A White Matter Connection of Schizophrenia and Alzheimer’s Disease

Author:

Kochunov Peter1,Zavaliangos-Petropulu Artemis2,Jahanshad Neda2,Thompson Paul M2,Ryan Meghann C1,Chiappelli Joshua1ORCID,Chen Shuo1,Du Xiaoming1ORCID,Hatch Kathryn1,Adhikari Bhim1,Sampath Hemalatha1,Hare Stephanie1,Kvarta Mark1,Goldwaser Eric1,Yang Fude3,Olvera Rene L4,Fox Peter T5,Curran Joanne E6,Blangero John6,Glahn David C7,Tan Yunlong3,Hong L Elliot1

Affiliation:

1. Department of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD

2. Imaging Genetics Center, Mark & Mary Stevens Neuroimaging & Informatics Institute, Keck School of Medicine, University of Southern California of USC, Marina del Rey, CA

3. Beijing Huilongguan Hospital, Peking University Huilongguan Clinical Medical School, Beijing, P. R. China

4. Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX

5. Research Imaging Institute, University of Texas Health Science Center at San Antonio, San Antonio, TX

6. Department of Human Genetics and South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX

7. Department of Psychiatry, Boston Children’s Hospital, Harvard Medical School, Boston, MA

Abstract

Abstract Schizophrenia (SZ) is a severe psychiatric illness associated with an elevated risk for developing Alzheimer’s disease (AD). Both SZ and AD have white matter abnormalities and cognitive deficits as core disease features. We hypothesized that aging in SZ patients may be associated with the development of cerebral white matter deficit patterns similar to those observed in AD. We identified and replicated aging-related increases in the similarity between white matter deficit patterns in patients with SZ and AD. The white matter “regional vulnerability index” (RVI) for AD was significantly higher in SZ patients compared with healthy controls in both the independent discovery (Cohen’s d = 0.44, P = 1·10–5, N = 173 patients/230 control) and replication (Cohen’s d = 0.78, P = 9·10–7, N = 122 patients/64 controls) samples. The degree of overlap with the AD deficit pattern was significantly correlated with age in patients (r = .21 and .29, P < .01 in discovery and replication cohorts, respectively) but not in controls. Elevated RVI-AD was significantly associated with cognitive measures in both SZ and AD. Disease and cognitive specificities were also tested in patients with mild cognitive impairment and showed intermediate overlap. SZ and AD have diverse etiologies and clinical courses; our findings suggest that white matter deficits may represent a key intersecting point for these 2 otherwise distinct diseases. Identifying mechanisms underlying this white matter deficit pattern may yield preventative and treatment targets for cognitive deficits in both SZ and AD patients.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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