TY - JOUR
T1 - Consensus paper of the WFSBP Task Force on Biological Markers
T2 - Criteria for biomarkers and endophenotypes of schizophrenia, part III: Molecular mechanisms
AU - The Members of the WFSBP Task Force on Biological Markers
AU - Schmitt, Andrea
AU - Martins-de-Souza, Daniel
AU - Akbarian, Schahram
AU - Cassoli, Juliana S.
AU - Ehrenreich, Hannelore
AU - Fischer, Andre
AU - Fonteh, Alfred
AU - Gattaz, Wagner F.
AU - Gawlik, Michael
AU - Gerlach, Manfred
AU - Grünblatt, Edna
AU - Halene, Tobias
AU - Hasan, Alkomiet
AU - Hashimoto, Kenij
AU - Kim, Yong Ku
AU - Kirchner, Sophie Kathrin
AU - Kornhuber, Johannes
AU - Kraus, Theo F.J.
AU - Malchow, Berend
AU - Nascimento, Juliana M.
AU - Rossner, Moritz
AU - Schwarz, Markus
AU - Steiner, Johann
AU - Talib, Leda
AU - Thibaut, Florence
AU - Riederer, Peter
AU - Falkai, Peter
N1 - Publisher Copyright:
© 2016 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2017/7/4
Y1 - 2017/7/4
N2 - Objectives: Despite progress in identifying molecular pathophysiological processes in schizophrenia, valid biomarkers are lacking for both the disease and treatment response. Methods: This comprehensive review summarises recent efforts to identify molecular mechanisms on the level of protein and gene expression and epigenetics, including DNA methylation, histone modifications and micro RNA expression. Furthermore, it summarises recent findings of alterations in lipid mediators and highlights inflammatory processes. The potential that this research will identify biomarkers of schizophrenia is discussed. Results: Recent studies have not identified clear biomarkers for schizophrenia. Although several molecular pathways have emerged as potential candidates for future research, a complete understanding of these metabolic pathways is required to reveal better treatment modalities for this disabling condition. Conclusions: Large longitudinal cohort studies are essential that pair a thorough phenotypic and clinical evaluation for example with gene expression and proteome analysis in blood at multiple time points. This approach might identify biomarkers that allow patients to be stratified according to treatment response and ideally also allow treatment response to be predicted. Improved knowledge of molecular pathways and epigenetic mechanisms, including their potential association with environmental influences, will facilitate the discovery of biomarkers that could ultimately be effective tools in clinical practice.
AB - Objectives: Despite progress in identifying molecular pathophysiological processes in schizophrenia, valid biomarkers are lacking for both the disease and treatment response. Methods: This comprehensive review summarises recent efforts to identify molecular mechanisms on the level of protein and gene expression and epigenetics, including DNA methylation, histone modifications and micro RNA expression. Furthermore, it summarises recent findings of alterations in lipid mediators and highlights inflammatory processes. The potential that this research will identify biomarkers of schizophrenia is discussed. Results: Recent studies have not identified clear biomarkers for schizophrenia. Although several molecular pathways have emerged as potential candidates for future research, a complete understanding of these metabolic pathways is required to reveal better treatment modalities for this disabling condition. Conclusions: Large longitudinal cohort studies are essential that pair a thorough phenotypic and clinical evaluation for example with gene expression and proteome analysis in blood at multiple time points. This approach might identify biomarkers that allow patients to be stratified according to treatment response and ideally also allow treatment response to be predicted. Improved knowledge of molecular pathways and epigenetic mechanisms, including their potential association with environmental influences, will facilitate the discovery of biomarkers that could ultimately be effective tools in clinical practice.
KW - Schizophrenia
KW - biomarkers
KW - epigenetics
KW - lipids
KW - proteomics
UR - http://www.scopus.com/inward/record.url?scp=84992417466&partnerID=8YFLogxK
U2 - 10.1080/15622975.2016.1224929
DO - 10.1080/15622975.2016.1224929
M3 - Review article
C2 - 27782767
AN - SCOPUS:84992417466
SN - 1562-2975
VL - 18
SP - 330
EP - 356
JO - World Journal of Biological Psychiatry
JF - World Journal of Biological Psychiatry
IS - 5
ER -