Literature DB >> 28515637

Ultrasound biomicroscopy value in evaluation of restoration of ciliary muscles contractility after cataract extraction.

Ayser Abd El-Hameed Fayed1.   

Abstract

PURPOSE: To assess the changes in the contractility of the ciliary muscle in eyes with presbyopia before and after phacoemulsification and intracapsular lens implantation using ultrasound biomicroscopy (UBM). PATIENTS AND METHODS: This prospective study included 50 eyes of 30 consecutive subjects operated at the Department of Ophthalmology. Patients with any ocular disorder affecting visual acuity, corneal surface irregularities, had posterior capsular perforation or intensive postoperative corneal edema, or were <35 years of age, were excluded. A clear corneal phacoemulsification and posterior chamber intraocular lens were implanted. UBM was performed with and without instilling 2% pilocarpine. Ciliary body axial length (CBAXL), anterior chamber depth, and angle were measured before and 1 month after surgery.
RESULTS: The CBAXL showed a greater contractile shortening (P<0.5), with centripetal, contractile shift of ciliary muscle mass.
CONCLUSION: After phacoemulsification and intracapsular lens implantation, ultrasonic biomicroscopy showed significant centripetal movement of the ciliary body compared with that before surgery. This shows that a lenticular sclerotic component may influence both lens movement and the contractility of the ciliary muscle and is believed to be related to the presbyopia.

Entities:  

Keywords:  accommodation; ciliary body; intraocular lens; pilocarpine; presbyopia

Year:  2017        PMID: 28515637      PMCID: PMC5424599          DOI: 10.2147/OPTH.S131399

Source DB:  PubMed          Journal:  Clin Ophthalmol        ISSN: 1177-5467


Introduction

Accommodation is the ability of the eye to modify the overall refractive power to deliver a sharp, image of near objects on the retina.1,2 The procedure is unquestionably administered by ciliary muscle contraction, the ciliary body moves and releases strain on the zonules that allow the lens equator to move away from the sclera, which allows the capsule to mold the young lens into a thicker, more convex, and dioptrically powerful form.3,4 Details concerning how ciliary muscle contraction influences zonular tension and the roles of the posterior zonules, iris, and vitreous body in accommodation remain unclear.1,5,6 During accommodation, the ciliary muscles contract and the ciliary body moves forward and inward, releasing tension on the zonules, which allows the lens equatorial diameter to decrease with an increase in the lens anteroposterior thickness.1,2 Magnetic resonance imaging has shown age-related decreases in the ciliary ring diameter in humans, which might affect accommodation and presbyopia.2 Ultrasound biomicroscopy (UBM) has shown greater displacement of the characteristics contour points of the ciliary body in younger volunteers than in older volunteers during accommodation.1,3 The goal of this in vivo study was to analyze the configurational changes of human ciliary muscles with accommodation before and after cataract surgery.

Patients and methods

Fifty eyes of 30 patients aged between 48 and 70 years with cataracts were included. Each eye underwent complete ophthalmic examination that included the best-corrected visual acuity, refraction, and indirect ophthalmoscopy. Subjects with eye disease affecting visual acuity, corneal surface irregularities, spherical refraction >−2.0 D, posterior capsular perforation, or intensive postoperative corneal edema, or were aged <35 years, were excluded. A clear corneal phacoemulsification was performed, and posterior chamber intraocular lens (AcrySof SA60AT; Alcon Laboratories, Fort Worth, TX, USA) were implanted. UBM was performed using an UBM 45 system (paradigm) 50 MHz transducer probe that allowed for a 4–5 mm tissue penetration and ~50 μm resolution. The UBM examination was performed before and 30 minutes after instilling 2% pilocarpine hydrochloride to induce accommodative changes in the ciliary body. Scanning of the iridocorneal angle, including the ciliary body, was acquired at nasal and temporal quadrants. Image analysis was performed using software caliper to measure the following parameters: width measurements with caliper positioned perpendicular to the ciliary muscle–sclera boundary (Figure 1A); overall visible ciliary muscle length that was defined as the anteroposterior distance from the scleral spur to the posterior tip of the ciliary muscle (Figure 1B); ACD (anterior chamber depth) (Figure 2A and B); CBAXL (ciliary body axial length), which was defined as a line passing through the apex of the dome-shaped ciliary body and the center of ciliary body (Figure 3); SCPA (scleral ciliary process angle); three width measures were acquired, selected because of the known anterior shift of the ciliary muscle with contraction.7,8 The parameters were measured using the methods reported by Pavlin et al.9 The average of the parameters from the temporal quadrants was used in the analysis. Two months after the operation, the same parameters were measured again using UBM.
Figure 1

(A) Width measurements with caliper positioned perpendicular to the ciliary muscle–sclera and (B) visible ciliary muscle length from the scleral spur to the posterior tip of the ciliary muscle (red line).

Abbreviation: CB, ciliary body.

Figure 2

Anterior chamber depth (A) before and (B) after cataract surgery (red line extends from corneal endothelium to the anterior lens surface).

Figure 3

Ciliary body axial length, line passing through the apex of the dome-shaped ciliary body and the center of ciliary body (red line).

The participants provided written informed consent before examination. The consent form was approved by the ethics committee. The study was approved by the Review Boards and Ethics Committee of Banha University. This study adhered to the tenants of the Declaration of Helsinki.

Results

Mean objective accommodative changes after pilocarpine instillation are summarized in Table 1.
Table 1

The ultrasound biomicroscopy measurement of the angle configuration of the eyes with and without pilocarpine instillation before and after cataract surgery

ParameterPreoperative
P-valuePostoperative
P-value
Pilocarpine −Pilocarpine +Pilocarpine −Pilocarpine +
ACD3.533 mm2.968 mm<0.53.870 mm3.690 mm<0.5
CBAXL1.699 mm1.685 mm0.21.898 mm1.668 mm<0.5
SCPA40.1139.500.341.9536.67<0.5

Abbreviations: ACD, anterior chamber depth; CBAXL, ciliary body axial length; SCPA, scleral ciliary process angle; pilocarpine (−), before pilocarpine; pilocarpine (+), after pilocarpine.

The UBM parameters from the temporal quadrants were used for statistical analysis. Considering ciliary muscle thickness, the CBAXL value with and without pilocarpine before cataract extraction was 1.699±0.150 mm and 1.685±0.180 mm, respectively. Applying unpaired Student’s t-test, there was no statistically significant difference in the mean CBAXL with and without pilocarpine before cataract extraction (P=0.2). There was a statistically significant difference in CBAXL value with and without pilocarpine after cataract extraction (P<0.5; Figures 4 and 5).
Figure 4

The CB appearance postoperative (after cataract surgery) before (A) and after (B) pilocarpine.

Abbreviation: CB, ciliary body.

Figure 5

Difference of CBAXL postoperative, before (A) and after (B) pilocarpine.

Abbreviation: CBAXL, ciliary body axial length.

The central ACD decreased significantly after pilocarpine instillation was 3.533 and 2.968 mm before and after pilocarpine, respectively. Cataract surgery deepened the anterior chamber significantly, the ACD before and after pilocarpine instillation was 3.870 and 3.690 mm, respectively, which contribute to the process of accommodation. With regard to mean relaxed ciliary muscle, the overall length was 3.950±4.3 mm. A statistically significant reduction in the overall ciliary muscle length during accommodation (3.800 mm) (after pilocarpine) was found (P<0.05). The shortening with accommodation was significant after cataract extraction (3.542 mm) (P<0.001).

Discussion

Recent advances in ophthalmic imaging technology allow the ciliary muscle to be more easily visualized and imaged with sufficient resolution to detect accommodative changes.1,7,9–11 The amount of ciliary muscle contraction needed to produce a unit change in accommodation progressively increases with age.8 The precise role and functional relationships between the age-related changes in the ciliary muscles, zonular fibers, and lens are unclear due to the lack of dynamic measurement and difficulties in imaging the ocular element.8,10 In this study, we aimed to assess the changes in contractility of the ciliary muscle in eyes with presbyopia before and after phacoemulsification and intracapsular lens implantation using UBM. The CBAXL was used together with SCPA as an indicator of centripetal ciliary body movement during accommodation. A key finding in this study is that the centripetal CBAXL decreases significantly after cataract surgery. These findings are in agreement with previous studies done by Koeppl et al10 and Park et al.12 The accommodative shortening of the centripetal axial length of the ciliary muscle (P≤0.5) observed in this study supports the premise that suggests that cataract extraction results in a decrease in lens thickness, which leads to the improvement of ciliary body movement. This study reports a distinct decrease in accommodative SCPA after cataract extraction. These changes were reported by Kim et al13 and Park et al.12 The observed changes can be explained by iris posterior displacement that altered the ciliary body shape. After cataract surgery, the pilocarpine induced decrease (−0.180 mm) in the ACD that was in agreement with Koeppl et al.10

Conclusion

The absolute and percentage variation between active and relaxed accommodation including inward shift of human ciliary muscle mass during accommodation and optic movement forward supports the premise of the recovery of ciliary body contractility after cataract surgery.
  12 in total

1.  Scanning electron microscopic studies of the zonular apparatus in human and monkey eyes.

Authors:  J W Rohen
Journal:  Invest Ophthalmol Vis Sci       Date:  1979-02       Impact factor: 4.799

2.  Clinical use of ultrasound biomicroscopy.

Authors:  C J Pavlin; K Harasiewicz; M D Sherar; F S Foster
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3.  Ultrasound biomicroscopy of anterior segment structures in normal and glaucomatous eyes.

Authors:  C J Pavlin; K Harasiewicz; F S Foster
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4.  [Dynamic changes of configuration and position of human ciliary body during accommodation].

Authors:  Jia Ma; Xiao-ming Chen
Journal:  Zhonghua Yan Ke Za Zhi       Date:  2004-09

5.  Comparison of pilocarpine-induced and stimulus-driven accommodation in phakic eyes.

Authors:  Christina Koeppl; Oliver Findl; Katharina Kriechbaum; Wolfgang Drexler
Journal:  Exp Eye Res       Date:  2005-01-04       Impact factor: 3.467

6.  Biomechanical analysis of the accommodative apparatus in primates.

Authors:  Klaus Ehrmann; Arthur Ho; Jean-Marie Parel
Journal:  Clin Exp Optom       Date:  2008-02-15       Impact factor: 2.742

Review 7.  Ciliary body.

Authors:  E R Tamm; E Lütjen-Drecoll
Journal:  Microsc Res Tech       Date:  1996-04-01       Impact factor: 2.769

8.  Imaging of cyclodialysis cleft by ultrasound biomicroscope.

Authors:  W S Karwatowski; R N Weinreb
Journal:  Am J Ophthalmol       Date:  1994-04-15       Impact factor: 5.258

9.  Changes in anterior chamber configuration after cataract surgery as measured by anterior segment optical coherence tomography.

Authors:  Martha Kim; Ki Ho Park; Tae-Woo Kim; Dong Myung Kim
Journal:  Korean J Ophthalmol       Date:  2011-03-11

10.  The effect of cataract extraction on the contractility of ciliary muscle.

Authors:  Kyung-Ah Park; Jae-Ha Yun; Changwon Kee
Journal:  Am J Ophthalmol       Date:  2008-04-24       Impact factor: 5.258

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Authors:  Yu-Cherng Chang; Keke Liu; Florence Cabot; Sonia H Yoo; Marco Ruggeri; Arthur Ho; Jean-Marie Parel; Fabrice Manns
Journal:  Biomed Opt Express       Date:  2018-01-25       Impact factor: 3.732

2.  Ciliochoroidal detachment after Ahmed glaucoma valve implantation: a retrospective study.

Authors:  Lin Fu; Yau Kei Chan; Li Nie; Qi Dai; Zhenbin Qian; Kendrick Co Shih; Jimmy Shiu Ming Lai; Rong Huang; Weihua Pan
Journal:  BMC Ophthalmol       Date:  2019-02-06       Impact factor: 2.209

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