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   Table of Contents      
Year : 2020  |  Volume : 68  |  Issue : 1  |  Page : 168-169

Commentary: Assessing the lamina cribrosa in idiopathic intracranial hypertension

Department of Ophthalmology and Neurology, University of Lexington, KY, USA

Date of Web Publication19-Dec-2019

Correspondence Address:
Dr. Padmaja Sudhakar
Department of Ophthalmology and Neurology, University of Kentucky, 740 S Limestone, Lexington, KY 40536
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijo.IJO_1435_19

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How to cite this article:
Sudhakar P. Commentary: Assessing the lamina cribrosa in idiopathic intracranial hypertension. Indian J Ophthalmol 2020;68:168-9

How to cite this URL:
Sudhakar P. Commentary: Assessing the lamina cribrosa in idiopathic intracranial hypertension. Indian J Ophthalmol [serial online] 2020 [cited 2020 Sep 20];68:168-9. Available from: http://www.ijo.in/text.asp?2020/68/1/168/273195

The lamina cribrosa (LC) is a connective tissue mesh in the scleral canal of the optic nerve head that contains retinal ganglion cell axons and retinal blood vessels.[1] LC forms a barrier between 2 pressure compartments in the eye: intraocular pressure (IOP) in the intraocular space and cerebrospinal fluid pressure in the intraorbital subarachnoid space. A pressure difference between the intraocular and intracranial compartments at the site of the LC is called the translaminar pressure. This has been hypothesized to play a pathophysiological role in several optic nerve head diseases including papilledema. A change in either IOP or intracranial pressure may affect the homeostasis of the optic nerve head. LC has been known to undergo morphologic changes in papilledema.

Idiopathic intracranial hypertension (IIH) is characterized by elevated intracranial pressure of unclear cause manifesting with papilledema. Symptoms include headache, pulsatile tinnitus, transient visual obscurations, and diplopia from sixth nerve palsy. The basic hypothesis in IIH has been that increased translaminar pressure difference is detrimental to the axons of the optic nerve producing a mechanical insult and a disturbed axoplasmic transport. This leads to axoplasmic stasis, causing optic disc edema, eventually resulting in axonal death and visual loss.[2]

High-resolution techniques to study the accurate thickness of LC are both limited and difficult in human beings. Spectral domain-optical coherence tomography (SD-OCT) has been used to image the optic nerve head in papilledema. But a disadvantage of conventional OCT technology is that as depth increases, the resolution decreases, thus, imaging of deeper structures such as LC becomes challenging.

Enhanced depth imaging (EDI)-OCT was first reported in 2008 by Spaide et al.[3] to address the limitations of conventional SD-OCT for imaging deep ocular structures and to improve the image quality of deeper structures of the posterior pole.[4],[5] This method involves placing the OCT apparatus close enough to the eye to create an inverted view of the fundus.[3],[4] This places the coherence gate at a deeper plane than its usual position in the vitreous and moves the position of peak sensitivity from near the posterior vitreous in conventional OCT to the inner sclera for EDI-OCT. Using EDI-OCT, it is possible to visualize structures 500–800 μm deeper than with conventional OCT.

Another imaging tool is the swept-source optic coherence tomography (SS-OCT), also known as high-penetration OCT, that can enhance the visualization of deep ocular structures like the LC.[6],[7] This uses longer wavelength light to study the deeper ocular structures.

There are not many studies that have used EDI-SD-OCT to study the LC in IIH. The present article is unique in that EDI-OCT was used to show several structural changes in LC from intracranial pressure alterations namely the depth, Bruch's membrane opening (BMO), and prelaminar tissue thickness. Undoubtedly their series is the largest in literature to elaborate on various morphologic changes of LC in IIH.[8]

Anterior displacement of the LC has been demonstrated using EDI-SD-OCT [9] and SS-OCT [7] in IIH compared with controls. Both studies suggest that increased intracranial pressure affecting the translaminar pressure creates anterior displacement of the LC. The present study has demonstrated 2 morphologic changes in support of this concept. The prelaminar tissue thickness measured as the area from the optic nerve head surface to the beginning of high reflectance of LC was found to be increased in IIH compared with controls. The anterior LC surface depth measured from the distance between the imaginary line passing through Bruch's membrane level and the anterior border of LC was shown to be reduced in IIH compared with controls. These features reflect the anterior displacement of the LC in IIH.

In contrast, EDI-OCT has shown posterior displacement of the LC in glaucoma.[9] The increased IOP compared with intracranial pressure affects the translaminar pressure causing the posterior displacement.

This study also demonstrated that BMO was significantly greater in IIH than the control group. Other studies using EDI-SD OCT have shown BMO was greater in papilledema patients with higher translaminar pressure difference. This reversed with reduction in that pressure.[10] Sibony et al. reported no statistically significant difference in BMO between the measurements before the treatment and after the treatment when the optic disc edema resolved, in their study of 23 IIH patients with optic disc edema.[11] However, the measurements were taken with SD-OCT, not with EDI-OCT.

No statistical difference was found in the LC thickness between IIH and healthy subjects in this study, just as demonstrated in another study using SS -OCT.[7] This favors the concept that translaminar pressure may play a more important role.

Overall this study implies that analysis of the morphologic changes of LC using EDI-OCT could be implemented as a valuable diagnostic and monitoring tool in intracranial hypertension.

  References Top

Wilczek M. The lamina cribrosa and its nature. Br J Ophthalmol 1947;31:551-65.  Back to cited text no. 1
Hedges TR. Papilledema: Its recognition and relation to increased intracranial pressure. Surv Ophthalmol 1975;19:201-23.  Back to cited text no. 2
Spaide RF, Koizumi H, Pozzoni MC. Enhanced depth imaging spectral-domain optical coherence tomography. Am J Ophthalmol 2008;146:496-500.  Back to cited text no. 3
Park SC, De Moraes CG, Teng CC, Tello C, Liebmann JM, Ritch R. Enhanced depth imaging optical coherence tomography of deep optic nerve complex structures in glaucoma. Ophthalmology 2012;119:3-9.  Back to cited text no. 4
Mrejen S, Spaide RF. Optical coherence tomography: Imaging of the choroid and beyond. Surv Ophthalmol 2013;58:387-429.  Back to cited text no. 5
Mansouri K, Nuyen B, N Weinreb R. Improved visualization of deep ocular structures in glaucoma using high penetration optical coherence tomography. Expert Rev Med Devices 2013;10:621-8.  Back to cited text no. 6
Pasaoglu I, Satana B, Altan C, Artunay O, Basarir B, Onmez FE, et al. Lamina cribrosa surface position in idiopathic intracranial hypertension with swept-source optical coherence tomography. Indian J Ophthalmol 2019;67:1085-8.  Back to cited text no. 7
[PUBMED]  [Full text]  
Tatar IT, Solmaz B, Erdem ZG, Pasaoglu I, Demircan A, Tülü Aygün B, et al. Morphological assessment of lamina cribrosa in idiopathic intracranial hypertension. Indian J Ophthalmol 202;68:164-7.  Back to cited text no. 8
Villarruel JM, Li XQ, Bach-Holm D, Hamann S. Anterior lamina cribrosa surface position in idiopathic intracranial hypertension and glaucoma. Eur J Ophthalmol 2017;27:55-61.  Back to cited text no. 9
García-Montesinos J, Munoz-Negrete FJ, de Juan V, Rebolleda G. Relationship between lamina cribrosa displacement and trans-laminar pressure difference in papilledema. Graefes Arch Clin Exp Ophthalmol 2017;255:1237-43.  Back to cited text no. 10
Sibony P, Kupersmith MJ, Honkanen R, Rohlf FJ, Torab-Parhiz A. Effects oflowering cerebrospinal fluid pressure on the shape of the peripapillary retina in intracranial hypertension. Invest Ophthalmol Vis Sci 2014;55:8223-31.  Back to cited text no. 11


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