Journal
HUMAN BRAIN MAPPING
Volume 43, Issue 16, Pages 4970-4983Publisher
WILEY
DOI: 10.1002/hbm.26056
Keywords
big data; DTI; ENIGMA; meta-analysis; RVI; structural deficit patterns
Funding
- National Institutes of Health [P50MH103222, R01AG095874, R01EB015611, R01MH112180, R01MH116147, R01MH116948, R01MH117601, R01MH123163, S10OD023696, U01MH108148]
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Severe mental illnesses (SMI), including major depressive (MDD), bipolar (BD), and schizophrenia spectrum (SSD) disorders have multifactorial risk factors. The regional vulnerability index (RVI) is a novel brain index that measures individual's brain-wide similarity to expected SMI patterns. The study found significant associations between RVI and MDD and SSD, as well as associations with childhood adversity and lower cognitive performance in nonpsychiatric controls. RVI shows similar or better specificity for SMI than polygenic risk scores (PRS).
Severe mental illnesses (SMI), including major depressive (MDD), bipolar (BD), and schizophrenia spectrum (SSD) disorders have multifactorial risk factors and capturing their complex etiopathophysiology in an individual remains challenging. Regional vulnerability index (RVI) was used to measure individual's brain-wide similarity to the expected SMI patterns derived from meta-analytical studies. It is analogous to polygenic risk scores (PRS) that measure individual's similarity to genome-wide patterns in SMI. We hypothesized that RVI is an intermediary phenotype between genome and symptoms and is sensitive to both genetic and environmental risks for SMI. UK Biobank sample of N = 17,053/19,265 M/F (age = 64.8 +/- 7.4 years) and an independent sample of SSD patients and controls (N = 115/111 M/F, age = 35.2 +/- 13.4) were used to test this hypothesis. UKBB participants with MDD had significantly higher RVI-MDD (Cohen's d = 0.20, p = 1 x 10(-23)) and PRS-MDD (d = 0.17, p = 1 x 10(-15)) than nonpsychiatric controls. UKBB participants with BD and SSD showed significant elevation in the respective RVIs (d = 0.65 and 0.60; p = 3 x 10(-5) and .009, respectively) and PRS (d = 0.57 and 1.34; p = .002 and .002, respectively). Elevated RVI-SSD were replicated in an independent sample (d = 0.53, p = 5 x 10(-5)). RVI-MDD and RVI-SSD but not RVI-BD were associated with childhood adversity (p < .01). In nonpsychiatric controls, elevation in RVI and PRS were associated with lower cognitive performance (p < 10(-5)) in six out of seven domains and showed specificity with disorder-associated deficits. In summary, the RVI is a novel brain index for SMI and shows similar or better specificity for SMI than PRS, and together they may complement each other in the efforts to characterize the genomic to brain level risks for SMI.
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