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Published in: Journal of Neurology 11/2015

01-11-2015 | Original Communication

Optical coherence tomography findings in Huntington’s disease: a potential biomarker of disease progression

Authors: Hannah M. Kersten, Helen V. Danesh-Meyer, Dean H. Kilfoyle, Richard H. Roxburgh

Published in: Journal of Neurology | Issue 11/2015

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Abstract

Previous reports of ocular abnormalities in Huntington’s disease (HD) have detailed eye movement disorders. The objective of this case–control study was to investigate optic nerve and macular morphology in HD using optical coherence tomography (OCT). A total of 26 HD patients and 29 controls underwent a thorough ophthalmic examination including spectral domain OCT scans of the macula and peripapillary retinal nerve fibre layer (RNFL). Genetic testing results, disease duration, HD disease burden scores and Unified HD Rating Scale motor scores were acquired for HD patients. Temporal RNFL thickness was significantly reduced in the HD group (62.3 vs. 69.8 μm, p = 0.005), and there was a significant negative correlation between temporal RNFL thickness and disease duration (R 2 = −0.51, p = 0.04). Average peripapillary RNFL thickness was not significantly different between the HD and control groups. There was a significant negative correlation between macular volume and disease duration (R 2 = −0.71, p = 0.002), and motor scores (R 2 = −0.56, p = 0.01). Colour vision was significantly poorer in the HD group. Temporal RNFL is preferentially thinned in HD patients, possibly implicating mitochondrial dysfunction as the temporal RNFL is reduced in the patients with some mitochondrial disorders, including Leber’s hereditary optic neuropathy. The correlation between the decrease in macular volume and temporal RNFL, and increasing disease severity suggests that OCT may be a useful biomarker for disease progression in HD. Larger, longitudinal studies are required.
Literature
1.
go back to reference Purdon SE, Mohr E, Ilivitsky V, Jones BD (1994) Huntington’s disease: pathogenesis, diagnosis and treatment. J Psychiatry Neurosci 19(5):359–367PubMedCentralPubMed Purdon SE, Mohr E, Ilivitsky V, Jones BD (1994) Huntington’s disease: pathogenesis, diagnosis and treatment. J Psychiatry Neurosci 19(5):359–367PubMedCentralPubMed
2.
go back to reference Martin JB, Gusella JF (1986) Huntington’s disease. Pathogenesis and management. N Engl J Med 315(20):1267–1276CrossRefPubMed Martin JB, Gusella JF (1986) Huntington’s disease. Pathogenesis and management. N Engl J Med 315(20):1267–1276CrossRefPubMed
3.
go back to reference The Huntington’s Disease Collaborative Research Group and The Hungtinton Study Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s disease collaborative research group. Cell 72(6):971–83 The Huntington’s Disease Collaborative Research Group and The Hungtinton Study Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s disease collaborative research group. Cell 72(6):971–83
4.
go back to reference Stout JC, Paulsen JS, Queller S, Solomon AC, Whitlock KB, Campbell JC et al (2011) Neurocognitive signs in prodromal Huntington disease. Neuropsychology 25(1):1–14PubMedCentralCrossRefPubMed Stout JC, Paulsen JS, Queller S, Solomon AC, Whitlock KB, Campbell JC et al (2011) Neurocognitive signs in prodromal Huntington disease. Neuropsychology 25(1):1–14PubMedCentralCrossRefPubMed
6.
go back to reference Blekher T, Johnson SA, Marshall J, White K, Hui S, Weaver M et al (2006) Saccades in presymptomatic and early stages of Huntington disease. Neurology 67(3):394–399CrossRefPubMed Blekher T, Johnson SA, Marshall J, White K, Hui S, Weaver M et al (2006) Saccades in presymptomatic and early stages of Huntington disease. Neurology 67(3):394–399CrossRefPubMed
7.
go back to reference Peltsch A, Hoffman A, Armstrong I, Pari G, Munoz DP (2008) Saccadic impairments in Huntington’s disease. Exp Brain Res 186(3):457–469CrossRefPubMed Peltsch A, Hoffman A, Armstrong I, Pari G, Munoz DP (2008) Saccadic impairments in Huntington’s disease. Exp Brain Res 186(3):457–469CrossRefPubMed
8.
go back to reference Lasker AG, Zee DS, Hain TC, Folstein SE, Singer HS (1988) Saccades in Huntington’s disease: slowing and dysmetria. Neurology 38(3):427–431CrossRefPubMed Lasker AG, Zee DS, Hain TC, Folstein SE, Singer HS (1988) Saccades in Huntington’s disease: slowing and dysmetria. Neurology 38(3):427–431CrossRefPubMed
9.
go back to reference Leigh RJ, Newman SA, Folstein SE, Lasker AG, Jensen BA (1983) Abnormal ocular motor control in Huntington’s disease. Neurology 33(10):1268–1275CrossRefPubMed Leigh RJ, Newman SA, Folstein SE, Lasker AG, Jensen BA (1983) Abnormal ocular motor control in Huntington’s disease. Neurology 33(10):1268–1275CrossRefPubMed
10.
go back to reference Anderson TJ, MacAskill MR (2013) Eye movements in patients with neurodegenerative disorders. Nat Rev Neurol 9(2):74–85CrossRefPubMed Anderson TJ, MacAskill MR (2013) Eye movements in patients with neurodegenerative disorders. Nat Rev Neurol 9(2):74–85CrossRefPubMed
11.
go back to reference Sakai RE, Feller DJ, Galetta KM, Galetta SL, Balcer LJ (2011) Vision in multiple sclerosis: the story, structure-function correlations, and models for neuroprotection. J Neuroophthalmol 31(4):362–373PubMedCentralCrossRefPubMed Sakai RE, Feller DJ, Galetta KM, Galetta SL, Balcer LJ (2011) Vision in multiple sclerosis: the story, structure-function correlations, and models for neuroprotection. J Neuroophthalmol 31(4):362–373PubMedCentralCrossRefPubMed
12.
go back to reference Huang D, Swanson EA, Lin CP, Schuman JS, Stinson WG, Chang W et al (1991) Optical coherence tomography. Science 254(5035):1178–1181CrossRefPubMed Huang D, Swanson EA, Lin CP, Schuman JS, Stinson WG, Chang W et al (1991) Optical coherence tomography. Science 254(5035):1178–1181CrossRefPubMed
13.
go back to reference Wojtkowski M, Srinivasan VJ, Ko TH, Fujimoto JG, Kowalczyk A, Duker JS (2004) Ultrahigh-resolution, high-speed, Fourier domain optical coherence tomography and methods for dispersion compensation. Opt Express 12(11):2404–2422CrossRefPubMed Wojtkowski M, Srinivasan VJ, Ko TH, Fujimoto JG, Kowalczyk A, Duker JS (2004) Ultrahigh-resolution, high-speed, Fourier domain optical coherence tomography and methods for dispersion compensation. Opt Express 12(11):2404–2422CrossRefPubMed
14.
go back to reference 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(2):137–146CrossRefPubMed 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(2):137–146CrossRefPubMed
15.
go back to reference Fisher JB, Jacobs DA, Markowitz CE, Galetta SL, Volpe NJ, Nano-Schiavi ML et al (2006) Relation of visual function to retinal nerve fiber layer thickness in multiple sclerosis. Ophthalmology 113(2):324–332CrossRefPubMed Fisher JB, Jacobs DA, Markowitz CE, Galetta SL, Volpe NJ, Nano-Schiavi ML et al (2006) Relation of visual function to retinal nerve fiber layer thickness in multiple sclerosis. Ophthalmology 113(2):324–332CrossRefPubMed
16.
go back to reference Gordon-Lipkin E, Chodkowski B, Reich DS, Smith SA, Pulicken M, Balcer LJ et al (2007) Retinal nerve fiber layer is associated with brain atrophy in multiple sclerosis. Neurology 69(16):1603–1609CrossRefPubMed Gordon-Lipkin E, Chodkowski B, Reich DS, Smith SA, Pulicken M, Balcer LJ et al (2007) Retinal nerve fiber layer is associated with brain atrophy in multiple sclerosis. Neurology 69(16):1603–1609CrossRefPubMed
17.
18.
go back to reference Iseri PK, Altinas O, Tokay T, Yuksel N (2006) Relationship between cognitive impairment and retinal morphological and visual functional abnormalities in Alzheimer disease. J Neuroophthalmol 26(1):18–24CrossRefPubMed Iseri PK, Altinas O, Tokay T, Yuksel N (2006) Relationship between cognitive impairment and retinal morphological and visual functional abnormalities in Alzheimer disease. J Neuroophthalmol 26(1):18–24CrossRefPubMed
19.
go back to reference Klistorner A, Garrick R, Barnett MH, Graham SL, Arvind H, Sriram P et al (2013) Axonal loss in nonoptic neuritis eyes of patients with multiple sclerosis linked to delayed visual evoked potential. Neurology 80(3):242–245CrossRefPubMed Klistorner A, Garrick R, Barnett MH, Graham SL, Arvind H, Sriram P et al (2013) Axonal loss in nonoptic neuritis eyes of patients with multiple sclerosis linked to delayed visual evoked potential. Neurology 80(3):242–245CrossRefPubMed
20.
go back to reference Lange AP, Sadjadi R, Zhu F, Alkabie S, Costello F, Traboulsee AL (2013) Spectral-domain optical coherence tomography of retinal nerve fiber layer thickness in NMO patients. J Neuroophthalmol 33(3):213–219CrossRefPubMed Lange AP, Sadjadi R, Zhu F, Alkabie S, Costello F, Traboulsee AL (2013) Spectral-domain optical coherence tomography of retinal nerve fiber layer thickness in NMO patients. J Neuroophthalmol 33(3):213–219CrossRefPubMed
21.
go back to reference Llufriu S, Sepulveda M, Blanco Y, Marin P, Moreno B, Berenguer J et al (2014) Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis. Plos One 9(12):e113936PubMedCentralCrossRefPubMed Llufriu S, Sepulveda M, Blanco Y, Marin P, Moreno B, Berenguer J et al (2014) Randomized placebo-controlled phase II trial of autologous mesenchymal stem cells in multiple sclerosis. Plos One 9(12):e113936PubMedCentralCrossRefPubMed
22.
go back to reference Merle H, Olindo S, Donnio A, Richer R, Smadja D, Cabre P (2008) Retinal peripapillary nerve fiber layer thickness in neuromyelitis optica. Invest Ophthalmol Vis Sci 49(10):4412–4417CrossRefPubMed Merle H, Olindo S, Donnio A, Richer R, Smadja D, Cabre P (2008) Retinal peripapillary nerve fiber layer thickness in neuromyelitis optica. Invest Ophthalmol Vis Sci 49(10):4412–4417CrossRefPubMed
23.
go back to reference Polo V, Garcia-Martin E, Bambo MP, Pinilla J, Larrosa JM, Satue M et al (2014) Reliability and validity of Cirrus and Spectralis optical coherence tomography for detecting retinal atrophy in Alzheimer’s disease. Eye (Basingstoke) 28(6):680–690 Polo V, Garcia-Martin E, Bambo MP, Pinilla J, Larrosa JM, Satue M et al (2014) Reliability and validity of Cirrus and Spectralis optical coherence tomography for detecting retinal atrophy in Alzheimer’s disease. Eye (Basingstoke) 28(6):680–690
24.
go back to reference Satue M, Garcia-Martin E, Fuertes I, Otin S, Alarcia R, Herrero R et al (2013) Use of Fourier-domain OCT to detect retinal nerve fiber layer degeneration in Parkinson’s disease patients. Eye 27(4):507–514PubMedCentralCrossRefPubMed Satue M, Garcia-Martin E, Fuertes I, Otin S, Alarcia R, Herrero R et al (2013) Use of Fourier-domain OCT to detect retinal nerve fiber layer degeneration in Parkinson’s disease patients. Eye 27(4):507–514PubMedCentralCrossRefPubMed
25.
go back to reference Galetta KM, Calabresi PA, Frohman EM, Balcer LJ (2011) Optical coherence tomography (OCT): imaging the visual pathway as a model for neurodegeneration. Neurotherapeutics 8(1):117–132PubMedCentralCrossRefPubMed Galetta KM, Calabresi PA, Frohman EM, Balcer LJ (2011) Optical coherence tomography (OCT): imaging the visual pathway as a model for neurodegeneration. Neurotherapeutics 8(1):117–132PubMedCentralCrossRefPubMed
26.
go back to reference Reilmann R, Bohlen S, Kirsten F, Ringelstein EB, Lange HW (2011) Assessment of involuntary choreatic movements in Huntington’s disease–toward objective and quantitative measures. Mov Disord 26(12):2267–2273CrossRefPubMed Reilmann R, Bohlen S, Kirsten F, Ringelstein EB, Lange HW (2011) Assessment of involuntary choreatic movements in Huntington’s disease–toward objective and quantitative measures. Mov Disord 26(12):2267–2273CrossRefPubMed
27.
go back to reference Penney JB Jr, Vonsattel JP, MacDonald ME, Gusella JF, Myers RH (1997) CAG repeat number governs the development rate of pathology in Huntington’s disease. Ann Neurol 41(5):689–692CrossRefPubMed Penney JB Jr, Vonsattel JP, MacDonald ME, Gusella JF, Myers RH (1997) CAG repeat number governs the development rate of pathology in Huntington’s disease. Ann Neurol 41(5):689–692CrossRefPubMed
28.
go back to reference Kersten HM, Roxburgh RH, Danesh-Meyer HV (2014) Ophthalmic manifestations of inherited neurodegenerative disorders. Nat Rev Neurol 10(6):349–362CrossRefPubMed Kersten HM, Roxburgh RH, Danesh-Meyer HV (2014) Ophthalmic manifestations of inherited neurodegenerative disorders. Nat Rev Neurol 10(6):349–362CrossRefPubMed
29.
go back to reference Fortuna F, Barboni P, Liguori R, Valentino ML, Savini G, Gellera C et al (2009) Visual system involvement in patients with Friedreich’s ataxia. Brain 132(Pt 1):116–123PubMed Fortuna F, Barboni P, Liguori R, Valentino ML, Savini G, Gellera C et al (2009) Visual system involvement in patients with Friedreich’s ataxia. Brain 132(Pt 1):116–123PubMed
30.
go back to reference Sitarz KS, Chinnery PF, Yu-Wai-Man P (2012) Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets. Curr Neurol Neurosci Rep 12(3):308–317PubMedCentralCrossRefPubMed Sitarz KS, Chinnery PF, Yu-Wai-Man P (2012) Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets. Curr Neurol Neurosci Rep 12(3):308–317PubMedCentralCrossRefPubMed
31.
go back to reference Barboni P, Savini G, Valentino ML, Montagna P, Cortelli P, De Negri AM et al (2005) Retinal nerve fiber layer evaluation by optical coherence tomography in Leber’s hereditary optic neuropathy. Ophthalmology 112(1):120–126CrossRefPubMed Barboni P, Savini G, Valentino ML, Montagna P, Cortelli P, De Negri AM et al (2005) Retinal nerve fiber layer evaluation by optical coherence tomography in Leber’s hereditary optic neuropathy. Ophthalmology 112(1):120–126CrossRefPubMed
32.
go back to reference Klebe S, Depienne C, Gerber S, Challe G, Anheim M, Charles P et al (2012) Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy. Brain 135(Pt 10):2980–2993PubMedCentralCrossRefPubMed Klebe S, Depienne C, Gerber S, Challe G, Anheim M, Charles P et al (2012) Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy. Brain 135(Pt 10):2980–2993PubMedCentralCrossRefPubMed
34.
go back to reference Sadun AA, Win PH, Ross-Cisneros FN, Walker SO, Carelli V (2000) Leber’s hereditary optic neuropathy differentially affects smaller axons in the optic nerve. Trans Am Ophthalmol Soc 98:223–232PubMedCentralPubMed Sadun AA, Win PH, Ross-Cisneros FN, Walker SO, Carelli V (2000) Leber’s hereditary optic neuropathy differentially affects smaller axons in the optic nerve. Trans Am Ophthalmol Soc 98:223–232PubMedCentralPubMed
35.
go back to reference Zuccato C, Valenza M, Cattaneo E (2010) Molecular mechanisms and potential therapeutical targets in Huntington’s disease. Physiol Rev 90(3):905–981CrossRefPubMed Zuccato C, Valenza M, Cattaneo E (2010) Molecular mechanisms and potential therapeutical targets in Huntington’s disease. Physiol Rev 90(3):905–981CrossRefPubMed
36.
go back to reference Shirendeb U, Reddy AP, Manczak M, Calkins MJ, Mao P, Tagle DA et al (2011) Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington’s disease: implications for selective neuronal damage. Hum Mol Genet 20(7):1438–1455PubMedCentralCrossRefPubMed Shirendeb U, Reddy AP, Manczak M, Calkins MJ, Mao P, Tagle DA et al (2011) Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington’s disease: implications for selective neuronal damage. Hum Mol Genet 20(7):1438–1455PubMedCentralCrossRefPubMed
37.
go back to reference Orr AL, Li S, Wang CE, Li H, Wang J, Rong J et al (2008) N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking. J Neurosci 28(11):2783–2792PubMedCentralCrossRefPubMed Orr AL, Li S, Wang CE, Li H, Wang J, Rong J et al (2008) N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking. J Neurosci 28(11):2783–2792PubMedCentralCrossRefPubMed
39.
go back to reference Helmlinger D, Yvert G, Picaud S, Merienne K, Sahel J, Mandel J-L et al (2002) Progressive retinal degeneration and dysfunction in R6 Huntington’s disease mice. Hum Mol Genet 11(26):3351–3359CrossRefPubMed Helmlinger D, Yvert G, Picaud S, Merienne K, Sahel J, Mandel J-L et al (2002) Progressive retinal degeneration and dysfunction in R6 Huntington’s disease mice. Hum Mol Genet 11(26):3351–3359CrossRefPubMed
40.
go back to reference Paulus W, Schwarz G, Werner A, Lange H, Bayer A, Hofschuster M et al (1993) Impairment of retinal increment thresholds in Huntington’s disease. Ann Neurol 34(4):574–578CrossRefPubMed Paulus W, Schwarz G, Werner A, Lange H, Bayer A, Hofschuster M et al (1993) Impairment of retinal increment thresholds in Huntington’s disease. Ann Neurol 34(4):574–578CrossRefPubMed
41.
go back to reference Petrasch-Parwez E, Saft C, Schlichting A, Andrich J, Napirei M, Arning L et al (2005) Is the retina affected in Huntington disease? Acta Neuropathol 110(5):523–525CrossRefPubMed Petrasch-Parwez E, Saft C, Schlichting A, Andrich J, Napirei M, Arning L et al (2005) Is the retina affected in Huntington disease? Acta Neuropathol 110(5):523–525CrossRefPubMed
42.
go back to reference Petrasch-Parwez E, Habbes H-W, Weickert S, Lobbecke-Schumacher M, Striedinger K, Wieczorek S et al (2004) Fine-structural analysis and connexin expression in the retina of a transgenic model of Huntington’s disease. J Comp Neurol 479(2):181–197CrossRefPubMed Petrasch-Parwez E, Habbes H-W, Weickert S, Lobbecke-Schumacher M, Striedinger K, Wieczorek S et al (2004) Fine-structural analysis and connexin expression in the retina of a transgenic model of Huntington’s disease. J Comp Neurol 479(2):181–197CrossRefPubMed
43.
go back to reference Batcha AH, Greferath U, Jobling AI, Vessey KA, Ward MM, Nithianantharajah J et al (2012) Retinal dysfunction, photoreceptor protein dysregulation and neuronal remodelling in the R6/1 mouse model of Huntington’s disease. Neurobiol Dis 45(3):887–896CrossRefPubMed Batcha AH, Greferath U, Jobling AI, Vessey KA, Ward MM, Nithianantharajah J et al (2012) Retinal dysfunction, photoreceptor protein dysregulation and neuronal remodelling in the R6/1 mouse model of Huntington’s disease. Neurobiol Dis 45(3):887–896CrossRefPubMed
44.
go back to reference Li M, Yasumura D, Ma AAK, Matthes MT, Yang H, Nielson G et al (2013) Intravitreal administration of HA-1077, a ROCK inhibitor, improves retinal function in a mouse model of huntington disease. Plos One 8(2):e56026PubMedCentralCrossRefPubMed Li M, Yasumura D, Ma AAK, Matthes MT, Yang H, Nielson G et al (2013) Intravitreal administration of HA-1077, a ROCK inhibitor, improves retinal function in a mouse model of huntington disease. Plos One 8(2):e56026PubMedCentralCrossRefPubMed
45.
go back to reference Ragauskas S, Leinonen H, Puranen J, Ronkko S, Nymark S, Gurevicius K et al (2014) Early retinal function deficit without prominent morphological changes in the R6/2 mouse model of Huntington’s disease. Plos One 9(12):e113317PubMedCentralCrossRefPubMed Ragauskas S, Leinonen H, Puranen J, Ronkko S, Nymark S, Gurevicius K et al (2014) Early retinal function deficit without prominent morphological changes in the R6/2 mouse model of Huntington’s disease. Plos One 9(12):e113317PubMedCentralCrossRefPubMed
46.
go back to reference Mizuno K, Asaoka M (1976) Cycloscopy and fluorescein cycloscopy. Investig Ophthalmol 15(7):561–564 Mizuno K, Asaoka M (1976) Cycloscopy and fluorescein cycloscopy. Investig Ophthalmol 15(7):561–564
47.
go back to reference Dorsey ER, Beck CA, Darwin K, Nichols P, Brocht AFD, Biglan KM et al (2013) Natural history of Huntington disease. JAMA Neurol 70(12):1520–1530PubMed Dorsey ER, Beck CA, Darwin K, Nichols P, Brocht AFD, Biglan KM et al (2013) Natural history of Huntington disease. JAMA Neurol 70(12):1520–1530PubMed
48.
go back to reference The Huntington’s Disease Collaborative Research Group and The Hungtinton Study Group (1996) Unified Huntington’s disease rating scale: reliability and consistency. Huntington Study Group. Mov Disord 11(2):136–42 The Huntington’s Disease Collaborative Research Group and The Hungtinton Study Group (1996) Unified Huntington’s disease rating scale: reliability and consistency. Huntington Study Group. Mov Disord 11(2):136–42
49.
go back to reference Stroet A, Linker RA, Gold R (2013) Advancing therapeutic options in multiple sclerosis with neuroprotective properties. J Neural Transm 120(Suppl 1):S49–S53CrossRefPubMed Stroet A, Linker RA, Gold R (2013) Advancing therapeutic options in multiple sclerosis with neuroprotective properties. J Neural Transm 120(Suppl 1):S49–S53CrossRefPubMed
Metadata
Title
Optical coherence tomography findings in Huntington’s disease: a potential biomarker of disease progression
Authors
Hannah M. Kersten
Helen V. Danesh-Meyer
Dean H. Kilfoyle
Richard H. Roxburgh
Publication date
01-11-2015
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 11/2015
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-015-7869-2

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