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Published on: October 12, 2017
Relationship between serum homocysteine, fibrinogen, lipoprotein-a level, and peripheral arterial disease: a
Hecheng Wang1, Pengpeng Wu1, Deying Jiang2
1School of Life and Pharmaceutical Sciences, Dalian University of Technology, Dalian, China.
Insights
Elevated serum homocysteine (Hcy), fibrinogen (FIB), and lipoprotein-a (LPa) are linked to increased peripheral artery disease (PAD) risk. Controlling Hcy levels may help reduce PAD incidence.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Epidemiology
Background:
- The association between serum homocysteine (Hcy), fibrinogen (FIB), and lipoprotein-a (LPa) and peripheral artery disease (PAD) requires further clarification.
- A comprehensive meta-analysis to establish dose-response relationships is lacking.
Purpose of the Study:
- To investigate the dose-response relationship between serum Hcy, FIB, LPa levels and the risk of PAD.
- To provide evidence for potential therapeutic targets in PAD prevention.
Main Methods:
- A systematic literature search was conducted across PubMed, Embase, and Web of Science.
- A robust error meta-regression method was employed to assess linear and non-linear dose-response relationships.
- 68 articles involving 565,209 participants were included in the meta-analysis.
Main Results:
- Serum Hcy, FIB, and LPa levels were significantly higher in PAD patients compared to controls.
- Elevated Hcy, FIB, and LPa were associated with increased PAD risk (ORs: 1.47, 1.14, 1.76, respectively).
- A U-shaped distribution was observed between Hcy levels and PAD risk; each 1 μmol/L increase in Hcy correlated with a 7% PAD risk increase.
Conclusions:
- Elevated serum Hcy, FIB, and LPa levels are associated with an increased risk of PAD.
- The risk of PAD escalates with increasing serum exposure levels within a defined range.
- Managing Hcy levels presents a potential strategy to mitigate the growing epidemic of PAD.
Aim:
At present, the relationship between serum homocysteine (Hcy), fibrinogen (FIB), lipoprotein-a (LPa), and PAD is uncertain, and there has been no meta-analysis to establish the dose-response relationship between their exposure levels and PAD.
Methods And Results:
Relevant literature published in PubMed, Embase, and Web of Science was retrieved. The robust error meta-regression method was used to assess the linear and non-linear dose-response relationship between exposure level and PAD risk. A total of 68 articles, involving 565,209 participants, were included. Combined with continuous variables, the serum Hcy, FIB, and LPa levels of PAD patients were significantly higher than those of healthy individuals. The odds ratios (ORs) of PAD for individuals with high Hcy, FIB, and LPa levels compared with those with low levels were 1.47, 1.14, and 1.76, respectively. The study also showed that circulating Hcy, FIB, and LPa were significantly elevated in patients with PAD compared with controls. The level of Hcy and the risk of PAD presented a U-shaped distribution. The nonlinear dose-response model showed that each 1 μmol/L increase in serum Hcy increased the risk of PAD by 7%. Similarly, for each 10 mg/dL FIB and 10 mg/dL LPa increases, the risk of PAD increased by 3% and 6%, respectively.
Conclusions:
This meta-analysis provided evidence that elevated Hcy, PIB, and LPa levels may increase the risk of PAD, and the risk of PAD increases with the increase in serum exposure within a certain range. By controlling Hcy level, the incidence of PAD may be reduced to control the PAD growing epidemic.
Trial Registration Number:
PROSPERO (CRD42021250501), https://www.crd.york.ac.uk/prospero/.
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