagnosis and follow-up of RP. Visual field monitoring and
electroretinography (ERG) are indirect signs of EZ loss and correlated with EZ width.
Mutations in RPE disrupt the synthesis of some vital peptide and growth factors for
photoreceptors.
Platelet-rich plasma (PRP) is a good source of growth factors. Platelets have more than 30
growth factors and cytokines in α-granules such as neurotrophic growth factor (NGF), neural
factor (NF), brain derived neurotrophic factor (BDNF), basic fibroblast growth factor (bFGF),
insulin-like growth factor (IGF), transforming growth factor (TGF-β), vascular endothelial
growth factor (VEGF), platelet derived growth factor (PDGF) etc. These peptides regulate the
energy cycle at the cellular level, local capillary blood flow, neurogenesis and cellular
metabolism. Anti-inflammatory effects of PRP are also associated with soluble cytokines.
Repetitive electromagnetic stimulation (rEMS), increases binding affinity and the synthesis
of growth factor receptors on neural tissues. It provides electromagnetic iontophoresis by
changing the electrical charges of tyrosine kinase receptors (Trk). rEMS forms
hyperpolarization-depolarization waves in neurons, thereby increasing neurotransmission and
capillary blood flow. Trk receptors are commonly found around limbus, extraocular muscle
insertions and the optic nerve. Molecules smaller than 75 kD can pass from the sclera
passively to the suprachoroidal space. Electrical or electromagnetic iontophoresis is
required for molecules larger than 75kD such as BDNF and IGF to pass through the sclera.
The aim of this study is to investigate whether natural progression rate can be slowed down
with subtenon PRP or PRP application combined with rEMS in retinitis pigmentosa cases.
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