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. 2022 Aug 4;22(1):355.
doi: 10.1186/s12872-022-02762-y.

Association of serum apoA-I with in-stent restenosis in coronary heart disease

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Association of serum apoA-I with in-stent restenosis in coronary heart disease

Xin Wang et al. BMC Cardiovasc Disord. .

Abstract

Background: Despite use of drug-eluting stents (DES), in-stent restenosis (ISR) continues adversely affecting clinical outcomes of patients undergoing percutaneous coronary intervention (PCI). Apolipoprotein A-I (apoA-I) has athero-protective effects. However, there is a paucity of clinical data regarding the association between apoA-I and ISR. We sought to investigate whether serum apoA-I is related to ISR after DES-based PCI.

Methods: In this retrospective case control study, 604 consecutive patients who underwent DES implantation before were enrolled. Patients who underwent repeat angiography within 12 months were included in the early ISR study (n = 205), while those beyond 12 months were included in the late ISR study (n = 399). ISR was defined as the presence of > 50% diameter stenosis at the stent site or at its edges. Clinical characteristics were compared between ISR and non-ISR patients in the early and late ISR study, respectively, after adjusting for confounding factors by multivariate logistic regression, stratified analysis, and propensity score matching. The predictive value was assessed by univariate and multivariate logistic regression analysis, receiver operating characteristic (ROC) curve analysis, and quartile analysis.

Results: In the early ISR study, 8.8% (18 of 205) patients developed ISR. Serum apoA-I in the ISR group was lower than that in the non-ISR group (1.1 ± 0.26 vs. 1.24 ± 0.23, P < 0.05). On multivariate logistic regression analysis, apoA-I was an independent risk factor for early ISR. Incidence of early ISR showed negative correlation with apoA-I and could be predicted by the combined use of apoA-I and glycosylated hemoglobin (HbA1c) level. In the late ISR study, 21.8% (87 of 399) patients developed ISR. On subgroup analysis, late ISR showed negative correlation with apoA-I irrespective of intensive lipid lowering; on multivariate logistic regression analysis, apoA-I was also an independent risk factor for late ISR. In patients with intensive lipid lowering, combined use of apoA-I, stenting time, and diabetes predicted the incidence of late ISR.

Conclusions: ApoA-I was an independent risk factor for ISR, and showed a negative correlation with ISR after DES-based PCI. Combined use of apoA-I and clinical indicators may better predict the incidence of ISR under certain circumstances.

Keywords: Drug-eluting stents; In-stent restenosis; Prediction; apoA-I.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Flowchart of patient enrollment
Fig. 2
Fig. 2
Receiver operating characteristic (ROC) analysis using A apoA-I, B HbA1c, C apoA-I and HbA1c combined, to estimate the strength of the model predicting the incidence of early in-stent restenosis
Fig. 3
Fig. 3
Association of each apoA-I quartile with early ISR incidence, adjusted by three models
Fig. 4
Fig. 4
Receiver operating characteristic (ROC) curve analysis using A apoA-I, B stenting time, C apoA-I and diabetes combined, D apoA-I and stenting time combined, E apoA-I and stenting time and diabetes combined, to estimate the strength of the model predicting the incidence of late in-stent restenosis
Fig. 5
Fig. 5
Association of each apoA-I quartile with late ISR incidence in patients with intensive lipid-lowering, adjusted by three models
Fig. 6
Fig. 6
Receiver operating characteristic (ROC) analysis using apoA-I, to estimate the strength of the model predicting the incidence of late in-stent restenosis after PS matching
Fig. 7
Fig. 7
Association of each apoA-I quartile with late ISR incidence after PS matching, adjusted by three models

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