Abstract

Background: Plasma metabolites are associated with cognitive and physical function in the elderly. Because cerebral small vessel disease (SVD) and neurodegeneration are common causes of cognitive and physical function decline, the primary objective of this study was to investigate the associations of six plasma metabolites (two plasma phosphatidylcholines [PCs]: PC aa C36:5 and PC aa 36:6 and four sphingomyelins [SMs]: SM C26:0, SM [OH] C22:1, SM [OH] C22:2, SM [OH] C24:1) with magnetic resonance imaging (MRI) features of cerebral SVD and neurodegeneration in older adults. Methods: This study included 238 older adults in the Atherosclerosis Risk in Communities study at the fifth exam. Multiple linear regression was used to assess the association of each metabolite (log-transformed) in separate models with MRI measures except lacunar infarcts, for which binary logistic regression was used. Results: Higher concentrations of plasma PC aa C36:5 had adverse associations with MRI features of cerebral SVD (odds ratio of 1.69 [95% confidence interval: 1.01, 2.83] with lacunar infarct, and beta of 0.16 log [cm3] [0.02, 0.30] with log [White Matter Hyperintensities (WMH) volume]) while higher concentrations of 3 plasma SM (OH)s were associated with higher total brain volume (beta of 12.0 cm3 [5.5, 18.6], 11.8 cm3 [5.0, 18.6], and 7.3 cm3 [1.2, 13.5] for SM [OH] C22:1, SM [OH] C22:2, and SM [OH] C24:1, respectively). Conclusions: This study identified associations between certain plasma metabolites and brain MRI measures of SVD and neurodegeneration in older adults, particularly higher SM (OH) concentrations with higher total brain volume.

Highlights

  • Cerebral small vessel diseases (SVD) and neurodegeneration frequently coexist and are common causes of poor physical and cognitive function in the elderly [1]

  • The objective of this study is to examine the plausible associations between six plasma phospholipids and sphingolipids (PC aa C36:5, PC aa C36:6, SM C26:0, SM [OH] C22:1, SM [OH] C22:2, and SM [OH] C24:1) and neuroimaging features of cerebral SVD and neurodegeneration in older adults

  • Since cerebral SVD frequently coexists with neurodegenerative disease such as Alzheimer’s disease (AD) [8], this study examines the associations of these six plasma metabolites with AD-associated neurodegeneration

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Summary

Introduction

Cerebral small vessel diseases (SVD) and neurodegeneration frequently coexist and are common causes of poor physical and cognitive function in the elderly [1]. Previous studies of plasma molecular components and neuroimaging features of SVD examined markers of inflammation (i.e., TGF-beta, C-reactive protein, interleukin-6, YKL-40) [1,5,6], endothelial dysfunction (i.e., intercellular adhesion molecule, thrombomodulin, tissue factor, and tissue factor pathway inhibitor, homocysteine) [3,4], and well-established lipid biomarkers of cardiovascular disease risk (triglycerides and cholesterol) [7]. Because cerebral small vessel disease (SVD) and neurodegeneration are common causes of cognitive and physical function decline, the primary objective of this study was to investigate the associations of six plasma metabolites (two plasma phosphatidylcholines [PCs]: PC aa C36:5 and PC aa 36:6 and four sphingomyelins [SMs]: SM C26:0, SM [OH] C22:1, SM [OH] C22:2, SM [OH] C24:1) with magnetic resonance imaging (MRI) features of cerebral SVD and neurodegeneration in older adults. Conclusions: This study identified associations between certain plasma metabolites and brain MRI measures of SVD and neurodegeneration in older adults, higher SM (OH) concentrations with higher total brain volume

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