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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6349208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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