Biomedicines (Jul 2021)

Relationship between Circulating PCSK9 and Markers of Subclinical Atherosclerosis—The IMPROVE Study

  • Daniela Coggi,
  • Beatrice Frigerio,
  • Alice Bonomi,
  • Massimiliano Ruscica,
  • Nicola Ferri,
  • Daniela Sansaro,
  • Alessio Ravani,
  • Palma Ferrante,
  • Manuela Damigella,
  • Fabrizio Veglia,
  • Nicolò Capra,
  • Maria Giovanna Lupo,
  • Chiara Macchi,
  • Kai Savonen,
  • Angela Silveira,
  • Sudhir Kurl,
  • Philippe Giral,
  • Matteo Pirro,
  • Rona Juliette Strawbridge,
  • Bruna Gigante,
  • Andries Jan Smit,
  • Elena Tremoli,
  • Mauro Amato,
  • Damiano Baldassarre,
  • on behalf of the IMPROVE Study Group

DOI
https://doi.org/10.3390/biomedicines9070841
Journal volume & issue
Vol. 9, no. 7
p. 841

Abstract

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(1) Background and purpose: circulating proprotein convertase subtilisin/kexin type 9 (PCSK9) is one of the key regulators of cholesterol metabolism. Despite this, its role as a player in atherosclerosis development is still matter of debate. Here, we investigated the relationships between this protein and several markers of subclinical atherosclerosis. (2) Methods: the IMPROVE study enrolled 3703 European subjects (54–79 years; 48% men; with ≥3 vascular risk factors), asymptomatic for cardiovascular diseases. PCSK9 levels were measured by ELISA. B-mode ultrasound was used to measure markers of carotid subclinical atherosclerosis. (3) Results: in the crude analysis, PCSK9 levels were associated with several baseline measures of carotid intima-media thickness (cIMT) (all p p = 0.01); with inter-adventitia common carotid artery diameter (ICCAD) (p p < 0.0001). However, after adjustment for age, sex, latitude, and pharmacological treatment, all the afore-mentioned correlations were no longer statistically significant. The lack of correlation was also observed after stratification for sex, latitude, and pharmacological treatments. (4) Conclusions: in subjects who are asymptomatic for cardiovascular diseases, PCSK9 plasma levels do not correlate with vascular damage and/or subclinical atherosclerosis of extracranial carotid arteries.

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