Literature DB >> 9088735

Quasielastic light scattering study of the living human lens as a function of age.

G M Thurston1, D L Hayden, P Burrows, J I Clark, V G Taret, J Kandel, M Courogen, J A Peetermans, M S Bowen, D Miller, K M Sullivan, R Storb, H Stern, G B Benedek.   

Abstract

PURPOSE: To determine contributions of molecular scattering elements to the increase with age in the light scattered from the human ocular lens in vivo.
METHODS: We used quasielastic light scattering to measure autocorrelation functions of the intensity of light scattered in vivo from three locations (anterior, nuclear and posterior) along the optic axis in ocular lenses of 225 subjects, ranging from 17 to 63 years of age. We deduced probability distributions of key parameters (Is, If, Ii, IT), which describe contributions of slowly diffusing (Is), rapidly diffusing (If) and relatively immobile (Ii) scattering elements to the total light intensity (IT) scattered into the collection optics. We deduced characteristic time tau s and tau f that describe the Brownian motion of scattering elements.
RESULTS: Probability distributions for each age decile show clearly defined shifts in key parameters with age. IT at the nucleus increases by a factor of three from age 20 to 60 years. This increase is produced principally by an approximate five-fold increase is Is. IT and Is and can be detected with an accuracy of approximately +/- 10%. We estimate threshold values for IT, which mark the boundary beyond which clinical cataract becomes manifest. This boundary represents 6 to 8 times the light scattering efficiency expected from the newborn lens.
CONCLUSIONS: This methodology permits a sensitive, quantitative, clinically useful representation of the pre-cataractous molecular changes associated with aging in the living human lens.

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Year:  1997        PMID: 9088735     DOI: 10.1076/ceyr.16.3.197.15410

Source DB:  PubMed          Journal:  Curr Eye Res        ISSN: 0271-3683            Impact factor:   2.424


  11 in total

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3.  Self-assembly of protein aggregates in ageing disorders: the lens and cataract model.

Authors:  John I Clark
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-03-25       Impact factor: 6.237

4.  Mechanism of insolubilization by a single-point mutation in alphaA-crystallin linked with hereditary human cataracts.

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5.  RETRACTED: Peptide-induced formation of protein aggregates and amyloid fibrils in human and guinea pig αA-crystallins under physiological conditions of temperature and pH.

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6.  Analysis of nuclear fiber cell cytoplasmic texture in advanced cataractous lenses from Indian subjects using Debye-Bueche theory.

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7.  Automated, computerized, feature-based phenotype analysis of slit lamp images of the mouse lens.

Authors:  Jenny Yuen; Yi Li; Linda G Shapiro; John I Clark; Ernest Arnett; E Helene Sage; James F Brinkley
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8.  In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in Humans.

Authors:  Olga Minaeva; Srikant Sarangi; Danielle M Ledoux; Juliet A Moncaster; Douglas S Parsons; Kevin J Washicosky; Caitlin A Black; Frank J Weng; Maria Ericsson; Robert D Moir; Yorghos Tripodis; John I Clark; Rudolph E Tanzi; David G Hunter; Lee E Goldstein
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2020-09-16       Impact factor: 6.053

9.  Clinical detection of precataractous lens protein changes using dynamic light scattering.

Authors:  Manuel B Datiles; Rafat R Ansari; Kwang I Suh; Susan Vitale; George F Reed; J Samuel Zigler; Frederick L Ferris
Journal:  Arch Ophthalmol       Date:  2008-12

10.  Observational Clinical Studies of Human Lens Transparency Using the Vision Index Pen.

Authors:  Azin Abazari; Harbans S Dhadwal; John Wittpenn
Journal:  Transl Vis Sci Technol       Date:  2019-11-15       Impact factor: 3.283

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