One in four adult Americans experiences a mental health disorder in a given year. About 2.4 million Americans live with schizophrenia. There are considerable and growing evidences suggesting schizophrenia may originate from early neurodevelopment involving abnormal neuronal circuits. However, schizophrenia still cannot be diagnosed until young adulthood at the earliest when the most rapid phase of neurodevelopment has already completed. The lack of earlier risk assessment has severely limited our understanding of the developmental trajectory of the disease thus preventing more effective intervention before symptom onset. This project will develop a novel non-invasive MRI technique that will provide the necessary sensitivity and resolution (10 micron) to detect potential developmental abnormalities associated with neuronal circuits. Our preliminary studies have demonstrated a markedly improved sensitivity and resolution compared to state-of- the-art MRI techniques. We will further develop this novel technique and determine its molecular basis of the improved sensitivity. We will test the technique on transgenic mouse models of schizophrenia and investigate its ability to detect abnormalities in neuronal circuits before symptoms occur. In particular, we will determine the relationship between the new image contrast and abnormalities of myelination and synapses associated with corticostriatal and corticohippocampal connectivity. The rationale of the research is that the proposed multidisciplinary imaging-genetics study would help us to better understand the genetic and developmental components of the disease, to detect circuit abnormalities before behavioral symptoms, and to eventually guide treatment strategies.

Public Health Relevance

This research will develop an in vivo MRI-based technique for assessing brain development. In addition to the study of normal brain development and schizophrenia, this technique could be relevant for applications to many brain disorders, including demyelination diseases and brain trauma. If our hypotheses are correct, this may save lives by providing earlier diagnosis of developmental brain disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH096979-01A1
Application #
8506266
Study Section
Developmental Brain Disorders Study Section (DBD)
Program Officer
Freund, Michelle
Project Start
2013-05-03
Project End
2018-01-31
Budget Start
2013-05-03
Budget End
2014-01-31
Support Year
1
Fiscal Year
2013
Total Cost
$392,500
Indirect Cost
$142,500
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Wei, Hongjiang; Lin, Huimin; Qin, Le et al. (2018) Quantitative susceptibility mapping of articular cartilage in patients with osteoarthritis at 3T. J Magn Reson Imaging :
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Wei, Hongjiang; Dibb, Russell; Decker, Kyle et al. (2017) Investigating magnetic susceptibility of human knee joint at 7 Tesla. Magn Reson Med 78:1933-1943
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