Correction
19 Jun 2015: Zhu H, Yu JJ, Yu RB, Ding H, Bai J, et al. (2015) Correction: Association between Childhood Strabismus and Refractive Error in Chinese Preschool Children. PLOS ONE 10(6): e0130914. https://doi.org/10.1371/journal.pone.0130914 View correction
Figures
Abstract
Purpose
To investigate the association between concomitant esotropia or concomitant exotropia and refractive error in preschool children
Methods
A population-based sample of 5831 children aged 3 to 6 years was selected from all kindergartens in a representative county (Yuhuatai District, Nanjing, Jiangsu Province) of Nanjing, China. Clinical examinations including ocular alignment, ocular motility, visual acuity, optometry, stereopsis screening, slit lamp examination and fundus examination were performed by trained ophthalmologists and optometrists. Odd ratios (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the association of refractive error with concomitant esotropia and concomitant exotropia.
Results
In multivariate logistic regression analysis, concomitant esotropia was associated independently with spherical equivalent anisometropia (OR, 3.15 for 0.50 to <1.00 diopter (D) of anisometropia, and 7.41 for > = 1.00 D of anisometropia) and hyperopia. There was a severity-dependent association of hyperopia with the development of concomitant esotropia, with ORs increasing from 9.3 for 2.00 to <3.00 D of hyperopia, to 180.82 for > = 5.00 D of hyperopia. Concomitant exotropia was associated with astigmatism (OR, 3.56 for 0.50 to 1.00 D of astigmatism, and 1.9 for <0.00 D of astigmatism), myopia (OR, 40.54 for -1.00 to <0.00 D of myopia, and 18.93 for <-1.00 D of myopia), and hyperopia (OR, 67.78 for 1.00 to <2.00 D of hyperopia, 23.13 for 2.00 to <3.00 D of hyperopia, 25.57 for 3.00 to <4.00 D of hyperopia, and 8.36 for 4.00 to <5.00 D of hyperopia).
Citation: Zhu H, Yu J-J, Yu R-B, Ding H, Bai J, Chen J, et al. (2015) Association between Childhood Strabismus and Refractive Error in Chinese Preschool Children. PLoS ONE 10(3): e0120720. https://doi.org/10.1371/journal.pone.0120720
Academic Editor: Chen-Wei Pan, Medical College of Soochow University, CHINA
Received: November 4, 2014; Accepted: January 25, 2015; Published: March 20, 2015
Copyright: © 2015 Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: The authors received funding from the Science and Technology Bureau of Yuhuatai District. The grant numbers are 201001110 and the URL is http://www.njkj.gov.cn/. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Strabismus is a common childhood ocular disorder with population-based prevalence estimates ranging from 1.2% to 5% in Chinese children [1, 2]. The manifest misalignment of the eyes often results in deficient binocular depth perception and even amblyopia. Besides these functional effects, there are psychological distresses because of strabismus, such as depression and anxiety, impaired self-esteem and self-confidence, unsatisfied interpersonal relationships and social prejudice [3–7]. Surgical or optical therapy is necessary in many patients with strabismus.
The cause of strabismus has not yet been clearly understood and many factors may contribute. Children who were hyperopia in infancy have been found to be more likely to become strabismus [8]. Refractive accommodative esotropia has been identified to be the consequence of childhood hyperopia [9, 10]. However, how hyperopia influences other strabismus and how other types of ametropia influence strabismus are not known very well. Population-based research is significant in exploring the effect of refractive error on the development of various types of childhood strabismus. Confirming the relationship is very helpful to guide eye care providers to manage childhood refractive error and to influence public health policy-making. The present study aimed to analyze associations between refractive error and different types of strabismus in preschool children aged 3 to 6 years enrolled in the population-based Nanjing Pediatric Vision Project (NPVP).
Methods
Sample Selection
The NPVP was conducted from 2011 to 2012 and aimed to estimate the burden of common pediatric ocular disorders of preschool children aged 3–6 years in the Yuhuatai District, Nanjing, China. Nanjing City is the capital of Jiangsu Province, a traditional economic and cultural hub of eastern China and has a population of 8.1 million according to the China Sixth National Population Census (2010). Yuhuatai District is one of 11 municipal districts of Nanjing and has a relatively stable population structure (approximately 413 thousand residents) and a medium socioeconomic status in eastern China, which makes it representative of that area. The study adhered to the Declaration of Helsinki and was approved by the Institutional Review Board of Jiangsu Province Hospital. Written informed consent was obtained from parents or legal representatives of all participating children.
Every 150 to 250 children who studied in the 43 kindergartens in Yuhuatai District were grouped according to geographic location, which were defined as clusters. In total, 48 clusters were established, and every cluster had 200 children on average. All of the clusters were numbered according to their locations and were randomly selected using a random numbers table.
Ocular Alignment and Movement
The eye examinations were performed by a team of two senior ophthalmologists, two junior ophthalmologists, two assistants and two optometrists. If glasses were worn, testing was performed with and without correction both. Ocular alignment was assessed using the Hirschberg light reflex test at a distance of 33 cm, the cover-uncover test and the alternate cover test with fixation targets at both 33 cm and 6 m [11]. Binocular and monocular ocular movements were examined at nine diagnostic positions of gaze with the head in a stationary position. If strabismus was suspected, a prism cover test was performed to detect the degree of eye misalignment.
Distance Visual Acuity (VA)
All children had distance VA measured, with or without spectacles, using the Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity chart (Precision, Vision, LaSalle, IL, USA) at a distance of 4 m. For children with distance VA < 6/12 or a two or more lines difference between eyes, subjective refraction was performed to obtain best corrected VA.
Optometry
All participants had the measurement of refractive error using an autorefractor (Suresight, Welch Allyn, USA) under non-cycloplegic conditions. The refraction status of children who were found abnormal in the examinations of ocular alignment, ocular movement and distance VA, was further evaluated under cycloplegic conditions if agreement was obtained from parents or legal representatives. One drop of topical 1.0% cyclopentolate (Cyclogyl, Alcon Pharmaceuticals) was administered to each eye twice at 5-minute intervals. Fifteen minutes later, a third drop of cyclopentolate was administered if the pupil size was < 6 mm or if the papillary light reflex was still present.
Ocular Examination
Children with abnormalities found in the examinations of ocular alignment, ocular movement and distance VA needed to have further ocular examinations, including stereopsis screening using children random-dot stereograms (edited by Shaoming Yan, People’s Medical Publishing House, 2006, China), slit lamp examination, and fundus examination.
Definition of Strabismus
Strabismus was determined if any tropia was present at distance or near, with or without spectacles and then classified according to the primary direction (esotropia, exotropia, vertical) of the tropia. Constant or intermittent heterotropia was defined as well.
Statistical Analysis
Vector analysis was used to determine the J0 (power in the vertical or horizontal meridian) and J45 (power in the oblique meridian) vector components of astigmatism [12]. Potential risk factors were spherical equivalent (SE) refractive error of less hyperopia eye, astigmatism of less astigmatic eye, SE anisometropia, J0 anisometropia (interocular difference in J0), and J45 anisometropia (interocular difference in J45). The dioptric criteria for levels of magnitude are provided in Table 1. The less hyperopic eye was chosen for analysis because that accommodative convergence (a potential contributor to convergent strabismus) is likely to be caused by accommodation in the less hyperopic eye if anisometropia is present.
Binary logistic regression model was fitted to explore the associations of potential risk factors separately for concomitant esotropia and concomitant exotropia. Only age, gender and factors that were significant at the P<0.10 level were retained in further stepwise multiple logistic analyses. All analyses were performed using SPSS software (version 17.0, IBM, China) for Windows 7.0.
Results
A total of 30 clusters including 5980 children were enrolled in this study and 5862 accepted eye examinations. Among the 5862 children, 31 were excluded from the data analysis for the following reasons: ages of 20 children were beyond the range of 3–6 years old, and 11 children had missing information. There were no significant differences in characteristics of children included in the data analysis compared with those excluded. Ultimately, 5831 children were analyzed, including 3118 boys (53.48%) and 2713 girls (46.52%), and the detection rate was 97.5%. The mean age of the children was 4.90±0.74 years.
337 children were found to have strabismus (prevalence, 5.8%, 95% CI 5.2%–6.4%) with no sex differences (5.9% [95%CI 5.07%-6.73%] in boys and 5.7% [95%CI 4.83%-6.57%] in girls). Among these, 6 had already undergone strabismus surgery and were orthophoria when examined. Of the 331 children having no history of surgery, 45 were concomitant esotropia, 270 were concomitant exotropia, 8 were microtropia, 7 were vertical strabismus and 1 were Duane retraction syndrome. The last three types of strabismus were excluded from analysis because of small numbers. Among children with concomitant esotropia, 80% were constant and 20% were intermittent. Among children with concomitant exotropia, 30% were constant and 70% were intermittent.
Agreement of cycloplegic optometry was obtained from parents or legal representatives of 370 children and refraction status of these children was measured under cycloplegic conditions. Among them, 41.6% had strabismus. The rest children only had the measurement of refractive error under non-cycloplegic conditions.
The univariate and multivariate analysis results for associations between refractive error and concomitant esotropia are provided in Table 2. After adjustment for other variables in the multivariate analysis, the following were identified as independent indicators of a greater risk for concomitant esotropia: SE anisometropia starting at the 0.50 to less than 1.00 D level (OR, 3.15–7.14 for different levels of SE anisometropia, relative to reference level of <0.50 D), and SE hyperopia starting at the 2.00 to less than 3.00 D level (OR, 9.28–180.82 for different levels of hyperopia, relative to reference level of 0.00 to <1.00 D).
Table 3 shows the univariate and multivariate analysis results for associations between refractive error and concomitant exotropia. In the multivariate analysis adjusted for all factors involved, SE hyperopia starting from the 1.00-<2.00 D level to the 4.00-<5.00 D level (OR, 8.36–67.78 for different levels of hyperopia, relative to reference level of 0.00 to <1.00 D), SE myopia starting at the -1.00 to less than 0.00 D level (OR, 18.93–40.54 for different levels of myopia, relative to reference level of 0.00 to <1.00 D), and astigmatism of 0.50 to less than 1.00 D and of less than 0.00 D (OR, 3.56 and 1.90 respectively, relative to reference level of 0.00 to <0.50 D) were identified as independent indicators of a greater risk for concomitant exotropia.
Discussion
The present study used a large population-based cohort of children 3 to 6 years of age to identify the association between refractive error and childhood concomitant esotropia and concomitant exotropia. The major potentially risky refractive errors for concomitant esotropia were SE anisometropia of 0.5 D or more and hyperopia of 2.00 D or more. For concomitant exotropia, myopia, hyperopia of 1.00 to less than 5.00 D, hyperopic astigmatism of 0.50 to less than 1.00 D, and myopic astigmatism were independent risk factors. Several previous population-based studies also explored the relationship between refractive error and strabismus (Table 4) [1, 13, 14]. However, in SMS and STARS, a separate analysis of esotropia and exotropia was not reported. MEPEDS & BPEDS detected esotropia and exotropia separately and found that hyperopia and SE anisometropia are risk factors for esotropia and astigmatism increases the risk of developing exotropia, which is partially consistent with our data.
Esotropia has been found to occur more frequently in children with hyperopia than in those without and infants with moderate hyperopia have been reported to be more likely to develop esotropia than emmetropic controls [8, 15–21]. However, the risk of developing esotropia associated with different levels of hyperopia hasn’t been quantified well. Limited evidence-based researches have been conducted to explore this question. The present population-based data show that hyperopia starting at the 2.00 to less than 3.00 D level pose more than a 9-fold increase in concomitant esotropia risk and a marked rise in this risk is associated with nearly each diopter of increasing hyperopia (Table 2). The odds of having concomitant esotropia in children with hyperopia of 5.00 D or more are 180 times greater than in children with 0.00 to less than 1.00 D of hyperopia. These findings implied the importance of correction of childhood hyperopia starting at the level of 2.00 D. Eye care providers and parents might take advantage of the present data to make proper decisions about whether to monitor or correct childhood hyperopia, even though the benefits of prophylactic optical correction haven’t been determined.
In the case of exotropia, mild to moderate hyperopia showed a strong association with exotropia. Previous studies reported the association between hyperopia and the development of strabismus in general and did not analyze esotropia and exotropia separately [1, 14, 22]. There are few studies with which this risk association can be compared.
Anisometropia has been observed to reduce binocularity in people without strabismus [23, 24]. It makes the association between anisometropia and esotropia, which was shown from the present data, highly plausible. Previous studies also implied this kind of relationship even though they analyzed strabismus in general [14, 25, 26]. MEPEDS & BPEDS detected associations between anisometropia and esotropia and supported our findings strongly [13]. Anisometropia wasn’t found to be associated with exotropia in our study, while anisoastigmatism in the J0 component and exotropia were related in MEPEDS & BPEDS [13].
Myopia was shown to be related with the occurrence of exotropia in the present study. Data from a population-based observational study indicated that children with intermittent exotropia showed a significant trend toward myopia over time [27]. The reason of the association between intermittent exotropia and myopia hasn’t been clarified. One potential explanation is that intermittent exotropia might increase accommodative demand [28] and reduction of accommodation has been found to slow the progression of moderate myopia [29]. That is, intermittent exotropia may promote the development of myopia through increasing accommodation. Thus, we are unable to state that myopia is a risk factor for exotropia. Instead, it is likely that intermittent exotropia might be a risk factor for myopia. Further study is needed to clarify the link between myopia and exotropia.
Astigmatism was also related to exotropia in our analysis, which was reported in MEPEDS & BPEDS as well. However, MEPEDS & BPEDS detected association between the absolute astigmatism and strabismus, while we didn’t. Hyperopic astigmatism and myopic astigmatism are likely to have different effects on the development of strabismus. Therefore, it might be more reasonable to analyze them separately, which needs to be explored further in the future.
There are a number of limitations in our study. Most participants just underwent optometry under non-cycloplegic conditions, which might not reveal the real refraction status of these children, especially hyperopia. We just included age, gender and associated refractive errors into the multivariate analysis. It is possible that other unknown or unexplored factors also may contribute to strabismus. Because that confirmation of refractive error and alignment was available only for the time of clinical examination, older children’s refractive error may have been different from that at an earlier age when strabismus first occurred. Meanwhile, younger children who were at risk for strabismus might have yet to develop strabismus, which might lead to underestimate the strength of associations with refractive error. The principal strengths of the present study are the large cohort of children aged 3–6 years old from a representative area in China and the strict population-based design. Compared with clinic-based studies that might overrepresent severe disease, this research is more likely to explore real risk associations in the population. All participants received comprehensive eye examinations by qualified experienced ophthalmologists and optometrists who followed a standardized protocol of examination. Thus, it is less likely to misclassify strabismus and refractive error.
In conclusion, this population-based study of childhood strabismus found a strong link between refractive error and strabismus. It is helpful to guide eye care providers and parents in making informed decisions regarding management of early refractive error. However, further study is needed to clarify the association between refractive error and strabismus and to evaluate the benefits of prophylactic optical correction of early refractive error.
Acknowledgments
The Nanjing Pediatric Vision Project thanks all the members of the Maternal and Child Healthcare Hospital of Yuhua District, Nanjing, China, for helpful advice and support.
Author Contributions
Conceived and designed the experiments: HL JJY HZ RBY JB HD JC. Performed the experiments: HL JJY HZ RBY JB HD JC. Analyzed the data: HL JJY HZ RBY. Contributed reagents/materials/analysis tools: HZ RBY. Wrote the paper: HZ HL.
References
- 1.
Von Noorden GK, Campos EC. Binocular Vision and Ocular Motility: Theory and Management of Strabismus. 6th ed. St. Louis: Mosby; 2002. https://doi.org/10.3368/aoj.51.1.161 pmid:21149051
- 2. Kushner BJ, Morton GV. Distance/near differences in intermittent exotropia. Arch Ophthalmol. 1998; 116(4): 478–486. pmid:9565045
- 3. Ip JM, Robaei D, Kifley A, Wang JJ, Rose KA, Mitchell P. Prevalence of hyperopia and associations with eye findings in 6- and 12-year-olds. Ophthalmology. 2008; 115(4): 678–685. pmid:17664011
- 4. Ingram RM, Arnold PE, Dally S, Lucas J. Results of a randomised trial of treating abnormal hypermetropia from the age of 6 months. Br J Ophthalmol. 1990; 74(3): 158–159. pmid:2182103
- 5. Ingram RM, Walker C, Wilson JM, Arnold PE, Dally S. Prediction of amblyopia and squint by means of refraction at age 1 year. Br J Ophthalmol. 1986; 70(1): 12–15. pmid:3947594
- 6. Weakley DR. The association between anisometropia, amblyopia, and binocularity in the absence of strabismus. Trans Am Ophthalmol Soc. 1999; 97: 987–1021. pmid:10703148
- 7. Ekdawi NS, Nusz KJ, Diehl NN, Mohney BG. The development of myopia among children with intermittent exotropia. Am J Ophthalmol. 2010; 149(3): 503–507. pmid:20172074
- 8. Walsh LA, Laroche GR, Tremblay F. The use of binocular visual acuity in the assessment of intermittent exotropia. J AAPOS. 2000; 4(3): 154–157. pmid:10849391
- 9. Chia A, Lin XY, Dirani M, Gazzard G, Ramamurthy D, Quah BL, et al. Risk factors for strabismus and amblyopia in young singapore chinese children. Ophthalmic Epidemiology. 2013; 20(3): 138–147. pmid:23713916
- 10. Fu J, Li SM, Liu LR, Li JL, Li SY, Zhu BD, et al. Prevalence of amblyopia and strabismus in a population of 7th-grade junior high school students in Central China: the Anyang Childhood Eye Study (ACES). Ophthalmic Epidemiology. 2014; 21(3): 197–203. pmid:24742059
- 11. Satterfield D, Keltner JL, Morrison TL. Psychosocial aspects of strabismus study. Arch Ophthalmol. 1993; 111(8): 1100–1105. pmid:8166786
- 12. Menon V, Saha J, Tandon R, Mehta M, Khokhar S. Study of the psychosocial aspects of strabismus. J Pediatr Ophthalmol Strabismus. 2002; 39(4): 203–208. pmid:12148552
- 13. Nelson BA, Gunton KB, Lasker JN, Nelson LB, Drohan LA. The psychosocial aspects of strabismus in teenagers and adults and the impact of surgical correction. J AAPOS. 2008; 12(1):72–76. pmid:18314071
- 14. Xu J, Yu X, Huang Y, Chen J, Yu H, Wang Y, et al. The psychosocial effects of strabismus before and after surgical correction in Chinese adolescents and adults. J Pediatr Ophthalmol Strabismus. 2012; 49(3): 170–175. pmid:22909123
- 15. Lin S, Congdon N, Yam JC, Huang Y, Qiu K, Ma D, et al. Alcohol use and positive screening results for depression and anxiety are highly prevalent among chinese children with strabismus. Am J Ophthalmol. 2014; 157(4): 894–900. pmid:24445033
- 16. Atkinson J, Braddick O, Robier B, Anker S, Ehrlich D, King J, et al. Two infant vision screening programmes: prediction and prevention of strabismus and amblyopia from photo- and videorefractive screening. Eye (Lond). 1996; 10(2): 189–198.
- 17. Raab EL. Etiologic factors in accommodative esodeviation. Trans Am Ophthalmol Soc. 1982; 80: 657–694. pmid:7182971
- 18. Ojaimi E, Rose KA, Smith W, Morgan IG, Martin FJ, Mitchell P. Methods for a population-based study of myopia and other eye conditions in school children: the Sydney Myopia Study. Ophthalmic Epidemiol. 2005; 12(1): 59–69. pmid:15848921
- 19. Miller J. Clinical applications of power vectors. Optom Vis Sci. 2008; 86(6): 599–602. pmid:19390467
- 20. Cotter SA, Varma R, Tarczy-Hornoch K, McKean-Cowdin R, Lin J, Wen G, et al. Risk factors associated with childhood strabismus: the multi-ethnic pediatric eye disease and Baltimore pediatric eye disease studies. Ophthalmology. 2011; 118(11): 2251–2261. pmid:21856012
- 21. Robaei D, Rose KA, Kifley A, Cosstick M, Ip JM, Mitchell P. Factors associated with childhood strabismus: findings from a population-based study. Ophthalmology. 2006; 113(7): 1146–1153. pmid:16675019
- 22. Colburn JD, Morrison DG, Estes RL, Li C, Lu P, Donahue SP. Longitudinal follow-up of hypermetropic children identified during preschool vision screening. J AAPOS. 2010; 14(3): 211–215. pmid:20603055
- 23. Robaei D, Rose KA, Ojaimi E, Kifley A, Martin FJ, Mitchell P. Causes and associations of amblyopia in a population-based sample of 6-year-old Australian children. Arch Ophthalmol. 2006; 124(6): 878–884. pmid:16769842
- 24. Anker S, Atkinson J, Braddick O, Ehrlich D, Hartley T, Nardini M, et al. Identification of infants with significant refractive error and strabismus in a population screening program using noncycloplegic videorefraction and orthoptic examination. Invest Ophthalmol Vis Sci. 2003; 44(2): 497–504. pmid:12556374
- 25. Atkinson J, Anker S, Bobier W, Braddick O, Durden K, Nardini M, et al. Normal emmetropization in infants with spectacle correction for hyperopia. Invest Ophthalmol Vis Sci. 2000; 41(12): 3726–3731. pmid:11053269
- 26. Holmström G, Rydberg A, Larsson E. Prevalence and development of strabismus in 10-year-old premature children: a population-based study. J Pediatr Ophthalmol Strabismus. 2006; 43(6): 345–352. pmid:17162970
- 27. Weakley DR. The association between nonstrabismic anisometropia, amblyopia, and subnormal binocularity. Ophthalmology. 2001; 108(1): 163–171. pmid:11150283
- 28. Huynh SC, Wang XY, Ip J, Robaei D, Kifley A, Rose KA, et al. Prevalence and associations of anisometropia and aniso-astigmatism in a population based sample of 6 year old children. Br J Ophthalmol. 2006; 90(5): 597–601. pmid:16622090
- 29. O'Connor AR, Stephenson TJ, Johnson A, Tobin MJ, Ratib S, Fielder AR. Strabismus in children of birth weight less than 1701 g. Arch Ophthalmol. 2002; 120(6): 767–773. pmid:12049582