ENIGMA-DTI: Translating reproducible white matter deficits into personalized vulnerability metrics in cross-diagnostic psychiatric research

Peter Kochunov, L. Elliot Hong, Emily L. Dennis, Rajendra A. Morey, David F. Tate, Elisabeth A. Wilde, Mark Logue, Sinead Kelly, Gary Donohoe, Pauline Favre, Josselin Houenou, Christopher R.K. Ching, Laurena Holleran, Ole A. Andreassen, Laura S. van Velzen, Lianne Schmaal, Julio E. Villalón-Reina, Carrie E. Bearden, Fabrizio Piras, Gianfranco SpallettaOdile A. van den Heuvel, Dick J. Veltman, Dan J. Stein, Meghann C. Ryan, Yunlong Tan, Theo G.M. van Erp, Jessica A. Turner, Liz Haddad, Talia M. Nir, David C. Glahn, Paul M. Thompson, Neda Jahanshad

Research output: Contribution to journalEditorialpeer-review

Abstract

The ENIGMA-DTI (diffusion tensor imaging) workgroup supports analyses that examine the effects of psychiatric, neurological, and developmental disorders on the white matter pathways of the human brain, as well as the effects of normal variation and its genetic associations. The seven ENIGMA disorder-oriented working groups used the ENIGMA-DTI workflow to derive patterns of deficits using coherent and coordinated analyses that model the disease effects across cohorts worldwide. This yielded the largest studies detailing patterns of white matter deficits in schizophrenia spectrum disorder (SSD), bipolar disorder (BD), major depressive disorder (MDD), obsessive–compulsive disorder (OCD), posttraumatic stress disorder (PTSD), traumatic brain injury (TBI), and 22q11 deletion syndrome. These deficit patterns are informative of the underlying neurobiology and reproducible in independent cohorts. We reviewed these findings, demonstrated their reproducibility in independent cohorts, and compared the deficit patterns across illnesses. We discussed translating ENIGMA-defined deficit patterns on the level of individual subjects using a metric called the regional vulnerability index (RVI), a correlation of an individual's brain metrics with the expected pattern for a disorder. We discussed the similarity in white matter deficit patterns among SSD, BD, MDD, and OCD and provided a rationale for using this index in cross-diagnostic neuropsychiatric research. We also discussed the difference in deficit patterns between idiopathic schizophrenia and 22q11 deletion syndrome, which is used as a developmental and genetic model of schizophrenia. Together, these findings highlight the importance of collaborative large-scale research to provide robust and reproducible effects that offer insights into individual vulnerability and cross-diagnosis features.

Original languageEnglish
JournalHuman Brain Mapping
DOIs
Publication statusE-pub ahead of print - Apr 2020

Keywords

  • big data
  • cross-disorder
  • DTI
  • ENIGMA
  • RVI
  • white matter deficit patterns

ASJC Scopus subject areas

  • Anatomy
  • Radiological and Ultrasound Technology
  • Radiology Nuclear Medicine and imaging
  • Neurology
  • Clinical Neurology

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