Brain deficit patterns of metabolic illnesses overlap with those for major depressive disorder: A new metric of brain metabolic disease

Author:

Hatch Kathryn S.1,Gao Si1,Ma Yizhou1,Russo Alessandro1,Jahanshad Neda2,Thompson Paul M.2,Adhikari Bhim M.1ORCID,Bruce Heather1,Van der Vaart Andrew1,Sotiras Aristeidis34ORCID,Kvarta Mark D.1ORCID,Nichols Thomas E.5ORCID,Schmaal Lianne67,Hong L. Elliot1,Kochunov Peter1ORCID

Affiliation:

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

2. Imaging Genetics Center, Stevens Neuroimaging and Informatics Institute Keck School of Medicine of USC Marina del Rey California USA

3. Institute of Informatics University of Washington, School of Medicine St. Louis Missouri USA

4. Department of Radiology University of Washington, School of Medicine St. Louis Missouri USA

5. Nuffield Department of Population Health of the University of Oxford Oxford UK

6. Centre for Youth Mental Health The University of Melbourne Melbourne Victoria Australia

7. Orygen Parkville Australia

Abstract

AbstractMetabolic illnesses (MET) are detrimental to brain integrity and are common comorbidities in patients with mental illnesses, including major depressive disorder (MDD). We quantified effects of MET on standard regional brain morphometric measures from 3D brain MRI as well as diffusion MRI in a large sample of UK BioBank participants. The pattern of regional effect sizes of MET in non‐psychiatric UKBB subjects was significantly correlated with the spatial profile of regional effects reported by the largest meta‐analyses in MDD but not in bipolar disorder, schizophrenia or Alzheimer's disease. We used a regional vulnerability index (RVI) for MET (RVI‐MET) to measure individual's brain similarity to the expected patterns in MET in the UK Biobank sample. Subjects with MET showed a higher effect size for RVI‐MET than for any of the individual brain measures. We replicated elevation of RVI‐MET in a sample of MDD participants with MET versus non‐MET. RVI‐MET scores were significantly correlated with the volume of white matter hyperintensities, a neurological consequence of MET and age, in both groups. Higher RVI‐MET in both samples was associated with obesity, tobacco smoking and frequent alcohol use but was unrelated to antidepressant use. In summary, MET effects on the brain were regionally specific and individual similarity to the pattern was more strongly associated with MET than any regional brain structural metric. Effects of MET overlapped with the reported brain differences in MDD, likely due to higher incidence of MET, smoking and alcohol use in subjects with MDD.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

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