Association of high level of hs-CRP with in-stent restenosis: A case-control study
- PMID: 30232022
- DOI: 10.1016/j.carrev.2018.08.015
Association of high level of hs-CRP with in-stent restenosis: A case-control study
Abstract
Background: In-stent restenosis (ISR) is one adverse outcome of coronary stent implantation. Although using drug-eluting stents has reduced the rate of ISR, it remains a major problem. Here, we have investigated the relationship between several patient characteristics including serum high sensitive C-reactive protein (hs-CRP) and ISR.
Methods: This was a case-control study comprising 104 individuals with ISR and 202 patients without. Baseline characteristics were collected using a questionnaire. Fasting blood glucose (FBG), serum triglycerides (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL-C) and serum high sensitivity C-reactive protein (hs-CRP) were measured using commercial kits on an auto-analyzer. Data were analyzed using SPSS software and a p value ≤ 0.05 was considered significant.
Results: Diabetes mellitus (p < 0.001), stent type (p = 0.005), serum hs-CRP (p = 0.006), FBG (p = 0.038) and serum TG (p = 0.039) were significantly associated with ISR. The association between hs-CRP and ISR remained significant after adjustment for stent type and DM. For patients with a serum hs-CRP <2.64 mg/dL, ISR was only associated with diabetes mellitus (p = 0.016); while for individuals with a serum hs-CRP ≥2.64 mg/dL, ISR was also associated with the presence of diabetes mellitus, serum triglycerides and stent type.
Conclusion: Higher levels of serum hs-CRP were significantly associated with the occurrence of ISR.
Keywords: Bare stent; Drug-eluting stent; Hs-CRP; In-stent restenosis (ISR).
Copyright © 2018 Elsevier Inc. All rights reserved.
Comment in
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In-Stent Restenosis, the Achilles' Heel of Percutaneous Coronary Intervention: The Predictive Role of High-Sensitivity C-Reactive Protein.Cardiovasc Revasc Med. 2019 Jul;20(7):542-543. doi: 10.1016/j.carrev.2019.05.008. Epub 2019 May 11. Cardiovasc Revasc Med. 2019. PMID: 31126807 No abstract available.
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