Korean J Ophthalmol.  2019 Oct;33(5):406-413. 10.3341/kjo.2019.0022.

Evaluation of Metabolite Changes in the Occipital Cortex of Patients with Idiopathic Infantile Nystagmus or Bilateral Ametropic Amblyopia by Magnetic Resonance Spectroscopy

Affiliations
  • 1Department of Ophthalmology, Kiziltepe Private Ipekyolu Hospital, Mardin, Turkey.
  • 2Department of Ophthalmology, Haseki Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. ercanozy@hotmail.com
  • 3Department of Ophthalmology, Private Goznuru Eye Hospital, Gaziantep, Turkey.
  • 4Department of Ophthalmology, Baskent University, Izmir, Turkey.
  • 5Department of Ophthalmology, Ataturk State Hospital, Antalya, Turkey.

Abstract

PURPOSE
To evaluate the effects of idiopathic infantile nystagmus (IN) and bilateral ametropic amblyopia on metabolites in the occipital cortex by magnetic resonance spectroscopy.
METHODS
The children included in this prospective study were divided into three groups. Group 1 consisted of 11 patients with idiopathic IN, group 2 consisted of 10 patients with bilateral ametropic amblyopia and group 3 consisted of nine normal children. A single-voxel magnetic resonance spectroscopy examination was performed by placing a region of interest on the occipital cortex of each participant. N-acetyl aspartate (NAA), creatine (Cr) and choline (Cho) concentrations were measured in the occipital cortex. This was followed by calculating and comparing the NAA/Cr and Cho/Cr ratios between the three groups. The Kruskal-Wallis test, Mann-Whitney U-test, and chi-square test were used for statistical analysis.
RESULTS
There was no statistically significant difference in NAA/Cr ratios between patients with idiopathic IN and normal children, but there was a statistically significant difference between these groups when Cho/Cr ratios were compared; the ratio was higher in the idiopathic IN group. There were no statistically significant differences in NAA/Cr or Cho/Cr ratios between patients with bilateral ametropic amblyopia and normal children.
CONCLUSIONS
Our findings suggest that the neurochemical profile of the occipital cortex is partially affected by idiopathic IN, but not by bilateral ametropic amblyopia.

Keyword

Amblyopia; Choline; Creatine; Resonance; Spectrum

MeSH Terms

Amblyopia*
Aspartic Acid
Child
Choline
Creatine
Humans
Magnetic Resonance Spectroscopy*
Occipital Lobe*
Prospective Studies
Aspartic Acid
Choline
Creatine

Figure

  • Fig. 1 (A) Axial, (B) sagittal, and (C) coronal views of the area where the region of interest was placed. Written informed consents were obtained from the parents of each child for the publication of the images.

  • Fig. 2 A spectrum obtained from the occipital cortex of a patient with idiopathic infantile nystagmus. Cho = choline; Cr = creatine; NAA = N-acetyl aspartate; ppm = parts per million. Intensity *10-3 arbitrary unit= relative proton concentration.

  • Fig. 3 A spectrum obtained from the occipital cortex of a patient with bilateral ametropic amblyopia. Cho = choline; Cr = creatine; NAA = N-acetyl aspartate; ppm = parts per million. Intensity *10-3 arbitrary unit= relative proton concentration.

  • Fig. 4 The mean N-acetyl aspartate (NAA)/creatine (Cr) ratios of groups 1, 2, and 3. Group 1, patients with idiopathic infantile nystagmus; group 2, patients with bilateral ametropic amblyopia; group 3, normal children.

  • Fig. 5 The mean choline (Cho)/creatine (Cr) ratios of groups 1, 2, and 3. Group 1, patients with idiopathic infantile nystagmus; group 2, patients with bilateral ametropic amblyopia; group 3, normal children.


Reference

1. Papageorgiou E, McLean RJ, Gottlob I. Nystagmus in childhood. Pediatr Neonatol. 2014; 55:341–351.
Article
2. Penix K, Swanson MW, DeCarlo DK. Nystagmus in pediatric patients: interventions and patient-focused perspectives. Clin Ophthalmol. 2015; 9:1527–1536.
3. Khanna S, Dell’Osso LF. The diagnosis and treatment of infantile nystagmus syndrome (INS). ScientificWorldJournal. 2006; 6:1385–1397.
Article
4. Sarvananthan N, Surendran M, Roberts EO, et al. The prevalence of nystagmus: the Leicestershire nystagmus survey. Invest Ophthalmol Vis Sci. 2009; 50:5201–5206.
Article
5. Abadi RV. Mechanisms underlying nystagmus. J R Soc Med. 2002; 95:231–234.
Article
6. Magdalene D, Bhattacharjee H, Choudhury M, et al. Community outreach: an indicator for assessment of prevalence of amblyopia. Indian J Ophthalmol. 2018; 66:940–944.
Article
7. Joly O, Franko E. Neuroimaging of amblyopia and binocular vision: a review. Front Integr Neurosci. 2014; 8:62.
Article
8. Firat PG, Ozsoy E, Demirel S, et al. Evaluation of peripapillary retinal nerve fiber layer, macula and ganglion cell thickness in amblyopia using spectral optical coherence tomography. Int J Ophthalmol. 2013; 6:90–94.
9. Gujar SK, Maheshwari S, Bjorkman-Burtscher I, Sundgren PC. Magnetic resonance spectroscopy. J Neuroophthalmol. 2005; 25:217–226.
Article
10. Simmons ML, Frondoza CG, Coyle JT. Immunocytochemical localization of N-acetyl-aspartate with monoclonal antibodies. Neuroscience. 1991; 45:37–45.
Article
11. Block W, Traber F, Flacke S, et al. In-vivo proton MR-spectroscopy of the human brain: assessment of N-acetylaspartate (NAA) reduction as a marker for neurodegeneration. Amino Acids. 2002; 23:317–323.
Article
12. Demougeot C, Garnier P, Mossiat C, et al. N-Acetylaspartate, a marker of both cellular dysfunction and neuronal loss: its relevance to studies of acute brain injury. J Neurochem. 2001; 77:408–415.
Article
13. Boucard CC, Hoogduin JM, van der Grond J, Cornelissen FW. Occipital proton magnetic resonance spectroscopy (1H-MRS) reveals normal metabolite concentrations in retinal visual field defects. PLoS One. 2007; 2:e222.
Article
14. Chan YL, Yeung DK, Leung SF, Cao G. Proton magnetic resonance spectroscopy of late delayed radiation-induced injury of the brain. J Magn Reson Imaging. 1999; 10:130–137.
Article
15. Schuff N, Amend D, Ezekiel F, et al. Changes of hippocampal N-acetyl aspartate and volume in Alzheimer’s disease. A proton MR spectroscopic imaging and MRI study. Neurology. 1997; 49:1513–1521.
Article
16. Zhang Y, Chen X, Wen G, et al. Proton magnetic resonance spectroscopy ((1)H-MRS) reveals geniculocalcarine and striate area degeneration in primary glaucoma. PLoS One. 2013; 8:e73197.
Article
17. Weaver KE, Richards TL, Saenz M, et al. Neurochemical changes within human early blind occipital cortex. Neuroscience. 2013; 252:222–233.
Article
18. Ozsoy E, Doganay S, Dogan M, et al. Evaluation of metabolite changes in visual cortex in diabetic retinopathy by MR-spectroscopy. J Diabetes Complications. 2012; 26:241–245.
Article
19. Sahin I, Alkan A, Keskin L, et al. Evaluation of in vivo cerebral metabolism on proton magnetic resonance spectroscopy in patients with impaired glucose tolerance and type 2 diabetes mellitus. J Diabetes Complications. 2008; 22:254–260.
Article
20. Behar KL, den Hollander JA, Stromski ME, et al. High-resolution 1H nuclear magnetic resonance study of cerebral hypoxia in vivo. Proc Natl Acad Sci U S A. 1983; 80:4945–4948.
Article
21. Berkowitz BA, Bansal N, Wilson CA. Non-invasive measurement of steady-state vitreous lactate concentration. NMR Biomed. 1994; 7:263–268.
Article
22. Rucker JC, Biousse V, Mao H, et al. Detection of lactate in the human vitreous body using proton magnetic resonance spectroscopy. Arch Ophthalmol. 2003; 121:909–911.
Article
23. Zhao H, Huang XF, Zheng ZL, et al. Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus. BMJ Open. 2016; 6:e010649.
Article
24. Watkins RJ, Patil R, Goult BT, et al. A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus. Hum Mol Genet. 2013; 22:2105–2118.
Article
25. Barrett BT, Bradley A, McGraw PV. Understanding the neural basis of amblyopia. Neuroscientist. 2004; 10:106–117.
Article
26. Barrett BT, Bradley A, Candy TR. The relationship between anisometropia and amblyopia. Prog Retin Eye Res. 2013; 36:120–158.
Article
27. Mangia S, Kumar AF, Moheet AA, et al. Neurochemical profile of patients with type 1 diabetes measured by 1H-MRS at 4 T. J Cereb Blood Flow Metab. 2013; 33:754–759.
Article
28. Coullon GS, Emir UE, Fine I, et al. Neurochemical changes in the pericalcarine cortex in congenital blindness attributable to bilateral anophthalmia. J Neurophysiol. 2015; 114:1725–1733.
Article
29. Castillo M, Kwock L, Mukherji SK. Clinical applications of proton MR spectroscopy. AJNR Am J Neuroradiol. 1996; 17:1–15.
30. Maheshwari SR, Fatterpekar GM, Castillo M, Mukherji SK. Proton MR spectroscopy of the brain. Semin Ultrasound CT MR. 2000; 21:434–451.
Article
31. Hufner K, Stephan T, Flanagin VL, et al. Cerebellar and visual gray matter brain volume increases in congenital nystagmus. Front Neurol. 2011; 2:60.
Article
Full Text Links
  • KJO
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr