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World Journal of Emergency Medicine ›› 2025, Vol. 16 ›› Issue (3): 256-261.doi: 10.5847/wjem.j.1920-8642.2025.045

• Original Article • Previous Articles     Next Articles

Exploring lipid-modifying therapies for sepsis through the modulation of circulating inflammatory cytokines: a Mendelian randomization study

Quan Li1, Yun Qu1, Jinfang Xue2, Hai Kang1(), Chuanzhu Lyu3()   

  1. 1Department of Emergency Medicie, Yantai Yuhuangding Hospital of Qingdao University, Yantai 264000, China
    2Emergency Department, the State Key Laboratory for Complex, Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100730, China
    3Emergency Medicine Center, Sichuan Provincial People’s Hospital, University of Electronic Science and Technology ofChina, Chengdu 610072, China
  • Received:2024-11-20 Accepted:2025-03-02 Online:2025-05-19 Published:2025-05-01
  • Contact: Hai Kang, Email: khyt058@163.com;Chuanzhu Lyu, Email: lvchuanzhu677@126.com

Abstract:

BACKGROUND: Whether lipid-modifying drugs directly impact the outcome of sepsis remains uncertain. Therefore, systematic investigations are needed to explore the potential impact of lipid-related therapies on sepsis outcomes and to elucidate the underlying mechanisms involving circulating inflammatory cytokines, which may play critical roles in the pathogenesis of sepsis. This study aimed to utilize drug-target Mendelian randomization to assess the direct causal effects of genetically proxied lipid-modifying therapies on sepsis outcomes.

METHODS: First, a two-sample Mendelian randomization study was conducted to validate the causal associations among high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and sepsis. A subsequent drug-target Mendelian randomization study assessed the direct causal effects of genetically proxied lipid-modifying therapies on the risk of sepsis, sepsis-related critical care admission, and sepsis-related death. The identified lipid-modifying drug targets were subsequently explored for direct causal relationships with 36 circulating inflammatory cytokines. Finally, enrichment analyses of the identified cytokines were conducted to explore the potential relationships of lipid-modifying drugs with the inflammatory response.

RESULTS: Genetically proxied cholesteryl ester transfer protein (CETP) inhibitors were significantly associated with sepsis-related critical care admission (OR=0.84, 95% CI [0.74, 0.95], P=0.008,) and sepsis-related death (OR=0.68, 95% CI [0.52, 0.88], P=0.004). The genetically proxied CETP inhibitors were strongly associated with the levels of 15 circulating inflammatory cytokines. Enrichment analyses indicated that CETP inhibitors may modulate inflammatory cytokines and influence the inflammatory response pathway.

CONCLUSION: This study supports a causal effect of genetically proxied CETP inhibitors in reducing the risk of sepsis-related critical care admission and death. These findings suggest that the underlying mechanism may involve the modulation of some circulating inflammatory cytokines, influencing the inflammatory response pathway.

Key words: Lipid-modifying therapies, Sepsis, Mendelian randomization