# Association of Alzheimer’s disease progression with YKL40 levels in peripheral blood and cerebrospinal fluid: a systematic review and meta-analysis

**Authors:** Qianwen Yang, Ruiqi Wang, Jian Pei, Qinhui Fu, Yijun Zhan, Wenyan Zhu

PMC · DOI: 10.3389/fneur.2026.1768353 · Frontiers in Neurology · 2026-02-05

## TL;DR

This study finds that YKL40 levels in the brain fluid and blood are higher in Alzheimer’s patients and early stages, suggesting it could help detect the disease early.

## Contribution

The study provides a meta-analysis showing YKL40 as a potential early biomarker for Alzheimer’s disease, though it cannot distinguish between early and later stages alone.

## Key findings

- CSF YKL40 levels were significantly higher in Alzheimer’s patients compared to healthy controls.
- Peripheral blood YKL40 levels were elevated in both Alzheimer’s and mild cognitive impairment patients.
- YKL40 levels did not significantly differ between Alzheimer’s and mild cognitive impairment groups in CSF.

## Abstract

Chitinase 3-like protein 1 (CHI3L1 or YKL40) is a potential neuroinflammatory biomarker linked to the pathogenesis of Alzheimer’s disease (AD). Previous studies have produced inconsistent results regarding YKL40 levels in various clinical stages of AD. This study aims to establish the correlation between YKL40 levels and AD progression through a meta-analysis of YKL40 levels in cerebrospinal fluid (CSF) and peripheral blood.

Comprehensive searches were conducted in PubMed, Medline, Web of Science, and the Cochrane Library to identify observational studies reporting CSF and peripheral blood YKL40 levels in AD patients, mild cognitive impairment (MCI) patients, preclinical AD (pre-AD) and healthy controls (HCs). A random effects meta-analysis was used to calculate the standardized mean difference (SMD) and 95% confidence intervals (CIs).

Thirty observational studies involving 2,102 AD patients, 1,504 MCI patients, 118 pre-AD individuals, and 2,091 HCs were included. Significant differences in CSF YKL-40 levels were observed in AD vs. HC (SMD = 1.37, 95%CI: [1.09, 1.65]; p = 0.000), MCI vs. HC (SMD = 0.96, 95%CI: [0.51, 1.41]; p = 0.000), and pre-AD vs. HC (SMD = 0.81, 95%CI: [0.39, 1.22]; p = 0.001) comparisons. Peripheral blood YKL-40 levels also demonstrated statistically significant elevations in both AD vs. HC (SMD = 0.40, 95%CI: [0.18, 0.63]; p = 0.000) and MCI vs. HC (SMD = 0.79, 95%CI: [0.03, 1.55]; p = 0.043) comparisons. However, CSF YKL-40 levels showed no statistically significant difference between AD and MCI groups (SMD = 0.25, 95%CI: [−0.08, 0.57]; p = 0.134).

Elevated YKL-40 levels in both CSF and peripheral blood are associated with the presence of Alzheimer’s disease and its early stages, indicating that YKL-40 reflects neuroinflammatory processes involved in AD onset. While YKL-40 shows potential value for early identification along the AD continuum, its limited ability to differentiate between MCI and AD highlights the need for its combined use with other biomarkers in disease staging and progression assessment.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251031837.

## Linked entities

- **Proteins:** CHI3L1 (chitinase 3 like 1), CHI3L1 (chitinase 3 like 1)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il1 (interleukin 1 complex) [NCBI Gene 111343] {aka Il-1}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, Chi3l1 (chitinase 3 like 1) [NCBI Gene 12654] {aka Brp39, Chil1, Gp39}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, CHI3L1 (chitinase 3 like 1) [NCBI Gene 1116] {aka ASRT7, CGP-39, GP-39, GP39, HC-gp39, HCGP-3P}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** neuroinflammation (MESH:D000090862), MCI (MESH:D060825), AD (MESH:D000544), neurodegeneration (MESH:D019636), inflammatory (MESH:D007249), A + T (MESH:D001260), Cognitive Impairment (MESH:D003072), Dementia (MESH:D003704), amyloid (MESH:C000718787), neuronal loss (MESH:D009410)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** R155C

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916370/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916370/full.md

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Source: https://tomesphere.com/paper/PMC12916370