TY - JOUR
T1 - An Introduction to the Human Connectome Project for Early Psychosis
AU - Jacobs, Grace R.
AU - Coleman, Michael J.
AU - Lewandowski, Kathryn E.
AU - Pasternak, Ofer
AU - Cetin-Karayumak, Suheyla
AU - Mesholam-Gately, Raquelle I.
AU - Wojcik, Joanne
AU - Kennedy, Leda
AU - Knyazhanskaya, Evdokiya
AU - Reid, Benjamin
AU - Swago, Sophia
AU - Lyons, Monica G.
AU - Rizzoni, Elizabeth
AU - John, Omar
AU - Carrington, Holly
AU - Kim, Nicholas
AU - Kotler, Elana
AU - Veale, Simone
AU - Haidar, Anastasia
AU - Prunier, Nicholas
AU - Haaf, Moritz
AU - Levitt, James J.
AU - Seitz-Holland, Johanna
AU - Rathi, Yogesh
AU - Kubicki, Marek
AU - Keshavan, Matcheri S.
AU - Holt, Daphne J.
AU - Seidman, Larry J.
AU - Öngür, Dost
AU - Breier, Alan
AU - Bouix, Sylvain
AU - Shenton, Martha E.
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. All rights reserved
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Background: The time following a recent onset of psychosis is a critical period during which intervention may be maximally effective. Studying individuals in this period also offers an opportunity to investigate putative brain biomarkers of illness prior to the long-term effects of chronicity and medication. The Human Connectome Project for Early Psychosis (HCP-EP) was funded by the National Institutes of Mental Health (NIMH) as an extension of the original Human Connectome Project's approach to understanding the human brain and its structural and functional connections. Design: The HCP-EP data were collected at 3 sites in Massachusetts (Beth Israel Deaconess Medical Center, McLean Hospital, and Massachusetts General Hospital), and one site in Indiana (Indiana University). Brigham and Women's Hospital served as the data coordination center and as an imaging site. Results: The HCP-EP dataset includes high-quality clinical, cognitive, functional, neuroimaging, and blood specimen data acquired from 303 individuals between the ages of 16-35 years old with affective psychosis (nâ...=â...75), non-affective psychosis (nâ...=â...148), and healthy controls (nâ...=â...80). Participants with early psychosis were within 5 years of illness onset (mean durationâ...=â...1.9 years, standard deviationâ...=â...1.4 years). All data and novel or modified analytic tools developed as part of the study are publicly available to the research community through the NIMH Data Archive (NDA) or GitHub (https://github.com/pnlbwh). Conclusions: This paper provides an overview of the specific HCP-EP procedures, assessments, and protocols, as well as a brief characterization of the study participants to make it easier for researchers to use this rich dataset. Although we focus here on discussing and comparing affective and non-affective psychosis groups, the HCP-EP dataset also provides sufficient information for investigators to group participants differently.
AB - Background: The time following a recent onset of psychosis is a critical period during which intervention may be maximally effective. Studying individuals in this period also offers an opportunity to investigate putative brain biomarkers of illness prior to the long-term effects of chronicity and medication. The Human Connectome Project for Early Psychosis (HCP-EP) was funded by the National Institutes of Mental Health (NIMH) as an extension of the original Human Connectome Project's approach to understanding the human brain and its structural and functional connections. Design: The HCP-EP data were collected at 3 sites in Massachusetts (Beth Israel Deaconess Medical Center, McLean Hospital, and Massachusetts General Hospital), and one site in Indiana (Indiana University). Brigham and Women's Hospital served as the data coordination center and as an imaging site. Results: The HCP-EP dataset includes high-quality clinical, cognitive, functional, neuroimaging, and blood specimen data acquired from 303 individuals between the ages of 16-35 years old with affective psychosis (nâ...=â...75), non-affective psychosis (nâ...=â...148), and healthy controls (nâ...=â...80). Participants with early psychosis were within 5 years of illness onset (mean durationâ...=â...1.9 years, standard deviationâ...=â...1.4 years). All data and novel or modified analytic tools developed as part of the study are publicly available to the research community through the NIMH Data Archive (NDA) or GitHub (https://github.com/pnlbwh). Conclusions: This paper provides an overview of the specific HCP-EP procedures, assessments, and protocols, as well as a brief characterization of the study participants to make it easier for researchers to use this rich dataset. Although we focus here on discussing and comparing affective and non-affective psychosis groups, the HCP-EP dataset also provides sufficient information for investigators to group participants differently.
KW - bipolar disorder
KW - cognition
KW - diffusion
KW - neuroimaging
KW - resting-state fMRI
KW - schizophrenia
UR - https://www.scopus.com/pages/publications/105004811660
U2 - 10.1093/schbul/sbae123
DO - 10.1093/schbul/sbae123
M3 - Journal Article
C2 - 39036958
AN - SCOPUS:105004811660
SN - 0586-7614
VL - 51
SP - 658
EP - 671
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
IS - 3
ER -