# The relationship between fibrinogen-to-albumin ratio and brachial-ankle pulse wave velocity in elderly individuals in China: a cross-sectional study

**Authors:** Yang Zhang, Nan Lu, Yucheng Liu, Jiaxing Ke, Ende Hu, Shanni Chai, Haifeng Chen

PMC · DOI: 10.3389/fcvm.2026.1737344 · Frontiers in Cardiovascular Medicine · 2026-02-09

## TL;DR

This study finds that a higher fibrinogen-to-albumin ratio is linked to increased vascular aging in elderly Chinese individuals.

## Contribution

The study establishes a novel association between the fibrinogen-to-albumin ratio and brachial-ankle pulse wave velocity in elderly populations.

## Key findings

- Higher fibrinogen-to-albumin ratio quartiles correlate with increased arteriosclerosis prevalence.
- Fibrinogen-to-albumin ratio independently predicts brachial-ankle pulse wave velocity in elderly individuals.
- The association between fibrinogen-to-albumin ratio and arteriosclerosis is linear and dose-dependent.

## Abstract

Arteriosclerosis, a hallmark of vascular aging, can be assessed using brachial-ankle pulse wave velocity (baPWV). The fibrinogen-to-albumin ratio (FAR), a novel marker reflecting inflammation and hemodynamics, has been proposed as a potential indicator for cardiovascular disease (CVD). However, the association between FAR and baPWV has not been fully elucidated. This study seeks to investigate this association.

A total of 389 elderly patients were enrolled. Arteriosclerosis was defined as a baPWV ≥1,800 cm/s. Participants were divided into four groups according to FAR quartiles. Multivariate logistic regression was used to assess the association between FAR quartiles and arteriosclerosis. Restricted cubic spline (RCS) analysis was additionally employed to examine the dose–response relationship between continuous FAR and arteriosclerosis risk.

The prevalence of arteriosclerosis increased significantly with increasing FAR quartiles (61.2%, 61.9%, 77.3%, 86.6%; p < 0.001). Multivariate linear regression demonstrated an independent positive correlation between FAR and baPWV (β = 13.283, 95% CI: 0.286–26.281, p = 0.046). In multivariate logistic regression, higher FAR quartiles were linked to higher odds ratios (ORs) for arteriosclerosis (Q2: OR = 0.997, 95% CI: 0.521–1.907, p = 0.992; Q3: OR = 2.094, 95% CI: 1.048–4.186, p = 0.036; Q4: OR = 2.804, 95% CI: 1.258–6.248, p = 0.012) with a significant trend (p for trend = 0.002). RCS analysis further confirmed a linear association between FAR and arteriosclerosis risk (p for non-linearity >0.05).

In elderly adults, FAR is independently and positively associated with baPWV, suggesting its potential as an additional biomarker for evaluating vascular aging.

## Linked entities

- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** malignancies (MESH:D009369), DM (MESH:D003920), valvular heart disease (MESH:D006349), Arteriosclerosis (MESH:D001161), coronary heart disease (MESH:D003327), Dyslipidemia (MESH:D050171), peripheral vascular disease (MESH:D016491), Inflammation (MESH:D007249), systemic lupus erythematosus (MESH:D008180), ischemia (MESH:D007511), myocarditis (MESH:D009205), Hypoalbuminemia (MESH:D034141), acute cerebral infarction (MESH:D056989), cerebrovascular disease (MESH:D002561), cerebral infarction (MESH:D002544), atrial fibrillation (MESH:D001281), infections (MESH:D007239), coagulation (MESH:D001778), CVD (MESH:D002318), acute myocardial infarction (MESH:D009203), Atherosclerosis (MESH:D050197), hypertension (MESH:D006973), thrombosis (MESH:D013927), carotid atherosclerosis (MESH:D002340), rheumatoid arthritis (MESH:D001172), lacunar stroke (MESH:D059409), liver dysfunction (MESH:D017093), CAD (MESH:D003324), type 2 diabetes mellitus (MESH:D003924)
- **Chemicals:** TG (MESH:D014280), UA (MESH:D014527), cholesterol (MESH:D002784), FAR (-), ROS (MESH:D017382), glucose (MESH:D005947), creatinine (MESH:D003404)
- **Species:** HC [taxon 11103], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** -455G/A, -148C/T

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926422/full.md

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Source: https://tomesphere.com/paper/PMC12926422