Abstract
Objective
To analyse macular retinal and choroidal layer thickness in former preterm and full-term infants and to assess associated perinatal influence factors and functional correlation.
Methods
This prospective controlled, cross-sectional, hospital-based study in a tertiary center of maximum care examined former preterm infants with a gestational age (GA) ≤ 32 weeks and full-term neonates currently aged 4 to 10 years. We investigated data from 397 infants, analysing total foveal retinal thickness and six distinct macular retinal layer and choroidal layer measurements via spectral-domain optical coherence tomography. Multivariable linear regression analysis was performed to investigate associations of layer thickness with GA and retinopathy of prematurity (ROP).
Results
Total retinal thickness in the fovea was thicker in former preterm infants with GA ≤ 28 weeks and in those with GA between 29–32 weeks compared to full-term infants independently of ROP. Occurrence of ROP was also associated with increased foveal thickness. Ganglion cell layer together with inner plexiform layer (GCL+IPL) was thinner in infants with GA ≤ 28 weeks than in full-term infants at 1000 and 2000μm distance from the fovea, but no association with ROP was present. Similar results were found for the photoreceptor layer. Total foveal retinal thickness was associated with low visual function.
Conclusion
This study identified low gestational age and ROP occurrence as main determinants for foveal thickening. Furthermore, thinned GCL+IPL measurements were associated with lower gestational age. This study highlights the prognostic value of these maturity parameters influencing retinal morphology, which may affect visual function.
Similar content being viewed by others
References
Wang J, Spencer R, Leffler JN et al (2012) Critical period for foveal fine structure in children with regressed retinopathy of prematurity. Retina 32:330–339
Yuodelis C, Hendrickson A (1986) A qualitative and quantitative analysis of the human fovea during development. Vis Res 26:847–855
Hendrickson AE, Yuodelis C (1984) The morphological development of the human fovea. Ophthalmology 91:603–612
Provis JM, Diaz CM, Dreher B (1998) Ontogeny of the primate fovea: a central issue in retinal development. Prog Neurobiol 54:549–580
Springer AD (1999) New role for the primate fovea: a retinal excavation determines photoreceptor deployment and shape. Vis Neurosci 16:629–636
Akerblom H, Larsson E, Eriksson U et al (2011) Central macular thickness is correlated with gestational age at birth in prematurely born children. Br J Ophthalmol 95:799–803
Bowl W, Stieger K, Bokun M et al (2016) OCT-based macular structure-function correlation in dependence on birth weight and gestational age-the Giessen long-term ROP study. Invest Ophthalmol Vis Sci 57:235–241
Park KA, Oh SY (2012) Analysis of spectral-domain optical coherence tomography in preterm children: retinal layer thickness and choroidal thickness profiles. Invest Ophthalmol Vis Sci 53:7201–7207
Yanni SE, Wang J, Chan M et al (2012) Foveal avascular zone and foveal pit formation after preterm birth. Br J Ophthalmol 96:961–966
Pueyo V, Gonzalez I, Altemir I et al (2015) Microstructural changes in the retina related to prematurity. Am J Ophthalmol 159:797–802
Nickla DL, Wallman J (2010) The multifunctional choroid. Prog Retin Eye Res 29:144–168
Moreno TA, O’Connell RV, Chiu SJ et al (2013) Choroid development and feasibility of choroidal imaging in the preterm and term infants utilizing SD-OCT. Invest Ophthalmol Vis Sci 54:4140–4147
Anderson MF, Ramasamy B, Lythgoe DT et al (2014) Choroidal thickness in regressed retinopathy of prematurity. Eye (Lond) 28:1461–1468
Wu WC, Shih CP, Wang NK et al (2013) Choroidal thickness in patients with a history of retinopathy of prematurity. JAMA Ophthalmol 131:1451–1458
Mohammad S, Gottlob I, Kumar A et al (2011) The functional significance of foveal abnormalities in albinism measured using spectral-domain optical coherence tomography. Ophthalmology 118:1645–1652
Jandeck C (2008) [Guidelines for ophthalmological screening of premature infants]. Ophthalmologe 105: 81–86, 88–90
Hammer DX, Iftimia NV, Ferguson RD et al (2008) Foveal fine structure in retinopathy of prematurity: an adaptive optics Fourier domain optical coherence tomography study. Invest Ophthalmol Vis Sci 49:2061–2070
Recchia FM, Recchia CC (2007) Foveal dysplasia evident by optical coherence tomography in patients with a history of retinopathy of prematurity. Retina 27:1221–1226
Ecsedy M, Szamosi A, Karko C et al (2007) A comparison of macular structure imaged by optical coherence tomography in preterm and full-term children. Invest Ophthalmol Vis Sci 48:5207–5211
Lago A, Matieli L, Gomes M et al (2007) Stratus optical coherence tomography findings in patients with retinopathy of prematurity. Arq Bras Oftalmol 70:19–21
Villegas VM, Capo H, Cavuoto K, et al. (2014) Foveal structure-function correlation in children with history of retinopathy of prematurity. Am J Ophthalmol 158: 508–512 e502
Fieß A, Christian L, Janz J et al (2017) Functional analysis and associated factors of the peripapillary retinal nerve fibre layer in former preterm and full-term infants. Br JOphthalmol. doi:10.1136/bjophthalmol-2016-309622
Wang J, Spencer R, Leffler JN, et al. (2012) Characteristics of peripapillary retinal nerve fiber layer in preterm children. Am J Ophthalmol 153: 850–855 e851
Rothman AL, Sevilla MB, Mangalesh S, et al. (2015) Thinner retinal nerve fiber layer in very preterm versus term infants and relationship to brain anatomy and neurodevelopment. Am J Ophthalmol 160: 1296–1308.e1292
Li XQ, Munkholm A, Larsen M et al (2015) Choroidal thickness in relation to birth parameters in 11- to 12-year-old children: the Copenhagen child cohort 2000 eye study. Invest Ophthalmol Vis Sci 56:617–624
Shao Z, Dorfman AL, Seshadri S et al (2011) Choroidal involution is a key component of oxygen-induced retinopathy. Invest Ophthalmol Vis Sci 52:6238–6248
Alasil T, Wang K, Keane PA et al (2013) Analysis of normal retinal nerve fiber layer thickness by age, sex, and race using spectral domain optical coherence tomography. J Glaucoma 22:532–541
Bendschneider D, Tornow RP, Horn FK et al (2010) Retinal nerve fiber layer thickness in normals measured by spectral domain OCT. J Glaucoma 19:475–482
Budenz DL, Anderson DR, Varma R et al (2007) Determinants of normal retinal nerve fiber layer thickness measured by stratus OCT. Ophthalmology 114:1046–1052
Parikh RS, Parikh SR, Sekhar GC et al (2007) Normal age-related decay of retinal nerve fiber layer thickness. Ophthalmology 114:921–926
Oner V, Ozgur G, Turkyilmaz K et al (2014) Effect of axial length on retinal nerve fiber layer thickness in children. Eur J Ophthalmol 24:265–272
Barteselli G, Chhablani J, El-Emam S et al (2012) Choroidal volume variations with age, axial length, and sex in healthy subjects: a three-dimensional analysis. Ophthalmology 119:2572–2578
Tan CS, Ouyang Y, Ruiz H et al (2012) Diurnal variation of choroidal thickness in normal, healthy subjects measured by spectral domain optical coherence tomography. Invest Ophthalmol Vis Sci 53:261–266
Fujiwara T, Imamura Y, Margolis R et al (2009) Enhanced depth imaging optical coherence tomography of the choroid in highly myopic eyes. Am J Ophthalmol 148:445–450
Shao L, Xu L, Chen CX et al (2013) Reproducibility of subfoveal choroidal thickness measurements with enhanced depth imaging by spectral-domain optical coherence tomography. Invest Ophthalmol Vis Sci 54:230–233
Sander BP, Collins MJ, Read SA (2014) The effect of topical adrenergic and anticholinergic agents on the choroidal thickness of young healthy adults. Exp Eye Res 128:181–189
Acknowledgements
Participating investigators or Collaborators who collected data or provided and cared for study patients (in alphabetical order): Luca Christian, Serife Demirbas, Paula Divis Di Oliveira, Lisa Ernst, Shirin Ghafoori, Saskia Jordan, Petra Nikolic, David Scheele, Florian Tlucynski, Christine Zeymer.
This study contains parts of the thesis of Johannes Janz.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
No funding was received for the study. The authors report no conflicts of interest. The authors declare that they have no competing interests.
Conflict of interest
All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licencing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.
Ethical approval
“All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.”
Informed consent
“Informed consent was obtained from all individual participants included in the study.”
Rights and permissions
About this article
Cite this article
Fieß, A., Janz, J., Schuster, A.K. et al. Macular morphology in former preterm and full-term infants aged 4 to 10 years. Graefes Arch Clin Exp Ophthalmol 255, 1433–1442 (2017). https://doi.org/10.1007/s00417-017-3662-5
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00417-017-3662-5