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Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease
SIGNIFICANCE: Sickle cell disease (SCD), characterized by painful vaso-occlusive crises, is associated with cognitive decline. However, objective quantification of cognitive decline in SCD remains a challenge, and the associated hemodynamics are unknown. AIM: To address this, we utilized functional...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581024/ https://www.ncbi.nlm.nih.gov/pubmed/37854507 http://dx.doi.org/10.1117/1.NPh.10.4.045004 |
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author | Sunwoo, John Shah, Payal Thuptimdang, Wanwara Khaleel, Maha Chalacheva, Patjanaporn Kato, Roberta M. Coates, Thomas D. Khoo, Michael C. K. |
author_facet | Sunwoo, John Shah, Payal Thuptimdang, Wanwara Khaleel, Maha Chalacheva, Patjanaporn Kato, Roberta M. Coates, Thomas D. Khoo, Michael C. K. |
author_sort | Sunwoo, John |
collection | PubMed |
description | SIGNIFICANCE: Sickle cell disease (SCD), characterized by painful vaso-occlusive crises, is associated with cognitive decline. However, objective quantification of cognitive decline in SCD remains a challenge, and the associated hemodynamics are unknown. AIM: To address this, we utilized functional near-infrared spectroscopy (fNIRS) to measure prefrontal cortex (PFC) oxygenation responses to [Formula: see text]-back working memory tasks in SCD patients and compared them with healthy controls. APPROACH: We quantified the PFC oxygenation rate as an index of cognitive activity in each group and compared them. In half of the participants, a Stroop test was administered before they started [Formula: see text]-back to elevate their baseline stress level. RESULTS: In SCD compared to healthy controls, we found that (1) under a high baseline stress level, there were significantly greater oxygenation responses during the 2-back task, further elevated with histories of stroke; (2) there was a marginally slower [Formula: see text]-back response time, and it was even slower with a history of stroke; and (3) the task accuracy was not different. CONCLUSIONS: Additional requirements for processing time, PFC resources, and PFC oxygenation in SCD patients offer an important basis for understanding their cognitive decline and highlight the potential of fNIRS for evaluating cognitive functions. |
format | Online Article Text |
id | pubmed-10581024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-105810242023-10-18 Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease Sunwoo, John Shah, Payal Thuptimdang, Wanwara Khaleel, Maha Chalacheva, Patjanaporn Kato, Roberta M. Coates, Thomas D. Khoo, Michael C. K. Neurophotonics Research Papers SIGNIFICANCE: Sickle cell disease (SCD), characterized by painful vaso-occlusive crises, is associated with cognitive decline. However, objective quantification of cognitive decline in SCD remains a challenge, and the associated hemodynamics are unknown. AIM: To address this, we utilized functional near-infrared spectroscopy (fNIRS) to measure prefrontal cortex (PFC) oxygenation responses to [Formula: see text]-back working memory tasks in SCD patients and compared them with healthy controls. APPROACH: We quantified the PFC oxygenation rate as an index of cognitive activity in each group and compared them. In half of the participants, a Stroop test was administered before they started [Formula: see text]-back to elevate their baseline stress level. RESULTS: In SCD compared to healthy controls, we found that (1) under a high baseline stress level, there were significantly greater oxygenation responses during the 2-back task, further elevated with histories of stroke; (2) there was a marginally slower [Formula: see text]-back response time, and it was even slower with a history of stroke; and (3) the task accuracy was not different. CONCLUSIONS: Additional requirements for processing time, PFC resources, and PFC oxygenation in SCD patients offer an important basis for understanding their cognitive decline and highlight the potential of fNIRS for evaluating cognitive functions. Society of Photo-Optical Instrumentation Engineers 2023-10-17 2023-10 /pmc/articles/PMC10581024/ /pubmed/37854507 http://dx.doi.org/10.1117/1.NPh.10.4.045004 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Research Papers Sunwoo, John Shah, Payal Thuptimdang, Wanwara Khaleel, Maha Chalacheva, Patjanaporn Kato, Roberta M. Coates, Thomas D. Khoo, Michael C. K. Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title | Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title_full | Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title_fullStr | Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title_full_unstemmed | Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title_short | Functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
title_sort | functional near-infrared spectroscopy-based prefrontal cortex oxygenation during working memory tasks in sickle cell disease |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581024/ https://www.ncbi.nlm.nih.gov/pubmed/37854507 http://dx.doi.org/10.1117/1.NPh.10.4.045004 |
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