Frontiers in Cardiovascular Medicine (Oct 2024)

PD-1/PD-L1 and coronary heart disease: a mendelian randomization study

  • Liangjia Zeng,
  • Liangjia Zeng,
  • Liangjia Zeng,
  • Yinglan Liang,
  • Yinglan Liang,
  • Ruoyun Zhou,
  • Ruoyun Zhou,
  • Wenting Yang,
  • Wenting Yang,
  • Kexin Chen,
  • Kexin Chen,
  • Baixin He,
  • Baixin He,
  • Yuqing Qiu,
  • Yuqing Qiu,
  • Linglong Liu,
  • Linglong Liu,
  • Deyang Zhou,
  • Deyang Zhou,
  • Zhaolin Xiao,
  • Zhaolin Xiao,
  • Haowen Liang,
  • Haowen Liang,
  • Binghua Zhang,
  • Binghua Zhang,
  • Renyu Li,
  • Renyu Li,
  • Lihong Yu,
  • Min Yi,
  • Xiaozhen Lin

DOI
https://doi.org/10.3389/fcvm.2024.1424770
Journal volume & issue
Vol. 11

Abstract

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IntroductionIt has been found that programmed cell death protein-1 (PD-1) or its ligand PD-L1 may play an important role in the onset and progression of coronary heart disease (CHD). Thus, we conducted this mendelian randomization analysis (MR) to estimate the causal relationship between PD-1/PD-L1 and 5 specific CHDs (chronic ischemic heart disease, acute myocardial infarction, angina pectoris, coronary atherosclerosis, and unstable angina pectoris), complemented by gene set enrichment analysis (GSEA) for further validation.MethodsPublicly available summary-level data were attained from the UK Biobank with genetic instruments obtained from the largest available, nonoverlapping genome-wide association studies (GWAS). Our analysis involved various approaches including inverse variance-weighted meta-analysis, alternative techniques like weighted median, MR-Egger, MR-multipotency residuals and outliers detection (PRESSO), along with multiple sensitivity assessments such as MR-Egger intercept test, Cochran's Q test, and leave-one-out sensitivity analysis to evaluate and exclude any anomalies.ResultsGene expression profile (GSE71226) was obtained from Gene Expression Omnibus (GEO) database for GSEA. IVW analysis showed a causal association between PD-1 and chronic ischemic heart disease (OR, 0.997; 95%CI, 0.995-0.999; P, 0.009), chronic ischemic heart disease and PD-1 (beta, −3.1; 95%CI, −6.017 to −0.183; P, 0.037), chronic ischemic heart disease and PD-L1 (beta, −3.269; 95%CI, −6.197 to −0.341; P, 0.029). No significant causal relationship was found between PD-1/PD-L1 and other 4 CHDs. The accuracy and robustness of these findings were confirmed by sensitivity tests. GSEA found that the KEGG pathway and related core genes of “PD-L1 expression and PD-1 checkpoint pathway in cancer” pathway were downregulated in CHD.DiscussionThis study provided evidence of a bidirectional causal relationship between PD-1 and chronic ischemic heart disease and a protective association between chronic ischemic heart disease and PD-L1.

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