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Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia

BACKGROUND: Diabetes often occurs together with tuberculosis (TB) and both may affect each other negatively. Diabetes may be associated with neurocognitive dysfunctioning in affected patients and may negatively impact treatment adherence and outcomes. This study compared the neurocognitive status be...

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Autores principales: Yorke, Ernest, Boima, Vincent, Dey, Ida Dzifa, Ganu, Vincent, Nkornu, Norah, Acquaye, Kelvin Samuel, Mate-Kole, C. Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119271/
https://www.ncbi.nlm.nih.gov/pubmed/32245444
http://dx.doi.org/10.1186/s12888-020-02570-8
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author Yorke, Ernest
Boima, Vincent
Dey, Ida Dzifa
Ganu, Vincent
Nkornu, Norah
Acquaye, Kelvin Samuel
Mate-Kole, C. Charles
author_facet Yorke, Ernest
Boima, Vincent
Dey, Ida Dzifa
Ganu, Vincent
Nkornu, Norah
Acquaye, Kelvin Samuel
Mate-Kole, C. Charles
author_sort Yorke, Ernest
collection PubMed
description BACKGROUND: Diabetes often occurs together with tuberculosis (TB) and both may affect each other negatively. Diabetes may be associated with neurocognitive dysfunctioning in affected patients and may negatively impact treatment adherence and outcomes. This study compared the neurocognitive status between newly diagnosed smear positive tuberculosis patients with dysglycaemia and those with normoglycaemia. METHODS: The current study was a cross-sectional study involving one hundred and forty-six (146) newly diagnosed smear positive TB patients. Oral glucose tolerance test (OGTT) was performed and the results were categorized as either normoglycaemia, impaired glucose tolerance (IGT), impaired fasting glucose (IFG) or diabetes. Neurocognitive functioning among study participants was assessed at the time of TB diagnosis using Cognitive Failure Questionnaire (CFQ), Montreal Cognitive Assessment tool (MoCA), California Verbal Learning Test (CVLT), Brief Symptom Inventory (BSI) and the Spitzer Quality of Life Index (QLI). RESULTS: The mean age of the participants (n = 146) was 38.7 years with 78.8% being males and 21.2% females. Using the fasting blood glucose test, the prevalence of impaired fasting glucose and diabetes were 5.5 and 3.4% respectively, both representing a total of 13 out of the 146 participants; whilst the prevalence of impaired glucose tolerance and diabetes using 2-h post-glucose values were 28.8 and 11.6% respectively, both representing a total of 59 out of the 146 participants. There were no significant differences in the mean scores on the neurocognitive measures between the dysglaycaemia and normoglycamic groups using fasting plasma glucose (FPG). However, there were significant differences in the mean scores between the dysglycaemia and normal groups using 2-h postprandial (2HPP) glucose values on Phobic Anxiety (Normal, Mean = 0.38 ± 0.603; dysglycaemia, Mean = 0.23 ± 0.356; p = 0.045), and Montreal Cognitive Assessment (MoCA) scores (17.26 ± 5.981 vs. 15.04 ± 5.834, p = 0.037). CONCLUSION: Newly diagnosed smear positive patients with dysglycaemia were associated with significantly lower mean cognitive scores and scores on phobic anxiety than those with normoglyacaemia. The latter finding must be further explored.
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spelling pubmed-71192712020-04-07 Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia Yorke, Ernest Boima, Vincent Dey, Ida Dzifa Ganu, Vincent Nkornu, Norah Acquaye, Kelvin Samuel Mate-Kole, C. Charles BMC Psychiatry Research Article BACKGROUND: Diabetes often occurs together with tuberculosis (TB) and both may affect each other negatively. Diabetes may be associated with neurocognitive dysfunctioning in affected patients and may negatively impact treatment adherence and outcomes. This study compared the neurocognitive status between newly diagnosed smear positive tuberculosis patients with dysglycaemia and those with normoglycaemia. METHODS: The current study was a cross-sectional study involving one hundred and forty-six (146) newly diagnosed smear positive TB patients. Oral glucose tolerance test (OGTT) was performed and the results were categorized as either normoglycaemia, impaired glucose tolerance (IGT), impaired fasting glucose (IFG) or diabetes. Neurocognitive functioning among study participants was assessed at the time of TB diagnosis using Cognitive Failure Questionnaire (CFQ), Montreal Cognitive Assessment tool (MoCA), California Verbal Learning Test (CVLT), Brief Symptom Inventory (BSI) and the Spitzer Quality of Life Index (QLI). RESULTS: The mean age of the participants (n = 146) was 38.7 years with 78.8% being males and 21.2% females. Using the fasting blood glucose test, the prevalence of impaired fasting glucose and diabetes were 5.5 and 3.4% respectively, both representing a total of 13 out of the 146 participants; whilst the prevalence of impaired glucose tolerance and diabetes using 2-h post-glucose values were 28.8 and 11.6% respectively, both representing a total of 59 out of the 146 participants. There were no significant differences in the mean scores on the neurocognitive measures between the dysglaycaemia and normoglycamic groups using fasting plasma glucose (FPG). However, there were significant differences in the mean scores between the dysglycaemia and normal groups using 2-h postprandial (2HPP) glucose values on Phobic Anxiety (Normal, Mean = 0.38 ± 0.603; dysglycaemia, Mean = 0.23 ± 0.356; p = 0.045), and Montreal Cognitive Assessment (MoCA) scores (17.26 ± 5.981 vs. 15.04 ± 5.834, p = 0.037). CONCLUSION: Newly diagnosed smear positive patients with dysglycaemia were associated with significantly lower mean cognitive scores and scores on phobic anxiety than those with normoglyacaemia. The latter finding must be further explored. BioMed Central 2020-04-03 /pmc/articles/PMC7119271/ /pubmed/32245444 http://dx.doi.org/10.1186/s12888-020-02570-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Yorke, Ernest
Boima, Vincent
Dey, Ida Dzifa
Ganu, Vincent
Nkornu, Norah
Acquaye, Kelvin Samuel
Mate-Kole, C. Charles
Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title_full Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title_fullStr Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title_full_unstemmed Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title_short Comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
title_sort comparison of neurocognitive changes among newly diagnosed tuberculosis patients with and without dysglycaemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119271/
https://www.ncbi.nlm.nih.gov/pubmed/32245444
http://dx.doi.org/10.1186/s12888-020-02570-8
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