Key result
Genetically predicted NT-proBNP levels show no link to ischemic stroke risk.
Why the study?
To evaluate the potential causal association between circulating NT-proBNP levels and ischemic stroke and its subtypes using genetic data.
Do genetically determined NT-proBNP levels affect the risk of ischemic stroke and its subtypes?
Observational (n=446,696)
Mendelian Randomization
Yes
Do genetically determined NT-proBNP levels affect the risk of ischemic stroke and its subtypes?
Genetically determined NT-proBNP levels do not show a significant causal association with overall ischemic stroke, but may have suggestive associations with specific subtypes such as small-vessel occlusion stroke.
No causal link to ischemic stroke risk; leaves open subtype-specific effects for further study.
Mendelian randomization was used to evaluate the potential causal association between N-terminal probrain natriuretic peptide (NT-proBNP) and ischemic stroke based on summary statistics data from large-scale genome-wide association studies. Three single-nucleotide polymorphisms (SNPs) rs198389, rs13107325, and rs11105306 associated with NT-proBNP levels found in large general populations and in patients with acute heart disease were used as instrumental variables. The results of genetic association analysis of each single SNP show that there is no significant association between NT-proBNP levels and ischemic stroke or its subtypes, whereas rs198389 alone has a suggestive association with large-artery atherosclerosis stroke. The MR analysis of three SNPs shows that NT-proBNP levels may reduce the risk of small-vessel occlusion stroke suggestively. This genetic analysis provides insights into the pathophysiology and treatment of ischemic stroke.
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Li et al. (2022) conducted an observational in Ischemic stroke and its subtypes (n=446,696). Genetically predicted N-terminal probrain natriuretic peptide (NT-proBNP) levels vs. Control was evaluated on Ischemic stroke (OR -0.044, 95% CI -0.129, 0.041, p=0.313). Genetically predicted NT-proBNP levels showed no significant causal association with the risk of ischemic stroke (OR -0.044, 95% CI -0.129 to 0.041, p=0.313).
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