Abstract:Accommodation in the human eye occurs through controlled changes in crystalline lens shape, thickness, and refractive surface placement relative to the cornea. The changes in lens curvatures, whether surface or internal, have been characterized as a function of accommodation and subject age by use of quantitative analysis of Scheimpflug slit-lamp photographic images. Radii of curvature of the major lens refractive surfaces--the external and nuclear boundaries--decrease linearly with increasing accommodation in… Show more
“…The age-related in vivo decline has been variously attributed to changes in lens surface curvature and refractive index distributions as well as, but less likely, alterations in other ocular components ([Atchison, 1995], [Fincham, 1937], [Glasser and Kaufman, 2003] and [Strenk et al ., 2005]). Recent studies on isolated lenses ([Borja et al ., 2008] and [Jones et al ., 2005]) indicate that the surfaces contribute only 20-40% of accommodated power change, most from the anterior surface ([Dubbleman et al ., 2005], [Fincham, 1937], [Garner and Yap, 1997] and [Koretz et al ., 2002]) and this changes little with age. Thus, alterations in the refractive index distribution, such as the development of the nuclear refractive index plateau (Augusteyn et al ., 2008), would be major factors responsible for the loss of power.…”
The purpose of this study was to study the age-dependence of the optomechanical properties of human lenses during simulated disaccommodation in a mechanical lens stretcher, designed to determine accommodative forces as a function of stretch distance, to compare the results with in vivo disaccommodation and to examine whether differences exist between eyes harvested in the USA and India.
Post-mortem human eyes obtained in the USA (n=46, age = 6 to 83 years) and India (n=91, age = 1 day to 85 years) were mounted in an optomechanical lens stretching system and dissected to expose the lens complete with its accommodating framework, including zonules, ciliary body, anterior vitreous and a segmented rim of sclera. Disaccommodation was simulated through radial stretching of the sectioned globe by 2 mm in increments of 0.25 mm. The load, inner ciliary ring diameter, lens equatorial diameter, central thickness and power were measured at each step. Changes in these parameters were examined as a function of age, as were the dimension/load and power/load responses.
Unstretched lens diameter and thickness increased over the whole age range examined and were indistinguishable from those of in vivo lenses as well as those of in vitro lenses freed from zonular attachments. Stretching increased the diameter and decreased the thickness in all lenses examined but the amount of change decreased with age. Unstretched lens power decreased with age and the accommodative amplitude decreased to zero by age 45-50. The load required to produce maximum stretch was independent of age (median 80 mN) whereas the change in lens diameter and power per unit load decreased significantly with age.
The age related changes in the properties of human lenses, as observed in the lens stretching device, are similar to those observed in vivo and are consistent with the classical Helmholtz theory of accommodation. The response of lens diameter and power to disaccommodative (stretching) forces decreases with age, consistent with lens nuclear stiffening.
“…The age-related in vivo decline has been variously attributed to changes in lens surface curvature and refractive index distributions as well as, but less likely, alterations in other ocular components ([Atchison, 1995], [Fincham, 1937], [Glasser and Kaufman, 2003] and [Strenk et al ., 2005]). Recent studies on isolated lenses ([Borja et al ., 2008] and [Jones et al ., 2005]) indicate that the surfaces contribute only 20-40% of accommodated power change, most from the anterior surface ([Dubbleman et al ., 2005], [Fincham, 1937], [Garner and Yap, 1997] and [Koretz et al ., 2002]) and this changes little with age. Thus, alterations in the refractive index distribution, such as the development of the nuclear refractive index plateau (Augusteyn et al ., 2008), would be major factors responsible for the loss of power.…”
The purpose of this study was to study the age-dependence of the optomechanical properties of human lenses during simulated disaccommodation in a mechanical lens stretcher, designed to determine accommodative forces as a function of stretch distance, to compare the results with in vivo disaccommodation and to examine whether differences exist between eyes harvested in the USA and India.
Post-mortem human eyes obtained in the USA (n=46, age = 6 to 83 years) and India (n=91, age = 1 day to 85 years) were mounted in an optomechanical lens stretching system and dissected to expose the lens complete with its accommodating framework, including zonules, ciliary body, anterior vitreous and a segmented rim of sclera. Disaccommodation was simulated through radial stretching of the sectioned globe by 2 mm in increments of 0.25 mm. The load, inner ciliary ring diameter, lens equatorial diameter, central thickness and power were measured at each step. Changes in these parameters were examined as a function of age, as were the dimension/load and power/load responses.
Unstretched lens diameter and thickness increased over the whole age range examined and were indistinguishable from those of in vivo lenses as well as those of in vitro lenses freed from zonular attachments. Stretching increased the diameter and decreased the thickness in all lenses examined but the amount of change decreased with age. Unstretched lens power decreased with age and the accommodative amplitude decreased to zero by age 45-50. The load required to produce maximum stretch was independent of age (median 80 mN) whereas the change in lens diameter and power per unit load decreased significantly with age.
The age related changes in the properties of human lenses, as observed in the lens stretching device, are similar to those observed in vivo and are consistent with the classical Helmholtz theory of accommodation. The response of lens diameter and power to disaccommodative (stretching) forces decreases with age, consistent with lens nuclear stiffening.
“…Although a Scheimpfl ug system could not compete in resolution with anterior segment optical coherence tomography (OCT), 15 which otherwise should also be corrected from optical distortion, 16,17 the large depth of focus in Scheimpfl ug images allows full cross-sections of the anterior segment, from the anterior cornea to the posterior lens, in a single snapshot generally not possible with OCT. Applications of corrected Scheimpfl ug crystalline lens/IOL in vivo imaging include customized eye modeling, 18,19 studies of quantitative changes of crystalline lens morphology with accommodation, 11,[20][21][22] aging, 6,23 or disease, 24 and assessment of new intraocular implants and surgical approaches for the correction of presbyopia. 25 …”
PURPOSE: To implement geometrical and optical distortion correction methods for anterior segment Scheimpfl ug images obtained with a commercially available system (Pentacam, Oculus Optikgeräte GmbH).
METHODS:Ray tracing algorithms were implemented to obtain corrected ocular surface geometry from the original images captured by the Pentacam's CCD camera. As details of the optical layout were not fully provided by the manufacturer, an iterative procedure (based on imaging of calibrated spheres) was developed to estimate the camera lens specifi cations. The correction procedure was tested on Scheimpfl ug images of a physical water cell model eye (with polymethylmethacrylate cornea and a commercial IOL of known dimensions) and of a normal human eye previously measured with a corrected optical and geometrical distortion Scheimpfl ug camera (Topcon SL-45 [Topcon Medical Systems Inc] from the Vrije University, Amsterdam, Holland).
RESULTS:Uncorrected Scheimpfl ug images show fl atter surfaces and thinner lenses than in reality. The application of geometrical and optical distortion correction algorithms improves the accuracy of the estimated anterior lens radii of curvature by 30% to 40% and of the estimated posterior lens by 50% to 100%. The average error in the retrieved radii was 0.37 and 0.46 mm for the anterior and posterior lens radii of curvature, respectively, and 0.048 mm for lens thickness.
CONCLUSIONS:The Pentacam Scheimpfl ug system can be used to obtain quantitative information on the geometry of the crystalline lens, provided that geometrical and optical distortion correction algorithms are applied, within the accuracy of state-of-the art phakometry and biometry. The techniques could improve with exact knowledge of the technical specifi cations of the instrument, improved edge detection algorithms, consideration of aspheric and non-rotationally symmetrical surfaces, and introduction of a crystalline gradient index.
“…This reshaping results from a reorganization of the lens cortical fibers and nucleus (Koretz and Handelman, 1982). Coordinated sliding of the fiber cell basal and apical tips (Kuszak et al, 2006) gives the lens the ability to mold around the shape of the lens nucleus (Brown, 1973; Koretz et al, 2002). …”
Section: The Role Of the Capsule In Lens Accommodationmentioning
The lens capsule is a modified basement membrane that completely surrounds the ocular lens. It is known that this extracellular matrix is important for both the structure and biomechanics of the lens in addition to providing informational cues to maintain lens cell phenotype. This review covers the development and structure of the lens capsule, lens diseases associated with mutations in extracellular matrix genes and the role of the capsule in lens function including those proposed for visual accommodation, selective permeability to infectious agents, and cell signaling.
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