The two ends of the spectrum: comparing chronic schizophrenia and premorbid latent schizotypy by actigraphy.

Journal: BMC psychiatry
Published Date:

Abstract

Motor activity alterations are key symptoms of psychiatric disorders like schizophrenia. Actigraphy, a non-invasive monitoring method, shows promise in early identification. This study characterizes Positive Schizotypy Factor (PSF) and Chronic Schizophrenia (CS) groups using actigraphic data from two databases. At Hauke Land University Hospital, data from patients with chronic schizophrenia were collected; separately, at the University of Szeged, healthy university students were recruited and screened for PSF tendencies toward schizotypy. Several types of features are extracted from both datasets. Machine learning algorithms using different feature sets achieved nearly 90-95% for the CS group and 70-85% accuracy for the PSF. By applying model-explaining tools to the well-performing models, we could conclude the movement patterns and characteristics of the groups. Our study indicates that in the PSF liability phase of schizophrenia, actigraphic features related to sleep are most significant, but as the disease progresses, both sleep and daytime activity patterns are crucial. These variations might be influenced by medication effects in the CF group, reflecting the broader challenges in schizophrenia research, where the drug-free study of patients remains difficult. Further studies should explore these features in the prodromal and clinical High-Risk groups to refine our understanding of the development of the disorder.

Authors

  • Szandra László
    Doctoral School of Interdisciplinary Medicine, Department of Medical Genetics, University of Szeged, Somogyi Béla Street 4., Szeged, 6720, Csongrád-Csanád, Hungary.
  • Ádám Nagy
    Department of Software Engineering, University of Szeged, Szeged, 6720, Csongrád-Csanád, Hungary. adam.nagy@inclouded.hu.
  • József Dombi
    University of Szeged, Interdisciplinary Excellence Centre, Hungary.
  • Emőke Adrienn Hompoth
    Department of Software Engineering, University of Szeged, Szeged, 6720, Csongrád-Csanád, Hungary.
  • Emese Rudics
    Doctoral School of Interdisciplinary Medicine, Department of Medical Genetics, University of Szeged, Somogyi Béla Street 4., Szeged, 6720, Csongrád-Csanád, Hungary.
  • Zoltán Szabó
    Department of Software Engineering, University of Szeged, Szeged, 6720, Csongrád-Csanád, Hungary.
  • András Dér
    HUN-REN Biological Research Centre, Institute of Biophysics, Temesvári Boulevard 62., Szeged, 6726, Csongrád-Csanád, Hungary.
  • András Búzás
    HUN-REN Biological Research Centre, Institute of Biophysics, Temesvári Boulevard 62., Szeged, 6726, Csongrád-Csanád, Hungary.
  • Zsolt János Viharos
    Institute for Computer Science and Control (SZTAKI), Center of Excellence in Production Informatics and Control, Hungarian Research Network (HUN-REN), Centre of Excellence of the Hungarian Academy of Sciences (MTA), Kende Street 13-17., H-1111, Budapest, Hungary.
  • Anh Tuan Hoang
    Institute of Engineering, HUTECH University, Ho Chi Minh City, Viet Nam.
  • Vilmos Bilicki
    Department of Software Engineering, University of Szeged, Dugonics tér 13, Szeged, 6720, Hungary.
  • István Szendi
    Department of Psychiatry, Kiskunhalas Semmelweis Hospital, Dr. Monszpart László Street 1., Kiskunhalas, 6400, Bács-Kiskun, Hungary.