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Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study

BACKGROUND: With the advance of subthalamic nucleus (STN) deep brain stimulation (DBS) in the treatment of Parkinson’s disease (PD), it is desired to identify objective criteria for the monitoring of the therapy outcome. This paper explores the feasibility of metabolic network derived from positron...

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Autores principales: Ge, Jingjie, Wang, Min, Lin, Wei, Wu, Ping, Guan, Yihui, Zhang, Huiwei, Huang, Zhemin, Yang, Likun, Zuo, Chuantao, Jiang, Jiehui, Rominger, Axel, Shi, Kuangyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596139/
https://www.ncbi.nlm.nih.gov/pubmed/33119814
http://dx.doi.org/10.1186/s13550-020-00722-1
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author Ge, Jingjie
Wang, Min
Lin, Wei
Wu, Ping
Guan, Yihui
Zhang, Huiwei
Huang, Zhemin
Yang, Likun
Zuo, Chuantao
Jiang, Jiehui
Rominger, Axel
Shi, Kuangyu
author_facet Ge, Jingjie
Wang, Min
Lin, Wei
Wu, Ping
Guan, Yihui
Zhang, Huiwei
Huang, Zhemin
Yang, Likun
Zuo, Chuantao
Jiang, Jiehui
Rominger, Axel
Shi, Kuangyu
author_sort Ge, Jingjie
collection PubMed
description BACKGROUND: With the advance of subthalamic nucleus (STN) deep brain stimulation (DBS) in the treatment of Parkinson’s disease (PD), it is desired to identify objective criteria for the monitoring of the therapy outcome. This paper explores the feasibility of metabolic network derived from positron emission tomography (PET) with (18)F-fluorodeoxyglucose in monitoring the STN DBS treatment for PD. METHODS: Age-matched 33 PD patients, 33 healthy controls (HCs), 9 PD patients with bilateral DBS surgery and 9 controls underwent (18)F-FDG PET scans. The DBS patients were followed longitudinally to investigate the alternations of the PD-related metabolic covariance pattern (PDRP) expressions. RESULTS: The PDRP expression was abnormally elevated in PD patients compared with HCs (P < 0.001). For DBS patients, a significant decrease in the Unified Parkinson’s Disease Rating Scale (UPDRS, P = 0.001) and PDRP expression (P = 0.004) was observed 3 months after STN DBS treatment, while a rollback was observed in both UPDRS and PDRP expressions (both P < 0.01) 12 months after treatment. The changes in PDRP expression mediated by STN DBS were generally in line with UPDRS improvement. The graphical network analysis shows increased connections at 3 months and a return at 12 months confirmed by small-worldness coefficient. CONCLUSIONS: The preliminary results demonstrate the potential of metabolic network expression as complimentary objective biomarker for the assessment and monitoring of STN DBS treatment in PD patients. Clinical Trial Registration ChiCTR-DOC-16008645. http://www.chictr.org.cn/showproj.aspx?proj=13865.
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spelling pubmed-75961392020-11-02 Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study Ge, Jingjie Wang, Min Lin, Wei Wu, Ping Guan, Yihui Zhang, Huiwei Huang, Zhemin Yang, Likun Zuo, Chuantao Jiang, Jiehui Rominger, Axel Shi, Kuangyu EJNMMI Res Original Research BACKGROUND: With the advance of subthalamic nucleus (STN) deep brain stimulation (DBS) in the treatment of Parkinson’s disease (PD), it is desired to identify objective criteria for the monitoring of the therapy outcome. This paper explores the feasibility of metabolic network derived from positron emission tomography (PET) with (18)F-fluorodeoxyglucose in monitoring the STN DBS treatment for PD. METHODS: Age-matched 33 PD patients, 33 healthy controls (HCs), 9 PD patients with bilateral DBS surgery and 9 controls underwent (18)F-FDG PET scans. The DBS patients were followed longitudinally to investigate the alternations of the PD-related metabolic covariance pattern (PDRP) expressions. RESULTS: The PDRP expression was abnormally elevated in PD patients compared with HCs (P < 0.001). For DBS patients, a significant decrease in the Unified Parkinson’s Disease Rating Scale (UPDRS, P = 0.001) and PDRP expression (P = 0.004) was observed 3 months after STN DBS treatment, while a rollback was observed in both UPDRS and PDRP expressions (both P < 0.01) 12 months after treatment. The changes in PDRP expression mediated by STN DBS were generally in line with UPDRS improvement. The graphical network analysis shows increased connections at 3 months and a return at 12 months confirmed by small-worldness coefficient. CONCLUSIONS: The preliminary results demonstrate the potential of metabolic network expression as complimentary objective biomarker for the assessment and monitoring of STN DBS treatment in PD patients. Clinical Trial Registration ChiCTR-DOC-16008645. http://www.chictr.org.cn/showproj.aspx?proj=13865. Springer Berlin Heidelberg 2020-10-29 /pmc/articles/PMC7596139/ /pubmed/33119814 http://dx.doi.org/10.1186/s13550-020-00722-1 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/.
spellingShingle Original Research
Ge, Jingjie
Wang, Min
Lin, Wei
Wu, Ping
Guan, Yihui
Zhang, Huiwei
Huang, Zhemin
Yang, Likun
Zuo, Chuantao
Jiang, Jiehui
Rominger, Axel
Shi, Kuangyu
Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title_full Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title_fullStr Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title_full_unstemmed Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title_short Metabolic network as an objective biomarker in monitoring deep brain stimulation for Parkinson’s disease: a longitudinal study
title_sort metabolic network as an objective biomarker in monitoring deep brain stimulation for parkinson’s disease: a longitudinal study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596139/
https://www.ncbi.nlm.nih.gov/pubmed/33119814
http://dx.doi.org/10.1186/s13550-020-00722-1
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