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Abstract
Background and Objectives Alzheimer dementia is a complex clinical syndrome that can be defined broadly as an amnestic multidomain dementia. We previously reported human cortical proteins that are implicated in Alzheimer dementia. To understand the pathologic correlates of these proteins for underlying disease mechanisms, we investigated cortical protein associations with common age-related neuropathologies.
Methods Participants were community-dwelling older adults from 2 cohort studies of aging and dementia. All underwent detailed annual clinical evaluations, and brain autopsies were performed after death. We use Alzheimer disease (AD) to refer to pathologically defined disease and Alzheimer dementia to refer to the clinical syndrome. Indices for AD, cortical Lewy bodies, limbic predominant age-related TAR DNA binding protein 43 encephalopathy neuropathologic changes (LATE-NC), hippocampal sclerosis, macroscopic infarcts, microinfarcts, cerebral amyloid angiopathy, atherosclerosis, and arteriolosclerosis were quantified during uniform structured neuropathologic evaluations. High-throughput protein abundances from frozen dorsolateral prefrontal cortex were quantified with mass spectrometry–based tandem mass tag proteomics analysis. Eleven human cortical proteins implicated in Alzheimer dementia, including angiotensin-converting enzyme, calcium-regulated heat-stable protein 1 (CHSP1), procathepsin H (CATH), double C2-like domain-containing protein α, islet cell autoantigen 1–like protein, serine β-lactamase–like protein LACTB, mitochondrial, pleckstrin homology domain–containing family A member 1, replication termination factor 2, sorting nexin-32, syntaxin-4, and syntaxin-6 (STX6), were previously identified with an integrative approach. Logistic regression analysis examined the association of protein expression with each of the neuropathologic indices.
Results A total of 391 older adults were included. We did not observe associations of these protein targets with pathologic diagnosis of AD. In contrast, multiple proteins were associated with non-AD neurodegenerative and cerebrovascular conditions. In particular, higher CHSP1 expression was associated with cortical Lewy bodies and macroscopic infarcts, and higher CATH expression was associated with LATE-NC and arteriolosclerosis. Furthermore, while higher STX6 expression increased the risk of Alzheimer dementia, the protein was not associated with any of the neuropathologic indices investigated.
Discussion Cortical proteins implicated in Alzheimer dementia do not necessarily work through AD pathogenesis; rather, non-AD neurodegenerative and vascular diseases and other pathways are at play. Furthermore, some proteins are pleiotrophic and associated with both neurodegenerative and cerebrovascular pathologies.
Glossary
- ACE=
- angiotensin-converting enzyme;
- AD=
- Alzheimer disease;
- CATH=
- procathepsin H;
- CHSP1=
- calcium-regulated heat-stable protein 1;
- CI=
- confidence interval;
- DOC2A=
- double C2-like domain-containing protein α;
- GIS=
- global internal standard;
- GWAS=
- genome-wide association study;
- H&E=
- hematoxylin & eosin;
- ICA1L=
- islet cell autoantigen 1–like protein;
- LACTB=
- serine β-lactamase–like protein LACTB, mitochondrial;
- LATE-NC=
- limbic-predominant age-related TDP-43 encephalopathy neuropathologic changes;
- NIA=
- National Institute on Aging;
- OR=
- odds ratio;
- ROSMAP=
- Religious Orders Study and Rush Memory and Aging Project;
- SNX32=
- sorting nexin-32;
- STX4=
- syntaxin-4;
- STX6=
- syntaxin-6;
- TDP-43=
- TAR DNA binding protein 43
Footnotes
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received August 3, 2021.
- Accepted in final form December 13, 2021.
- © 2021 American Academy of Neurology
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