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The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis
The mean kurtosis (MK) and fractional anisotropy (FA) in patients of Parkinson’s disease (PD) are usually measured by diffusion kurtosis imaging (DKI) and diffusion tensor imaging (DTI), separately. METHODS: In this study we perform a meta-analysis to discuss which noninvasive biomarker is more adva...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666087/ https://www.ncbi.nlm.nih.gov/pubmed/36397320 http://dx.doi.org/10.1097/MD.0000000000031312 |
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author | Huang, Songtao Dong, Yanchao Zhao, Jiaying |
author_facet | Huang, Songtao Dong, Yanchao Zhao, Jiaying |
author_sort | Huang, Songtao |
collection | PubMed |
description | The mean kurtosis (MK) and fractional anisotropy (FA) in patients of Parkinson’s disease (PD) are usually measured by diffusion kurtosis imaging (DKI) and diffusion tensor imaging (DTI), separately. METHODS: In this study we perform a meta-analysis to discuss which noninvasive biomarker is more advantageous for PD, MK, or FA. Databases including Medline via PubMed, the Cochrane Central Register of Controlled Trials, Embase via OVID and China National Knowledge Infrastructure. Databases are searched up to December 31st, 2019. Four brain regions are identified for analysis based on data extracted from articles. RESULTS: The articles contain 5 trials with 274 total PD patients and 189 healthy controls (HCs). The results show not only significantly higher MK values of putamen, caudate, globus pallidus in PD compared to that of HCs (weighted mean difference [WMD] = 0.06, 95% CI = 0.02–0.09, P = .002, WMD = 0.03, 95% CI = 0.01–0.067, P = .01, WMD = 0.18, 95% CI = 0.11–0.24, P < .00001), but also a significantly higher FA in caudate of PD compared to HCs (WMD = 0.02, 95% CI = 0.00–0.03, P = .006). CONCLUSION: This indicates that the sharp difference detected between PD patients and HCs can be detected by DKI and DTI. By further discussing results, we found that MK could be more sensitive diagnostic biomarker than FA toward PD diagnosis. |
format | Online Article Text |
id | pubmed-9666087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-96660872022-11-16 The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis Huang, Songtao Dong, Yanchao Zhao, Jiaying Medicine (Baltimore) 6800 The mean kurtosis (MK) and fractional anisotropy (FA) in patients of Parkinson’s disease (PD) are usually measured by diffusion kurtosis imaging (DKI) and diffusion tensor imaging (DTI), separately. METHODS: In this study we perform a meta-analysis to discuss which noninvasive biomarker is more advantageous for PD, MK, or FA. Databases including Medline via PubMed, the Cochrane Central Register of Controlled Trials, Embase via OVID and China National Knowledge Infrastructure. Databases are searched up to December 31st, 2019. Four brain regions are identified for analysis based on data extracted from articles. RESULTS: The articles contain 5 trials with 274 total PD patients and 189 healthy controls (HCs). The results show not only significantly higher MK values of putamen, caudate, globus pallidus in PD compared to that of HCs (weighted mean difference [WMD] = 0.06, 95% CI = 0.02–0.09, P = .002, WMD = 0.03, 95% CI = 0.01–0.067, P = .01, WMD = 0.18, 95% CI = 0.11–0.24, P < .00001), but also a significantly higher FA in caudate of PD compared to HCs (WMD = 0.02, 95% CI = 0.00–0.03, P = .006). CONCLUSION: This indicates that the sharp difference detected between PD patients and HCs can be detected by DKI and DTI. By further discussing results, we found that MK could be more sensitive diagnostic biomarker than FA toward PD diagnosis. Lippincott Williams & Wilkins 2022-11-11 /pmc/articles/PMC9666087/ /pubmed/36397320 http://dx.doi.org/10.1097/MD.0000000000031312 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 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 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 6800 Huang, Songtao Dong, Yanchao Zhao, Jiaying The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title | The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title_full | The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title_fullStr | The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title_full_unstemmed | The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title_short | The mean kurtosis (MK) is more sensitive diagnostic biomarker than fractional anisotropy (FA) for Parkinson’s disease: A diagnostic performance study and meta-analysis |
title_sort | mean kurtosis (mk) is more sensitive diagnostic biomarker than fractional anisotropy (fa) for parkinson’s disease: a diagnostic performance study and meta-analysis |
topic | 6800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666087/ https://www.ncbi.nlm.nih.gov/pubmed/36397320 http://dx.doi.org/10.1097/MD.0000000000031312 |
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