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Prediabetes and structural brain abnormalities: Evidence from observational studies

Type 2 diabetes mellitus has been linked to structural brain abnormalities, but evidence of the association among prediabetes and structural brain abnormalities has not been systematically evaluated. Comprehensive searching strategies and relevant studies were systematically retrieved from PubMed, E...

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Autores principales: Zhou, Jian‐Bo, Tang, Xing‐Yao, Han, Yi‐Peng, Luo, Fu‐qiang, Cardoso, Marly Augusto, Qi, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685098/
https://www.ncbi.nlm.nih.gov/pubmed/31856401
http://dx.doi.org/10.1002/dmrr.3261
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author Zhou, Jian‐Bo
Tang, Xing‐Yao
Han, Yi‐Peng
Luo, Fu‐qiang
Cardoso, Marly Augusto
Qi, Lu
author_facet Zhou, Jian‐Bo
Tang, Xing‐Yao
Han, Yi‐Peng
Luo, Fu‐qiang
Cardoso, Marly Augusto
Qi, Lu
author_sort Zhou, Jian‐Bo
collection PubMed
description Type 2 diabetes mellitus has been linked to structural brain abnormalities, but evidence of the association among prediabetes and structural brain abnormalities has not been systematically evaluated. Comprehensive searching strategies and relevant studies were systematically retrieved from PubMed, Embase, Medline and web of science. Twelve articles were included overall. Stratified analyses and regression analyses were performed. A total of 104 468 individuals were included. The risk of infarct was associated with continuous glycosylated haemoglobin (HbA(1c)) [adjusted odds ratio (OR) 1.19 (95% confidence interval [CI]: 1.05‐1.34)], or prediabetes [adjusted OR 1.13 (95% CI: 1.00‐1.27)]. The corresponding ORs associated with white matter hyperintensities were 1.08 (95%CI: 1.04‐1.13) for prediabetes, and 1.10 (95%CI: 1.08‐1.12) for HbA(1c). The association was significant between the decreased risk of brain volume with continuous HbA(1c) (the combined OR 0.92, 95% CI: 0.87‐0.98). Grey matter volume and white matter volume were inversely associated with prediabetes [weighted mean deviation (WMD), −9.65 (95%CI: −15.25 to −4.04) vs WMD, −9.25 (95%CI: −15.03 to −3.47)]. There were no significant association among cerebral microbleeds, hippocampal volume, continuous total brain volume, and prediabetes. Our findings demonstrated that (a) both prediabetes and continuous HbA(1c) were significantly associated with increasing risk of infarct or white matter hyperintensities; (b) continuous HbA(1c) was associated with a decreased risk of brain volume; (c) prediabetes was inversely associated with grey matter volume and white matter volume. To confirm these findings, further studies on early diabetes onset and structural brain abnormalities are needed.
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spelling pubmed-76850982020-12-03 Prediabetes and structural brain abnormalities: Evidence from observational studies Zhou, Jian‐Bo Tang, Xing‐Yao Han, Yi‐Peng Luo, Fu‐qiang Cardoso, Marly Augusto Qi, Lu Diabetes Metab Res Rev Review Articles Type 2 diabetes mellitus has been linked to structural brain abnormalities, but evidence of the association among prediabetes and structural brain abnormalities has not been systematically evaluated. Comprehensive searching strategies and relevant studies were systematically retrieved from PubMed, Embase, Medline and web of science. Twelve articles were included overall. Stratified analyses and regression analyses were performed. A total of 104 468 individuals were included. The risk of infarct was associated with continuous glycosylated haemoglobin (HbA(1c)) [adjusted odds ratio (OR) 1.19 (95% confidence interval [CI]: 1.05‐1.34)], or prediabetes [adjusted OR 1.13 (95% CI: 1.00‐1.27)]. The corresponding ORs associated with white matter hyperintensities were 1.08 (95%CI: 1.04‐1.13) for prediabetes, and 1.10 (95%CI: 1.08‐1.12) for HbA(1c). The association was significant between the decreased risk of brain volume with continuous HbA(1c) (the combined OR 0.92, 95% CI: 0.87‐0.98). Grey matter volume and white matter volume were inversely associated with prediabetes [weighted mean deviation (WMD), −9.65 (95%CI: −15.25 to −4.04) vs WMD, −9.25 (95%CI: −15.03 to −3.47)]. There were no significant association among cerebral microbleeds, hippocampal volume, continuous total brain volume, and prediabetes. Our findings demonstrated that (a) both prediabetes and continuous HbA(1c) were significantly associated with increasing risk of infarct or white matter hyperintensities; (b) continuous HbA(1c) was associated with a decreased risk of brain volume; (c) prediabetes was inversely associated with grey matter volume and white matter volume. To confirm these findings, further studies on early diabetes onset and structural brain abnormalities are needed. John Wiley & Sons, Inc. 2019-12-19 2020-05 /pmc/articles/PMC7685098/ /pubmed/31856401 http://dx.doi.org/10.1002/dmrr.3261 Text en © 2019 The Authors. Diabetes/Metabolism Research and Reviews published by John Wiley & Sons Ltd 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 Review Articles
Zhou, Jian‐Bo
Tang, Xing‐Yao
Han, Yi‐Peng
Luo, Fu‐qiang
Cardoso, Marly Augusto
Qi, Lu
Prediabetes and structural brain abnormalities: Evidence from observational studies
title Prediabetes and structural brain abnormalities: Evidence from observational studies
title_full Prediabetes and structural brain abnormalities: Evidence from observational studies
title_fullStr Prediabetes and structural brain abnormalities: Evidence from observational studies
title_full_unstemmed Prediabetes and structural brain abnormalities: Evidence from observational studies
title_short Prediabetes and structural brain abnormalities: Evidence from observational studies
title_sort prediabetes and structural brain abnormalities: evidence from observational studies
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685098/
https://www.ncbi.nlm.nih.gov/pubmed/31856401
http://dx.doi.org/10.1002/dmrr.3261
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