Cargando…
HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis
OBJECTIVE: To explore the association between glycated hemoglobin (A1C) variability and renal disease progression in patients with diabetes mellitus. METHODS: A comprehensive search was performed using the PubMed and Embase databases (up to April 26, 2014). The hazard ratio (HR) was pooled per unit...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270779/ https://www.ncbi.nlm.nih.gov/pubmed/25521346 http://dx.doi.org/10.1371/journal.pone.0115509 |
_version_ | 1782349540448272384 |
---|---|
author | Cheng, Dongsheng Fei, Yang Liu, Yumei Li, Junhui Xue, Qin Wang, Xiaoxia Wang, Niansong |
author_facet | Cheng, Dongsheng Fei, Yang Liu, Yumei Li, Junhui Xue, Qin Wang, Xiaoxia Wang, Niansong |
author_sort | Cheng, Dongsheng |
collection | PubMed |
description | OBJECTIVE: To explore the association between glycated hemoglobin (A1C) variability and renal disease progression in patients with diabetes mellitus. METHODS: A comprehensive search was performed using the PubMed and Embase databases (up to April 26, 2014). The hazard ratio (HR) was pooled per unit increase in the standard deviation of A1C (A1C-SD) to evaluate the dose-response relationship between A1C-SD and the risk of nephropathy. RESULTS: Eight studies with a total of 17,758 subjects provided the HR for A1C-SD and were included in the final meta-analysis. The pooled HR results demonstrated that A1C-SD was significantly associated with the progression of renal status (HR for both T1DM and T2DM 1.43, 95% confidence interval [CI] 1.24–1.64; HR for T1DM 1.70, 95%CI 1.41–2.05; HR for T2DM 1.20, 95%CI 1.12–1.28). A1C-SD was significantly correlated with new-onset microalbuminuria (HR for T1DM 1.63, 95%CI 1.28–2.07; HR for T2DM 1.23, 95%CI 1.08–1.39). These outcomes were also supported in subgroup analyses. Furthermore, sensitivity analyses demonstrated that the results were robust. CONCLUSIONS: A1C variability is independently associated with the development of microalbuminuria and the progression of renal status in both type 1 and 2 diabetes patients. A standard method for measuring A1C variability is essential for further and deeper analyses. In addition, future studies should assess the effect of reducing A1C variability on nephropathy complication. |
format | Online Article Text |
id | pubmed-4270779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42707792014-12-26 HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis Cheng, Dongsheng Fei, Yang Liu, Yumei Li, Junhui Xue, Qin Wang, Xiaoxia Wang, Niansong PLoS One Research Article OBJECTIVE: To explore the association between glycated hemoglobin (A1C) variability and renal disease progression in patients with diabetes mellitus. METHODS: A comprehensive search was performed using the PubMed and Embase databases (up to April 26, 2014). The hazard ratio (HR) was pooled per unit increase in the standard deviation of A1C (A1C-SD) to evaluate the dose-response relationship between A1C-SD and the risk of nephropathy. RESULTS: Eight studies with a total of 17,758 subjects provided the HR for A1C-SD and were included in the final meta-analysis. The pooled HR results demonstrated that A1C-SD was significantly associated with the progression of renal status (HR for both T1DM and T2DM 1.43, 95% confidence interval [CI] 1.24–1.64; HR for T1DM 1.70, 95%CI 1.41–2.05; HR for T2DM 1.20, 95%CI 1.12–1.28). A1C-SD was significantly correlated with new-onset microalbuminuria (HR for T1DM 1.63, 95%CI 1.28–2.07; HR for T2DM 1.23, 95%CI 1.08–1.39). These outcomes were also supported in subgroup analyses. Furthermore, sensitivity analyses demonstrated that the results were robust. CONCLUSIONS: A1C variability is independently associated with the development of microalbuminuria and the progression of renal status in both type 1 and 2 diabetes patients. A standard method for measuring A1C variability is essential for further and deeper analyses. In addition, future studies should assess the effect of reducing A1C variability on nephropathy complication. Public Library of Science 2014-12-18 /pmc/articles/PMC4270779/ /pubmed/25521346 http://dx.doi.org/10.1371/journal.pone.0115509 Text en © 2014 Cheng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Cheng, Dongsheng Fei, Yang Liu, Yumei Li, Junhui Xue, Qin Wang, Xiaoxia Wang, Niansong HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title | HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title_full | HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title_fullStr | HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title_full_unstemmed | HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title_short | HbA1C Variability and the Risk of Renal Status Progression in Diabetes Mellitus: A Meta-Analysis |
title_sort | hba1c variability and the risk of renal status progression in diabetes mellitus: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270779/ https://www.ncbi.nlm.nih.gov/pubmed/25521346 http://dx.doi.org/10.1371/journal.pone.0115509 |
work_keys_str_mv | AT chengdongsheng hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT feiyang hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT liuyumei hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT lijunhui hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT xueqin hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT wangxiaoxia hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis AT wangniansong hba1cvariabilityandtheriskofrenalstatusprogressionindiabetesmellitusametaanalysis |