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Refractive error characteristics and influence on ocular parameters in patients with unilateral congenital ptosis

Abstract

Background

The study aimed to investigate the difference in refractive status and ocular parameters between ptotic and fellow eyes in patients with unilateral congenital ptosis.

Methods

Thirty patients (53% males, age 22.00 ± 11.41 years) with unilateral congenital ptosis diagnosed and treated at the First Affiliated Hospital of Sun-yat Sen University were enrolled and underwent detailed refractive examinations from March 2019 to February 2022. Ocular biometric measurements were performed by an IOL Master 700 biometer. The differences in refractive error characteristics, best-corrected visual acuity (BCVA), and ocular parameters including axial length (AL), central corneal thickness (CCT), aqueous depth (AQD), anterior chamber depth (ACD), lens thickness (LT), and keratometry values between ptotic and fellow eyes were analysed.

Results

A lower BCVA (logMAR, median (IQR), 0.00 (− 0.13,0.00), P = 0.009) and a higher incidence of amblyopia (n (%), 7(23%), P = 0.016) were observed in ptotic eyes. The CCT of ptotic eyes was greater than that of fellow eyes (mean ± SD, 539.83 ± 26.73 μm, P < 0.001). The keratometry values at the flat axis (K1) and mean corneal power (Km) were smaller in ptotic eyes (mean ± SD, 42.11 ± 1.49 D, 42.68 ± 1.52 D, respectively, both P = 0.001). There was no significant difference in AL between ptotic and fellow eyes.

Conclusions

Congenital ptosis influences ocular parameters, mainly causing a thicker and flatter cornea. Patients with unilateral congenital ptosis might have lower BCVA in the ptotic eyes.

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Introduction

Congenital ptosis is a relatively normal ocular abnormality caused by a drooping eyelid within the first year of life, characterized as a narrow palpebral fissure and more coverage by the upper eyelid on the cornea. Several studies have reported that congenital ptosis can increase the incidence of myopia, hyperopia, astigmatism, anisometropia and amblyopia [1,2,3,4,5]. Previous studies have shown that pressure from the upper eyelid may alter corneal shape [6]. In animal experiments, axial elongation was induced by covering the pupil was observed [7,8,9]. This effect was also illustrated in human infants [10]. However, under long-term pressure and coverage from the upper eyelid, the effect of congenital ptosis on ocular structure remains unclear.

Recently, the IOL Master 700 (Carl Zeiss AG, Jena, Germany), a highly advanced, noncontact biometer, was introduced, allowing accurate ocular parameter testing on patients with congenital ptosis [11]. It is based on swept-source optical coherence tomography (SS-OCT), providing fixation points for the patients and retinal OCT images for technicians when testing to gain accurate axial measurements from the posterior cornea to the fovea [12]. In addition, it also provides measurements of central corneal thickness, lens thickness, anterior chamber depth, and corneal power.

In this study, we focus on both refractive status and the ocular biological parameters of unilateral congenital ptosis to compare the refractive error between ptotic eyes and fellow eyes and to investigate the influence of congenital ptosis on the ocular structure during eyeball growth.

Materials and methods

Patients

We enrolled 30 patients with unilateral congenital ptosis who were diagnosed and treated at the Ophthalmology Department of the First Affiliated Hospital of Sun Yat-sen University between March 2019 and February 2022. This study was approved by the Ethics Committee of the First Affiliated Hospital of Sun Yat-sen University in China ([2021]544) and complied with the tenets of the Declaration of Helsinki for biomedical research involving human subjects.

The normal position of the upper lid covers the cornea by less than 2 mm, and ptosis can be diagnosed when the upper lid is below its normal position. The severity of ptosis can be classified as mild (1–2 mm), when the upper lid does not cover the pupil, moderate (3–4 mm), when the upper lid partially covers the pupil, and severe (more than 4 mm), when the pupil is completely covered by the eyelid [13].

The inclusion criteria included unilateral congenital ptosis, age greater than 5 years, absence of other ocular pathology, and reliable measurement results. The exclusion criteria were acquired ptosis, patients younger than 5 years and inability to cooperate with the examination, a history of eye trauma, previous ocular surgery (including ptosis correction surgery), corneal opacity, wearing of an eye contact lens in the last 3 months, and other ophthalmic or systemic disorders.

Ophthalmic examination

All patients were examined by the same trained examiner. Routine ophthalmic examinations were performed for all patients, including best-corrected visual acuity (BCVA) measurements using a Snellen chart, detailed slit-lamp examination of the anterior segment, fundus examination with dilated pupils, and measurement of intraocular pressure (Topcon CT-80A, Tokyo, Japan). Complete evaluation of ptosis, including measurement of the height of the palpebral fissure (HPF) and levator functions (LF), was performed by the lid excursion method, involving measurement of the upper lid from extreme downgaze to extreme upgaze with the frontalis muscle fixed.

Refractive error examination

Cycloplegic refraction was performed for all patients. Children younger than 10 years were given 1% atropine ointment once a day for 3 days and were examined on the fourth day. Patients older than 10 years were examined following administration of combined 0.5% phenylephrine hydrochloride and 0.5% tropicamide eye drops three times every 5 minutes. We calculated the refraction by the spherical equivalent refraction (SER) and defined myopia as an SER of at least − 0.50 D and hyperopia as an SER of + 2.00 D or more. Astigmatism was defined as 0.75 DC or more. Anisometropia was defined as at least a 1.00 D difference with the opposite eye. We defined amblyopia as a visual acuity of 6/9 or less and a difference of more than two Snellen lines between the fellow and ptotic eyes, excluding any other ocular abnormalities [1, 14].

Ocular biometric measurements

Biometric measurements were performed using an IOL Master 700 three times by the same well-trained technician before pupillary dilatation in all patients. Each time before the examination, the device was recalibrated. During the measurement, the examinees were asked to position their heads on a headrest and look at a fixation point for foveal scans. Poor-quality results were deleted, and new measurements were obtained until the readings were reliable.

The axial length (AL), central corneal thickness (CCT), aqueous depth (AQD), anterior chamber depth (ACD), lens thickness (LT), keratometry values at the flat (K1) and steep (K2) axis, and mean corneal power (Km) were obtained. AL was defined as the distance from the tear film to the retinal pigment epithelium (RPE) of the fovea. CCT was defined as the distance from the anterior to the posterior cornea [15]. AQD was measured using signals from the posterior face of the cornea to the anterior surface of the lens. The ACD was defined as the distance from the central corneal epithelium to the anterior surface of the lens and calculated by adding the CCT and AQD (CCT + AQD) [16]. LT was defined as the distance between the anterior and posterior lens surfaces. Corneal power included K1, K2 and Km, where K1 was defined as the corneal power at the flat axis and K2 at the steep axis, and Km was the average value of K1 and K2 [17, 18].

Statistical analysis

Statistical analysis was performed by using SPSS version 22.0. The Snellen VA was converted to the logarithm of the minimum angle of resolution (logMAR) value. The Shapiro–Wilk test was used to examine whether the measured values followed a normal distribution. Descriptive results for continuous variables are expressed as the mean ± standard deviation (SD) or median and interquartile range (IQR) depending on the normality of the distribution. Differences were compared using paired t tests for data with a normal distribution and Wilcoxon rank-sum tests for those with a nonnormal distribution. McNemar’s tests were used to compare the frequencies of refractive types between the fellow and ptotic eyes. A P value less than 0.05 was considered statistically significant.

Results

In total, 30 eyes of 30 patients with unilateral congenital ptosis in this study were analysed, and the 30 fellow eyes without ptosis served as controls. The distribution of sex was 16 (53%) males and 14 (47%) females. The average age was 22.00 ± 11.41 years, ranging from 5 to 46 years old. Out of 30 patients, 8 (27%) had mild ptosis, 15 (50%) had moderate ptosis, and 7 (23%) had severe ptosis. Fifteen (50%) had the right eye affected, while 15 (50%) had the left eye affected. Table 1 shows the demographics of the patients.

Table 1 Demographic characteristics of the participants (N = 30)

The BCVA of the ptotic eyes was significantly lower (logMAR, median (IQR), 0.00 (−0.13, 0.00), p = 0.009) than that of the fellow eyes. The incidence of myopia and astigmatism did not differ significantly between ptotic eyes and fellow eyes. However, the prevalence of amblyopia in the ptotic eyes (n (%), 7(23%), p = 0.016) was higher than that in the fellow eyes (n (%), 0). All 7 amblyopic eyes were ptotic, 3 severe and 4 moderate. The results are shown in Table 2.

Table 2 Differences in BCVA and refractive status between fellow and ptotic eyes (N = 30)

Ocular biometric parameters in eyes with ptosis were compared with those of the fellow normal eyes and are summarized in Table 3. The CCT was greater in the ptotic eyes than in the fellow eyes (539.83 ± 26.73 μm vs. 530.03 ± 27.43 μm, p < 0.001). The K1 (42.11 ± 1.49 D vs. 42.52 ± 1.41 D, p = 0.001) and SE (42.68 ± 1.52 D vs. 43.02 ± 1.41 D, p = 0.001) of ptotic eyes were lower than those of fellow eyes, which means that the corneas of the former were thicker and flatter. The parameters AL, AQD, ACD, LT, K2 and IOP were not significantly different between the ptotic and fellow eyes.

Table 3 Comparison of ocular biometric parameters between ptotic and fellow eyes (N = 30)

Discussion

It has been established that congenital ptosis may increase the incidence of refractive errors, including myopia, hyperopia, and astigmatism, as well as the incidence of amblyopia and anisometropia [1, 19, 20]. In addition, due to amblyopia or deprivation caused by a drooping eyelid covering the pupil, congenital ptosis may have a negative influence on visual acuity [21]. Our study revealed that patients with congenital ptosis are more likely to experience visual impairment. Among the 30 patients with unilateral ptosis, the BCVA in ptotic eyes was lower than that in fellow normal eyes, which indicated that congenital ptosis may lead to visual defects.

In the present study, the incidence of amblyopia in patients with congenital ptosis was 23%, similar to previous reports [21,22,23]. In addition, all amblyopic eyes in this study were ptotic, revealing that in patients with unilateral congenital ptosis, amblyopia was found more often in ptotic eyes. In regard to the causes of amblyopia in patients with congenital ptosis, astigmatism accounted for the largest proportion. Ugurbas et al. observed that among patients with congenital ptosis, ptotic eyes had more asymmetric and irregular corneas, resulting in an increased magnitude of astigmatism, which may be associated with a higher incidence of amblyopia [3]. The reports by Huo et al. and Paik et al. independently found that in patients with congenital ptosis, ptotic eyes had a higher frequency of astigmatism and amblyopia [1, 23]. In our study, the 7 amblyopic eyes were ptotic, which may to some extent be related to astigmatism; however, larger samples may be needed to verify this assumption.

In normal human eyes, the upper eyelid covers 1–2 mm of the cornea, while the lower eyelid covers none of it. A previous study showed that the superior cornea is thicker than the inferior cornea [24]. Under the coverage and pressure of the upper eyelid, the superior cornea is chronically hypoxic. This finding can be explained by research showing that compared with the central and inferior corneas, the superior cornea demands more oxygen after lifting the upper eyelid [25, 26]. Consequently, we presumed that the chronic hypoxia induced by a constantly drooped eyelid may cause chronic corneal oedema, leading to thickening of the cornea. In the current study, a thicker central cornea was found in ptotic eyes, which was consistent with the findings of Li X et al. [27] We speculated that in congenital ptosis, ptotic eyes are covered more by the drooping eyelids and are subject to mechanical stress, resulting in chronic hypoxia of the cornea and thus leading to a thicker cornea.

In our study, among the 30 patients with unilateral congenital ptosis, no difference in axial length between ptotic eyes and fellow normal eyes was observed, which is consistent with the reports individually by von Noorden et al. and Takahashi et al. [28, 29] One possible explanation is that by adjusting the head posture, patients with congenital ptosis are able to offset the covering of the upper eyelid, thus avoiding occlusion when looking. This indicates that in human eyes, ocular axial elongation does not arise from a similar mechanism to that in animal models [7,8,9].

A previous study showed that the pressure from the upper eyelids may influence the shape of the cornea, causing it to steepen [30]. In another study, the authors stated that at primary gaze, the wider the horizontal palpebral fissure was, the flatter the cornea [31]. However, in the current study, we found that both the horizontal corneal power and mean corneal power of ptotic eyes were lower than those of fellow eyes, which indicates that congenital ptosis, with a narrower palpebral fissure and under more pressure from the upper eyelid, may lead to flattening of the cornea.

Several limitations of this research need to be considered. First, the average age of these patients (22.00 ± 11.41 years) is relatively high, since people at these ages in China typically have myopia. It is possible that different results regarding the refractive error and axial length could be obtained from younger patients. The second limitation is that the number of patients included in this study was small despite our having calculated the minimum required sample size in advance. Future research needs to be done to determine additional abnormalities induced by congenital ptosis, providing more useful information for treatment. Third, the ocular parameters in this study seem to be limited, and more parameter testing and more accurate techniques should be applied for patients with congenital ptosis. Finally, in order to better control the study findings, only patients with unilateral congenital ptosis were enrolled, and ocular changes caused by acquired ptosis remain unknown; therefore, further studies are needed.

In summary, we confirmed that congenital ptosis may not only have an influence on refractive error and increase the prevalence of amblyopia but also cause the cornea to become thicker and flatter. The impact of congenital ptosis on axial length seems to be minimal in humans.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

SS-OCT:

Swept-source optical coherence tomography

BCVA:

Best-corrected visual acuity

HPF:

Height of the palpebral fissure

LF:

Levator function

logMAR:

Logarithm of the minimum angle of resolution

SER:

Spherical equivalent refraction

DS:

Dioptre of spherical power

DC:

Dioptre of cylindrical power

AL:

Axial length

CCT:

Central corneal thickness

AQD:

Aqueous depth

ACD:

Anterior chamber depth

LT:

Lens thickness

K1:

Keratometry values at the flat axis

K2:

Keratometry values at the steep axis

Km:

Mean corneal power

RPE:

Retinal pigment epithelium

References

  1. Huo L, Cui D, Yang X, et al. A retrospective study: form-deprivation myopia in unilateral congenital ptosis. Clin Exp Optom. 2012;95(4):404–9. https://doi.org/10.1111/j.1444-0938.2012.00716.x.

    Article  PubMed  Google Scholar 

  2. Gusek-Schneider GC, Martus P. Stimulus deprivation myopia in human congenital ptosis: a preliminary report of 50 unilateral cases. Strabismus. 2000;8(3):169–77.

    CAS  Article  Google Scholar 

  3. Uğurbaş SH, Zilelioğlu G. Corneal topography in patients with congenital ptosis. Eye (London, England). 1999;13(Pt 4):550–4. https://doi.org/10.1038/eye.1999.136.

    Article  Google Scholar 

  4. Merriam WW, Ellis FD, Helveston EM. Congenital blepharoptosis, anisometropia, and amblyopia. Am J Ophthalmol. 1980;89(3):401–7. https://doi.org/10.1016/0002-9394(80)90011-2.

    CAS  Article  PubMed  Google Scholar 

  5. Griepentrog GJ, Diehl N, Mohney BG. Amblyopia in childhood eyelid ptosis. Am J Ophthalmol. 2013;155(6):1125–1128.e1121. https://doi.org/10.1016/j.ajo.2012.12.015.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Lieberman DM, Grierson JW. The lids influence on corneal shape. Cornea. 2000;19(3):336–42. https://doi.org/10.1097/00003226-200005000-00016.

    CAS  Article  PubMed  Google Scholar 

  7. Smith EL 3rd, Bradley DV, Fernandes A, et al. Form deprivation myopia in adolescent monkeys. Optom Vis Sci. 1999;76(6):428–32. https://doi.org/10.1097/00006324-199906000-00023.

    Article  PubMed  Google Scholar 

  8. Troilo D, Nickla DL, Wildsoet CF. Form deprivation myopia in mature common marmosets (Callithrix jacchus). Invest Ophthalmol Vis Sci. 2000;41(8):2043–9.

    CAS  PubMed  Google Scholar 

  9. Howlett MH, McFadden SA. Form-deprivation myopia in the guinea pig (Cavia porcellus). Vis Res. 2006;46(1–2):267–83. https://doi.org/10.1016/j.visres.2005.06.036.

    Article  PubMed  Google Scholar 

  10. Hoyt CS, Stone RD, Fromer C, et al. Monocular axial myopia associated with neonatal eyelid closure in human infants. Am J Ophthalmol. 1981;91(2):197–200. https://doi.org/10.1016/0002-9394(81)90173-2.

    CAS  Article  PubMed  Google Scholar 

  11. Huang J, Chen H, Li Y, et al. Comprehensive Comparison of Axial Length Measurement With Three Swept-Source OCT-Based Biometers and Partial Coherence Interferometry. J Refract Surg (Thorofare, N.J. : 1995). 2019;35(2):115–20. https://doi.org/10.3928/1081597x-20190109-01.

    Article  Google Scholar 

  12. Yang JY, Kim HK, Kim SS. Axial length measurements: comparison of a new swept-source optical coherence tomography-based biometer and partial coherence interferometry in myopia. J Cataract Refract Surg. 2017;43(3):328–32. https://doi.org/10.1016/j.jcrs.2016.12.023.

    Article  PubMed  Google Scholar 

  13. Díaz-Manera J, Luna S, Roig C. Ocular ptosis: differential diagnosis and treatment. Curr Opin Neurol. 2018;31(5):618–27. https://doi.org/10.1097/wco.0000000000000600.

    Article  PubMed  Google Scholar 

  14. Anderson RL, Baumgartner SA. Amblyopia in ptosis. Arch Ophthalmol (Chicago, Ill. : 1960). 1980;98(6):1068–9. https://doi.org/10.1001/archopht.1980.01020031058009.

    CAS  Article  Google Scholar 

  15. Hughes RPJ, Read SA, Collins MJ, et al. Changes in ocular biometry during short-term accommodation in children. Ophthalmic Physiol Opt. 2020;40(5):584–94. https://doi.org/10.1111/opo.12711.

    Article  PubMed  Google Scholar 

  16. Fukuda S, Ueno Y, Fujita A, et al. Comparison of anterior segment and lens biometric measurements in patients with cataract. Graefes Arch Clin Exp Ophthalmol. 2020;258(1):137–46. https://doi.org/10.1007/s00417-019-04482-0.

    Article  PubMed  Google Scholar 

  17. Akman A, Asena L, Güngör SG. Evaluation and comparison of the new swept source OCT-based IOLMaster 700 with the IOLMaster 500. Br J Ophthalmol. 2016;100(9):1201–5. https://doi.org/10.1136/bjophthalmol-2015-307779.

    Article  PubMed  Google Scholar 

  18. Asena L, Akman A, Güngör SG, et al. Comparison of Keratometry obtained by a swept source OCT-based biometer with a standard optical biometer and Scheimpflug imaging. Curr Eye Res. 2018;43(7):882–8. https://doi.org/10.1080/02713683.2018.1458881.

    Article  PubMed  Google Scholar 

  19. Gusek-Schneider GC, Martus P. Stimulus deprivation myopia in human congenital ptosis: a study of 95 patients. J Pediatr Ophthalmol Strabismus. 2001;38(6):340–8.

    CAS  Article  Google Scholar 

  20. Srinagesh V, Simon JW, Meyer DR, et al. The association of refractive error, strabismus, and amblyopia with congenital ptosis. J AAPOS. 2011;15(6):541–4. https://doi.org/10.1016/j.jaapos.2011.08.006.

    Article  PubMed  Google Scholar 

  21. Ural O, Mocan MC, Erdener U. Evaluation of all causes of visual function loss in children with congenital Blepharoptosis. J Pediatr Ophthalmol Strabismus. 2020;57(2):97–102. https://doi.org/10.3928/01913913-20200120-01.

    Article  PubMed  Google Scholar 

  22. Dray JP, Leibovitch I. Congenital ptosis and amblyopia: a retrospective study of 130 cases. J Pediatr Ophthalmol Strabismus. 2002;39(4):222–5.

    Article  Google Scholar 

  23. Paik JS, Kim SA, Park SH, et al. Refractive error characteristics in patients with congenital blepharoptosis before and after ptosis repair surgery. BMC Ophthalmol. 2016;16(1):177. https://doi.org/10.1186/s12886-016-0351-9.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Haque S, Jones L, Simpson T. Thickness mapping of the cornea and epithelium using optical coherence tomography. Optom Vis Sci. 2008;85(10):E963–76. https://doi.org/10.1097/OPX.0b013e318188892c.

    Article  PubMed  Google Scholar 

  25. Benjamin WJ, Hill RM. Human cornea: superior and central oxygen demands. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle. Ophthalmologie. 1988;226(1):41–4. https://doi.org/10.1007/bf02172716.

    CAS  Article  Google Scholar 

  26. Benjamin WJ, Ruben CM. Human corneal oxygen demands at superior, central, and inferior sites. J Am Optom Assoc. 1995;66(7):423–8.

    CAS  PubMed  Google Scholar 

  27. Li X, Liu C, Mao Z, et al. Effect of congenital blepharoptosis on corneal biomechanical properties and changes after ptosis surgery. Eye (London, England). 2020;34(6):1055–62. https://doi.org/10.1038/s41433-019-0586-9.

    Article  Google Scholar 

  28. von Noorden GK, Lewis RA. Ocular axial length in unilateral congenital cataracts and blepharoptosis. Invest Ophthalmol Vis Sci. 1987;28(4):750–2.

    Google Scholar 

  29. Takahashi Y, Kang H, Kakizaki H. Axial globe length in congenital ptosis. J Pediatr Ophthalmol Strabismus. 2015;52(3):177–82. https://doi.org/10.3928/01913913-20150326-11.

    Article  PubMed  Google Scholar 

  30. Read SA, Collins MJ, Carney LG. A review of astigmatism and its possible genesis. Clin Exp Optom. 2007;90(1):5–19. https://doi.org/10.1111/j.1444-0938.2007.00112.x.

    Article  PubMed  Google Scholar 

  31. Read SA, Collins MJ, Carney LG. The influence of eyelid morphology on normal corneal shape. Invest Ophthalmol Vis Sci. 2007;48(1):112–9. https://doi.org/10.1167/iovs.06-0675.

    Article  PubMed  Google Scholar 

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Acknowledgements

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Funding

This study did not receive external funding.

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Authors and Affiliations

Authors

Contributions

HLJ and CTT designed the study; LYL, HJW, CYL and LWT collected data. LYL managed the data and wrote the manuscript; CTT analysed the data; HLJ and CTT reviewed the manuscript. All authors read and approved the final version of the manuscript.

Corresponding author

Correspondence to Lijun Huo.

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Ethics approval and consent to participate

This study was approved by the Ethics Committee of the First Affiliated Hospital of Sun Yat-sen University in China ([2021]544) and conducted in compliance with the Declaration of Helsinki.

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Written informed consent for publication was obtained from the participants.

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The authors declare that they have no competing interests.

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Liu, Y., Chen, T., Huang, J. et al. Refractive error characteristics and influence on ocular parameters in patients with unilateral congenital ptosis. BMC Ophthalmol 22, 291 (2022). https://doi.org/10.1186/s12886-022-02511-x

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Keywords

  • Congenital ptosis
  • Refractive error
  • Ocular parameters
  • IOL master700