Cargando…
Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control
BACKGROUND: Risky health decisions and impulse control profiles may impact on metabolic control in type 1 diabetes mellitus (T1DM). We hypothesize that the neural correlates of cognitive impulsivity and decision-making in T1DM relate to metabolic control trajectories. METHODS: We combined functional...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Diabetes Association
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723195/ https://www.ncbi.nlm.nih.gov/pubmed/35313394 http://dx.doi.org/10.4093/dmj.2021.0307 |
_version_ | 1784844113213915136 |
---|---|
author | Jorge, Helena Duarte, Isabel C. Paiva, Sandra Relvas, Ana Paula Castelo-Branco, Miguel |
author_facet | Jorge, Helena Duarte, Isabel C. Paiva, Sandra Relvas, Ana Paula Castelo-Branco, Miguel |
author_sort | Jorge, Helena |
collection | PubMed |
description | BACKGROUND: Risky health decisions and impulse control profiles may impact on metabolic control in type 1 diabetes mellitus (T1DM). We hypothesize that the neural correlates of cognitive impulsivity and decision-making in T1DM relate to metabolic control trajectories. METHODS: We combined functional magnetic resonance imaging (fMRI), measures of metabolic trajectories (glycosylated hemoglobin [HbA1c] over multiple time points) and behavioral assessment using a cognitive impulsivity paradigm, the Balloon Analogue Risk Task (BART), in 50 participants (25 T1DM and 25 controls). RESULTS: Behavioral results showed that T1DM participants followed a rigid conservative risk strategy along the iterative game. Imaging group comparisons showed that patients showed larger activation of reward related, limbic regions (nucleus accumbens, amygdala) and insula (interoceptive saliency network) in initial game stages. Upon game completion differences emerged in relation to error monitoring (anterior cingulate cortex [ACC]) and inhibitory control (inferior frontal gyrus). Importantly, activity in the saliency network (ACC and insula), which monitors interoceptive states, was related with metabolic trajectories, which was also found for limbic/reward networks. Parietal and posterior cingulate regions activated both in controls and patients with adaptive decision-making, and positively associated with metabolic trajectories. CONCLUSION: We found triple converging evidence when comparing metabolic trajectories, patients versus controls or risk averse (non-learners) versus patients who learned by trial and error. Dopaminergic reward and saliency (interoceptive and error monitoring) circuits show a tight link with impaired metabolic trajectories and cognitive impulsivity in T1DM. Activity in parietal and posterior cingulate are associated with adaptive trajectories. This link between reward-saliency-inhibition circuits suggests novel strategies for patient management. |
format | Online Article Text |
id | pubmed-9723195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-97231952022-12-14 Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control Jorge, Helena Duarte, Isabel C. Paiva, Sandra Relvas, Ana Paula Castelo-Branco, Miguel Diabetes Metab J Original Article BACKGROUND: Risky health decisions and impulse control profiles may impact on metabolic control in type 1 diabetes mellitus (T1DM). We hypothesize that the neural correlates of cognitive impulsivity and decision-making in T1DM relate to metabolic control trajectories. METHODS: We combined functional magnetic resonance imaging (fMRI), measures of metabolic trajectories (glycosylated hemoglobin [HbA1c] over multiple time points) and behavioral assessment using a cognitive impulsivity paradigm, the Balloon Analogue Risk Task (BART), in 50 participants (25 T1DM and 25 controls). RESULTS: Behavioral results showed that T1DM participants followed a rigid conservative risk strategy along the iterative game. Imaging group comparisons showed that patients showed larger activation of reward related, limbic regions (nucleus accumbens, amygdala) and insula (interoceptive saliency network) in initial game stages. Upon game completion differences emerged in relation to error monitoring (anterior cingulate cortex [ACC]) and inhibitory control (inferior frontal gyrus). Importantly, activity in the saliency network (ACC and insula), which monitors interoceptive states, was related with metabolic trajectories, which was also found for limbic/reward networks. Parietal and posterior cingulate regions activated both in controls and patients with adaptive decision-making, and positively associated with metabolic trajectories. CONCLUSION: We found triple converging evidence when comparing metabolic trajectories, patients versus controls or risk averse (non-learners) versus patients who learned by trial and error. Dopaminergic reward and saliency (interoceptive and error monitoring) circuits show a tight link with impaired metabolic trajectories and cognitive impulsivity in T1DM. Activity in parietal and posterior cingulate are associated with adaptive trajectories. This link between reward-saliency-inhibition circuits suggests novel strategies for patient management. Korean Diabetes Association 2022-11 2022-03-22 /pmc/articles/PMC9723195/ /pubmed/35313394 http://dx.doi.org/10.4093/dmj.2021.0307 Text en Copyright © 2022 Korean Diabetes Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jorge, Helena Duarte, Isabel C. Paiva, Sandra Relvas, Ana Paula Castelo-Branco, Miguel Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title | Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title_full | Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title_fullStr | Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title_full_unstemmed | Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title_short | Abnormal Responses in Cognitive Impulsivity Circuits Are Associated with Glycosylated Hemoglobin Trajectories in Type 1 Diabetes Mellitus and Impaired Metabolic Control |
title_sort | abnormal responses in cognitive impulsivity circuits are associated with glycosylated hemoglobin trajectories in type 1 diabetes mellitus and impaired metabolic control |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723195/ https://www.ncbi.nlm.nih.gov/pubmed/35313394 http://dx.doi.org/10.4093/dmj.2021.0307 |
work_keys_str_mv | AT jorgehelena abnormalresponsesincognitiveimpulsivitycircuitsareassociatedwithglycosylatedhemoglobintrajectoriesintype1diabetesmellitusandimpairedmetaboliccontrol AT duarteisabelc abnormalresponsesincognitiveimpulsivitycircuitsareassociatedwithglycosylatedhemoglobintrajectoriesintype1diabetesmellitusandimpairedmetaboliccontrol AT paivasandra abnormalresponsesincognitiveimpulsivitycircuitsareassociatedwithglycosylatedhemoglobintrajectoriesintype1diabetesmellitusandimpairedmetaboliccontrol AT relvasanapaula abnormalresponsesincognitiveimpulsivitycircuitsareassociatedwithglycosylatedhemoglobintrajectoriesintype1diabetesmellitusandimpairedmetaboliccontrol AT castelobrancomiguel abnormalresponsesincognitiveimpulsivitycircuitsareassociatedwithglycosylatedhemoglobintrajectoriesintype1diabetesmellitusandimpairedmetaboliccontrol |