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Altered functional connectivity during hypoglycaemia in type 1 diabetes

Behavioural responses to hypoglycaemia require coordinated recruitment of broadly distributed networks of interacting brain regions. We investigated hypoglycaemia-related changes in brain connectivity in people without diabetes (ND) and with type 1 diabetes with normal (NAH) or impaired (IAH) hypogl...

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Autores principales: Jacob, Peter, Nwokolo, Munachiso, Cordon, Sally M, Macdonald, Ian A, Zelaya, Fernando O, Amiel, Stephanie A, O’Daly, Owen, Choudhary, Pratik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274862/
https://www.ncbi.nlm.nih.gov/pubmed/35209745
http://dx.doi.org/10.1177/0271678X221082911
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author Jacob, Peter
Nwokolo, Munachiso
Cordon, Sally M
Macdonald, Ian A
Zelaya, Fernando O
Amiel, Stephanie A
O’Daly, Owen
Choudhary, Pratik
author_facet Jacob, Peter
Nwokolo, Munachiso
Cordon, Sally M
Macdonald, Ian A
Zelaya, Fernando O
Amiel, Stephanie A
O’Daly, Owen
Choudhary, Pratik
author_sort Jacob, Peter
collection PubMed
description Behavioural responses to hypoglycaemia require coordinated recruitment of broadly distributed networks of interacting brain regions. We investigated hypoglycaemia-related changes in brain connectivity in people without diabetes (ND) and with type 1 diabetes with normal (NAH) or impaired (IAH) hypoglycaemia awareness. Two-step hyperinsulinaemic hypoglycaemic clamps were performed in 14 ND, 15 NAH and 22 IAH participants. BOLD timeseries were acquired at euglycaemia (5.0 mmol/L) and hypoglycaemia (2.6 mmol/L), with symptom and counter-regulatory hormone measurements. We investigated hypoglycaemia-related connectivity changes using established seed regions for the default mode (DMN), salience (SN) and central executive (CEN) networks and regions whose activity is modulated by hypoglycaemia: the thalamus and right inferior frontal gyrus (RIFG). Hypoglycaemia-induced changes in the DMN, SN and CEN were evident in NAH (all p < 0.05), with no changes in ND or IAH. However, in IAH there was a reduction in connectivity between regions within the RIFG (p = 0.001), not evident in the ND or NAH groups. We conclude that hypoglycaemia induces coordinated recruitment of the DMN and SN in diabetes with preserved hypoglycaemia awareness which is absent in IAH and ND. Changes in connectivity in the RIFG, a region associated with attentional modulation, may be key in impaired hypoglycaemia awareness.
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spelling pubmed-92748622022-07-13 Altered functional connectivity during hypoglycaemia in type 1 diabetes Jacob, Peter Nwokolo, Munachiso Cordon, Sally M Macdonald, Ian A Zelaya, Fernando O Amiel, Stephanie A O’Daly, Owen Choudhary, Pratik J Cereb Blood Flow Metab Original Articles Behavioural responses to hypoglycaemia require coordinated recruitment of broadly distributed networks of interacting brain regions. We investigated hypoglycaemia-related changes in brain connectivity in people without diabetes (ND) and with type 1 diabetes with normal (NAH) or impaired (IAH) hypoglycaemia awareness. Two-step hyperinsulinaemic hypoglycaemic clamps were performed in 14 ND, 15 NAH and 22 IAH participants. BOLD timeseries were acquired at euglycaemia (5.0 mmol/L) and hypoglycaemia (2.6 mmol/L), with symptom and counter-regulatory hormone measurements. We investigated hypoglycaemia-related connectivity changes using established seed regions for the default mode (DMN), salience (SN) and central executive (CEN) networks and regions whose activity is modulated by hypoglycaemia: the thalamus and right inferior frontal gyrus (RIFG). Hypoglycaemia-induced changes in the DMN, SN and CEN were evident in NAH (all p < 0.05), with no changes in ND or IAH. However, in IAH there was a reduction in connectivity between regions within the RIFG (p = 0.001), not evident in the ND or NAH groups. We conclude that hypoglycaemia induces coordinated recruitment of the DMN and SN in diabetes with preserved hypoglycaemia awareness which is absent in IAH and ND. Changes in connectivity in the RIFG, a region associated with attentional modulation, may be key in impaired hypoglycaemia awareness. SAGE Publications 2022-02-25 2022-08 /pmc/articles/PMC9274862/ /pubmed/35209745 http://dx.doi.org/10.1177/0271678X221082911 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Jacob, Peter
Nwokolo, Munachiso
Cordon, Sally M
Macdonald, Ian A
Zelaya, Fernando O
Amiel, Stephanie A
O’Daly, Owen
Choudhary, Pratik
Altered functional connectivity during hypoglycaemia in type 1 diabetes
title Altered functional connectivity during hypoglycaemia in type 1 diabetes
title_full Altered functional connectivity during hypoglycaemia in type 1 diabetes
title_fullStr Altered functional connectivity during hypoglycaemia in type 1 diabetes
title_full_unstemmed Altered functional connectivity during hypoglycaemia in type 1 diabetes
title_short Altered functional connectivity during hypoglycaemia in type 1 diabetes
title_sort altered functional connectivity during hypoglycaemia in type 1 diabetes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274862/
https://www.ncbi.nlm.nih.gov/pubmed/35209745
http://dx.doi.org/10.1177/0271678X221082911
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