fNIRS-based brain state transition features to signify functional degeneration after Parkinson's disease

J Neural Eng. 2022 Aug 12;19(4). doi: 10.1088/1741-2552/ac861e.

Abstract

Objective.Parkinson's disease (PD) is a common neurodegenerative brain disorder, and early diagnosis is of vital importance for treatment. Existing methods are mainly focused on behavior examination, while the functional neurodegeneration after PD has not been well explored. This paper aims to investigate the brain functional variation of PD patients in comparison with healthy controls.Approach.In this work, we propose brain hemodynamic states and state transition features to signify functional degeneration after PD. Firstly, a functional near-infrared spectroscopy (fNIRS)-based experimental paradigm was designed to capture brain activation during dual-task walking from PD patients and healthy controls. Then, three brain states, named expansion, contraction, and intermediate states, were defined with respect to the oxyhemoglobin and deoxyhemoglobin responses. After that, two features were designed from a constructed transition factor and concurrent variations of oxy- and deoxy-hemoglobin over time, to quantify the transitions of brain states. Further, a support vector machine classifier was trained with the proposed features to distinguish PD patients and healthy controls.Main results.Experimental results showed that our method with the proposed brain state transition features achieved classification accuracy of 0.8200 andFscore of 0.9091, and outperformed existing fNIRS-based methods. Compared with healthy controls, PD patients had significantly smaller transition acceleration and transition angle.Significance.The proposed brain state transition features well signify functional degeneration of PD patients and may serve as promising functional biomarkers for PD diagnosis.

Keywords: Parkinson’s disease; brain hemodynamic states; brain state transition; fNIRS; functional degeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain
  • Humans
  • Oxyhemoglobins
  • Parkinson Disease* / diagnosis
  • Support Vector Machine
  • Walking

Substances

  • Oxyhemoglobins