4.7 Article

The additive impact of cardio-metabolic disorders and psychiatric illnesses on accelerated brain aging

期刊

HUMAN BRAIN MAPPING
卷 43, 期 6, 页码 1997-2010

出版社

WILEY
DOI: 10.1002/hbm.25769

关键词

accelerated brain aging; cardio-metabolic disorders; MRI; quantile regression index; severe mental illness; UK Biobank

资金

  1. National Institutes of Health [R01AG059874, R01EB015611, R01MH112180, R01MH116948, R01MH117601, S10OD023696, U01MH108148, U54 EB020403]

向作者/读者索取更多资源

Severe mental illnesses, such as major depressive disorder, bipolar disorder, and schizophrenia spectrum disorder, increase the risk of accelerated brain aging. These illnesses have independent effects on whole-brain quantile regression index (QRI), with schizophrenia spectrum disorder having the greatest impact. Hypertension has a significant effect on both individuals with and without severe mental illnesses. The volume of white matter hyperintensities is associated with QRI, primarily influenced by cardio-metabolic disorders, especially hypertension.
Severe mental illnesses (SMI) including major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia spectrum disorder (SSD) elevate accelerated brain aging risks. Cardio-metabolic disorders (CMD) are common comorbidities in SMI and negatively impact brain health. We validated a linear quantile regression index (QRI) approach against the machine learning BrainAge index in an independent SSD cohort (N = 206). We tested the direct and additive effects of SMI and CMD effects on accelerated brain aging in the N = 1,618 (604 M/1,014 F, average age = 63.53 +/- 7.38) subjects with SMI and N = 11,849 (5,719 M/6,130 F; 64.42 +/- 7.38) controls from the UK Biobank. Subjects were subdivided based on diagnostic status: SMI+/CMD+ (N = 665), SMI+/CMD- (N = 964), SMI-/CMD+ (N = 3,765), SMI-/CMD- (N = 8,083). SMI (F = 40.47, p = 2.06 x 10(-10)) and CMD (F = 24.69, p = 6.82 x 10(-7)) significantly, independently impacted whole-brain QRI in SMI+. SSD had the largest effect (Cohen's d = 1.42) then BD (d = 0.55), and MDD (d = 0.15). Hypertension had a significant effect on SMI+ (d = 0.19) and SMI- (d = 0.14). SMI effects were direct, independent of MD, and remained significant after correcting for effects of antipsychotic medications. Whole-brain QRI was significantly (p < 10(-16)) associated with the volume of white matter hyperintensities (WMH). However, WMH did not show significant association with SMI and was driven by CMD, chiefly hypertension (p < 10(-16)). We used a simple and robust index, QRI, the demonstrate additive effect of SMI and CMD on accelerated brain aging. We showed a greater effect of psychiatric illnesses on QRI compared to cardio-metabolic illness. Our findings suggest that subjects with SMI should be among the targets for interventions to protect against age-related cognitive decline.

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