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Glycocalyx shedding patterns identifies antipsychotic-naïve patients with first-episode psychosis.
Andersen, Helle G; DellaValle, Brian; Bøgehave, Hjalte; Mogensen, Phillip Bredahl; Hahn, Margaret K; Goth, Christoffer K; Sørensen, Mikkel E; Sigvard, Anne K; Tangmose, Karen; Bojesen, Kirsten B; Nielsen, Mette Ø; Tonetto, Simone; Jørgensen, Mathias L; Hempel, Casper; Rungby, Jørgen; Glenthøj, Birte Y; Ambrosen, Karen S; Ebdrup, Bjørn H.
  • Andersen HG; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark; Copenhagen Research Centre for Mental Health and VIRTU Research Group, Mental Health
  • DellaValle B; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; GLX Analytix ApS, Copenhagen, Denmark.
  • Bøgehave H; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; GLX Analytix ApS, Copenhagen, Denmark.
  • Mogensen PB; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; GLX Analytix ApS, Copenhagen, Denmark.
  • Hahn MK; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark; Department of Psychiatry, University of Toronto, Toronto, ON, Canada; Centre for Addi
  • Goth CK; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; GLX Analytix ApS, Copenhagen, Denmark.
  • Sørensen ME; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
  • Sigvard AK; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
  • Tangmose K; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
  • Bojesen KB; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
  • Nielsen MØ; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University o
  • Tonetto S; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; Laboratory of Neuropsychiatry, Psychiatric Center Copenhagen, Copenhagen University Hospital, Copenhagen, Denmark; Department of Neuroscience, Faculty of Health and Medical S
  • Jørgensen ML; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark; GLX Analytix ApS, Copenhagen, Denmark.
  • Hempel C; GLX Analytix ApS, Copenhagen, Denmark; DTU Health, Department of Health Technology, Technical University of Denmark, Kgs. Lyngby, Denmark.
  • Rungby J; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark; Copenhagen Center for Translational Research, Copenhagen University Hospital, Bispebjerg and Frederiksberg Hospital, Denmark.
  • Glenthøj BY; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University o
  • Ambrosen KS; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
  • Ebdrup BH; Center for Neuropsychiatric Schizophrenia Research and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University o
Psychiatry Res ; 339: 116037, 2024 Jun 21.
Article en En | MEDLINE | ID: mdl-38959578
ABSTRACT
Psychotic disorders have been linked to immune-system abnormalities, increased inflammatory markers, and subtle neuroinflammation. Studies further suggest a dysfunctional blood brain barrier (BBB). The endothelial Glycocalyx (GLX) functions as a protective layer in the BBB, and GLX shedding leads to BBB dysfunction. This study aimed to investigate whether a panel of 11 GLX molecules derived from peripheral blood could differentiate antipsychotic-naïve first-episode psychosis patients (n47) from healthy controls (HC, n49) and whether GLX shedding correlated with symptom severity. Blood samples were collected at baseline and serum was isolated for GLX marker detection. Machine learning models were applied to test whether patterns in GLX markers could classify patient groups. Associations between GLX markers and symptom severity were explored. Patients showed significantly increased levels of three GLX markers compared to HC. Based on the panel of 11 GLX markers, machine learning models achieved a significant mean classification accuracy of 81%. Post hoc analysis revealed associations between increased GLX markers and symptom severity. This study demonstrates the potential of GLX molecules as immuno-neuropsychiatric biomarkers for early diagnosis of psychosis, as well as indicate a compromised BBB. Further research is warranted to explore the role of GLX in the early detection of psychotic disorders.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article