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Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes
AIMS: Increased visit‐to‐visit glycaemic variability is independently associated with adverse outcomes in Type 2 diabetes. Our aim was to identify the patient characteristics associated with raised visit‐to‐visit glycaemic variability in people with Type 2 diabetes. METHODS: A case–control study was...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811920/ https://www.ncbi.nlm.nih.gov/pubmed/28755478 http://dx.doi.org/10.1111/dme.13435 |
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author | Noyes, J. D. Soto‐Pedre, E. Donnelly, L. A. Pearson, E. R. |
author_facet | Noyes, J. D. Soto‐Pedre, E. Donnelly, L. A. Pearson, E. R. |
author_sort | Noyes, J. D. |
collection | PubMed |
description | AIMS: Increased visit‐to‐visit glycaemic variability is independently associated with adverse outcomes in Type 2 diabetes. Our aim was to identify the patient characteristics associated with raised visit‐to‐visit glycaemic variability in people with Type 2 diabetes. METHODS: A case–control study was conducted to establish associations between HbA(1c) variability and clinical covariates in 10 130 people with Type 2 diabetes. Variability was calculated by two metrics [sd and coefficient of variation (CV)] from a minimum of four HbA(1c) readings obtained over a 4‐year period. High and low variability groups were defined as the top and bottom tertile of the sd or CV, and used in logistic regression analyses including a number of clinical and biochemical covariates. The analyses were stratified into low mean (< 53 mmol/mol; 7%) and high mean (≥ 53 mmol/mol; 7%) HbA(1c) groups. RESULTS: Findings were consistent across both HbA(1c) groups and variability metrics. Treatment, independent of other factors, was the most strongly associated covariate for the risk of high HbA(1c) variability. A six‐fold increased risk was observed in the low HbA(1c) group, between the most and least intense treatment regimens (P < 0.001). Similar findings were present in the high HbA(1c) group with a three‐fold increase in risk (P < 0.001). In addition, male gender, younger age, reduced HDL‐cholesterol and increased BMI were all found to be independently associated with raised visit‐to‐visit glycaemic variability. CONCLUSIONS: Intensive treatment resulting in low mean HbA(1c) was associated with marked increase in HbA(1c) variability. Irrespective of diabetes control, the greatest visit‐to‐visit variability was observed in young, insulin resistant men. |
format | Online Article Text |
id | pubmed-5811920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58119202018-02-16 Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes Noyes, J. D. Soto‐Pedre, E. Donnelly, L. A. Pearson, E. R. Diabet Med Research Articles AIMS: Increased visit‐to‐visit glycaemic variability is independently associated with adverse outcomes in Type 2 diabetes. Our aim was to identify the patient characteristics associated with raised visit‐to‐visit glycaemic variability in people with Type 2 diabetes. METHODS: A case–control study was conducted to establish associations between HbA(1c) variability and clinical covariates in 10 130 people with Type 2 diabetes. Variability was calculated by two metrics [sd and coefficient of variation (CV)] from a minimum of four HbA(1c) readings obtained over a 4‐year period. High and low variability groups were defined as the top and bottom tertile of the sd or CV, and used in logistic regression analyses including a number of clinical and biochemical covariates. The analyses were stratified into low mean (< 53 mmol/mol; 7%) and high mean (≥ 53 mmol/mol; 7%) HbA(1c) groups. RESULTS: Findings were consistent across both HbA(1c) groups and variability metrics. Treatment, independent of other factors, was the most strongly associated covariate for the risk of high HbA(1c) variability. A six‐fold increased risk was observed in the low HbA(1c) group, between the most and least intense treatment regimens (P < 0.001). Similar findings were present in the high HbA(1c) group with a three‐fold increase in risk (P < 0.001). In addition, male gender, younger age, reduced HDL‐cholesterol and increased BMI were all found to be independently associated with raised visit‐to‐visit glycaemic variability. CONCLUSIONS: Intensive treatment resulting in low mean HbA(1c) was associated with marked increase in HbA(1c) variability. Irrespective of diabetes control, the greatest visit‐to‐visit variability was observed in young, insulin resistant men. John Wiley and Sons Inc. 2017-08-17 2018-02 /pmc/articles/PMC5811920/ /pubmed/28755478 http://dx.doi.org/10.1111/dme.13435 Text en © 2017 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK This is an open access article under the terms of the Creative Commons Attribution (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 | Research Articles Noyes, J. D. Soto‐Pedre, E. Donnelly, L. A. Pearson, E. R. Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title | Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title_full | Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title_fullStr | Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title_full_unstemmed | Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title_short | Characteristics of people with high visit‐to‐visit glycaemic variability in Type 2 diabetes |
title_sort | characteristics of people with high visit‐to‐visit glycaemic variability in type 2 diabetes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811920/ https://www.ncbi.nlm.nih.gov/pubmed/28755478 http://dx.doi.org/10.1111/dme.13435 |
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