YKL-40 is an acute phase protein elevated in patients with infectious and inflammatory diseases. We tested the hypothesis that baseline elevated YKL-40 is associated with increased risk of future infectious disease in healthy individuals in the general population.
We followed prospectively 94665 individuals from the Danish general population for up to 23 years and analyzed for plasma YKL-40 levels (n=21584) and CHI3L1 rs4950928 genotype (n=94184). Endpoints were any infection, bacterial pneumonia, urinary tract infection, skin infection, sepsis, diarrhoeal disease, and other infections.
For YKL-40 percentile category 91-100% versus 0-33%, the multifactorially and C-reactive protein (CRP) adjusted hazard ratios were 1.71 (95% confidence interval: 1.50-1.96; P-value=4×10) for any infection, 1.97 (1.64-2.37; P=4×10) for bacterial pneumonia, 1.62 (1.24-2.11; P=0.002) for urinary tract infection, 1.74 (1.31-2.32;P=2×10) for skin infection, 1.76 (1.25-2.46; P=0.004) for sepsis, 1.90 (1.29-2.78; P=0.002) for diarrhoeal disease, and 2.71 (1.38-5.35; P=0.01) for other infections. In multifactorially and CRP adjusted models, a two-fold increase in YKL-40 was associated with increased risk of all infectious disease endpoints. Mendelian randomization did not support causality, as CHI3L1 rs4950928 was associated with 94% and 190% higher YKL-40 levels (for CG and CC versus GG genotype), but not with increased risk of any infectious disease endpoint.
Baseline elevated plasma YKL-40 was not a cause, but a strong marker of increased risk of future infectious diseases in individuals in the general population.

Copyright © 2020 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

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