Retinal Detachment
Conditions
Keywords
Retinal detachment, Photoreceptor apoptosis, Cytokine
Brief summary
Photoreceptor apoptosis is the basis for permanent visual loss in a number of retinal disorders including age-related macular degeneration (AMD) and retinal detachment (RD). Thus, despite tremendous advances in vitreoretinal surgery and management of rhegmatogenous RD leading to a primary reattachment rate over 95%, some patients show poor visual recovery because of photoreceptor apoptosis. Physiologically, microglial cells (resident macrophages) are present only in the inner retina. The subretinal space, located between the retinal pigment epithelium (RPE) and the photoreceptor outer segments (POS), is devoid of all mononuclear phagocytes and form a zone of immune privilege. In AMD, several studies showed a strong association between subretinal mononuclear phagocytes infiltration and advanced forms of AMD. Experimental work in mice suggest that this infiltration plays an important role in the pathogenesis of this condition by producing inflammatory cytokines. RD-induced photoreceptor apoptosis might result from similar mechanisms. The aim of this study is to determine the cytokine profile in vitreous samples from patients with RD and to compare it with those from control patients with macular hole.
Interventions
Pars plana vitrectomy
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with primary retinal detachment requiring vitrectomy * Patients with idiopathic macular hole requiring vitrectomy
Exclusion criteria
* History of retinal detachment or intraocular inflammatory diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intravitreous cytokine levels | up to one month after surgery |
Countries
France