# Proprotein convertase subtilisin/kexin type 9: a promising marker of cardiovascular risk in post-menopausal diabetic women in primary prevention

**Authors:** Michelangelo Rottura, Maria Antonietta Barbieri, Carmine Siniscalchi, Pierpaolo Di Micco, Selene Francesca Anna Drago, Marianna Gigliotti De Fazio, Arrigo Francesco Giuseppe Cicero, Federica Fogacci, Giuseppe Armentaro, Angela Sciacqua, Vincenzo Arcoraci, Natasha Irrera, Egidio Imbalzano

PMC · DOI: 10.3389/fmed.2025.1521344 · 2025-03-12

## TL;DR

This study explores how PCSK9 levels relate to cardiovascular risk in post-menopausal diabetic women, finding a link with blood pressure and cholesterol markers.

## Contribution

The study identifies ApoB and LDL as factors influencing PCSK9 levels and shows PCSK9's direct effect on pulse wave velocity in diabetic women.

## Key findings

- Apolipoprotein B is an independent predictor of PCSK9 levels.
- PCSK9 levels are inversely related to LDL cholesterol levels.
- PCSK9 levels directly influence pulse wave velocity in post-menopausal diabetic women.

## Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) increases circulating LDL levels and cardiovascular disease (CVD) risk; its levels may be related to the dysregulation of glycemic control and may be affected by estrogens. The aim of this study was to assess factors related to PCSK9 levels, and to evaluate the correlation between PCSK9 levels and CV parameters in post-menopausal diabetic women in primary prevention.

Generalized linear models (GLM) were adopted to evaluate predictors of PCSK9 levels as well as factors related to CV outcomes, such as pulse wave velocity (PWV), pulse pressure (PP), and augmentation index (AI).

A total of 135 post-menopausal diabetic women, with a median (Q1-Q3) serum PCSK9 levels of 370.3 (344.0–409.4) ng/ml were enrolled. Apolipoprotein B values resulted an independent predictor of PCSK9 levels (B = 1.023; p < 0.001). However, LDL values were inversely related to PCSK9 levels (B = −0.578; p < 0.001). PCSK9 levels influenced PWV (B = 0.010; p = 0.010), but did not influence other CV outcomes.

ApoB and LDL may influence PCSK9 levels and PCSK9 directly influence PWV in post-menopausal diabetic women in primary prevention. Therefore, the relationship between PCSK9 and primary prevention cannot be excluded, thus highlighting its role as biomarker of CV risk.

## Linked entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738]
- **Proteins:** LDL (LDL cholesterol), APOB (apolipoprotein B)
- **Diseases:** diabetes (MONDO:0005015), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}
- **Diseases:** CVD (MESH:D002318), diabetic (MESH:D003920)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11936939/full.md

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Source: https://tomesphere.com/paper/PMC11936939