Evaluation of choroidal thickness in retinitis pigmentosa using enhanced depth imaging optical coherence tomography

Objective To describe the choroidal characteristics of patients with retinitis pigmentosa (RP) using enhanced depth imaging (EDI) and spectral domain (SD) optical coherence tomography (OCT). Purpose To investigate the spectral-domain ocular coherence tomography features of the choroid in patients with RP using EDI. Methods A prospective, case–control study of 21 patients from the Cole Eye Institute with RP imaged using the Spectralis OCT and an EDI protocol. Submacular choroidal thickness measurements were obtained beneath the fovea and at 500 µm intervals for 2.5 mm nasal and temporal to the centre of the fovea. These measurements were compared to choroidal thickness measurements from 25 healthy age-matched controls with similar refractive error range and no clinical evidence of retinal or glaucomatous disease. Statistical analysis was performed to compare choroidal thickness at each location between the two groups and to correlate choroidal thickness with best-corrected visual acuity and central retinal thickness. Results Mean ages were 40.6 years for control patients and 45.1 years for RP patients (p>0.05). Mean choroidal thickness measurements were 245.6±103 µm in RP patients and 337.8.2±109 µm in controls (p<0.0001). There was no correlation between subfoveal choroidal thickness and visual acuity or retinal thickness in the RP patients when compared to the control group. Conclusions Submacular choroidal thickness, as measured by SD–OCT EDI, is significantly reduced in patients with RP, but did not correlate with visual acuity or retinal thickness in RP patients. Further research is needed to understand better the pathophysiological significance of the choroidal alterations present in RP.

[1]  Boris Hermann,et al.  Wide-field optical coherence tomography of the choroid in vivo. , 2008, Investigative ophthalmology & visual science.

[2]  T. Rosenberg,et al.  Prevalence of retinitis pigmentosa and allied disorders in Denmark , 1992, Acta ophthalmologica.

[3]  M. Horneber,et al.  Quantitative and morphological changes of the choroid vasculature in RCS rats and their congenic controls. , 1996, Experimental eye research.

[4]  Magali Saint-Geniez,et al.  An essential role for RPE-derived soluble VEGF in the maintenance of the choriocapillaris , 2009, Proceedings of the National Academy of Sciences.

[5]  R. Spaide,et al.  A pilot study of enhanced depth imaging optical coherence tomography of the choroid in normal eyes. , 2009, American journal of ophthalmology.

[6]  E. Stone,et al.  ELECTRORETINOGRAPHIC FINDINGS IN PATIENTS WITH STARGARDT DISEASE AND FUNDUS FLAVIMACULATUS , 2002, Retina.

[7]  E. Berson Retinitis pigmentosa. The Friedenwald Lecture. , 1993, Investigative ophthalmology & visual science.

[8]  M. Haim Prevalence of retinitis pigmentosa and allied disorders in Denmark , 1992, Acta ophthalmologica.

[9]  S. Liebowitz Retinitis pigmentosa. , 1979, Journal - American Intra-Ocular Implant Society.

[10]  S. Bhattacharya,et al.  Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8). , 1993, Human molecular genetics.

[11]  C. Costagliola,et al.  Enhanced depth imaging spectral-domain optical coherence tomography. , 2010, Retina.

[12]  V. Reppucci,et al.  RPE destruction causes choriocapillary atrophy. , 1984, Investigative ophthalmology & visual science.

[13]  A E Maumenee,et al.  Fluorescein angiography of the choriocapillaris. , 1969, American journal of ophthalmology.

[14]  Qiuyun Chen,et al.  Update on the molecular genetics of retinitis pigmentosa , 2001, Ophthalmic genetics.

[15]  Adnan Tufail,et al.  Choroidal imaging in inherited retinal disease using the technique of enhanced depth imaging optical coherence tomography , 2010, Graefe's Archive for Clinical and Experimental Ophthalmology.

[16]  J. Grunwald,et al.  Retinal hemodynamics in retinitis pigmentosa. , 1996, American journal of ophthalmology.

[17]  P. Humphries,et al.  On the molecular genetics of retinitis pigmentosa. , 1992, Science.

[18]  E. Campos,et al.  Subfoveal choroidal blood flow and central retinal function in retinitis pigmentosa. , 2009, Investigative ophthalmology & visual science.

[19]  J. Heckenlively,et al.  Clinical findings and common symptoms in retinitis pigmentosa. , 1988, American journal of ophthalmology.

[20]  J. Flammer,et al.  Ocular pulse amplitude is reduced in patients with advanced retinitis pigmentosa , 2001, The British journal of ophthalmology.

[21]  E. Lütjen-Drecoll,et al.  Morphological changes of retinal pigment epithelium and choroid in rd-mice. , 1999, Experimental eye research.

[22]  F. Newell,et al.  Fluorescein angiography in retinitis pigmentosa. , 1970, American journal of ophthalmology.

[23]  M. Langham,et al.  Decreased choroidal blood flow associated with retinitis pigmentosa , 1990, Eye.

[24]  K. Narfström,et al.  Choroidal microcirculation in Abyssinian cats with hereditary rod-cone degeneration. , 2008, Experimental eye research.