Trial Analysis of Brain Activity Information for the Presymptomatic Disease Detection of Rheumatoid Arthritis

Author:

Maeda Keisuke1ORCID,Ogawa Takahiro2ORCID,Kayama Tasuku3,Sasaki Takuya34,Tainaka Kazuki5,Murakami Masaaki6789,Haseyama Miki2ORCID

Affiliation:

1. Data-Driven Interdisciplinary Research Emergence Department, Hokkaido University, N-13, W-10, Kita-ku, Sapporo 060-0813, Japan

2. Faculty of Information Science and Technology, Hokkaido University, N-14, W-9, Kita-ku, Sapporo 060-0814, Japan

3. Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aramaki-Aoba, Aoba-ku, Sendai 980-8578, Japan

4. Department of Neuropharmacology, Tohoku University School of Medicine, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan

5. Department of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, 1-757 Asahimachi-dori, Chuo-ku, Niigata 951-8585, Japan

6. Division of Molecular Psychoimmunology, Institute for Genetic Medicine and Graduate School of Medicine, Hokkaido University, Kita-15, Nishi-7, Kita-ku, Sapporo 060-0815, Japan

7. Division of Molecular Neuroimmunology, National Institute for Physiological Sciences, Myodaiji, Okazaki 444-8585, Japan

8. Group of Quantum Immunology, National Institute for Quantum and Radiological Science and Technology (QST), 4-9-1 Anagawa, Inage 263-8555, Japan

9. Institute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Kita-21, Nishi-11, Kita-ku, Sapporo 001-0021, Japan

Abstract

This study presents a trial analysis that uses brain activity information obtained from mice to detect rheumatoid arthritis (RA) in its presymptomatic stages. Specifically, we confirmed that F759 mice, serving as a mouse model of RA that is dependent on the inflammatory cytokine IL-6, and healthy wild-type mice can be classified on the basis of brain activity information. We clarified which brain regions are useful for the presymptomatic detection of RA. We introduced a matrix completion-based approach to handle missing brain activity information to perform the aforementioned analysis. In addition, we implemented a canonical correlation-based method capable of analyzing the relationship between various types of brain activity information. This method allowed us to accurately classify F759 and wild-type mice, thereby identifying essential features, including crucial brain regions, for the presymptomatic detection of RA. Our experiment obtained brain activity information from 15 F759 and 10 wild-type mice and analyzed the acquired data. By employing four types of classifiers, our experimental results show that the thalamus and periaqueductal gray are effective for the classification task. Furthermore, we confirmed that classification performance was maximized when seven brain regions were used, excluding the electromyogram and nucleus accumbens.

Funder

AMED Moonshot

JSPS KAKENHI

Publisher

MDPI AG

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