Neurotrophic keratitis

Neurotrophic keratitis
Other names: Neurotrophic keratopathy
a)Neurotrophic ulcer before treatment b) after 1 month of treatment with topical E-PRP
SpecialtyOphthalmology

Neurotrophic keratitis (NK) is a degenerative disease of the cornea caused by damage of the trigeminal nerve,[1] which results in impairment of corneal sensitivity, spontaneous corneal epithelium breakdown, poor corneal healing and development of corneal ulceration, melting and perforation.[2] This is because, in addition to the primary sensory role, the nerve also plays a role maintaining the integrity of the cornea by supplying it with trophic factors and regulating tissue metabolism.[3]

Neurotrophic keratitis is classified as a rare disease, with an estimated prevalence of less than 5 in 10,000 people in Europe. It has been recorded that on average, 6% of herpetic keratitis cases may evolve to this disease, with a peak of 12.8% of cases of keratitis due to varicella zoster virus.[4]

The diagnosis, and particularly the treatment of neurotrophic keratitis are the most complex and challenging aspects of this disease, as a satisfactory therapeutic approach is not yet available.[5]

Signs and symptoms

The clinical presentation of this condition is as follows:[6]

  • Blurred vision
  • Red eyes
  • Dry eye
  • Decreased clarity
  • Photophobia

Causes

The cornea lacks blood vessels and is among the most densely innervated structures of the human body. Corneal nerves are responsible for maintaining the anatomical and functional integrity of the cornea, conveying tactile, temperature and pain sensations, playing a role in the blink reflex, in wound healing and in the production and secretion of tears.[7]

Most corneal nerve fibres are sensory in origin and are derived from the ophthalmic branch of the trigeminal nerve.[8] Congenital or acquired ocular and systemic diseases[9] can determine a lesion at different levels of the trigeminal nerve, which can lead to a reduction (hypoesthesia) or loss (anesthesia) of sensitivity of the cornea.[10] The most common causes of loss of corneal sensitivity are viral infections (herpes simplex[11] and herpes zoster ophthalmicus),[12] chemical burns, physical injuries, corneal surgery, neurosurgery,[13] chronic use of topical medications, or chronic use of contact lenses.[14]

Possible causes also include systemic diseases such as diabetes mellitus,[15] multiple sclerosis or leprosy.

Other, albeit less frequent, potential causes of the disease are: intracranial space-occupying lesions such as neuroma, meningioma and aneurysms, which may compress the trigeminal nerve and reduce corneal sensitivity.[16]

Conversely, congenital conditions that may lead to this disorder are very rare.[17]

Diagnosis

NK is diagnosed on the basis of the patient's medical history and a careful examination of the eye and surrounding area.

With regard to the patient's medical history, special attention should be paid to any herpes virus infections and possible surgeries on the cornea, trauma, abuse of anaesthetics or chronic topical treatments, chemical burns or, use of contact lenses.[18] It is also necessary to investigate the possible presence of diabetes[19] or other systemic diseases such as multiple sclerosis.

The clinical examination is usually performed through a series of assessments and tools:[20]

  • General examination of cranial nerves, to determine the presence of nerve damage.
  • Eye examinations:
  1. Complete eye examination: examination of the eyelids, blink rate, presence of inflammatory reactions and secretions, corneal epithelial alterations.
  2. Corneal sensitivity test: performed by placing a cotton wad or cotton thread in contact with the corneal surface: this only allows to determine whether corneal sensitivity is normal, reduced or absent; or using an esthesiometer that allows to assess corneal sensitivity.
  3. Tear film function test, such as Schirmer's test, and tear film break-up time.
  4. Fluorescein eye stain test, which shows any damage to the corneal and conjunctival epithelium

Classification

According to Mackie's classification, neurotrophic keratitis can be divided into three stages based on severity:

  1. Stage I: characterized by alterations of the corneal epithelium, which is dry and opaque, with superficial punctate keratopathy and corneal oedema. Long-lasting neurotrophic keratitis may also cause hyperplasia of the epithelium, stromal scarring and neovascularization of the cornea.
  2. Stage II: characterized by development of epithelial defects, often in the area near the centre of the cornea.
  3. Stage III: characterized by ulcers of the cornea accompanied by stromal oedema and/or melting that may result in corneal perforation.[21]

Treatment

Early diagnosis, targeted treatment according to the severity of the disease, and regular monitoring of patients with neurotrophic keratitis are critical to prevent damage progression and the occurrence of corneal ulcers, especially considering that the deterioration of the condition is often poorly symptomatic.[22]

The purpose of treatment is to prevent the progression of corneal damage and promote healing of the corneal epithelium. The treatment should always be personalized according to the severity of the disease. Conservative treatment is typically the best option.

In stage I, the least serious, treatment consists of the administration of preservative-free artificial tears several times a day in order to lubricate and protect the ocular surface, improving the quality of the epithelium and preventing the possible loss of transparency of the cornea.

In stage II, treatment should be aimed at preventing the development of corneal ulcers and promoting the healing of epithelial lesions. In addition to artificial tears, topical antibiotics may also be prescribed to prevent possible infections. Patients should be monitored very carefully since, being the disease poorly symptomatic, the corneal damage may progress without the patient noticing any worsening of the symptoms. Corneal contact lenses can also be used in this stage of the disease, for their protective action to improve corneal healing.[23]

In the most severe forms (stage III), it is necessary to stop the progression towards corneal perforation: in these cases, a possible surgical treatment option is tarsorrhaphy, i.e. the temporary or permanent closure of the eyelids by means of sutures or botulinum toxin injection. This protects the cornea, although the aesthetic result of these procedures may be difficult to accept for patients. Similarly, a procedure that entails the creation of a conjunctival flap has been shown to be effective in the treatment of chronic corneal ulcers with or without corneal perforation.[24]

In addition, another viable therapeutic option is amniotic membrane graft, which has recently been shown to play a role in stimulating corneal epithelium healing and in reducing vascularisation and inflammation of the ocular surface.[25] Other approaches used in severe forms include the administration of autologous serum eye drops.[26]

Research studies have focused on developing novel treatments for neurotrophic keratitis, and several polypeptides, growth factors and neuromediators have been proposed.[27] Studies were conducted on topical treatment with Substance P and IGF-1 (insulin-like growth factor-1), demonstrating an effect on epithelial healing.[28] Nerve Growth Factor (NGF) play a role in the epithelial proliferation and differentiation and in the survival of corneal sensory nerves. Topical treatment with murine NGF showed to promote recovery of epithelial integrity and corneal sensitivity in NK patients.[29] Recently, a recombinant human nerve growth factor eye drop formulation has been developed for clinical use.[30]

Cenegermin, a recombinant form of human NGF, has recently been approved in Europe in an eye drop formulation for neurotrophic keratitis.[31] Cenegermin as an eye drop formulation for treatment of NK is approved by FDA in August 2018

See also

References

  1. ↑ Bonini S, Rama P, Olzi D, Lambiase A, Neurotrophic keratitis. Eye 17 (2003) 989-995
  2. ↑ Sacchetti M, Lambiase A, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  3. ↑ Sacchetti, M; Lambiase, A (2014). "Diagnosis and management of neurotrophic keratitis". Clinical Ophthalmology. 8: 571–579. doi:10.2147/OPTH.S45921. PMC 3964170. PMID 24672223.
  4. ↑ Sacchetti M, Lambiase A, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  5. ↑ Bonini S, Rama P, Olzi D, Lambiase A, Neurotrophic keratitis. Eye 17 (2003) 989-995.
  6. ↑ "Neurotrophic Keratitis". NORD (National Organization for Rare Disorders). Archived from the original on 19 April 2021. Retrieved 17 March 2022.
  7. ↑ B.S. Shaheen, M. Bakir, and S. Jain, Corneal nerves in health and disease. Surv Ophthalmol 59 (2014) 263-85.
  8. ↑ L. J. Muller et al., Corneal nerves: structure, contents and function. Experimental Eye Research, 76 (2003) 521-542.
  9. ↑ F. Semeraro, E. Forbice, V. Romano, M. Angi, M.R. Romano, M. E. Filippelli, R. Di Iorio, and C. Costagliola, Neurotrophic keratitis. Ophthalmologica 231 (2014) 191-7; L. J. Muller et al., Corneal nerves: structure, contents and function. Experimental Eye Research, 76(2003) 521-542.
  10. ↑ F. Semeraro, E. Forbice, V. Romano, M. Angi, M.R. Romano, M. E. Filippelli, R. Di Iorio, and C. Costagliola, Neurotrophic keratitis. Ophthalmologica 231 (2014) 191-7; L. J. Muller et al., Corneal nerves: structure, contents and function. Experimental Eye Research, 76(2003) 521-542.
  11. ↑ J. Gallar, T. M. Tervo, W. Neira, J. M. Holopainen, M. E. Lamberg, F. Minana, M. C. Acosta, and C. Belmonte, Selective changes in human corneal sensation associated with herpes simplex virus keratitis. Invest Ophthalmol Vis Sci 51 (2010) 4516-22.
  12. ↑ T. J. Liesegang, Corneal complications from herpes zoster ophthalmicus. Ophthalmology 92 (1985) 316-24.
  13. ↑ S. Bonini, P. Rama, D. Olzi, and A. Lambiase, Neurotrophic keratitis. Eye 17 (2003) 989-995.
  14. ↑ M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  15. ↑ R. A. Hyndiuk, E. L. Kazarian, R. O. Schultz, and S. Seideman, Neurotrophic corneal ulcers in diabetes mellitus. Arch Ophthalmol 95 (1977) 2193-6.
  16. ↑ S. Bonini, P. Rama, D. Olzi, and A. Lambiase, Neurotrophic keratitis. Eye 17 (2003) 989-995.
  17. ↑ D. John, M. Thomas, and P. Jacob, Neurotrophic keratitis and congenital insensitivity to pain with anhidrosis—a case report with 10-year follow-up. Cornea 30 (2011) 100-2.
  18. ↑ S. Bonini, P. Rama, D. Olzi, and A. Lambiase, Neurotrophic keratitis. Eye 17 (2003) 989-995.
  19. ↑ F. Semeraro, E. Forbice, V. Romano, M. Angi, M.R. Romano, M.E. Filippelli, R. Di Iorio, and C. Costagliola, Neurotrophic keratitis. Ophthalmologica 231 (2014) 191-7.
  20. ↑ M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  21. ↑ M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  22. ↑ M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  23. ↑ H. L. Gould, Treatment of neurotrophic keratitis with scleral contact lenses. Eye Ear Nose Throat Mon 46 (1967) 1406-14.
  24. ↑ M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  25. ↑ Turkoglu E, Celik E, and Alagoz G, A comparison of the efficacy of autologous serum eye drops with amniotic membrane transplantation in neurotrophic keratitis. Semin Ophthalmol 29 (2014) 119-26.
  26. ↑ Turkoglu E, Celik E, and Alagoz G, A comparison of the efficacy of autologous serum eye drops with amniotic membrane transplantation in neurotrophic keratitis. Semin Ophthalmol 29 (2014) 119-26.
  27. ↑ Mastropasqua L, Massaro-Giordano G, Nubile M, Sacchetti M, Understanding the Pathogenesis of Neurotrophic Keratitis: The Role of Corneal Nerves. J Cell Physiol. 2017 Apr; 232(4):717-724
  28. ↑ Yanai R, Nishida R, Chikama T, Morishige N, Yamada N, Sonoda KH, Potential New Modes of Treatment of Neurotrophic Keratopathy. Cornea 34 Suppl 11 (2015) S121-7
  29. ↑ Lambiase A, Rama P, Bonini S, Caprioglio G, Aloe L. Topical treatment with nerve growth factor for corneal neurotrophic ulcers. N Engl J Med. 1998;338(17):1174-80.
  30. ↑ Sacchetti M, Lambiase A, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
  31. ↑ Archived 2018-06-20 at the Wayback Machine European Medicines Agency, New medicine for rare eye disease
Classification
External resources
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.