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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...

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Detalles Bibliográficos
Autores principales: Noyes, J. D., Soto‐Pedre, E., Donnelly, L. A., Pearson, E. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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