Mendelian randomization demonstrates a causal link between peripheral circulating acylcarnitines and intracranial aneurysms

孟德尔随机化 神经学 随机化 神经外科 医学 外围设备 因果推理 内科学 随机对照试验 神经科学 心理学 生物 遗传学 外科 遗传变异 基因 病理 基因型
作者
Ying Wang,Kang Xie,Junyu Wang,Fenghua Chen,Xi Li,Longbo Zhang
出处
期刊:Neurotherapeutics [Springer Science+Business Media]
卷期号:: e00428-e00428
标识
DOI:10.1016/j.neurot.2024.e00428
摘要

Intracranial aneurysm (IA) is the most prevalent type of cerebral vascular disease causing life-threatening subarachnoid hemorrhages (SAH). A long-term vascular structure remodeling is considered as the main pathophysiological feature of IAs. However, the causal factors triggering the pathophysiological process are not clear. Recently, the abnormalities of peripheral circulating proteins and metabolites have been found in IAs patients and associated with the ruptures. We comprehensively investigated the potential causal relationship between blood metabolites and proteins and IAs using the mendelian randomization (MR) analysis. We applied two-sample MR to explore the potential causal association between peripheral circulating metabolites (191 blood metabolites) and proteins (1398 proteins) and IAs using data from the FinnGen study and the GWAS datasets published by Bakker et al. We identified palmitoylcarnitine, stearoylcarnitine and 2-tetradecenoylcarnitine as causal contributors of IAs and ruptures. Further two-step mediation MR analysis suggested that hypertension as one of the contributors of IAs and ruptures mediated the causal relationship between palmitoylcarnitine, stearoylcarnitine and 2-tetradecenoylcarnitine and IAs. Together, our study demonstrates that blood metabolic palmitoylcarnitine, stearoylcarnitine and 2-tetradecenoylcarnitine are causally linked to the formation and rupture of IAs. Hypertension partially mediates the causal effects.
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