4.7 Article

Weighted network measures reveal differences between dementia types: An EEG study

期刊

HUMAN BRAIN MAPPING
卷 41, 期 6, 页码 1573-1590

出版社

WILEY
DOI: 10.1002/hbm.24896

关键词

Alzheimer's disease; biomarker; brain connectivity; graph theory; Lewy body; Parkinson's disease; proportional thresholding

资金

  1. National Institute for Health Research (NIHR) Newcastle Biomedical Research Centre (BRC)
  2. Wellcome Trust [WT088441MA]
  3. Medical Research Council [MR/T004347/1]
  4. MRC [MR/T004347/1] Funding Source: UKRI

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The diagnosis of dementia with Lewy bodies (DLB) versus Alzheimer's disease (AD) can be difficult especially early in the disease process. However, one inexpensive and non-invasive biomarker which could help is electroencephalography (EEG). Previous studies have shown that the brain network architecture assessed by EEG is altered in AD patients compared with age-matched healthy control people (HC). However, similar studies in Lewy body diseases, that is, DLB and Parkinson's disease dementia (PDD) are still lacking. In this work, we (a) compared brain network connectivity patterns across conditions, AD, DLB and PDD, in order to infer EEG network biomarkers that differentiate between these conditions, and (b) tested whether opting for weighted matrices led to more reliable results by better preserving the topology of the network. Our results indicate that dementia groups present with reduced connectivity in the EEG alpha band, whereas DLB shows weaker posterior-anterior patterns within the beta-band and greater network segregation within the theta-band compared with AD. Weighted network measures were more consistent across global thresholding levels, and the network properties reflected reduction in connectivity strength in the dementia groups. In conclusion, beta- and theta-band network measures may be suitable as biomarkers for discriminating DLB from AD, whereas the alpha-band network is similarly affected in DLB and PDD compared with HC. These variations may reflect the impairment of attentional networks in Parkinsonian diseases such as DLB and PDD.

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