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Published on: October 12, 2017
Serum lipoprotein (a) level and restenosis after percutaneous coronary intervention
P Lolekha1, W Leowattana, C Kangkagate
1Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Insights
This study investigated lipoprotein (a) (Lp (a)) as a predictor of restenosis after percutaneous coronary intervention (PCI). Researchers found no significant correlation between serum Lp (a) levels and restenosis risk in patients undergoing PCI.
Area of Science:
- Cardiology
- Vascular Biology
- Biochemistry
Background:
- Restenosis after percutaneous coronary intervention (PCI) is a complex pathological process.
- Lipoprotein (a) (Lp (a)) is an emerging risk factor for atherosclerotic vascular disease.
- The association between elevated Lp (a) levels and restenosis post-PCI remains controversial.
Purpose of the Study:
- To investigate the relationship between serum Lp (a) levels and the occurrence of restenosis after PCI.
- To determine if serum Lp (a) concentration can serve as a predictor for restenosis following PCI.
Main Methods:
- A cohort of 100 patients undergoing PCI was studied.
- Patients were categorized into restenosis (31%) and non-restenosis (69%) groups.
- Serum levels of Lp (a), total cholesterol, triglyceride, HDL-C, and LDL-C were measured and compared between groups.
Main Results:
- No significant difference in serum Lp (a) levels was observed between the restenosis and non-restenosis groups (p=0.06).
- Using a cutoff of 30 mg/dL for high Lp (a), no significant correlation with restenosis was found (p=0.08).
- Lipid profiles (total cholesterol, triglyceride, HDL-C, LDL-C) did not significantly differ between the groups.
Conclusions:
- Serum Lp (a) levels do not appear to be a significant predictor of restenosis after PCI in this study population.
- Further research may be needed to elucidate the role of Lp (a) in post-PCI restenosis.
Abstract:
Restenosis is regarded as the result of a combination of various pathological events. The mechanisms are complex and not completely understood. In this study, the authors focused on the lipoprotein (a) (Lp (a)). It is one of the novel risk factors in atherosclerotic vascular disease. Numerous clinical studies suggest that individuals with elevated blood levels of Lp (a) have been shown to be associated with atherosclerotic vascular disease. However, whether a high serum concentration of Lp (a) affects restenosis after PCI remains controversial. In this study, the relationship between serum Lp (a) levels and restenosis after PCI was examined to investigate whether serum Lp (a) levels may be a predictor of restenosis after PCI. Of the 100 patients studied, 31 patients (31%) were classified as the restenosis group and 69 patients (69%) the non-restenosis group. Both groups did not significantly differ in serum concentration of total cholesterol, triglyceride, HDL-C, and LDL-C. The mean serum Lp (a) concentration in patients with restenosis was 41.50 +/- 34.99 mg/dL compared with a mean serum Lp (a) concentration of 29.87 +/- 25.47 mg/dL in those without restenosis. There was no statistical significance of Lp (a) level between the restenosis and non-restenosis groups (p=0.06). In healthy subjects, the normal reference range of serum Lp (a) concentration is below 30 mg/dL. From this reference, if a cut off point of serum Lp (a) concentration equal to 30 mg/dL or above to identify high Lp (a) level group was used. High serum Lp (a) level was established in 15 patients with restenosis versus 21 patients without restenosis. From this cut off point of serum Lp (a) level, the authors did not find a correlation between serum Lp (a) level and the restenosis group. (p=0.08).
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