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Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy

MicroRNAs (miRNAs/miRs) are involved in the pathogenesis of diabetes mellitus and its chronic complications, and their circulating levels have emerged as potential biomarkers for the development and progression of diabetes. However, few studies have examined the expression of miRNAs in diabetic reti...

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Autores principales: Dantas da Costa e Silva, Maria Enoia, Polina, Evelise Regina, Crispim, Daisy, Sbruzzi, Renan Cesar, Lavinsky, Daniel, Mallmann, Felipe, Martinelli, Nidiane Carla, Canani, Luis Henrique, dos Santos, Katia Gonçalves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349208/
https://www.ncbi.nlm.nih.gov/pubmed/30467971
http://dx.doi.org/10.1111/jcmm.14030
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author Dantas da Costa e Silva, Maria Enoia
Polina, Evelise Regina
Crispim, Daisy
Sbruzzi, Renan Cesar
Lavinsky, Daniel
Mallmann, Felipe
Martinelli, Nidiane Carla
Canani, Luis Henrique
dos Santos, Katia Gonçalves
author_facet Dantas da Costa e Silva, Maria Enoia
Polina, Evelise Regina
Crispim, Daisy
Sbruzzi, Renan Cesar
Lavinsky, Daniel
Mallmann, Felipe
Martinelli, Nidiane Carla
Canani, Luis Henrique
dos Santos, Katia Gonçalves
author_sort Dantas da Costa e Silva, Maria Enoia
collection PubMed
description MicroRNAs (miRNAs/miRs) are involved in the pathogenesis of diabetes mellitus and its chronic complications, and their circulating levels have emerged as potential biomarkers for the development and progression of diabetes. However, few studies have examined the expression of miRNAs in diabetic retinopathy (DR) in humans. This case‐control study aimed to investigate whether the plasma levels of miR‐29b and miR‐200b are associated with DR in 186 South Brazilians with type 2 diabetes (91 without DR, 46 with non‐proliferative DR and 49 with proliferative DR). We also included 20 healthy blood donors to determine the miRNA expression in the general population. Plasma levels of miR‐29b and miR‐200b were quantified by reverse transcription‐quantitative polymerase chain reaction (RT‐qPCR). Proliferative DR was inversely associated with plasma levels of miR‐29b (unadjusted OR = 0.694, 95% CI: 0.535‐0.900, P = 0.006) and miR‐200b (unadjusted OR = 0.797, 95% CI: 0.637‐0.997, P = 0.047). However, these associations were lost after controlling for demographic and clinical covariates. In addition, patients with type 2 diabetes had lower miR‐200b levels than blood donors. Our findings reinforce the importance of addressing the role of circulating miRNAs, including miR‐29 and miR‐200b, in DR.
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spelling pubmed-63492082019-02-01 Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy Dantas da Costa e Silva, Maria Enoia Polina, Evelise Regina Crispim, Daisy Sbruzzi, Renan Cesar Lavinsky, Daniel Mallmann, Felipe Martinelli, Nidiane Carla Canani, Luis Henrique dos Santos, Katia Gonçalves J Cell Mol Med Original Articles MicroRNAs (miRNAs/miRs) are involved in the pathogenesis of diabetes mellitus and its chronic complications, and their circulating levels have emerged as potential biomarkers for the development and progression of diabetes. However, few studies have examined the expression of miRNAs in diabetic retinopathy (DR) in humans. This case‐control study aimed to investigate whether the plasma levels of miR‐29b and miR‐200b are associated with DR in 186 South Brazilians with type 2 diabetes (91 without DR, 46 with non‐proliferative DR and 49 with proliferative DR). We also included 20 healthy blood donors to determine the miRNA expression in the general population. Plasma levels of miR‐29b and miR‐200b were quantified by reverse transcription‐quantitative polymerase chain reaction (RT‐qPCR). Proliferative DR was inversely associated with plasma levels of miR‐29b (unadjusted OR = 0.694, 95% CI: 0.535‐0.900, P = 0.006) and miR‐200b (unadjusted OR = 0.797, 95% CI: 0.637‐0.997, P = 0.047). However, these associations were lost after controlling for demographic and clinical covariates. In addition, patients with type 2 diabetes had lower miR‐200b levels than blood donors. Our findings reinforce the importance of addressing the role of circulating miRNAs, including miR‐29 and miR‐200b, in DR. John Wiley and Sons Inc. 2018-11-23 2019-02 /pmc/articles/PMC6349208/ /pubmed/30467971 http://dx.doi.org/10.1111/jcmm.14030 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Dantas da Costa e Silva, Maria Enoia
Polina, Evelise Regina
Crispim, Daisy
Sbruzzi, Renan Cesar
Lavinsky, Daniel
Mallmann, Felipe
Martinelli, Nidiane Carla
Canani, Luis Henrique
dos Santos, Katia Gonçalves
Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title_full Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title_fullStr Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title_full_unstemmed Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title_short Plasma levels of miR‐29b and miR‐200b in type 2 diabetic retinopathy
title_sort plasma levels of mir‐29b and mir‐200b in type 2 diabetic retinopathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349208/
https://www.ncbi.nlm.nih.gov/pubmed/30467971
http://dx.doi.org/10.1111/jcmm.14030
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