# Plasma Proteome Signature for Leukocyte Telomere Length and Its Link to Abdominal Aortic Aneurysm

## TL;DR

This study identifies plasma proteins linked to leukocyte telomere length and shows how one protein, GDF15, connects telomere shortening to abdominal aortic aneurysm risk.

## Contribution

The paper discovers five proteins causally influenced by telomere length and identifies GDF15 as a mediator of aneurysm risk.

## Key findings

- Fifteen proteins were associated with leukocyte telomere length in White participants.
- GDF15 mediates 12.4% of the link between telomere length and abdominal aortic aneurysm risk.
- Three proteins (MZB1, PLOD3, COL28A1) showed consistent associations across different populations.

## Abstract

Shorter leukocyte telomere length (LTL) is an aging biomarker and risk factor for aging‐related diseases, including abdominal aortic aneurysm (AAA). This study aimed to identify plasma proteins causally associated with LTL and investigate their roles in linking LTL to AAA. A proteomics analysis was conducted for LTL and a polygenic risk score (PRS) for LTL using 4955 plasma proteins by SomaScan in self‐identified White participants (N = 7587–8055) from the Atherosclerosis Risk in Communities (ARIC) study. Replications were evaluated in self‐identified Black participants (N = 1668–2094) from ARIC and White participants (N = 2333–2431) from the Cardiovascular Health Study (CHS). Mendelian randomization (MR) analysis assessed causality between LTL and proteins. Survival and mediation analyses explored protein‐mediated associations between LTL and AAA risk. In ARIC White participants, 15 unique proteins were identified for LTL or LTL PRS. Three LTL‐associated proteins (MZB1, PLOD3, COL28A1) replicated in ARIC Black participants, and six (TNFRSF17, MZB1, CHL1, GDF15, THPO and PLOD3) in CHS White participants. Three proteins associated with LTL PRS (THPO, GP1Bα, PEAR1) replicated in CHS White participants. MR analysis supported causal associations between LTL and five proteins (KDR, TNFRSF17, GDF15, ST3GAL6, CHL1) with all except GDF15 being novel to LTL. LTL was associated with AAA risk (HR = 0.873, 95% CI: 0.803–0.950), with GDF15 mediating 12.4% of this association (p = 0.028). We identified five proteins causally influenced by LTL and highlighted GDF15 as a mediator linking LTL to AAA risk, offering novel insights into aging biology and AAA pathogenesis.