Cerebrospinal Fluid C1-Esterase Inhibitor and Tie-1 Levels Affect Cognitive Performance: Evidence from Proteome-Wide Mendelian Randomization

Author:

Zagkos Loukas1ORCID,Dib Marie-Joe2,Cronjé Héléne T.3,Elliott Paul145,Dehghan Abbas145,Tzoulaki Ioanna1456ORCID,Gill Dipender1ORCID,Daghlas Iyas7

Affiliation:

1. Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London SW7 2BX, UK

2. Division of Cardiovascular Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA

3. Department of Public Health, Section of Epidemiology, University of Copenhagen, 1165 Copenhagen, Denmark

4. UK Dementia Research Institute at Imperial College London, Hammersmith Hospital, London W1T 7NF, UK

5. Medical Research Council Centre for Environment and Health, School of Public Health, Imperial College London, London SW7 2AZ, UK

6. Centre for Systems Biology, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece

7. Department of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA

Abstract

Objective: The association of cerebrospinal fluid (CSF) protein levels with cognitive function in the general population remains largely unexplored. We performed Mendelian randomization (MR) analyses to query which CSF proteins may have potential causal effects on cognitive performance. Methods and analysis: Genetic associations with CSF proteins were obtained from a genome-wide association study conducted in up to 835 European-ancestry individuals and for cognitive performance from a meta-analysis of GWAS including 257,841 European-ancestry individuals. We performed Mendelian randomization (MR) analyses to test the effect of randomly allocated variation in 154 genetically predicted CSF protein levels on cognitive performance. Findings were validated by performing colocalization analyses and considering cognition-related phenotypes. Results: Genetically predicted C1-esterase inhibitor levels in the CSF were associated with a better cognitive performance (SD units of cognitive performance per 1 log-relative fluorescence unit (RFU): 0.23, 95% confidence interval: 0.12 to 0.35, p = 7.91 × 10−5), while tyrosine-protein kinase receptor Tie-1 (sTie-1) levels were associated with a worse cognitive performance (−0.43, −0.62 to −0.23, p = 2.08 × 10−5). These findings were supported by colocalization analyses and by concordant effects on distinct cognition-related and brain-volume measures. Conclusions: Human genetics supports a role for the C1-esterase inhibitor and sTie-1 in cognitive performance.

Funder

UK Medical Research Council (MRC), Alzheimer’s Society, and Alzheimer’s Research UK

Novo Nordic Foundation

Wellcome Trust seed award

Publisher

MDPI AG

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