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Association between Lipid Levels and Risk for Different Types of Aneurysms: A Mendelian Randomization Study

Background: Although the associations between serum lipid levels and aneurysms have been investigated in epidemiological studies, causality remains unknown. Thus, this study aimed to investigate the causal relationships of serum high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein c...

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Detalles Bibliográficos
Autores principales: Chen, Yanghui, Huang, Man, Xuan, Yunling, Li, Ke, Xu, Xin, Wang, Linlin, Sun, Yang, Xiao, Lei, Xu, Ping, Kong, Wei, Wang, Dao Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621501/
https://www.ncbi.nlm.nih.gov/pubmed/34834523
http://dx.doi.org/10.3390/jpm11111171
Descripción
Sumario:Background: Although the associations between serum lipid levels and aneurysms have been investigated in epidemiological studies, causality remains unknown. Thus, this study aimed to investigate the causal relationships of serum high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), and triglyceride (TG) levels on five types of aneurysms, using genetic variants associated with four lipid traits as instrumental variables in a Mendelian randomization (MR) analysis. Methods: We performed two-sample Mendelian randomization (MR) analyses to evaluate the associations of HDL-C, LDL-C, TC, and TG levels with risks for five types of aneurysms and those of LDL-C- (HMGCR, NPC1L1, PCSK9, CETP, and LDLR) and TG-lowering targets (ANGPTL3 and LPL) with aneurysms. Results: The sample sizes of the included studies ranged from nearly 80,000 to 410,000. We found inverse associations between genetically predicted HDL-C levels and aortic (OR = 0.74, 95% CI = 0.65–0.85) and abdominal aortic aneurysms (0.58, 0.45–0.75). A 1-SD increase in LDL-C and TC levels was associated with increased risks for aortic (1.41, 1.26–1.58 and 1.36, 1.18–1.56, respectively) and abdominal aortic aneurysms (1.82, 1.48–2.22 and 1.55, 1.25–1.93, respectively). TG levels were significantly associated with aortic (1.36, 1.18–1.56) and lower extremity artery aneurysms (2.76, 1.48–5.14), but limited to cerebral aneurysm (1.23, 1.06–1.42). Secondary analyses revealed a relationship between genetically proxied LDL-C-lowering targets and all types of aneurysms; however, the drug targets remained heterogeneous. We found a weak association between TG-lowering therapies and aortic (ANGPTL3, 0.51, 0.29–0.89) and abdominal aortic aneurysms (LPL, 0.64, 0.44–0.94). Conclusion: According to genetic evidence, lipid dysfunction is a causal risk factor for aneurysms. Lipid-lowering drugs may be a potential effective strategy in preventing and managing aneurysms.