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Hypertriglyceridemia as a Key Contributor to Abdominal Aortic Aneurysm Development and Rupture: Insights from Genetic and Experimental Models. | LitMetric

AI Article Synopsis

  • Abdominal aortic aneurysm (AAA) is a serious vascular disease that currently lacks effective treatments, prompting research into its causative factors.
  • This study used genetic, proteomic, and metabolomic approaches along with mouse models to show that high levels of triglycerides (TG) contribute significantly to the development and rupture of AAA.
  • The findings highlight that managing triglyceride-rich lipoproteins could be crucial for treating AAA and suggest that targeting TG pathways may inhibit AAA progression.

Article Abstract

Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease without effective medications. This study integrated genetic, proteomic, and metabolomic data to identify causation between increased triglyceride (TG)-rich lipoproteins and AAA risk. Three hypertriglyceridemia mouse models were employed to test the hypothesis that increased plasma TG concentrations accelerate AAA development and rupture. In the angiotensin II-infusion AAA model, most -deficient mice with severely high plasma TG concentrations died of aortic rupture. Consistently, -deficient mice with moderately increased TG concentrations had accelerated AAA development, while human transgenic mice with dramatically increased TG concentrations exhibited aortic dissection and rupture. Increased TG concentrations and palmitate inhibited lysyl oxidase maturation. Administration of antisense oligonucleotide targeting profoundly inhibited AAA progression in human transgenic mice and -deficient mice. These results indicate that hypertriglyceridemia is a key contributor to AAA pathogenesis, highlighting the importance of triglyceride-rich lipoprotein management in treating AAA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11361217PMC
http://dx.doi.org/10.1101/2024.08.07.24311621DOI Listing

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