Raman spectroscopy of human vitreous collagen in diabetic retinopathy

Jerry M.D. Sebag*, Shuming Nie, K. Reiser, Nai Teng Yu

*Corresponding author for this work

Research output: Chapter in Book/Conference Proceeding/ReportConference Paper published in a bookpeer-review

Abstract

In diabetes nonenzymatic glycation alters collagen throughout the body resulting in the histopathology that underlies diabetic disease in several organs. In the eye such changes in vitreous collagen could contribute to vitreous degeneration and the progression of proliferative diabetic retinopathy. Previous studies have demonstrated early glycation and advanced endproducts in the vitreous of humans with proliferative diabetic retinopathy. Near-infrared Fourier-transform Raman spectroscopy was performed on vitreous obtained at surgery from diabetic patients and from non-diabetic control subjects. The findings were compared to measurements obtained in untreated and glycated (in vitro) rat-tail tendon collagen. The results demonstrated substantial changes in diabetic vitreous collagen resulting from glycation, most likely advanced glycation endproducts. This approach appears to be useful as a means of characterizing the molecular changes induced by diabetes. Furthermore, this technique could be developed as a way of quantifying these changes in vivo in several tissues, so as to gauge the severity of non-enzymatic glycation and monitor the response to therapy.

Original languageEnglish
Title of host publicationProceedings of SPIE - The International Society for Optical Engineering
PublisherPubl by Int Soc for Optical Engineering
Pages202-205
Number of pages4
ISBN (Print)0819407909
Publication statusPublished - 1992
Externally publishedYes
EventOphthalmic Technologies II - Los Angeles, CA, USA
Duration: 19 Jan 199221 Jan 1992

Publication series

NameProceedings of SPIE - The International Society for Optical Engineering
Volume1644
ISSN (Print)0277-786X

Conference

ConferenceOphthalmic Technologies II
CityLos Angeles, CA, USA
Period19/01/9221/01/92

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