1.Fusion of electroencephalography multi-domain features and functional connectivity for early dementia recognition.
Wenwen CHANG ; Lei ZHENG ; Guanghui YAN ; Renjie LYU ; Wenchao NIE ; Bin GUO
Journal of Biomedical Engineering 2024;41(6):1119-1127
Dementia is a neurodegenerative disease closely related to brain network dysfunction. In this study, we assessed the interdependence between brain regions in patients with early-stage dementia based on phase-lock values, and constructed a functional brain network, selecting network feature parameters for metrics based on complex network analysis methods. At the same time, the entropy information characterizing the EEG signals in time domain, frequency domain and time-frequency domain, as well as the nonlinear dynamics features such as Hjorth and Hurst indexes were extracted, respectively. Based on the statistical analysis, the feature parameters with significant differences between different conditions were screened to construct feature vectors, and finally multiple machine learning algorithms were used to realize the recognition of early categories of dementia patients. The results showed that the fusion of multiple features performed well in the categorization of Alzheimer's disease, frontotemporal lobe dementia and healthy controls, especially in the identification of Alzheimer's disease and healthy controls, the accuracy of β-band reached 98%, which showed its effectiveness. This study provides new ideas for the early diagnosis of dementia and computer-assisted diagnostic methods.
Humans
;
Electroencephalography/methods*
;
Alzheimer Disease/physiopathology*
;
Dementia/physiopathology*
;
Early Diagnosis
;
Algorithms
;
Brain/physiopathology*
;
Machine Learning
;
Frontotemporal Dementia/physiopathology*
;
Diagnosis, Computer-Assisted
2.Identification of a rare platelet-specific antigen HPA-10bw allele among ethnic Han Chinese population in Shandong.
Jingru SHAO ; Wenchao LI ; Yingfang PAN ; Wenben QIAO ; Chuanfu ZHU ; Xiangmin NIE ; Yan LIU
Chinese Journal of Medical Genetics 2022;39(2):231-233
OBJECTIVE:
To study the polymorphism of human platelet antigen (HPA) system 10 among ethnic Han Chinese from Shandong, China so as to supplement the data of platelet donor bank in the region.
METHODS:
Peripheral blood samples of platelet donors from the region were genotyped for HPA-10 alleles by PCR-sequence specific primer (PCR-SSP) and direct sequencing.
RESULTS:
Among 1401 donors, a rare heterozygote carrier of HPA-10w (a+b+) was identified, which gave an allelic frequency of approximately 0.035%.
CONCLUSION
The detection of rare HPA-10bw antigen allele among ethnic Han Chinese from Shandong is useful for the diagnosis and prevention of neonatal alloimmune thrombocytopenia and post-transfusion purpura in the region.
Alleles
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Antigens, Human Platelet/genetics*
;
Asians/genetics*
;
Gene Frequency
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Genotype
;
Humans
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Infant, Newborn
;
Polymorphism, Genetic

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