Growth in foetal life, infancy, and early childhood and the association with ocular biometry

Jan Willem L Tideman, Jan Roelof Polling, Vincent W V Jaddoe, Johannes R Vingerling, Caroline C W Klaver, Jan Willem L Tideman, Jan Roelof Polling, Vincent W V Jaddoe, Johannes R Vingerling, Caroline C W Klaver

Abstract

Purpose: Ocular biometry varies within groups of emmetropic, hyperopic or myopic children. The aim of this study was to quantify the effect of foetal and infant growth on ocular biometry in early childhood, to determine the most important period for this association, and to examine genetic overlap with height and birth weight.

Methods: 5931 children (50.1% girls) from a population-based prospective birth cohort study underwent intra-uterine and infant growth measurements at second and third trimester, and from birth to 72 months. An ophthalmic examination including axial length (mm) and corneal radius of curvature (mm) was performed at 6 years of age. The associations between prenatal and postnatal growth variables and axial length and corneal radius of curvature were assessed with conditional linear regression analyses. Weighted genetic risk scores for birth weight and height were calculated and causality was tested with Mendelian randomisation.

Results: Weight and length from mid-pregnancy to 2 years of age were most important prognostic factors for axial length and corneal radius of curvature at age 4.9-9 years (mean 6.2 years S.D. 0.5). For height (Standard deviation score), the association with axial length and corneal radius of curvature was highest for the measurement at 12 months (β 0.171 p < 0.001 and 0.070 p < 0.001). The genetic height and birth weight risk scores were both significantly associated with ocular biometry.

Conclusions: Larger neonates had longer axial length and greater corneal radius of curvature. Growth during pregnancy and 2 years postnatally is the most important period underlying this association and may be partly genetically determined by genes associated with height.

Keywords: epidemiology; genetics; myopia; optics; orthokeratology.

Conflict of interest statement

The authors report no conflicts of interest and have no proprietary interest in any of the materials mentioned in this article.

© 2019 The Authors. Ophthalmic & Physiological Optics published by John Wiley & Sons Ltd on behalf of College of Optometrists.

Figures

Figure 1
Figure 1
Non‐linearity in the association between axial length (left), corneal radius (middle) and AL/CR ratio (right) and birth weight for gestational age adjusted for age, gender and ethnicity.
Figure 2
Figure 2
The association between foetal and infant weight SDS (standard deviation score) per time period with (a) axial length (mm), (b) corneal radius of curvature (mm) and (c) AL/CR ratio (mm mm−1) (N = 1595).

References

    1. Mutti DO, Mitchell GL, Jones LA et al Axial growth and changes in lenticular and corneal power during emmetropization in infants. Invest Ophthalmol Vis Sci 2005; 46: 3074–3080.
    1. Tideman JWL, Polling JR, Vingerling JR et al Axial length growth and the risk of developing myopia in European children. Acta Ophthalmol 2018; 96: 301–309.
    1. Brown NP, Koretz JF & Bron AJ. The development and maintenance of emmetropia. Eye (Lond) 1999; 13: 83–92.
    1. Hashemi H, Khabazkhoob M, Miraftab M et al Axial length to corneal radius of curvature ratio and refractive errors. J Ophthalmic Vis Res 2013; 8: 220–226.
    1. Ojaimi E, Rose KA, Morgan IG et al Distribution of ocular biometric parameters and refraction in a population‐based study of Australian children. Invest Ophthalmol Vis Sci 2005; 46: 2748–2754.
    1. Saw SM, Tong L, Chia KS et al The relation between birth size and the results of refractive error and biometry measurements in children. Br J Ophthalmol 2004; 88: 538–542.
    1. Ojaimi E, Robaei D, Rochtchina E, Rose KA, Morgan IG & Mitchell P. Impact of birth parameters on eye size in a population‐based study of 6‐year‐old Australian children. Am J Ophthalmol 2005; 140: 535–537.
    1. Northstone K, Guggenheim JA, Howe LD et al Body stature growth trajectories during childhood and the development of myopia. Ophthalmology 2013; 120: e1.
    1. Lim LS, Chua S, Tan PT et al Eye size and shape in newborn children and their relation to axial length and refraction at 3 years. Ophthalmic Physiol Opt 2015; 35: 414–423.
    1. Jaddoe VW, van Duijn CM, Franco OH et al The Generation R Study: design and cohort update 2012. Eur J Epidemiol 2012; 27: 739–756.
    1. Verburg BO, Steegers EA, De Ridder M et al New charts for ultrasound dating of pregnancy and assessment of fetal growth: longitudinal data from a population‐based cohort study. Ultrasound Obstet Gynecol 2008; 31: 388–396.
    1. Hadlock FP, Harrist RB, Carpenter RJ, Deter RL & Park SK. Sonographic estimation of fetal weight. The value of femur length in addition to head and abdomen measurements. Radiology 1984; 150: 535–540.
    1. Niklasson A, Ericson A, Fryer JG, Karlberg J, Lawrence C & Karlberg P. An update of the Swedish reference standards for weight, length and head circumference at birth for given gestational age (1977‐1981). Acta Paediatr Scand 1991; 80: 756–762.
    1. Allochtonen in Nederland 2004. Voorburg/Heerlen: Statistics Netherlands, 2004.
    1. Keijzer‐Veen MG, Euser AM, van Montfoort N, Dekker FW, Vandenbroucke JP & Van Houwelingen HC. A regression model with unexplained residuals was preferred in the analysis of the fetal origins of adult diseases hypothesis. J Clin Epidemiol 2005; 58: 1320–1324.
    1. Wood AR, Esko T, Yang J et al Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet 2014; 46: 1173–1186.
    1. Horikoshi M, Beaumont RN, Day FR et al Genome‐wide associations for birth weight and correlations with adult disease. Nature 2016; 538: 248–252.
    1. Johnson TS, Engstrom JL & Gelhar DK. Intra‐ and interexaminer reliability of anthropometric measurements of term infants. J Pediatr Gastroenterol Nutr 1997; 24: 497–505.
    1. Wood AJ, Raynes‐Greenow CH, Carberry AE & Jeffery HE. Neonatal length inaccuracies in clinical practice and related percentile discrepancies detected by a simple length‐board. J Paediatr Child Health 2013; 49: 199–203.
    1. Ophthalmology AAO . Clinical Optics Basic and Clinical Science Course 2017 ‐ 2018:200.
    1. Tideman JW, Polling JR, Voortman T et al Low serum vitamin D is associated with axial length and risk of myopia in young children. Eur J Epidemiol 2016; 31: 491–499.
    1. Augusteyn RC, Nankivil D, Mohamed A, Maceo B, Pierre F & Parel JM. Human ocular biometry. Exp Eye Res 2012; 102: 70–75.
    1. Inagaki Y. The rapid change of corneal curvature in the neonatal period and infancy. Arch Ophthalmol 1986; 104: 1026–1027.
    1. Zadnik K, Manny RE, Yu JA et al Ocular component data in schoolchildren as a function of age and gender. Optom Vis Sci 2003; 80: 226–236.
    1. He M, Xiang F, Zeng Y et al Effect of time spent outdoors at school on the development of myopia among children in China: a randomized clinical trial. JAMA 2015; 314: 1142–1148.
    1. Rose KA, Morgan IG, Ip J et al Outdoor activity reduces the prevalence of myopia in children. Ophthalmology 2008; 115: 1279–1285.
    1. Sherwin JC, Reacher MH, Keogh RH, Khawaja AP, Mackey DA & Foster PJ. The association between time spent outdoors and myopia in children and adolescents: a systematic review and meta‐analysis. Ophthalmology 2012; 119: 2141–2151.
    1. Tideman JWL, Polling JR, Hofman A, Jaddoe VW, Mackenbach JP & Klaver CC. Environmental factors explain socioeconomic prevalence differences in myopia in 6‐year‐old children. Br J Ophthalmol 2018; 102: 243–247.
    1. Verhoeven VJ, Hysi PG, Wojciechowski R et al Genome‐wide meta‐analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet 2013; 45: 314–318.
    1. Feldkaemper M & Schaeffel F. An updated view on the role of dopamine in myopia. Exp Eye Res 2013; 114: 106–119.
    1. Tideman JW, Fan Q, Polling JR et al When do myopia genes have their effect? Comparison of genetic risks between children and adults. Genet Epidemiol 2016; 40: 756–766.
    1. Zhou X, Pardue MT, Iuvone PM & Qu J. Dopamine signaling and myopia development: what are the key challenges. Prog Retin Eye Res 2017; 61: 60–71.
    1. Wildsoet CF & Schmid KL. Optical correction of form deprivation myopia inhibits refractive recovery in chick eyes with intact or sectioned optic nerves. Vision Res 2000; 40: 3273–3282.

Source: PubMed

3
Iratkozz fel