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Functional connectivity markers of depression in advanced Parkinson's disease
BACKGROUND: Depression is a common comorbid condition in Parkinson's disease and a major contributor to poor quality of life. Despite this, depression in PD is under-diagnosed due to overlapping symptoms and difficulties in the assessment of depression in cognitively impaired old patients. OBJE...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931212/ https://www.ncbi.nlm.nih.gov/pubmed/31869768 http://dx.doi.org/10.1016/j.nicl.2019.102130 |
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author | Lin, Hai Cai, Xiaodong Zhang, Doudou Liu, Jiali Na, Peng Li, Weiping |
author_facet | Lin, Hai Cai, Xiaodong Zhang, Doudou Liu, Jiali Na, Peng Li, Weiping |
author_sort | Lin, Hai |
collection | PubMed |
description | BACKGROUND: Depression is a common comorbid condition in Parkinson's disease and a major contributor to poor quality of life. Despite this, depression in PD is under-diagnosed due to overlapping symptoms and difficulties in the assessment of depression in cognitively impaired old patients. OBJECTIVES: This study is to explore functional connectivity markers of depression in PD patients using resting-state fMRI and help diagnose whether patients have depression or not. METHODS: We reviewed 156 advanced PD patients (duration > 5 years; 59 depressed ones) and 45 healthy control subjects who underwent a resting-state fMRI scanning. Functional connectivity analysis was employed to characterize intrinsic connectivity networks using group independent component analysis and extract connectivity features. Features were put into an all-relevant feature selection procedure within cross-validation loops, to identify features with significant discriminative power for classification. Random forest classifiers were built for depression diagnosis, on the basis of identified features. RESULTS: 42 intrinsic connectivity networks were identified and arranged into subcortical, auditory, somatomotor, visual, cognitive control, default-mode and cerebellar networks. Six features were significantly relevant to classification. They were connectivity within posterior cingulate cortex, within insula, between posterior cingulate cortex and insula/hippocampus+amygdala, between insula and precuneus, and between superior parietal lobule and medial prefrontal cortex. The mean accuracy achieved with classifiers to discriminate depressed patients from the non-depressed was 82.4%. CONCLUSIONS: Our findings provide preliminary evidence that resting-state functional connectivity can characterize depressed PD patients and help distinguish them from non-depressed ones. |
format | Online Article Text |
id | pubmed-6931212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-69312122019-12-30 Functional connectivity markers of depression in advanced Parkinson's disease Lin, Hai Cai, Xiaodong Zhang, Doudou Liu, Jiali Na, Peng Li, Weiping Neuroimage Clin Regular Article BACKGROUND: Depression is a common comorbid condition in Parkinson's disease and a major contributor to poor quality of life. Despite this, depression in PD is under-diagnosed due to overlapping symptoms and difficulties in the assessment of depression in cognitively impaired old patients. OBJECTIVES: This study is to explore functional connectivity markers of depression in PD patients using resting-state fMRI and help diagnose whether patients have depression or not. METHODS: We reviewed 156 advanced PD patients (duration > 5 years; 59 depressed ones) and 45 healthy control subjects who underwent a resting-state fMRI scanning. Functional connectivity analysis was employed to characterize intrinsic connectivity networks using group independent component analysis and extract connectivity features. Features were put into an all-relevant feature selection procedure within cross-validation loops, to identify features with significant discriminative power for classification. Random forest classifiers were built for depression diagnosis, on the basis of identified features. RESULTS: 42 intrinsic connectivity networks were identified and arranged into subcortical, auditory, somatomotor, visual, cognitive control, default-mode and cerebellar networks. Six features were significantly relevant to classification. They were connectivity within posterior cingulate cortex, within insula, between posterior cingulate cortex and insula/hippocampus+amygdala, between insula and precuneus, and between superior parietal lobule and medial prefrontal cortex. The mean accuracy achieved with classifiers to discriminate depressed patients from the non-depressed was 82.4%. CONCLUSIONS: Our findings provide preliminary evidence that resting-state functional connectivity can characterize depressed PD patients and help distinguish them from non-depressed ones. Elsevier 2019-12-13 /pmc/articles/PMC6931212/ /pubmed/31869768 http://dx.doi.org/10.1016/j.nicl.2019.102130 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Lin, Hai Cai, Xiaodong Zhang, Doudou Liu, Jiali Na, Peng Li, Weiping Functional connectivity markers of depression in advanced Parkinson's disease |
title | Functional connectivity markers of depression in advanced Parkinson's disease |
title_full | Functional connectivity markers of depression in advanced Parkinson's disease |
title_fullStr | Functional connectivity markers of depression in advanced Parkinson's disease |
title_full_unstemmed | Functional connectivity markers of depression in advanced Parkinson's disease |
title_short | Functional connectivity markers of depression in advanced Parkinson's disease |
title_sort | functional connectivity markers of depression in advanced parkinson's disease |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931212/ https://www.ncbi.nlm.nih.gov/pubmed/31869768 http://dx.doi.org/10.1016/j.nicl.2019.102130 |
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