Increased levels of N(ε)- Carboxy methyl lysine (N(ε)-CML) are associated with topographic alterations in retinal pigment epithelium: A preliminary study
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
27039312
DOI
10.1016/j.jdiacomp.2016.03.011
PII: S1056-8727(16)30048-4
Knihovny.cz E-resources
- Keywords
- Advanced glycation end product, Diabetic retinopathy, N(ε)- Carboxy methyl lysine, Retinal pigment epithelium, Spectral domain optical coherence tomography,
- MeSH
- Biomarkers blood MeSH
- Tertiary Care Centers MeSH
- Diabetes Mellitus, Type 2 complications MeSH
- Diabetic Retinopathy blood diagnostic imaging physiopathology MeSH
- Adult MeSH
- Glycated Hemoglobin analysis MeSH
- Middle Aged MeSH
- Humans MeSH
- Lysine analogs & derivatives blood MeSH
- Disease Progression MeSH
- Vitreoretinopathy, Proliferative blood complications diagnostic imaging physiopathology MeSH
- Prospective Studies MeSH
- Cross-Sectional Studies MeSH
- Regression Analysis MeSH
- Retinal Pigment Epithelium diagnostic imaging physiopathology MeSH
- Case-Control Studies MeSH
- Severity of Illness Index MeSH
- Up-Regulation * MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- Glycated Hemoglobin A MeSH
- hemoglobin A1c protein, human MeSH Browser
- Lysine MeSH
- N(6)-carboxymethyllysine MeSH Browser
PURPOSE: To evaluate the association of serum levels of N(ε)- Carboxy methyl lysine (N(ε)-CML), an advanced glycation end product with topographic alterations in retinal pigment epithelium (RPE) in diabetic retinopathy on spectral domain optical coherence tomography (SD-OCT). METHOD: Consecutive cases of type 2 diabetes mellitus with no retinopathy (n=20); non-proliferative diabetic retinopathy (n=20); proliferative diabetic retinopathy (n=20) and healthy controls (n=20) between the ages of 40 and 65years were included. RPE alterations were graded on segmentation map of SD-OCT: grade 0, No RPE alterations; grade 1, RPE alterations in up to two quadrants and grade 2, RPE alterations in more than two quadrants. Serum level of N(ε)-CML and glycated hemoglobin (HbA1c) was analyzed using the standard protocol. Statistical analysis was done. RESULTS: Significant increase in N(ε)-CML was observed with increased severity of diabetic retinopathy (F=34.1; p<0.0001). Fisher exact test revealed significant increase in grades of RPE alterations with increased severity of diabetic retinopathy (p<0.001). Univariate ordinal regression analysis was done to calculate the risk of progression in grades of RPE alteration with individual changes in variables like duration of diabetes (odds ratio=1.37; p=0.001), HbA1c (odds ratio=1.37; p=0.002) and Nε-CML (odds ratio=1.37; p<0.0001). Multivariate ordinal regression analysis for predicting progression in grades of RPE alteration revealed Nε-CML to be an independent predictor of increase in grades of RPE alteration (adjusted odds ratio=1.07; p<0.01) when duration of diabetes and HbA1c were held constant. CONCLUSION: Increase in serum levels of N(ε)- Carboxy methyl lysine is significantly associated with topographic alterations in RPE. Grades of RPE alteration increase significantly with increased severity of diabetic retinopathy.
Department of Community Medicine King George's Medical University Lucknow India
Department of Ophthalmology King George's Medical University Lucknow India
Developmental Toxicology Division Indian Institute of Toxicology Research Lucknow India
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