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Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus

BACKGROUND: Type 2 diabetes mellitus (T2DM) is a major cause of heart failure (HF) with preserved ejection fraction (HFpEF), usually presenting as left ventricular (LV) diastolic dysfunction. Thus, LV diastolic function should be considered a crucial marker of a preclinical form of DM-related cardia...

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Autores principales: Yokota, Shun, Tanaka, Hidekazu, Mochizuki, Yasuhide, Soga, Fumitaka, Yamashita, Kentaro, Tanaka, Yusuke, Shono, Ayu, Suzuki, Makiko, Sumimoto, Keiko, Mukai, Jun, Suto, Makiko, Takada, Hiroki, Matsumoto, Kensuke, Hirota, Yushi, Ogawa, Wataru, Hirata, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894492/
https://www.ncbi.nlm.nih.gov/pubmed/31805945
http://dx.doi.org/10.1186/s12933-019-0971-5
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author Yokota, Shun
Tanaka, Hidekazu
Mochizuki, Yasuhide
Soga, Fumitaka
Yamashita, Kentaro
Tanaka, Yusuke
Shono, Ayu
Suzuki, Makiko
Sumimoto, Keiko
Mukai, Jun
Suto, Makiko
Takada, Hiroki
Matsumoto, Kensuke
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
author_facet Yokota, Shun
Tanaka, Hidekazu
Mochizuki, Yasuhide
Soga, Fumitaka
Yamashita, Kentaro
Tanaka, Yusuke
Shono, Ayu
Suzuki, Makiko
Sumimoto, Keiko
Mukai, Jun
Suto, Makiko
Takada, Hiroki
Matsumoto, Kensuke
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
author_sort Yokota, Shun
collection PubMed
description BACKGROUND: Type 2 diabetes mellitus (T2DM) is a major cause of heart failure (HF) with preserved ejection fraction (HFpEF), usually presenting as left ventricular (LV) diastolic dysfunction. Thus, LV diastolic function should be considered a crucial marker of a preclinical form of DM-related cardiac dysfunction. However, the impact of glycemic variability (GV) on LV diastolic function in such patients remains unclear. METHODS: We studied 100 asymptomatic T2DM patients with preserved LV ejection fraction (LVEF) without coronary artery disease (age: 60 ± 14 years, female: 45%). GV was evaluated as standard deviation of blood glucose level using continuous glucose monitoring system for at least 72 consecutive hours. LV diastolic function was defined as mitral inflow E and mitral e’ annular velocities (E/e’), and > 14 was determined as abnormal. RESULTS: E/e’ in patients with high GV (≥ 35.9 mg/dL) was significantly higher than that in patients with low GV (11.3 ± 3.9 vs. 9.8 ± 2.8, p = 0.03) despite similar age, gender-distribution, and hemoglobin A1c (HbA1c). Multivariate logistic regression analysis showed that GV ≥ 35.9 mg/dL (odds ratio: 3.67; 95% confidence interval: 1.02–13.22; p < 0.05) was an independently associated factor, as was age, of E/e’ > 14. In sequential logistic models for the associations of LV diastolic dysfunction, one model based on clinical variables including age, gender and hypertension was not improved by addition of HbA1c (p = 0.67) but was improved by addition of high GV (p = 0.04). CONCLUSION: Since HFpEF is a syndrome caused by diverse agents, reducing GV may represent a potential new therapeutic strategy for the prevention of the development of HFpEF in T2DM patients.
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spelling pubmed-68944922019-12-11 Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus Yokota, Shun Tanaka, Hidekazu Mochizuki, Yasuhide Soga, Fumitaka Yamashita, Kentaro Tanaka, Yusuke Shono, Ayu Suzuki, Makiko Sumimoto, Keiko Mukai, Jun Suto, Makiko Takada, Hiroki Matsumoto, Kensuke Hirota, Yushi Ogawa, Wataru Hirata, Ken-ichi Cardiovasc Diabetol Original Investigation BACKGROUND: Type 2 diabetes mellitus (T2DM) is a major cause of heart failure (HF) with preserved ejection fraction (HFpEF), usually presenting as left ventricular (LV) diastolic dysfunction. Thus, LV diastolic function should be considered a crucial marker of a preclinical form of DM-related cardiac dysfunction. However, the impact of glycemic variability (GV) on LV diastolic function in such patients remains unclear. METHODS: We studied 100 asymptomatic T2DM patients with preserved LV ejection fraction (LVEF) without coronary artery disease (age: 60 ± 14 years, female: 45%). GV was evaluated as standard deviation of blood glucose level using continuous glucose monitoring system for at least 72 consecutive hours. LV diastolic function was defined as mitral inflow E and mitral e’ annular velocities (E/e’), and > 14 was determined as abnormal. RESULTS: E/e’ in patients with high GV (≥ 35.9 mg/dL) was significantly higher than that in patients with low GV (11.3 ± 3.9 vs. 9.8 ± 2.8, p = 0.03) despite similar age, gender-distribution, and hemoglobin A1c (HbA1c). Multivariate logistic regression analysis showed that GV ≥ 35.9 mg/dL (odds ratio: 3.67; 95% confidence interval: 1.02–13.22; p < 0.05) was an independently associated factor, as was age, of E/e’ > 14. In sequential logistic models for the associations of LV diastolic dysfunction, one model based on clinical variables including age, gender and hypertension was not improved by addition of HbA1c (p = 0.67) but was improved by addition of high GV (p = 0.04). CONCLUSION: Since HFpEF is a syndrome caused by diverse agents, reducing GV may represent a potential new therapeutic strategy for the prevention of the development of HFpEF in T2DM patients. BioMed Central 2019-12-05 /pmc/articles/PMC6894492/ /pubmed/31805945 http://dx.doi.org/10.1186/s12933-019-0971-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Yokota, Shun
Tanaka, Hidekazu
Mochizuki, Yasuhide
Soga, Fumitaka
Yamashita, Kentaro
Tanaka, Yusuke
Shono, Ayu
Suzuki, Makiko
Sumimoto, Keiko
Mukai, Jun
Suto, Makiko
Takada, Hiroki
Matsumoto, Kensuke
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title_full Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title_fullStr Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title_full_unstemmed Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title_short Association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
title_sort association of glycemic variability with left ventricular diastolic function in type 2 diabetes mellitus
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894492/
https://www.ncbi.nlm.nih.gov/pubmed/31805945
http://dx.doi.org/10.1186/s12933-019-0971-5
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