Skip to main content

Advertisement

We’d like to understand how you use our websites in order to improve them. Register your interest.

Effects of angiotensin receptor blockers on neointimal characteristics in angina patients requiring stent implantation: optical coherence tomography analysis

Abstract

Background

Angiotensin receptor blockers (ARBs) are known for its anti-inflammatory and anti-proliferative effects. The aim of the study was to evaluate long-term effects of ARBs on morphologic characteristics of stent restenosis in patients with coronary artery disease requiring stent implantation by optical coherence tomography (OCT).

Methods

Patients with coronary artery disease having history of drug-eluting stent implantation (n = 407) were analyzed on the basis of ARB therapy as the ARB group (n = 162) and the non-ARB group (n = 245). Neointimal characterizations were performed at lesions with diameter stenosis >30% with OCT in each group. Major adverse cardiovascular events (MACEs), lumen area, stent area, neointimal area, neointimal thickness, nonapposed struts, uncovered struts, and intraluminal mass between two groups were also observed.

Results

More patients in the ARB group revealed homogeneous and layered neointimal pattern (44.9% vs. 35.6%, P < 0.001, and 16.8% vs. 10.6%, P < 0.001, respectively), and whereas patients in the non-ARB group revealed heterogeneous neointimal pattern (1.1% vs. 7.6%, P < 0.001). Mean neointimal area (1.09 ± 1.00 mm2 vs. 1.38 ± 1.24 mm2) and mean neointimal thickness (140.6 ± 112.0 μm vs. 189.6 ± 423.1 μm) with OCT were smaller in the ARB group when compared to the non-ARB group. Percentage of covered stents was significantly higher in the ARB group when compared to the Non-ARB group (97.3% vs. 92.6%, P = 0.015). Other factors such as follow-up % diameter stenosis, late lumen loss, binary restenosis, MACEs, various neointimal characteristics analyzed by image analyzing software did not show significant differences.

Conclusion

The use of ARBs after drug-eluting stent implantation demonstrated difference in neointimal characteristics, less amount of neointimal area and fewer number of uncovered stent struts during the follow-up OCT, indicating the anti-proliferative and anti-inflammatory effects of ARBs.

Peer Review reports

Background

Angiotensin receptor blockers (ARBs) have been widely used in hypertensive patients with coronary artery disease (CAD) requiring stent implantation. In addition to its antihypertensive effect, ARBs are also known for their anti-inflammatory and anti-proliferative effects. The renin–angiotensin system has been implicated in the pathogenesis of restenosis and acute coronary syndrome [1,2,3,4,5,6] and, thus, may be a potential target for the prevention of in-stent restenosis and atherothrombotic events in patients who have CAD. It is well known that direct vascular effects of angiotensin II include vasoconstriction, inflammation, endothelial dysfunction, and stimulation of growth processes and remodeling, which are mediated by type 1 receptors [3, 7]. The single-center VALsartan for Prevention of REstenosis after Stenting of Type B2/C lesions (VAL-PREST) trial documented the remarkable therapeutic effects of the ARB valsartan on restenosis after stenting in complex coronary lesions [8]. In that trial, the ARB was more effective than placebo for preventing in-stent intimal proliferation and its superiority over an angiotensin-converting enzyme (ACE) inhibitor can be predicted from the result that 68% of patients in the placebo group were taking an ACE inhibitor.

Optical coherence tomography (OCT) is an emerging intracoronary diagnostic modality that provides high-resolution images of coronary artery in vivo [9]. In addition to tissue characterization in native coronary plaques, OCT has been applied to characterize neointima after stent implantation [10]. Indeed, several OCT studies revealed the development of lipid-laden neointima inside the stents, and OCT has become the modality of choice to study atherosclerotic change of neointima [11,12,13]. However, correlation between anti-proliferative effect of ARB and change of neointimal characterization has not been studied yet. We investigated and compared the long-term effects of ARBs on neointimal characteristics in patients with CAD requiring stent implantation by OCT image analysis.

Methods

Study design and patients

This study was based on a retrospective observational data on patients who underwent OCT in Korea university Anam hospital between January 2011 and December 2012. Patients with CAD having history of drug-eluting stent (DES) implantation were analyzed on the basis of ARB therapy. Type of ARB or DES was not limited and administering other medications such as aspirin, β-blocker, calcium channel blocker for angina was not prohibited. Patients were divided in terms of taking ARBs as the ARB group and the non-ARB group. Inclusion criteria were: age between 40 to 75 years, CAD requiring drug-eluting stent implantation, diagnosed with hypertension or under antihypertensive medications, and OCT measurements during the follow-up. Patients with left main CAD, previous history of coronary artery bypass graft, acute myocardial infarction (MI), chronic total occlusion, ejection fraction <50%, unsuccessful reperfusion after coronary stent implantation, and liver or renal dysfunction were excluded from this study. Age and risk factor matching (diabetes, hyperlipidemia, smoking, family history of CAD) was performed. Major adverse cardiovascular events (MACEs) such as all-cause death, non-fatal MI, stroke, and target lesion revascularization (TLR) were compared between the two groups during the follow-up.

Quantitative coronary angiography

Offline quantitative coronary angiography (QCA) was conducted using the view that revealed the highest degree of stenosis. Severity of coronary stenosis was measured using the Cardiovascular Measurement System (MEDIS Medical Imaging System; Leiden, The Netherlands). For every patient, angiograms were analyzed at the time of OCT examination. Lesion length, reference diameter, minimal luminal diameter, and percent diameter stenosis were calculated by a single operator who was blinded to clinical characteristics. Analysis of angiographic frames was performed in the end-diastolic stage. Angiographic restenotic lesion type was classified as follows: focal restenosis, <10 mm in length (A) (articulation or gap [IA], margin [IB], focal body [IC], multifocal [ID]), or diffuse intrastent restenosis (B), >10 mm in length (intrastent [II], proliferative [III]) [14].

OCT examination and analysis

OCT examination and analysis was performed during the follow-up (LightLab Imaging Inc., Ilumien Offline review workstation, Ver D.O 2, MA, USA). Under guidance of a 0.014 in. angioplasty wire, OCT imaging catheter (C7 DragonflyTM, LightLab Imaging Inc., MA, USA) was advanced into the distal end of the DES implantation site. The entire length of the stent was imaged with an automatic pullback device moving at 15 mm/s and the OCT image clearly visualized the stent cross-section.

Neointimal characterizations were performed with OCT images at lesions of diameter stenosis >30% and were analyzed into two groups with same lesions by experienced observers using established criteria [10, 15]. The first group was categorized simply with patterns defining neointimal tissue structure of homogeneous, heterogeneous or layered (Fig. 1). Another group was classified into seven categories using densitometric analysis with image analyzing software (Image Pro Plus 7.0, Media cybernetics Inc., Bethesda, MD, USA): (1) macrophage, (2) cholesterol plaque, (3) fibrous plaque, (4) proteoglycan rich plaque, (5) calcified plaque, (6) lipid plaque, and (7) neovascularization. With densitometry, ranging from contrast of minimum 0(darkest) to maximum 255(brightest), lipid or calcified plaque or neovascularization was set to 0–69 (purple), proteoglycan plaque to 70–108 (yellow), fibrous plaque to 109–194 (orange) and macrophage or cholesterol crystal to 195–255 (red) (Fig. 2). Overlapping categories (macrophage or cholesterol crystal and lipid plaque or calcified plaque or neovascularization) could not be differentiated by densitometry; therefore, setting boundaries manually between overlapping categories and calculating ratio with pixels was done manually (Fig. 3). Lumen area, stent area, neointimal area, neointimal thickness, nonapposed struts, uncovered struts, and intraluminal mass were also observed.

Fig. 1
figure1

Neointimal characterizations. a Homogeneous b Heterogeneous c Layered

Fig. 2
figure2

Neointimal characterizations categorizing by contrast-color matching. a Original OCT finding b Macrophage or cholesterol crystal c Fibrous plaque d Proteoglycan plaque e Lipid or calcified plaque or neovascularization f Whole image of analysis

Fig. 3
figure3

Neointimal characterizations categorizing by contrast-color matching. a original OCT finding filled with contrast-color category b Count whole contrast-color pixels (color pink) c Set boundary of corresponding lesion (green)

Study endpoints

Primary end point was to compare neointimal characteristics and neointimal area with OCT during the follow-up. The secondary end point was to compare major adverse cardiovascular events (MACEs defined as non-fatal MI, death, stroke, and TLR) and late lumen loss, diameter stenosis, in-stent restenosis (defined according to the Academic Research Consortium criterion) [16] during the follow-up.

Statistical analysis

Categorical variables are expressed as numbers and percentages. Continuous variables are expressed as mean ± SD. Comparisons between groups were performed with 2-tailed Student t test for continuous variables and with χ2 or Fisher exact test for categorical variables. The reproducibility of qualitative variables was assessed with κ test. A P < 0.05 was considered statistically significant. All statistical analyses were performed using SPSS (SPSS 12.0; Chicago, IL) software.

Results

Participant characteristics and baseline assessments

In total, we included 407 patients who were diagnosed as CAD having history of DES implantation and underwent OCT. Of these patients, 162 (39.8%) were in ARB group and 245 (60.2%) were in non-ARB group. Patient baseline characteristics were well matched in the study groups except sex. In the ARB group, fewer patients were male compared with the non-ARB group (66.0% vs. 79.6%, P = 0.002). Regarding as a retrospective data, various types of ARB were used in this study but difference of other medication use for angina was not statistically significant except CCB (24.1% vs. 68.9%, P < 0.001) (Table 1).

Table 1 Baseline patient characteristics

Target lesion characteristics and QCA analysis

Target arteries or types of target lesion did not differ within both groups (Table 2). Atherosclerotic lesions were located in left anterior descending artery (LAD) mainly (72.8% vs. 68.7%, P = 0.129), and angiographic restenotic lesion type C took the largest portion in both groups (44.1% vs. 43.3%, P = 0.939). Although several types of DES used in the study, there was no significant difference. Also, QCA findings on baseline, postprocedure and OCT follow-up revealed no significant differences in any parameters between the 2 groups (Table 3).

Table 2 Target lesion characteristics
Table 3 QCA Measurements at baseline

Endpoints

Descripted above, neointimal characteristics obtained by OCT were analyzed in two different methods, three patterns of homogenous, heterogeneous or layered and seven categories of using image analyzing software. As we analyzed with former method, all three patterns were differed with statistical significance between two groups (Table 4). Homogeneous and layered pattern existed more in the ARB group (44.9% vs. 35.6%, P < 0.001 and 16.8% vs. 10.6%, P < 0.001, respectively), whereas heterogeneous pattern was more seen in the non-ARB group (1.1% vs. 7.6%, P < 0.001). By using latter method, both groups were statistically similar (Table 4), but macrophage seemed to be lower in the ARB group (0.98% vs. 1.23%, P = 0.225). Secondary endpoints consist with comparing major adverse cardiovascular events and late lumen loss, diameter stenosis, in-stent restenosis during the follow-up did not show any statistical significance, although patients in the ARB group were more likely to occur TLR than the non-ARB group (15.4% vs. 9.4%, P = 0.077). In quantitive OCT findings, stent struts were covered more likely in the ARB group than the non-ARB group (97.3% vs. 92.6%, P = 0.015) (Table 5).

Table 4 Primary endpoint. Neointimal characterization by OCT
Table 5 Secondary endpoint. Cardiovascular events, QCA measurements and quantitative OCT findings during the follow-up period

Discussion

Stent restenosis is an infrequent but poorly understood clinical problem in the drug-eluting stent era and its treatment is challenging. Experimental and clinical studies have identified excessive neointimal hyperplasia as leading cause of stent restenosis [17,18,19]. Neointima was composed of various characteristic lesions, such as fibrous tissue, proteoglycan-rich tissue, approved by pathologic examination of restenosis in bare-metal stent (BMS) and in DES in tissue samples obtained by atherectomy [20]. In the other hand, ARBs inhibit atherosclerosis as reduced plaque burden in atherosclerotic vessels and reduced incidence of in-stent restenosis [21]. In this concept of anti-inflammatory and anti-proliferative effect of ARBs toward atherosclerosis and neointimal growth, our present study assessed difference of neointimal characterization in use of long term ARBs by OCT. Furthermore, we tried to discover changes of specific neointimal component related to ARBs use.

Neointimal characterization in OCT was analyzed into two groups: a group which is classified conventionally into three patterns of homogeneous, heterogeneous and layered, and another group of specific neointimal component described above in methods. Considering former group, although currently no OCT criteria have been validated with histology for the identification of these tissue types, there are consumptions of each pattern correlating with neointimal characteristics. Homogeneous pattern is regarded identical to fibrous plaque, which was shown predominance in DES comparing with BMS [20]. Heterogeneous pattern is believed to be a mixture of various neointimal components within whole portion of neointimal growth that might result to show different optical properties [10]. Layered pattern could be visualized in OCT based on pathologic examinations that have demonstrated the density and orientation of smooth muscle cells vary within restenotic tissue compared to the inner luminal border and tissue located far from the lumen [22]. In the current study, homogeneous and layered pattern of neointima were more likely to be present in use of ARBs. Considering an experimental data that ARBs increased the thickness of the fibrous cap and collagen content in the plaque resulting in reduce of plaque vulnerability [23] and homogeneous pattern is identical to fibrous plaque, our result suggests neointimal change seen in OCT by ARBs may have correlation histopathology. As layered pattern is known to be divided into the inner luminal border, which the smooth muscle cells are more compact and show a homogeneous concentric orientation, whereas the density of cells decreases and the orientation becomes more heterogeneous in the tissue located far from the lumen, it can be assumed that stabilized neointima by ARBs can be explained as homogeneous portion. In contrast, heterogeneous pattern was more appeared in the non-ARB group. This can mean in an opposite view that anti-inflammatory effect of ARBs play a role for less appearing of heterogeneous pattern in long-term ARBs use.

Another goal was to objectify and quantify specific neointimal component by using image analyzing software, so as to classify lesions easily. However, an attempt to discover changes of specific neointimal component related to ARBs use has failed, although macrophage seemed to be lower in the ARB group (0.98% vs. 1.23%, P = 0.225), but in other hand, recent study showed decreased plaque macrophages after use of ARBs in histological evaluation [23]. Main cause of the difference between histological finding and result OCT analysis by densitometry can be thought as the measurement bias, as lesions were defined not by characteristic morphology but brightness.

Interestingly, stent struts were covered more likely in the ARB group than the non-ARB group (97.3% vs. 92.6%, P = 0.015). Degree of reendothelialization, which is identical with coverage of stent struts, is regarded as the most powerful predictor of stent thrombosis proven by an autopsy or animal study [24, 25]. ARBs attenuate in-stent neointima formation by inhibiting inflammation and progenitor cells, and in other hand, angiotensin II is known to exert an inhibitory effect on thrombolysis, stimulating thrombus formation, suggesting that ARBs may have an anti-thrombotic effect also [26, 27]. Contradiction of opposing effects of ARBs may have caused the situation that there was no difference of cardiovascular event including thrombotic diseases between the ARB and non-ARB group.

Study limitations

Present study has several limitations. Unlike prior studies that revealed ARBs reduced incidence of in-stent restenosis, difference of TLR between two groups in our result did not show any statistical significance. It may be because of the retrospective character, the limited sample size, or different types of ARBs were used in this study. Available data suggest that the beneficial effects of ARBs on atherosclerosis cannot be considered a class effect. Losartan and candesartan have not shown any effect on atherosclerosis or on in-stent restenosis, but valsartan, olmesartan and telmisartan appear to have a significant beneficial effect [21]. Also, various types of DES were used, from first generation (SES) to second generation (EES, BES, ZES), limiting this study that second-generation DES lead to a lower percentage of uncovered and malapposed struts, as well as a lower incidence of intra-stent thrombi, compared with first-generation DES [28, 29]. Measurement bias in analyzing densitometry with image analyzing software was described above in discussion.

Conclusions

In conclusion, the use of ARBs after DES implantation demonstrated different neointimal characteristics when compared with the non-ARB group, and stent struts were covered more likely with the use of ARBs during the follow-up OCT, indicating the anti-inflammatory effects of ARBs. For more definite conclusions, long-term clinical and serial OCT follow-up with a larger population will be needed in the future.

Abbreviations

ACE:

Angiotensin converting enzyme

ARB:

Angiotensin receptor blocker

BMS:

Bare-metal stent

CAD:

Coronary artery disease

DES:

Drug-eluting stent

MACE:

Major adverse cardiovascular event

OCT:

Optical coherence tomography

QCA:

Quantitative coronary angiography

TLR:

Target lesion revascularization

VAL-PREST:

Valsartan for prevention of restenosis after Stenting of Type B2/C lesions trial

References

  1. 1.

    Bell L, Madri JA. Influence of the angiotensin system on endothelial and smooth muscle cell migration. Am J Pathol. 1990;137(1):7–12.

  2. 2.

    Daemen MJ, Lombardi DM, Bosman FT, Schwartz SM. Angiotensin II induces smooth muscle cell proliferation in the normal and injured rat arterial wall. Circ Res. 1991;68(2):450–6.

  3. 3.

    Gibbons GH, Dzau VJ. The emerging concept of vascular remodeling. N Engl J Med. 1994;330(20):1431–8.

  4. 4.

    Prasad A, Koh KK, Schenke WH, Mincemoyer R, Csako G, Fleischer TA, Brown M, Selvaggi TA, Quyyumi AA. Role of angiotensin II type 1 receptor in the regulation of cellular adhesion molecules in atherosclerosis. Am Heart J. 2001;142(2):248–53.

  5. 5.

    Tharaux PL, Chatziantoniou C, Fakhouri F, Dussaule JC. Angiotensin II activates collagen I gene through a mechanism involving the MAP/ER kinase pathway. Hypertension (Dallas, Tex: 1979). 2000;36(3):330–6.

  6. 6.

    Wolf G. Free radical production and angiotensin. Curr Hypertens Rep. 2000;2(2):167–73.

  7. 7.

    Dzau VJ. Theodore Cooper lecture: tissue angiotensin and pathobiology of vascular disease: a unifying hypothesis. Hypertension (Dallas, Tex: 1979). 2001;37(4):1047–52.

  8. 8.

    Peters S, Gotting B, Trummel M, Rust H, Brattstrom A. Valsartan for prevention of restenosis after stenting of type B2/C lesions: the VAL-PREST trial. The Journal of invasive cardiology. 2001;13(2):93–7.

  9. 9.

    Yabushita H, Bouma BE, Houser SL, Aretz HT, Jang IK, Schlendorf KH, Kauffman CR, Shishkov M, Kang DH, Halpern EF, et al. Characterization of human atherosclerosis by optical coherence tomography. Circulation. 2002;106(13):1640–5.

  10. 10.

    Gonzalo N, Serruys PW, Okamura T, van Beusekom HM, Garcia-Garcia HM, van Soest G, van der Giessen W, Regar E. Optical coherence tomography patterns of stent restenosis. Am Heart J. 2009;158(2):284–93.

  11. 11.

    Habara M, Terashima M, Nasu K, Kaneda H, Inoue K, Ito T, Kamikawa S, Kurita T, Tanaka N, Kimura M, et al. Difference of tissue characteristics between early and very late restenosis lesions after bare-metal stent implantation: an optical coherence tomography study. Circulation Cardiovascular interventions. 2011;4(3):232–8.

  12. 12.

    Kang SJ, Mintz GS, Akasaka T, Park DW, Lee JY, Kim WJ, Lee SW, Kim YH, Whan Lee C, Park SW, et al. Optical coherence tomographic analysis of in-stent neoatherosclerosis after drug-eluting stent implantation. Circulation. 2011;123(25):2954–63.

  13. 13.

    Takano M, Yamamoto M, Inami S, Murakami D, Ohba T, Seino Y, Mizuno K. Appearance of lipid-laden intima and neovascularization after implantation of bare-metal stents extended late-phase observation by intracoronary optical coherence tomography. J Am Coll Cardiol. 2009;55(1):26–32.

  14. 14.

    Mehran R, Dangas G, Abizaid AS, Mintz GS, Lansky AJ, Satler LF, Pichard AD, Kent KM, Stone GW, Leon MB. Angiographic patterns of in-stent restenosis: classification and implications for long-term outcome. Circulation. 1999;100(18):1872–8.

  15. 15.

    Tearney GJ, Yabushita H, Houser SL, Aretz HT, Jang IK, Schlendorf KH, Kauffman CR, Shishkov M, Halpern EF, Bouma BE. Quantification of macrophage content in atherosclerotic plaques by optical coherence tomography. Circulation. 2003;107(1):113–9.

  16. 16.

    Cutlip DE, Windecker S, Mehran R, Boam A, Cohen DJ, van Es GA, Steg PG, Morel MA, Mauri L, Vranckx P, et al. Clinical end points in coronary stent trials: a case for standardized definitions. Circulation. 2007;115(17):2344–51.

  17. 17.

    Farb A, Sangiorgi G, Carter AJ, Walley VM, Edwards WD, Schwartz RS, Virmani R. Pathology of acute and chronic coronary stenting in humans. Circulation. 1999;99(1):44–52.

  18. 18.

    Hoffmann R, Mintz GS, Dussaillant GR, Popma JJ, Pichard AD, Satler LF, Kent KM, Griffin J, Leon MB. Patterns and mechanisms of in-stent restenosis. A serial intravascular ultrasound study. Circulation. 1996;94(6):1247–54.

  19. 19.

    Nakatani M, Takeyama Y, Shibata M, Yorozuya M, Suzuki H, Koba S, Katagiri T. Mechanisms of restenosis after coronary intervention: difference between plain old balloon angioplasty and stenting. Cardiovasc Pathol. 2003;12(1):40–8.

  20. 20.

    van Beusekom HM, Saia F, Zindler JD, Lemos PA, Swager-ten Hoor SL, van Leeuwen MA, de Feijter PJ, Serruys PW, van der Giessen WJ. drug-eluting stents show delayed healing: paclitaxel more pronounced than sirolimus. Eur Heart J. 2007;28(8):974–9.

  21. 21.

    Peters S. Inhibition of atherosclerosis by angiotensin II type 1 receptor antagonists. American journal of cardiovascular drugs: drugs, devices, and other interventions. 2013;13(4):221–4.

  22. 22.

    van Beusekom HM, van der Giessen WJ, van Suylen R, Bos E, Bosman FT, Serruys PW. Histology after stenting of human saphenous vein bypass grafts: observations from surgically excised grafts 3 to 320 days after stent implantation. J Am Coll Cardiol. 1993;21(1):45–54.

  23. 23.

    Hotchi J, Hoshiga M, Takeda Y, Yuki T, Fujisaka T, Ishihara T, Hanafusa T. Plaque-stabilizing effect of angiotensin-converting enzyme inhibitor and/or angiotensin receptor blocker in a rabbit plaque model. J Atheroscler Thromb. 2013;20(3):257–66.

  24. 24.

    Finn AV, Joner M, Nakazawa G, Kolodgie F, Newell J, John MC, Gold HK, Virmani R. Pathological correlates of late drug-eluting stent thrombosis: strut coverage as a marker of endothelialization. Circulation. 2007;115(18):2435–41.

  25. 25.

    Joner M, Nakazawa G, Finn AV, Quee SC, Coleman L, Acampado E, Wilson PS, Skorija K, Cheng Q, Xu X, et al. Endothelial cell recovery between comparator polymer-based drug-eluting stents. J Am Coll Cardiol. 2008;52(5):333–42.

  26. 26.

    Ohtani K, Egashira K, Ihara Y, Nakano K, Funakoshi K, Zhao G, Sata M, Sunagawa K. Angiotensin II type 1 receptor blockade attenuates in-stent restenosis by inhibiting inflammation and progenitor cells. Hypertension (Dallas, Tex: 1979). 2006;48(4):664–70.

  27. 27.

    Voors AA. Vascular benefits of angiotensin receptor blockers. Expert Opin Investig Drugs. 2007;16(7):987–97.

  28. 28.

    Kim BK, Kim JS, Park J, Ko YG, Choi D, Jang Y, Hong MK. Comparison of optical coherence tomographic assessment between first- and second-generation drug-eluting stents. Yonsei Med J. 2012;53(3):524–9.

  29. 29.

    Iannaccone M, D'Ascenzo F, Templin C, Omedè P, Montefusco A, Guagliumi G, Serruys PW, Di Mario C, Kochman J, Quadri G, et al. Optical coherence tomography evaluation of intermediate-term healing of different stent types: systemic review and meta-analysis. European heart journal cardiovascular imaging. 2017;18(2):159–66.

Download references

Acknowledgments

Not applicable.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Availability of data and materials

This research was performed utilizing existing data from multiple EMRs within Korea University Anam Hospital. Data supporting the results reported in the article are available from the corresponding author on reasonable request.

Author information

Affiliations

Authors

Contributions

All named authors were involved in this project. SJH and DSL conceived and designed the study, provided methodological advice, participated in data interpretation and provided guidance and revisions for final draft of the manuscript. JYC assisted with study design and data analysis, performed literature study and wrote the first several drafts of the manuscript. All authors have read and approved the final draft of this manuscript.

Corresponding author

Correspondence to Do-Sun Lim.

Ethics declarations

Ethics approval and consent to participate

The institutional review board (IRB) of Korea University Anam Hospital approved this study with a waiver of informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Cho, J.Y., Hong, S.J. & Lim, D. Effects of angiotensin receptor blockers on neointimal characteristics in angina patients requiring stent implantation: optical coherence tomography analysis. BMC Cardiovasc Disord 17, 278 (2017). https://doi.org/10.1186/s12872-017-0709-9

Download citation

Keywords

  • Angiotensin receptor blockers
  • Neointima
  • Drug-eluting stents
  • Optical coherence tomography