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Increased Lipoprotein (a) concentrations in patients with chronic venous leg ulcers: a study on patients with or
Markus Zutt1, Ulrich Krüger, Albert Rosenberger
1Department of Dermatology, Venereology and Allergology, University of Göttingen, Göttingen, Germany. mzutt@gwdg.de
Insights
Elevated Lipoprotein (a) [Lp(a)] levels are common in patients with chronic venous leg ulcers, suggesting it may be a novel pathogenic factor. This finding could improve understanding and treatment of these ulcers.
Area of Science:
- Vascular Medicine
- Thrombosis Research
- Dermatology
Background:
- Chronic venous leg ulcers represent a significant global health burden with complex, not fully understood pathophysiology.
- Current knowledge gaps exist regarding reliable pathogenic and prognostic markers for these ulcers.
- Existing data suggest a link between venous leg ulcers and thrombophilia.
Purpose of the Study:
- To investigate serum Lipoprotein (a) [Lp(a)] levels in patients with chronic venous leg ulcers.
- To determine if Lp(a) serves as a pathogenic or prognostic parameter in this patient population.
- To compare Lp(a) levels between patients with and without postthrombotic syndrome and healthy controls.
Main Methods:
- Serum Lp(a) levels were measured in 210 patients with chronic venous leg ulcers (stratified by postthrombotic syndrome) and 341 healthy controls.
- Statistical analysis was performed to compare Lp(a) concentrations across the groups.
- Correlation between Lp(a) and C-reactive protein (CRP) levels was assessed.
Main Results:
- Significantly higher Lp(a) serum concentrations (>0.3 g/L) were observed in 42% of patients with venous leg ulcers compared to 20% of healthy controls.
- Increased Lp(a) levels were found in 49% of patients without postthrombotic syndrome versus 35% with the syndrome.
- Significant differences in Lp(a) levels were noted among all three groups (p<0.001), with no correlation to CRP values.
Conclusions:
- Serum Lp(a) level is a potential novel pathogenic parameter for chronic venous leg ulcers.
- Elevated Lp(a) may contribute to ulcer pathogenesis via thrombogenic microcirculatory dysregulation or impaired fibrinolysis.
- Further research is warranted to elucidate the precise mechanisms of Lp(a) in venous leg ulcer development.
Abstract:
Chronic venous leg ulcers are common and cause considerable burden of disease for affected patients with significant costs for health care systems worldwide. The complex pathophysiology of chronic venous leg ulcers is still not entirely understood. In addition, reliable pathogenic and/or prognostic parameters are not known. Published data suggest that patients with chronic venous leg ulcers reveal congenital or acquired thrombophilia. We examined the serum Lipoprotein (a) [Lp(a)] level, a proatherogenic and prothrombotic risk factor, in patients with chronic venous leg ulcers (n=210, stratified into patients with postthrombotic syndrome or without) and in a healthy control group (n=341). Forty-two percent of all patients, compared with 20% of healthy controls, revealed significantly increased Lp(a) serum concentrations above 0.3 g/L. Furthermore, 49% without postthrombotic syndrome but only 35% with postthrombotic syndrome showed increased Lp(a) levels. The increase of Lp(a) level was significantly different between all three groups (p<0.001). There was no correlation of Lp(a) levels and CRP values in all groups. Based on these data, it is conceivable that Lp(a) plasma level is a novel pathogenic parameter for chronic venous leg ulcers. Elevated concentrations may contribute to the pathogenesis through induction of thrombogenic microcirculatory dysregulations, impaired extravascular fibrinolysis, or other mechanisms like proinflammatory effects.
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