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Cardiometabolic risk factors in adults with cystic fibrosis undergoing elexacaftor/tezacaftor/ivacaftor therapy. | LitMetric

AI Article Synopsis

  • - The introduction of ETI therapy has improved life expectancy for adults with cystic fibrosis, but it raises concerns about long-term health issues, particularly cardiovascular risks due to existing factors linked to CF.
  • - A study involving 58 adults with CF assessed changes in cardiac and metabolic biomarkers after 6 months on ETI therapy, revealing increased cholesterol and triglycerides levels while inflammatory markers decreased.
  • - The findings indicate a disruption in hormone regulation related to obesity and cardiovascular risk, suggesting that while ETI improves some aspects of health, it negatively affects lipid profiles in patients, leading to potential metabolic issues.

Article Abstract

The introduction of elexacaftor/tezacaftor/ivacaftor (ETI) therapy has further extended life expectancy of adults with cystic fibrosis (awCF), highlighting the need for increased attention to potential long-term health issues. Given the increasing prevalence of cardiovascular diseases in the ageing population and the presence of cardiovascular risk factors associated with CF, understanding the impact of ETI on cardiometabolic risk factors is a crucial clinical concern. The aim of our prospective observational study was to explore early changes in cardiac and metabolic biomarkers after 6 months of ETI therapy. A total of 58 consecutive awCF were enrolled during clinical stability at the Adult CF Center of the Policlinico Hospital in Milan, Italy between January 2021 and June 2022. Blood samples were obtained before ETI initiation and after 6 months, and underwent central processing for an extended panel of cardiometabolic biomarkers. We observed a rise in cholesterol, triglycerides, apolipoprotein-B and adipokine levels, while inflammatory markers decreased. The direct relationship between leptin and adiponectin suggest a disruption in the normal regulatory mechanisms that control these hormones, potentially leading to metabolic imbalances, such as increased risk of obesity and cardiovascular events. The impact of ETI on cardiovascular risk in awCF is heterogeneous and while it improves some risk factors, such as chronic inflammation, it has a worsening effect on lipoproteins. Our findings suggest that the dysregulation of adipokines could be a potential cause of the metabolic disturbances observed in awCF.

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Source
http://dx.doi.org/10.1016/j.jcf.2024.11.009DOI Listing

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