Development and Validation of a Clinical and Laboratory-Based Nomogram for Predicting Coronary Microvascular Obstruction in NSTEMI Patients After Primary PCI.

OBJECTIVE: Cardiac microvascular obstruction (CMVO) remains a severe complication in non-ST elevation myocardial infarction (NSTEMI) patients with reperfusion therapy. We aimed at developing and validating the nomogram to predict the possibility of CMVO after primary percutaneous coronary intervention (PCI) by integrating clinical and laboratory-based information.
METHODS: A total of 325 patients undergoing primary PCI for NSTEMI were recruited and divided into the training cohort (n=226) and the validating cohort (n = 99). The development of the nomogram was based on independent predictors of CMVO, and these variables were selected by multivariable logistic regression analysis.
RESULTS: Independent predictors contained in nomogram were identified by multivariable logistic regression analysis, and these independent predictors included neutrophils (OR 1.166, 95% CI 1.044-1.303, P<0.01), hemoglobin (OR 1.037, 95% CI 1.013-1.062, P<0.01), triglyceride (OR 1.343, 95% CI 1.059; 1.704, P=0.015), Killip grade (OR 2.190, 95% CI 1.065-4.503, P=0.033), high thrombus load (OR 3.146, 95% CI 1.424-6.952, P<0.01), no-reflow (OR 3.142, 95% CI 1.419-6.955, P<0.01) and ischemic postconditioning (OR 0.445, 95% CI 0.209-0.944, P=0.035). The nomogram accurately predicted the presentation of CMVO in both the training set and validating set (AUC, 0.835 and 0.881, respectively). The results predicted by nomogram were confirmed to be highly consistent with the results of DE-CMR, both the training and validating cohorts, by Calibration plot and Hosmer-Lemeshow test. Decision curve analysis (DCA) also suggested that the nomogram was applicable in the clinic.
CONCLUSION: The nomogram showed good performance in predicting CMVO, and it could help clinicians optimize the clinical treatments to improve the prognosis of NSTEMI patients.

Introduction

Non-ST segment elevation myocardial infarction (NSTEMI) is a severe type of acute coronary syndrome (ACS), and its incidence is growing.1 In a myocardial infarction registry, 63.1% were NSTEMI, and 4.2% of NSTEMI patients died in the hospital.2 Therefore, more attention should be paid to the treatment and prognosis of NOSTEMI patients. Currently, reperfusion therapy, as the main treatment for NSTEMI patients, is mainly aimed to prompt intervention for the culprit artery. However, in some circumstances, the culprit’s vessel is opened, yet main adverse cardiovascular events (MACE), such as death, rehospitalization, or heart failure, would still happen to patients due to coronary microvascular obstruction (CMVO).3 The occurrence of CMVO is a result of multiple factors. Mechanisms involved in pathogenesis of CMVO include blocking of the vascular lumen due to formation of leukocyte–platelet aggregates and erythrocyte aggregates, myocardial cell edema induced by coronary microvasculature compression after reperfusion injury, which will be aggravated by the lack of blood flow in functional vessels, and the distal microvascular embolization elicited by atherothrombotic debris during percutaneous coronary intervention (PCI).4 In addition, oxidative stress and intracardial hemorrhage after acute myocardial infarction (AMI), coronary spasm and dissection, endothelial dysfunction, inflammation in microvasculature, and individual susceptibility can also be implicated in CMVO.5,6

Currently, preventive treatment strategies for CMVO include ischemic postconditioning, drug treatment, and interventional procedures, and in order to translate clinically into effective treatment for AMI patients, especially, the elderly, with comorbidities, and with receiving several medications, we need to focus not only on the reduction in infarct size, but also on attenuation of CMVO size.7–9 In addition, studies showed that active and effective treatment early would make CMVO improved.10 Therefore, early detection of CMVO is particularly vital for the treatment and clinical prognosis of patients. Currently, diagnosis of CMVO includes invasive and non-invasive detection methods. In invasive detection methods, coronary flow reserve (CFR) is considered the gold standard for evaluating CMD, but it is difficult to be widely promoted in clinical practice due to trauma, time consumption, expensiveness, and many potential complications. Thrombolysis in myocardial infarction (TIMI), TIMI myocardial perfusion grade (TMPG), and myocardial blush grading (MBG) are the primary detection methods for CMVO during PCI. However, the results of angiography may not reflect the perfusion status of capillaries.11 Studies have confirmed that 29–38% of patients with TIMI 3 still have CMVO.12,13 Vicente et al found that MBG underestimated CMVO after optimal revascularization in AMI.14 In addition, Wu et al demonstrated that a noninvasive method for MRI-determined microvascular obstruction can predict prognosis within 2 years.15 Judd et al conducted a study in the dog model and confirmed that the coronary microvascular hypoperfusion area distinguished by delay-enhanced cardiovascular magnetic resonance (DE-CMR) corresponds to the coronary microvascular occlusion area of thioflavin-negative regions.16 Therefore, compared with invasive detection methods, DE-CMR has been regarded as the gold standard for noninvasive detecting CMVO. However, DE-CMR may have many shortcomings that make it less clinically used, such as high cost, time consumption, poor tolerance, Most current studies focus on looking for independent risk factors of arising CMVO after PCI, but the occurrence of CMVO is the result of multiple risk factors interacting, and not the result of a certain risk factor.3 Accordingly, one single indicator may not be valid enough to evaluate CMVO after PCI. According to the above statement, a simple scoring system needs to be established to assess quickly and easily whether NSTEMI patients have CMVO after PCI.

Nomogram, as a graphical tool, can be used to quickly calculate the morbidity of a certain disease in an individual patient, as well as evaluate the prognosis.17 To determine quickly and conveniently CMVO probability after primary PCI and stratify high-risk patients, this retrospective study based on the analysis of independent risk factors of laboratory examinations and clinical indicators aims to establish a nomogram that can quickly calculate the probability of CMVO individually.

Materials and Methods

Study Design and Participants

The consecutive patients were retrospectively reviewed for the data, which was recorded in the medical record management system of the Affiliated Hospital of Xuzhou Medical University and the Second Affiliated Hospital of Xuzhou Medical University from September 1, 2019, to September 31, 2021, and 1428 patients with NSTEMI were included in the study. According to the inclusion and exclusion criteria, 325 NSTEMI patients were eventually divided into the training cohort (70%, n=226) and validation cohort (30%, n=99), which were used for the development and verification of nomogram. Figure 1 showed the flow chart of the study. In additional, shows detailed design program for the study.

Figure 1

Flow chart.

Inclusion criteria were as follows: 1) The diagnosis of NSTEMI met the diagnostic criteria of the relevant guidelines;1 2) The patients were performed primary PCI within 24 hours of the onset of symptoms.

Meanwhile, exclusion criteria contain any one of the following: 1) age <18 years old; 2) Patients had not undergone DE-CMR; 3) Patients with any one of the following diseases: cardiogenic shock, immunological or rheumatic diseases, severe liver, and kidney dysfunction (require liver and kidney replacement therapy), malignant tumors, bleeding disorders, and contraindication for the anticoagulant or antiplatelet agents; 4) Killip IV grade; 5) Patients with severely missing clinical data.

Clinical Treatment Process

All patients were sent to digital subtraction angiography (DSA) room, and then underwent primary PCI treatment. Patients received 300 mg aspirin, 600 mg clopidogrel, or 180 mg ticagrelor as pre-treatment before primary coronary angiography and primary PCI. During the angiography, 3000U unfractionated heparin and 200ug of nitroglycerin were injected through the sheath and 100 IU/kg unfractionated heparin was injected through the sheath during primary PCI. Intraoperative medication including nitroprusside, nitroglycerin, tirofiban, and other drugs that improve the symptoms of coronary ischemia, and adjuvant therapy including thrombus aspiration and cardiac pacing was determined according to the patient’s condition and the operators. Patients who were not suitable for PCI should be treated with percutaneous transluminal coronary angioplasty (PTCA). They should be treated with regular programs after the operation, such as Dual antiplatelet [aspirin (100mg QD) combined with clopidogrel (75mg QD) or aspirin (100mg QD) combined with ticagrelor (90mg BID) and statins.

Collection of Candidate Variables

Relevant demographic variables included age, gender, height, weight, systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate (HR), smoking history, drinking status, pre-infarction angina, and Killip grade. Previous history contained hypertension, diabetes, cerebral infarction, and history of stent implantation. Laboratory examination was consist of white blood cell (WBC) count, neutrophil (N) count, lymphocyte (L) count, red blood cell (RBC) count, hemoglobin (Hb), platelet (PLT) count, high-sensitivity C-reactive protein (hs-CRP), albumin, creatinine, estimated glomerular filtration rate (eGFR), serum uric acid (SUA), glucose, glycated hemoglobin, total cholesterol, triglycerides, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein A, apolipoprotein B, lipoprotein a, small dense low-density lipoprotein cholesterol (sdLDL-C), lactate dehydrogenase, creatine kinase isoenzyme, high-sensitivity troponin T (hsTnT), cardiac troponin I (cTnI), N-terminal pro-brain natriuretic peptide (NT-proBNP), fibrinogen (FIB), and D-dimer. Image data during PCI included symptom onset-to-balloon time (SBT), door-to-balloon (D2B) time, history of stent implantation, multiple vascular disease, left anterior descending (LAD), left circumflex branch (LCX), right coronary artery (RCA), calcified lesions, proximal lesions, bifurcation lesion, stent length, stent diameter, number of stent, high thrombus load, no-reflow, ischemic postconditioning, temporary pacemaker, and the use drug of tirofiban, atropine, dopamine or hydroxylamine and nitroprusside.

Assessment of CMVO and Definitions

DE-CMR (3.0T) was performed to assess CMVO within 5–7 days after successful reperfusion. In DE-CMR, the infarct area shows as the high signal area in the enhanced area, and CMVO appears as a low signal area in the center of the high signal. Related definitions of important candidate variables included the following: History of CAD is defined as either one or more major epicardial coronary arteries that have more than 50% lumen stenosis on imaging. The multivessel disease is defined as more than 50% stenosis of either one or more main epicardial vessels. Bifurcation lesions are defined as coronary artery stenosis occurring nearing and/or involving the origin of important branch openings.18 If one of the following characteristics is met, it is indicated as a high thrombotic load: 1) The vessel diameter of the infarct-related arteries (IRA) ≥4.0 mm; 2) Thrombus length tripled the inner diameter of the reference vessel or more; 3) There is no tapering lumen proximal to the occlusion site for truncation-like occlusion; 4) Thrombus accumulation proximal to the occlusion site; 5) Floating thrombus presented near the proximal occlusion site; 6) Persistent contrast retention near the distal end of occlusion.19 “No reflow” was defined as TIMI flow grade <3 with the reopening of occluded coronary artery evidenced in angiography.20 After reperfusion by stents implantation, ischemic postconditioning was defined as inflation and deflation frequently (approximately four times) of the balloon within 1 minute of reperfusion.21

Statistical Analysis

Continuous variables were indicated as mean ± standard deviation, If the test of normality and the homogeneity test of variance is performed, the t-test is appropriate. Otherwise, the Mann–Whitney U-test is appropriate. Categorical variables were presented as percentages in the tables and compared by using the X2 test or Fisher exact test. The candidate variables were first selected by univariate logistic regression analysis in the train set, and the candidate variables from P-value < 0.05 in the univariate logistic regression analysis were analyzed in the multivariable logistic regression analysis. Finally, variables with a P-value < 0.05 in the multivariable logistic regression analysis were included in the nomogram. Nomogram evaluation consisted of discrimination capacity, calibration, and clinical effectiveness. The concordance index (C-index) was measured to quantify the discrimination capacity of the nomogram, and C-index is equal to the area under the receiver operating characteristics curve (AUC-ROC) in logistic regression analysis. A calibration plot was drawn to evaluate the prediction accuracy of the nomogram, and the Hosmer-Lemeshow test was calculated to assess the consistency of the predicted with actual probability. Decision curve analysis (DCA) was performed to evaluate Clinical effectiveness. Stata (Version 15.0, ) and R Studio (Version 4.1.1, ) were utilized to analyze data. All statistical tests with a P-value < 0.05 were significant.

Results

Participants Characteristics

From September 1, 2019, to September 31, 2021, 325 participants were enrolled in the testing dataset. 133 (41%) of 325 participants were diagnosed with CMVO by DE-CMR. Among all patients, 226 patients were placed in the train dataset and 99 in the validation dataset in chronological order (Table 1). The training set was divided into 98 patients with CMVO and 128 patients without CMVO, and the validating dataset was divided into 35 patients with CMVO and 64 patients without CMVO. The patients with CMVO after primary PCI had a higher level of Killip grade, higher using tirofiban, a higher proportion of No-reflow, heavier thrombus load, a higher baseline level of N, NLR, Hb, TG, LDH, CKMB, hsTnT, cTnI (all P<0.05). However, lower levels ofWBC, a lower proportion of women, a lower proportion of ischemic postconditioning were found in CMVO (all P<0.05).

Table 1

Patient Characteristics

Variables	Validation Cohort (N=99)	Training Cohort (N=226)	P value
Age, years	56.83 ± 11.85	57.33 ± 13.29	0.746
Sex			0.582
Male, n (%)	86 (86.87)	191 (84.51)
Female, n (%)	13 (13.13)	35 (15.49)
Height, cm	167.51 ± 6.69	167.51 ± 14.65	0.996
Weight, kg	73.47 ± 12.50	73.61 ± 13.16	0.931
SBP, mmHg	126.79 ± 16.53	125.83 ± 18.30	0.654
DBP, mmHg	82.86 ± 13.32	80.09 ± 12.65	0.075
HR, times/min	79.45 ± 11.94	79.53 ± 13.28	0.963
Smoking, n (%)			0.266
NO	42 (42.42)	111 (49.12)
Yes	57 (57.58)	115 (50.88)
Drinking, n (%)			0.795
NO	65 (65.66)	145 (64.16)
Yes	34 (34.34)	81 (35.84)
Hypertension, n (%)			0.353
NO	51 (51.52)	129 (57.08)
Yes	48 (48.48)	97 (42.92)
Diabete, n (%)			0.325
NO	74 (74.75)	180 (79.65)
Yes	25 (25.25)	46 (20.35)
Ischemic stroke, n (%)			0.886
NO	92 (92.93)	211 (93.36)
Yes	7 (7.07)	15 (6.64)
History of CAD, n (%)			0.599
NO	74 (74.75)	175 (77.43)
Yes	25 (25.25)	51 (22.57)
Laboratory test
WBC, ×109/L	9.95 ± 2.76	11.47 ± 11.39	0.191
N, ×109/L	7.78 ± 2.58	8.02 ± 3.34	0.522
L, ×109/L	1.59 ± 1.11	1.88 ± 1.37	0.063
NLR, %	6.19 ± 3.88	6.60 ± 8.28	0.637
RBC, ×109/L	4.68 ± 0.62	4.79 ± 0.55	0.096
Hb, g/L	143.61 ± 17.20	145.02 ± 17.22	0.495
PLT, ×109/L	214.88 ± 56.22	218.50 ± 61.93	0.618
HsCRP, mg/dl	10.11 ± 13.25	9.58 ± 17.31	0.786
Albumin, g/L	39.55 ± 5.32	39.51 ± 4.37	0.94
SCr, mmol/L	64.63 ± 16.31	64.27 ± 14.19	0.841
eGFR, mL/min/1.73m2	108.50 ± 15.95	107.52 ± 14.86	0.593
Glucose, mmol/L	6.63 ± 3.10	6.48 ± 2.49	0.634
TC, mmol/L	4.78 ± 1.04	4.60 ± 2.35	0.464
TG, mmol/L	1.99 ± 1.58	1.92 ± 1.70	0.714
HDL cholesterol, mmol/L	1.02 ± 0.26	0.99 ± 0.27	0.335
LDL cholesterol, mmol/L	3.01 ± 0.95	2.82 ± 1.06	0.127
sdLDL cholesterol, mmol/L	0.98 ± 0.57	1.04 ± 0.54	0.317
Apo A, g/L	1.16 ± 0.20	1.17 ± 0.21	0.633
Apo B, g/L	1.00 ± 0.25	0.95 ± 0.29	0.221
Lpa, mg/L	271.16 ± 193.63	250.57 ± 183.46	0.361
LDH, U/L	519.64 ± 345.65	654.85 ± 705.51	0.071
CKMB, ng/mL	99.15 ± 77.59	103.15 ± 83.33	0.685
hsTnT, ng/L	3040.03 ± 3044.39	3552.49 ± 2977.84	0.157
NT-proBNP, pg/mL	1348.87 ± 1527.45	1629.01 ± 2023.15	0.219
cTnI, ng/L	17.73 ± 15.36	19.11 ± 16.45	0.479
FIB, g/L	2.90 ± 1.10	2.72 ± 0.77	0.081
DD2, ug/mL	0.32 ± 0.31	0.39 ± 0.56	0.276
HbA1c (%)	6.59 ± 1.37	6.64 ± 1.38	0.759
sUA, umol/L	307.69 ± 99.31	297.00 ± 93.78	0.354
Angiographic features
SBT, h	4.55 ± 3.05	4.39 ± 2.69	0.623
D2B, min	72.81 ± 24.13	67.62 ± 44.38	0.275
Pre-AP, n (%)			0.623
NO	76 (76.77)	179 (79.20)
Yes	23 (23.23)	47 (20.80)
Killip grade			0.728
Grade I, n (%)	83 (83.84)	186 (82.30)
Grade II, n (%)	10 (10.10)	29 (12.83)
Grade III, n (%)	6 (6.06)	11 (4.87)
History of stent implantation, n (%)			0.076
NO	96 (96.97)	207 (91.59)
Yes	3 (3.03)	19 (8.41)
Multivascular disease, n (%)			0.719
NO	33 (33.33)	80 (35.40)
Yes	66 (66.67)	146 (64.60)
LAD, n (%)			0.95
NO	50 (50.51)	115 (50.88)
Yes	49 (49.49)	111 (49.12)
LCX, n (%)			0.302
NO	84 (84.85)	201 (88.94)
Yes	15 (15.15)	25 (11.06)
RCA, n (%)			0.29
NO	64 (64.65)	132 (58.41)
Yes	35 (35.35)	94 (41.59)
Calcified lesions, n (%)			0.662
NO	94 (94.95)	217 (96.02)
Yes	5 (5.05)	9 (3.98)
Proximal lesions, n (%)			0.591
NO	47 (47.47)	100 (44.25)
Yes	52 (52.53)	126 (55.75)
Bifurcation lesion, n (%)			0.717
NO	81 (81.82)	181 (80.09)
Yes	18 (18.18)	45 (19.91)
Stent length, mm	28.91 ± 12.86	28.09 ± 10.56	0.547
Stent diameter, mm	2.98 ± 0.41	3.05 ± 0.40	0.173
Number of stents, n (%)	1.20 ± 0.40	1.13 ± 0.34	0.112
High thrombus load, n (%)			0.91
NO	73 (73.74)	168 (74.34)
Yes	26 (26.26)	58 (25.66)
No-reflow, n (%)			0.891
NO	73 (73.74)	165 (73.01)
Yes	26 (26.26)	61 (26.99)
Ischemic postconditioning, n (%)			0.791
NO	62 (62.63)	145 (64.16)
Yes	37 (37.37)	81 (35.84)
Temporary pacemaker, n (%)			0.811
NO	98 (98.99)	223 (98.67)
Yes	1 (1.01)	3 (1.33)
Procedural medication
Tirofiban, n (%)			0.612
NO	80 (80.81)	177 (78.32)
Yes	19 (19.19)	49 (21.68)
Atropine, n (%)			0.886
NO	92 (92.93)	211 (93.36)
Yes	7 (7.07)	15 (6.64)
Dopamine or Hydroxylamine, n (%)			0.584
NO	94 (94.95)	211 (93.36)
Yes	5 (5.05)	15 (6.64)
Nitroprusside, n (%)			0.648
NO	60 (60.61)	143 (63.27)
Yes	39 (39.39)	83 (36.73)

Abbreviations: SBP, systolic blood pressure; DBP, diastolic blood pressure; WBC, white blood cell; N, neutrophils; L, lymphocytes; NLR, N/L ratio; RBC, red blood cell; Hb, hemoglobin; PLT, platelets; hsCRP, high-sensitivity C-reactive protein; sCr, serum creatinine; eGFR, estimated glomerular filtration rate; TC, total cholesterol; TG, triglycerides; HDL, high-density lipoprotein; LDL, low density lipoprotein; sdLDL, small dense low-density lipoprotein; Apo A, apolipoprotein A; Apo B, apolipoprotein B; Lpa, lipoprotein a; LDH, lactate dehydrogenase; CKMB, creatine kinase isoenzyme-MB; hsTnT, high-sensitivity troponin T; cTnI, cardiac troponin I; NT-proBNP, N-terminal pro-brain natriuretic peptide; FIB, fibrinogen; DD2, D-dimer; HbA1c, glycated hemoglobin; sUA, serum uric acid; SBT, symptom onset-to-balloon time; D2B, door-to-balloon time; pre-AP, pre-infarction angina; LAD, left anterior descending; LCX, left circumflex branch; RCA, right coronary artery.

Predictors of CMVO After Primary PCI

The predictors with P-value <0.05 in the univariate analysis results were sex (OR 0.397, 95% CI 0.177–0.891, P=0.025), N (OR 1.231, 95% CI 1.124–1.348, P<0.001), Hb (OR 1.048, 95% CI 1.028–1.067, P<0.001), TG (OR 1.387, 95% CI 1.154–1.667, P=0.001), LDH (OR 1.0006, 95% CI 1.0001–1.0012, P=0.015), CKMB (OR 1.005, 95% CI 1.002–1.008, P=0.003), hsTnT (OR 1.0002, 95% CI 1.0001–1.0003, P<0.001), cTnI (OR 1.022, 95% CI 1.005–1.038, P=0.01), SBT (OR 1.108, 95% CI 1.003–1.224, P=0.043), Killip grade (OR 2.098, 95% CI 1.222–3.602, P=0.007), high thrombus load (OR 3.42, 95% CI 1.827–6.400, P<0.001), no-reflow (OR 2.891, 95% CI 1.575–5.306, P=0.001) and ischemic postconditioning (OR 0.37, 95% CI 0.207–0.663, P=0.001) (Table 2). Finally, the following 7 variables selected by multivariate regression analysis were considered as independent influencing factors for CMVO in NSTEMI patients after primary PCI: N (OR 1.166, 95% CI 1.044–1.303, P<0.01), Hb (OR 1.037, 95% CI 1.013–1.062, P<0.01), TG (OR 1.343, 95% CI 1.059; 1.704, P=0.015), Killip grade (OR 2.190, 95% CI 1.065–4.503, P=0.033), high thrombus load (OR 3.146, 95% CI 1.424–6.952, P<0.01), no-reflow (OR 3.142, 95% CI 1.419–6.955, P<0.01) and ischemic postconditioning (OR 0.445, 95% CI 0.209–0.944, P=0.035) (Table 3).

Table 2

Univariate Logistic Regression Analysis of the Data from the Training Cohort

Variables	OR	95% CI	P value
Age, years	0.985	(0.965;1.004)	0.127
Sex	0.397	(0.177;0.891)	0.025
Height, cm	1.000	(0.982;1.018)	0.99
Weight, kg	1.004	(0.984;1.025)	0.674
SBP, mmHg	1.006	(0.991;1.02)	0.454
DBP, mmHg	1.009	(0.988;1.03)	0.418
HR, times/min	1.018	(0.997;1.038)	0.09
Smoking, n (%)	1.254	(0.74;2.124)	0.401
Drinking, n (%)	0.99	(0.572;1.714)	0.972
Hypertension, n (%)	0.798	(0.468;1.36)	0.407
Diabetes, n (%)	1.400	(0.731;2.68)	0.310
Stroke, n (%)	0.453	(0.14;1.467)	0.186
History of CAD, n (%)	1.488	(0.795;2.783)	0.214
Laboratory test
WBC, ×109/L	0.991	(0.963;1.019)	0.507
N, ×109/L	1.231	(1.124;1.348)	<0.001
L, ×109/L	0.889	(0.724;1.092)	0.263
NLR, %	1.017	(0.982;1.054)	0.345
RBC, ×109/L	1.534	(0.941;2.503)	0.086
Hb, g/L	1.048	(1.028;1.067)	<0.001
PLT, ×109/L	1.000	(0.995;1.004)	0.880
HsCRP, mg/dl	1.012	(0.996;1.028)	0.143
Albumin, g/L	1.024	(0.964;1.088)	0.440
SCr, mmol/L	1.006	(0.988;1.025)	0.503
eGFR, mL/min/1.73m2	1.014	(0.996;1.033)	0.133
Glucose, mmol/L	1.027	(0.924;1.141)	0.621
TC, mmol/L	1.122	(0.932;1.351)	0.224
TG, mmol/L	1.387	(1.154;1.667)	0.001
HDL cholesterol, mmol/L	2.036	(0.763;5.434)	0.156
LDL cholesterol, mmol/L	1.006	(0.785;1.288)	0.965
sdLDL cholesterol, mmol/L	0.988	(0.608;1.606)	0.962
Apo A, g/L	3.031	(0.845;10.866)	0.089
Apo B, g/L	1.292	(0.524;3.187)	0.578
Lpa, mg/L	0.9989	(0.9974;1.0004)	0.171
LDH, U/L	1.0006	(1.0001;1.0012)	0.015
CKMB, ng/mL	1.005	(1.002;1.008)	0.003
HsTnT, ng/L	1.0002	(1.0001; 1.0003)	<0.001
NT-proBNP, pg/mL	1.000	(0.9999; 1.0001)	0.899
CTNI, ng/L	1.022	(1.005;1.038)	0.010
FIB, g/L	1.002	(0.711;1.414)	0.989
DD2, ug/mL	0.750	(0.412;1.365)	0.347
HbA1c (%)	1.071	(0.885;1.296)	0.700
SUA, umol/L	1.001	(0.998;1.004)	0.572
Angiographic features
SBT, h	1.108	(1.003;1.224)	0.043
D2B, min	0.999	(0.993;1.005)	0.837
Pre-AP, n (%)	0.686	(0.353;1.332)	0.265
Killip grade	2.098	(1.222;3.602)	0.007
History of stent implantation, n (%)	0.744	(0.281;1.965)	0.550
Multivascular disease, n (%)	1.238	(0.712;2.152)	0.450
LAD, n (%)	1.23	(0.726;2.083)	0.442
LCX, n (%)	1.773	(0.767;4.098)	0.181
RCA, n (%)	0.65	(0.379;1.115)	0.117
Calcified lesions, n (%)	4.846	(0.984;23.87)	0.052
Proximal lesions, n (%)	0.887	(0.523;1.507)	0.658
Bifurcation lesion, n (%)	1.478	(0.767;2.845)	0.243
Stent length, mm	0.989	(0.964;1.014)	0.383
Stent diameter, mm	0.650	(0.334;1.266)	0.205
Number of stents, n (%)	0.725	(0.328;1.605)	0.428
High thrombus load, n (%)	3.420	(1.827;6.400)	<0.001
No-reflow, n (%)	2.891	(1.575;5.306)	0.001
Ischemic postconditioning, n (%)	0.370	(0.207;0.663)	0.001
Temporary pacemaker, n (%)	2.646	(0.236;29.608)	0.430
Procedural medication
Tirofiban, n (%)	1.336	(0.708;2.521)	0.371
Atropine, n (%)	1.154	(0.404;3.298)	0.789
Dopamine or Hydroxylamine, n (%)	0.634	(0.210;1.920)	0.421
Nitroprusside, n (%)	1.081	(0.627;1.865)	0.779

Abbreviations: SBP, systolic blood pressure; DBP, diastolic blood pressure; WBC, white blood cell; N, neutrophils; L, lymphocytes; NLR, N/L ratio; RBC, red blood cell; Hb, hemoglobin; PLT, platelets; hsCRP, high-sensitivity C-reactive protein; sCr, serum creatinine; eGFR, estimated glomerular filtration rate; TC, total cholesterol; TG, triglycerides; HDL, high-density lipoprotein; LDL, low density lipoprotein; sdLDL, small dense low-density lipoprotein; Apo A, apolipoprotein A; Apo B, apolipoprotein B; Lpa, lipoprotein a; LDH, lactate dehydrogenase; CKMB, creatine kinase isoenzyme-MB; hsTnT, high-sensitivity troponin T; cTnI, cardiac troponin I; NT-proBNP, N-terminal pro-brain natriuretic peptide; FIB, fibrinogen; DD2, D-dimer; HbA1c, glycated hemoglobin; sUA, serum uric acid; SBT, symptom onset-to-balloon time; D2B, door-to-balloon time; preAP, pre-infarction angina; LAD, left anterior descending; LCX, left circumflex branch; RCA, right coronary artery.

Table 3

Multivariate Logistic Regression Analysis of the Data from the Training Cohort

Variable	OR	95% CI	P value
Killip grade, n (%)	2.19	(1.065;4.503)	0.033
N, ×109/L	1.166	(1.044; 1.303)	0.006
Hb, g/L	1.037	(1.013; 1.062)	0.002
TG, mmol/L	1.343	(1.059; 1.704)	0.015
High thrombus load, n (%)	3.146	(1.424; 6.952)	0.005
No-reflow, n (%)	3.142	(1.419; 6.955)	0.005
Ischemic postconditioning, n (%)	0.445	(0.209; 0.944)	0.035

Abbreviations: N, neutrophils; Hb, hemoglobin; TG, triglycerides.

Development and Validation of Nomogram to the Predictive Probability of CMVO After Primary PCI

These 7 independent influencing factors selected by multivariate regression analysis were incorporated to generate a nomogram, and the nomogram was showed in Figure 2. The AUC for the nomogram of the training cohort and the validation cohort was 0.835 (95% CI: 0.780–0.882) and 0.881 (95% CI: 0.803–0.939), respectively, which suggested a nomogram with good discriminative capacity, and ROC curves were showed in Figure 3A and B. The calibration of the nomogram was assessed by using the calibration curve and Hosmer-Lemeshow test. The calibration plot showed good agreement between the nomogram and the validating sets (Figure 4A and B), and the Hosmer-Lemeshow test also suggested high consistency for predicted and actual probability in both the nomogram (P = 0.684) and validation (P = 0.727) cohort.

Figure 2

Nomogram for predicting the possibility of CMVO after primary PCI in NSTEMI patients.

Figure 3

ROC curves for the nomogram in the training cohort (A) and the validating cohort (B).

Figure 4

The calibration plot for the nomogram in the training cohort (A) and the validating cohort (B). The predicted probability of CMVO is plotted on the x-axis and the actual probability is plotted on the y-axis.

Use of the Nomogram

The possibility of CMVO after NSTEMI is predicted by combining N, Hb, TG, Killip grade, high thrombus load, No-reflow, and ischemic postconditioning. The score of each variable is calculated by drawing a vertical line between each variable axis and the top line of the nomogram. Then, we can add the scores of each variable and find the corresponding score on the total scoreline. Finally, we can draw a vertical line from the total scoreline to the bottom predicted probability scale to obtain the individual probability of CMVO in NSTEMI patients.

Clinical Effectiveness

The clinical validity of the nomogram was evaluated by the decision curve analysis (DCA). As shown decision curve, the blue dotted line represents the intervention-none and the net benefit with zero, the green dotted line shows intervention-all-patients. The upper part of the green dotted line represents positive income, meanwhile, the lower part represents negative income. Redline represents a threshold of the model. The threshold of the nomogram and validation sets exceed widely threshold range and all range shows from approximately 5% to 85%, which suggests that the nomogram was clinically useful (Figure 5A and B).

Figure 5

The decision curve analysis (DCA) for the nomogram in the training cohort (A) and the validating cohort (B). The blue dotted line represents the intervention-none and the net benefit with zero, the green dotted line shows intervention-all-patients. The upper part of the green dotted line represents positive income, meanwhile, the lower part represents negative income. The red line represents a threshold of the model.

Discussion

At present, in clinical practice, primary PCI is the main treatment method for NSTEMI. However, even after primary PCI, some NSTEMI patients still have main adverse cardiovascular events, which seriously affect people’s quality of life. However, the current evaluation of CMVO still lacks a unified prediction and scoring system. Therefore, the focus of the present study is to develop a nomogram and identify the possibility of CMVO after PCI for NSTEMI patients. Based on multivariate logistic regression analysis, we identified the following 7 independent influencing factors for CMVO: N, Hb, TG, Killip grade, high thrombus load, no-reflow and ischemic postconditioning. The present study demonstrates that a simple diagnostic score composed of the above independent risk factors is a valid clinical tool for calculating the possibility of CMVO after primary PCI. The excellent correspondence of results in both the nomogram and verification cohort demonstrated that the score is useful enough to provide accurate risk stratification of NSTEMI patients even among people in different periods.

For AMI, what was once considered to be a disease with a high risk for mortality have been treated effectively with low mortality because of primary PCI, during the past 2 decades. However, despite the general success of primary PCI, a large proportion of patients do not achieve myocardial reperfusion owing to CMVO after primary PCI.22 Several studies have clearly shown that CMVO is interrelated to various adverse prognoses, such as ventricular remodeling, heart failure, and death.3 Therefore, the diagnosis of CMVO is particularly important for clinicians. Xiao et al established a model for predicting CMVO after primary PCI in STEMI patients,23 but their results may have certain controversy. Firstly, they defined TMPG 3 grade as the gold standard for CMVO, however, the current gold standard for diagnosing CMVO is DE-CMR in our study. Early studies had shown that even if coronary angiography showed complete recovery of epicardial blood flow, a sizeable proportion of patients still had CMVO.11–14 And secondly, their model has not been tested for clinical effectiveness, whether the model can be effectively applied in a clinic is still unknown. Meanwhile, in the present study, not only do we regard DE-CMR as the gold standard for diagnosing CMVO, but also our model has good clinical effectiveness by conducting clinical effectiveness tests.

Previous studies have shown that the emergence of CMVO was caused by multiple interactive mechanisms, which makes the diagnosis of CMVO unable to be predicted by a single factor. Among the various CMVO mechanisms, the following four mechanisms are widely accepted: distant embolization, ischemia-related injury, reperfusion-related injury, and individual susceptibility.24–26 In this study, multiple risk factors were identified to develop a nomogram that can predict the possibility of CMVO after primary PCI. For the constituent elements of nomogram in the present study, neutrophils result in capillary blocking in the coronary microcirculation and can mediate endothelial function injury leading to the “no-reflow” phenomenon.27,28 As one of the major risk factors in cardiovascular disease, the mechanism of the contribution of dyslipidemia in atherosclerosis has been widely accepted. Hypertriglyceridaemia exerts detrimental effects on nitric oxide bioavailability resulting in endothelial dysfunction and stimulating the accumulation of inflammatory factors to the endothelial surface decreasing stability of coronary artery plaques.29,30 For AMI patients, the Killip grade indicates their quality of heart function, and the high Killip grade represents poor heart function and larger infarct size.31 Jang and De Luca et al found that high Killip grade was associated with a high coronary microcirculation resistance index and myocardial reperfusion injury.32,33

In addition, the study also found high thrombus load, no-reflow were independent risk factors and ischemic postconditioning was an independent protective factor for CMVO after primary PCI. The high-load thrombus may break up to form small or tiny thrombus to block the distal capillaries either spontaneously or after mechanical dilation of the culprit lesion, which can cause the “no-reflow” or slow-reflow of the culprit’s vessel during primary PCI,34 which may aggravate ischemia-reperfusion injury. In clinical practice, we often regard “no-reflow” phenomenon as CMVO, yet CMVO may be more complicated than the “no-reflow”.35 Most “no-reflow” phenomena are reversible by applying vasodilators into the coronary arteries,26 In addition, Kim and Vicente et al found that the possibility of CMVO diagnosed by coronary angiography is often lower than the actual incidence of CMVO.11–14 Meanwhile, Engstrøm et al found that ischemic postconditioning had no obvious positive effect on death and hospitalization,36 but the study from Zhao et al found that ischemic postconditioning was cardio-protective effect on the heart by attenuating myocardial edema after reperfusion injury.37 The cardioprotection by ischemic preconditioning could be achieved through several complex signal transduction pathways. Although several risk factors and comorbidities, including advanced age, diabetes, hypertension, and Hyperemia, may attenuate or abrogate the cardioprotection effects of ischemic postconditioning, this cardioprotection effect could be not affected by coronary microembolization.7,38 The protective effect of ischemic postconditioning is consistent with the results of this study.

Currently, some studies have proved that age, smoking, and other factors are independent risk factors for CMVO. With the increase of age, aging-related vascular endothelial dysfunction can induce coronary artery disease.39,40 In addition, endothelial dysfunction has been confirmed in the coronary arteries of long-term smokers, in whom coronary flow reserve was reduced by 21% by comparing with the value in nonsmoking.41 However, the present study did not get similar results with the above. We analyzed the following reasons for the above results: 1) In this study, only 30% of patients were elderly, which reduced the proportion of risk factors for advanced age. 2) In this study, about 97% of smoking patients were young and middle-aged, which may increase the influence of age as a risk factor on the results. 3) The data collection bias has a certain impact on the experimental results because of the retrospective study. Although the nomogram does not include the above influencing factors, it can still predict the occurrence of CMVO accurately.

Limitations

Several limitations should be pointed out. Firstly, the present study is a single-center retrospective design. The number of patients is small, and the selected population is relatively limited, which may lead to experimental bias. Further studies, especially multi-center registration, large-scale prospective research should be needed to verify the transportability and generalizability of our nomogram. Secondly, some indicators of echocardiography were not included in the nomogram. Finally, the nomogram cannot be applied to those patients with Killip IV grade, as these patients were excluded in this study.

Conclusions

The nomogram developed by using 7 factors, including N, Hb, TG, Killip grade, high thrombotic load, no-reflow, and ischemic post-treatment, could be used to calculate the possibility of CMVO in NSTEMI patients after primary PCI, and it could help clinicians contribute to the risk stratification, judge the prognosis and make a decision for treatment in NSTEMI patients.