Retinal nerve fiber layer thickness changes in Parkinson disease: a meta-analysis

Ji-Guo Yu, Yi-Fan Feng, Yi Xiang, Jin-Hai Huang, Giacomo Savini, Vincenzo Parisi, Wan-Ju Yang, Xun-An Fu, Ji-Guo Yu, Yi-Fan Feng, Yi Xiang, Jin-Hai Huang, Giacomo Savini, Vincenzo Parisi, Wan-Ju Yang, Xun-An Fu

Abstract

Background: Parkinson disease (PD) is a neurodegenerative process that leads to a selective loss of dopaminergic neurons, mainly in the basal ganglia of the brain. Numerous studies have analyzed the ability of optical coherence tomography (OCT) to detect retinal nerve fiber layer (RNFL) thickness abnormalities and changes in PD, but the results have not always been consistent. Therefore, we carried out a meta-analysis to evaluate the RNFL thickness measured with OCT in PD.

Methods and findings: Case-control studies were selected through an electronic search of the Cochrane Controlled Trials Register, PUBMED and EMBASE. For the continuous outcomes, we calculated the weighted mean difference (WMD) and 95% confidence interval (CI). The statistical analysis was performed by RevMan 5.0 software. Thirteen case-control studies were included in the present meta-analysis, containing a total of 644 eyes in PD patients and 604 eyes in healthy controls. The results of our study showed that there was a significant reduction in average RNFL thickness in patients with PD compared to healthy controls (WMD = -5.76, 95% CI: -8.99 to -2.53, P = 0.0005). Additionally, differences of RNFL thickness in superior quadrant (WMD = -4.44, 95% CI: -6.93 to -1.94, P = 0.0005), inferior quadrant (WMD = -7.56, 95% CI: -11.33 to -3.78, P<0.0001), nasal quadrant (WMD = -3.12, 95% CI: -5.63 to -0.61, P = 0.01) and temporal quadrant (WMD = -4.63, 95% CI: -7.20 to -2.06, P = 0.0004) were all significant between the two groups.

Conclusion: In view of these results and the noninvasive nature of OCT technology, we surmise that OCT could be a useful tool for evaluating the progression of the Parkinson disease.

Trial registration: ClinicalTrials.gov NCT01928212.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Search and study selection process.
Figure 1. Search and study selection process.
Figure 2. Meta-analysis of average RNFL thickness…
Figure 2. Meta-analysis of average RNFL thickness between PD patients and healthy controls.
Figure 3. Meta-analysis of RNFL thickness between…
Figure 3. Meta-analysis of RNFL thickness between PD patients and healthy controls: (A) superior, (B) inferior, (C) nasal and (D) temporal.
Figure 4. A funnel plot for evaluating…
Figure 4. A funnel plot for evaluating the publication bias: (A) average, (B) superior, (C) inferior, (D) nasal and (E) temporal.

References

    1. Parisi V, Manni G, Spadaro M, Colacino G, Restuccia R, et al. (1999) Correlation between morphological and functional retinal impairment in multiple sclerosis patients. Invest Ophthalmol Vis Sci 40: 2520–2527.
    1. Parisi V, Pierelli F, Coppola G, Restuccia R, Ferrazzoli D, et al. (2007) Reduction of optic nerve fiber layer thickness in CADASIL. Eur J Neurol 14: 627–631.
    1. Parisi V, Restuccia R, Fattapposta F, Mina C, Bucci MG, et al. (2001) Morphological and functional retinal impairment in Alzheimer's disease patients. Clin Neurophysiol 112: 1860–1867.
    1. Albrecht P, Muller AK, Sudmeyer M, Ferrea S, Ringelstein M, et al. (2012) Optical coherence tomography in parkinsonian syndromes. PLoS One 7: e34891.
    1. Moschos MM, Tagaris G, Markopoulos I, Margetis I, Tsapakis S, et al. (2011) Morphologic changes and functional retinal impairment in patients with Parkinson disease without visual loss. Eur J Ophthalmol 21: 24–29.
    1. Altintas O, Iseri P, Ozkan B, Caglar Y (2008) Correlation between retinal morphological and functional findings and clinical severity in Parkinson's disease. Doc Ophthalmol 116: 137–146.
    1. Archibald NK, Clarke MP, Mosimann UP, Burn DJ (2011) Retinal thickness in Parkinson's disease. Parkinsonism Relat Disord 17: 431–436.
    1. Parkinson J (2002) An essay on the shaking palsy. J Neuropsychiatry Clin Neurosci 14: 223–236 discussion 222.
    1. Aaker GD, Myung JS, Ehrlich JR, Mohammed M, Henchcliffe C, et al. (2010) Detection of retinal changes in Parkinson's disease with spectral-domain optical coherence tomography. Clin Ophthalmol 4: 1427–1432.
    1. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, et al. (2009) The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med 6: e1000100.
    1. Feng YF (2013) Retinal Nerve Fiber Layer Thickness Changes in Parkinson Disease: A Meta-analysis. Available: . Accessed 2013 Aug 22.
    1. Stang A (2010) Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol 25: 603–605.
    1. Wells GA, Shea B, O'Connell D, Peterson J, Welch V, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality if nonrandomized studies in meta-analyses.
    1. Higgins JP, Thompson SG, Deeks JJ, Altman DG (2003) Measuring inconsistency in meta-analyses. BMJ 327: 557–560.
    1. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634.
    1. Stuck AE, Rubenstein LZ, Wieland D (1998) Bias in meta-analysis detected by a simple, graphical test. Asymmetry detected in funnel plot was probably due to true heterogeneity. BMJ 316: 469 author reply 470–461.
    1. Satue M, Garcia-Martin E, Fuertes I, Otin S, Alarcia R, et al. (2013) Use of Fourier-domain OCT to detect retinal nerve fiber layer degeneration in Parkinson's disease patients. Eye (Basingstoke) 27: 507–514.
    1. Inzelberg R, Ramirez JA, Nisipeanu P, Ophir A (2004) Retinal nerve fiber layer thinning in Parkinson disease. Vision Res 44: 2793–2797.
    1. Kirbas S, Turkyilmaz K, Tufekci A, Durmus M (2013) Retinal nerve fiber layer thickness in Parkinson disease. J Neuroophthalmol 33: 62–65.
    1. Rohani M, Langroodi AS, Ghourchian S, Falavarjani KG, Soudi R, et al. (2012) Retinal nerve changes in patients with tremor dominant and akinetic rigid Parkinson's disease. Neurol Sci
    1. Tsironi EE, Dastiridou A, Katsanos A, Dardiotis E, Veliki S, et al. (2012) Perimetric and retinal nerve fiber layer findings in patients with Parkinson's disease. BMC Ophthalmol 12: 54.
    1. La Morgia C, Barboni P, Rizzo G, Carbonelli M, Savini G, et al. (2013) Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? Eur J Neurol 20: 198–201.
    1. Sen A, Tugcu B, Coskun C, Ekinci C, Nacaroglu SA (2013) Effects of levodopa on retina in Parkinson disease. Eur J Ophthalmol 0.
    1. Garcia-Martin E, Satue M, Fuertes I, Otin S, Alarcia R, et al. (2012) Ability and reproducibility of Fourier-domain optical coherence tomography to detect retinal nerve fiber layer atrophy in Parkinson's disease. Ophthalmology 119: 2161–2167.
    1. Garcia-Martin E, Pueyo V, Ara JR, Almarcegui C, Martin J, et al. (2011) Effect of optic neuritis on progressive axonal damage in multiple sclerosis patients. Mult Scler 17: 830–837.
    1. Garcia-Martin E, Pablo LE, Herrero R, Satue M, Polo V, et al. (2012) Diagnostic ability of a linear discriminant function for spectral-domain optical coherence tomography in patients with multiple sclerosis. Ophthalmology 119: 1705–1711.
    1. Martinez A, Proupim N, Sanchez M (2008) Retinal nerve fibre layer thickness measurements using optical coherence tomography in migraine patients. Br J Ophthalmol 92: 1069–1075.
    1. Kesler A, Vakhapova V, Korczyn AD, Naftaliev E, Neudorfer M (2011) Retinal thickness in patients with mild cognitive impairment and Alzheimer's disease. Clin Neurol Neurosurg 113: 523–526.
    1. Moreno-Ramos T, Benito-Leon J, Villarejo A, Bermejo-Pareja F (2013) Retinal nerve fiber layer thinning in dementia associated with parkinson's disease, dementia with lewy bodies, and alzheimer's disease. Journal of Alzheimer's Disease 34: 659–664.
    1. Gaenslen A, Berg D (2010) Early diagnosis of Parkinson's disease. Int Rev Neurobiol 90: 81–92.
    1. Thenganatt MA, Louis ED (2012) Distinguishing essential tremor from Parkinson's disease: bedside tests and laboratory evaluations. Expert Rev Neurother 12: 687–696.
    1. Carelli V, La Morgia C, Valentino ML, Barboni P, Ross-Cisneros FN, et al. (2009) Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders. Biochim Biophys Acta 1787: 518–528.
    1. Yavas GF, Yilmaz O, Kusbeci T, Ozturk F (2007) The effect of levodopa and dopamine agonists on optic nerve head in Parkinson disease. Eur J Ophthalmol 17: 812–816.
    1. Biousse V, Skibell BC, Watts RL, Loupe DN, Drews-Botsch C, et al. (2004) Ophthalmologic features of Parkinson's disease. Neurology 62: 177–180.
    1. Jackson GR, Owsley C (2003) Visual dysfunction, neurodegenerative diseases, and aging. Neurol Clin 21: 709–728.
    1. Bodis-Wollner I (1990) Visual deficits related to dopamine deficiency in experimental animals and Parkinson's disease patients. Trends Neurosci 13: 296–302.
    1. Frederick JM, Rayborn ME, Laties AM, Lam DM, Hollyfield JG (1982) Dopaminergic neurons in the human retina. J Comp Neurol 210: 65–79.
    1. Spund B, Ding Y, Liu T, Selesnick I, Glazman S, et al. (2013) Remodeling of the fovea in Parkinson disease. J Neural Transm 120: 745–753.
    1. Bayer AU, Keller ON, Ferrari F, Maag KP (2002) Association of glaucoma with neurodegenerative diseases with apoptotic cell death: Alzheimer's disease and Parkinson's disease. Am J Ophthalmol 133: 135–137.
    1. Rudnicka AR, Mt-Isa S, Owen CG, Cook DG, Ashby D (2006) Variations in primary open-angle glaucoma prevalence by age, gender, and race: a Bayesian meta-analysis. Invest Ophthalmol Vis Sci 47: 4254–4261.
    1. Hood DC, Cho J, Raza AS, Dale EA, Wang M (2011) Reliability of a computer-aided manual procedure for segmenting optical coherence tomography scans. Optom Vis Sci 88: 113–123.

Source: PubMed

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