Literature DB >> 25375841

Association between tissue characteristics of coronary plaque and distal embolization after coronary intervention in acute coronary syndrome patients: insights from a meta-analysis of virtual histology-intravascular ultrasound studies.

Song Ding1, Longwei Xu1, Fan Yang1, Lingcong Kong1, Yichao Zhao1, Lingchen Gao1, Wei Wang1, Rende Xu1, Heng Ge1, Meng Jiang1, Jun Pu1, Ben He1.   

Abstract

BACKGROUND AND OBJECTIVES: The predictive value of plaque characteristics assessed by virtual histology-intravascular ultrasound (VH-IVUS) including fibrous tissue (FT), fibrofatty (FF), necrotic core (NC) and dense calcium (DC) in identifying distal embolization after percutaneous coronary intervention (PCI) is still controversial. We performed a systematic review and meta-analysis to summarize the association of pre-PCI plaque composition and post-PCI distal embolization in acute coronary syndrome patients.
METHODS: Studies were identified in PubMed, OVID, EMBASE, the Cochrane Library, the Current Controlled Trials Register, reviews, and reference lists of relevant articles. A meta-analysis using both fixed and random effects models with assessment of study heterogeneity and publication bias was performed.
RESULTS: Of the 388 articles screened, 10 studies with a total of 872 subjects (199 with distal embolization and 673 with normal flow) met the eligibility of our study. Compared with normal flow groups, significant higher absolute volume of NC [weighted mean differences (WMD): 5.79 mm3, 95% CI: 3.02 to 8.55 mm3; p<0.001] and DC (WMD: 2.55 mm3, 95% CI: 0.22 to 4.88 mm3; p = 0.03) were found in acute coronary syndrome patients with distal embolization. Further subgroup analysis demonstrated that the predictive value of tissue characteristics in determining distal embolization was correlated to clinical scenario of the patients, definition of distal embolization, and whether the percutaneous aspiration thrombectomy was applied.
CONCLUSION: Our study that pooled current evidence showed that plaque components were closely related to the distal embolization after PCI, especially the absolute volume of NC and DC, supporting further studies with larger sample size and high-methodological quality.

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Mesh:

Year:  2014        PMID: 25375841      PMCID: PMC4222782          DOI: 10.1371/journal.pone.0106583

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Rationale

Distal embolization (DE) is a common complication after percutaneous coronary intervention (PCI), particularly in the setting of acute coronary syndrome (ACS) or vein graft intervention, which may result in microvascular obstruction and no-reflow phenomenon [1], [2]. This undesirable side effect of PCI has been confirmed to be associated with increased post-procedural myocardial infarction, in-hospital mortality, and long-term adverse events [3]–[5]. However, there is no effective strategy for prediction and prevention of DE, which is an important issue for interventional cardiology. Although several studies using grayscale intravascular ultrasound (IVUS) have indicated that plaque characteristics identified by pre-interventional IVUS (i.e., a large plaque burden, a lipid-pool-like image, and positive remodeling) maybe associated with the angiographic no-reflow phenomenon in ACS patients [6]–[10], gray-scale IVUS is dependent on the simple interpretation of acoustic reflections and of limited value for identifying specific plaque components [11]. Recently, some new methods able to assess both plaque morphology and tissue characteristics, such as virtual histology-IVUS (VH-IVUS), have become clinically available. VH-IVUS is based on spectral and amplitude analysis of IVUS backscattered radiofrequency that allows for characterization of in-vivo atherosclerotic plaque into four types: fibrous (FT), fibrofatty (FF), necrotic core (NC), and dense calcium (DC) [12]–[23]. However, whether pre-PCI plaque characteristics of culprit lesion assessed by VH-IVUS could predict post-PCI angiographic DE, and which plaque components are associated with no-reflow phenomenon remain debated. We therefore performed a systematic review that pooled current evidence to investigate the relationship between pre-PCI plaque composition characteristics assessed by VH-IVUS and post-PCI DE phenomenon in ACS patients.

Methods

Search strategy

PubMed, Ovid, EMBASE, and the Cochrane Library databases were searched in their entirety from January 2002 to April 2013. Complex search strategies were formulated using the following MESH terms and text words: intravascular ultrasound, virtual histology, IVUS, VH-IVUS, plaque component, plaque composition, plaque characteristic, no reflow, DE, microembolization, and obstruction. In order to identify any studies missed by the literature searches, we had searched reference lists of all eligible studies and relevant review articles. In addition, we searched from published and ongoing trials in clinical trial registries (ClinicalTrials.gov, Controlled-trials.com and the WHO International Clinical Trials Registry Platform). Searches were not restricted by language, time published, or publication status. Duplicate reports were eliminated (Appendix S1).

Study selection

We included studies when the following criteria were met:(1) Plaque characteristics were assessed by VH-IVUS; (2) VH-IVUS was performed before coronary intervention in ACS patients; and (3) DE was defined according to angiographic evidence or clinical relevancy. Studies without normal flow (NF) group were excluded from our analysis.

Data extraction

Two reviewers (D. S. and P. J.) assessed the eligibility of studies using a standardized form developed for this purpose in duplicate and independently. Disagreements were adjudicated by resolved by consensus. Data extraction was completed by the same observers using a standardized data extraction form developed for this study. The following information was extracted from each study: sample size, mean age, gender distribution, risk factors, clinical scenario, definition of DE, and the volume (mm3)and percentage of each tissue component of plaque (including FT, FF, NC, and DC). Several studies met our inclusion criteria but were missing data vital to our analysis; in these cases, we contacted the authors to obtain raw data whenever possible.

Statistical analysis

Statistical analysis in this study was carried out using RevMan software version 5.2 (The Cochrane Collaboration). Results were summarized as weighted mean differences (WMD) with their associated 95% confidence intervals (CI) using both fixed and random effects models, the latter was more conservative where heterogeneity beyond that expected by chance alone was encountered. In addition, the odds ratio (OR) was calculated for baseline comorbidities. Heterogeneity between studies was analyzed by the Q statistic and the I2 statistic. A p value of the Q statistic <0.1 was defined as an indicator of heterogeneity, and an I2 <50% indicated that the magnitude of the heterogeneity might not be significant. Funnel plots were plotted to investigate possible small study effects/publication bias by using Revman 5.2. Planned subgroup analyses were conducted based on the clinical scenario, definition of DE, and whether percutaneous aspiration thrombectomy was applied.

Quality assessment

Methodological quality was assessed independently by 2 reviewers (D. S. and P. J.) using the Newcastle-Ottawa Scale.

Results

Search result

After initial literature search, we identified 388 potential studies, of which 357 studies were excluded based on the title and abstracts, because they were unrelated papers, reviews, editorials, letters, case reports or animal studies. The remaining 31 articles were considered of interest and examined in full-text. Of these, 19 studies those were not IVUS-based were excluded. Of the remainder, 2 studies without DE data were excluded [12], [13]. Therefore, 10 observational studies were included in our final meta-analysis [14]–[23]. Figure 1 shows the study selection process.
Figure 1

Process of study selection.

Characteristics of included studies

Table 1 and 2 summarize the main features of the included studies. A total of 872 patients (199 patients in DE group and 673 patients in NF group) were enrolled in the 10 studies, and the sample sizes were 44–190 in each study. Among the included studies, 5 studies involved AMI patients [14], [18]–[21] (4 of them only involved STEMI patients), 3 studies enrolled unstable angina (UA) patients [16], [22], [23], and the remaining 2 studies involved ACS (including both AMI and UA) patients [15], [17]. Percutaneous aspiration thrombectomy was performed before IVUS examinations in 7 studies [14], [15], [18]–[21], [23]. There were no significant differences between DE and NF groups in age and gender of patients. Moreover, there was no significant difference in the incidence of hypertension (OR: 1.36, 95% CI: 0.95 to 1.95, p = 0.10), diabetes (OR: 1.36, 95% CI: 0.94 to 1.96, p = 0.10) and hyperlipidaemia (OR: 1.44, 95% CI: 0.89 to 2.31, p = 0.13) between the two groups. A Funnel plot for NC volume outcome data was used to assess any potential small study effects or publication bias (Figure 2). The Funnel plot was roughly symmetrical as to the mean-effect size line.
Table 1

Basical characteristics of studies included in meta-analysis (Normal flow vs. distal embolization).

StudyStudy intervalLocationSample size (n)DesignClinical scenarioPATDefinition of distal embolization
Bae 2008NRDaejeon, South Korea45/12RSCAMIYesTIMI flow grade ≤2
Higashikuni 20082005.6–2006.4Tokyo, Japan40/9RSCACS (AMI and UA)YesDecrease of at least 1 grade in TIMI
Hong 2009NRWashington DC, United States42/38RSCUANocTnI elevation >3X the ULN
Hong 20112006.2–2008.1Gwangju, South Korea166/24RSCACS (STEMI, NSTEMI and UA)NoTIMI flow grade ≤2
Kawaguchi 20072005.8–2006.12Gunma, Japan60/11PSCAMI (STEMI)YesST-segment re-elevation
Nakamura 20072006.1–2006.3Saitama, Japan42/8PSCAMI (STEMI)YesDecrease in TIMI flow grade
Ohshima 20092007.1–2007.12Ehime, Japan24/20PSCAMI (STEMI)YesTIMI flow grade ≤2
Ohshima 2011NREhime, Japan19/34RSCAMI (STEMI)YesTIMI flow grade ≤2
Shin 2011NRUlsan, South Korea90/22RSCUANoCK-MB elevation >1X the ULN
Zhao 20132010.9–2011.11Zhengzhou, China145/21RSCUAYesTIMI flow grade ≤2

ACS, acute coronary injury; AMI, acute myocardial infarction; NR, not reported; NSTEMI, non ST-segment elevation myocardial infarction; PAT, percutaneous aspiration thrombectomy; PSC, prospective single center; RSC, retrospective single center; STEMI, ST-segment elevation myocardial infarction; ULN, upper limit of normal.

Table 2

Clinical characteristics of studies included in meta-analysis (Normal flow vs. distal embolization).

StudyMean age (years)Males (%)ComorbiditiesPre-PCI use of Aspirin (%)Use of StatinsUse of GP IIb/IIIa inhibitorUse of StatinsUse of distal protectiondevices
HT (%)DM (%)HL (%)
Bae 200856.2/67.582.2/66.740.0/33.313.3/33.331.1/25.0100/100NR0/0NRNo
Higashikuni 200866.6/60.692.5/77.870.0/55.630.0/55.665.0/830.0/44.422.5/22.20/022.5/22.2No
Hong 200965/6347.6/76.364.3/73.723.8/31.6NR92.9/86.8NR14.3/10.5NRNo
Hong 201160.5/60.165.7/58.352.4/70.819.3/25NRNRNR23.5/29.2NRNR
Kawaguchi 2007NRNR68.3/81.841.7/9.145.0/81.8NRNR0/0NRNo
Nakamura 200765.3/58.585.7/87.542.9/25.023.8/37.561.9/62.5100/100NR0/0NRNo
Ohshima 200966.0/74.083.3/65.058.3/75.054.2/60.062.5/45.0100/100NRNRNRNo
Ohshima 201173/6768.4/85.378.9/70.626.3/38.247.4/61.8100/100NRNRNRNo
Shin 201161.4/65.561.1/50.051.1/72.732.2/22.753.3/63.6100/10021.1/27.30/021.1/27.3No
Zhao 201351/4966.2/66.659.3/61.926.9/47.6NR100/10098.6/95.2NR98.6/95.2No

DM, diabetes mellitus; HT, hypertension; HL, hyperlipidaemia; NR, not reported;

Figure 2

Funnel plot for necrotic core volume outcome data of involved studies.

ACS, acute coronary injury; AMI, acute myocardial infarction; NR, not reported; NSTEMI, non ST-segment elevation myocardial infarction; PAT, percutaneous aspiration thrombectomy; PSC, prospective single center; RSC, retrospective single center; STEMI, ST-segment elevation myocardial infarction; ULN, upper limit of normal. DM, diabetes mellitus; HT, hypertension; HL, hyperlipidaemia; NR, not reported; Moreover, we evaluated the quality of primary studies using the Newcastle–Ottawa Scale, a validated technique for assessing the quality of observational and non randomized studies. As shown in Table 3, all observational studies were intermediate to low intermediate bias risk as assessed by the Newcastle-Ottawa Scale for quality assessment risk evaluation of adequacy of selection, comparability of study groups, and assessment of outcome or exposure.
Table 3

Newcastle-Ottawa Scale of bias risk for the involved studies.

StudyAdequacy of selectionComparabilityOutcomes assessment
Representativeness of the exposed cohortSelection of the non-exposed cohortAscertainment of exposureAssessment of OutcomesFollow-up period long enough for outcome to occurAdequacy of follow-up period among cohorts
Bae 2008****************
Higashikuni 2008*****************
Hong 2009***************
Hong 2011****************
Kawaguchi 2007**************
Nakamura 2007*****************
Ohshima 2009****************
Ohshima 2011*****************
Shin 2011***************
Zhao 2013***************

Asterisks are the star rating as per the Newcastle-Ottawa Scale; ** and *** indicate highest rating for these categories.

Asterisks are the star rating as per the Newcastle-Ottawa Scale; ** and *** indicate highest rating for these categories.

Relationship between coronary plaque characteristics and DE

As shown in Table 4, Figure 3 and 4, the absolute volume and percentage of four different plaque compositions through the entire culprit lesion were assessed. Compared with NF group, the overall pooled results with random-effects analysis showed DE group had significant higher absolute volume of NC (WMD: 5.79 mm3, 95% CI: 3.02 to 8.55 mm3; p<0.001) and DC (WMD: 2.55 mm3, 95% CI: 0.22 to 4.88 mm3; p = 0.03). The difference between the two groups was not statistically significant with respect to percentage of NC (WMD: 4.35%, 95% CI: −1.44% to 10.15%; p = 0.14) and DC (WMD: 0.81%, 95% CI: −1.20% to 2.82%; p = 0.43). In addition, there were no significant differences in absolute volume and percentage of FT and FF at the entire culprit lesions between the two groups. Substantial statistical heterogeneity was detected in all of the comparisons among these trials, except for the absolute volume of FT (I2  = 0%).
Table 4

Composition of plaque by VH-IVUS.

StudyAbsolute volume (mm3)Percentage (%)
FTFFDCNCFTFFDCNC
Bae 2008Reflow83.8 (66.8)18.0 (18.6)12.7 (13.9)28.8 (26.0)NRNRNRNR
No reflow119.6 (61.7)36.7 (25.5)9.3 (8.9)26.1 (21.0)NRNRNRNR
Higashikuni 2008ReflowNRNRNRNR68.3 (10.2)15.5 (7.1)4.8 (3.6)11.7 (7.9)
No reflowNRNRNRNR59.6 (11.2)12.0 (9.7)4.7 (3.3)22.1 (9.3)
Hong 2009Reflow33.9(14.2)16.9(11.6)3.2(3.0)7.9(4.4)55.0(11.6)27.5(13.0)4.8(3.4)12.8(8.4)
No reflow38.4(19.0)13.1(9.9)3.8(3.0)13.6(6.4)55.7(13.1)19.0(9.3)5.5(3.9)19.8(10.4)
Hong 2011Reflow77 (75.4)20 (25.4)10 (11.5)16 (16.9)61 (9.9)16 (9.9)9 (6.8)14 (8.0)
No reflow76 (50.0)15 (18.5)19 (20.0)30 (23.8)55 (14.0)9 (6.1)14 (8.0)22 (11.0)
Kawaguchi 2007Reflow68.2 (35.3)13.2 (11.4)9.6 (13.9)20.4 (19.2)NRNRNRNR
No reflow67.1 (30.7)9.8 (10.4)12.2 (8.6)32.9 (14.1)NRNRNRNR
Nakamura 2007ReflowNRNRNRNR67.0 (1.5)17.0 (1.1)4.8 (0.6)11.2 (1.2)
No reflowNRNRNRNR68.3 (2.1)23.1 (3.5)2.6 (0.6)6.3 (1.0)
Ohshima 2009Reflow56.6 (21.8)8.6 (5.2)6.5 (5.3)12.0 (7.4)67.8 (10.2)10.1 (3.9)7.8 (5.2)14.3 (6.7)
No reflow56.2 (32.6)14.2 (11.4)10.3 (7.6)14.1 (6.7)57.5 (10.7)14.5 (9.6)11.8 (8.9)15.8 (7.4)
Ohshima 2011Reflow57.0 (33.3)14.7 (11.5)9.3 (6.0)13.7 (6.7)57.5 (11.0)14.8 (9.7)11.3 (9.0)15.8 (7.6)
No reflow67.5 (29.7)15.0 (11.7)11.0 (8.8)16.8 (10.0)61.2 (10.8)13.4 (8.1)10.2 (7.2)15.3 (6.0)
Shin 2011ReflowNRNR3.9 (3.7)8.8 (5.8)NRNRNRNR
No reflowNRNR9.1 (5.8)17.2 (8.8)NRNRNRNR
Zhao 2013ReflowNRNRNRNR59.24 (6.72)17.90 (3.21)8.36 (3.13)14.50 (5.48)
No reflowNRNRNRNR50.26 (8.72)15.29 (2.83)9.53 (2.99)24.92 (10.04)

Data are presented as mean (SD)

FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium.

Figure 3

Absolute volume comparison of four different plaque compositions through the entire culprit lesion between the normal flow group and the distal embolization group.

(A) Absolute fibrous volume comparison; (B) Absolute fibrofatty volume comparison; (C) Absolute dense calcium volume comparison; (D) Absolute necrotic core volume comparison;

Figure 4

Percentage comparison of four different plaque compositions through the entire culprit lesion between the normal flow group and the distal embolization group.

(A) Fibrous percentage comparison; (B) Fibrofatty percentage comparison; (C) Dense calcium percentage comparison; (D) Necrotic core percentage comparison.

Absolute volume comparison of four different plaque compositions through the entire culprit lesion between the normal flow group and the distal embolization group.

(A) Absolute fibrous volume comparison; (B) Absolute fibrofatty volume comparison; (C) Absolute dense calcium volume comparison; (D) Absolute necrotic core volume comparison;

Percentage comparison of four different plaque compositions through the entire culprit lesion between the normal flow group and the distal embolization group.

(A) Fibrous percentage comparison; (B) Fibrofatty percentage comparison; (C) Dense calcium percentage comparison; (D) Necrotic core percentage comparison. Data are presented as mean (SD) FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium.

Subgroup analysis

Planned subgroup analyses were conducted based on the different clinical scenario, definition of DE, and whether percutaneous aspiration thrombectomy was applied (Table 5 and 6). Subgroup analysis by different clinical scenario showed that patients with DE had significantly higher absolute volume and percentage of NC (WMD: 6.61 mm3, 95% CI: 4.11 to 9.12 mm3; p<0.001 and WMD: 8.64%, 95% CI: 5.29% to 11.99%; p<0.001) in subgroup of UA patients.
Table 5

Subgroup analyses of the association of the absolute volume of plaque components with the onset of distal embolization.

FTFFDCNC
SubgroupWMD (95% CI, mm3) p WMD (95% CI, mm3) p WMD (95% CI, mm3) p WMD (95% CI, mm3) p
Clinical scenario
AMI5.21 (−4.93, 15.35)0.313.17 (−3.25, 9.59)0.331.81 (−0.81, 4.44)0.183.56 (−0.37, 7.50)0.08
Unstable angina4.50 (−2.91, 11.91)0.23−3.80 (−8.51, 0.91)0.112.77 (−1.73, 7.27)0.236.61 (4.11, 9.12)<0.001
Definition of distal embolization
Angiographic evidence5.62 (−4.83, 16.07)0.293.11 (−3.77, 10.00)0.382.44 (−1.34, 6.22)0.213.88 (−0.62, 8.38)0.09
Clinical relevancy3.84 (−3.12, 10.80)0.28−3.67 (−7.54, 0.20)0.062.71 (−0.88, 6.29)0.147.13 (4.40, 9.87)<0.001
Thrombectomy
With thrombectomy−4.36 (−10.42, 1.71)0.160.80 (−3.89, 5.49)0.740.06 (−2.17, 2.30)0.963.56 (−0.37, 7.50)0.08
Without thrombectomy−2.57 (−9.14, 3.99)0.44−7.38 (−9.86, −4.90)<0.0012.59 (−1.60, 6.77)0.237.47 (4.25, 10.69)<0.001

FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium; WMD, weighted mean differences; AMI, acute myocardial infarction.

Table 6

Subgroup analyses of the association of the percentage of plaque components with the onset of distal embolization.

FTFFDCNC
SubgroupWMD (95% CI, %) p WMD (95% CI, %) p WMD (95% CI, %) p WMD (95% CI, %) p
Clinical scenario
AMI−1.48 (−8.40, 5.44)0.683.49 (−0.68, 7.66)0.10−0.18 (−3.89, 3.53)0.92−1.67 (−6.04, 2.70)0.45
Unstable angina−4.34 (−13.81, 5.14)0.37−5.06 (−10.75, 0.63)0.080.97 (−0.07, 2.02)0.078.64 (5.29, 11.99)<0.001
Definition of distal embolization
Angiographic evidence−4.60 (−9.87, 0.67)0.09−0.61 (−4.91, 3.70)0.780.87 (−1.49, 3.24)0.473.91 (−2.30, 10.11)0.22
Clinical relevancy0.70 (−4.75, 6.15)0.80−8.50 (−13.42, −3.58)<0.0010.70 (−0.91, 2.31)0.397.00 (2.83,11.17)0.001
Thrombectomy
With thrombectomy5.21 (−4.93, 15.35)0.313.17 (−3.25, 9.59)0.331.81 (−0.81, 4.44)0.183.07 (−3.45,9.59)0.36
Without thrombectomy3.98 (−3.07, 11.04)0.27−4.09 (−8.19, 0.01)0.053.85 (−0.46, 8.17)0.087.45 (4.38, 10.53)<0.001

FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium; WMD, weighted mean differences; AMI, acute myocardial infarction.

FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium; WMD, weighted mean differences; AMI, acute myocardial infarction. FT, fibrous tissue; FF, fibrofatty; NC, necrotic core; DC, dense calcium; WMD, weighted mean differences; AMI, acute myocardial infarction. In order to assess the impact of the definition of DE in determining DE on our analyses, subgroup analysis by angiographic or clinical relevance definition was performed. The results showed that there was significantly higher absolute volume of NC (WMD: 7.13 mm3, 95% CI: 4.40 to 9.87 mm3; p = 0.04) in subgroup of DE in clinical relevance definition. In order to investigate whether percutaneous aspiration thrombectomy would affect the outcomes, trials were divided into two subgroups according to whether thrombectomy was applied. The results showed that in the subgroup without thrombectomy, patients with DE had significantly higher absolute volume and percentage of NC (WMD: 7.47 mm3, 95% CI: 4.25 to 10.69 mm3; p<0.001 and WMD: −7.45%, 95% CI: 4.38% to 10.53%; p<0.001), and significantly lower absolute volume of FF (WMD: −7.38 mm3, 95% CI: −9.86 to −4.90 mm3; p<0.001).

Discussion

The present meta-analysis that pooled all currently available published data indicated that, among four phenotypes of coronary plaque composition assessed by VH-IVUS, absolute volume of NC components was closely related to the DE after PCI in ACS patients. Besides, absolute volume of DC component might also be related to the DE after PCI. Further subgroup analysis revealed that the predictive value of VH-IVUS plaque characteristics in determining DE was correlated to the clinical scenario of the patients, the definition of DE, and whether percutaneous aspiration thrombectomy was applied. Two recent review/meta-analyses [24], [25] that investigated the relationship between plaque characteristics and DE after PCI have also reported that the extent of NC was larger in patients with DE. The meta-analysis by Jang et al. [24] evaluated the effect of plaque characteristics on embolization after PCI by grayscale-IVUS and VH-IVUS, and found that the morphologic characteristics of plaque derived from grayscale-IVUS (i.e.,eccentric plaque, ruptured plaque, and attenuated plaque) and the NC component derived from VH-IVUS are closely related to the DE phenomenon after PCI. The systematic review by Claessen et al. [25] summarized the published data on the use of plaque composition assessment by VH-IVUS to predict the occurrence of DE, and found that the NC component was associated with DE in all but 2 of the 11 reviewed studies. In the present study, we performed a systematic review that pooled all the currently available published data investigating the relationship between pre-PCI plaque composition characteristics assessed by VH-IVUS and post-PCI DE phenomenon in ACS patients, and we updated the meta-analysis by adding two VH-IVUS studies [22], [23] that did not include in the previous meta-analysis by Jang et al. [24]. We found that absolute volume of NC component, but not percentage of NC component, was closely related to the DE after PCI in ACS patients, confirming the findings of previous review/meta-analyses. In addition, our analysis that pooled all current evidence found that besides NC volume, absolute DC volume was also closely related to the DE phenomenon after PCI. There is some evidence which indicated that DC might be related to DE. For example, pathologic studies revealed that coronary calcification is related to the total plaque burden, NC component, plaque erosion or rupture that is responsible for coronary thrombosis [26]–[29]. In addition, some studies have also reported that coronary calcium was associated with coronary event including myocardial infarction or death in symptomatic/asymptomatic persons [30]–[33]. In our analysis, we noted a considerable degree of heterogeneity among the included trials. Thus, we performed further subgroup analyses and tried to appraise the possible sources of differences and heterogeneity among trials. Our results suggested that the clinical scenario of the patients, the definition of DE and the use of thrombectomy may influence the correlation between tissue characteristics of coronary plaque and DE. When analyzed in the context of clinical scenario, increased absolute volume of NC was found in DE group in studies including UA patients, but not in those including AMI patients. This phenomenon might be explained by the rupture and migration of NC plaque in AMI patients. In addition, VH-IVUS is limited to detecting thrombus (in fact, thrombus appears as either fibrotic or fibrofatty plaque depending on the age of the thrombus) [34]. Moreover, large amount of NC may have migrated into the distal coronary bed before or during primary PCI in AMI patients [14]. An unexpected finding in our analysis was that no association was found between plaque components and DE in the subgroup of angiographically defined DE. Although angiography has been commonly used as a gold standard for assessing DE, TIMI flow grade is a subjective method to assess epicardial blood flow. As suggested by published literatures, the qualitative nature of TIMI grade renders it somewhat dependent on the technical skill of the observer, and significant differences were found in inter-observer variabilities among different reports, particularly for TIMI 2 grade (Kappa value was 0.4963 for inter-observer variability), which may introduce selection bias in the enrollment of the participants [35], [36]. In addition, our results indicated that pre-stent percutaneous aspiration thrombectomy may also be a important factor in determining the predictive value of VH-IVUS-derived plaque characteristics.

Study limitations

Several important limitations of our study should be taken into account, in order to place our findings in the proper context. Firstly, as mentioned above, there was considerable heterogeneity in patient characteristics, use of pre-stent thrombectomy, and definitions of DE among the included trials. Secondly, although the consensus document recommends measurement of the absolute and relative components of each plaque at the minimum lumen site and over the whole lesion, these measurements were not usually reported uniformly in the individual studies involved in our study. Thirdly, although our pooled analysis found that besides NC volume, absolute DC volume was also closely related to the DE phenomenon after PCI, more evidence should be obtained to confirm this finding because only two of the studies included in our meta-analysis reported statistically significant association between DC component and post-PCI DE. Finally, all of the involved trials were non-randomized studies and of small sample sizes, which might have brought some bias. Therefore further studies with larger sample size and high-methodological quality are needed. Search strategy. (DOC) Click here for additional data file. Meta-Analysis on Genetic Association Studies Checklist. (DOCX) Click here for additional data file.
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1.  Comparison of coronary arterial finding by intravascular ultrasound in patients with "transient no-reflow" versus "reflow" during percutaneous coronary intervention in acute coronary syndrome.

Authors:  Raisuke Iijima; Hideo Shinji; Nobutaka Ikeda; Hideki Itaya; Kunihiko Makino; Atsushi Funatsu; Itaru Yokouchi; Hirotaka Komatsu; Naoki Ito; Hiroya Nuruki; Rintaro Nakajima; Masato Nakamura
Journal:  Am J Cardiol       Date:  2005-11-02       Impact factor: 2.778

2.  Angiographic no-reflow phenomenon and plaque characteristics by virtual histology intravascular ultrasound in patients with acute myocardial infarction.

Authors:  Tomohiro Nakamura; Norifumi Kubo; Junya Ako; Shin-Ichi Momomura
Journal:  J Interv Cardiol       Date:  2007-10       Impact factor: 2.279

3.  Long-term prognostic value of coronary calcification detected by electron-beam computed tomography in patients undergoing coronary angiography.

Authors:  P C Keelan; L F Bielak; K Ashai; L S Jamjoum; A E Denktas; J A Rumberger; P F Sheedy II; P A Peyser; R S Schwartz
Journal:  Circulation       Date:  2001-07-24       Impact factor: 29.690

4.  No-reflow phenomenon and lesion morphology in patients with acute myocardial infarction.

Authors:  Atsushi Tanaka; Takahiko Kawarabayashi; Yoshiharu Nishibori; Toshihiko Sano; Yukio Nishida; Daiju Fukuda; Kenei Shimada; Junichi Yoshikawa
Journal:  Circulation       Date:  2002-05-07       Impact factor: 29.690

5.  Relation of atherothrombosis burden and volume detected by intravascular ultrasound to angiographic no-reflow phenomenon during stent implantation in patients with acute myocardial infarction.

Authors:  Takuji Katayama; Norifumi Kubo; Yosuke Takagi; Hiroshi Funayama; Nahoko Ikeda; Takeshi Ishida; Taishi Hirahara; Yoshitaka Sugawara; Takanori Yasu; Masanobu Kawakami; Muneyasu Saito
Journal:  Am J Cardiol       Date:  2005-11-28       Impact factor: 2.778

6.  Progression of coronary calcium on serial electron beam tomographic scanning is greater in patients with future myocardial infarction.

Authors:  Paolo Raggi; Bruce Cooil; Leslee J Shaw; Jamil Aboulhson; Junichiro Takasu; Matthew Budoff; Tracy Q Callister
Journal:  Am J Cardiol       Date:  2003-10-01       Impact factor: 2.778

7.  Usefulness of virtual histology intravascular ultrasound to predict distal embolization for ST-segment elevation myocardial infarction.

Authors:  Ren Kawaguchi; Shigeru Oshima; Masaaki Jingu; Hideki Tsurugaya; Takuji Toyama; Hiroshi Hoshizaki; Koichi Taniguchi
Journal:  J Am Coll Cardiol       Date:  2007-10-23       Impact factor: 24.094

8.  Impact of plaque rupture on infarct size in ST-segment elevation anterior acute myocardial infarction.

Authors:  Ikuyoshi Kusama; Kiyoshi Hibi; Masami Kosuge; Naoki Nozawa; Hiroyuki Ozaki; Hideto Yano; Shinnichi Sumita; Kengo Tsukahara; Jun Okuda; Toshiaki Ebina; Satoshi Umemura; Kazuo Kimura
Journal:  J Am Coll Cardiol       Date:  2007-09-10       Impact factor: 24.094

9.  Prognostic value of coronary calcification and angiographic stenoses in patients undergoing coronary angiography.

Authors:  R Detrano; T Hsiai; S Wang; G Puentes; J Fallavollita; P Shields; W Stanford; C Wolfkiel; D Georgiou; M Budoff; J Reed
Journal:  J Am Coll Cardiol       Date:  1996-02       Impact factor: 24.094

10.  TIMI frame count: a quantitative method of assessing coronary artery flow.

Authors:  C M Gibson; C P Cannon; W L Daley; J T Dodge; B Alexander; S J Marble; C H McCabe; L Raymond; T Fortin; W K Poole; E Braunwald
Journal:  Circulation       Date:  1996-03-01       Impact factor: 29.690

View more
  4 in total

1.  Impact of attenuated plaques on TIMI grade flow and clinical outcomes of coronary artery disease patients: a systematic review and meta analysis.

Authors:  Ruofei Jia; Xiaolu Nie; Hong Li; Huagang Zhu; Lianmei Pu; Xiang Li; Jing Han; Duo Yang; Shuai Meng; Zening Jin
Journal:  J Thorac Dis       Date:  2016-03       Impact factor: 2.895

2.  A meta-analytic review of prevalence for Brugada ECG patterns and the risk for death.

Authors:  Xiao-Qing Quan; Song Li; Rui Liu; Kai Zheng; Xiao-Fen Wu; Qiang Tang
Journal:  Medicine (Baltimore)       Date:  2016-12       Impact factor: 1.889

3.  Relationship between plaque composition by virtual histology intravascular ultrasound and clinical outcomes after percutaneous coronary intervention in saphenous vein graft disease patients: study protocol of a prospective cohort study.

Authors:  Yin Liu; Hai-Bo Wang; Xiang Li; Jian-Yong Xiao; Ji-Xiang Wang; Kathleen H Reilly; Bo Sun; Jing Gao
Journal:  BMC Cardiovasc Disord       Date:  2018-12-12       Impact factor: 2.298

4.  Impact of Early ST-Segment Changes on Cardiac Magnetic Resonance-Verified Intramyocardial Haemorrhage and Microvascular Obstruction in ST-Elevation Myocardial Infarction Patients.

Authors:  Song Ding; Zheng Li; Heng Ge; Zhi-Qing Qiao; Yi-Lin Chen; Ao-Lei Andong; Fan Yang; Ling-Cong Kong; Meng Jiang; Ben He; Jun Pu
Journal:  Medicine (Baltimore)       Date:  2015-09       Impact factor: 1.817

  4 in total

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