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147

Table 1. Spectral domain OCT systems commercially availables

 

 

 

 

 

 

Company

Name of device

Acquisition speed (A-scans/s)

Axial resolution (mm)

 

 

 

 

Bioptigen

3D SDOCT

20,000

B6

Carl Zeiss Meditec

Cirrus

27,000

B5

Heidelberg

Spectralis

40,000

B7

OTI

Spectral OCT/SLO

27,000

5–6

Optovue

RTVue-100

26,000

B5

Optopol

Copernicus

25,000

B6

Topcon

3D OCT 1000

20,000

5

 

 

 

 

Abbreviations

 

CSLO

confocal scanning laser ophthalmo-

 

scopy

OCT

optical coherence tomography

ONH

optic nerve head

ONHP

optic nerve head photographs

RNFL

retinal nerve fibers layer

SDOCT

spectral domain OCT

SLP

scanning laser polarimetry

UHR

ultra-high resolution

References

Airaksinen, P.J. and Drance, S.M. (1985) Neuroretinal rim area and retinal nerve fiber layer in glaucoma. Arch. Ophthalmol., 103: 203–204.

Airaksinen, P.J., Drance, S.M., Douglas, G.R., Mawson, D.K. and Nieminen, H. (1985) Diffuse and localized nerve fiber loss in glaucoma. Am. J. Ophthalmol., 98(5): 566–571.

Aydin, A., Wollstein, G., Price, L.L., Fujimoto, J.G. and Schuman, J.S. (2003) Optical coherence tomography assessment of retinal nerve fiber layer thickness changes after glaucoma surgery. Ophthalmology, 110(8): 1506–1511.

Balazsi, A.G., Drance, S.M., Schulzer, M. and Douglas, G.R. (1984) Neuroretinal rim area in suspected glaucoma and early chronic open angle glaucoma. Arch. Ophthalmol., 102(7): 1011–1014.

Bowd, C., Zangwill, L.M., Berry, C.C., Blumenthal, E.Z., Vasile, C., Sanchez-Galeana, C.A., Bosworth, C.F., Sample, P.A. and Weinreb, E.N. (2001) Detecting early glaucoma by assessment of retinal nerve fiber layer thickness and visual function. Invest. Ophthalmol. Vis. Sci., 42(9): 1993–2003.

Bowd, C., Zangwill, L.M., Blumenthal, E.Z., Vasile, C., Boehm, A.G., Gokhale, P.A., Mohammadi, K., Amini, P., Sankary, T.M. and Weinreb, R.N. (2002) Imaging of the optic disc and retinal nerve fiber layer: the effects of age, optic

disc area, refractive error, and gender. J. Opt. Soc. Am. A Opt. Image Sci. Vis., 19(1): 197–207.

Budenz, D.L., Michael, A., Chang, R.T., Chang, R.T., McSoley, J. and Katz, J. (2005) Sensitivity and specificity of the stratus OCT for perimetric glaucoma. Ophthalmology, 112: 3–9.

Caprioli, J. and Miller, J.M. (1990) Measurement of relative nerve fiber layer surface height in glaucoma. Ophthalmology, 97: 358–365.

Drexel, W., Morgner, U., Ghanta, R.K., Schuman, J.S., Kartbner, F.X. and Fujimoto, J.G. (2001) Ultrahigh resolution ophthalmological optical coherence tomography. Nat. Med., 7: 502–507.

Fujimoto, J.G., Huang, D., Hee, M.R., Ko, T., Swanson, E., Puliafito, C.A. and Schuman, J.S. (2004) Physical principles of optical coherence tomography. In: Schuman, J.S., Puliafito, C.A. and Fujimoto J.G. (Eds.), Optical coherence tomography of ocular diseases, 2nd ed., Appendix A. Slack Inc., Thorofare, NJ, pp. 677–688.

Greaney, M.J., Hoffman, D.C., Garway-Heath, D.F., Nakla, M., Coleman, A.L. and Caprioli, J. (2002) Comparison of optic nerve imaging methods to distinguish normal eyes from those with glaucoma. Invest. Ophthalmol. Vis. Sci., 43: 140–145.

Guedes, V., Schuman, J.S., Hertzmark, E., Wollstein, G., Correnti, A., Mancini, R., Lederer, D., Voskanian, S., Velasquez, L., Pakter, H.M., Pedut-Kloizman, T., Fujimoto, J.G. and Mattox, C. (2003) Optical coherence tomography measurement of macular and nerve fiber layer thickness in normal and glaucomatous human eyes. Ophthalmology, 110(1): 177–189.

Hougaard, J.L., Heijl, A. and Bengtsson, B. (2007) Glaucoma detection by Stratus OCT. J. Glaucoma, 16(3): 302–306.

Hoyt, W.F., Frisen, L. and Newman, N.M. (1973) Funduscopy of nerve fiber layer defects in glaucoma. Invest. Ophthalmol. Vis. Sci., 12: 814–829.

Hoyt, W.F. and Newmann, N.M. (1972) The earliest observable defects in glaucoma. Lancet, 1: 692–693.

Johnson, Z.K., Rehman Siddiqui, M.A. and Azuara-Blanco, A. (2007) The quality of reporting of diagnostic accuracy studies of optical coherence tomography in glaucoma. Ophthalmology, 114: 1607–1612.

148

Mikelberg, F.S., Yidegiligne, H.M. and Shulzer, M. (1995) Optic nerve axon count and axon diameter in patient with ocular hypertension and normal visual field. Ophthalmology, 102: 342–348.

Nouri-Madhavi, K., Hoffman, D.C., Tannenbaum, D.P., Law, S.K. and Caprioli, J. (2004) Identifying early glaucoma with optical coherence tomography. Am. J. Ophthalmol., 37: 228–235.

Parikh, R.S., Parikh, S., Sekhar, G.C., Kumar, R.S., Prabakaran, S., Babu, J.G. and Thomas, R. (2007) Diagnostic capability of optical coherence tomography (Stratus OCT 3) in early glaucoma. Ophthalmology, 114: 2238–2243.

Pieroth, L., Schuman, J.S., Hertzmark, E., Hee, M.R., Wilkins, J.R., Coker, J., Mattox, C., Pedut-Kloizman, T., Puliafito, C.A., Fujimoto, J.G. and Swanso, E. (1998) Evaluation of focal defects of the nerve fiber layer using optical coherence tomography. Ophthalmology, 106: 570–579.

Podoleanu, A.G., Dobre, G.M., Webb, D.J. and Jackson, D.A. (1997) Simultaneous en-face imaging for two layers in the human retina by low coherence interferometry. Opt. Lett., 22(13): 1039–1041.

Quigley, H.A. (1999) Neuronal death in glaucoma. Prog. Retin. Eye Res., 18: 39–57.

Quigley, H.A., Adicks, E.M. and Green, R. (1982) Optic nerve damage in human glaucoma. III: Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema and toxic neuropathy. Arch. Ophthalmol., 100: 135–146.

Quigley, H.A., Davis, E.B. and Anderson, E.R. (1977) Descending optic nerve degeneration in primates. Invest. Ophthalmol. Vis. Sci., 16: 841–849.

Radius, R.L. and Anderson, D.R. (1979) The histology of the retinal nerve fiber layer bundles and bundle defects. Arch. Ophthalmol., 97: 948–951.

Schuman, J.S., Hee, M.R., Puliafito, C.A., Wong, C., PedutKloizman, T., Lin, C.P., Hertzmark, E., Izatt, J.A., Swanson, E.A. and Fujimoto, J.G. (1995) Quantification of nerve fiber layer thickness in normal and glaucomatous eyes using optical coherence tomography. Arch. Ophthalmol., 113: 586–596.

Schuman, J.S., Pedut-Kloizman, T., Hertzmark, E., Hee, M.R., Wilkins, J.R., Coker, J.G., Puliafito, C.A., Fujimoto, J.G. and Swanson, E.A. (1996) Reproducibility of nerve fiber layer thickness measurements using optical coherence tomography. Ophthalmology, 103: 1889–1898.

Schuman, J.S., Wollstein, G., Farra, T., Hertzmark, E., Aydin, A., Fujimoto, J.G. and Paunescu, L.A. (2003) Comparison of optic nerve head measurements obtained by optical coherence tomography and confocal scanning laser ophthalmoscopy. Am. J. Ophthalmol., 135(4): 504–512.

Smith, M., Frost, A., Graham, C.M. and Shaw, S. (2007) Effect of pupillary dilatation on glaucoma assessments using optical coherence tomography. Br. J. Ophthalmol., 91: 1686–1690.

Soliman, M.A.E., Van den Berg, T.J.T.P., Ismaeil, A.A., De Jong, L.A.M.S. and De Smet, M.D. (2002) Retinal nerve fiber layer analysis: relationship between optical coherence tomography and red-free photography. Am. J. Ophthalmol., 133: 187–195.

Sommer, A., Katz, J., Quigley, H.A., Miller, N.R., Robin, A.L., Richter, R.C. and Witt, K.A. (1991) Clinically detectable nerve fiber atrophy precedes the onset of glaucomatous field loss. Arch. Ophthalmol., 109: 77–83.

Sommer, A., Quigley, H.A., Robin, A.L., Miller, N.R., Katz, J. and Arkell, S. (1984) Evaluation of nerve fiber layer assessment. Arch. Ophthalmol., 102(12): 1766–1771.

Varma, R., Skaf, M. and Barron, E. (1996) Retinal nerve fiber layer thickness in normal human eyes. Ophthalmology, 103: 2114–2119.

Vogt, A. (1913) Herstellung eines gelbblauen Lichtfiltrates, in welchem die macula centralis in vivo in gelber Farbung erscheint, die nervenfasern der netzhaut und andere feine einzelhelten derselben sichtbar warden und der grad der gelbfarbung der lines ophthalmoskopisch nachweisbar ist. Arch. Ophthalmol., 84: 293–311.

Williams, Z.Y., Schuman, J.S., Gamell, L., Nemi, A., Hertzmark, E., Fujimoto, J.G., Mattox, C., Simpson, J. and Wollstein, G. (2002) Optical coherence tomography measurement of nerve fiber layer thickness and the likelihood of a visual field defect. Am. J. Ophthalmol., 134(4): 538–546.

Wojtkoswki, M., Leitgeb, R., Kowalczyk, A., Bajraszewski, T. and Fercher, A.F. (2002) In vivo human retinal imaging by Fourier domain optical coherence tomography. J. Biomed. Opt., 7(3): 457–463.

Zangwill, L.M., Bowd, C., Berry, C.C., Williams, J., Blumenthal, E.Z., Sanchez-Galeana, C.A., Vasile, C. and Weinreb, E.N. (2001) Discriminating between normal and glaucomatous eyes using the Heidelberg retina tomograph, GDx nerve fiber analyzer, and optical coherence tomography. Arch. Ophthalmol., 119(7): 985–993.

C. Nucci et al. (Eds.)

Progress in Brain Research, Vol. 173

ISSN 0079-6123

Copyright r 2008 Elsevier B.V. All rights reserved

CHAPTER 11

Functional laser Doppler flowmetry of the optic nerve: physiological aspects and clinical applications

Charles E. Riva1 and Benedetto Falsini2,

1Dipartimento di Discipline Chirurgiche, Rianomatorie e dei Trapianti ‘‘Antonio Valsalva’’, Universita´ di Bologna, Bologna, Italy

2Istituto di Oftalmologia, Universita’ Cattolica del S. Cuore, Roma, Italy

Abstract: The present paper reviews the methodology and clinical results of recording, by laser Doppler flowmetry, the hemodynamic response of the optic nerve head elicited by visual stimulation. The basic mechanism underlying this novel technique (which is called here functional laser Doppler flowmetry (FLDF)) is the coupling between visually evoked neural activity and vascular activity within the neural tissue of the optic nerve (neurovascular coupling). The blood flow responses elicited by various visual stimuli (luminance and chromatic flicker, focal and pattern stimulation) have been characterized in humans by FLDF. These responses are similar to those assessed by electrophysiological methods (flicker and pattern electroretinography) evoked by the same stimuli. In addition, a significant correlation has been demonstrated between the hemodynamic responses and the neural activity induced electrical signals arising from the inner retina, providing evidence in support of the presence of a neurovascular coupling in humans. The application of FLDF in patients with ocular hypertension and early glaucoma demonstrates that the visually evoked hyperemic responses are significantly depressed even when neural retinal activity may be still relatively preserved, suggesting that abnormal optic nerve head autoregulation in response to visual stimuli may be altered early in the disease process. FLDF may open new avenues of investigation in the field of glaucoma and other neuro-ophthalmic disorders, providing new pathophysiological data and outcome measures for potential neuro-protective treatments.

Keywords: functional hyperemia; glaucoma; laser Doppler flowmetry; neural activity; optic nerve; ERG; neurovascular coupling

Introduction

Recent experimental data in both animals and humans indicate that visual stimulation by uniform field flicker or pattern contrast reversal induces an increase in optic nerve head blood flow (Fonh)

Corresponding author. Tel.: +39 06 30156344; Fax: +39 06 3051274; Email: bfalsini@rm.unicatt.it

coupled with an increase of retinal neural activity (Riva et al., 1991, 1992, 2001, 2005). These flow and activity responses are symbolized here as

RFonh and RA. In cats, the coupling between RFonh and RA is particularly tight when Fonh is

measured by laser Doppler flowmetry (LDF) and RA is derived from the electrical signal generated by the ganglion cells (Riva and Buerk, 1998) or from the K+ ion concentration (Buerk et al., 1995), both measured at the surface of the optic nerve.

DOI: 10.1016/S0079-6123(08)01111-4

149