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Review
. 2024 Apr 18:15:1362012.
doi: 10.3389/fimmu.2024.1362012. eCollection 2024.

Exploring causal correlations between inflammatory cytokines and knee osteoarthritis: a two-sample Mendelian randomization

Jiayu Zhang  1 , Kexuan Li  1 , Xiuyue Qiu  1
Affiliations
Review

Exploring causal correlations between inflammatory cytokines and knee osteoarthritis: a two-sample Mendelian randomization

Jiayu Zhang et al. Front Immunol. .

Abstract

Objectives: Knee osteoarthritis (KOA) and certain inflammatory cytokines (such as interleukin 1 [IL-1] and tumor necrosis factor alpha [TNF-a]) are related; however, the causal relationship remains unclear. Here, we aimed to assess the causal relationship between 41 inflammatory cytokines and KOA using Mendelian randomization (MR).

Methods: Two-sample bidirectional MR was performed using genetic variation data for 41 inflammatory cytokines that were obtained from European Genome-Wide Association Study (GWAS) data (n=8293). KOA-related genetic association data were also obtained from European GWAS data (n=40,3124). Inverse variance weighting (IVW), MR, heterogeneity, sensitivity, and multiple validation analyses were performed.

Results: Granulocyte colony-stimulating factor (G-CSF) or colony-stimulating factor 3 (CSF-3) levels were negatively associated with the risk of developing KOA (OR: 0.93, 95%CI:0.89-0.99, P=0.015). Additionally, macrophage inflammatory protein-1 alpha (MIP-1A/CCL3) was a consequence of KOA (OR: 0.72, 95%CI:0.54-0.97, P=0.032). No causal relationship was evident between other inflammatory cytokines and KOA development.

Conclusion: This study suggests that certain inflammatory cytokines may be associated with KOA etiology. G-CSF exerts an upstream influence on KOA development, whereas MIP-1A (CCL-3) acts as a downstream factor.

Keywords: Mendelian randomization; disease etiology; genetic variation; inflammatory cytokines; knee osteoarthritis.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Schematic representation of the study design in this bidirectional Mendelian randomization (MR) analysis.
Figure 2
Figure 2
Scatter and funnel plots of Mendelian randomization (MR) analyses for granulocyte colony-stimulating factor (G-CSF) and macrophage inflammatory protein-1 alpha (MIP-1A) in patients with knee osteoarthritis (KOA). (A) The exposure is G-CSF and outcome is KOA. (B) The exposure is KOA and outcome is MIP-1A. (C, D) Funnel plots show the inverse variance weighted MR estimate of each cytokine single-nucleotide polymorphism (SNP) with KOA versus 1/standard error (1/SEIV).
See this image and copyright information in PMC

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