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Association between Cystatin C and Peripheral Artery Disease in the Chinese Han Population
Jianqing Deng1, Jie Liu1, Dan Rong1
1Department of Vascular and Endovascular Surgery, Chinese PLA General Hospital, Beijing, China.
Insights
Elevated cystatin C levels are linked to a higher risk of peripheral artery disease (PAD) in the Chinese Han population. This study suggests cystatin C may serve as a biomarker for PAD risk.
Area of Science:
- Cardiovascular Research
- Biomarker Discovery
- Epidemiology
Background:
- Inconsistent findings exist regarding the association between cystatin C and peripheral artery disease (PAD).
- Limited research has explored this link specifically within the Chinese Han population.
Purpose of the Study:
- To investigate the relationship between serum cystatin C levels and PAD.
- To assess potential dose-dependent associations and explore the link with PAD severity in a Chinese cohort.
Main Methods:
- Secondary analysis of a case-control study involving 426 participants.
- Logistic regression, subgroup, and interaction analyses were employed.
- Propensity score matching and analysis of ankle-brachial index (ABI) strata were used to validate findings and explore severity.
Main Results:
- Serum cystatin C was significantly higher in PAD cases (1.24 ± 0.34 mg/L) versus controls (1.06 ± 0.19 mg/L).
- Elevated cystatin C (≥1.25 mg/L) was associated with increased PAD risk, with a 17% higher risk per 100-μg/L increase.
- Lower ABI (<0.4) correlated with higher cystatin C levels, suggesting a link to PAD severity.
Conclusions:
- Higher serum cystatin C levels are significantly associated with an increased risk of PAD in the Chinese Han population.
- Cystatin C may serve as a valuable biomarker for PAD risk in this demographic.
- Further prospective cohort studies in China are recommended for validation.
Background:
Recent studies of the association between cystatin C and peripheral artery disease (PAD) have produced inconsistent results, and few studies have been conducted to investigate this association in the Chinese Han population. Therefore, we evaluated the relationship between cystatin C and PAD using Chinese data.
Methods:
We performed a secondary analysis of the data from a previously published case-control study about PAD in our center. We examined the relationship between cystatin C and PAD by logistic regression models and subgroup and interaction analyses. We also constructed a propensity score-matched population by matching the conventional risk factors to further validate this association. In addition, we explored the relationship between cystatin C level and ankle-brachial index (ABI) strata (<0.4, ≥0.4) to shed light on a possible dose-dependent relationship between cystatin C levels and PAD severity.
Results:
In total, 426 participants were included for evaluation. The mean serum cystatin C concentration was significantly lower in the control group than that in the case group (1.06 ± 0.19 mg/L vs. 1.24 ± 0.34 mg/L, P < 0.001). After adjustment for conventional risk factors, the risk of PAD was significantly higher in individuals with a cystatin C level of ≥1.25 mg/L. A 17% higher risk of PAD was associated with each 100-μg/L increase in the serum cystatin C level. Similar results were seen in the analyses of the propensity score-matched population comprising 164 participants. Furthermore, patients with an ABI <0.4 had higher cystatin C level than those with an ABI ≥0.4 (1.31 ± 0.05 mg/L vs. 1.18 ± 0.03 mg/L, P = 0.03).
Conclusions:
Our analysis indicated that an elevated cystatin C level is significantly associated with an increased risk of PAD in the Chinese Han population. Larger Chinese prospective cohort studies are needed to validate these findings.
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