- Open Access
Variability in blood lipids affects the neutrophil to lymphocyte ratio in patients undergoing elective percutaneous coronary intervention: a retrospective study
Lipids in Health and Disease volume 19, Article number: 124 (2020)
Atherosclerosis is associated with chronic inflammation and lipid metabolism. The neutrophil to lymphocyte ratio (NLR) as an indicator of inflammation has been confirmed to be associated with cardiovascular disease prognosis. However, few studies have explored the effects of blood lipid variability on NLR. The aim of this study was to explore the relationship between variability in blood lipid levels and NLR.
The association between variability in blood lipids and NLR was assessed with both univariate and multivariate linear regression. Multivariate linear regression was also performed for a subgroup analysis.
The variability of high-density lipoprotein cholesterol (HDL-C) (regression coefficients [β] 4.008, standard error (SE) 0.503, P-value< 0.001) and low-density lipoprotein cholesterol (LDL-C) ([β] 0.626, SE 0.164, P-value< 0.001) were risk factors for the NLR value, although baseline LDL-C and HDL-C were not risk factors for NLR values. Variability of HDL-C ([β] 4.328, SE 0.578, P-value< 0.001) and LDL-C ([β] 0.660, SE 0.183, P-value< 0.001) were risk factors for NLR variability. Subgroup analysis demonstrated that the relationship between variability of LDL-C and NLR was consistent with the trend of the total sample for those with diabetes mellitus, controlled blood lipid, statins, atorvastatin. The relationship between the variability of HDL-C and NLR was consistent with the trend of the total sample in all subgroups.
The variability of HDL-C and LDL-C are risk factors for the value and variability of NLR, while the relationship between variability of HDL-C and NLR is more stable than the variability of LDL-C in the subgroup analysis, which provides a new perspective for controlling inflammation in patients undergoing PCI.
Atherosclerosis, which is associated with lipid metabolism, is a common disease characterized by lipid deposition of the arterial intimal layer as well as formation of atherosclerotic plaques [1, 2]. Atherosclerosis accounts for elevated morbidity and mortality worldwide . It has recently been found that blood lipid theory is key for the development of atherosclerosis and that low-density lipoprotein cholesterol (LDL-C) plays a key role in this . Indeed, elevated levels of triglyceride (TG) and LDL-C in serum and a decrease in high-density lipoprotein cholesterol (HDL-C) are considered the lipid triads of atherosclerosis .
Atherosclerosis is also an inflammatory process that responds to various risk factors . Chronic inflammation of the arterial wall is important for the development of atherosclerosis . As a cost-effective, readily available indicator of inflammation, the neutrophil to lymphocyte ratio (NLR) is predictive of patients’ prognosis in the metastatic urothelial cancer (mUC) following immune-checkpoint inhibitors  and shows prognostic value for predicting the 30-day mortality rate and 3-month readmission rate of community-acquired pneumonia (CAP) patients . More importantly, NLR has been shown to be associated with the severity and prognosis of many cardiovascular diseases, including coronary atherosclerosis [9, 10]. Authors of previous studies have confirmed that NLR is a predictor of in-hospital major adverse cardiovascular events  and long-term prognosis  in patients after PCI. Even in the typical white blood cell count range, a higher NLR is associated with atherosclerotic events . In both healthy people  and coronary artery disease (CAD) patients , low HDL-C has been shown to correlate with the rise of NLR, although whether the variability of lipid protein has any effect on NLR remains unclear.
The aim of this study was to investigate the relationship of blood lipids as well as their variability with NLR in patients who were undergoing elective percutaneous coronary intervention (PCI).
Population and procedures
This single center, observational, retrospective study analyzed data from 4445 patients consecutively admitted to the Sir Run Run Shaw Hospital, Zhejiang University in China between January 2009 and April 2019. Inclusion criteria were as follows: (1) patients must have undergone elective percutaneous coronary intervention; (2) NLR and lipid values during follow-up such as total cholesterol (TC), TG, LDL-C, HDL-C were available; (3) patients were followed up three times or more in the outpatient clinic within 1 year following PCI.
Participants were excluded if their C-reactive protein (CRP)>10 mg/L, their white blood cell count (WBC)>10 × 10^9/L, they had congenital heart disease, valvular heart disease, heart failure, peripheral arterial disease, severe renal or hepatic dysfunction, hematological disorders, history of malignancy, acute or chronic infection.
All PCI procedures were carried out by experienced interventional cardiologists using the femoral or radial artery approach, as recommended by current guidelines . Blood samples for baseline information were collected 24 h before PCI. Three or more follow-ups were carried out in 1 year for patients who have undergone PCI. After an overnight fast, blood samples were taken by antecubital vein puncture to measure routinely evaluated laboratory values. Total leucocyte count and its subtypes, including neutrophil and lymphocyte, as well as monocyte and platelet count were analyzed using an automated blood cell counter. Lipid values such as total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and very low-density lipoprotein (VLDL) were also measured by a blood chemistry analyzer (Hitachi 747; Hitachi, Tokyo, Japan). The study was given approval by the Ethics Committee of Sir Run Run Shaw Hospital of Zhejiang University.
Patients’ medical records from when they were hospitalized were used as baseline indicators and blood samples for baseline information were collected 24 h before PCI. HDL-C (STDEV), LDL-C (STDEV), TG (STDEV) and TC (STDEV) refer to the variability of HDL-C, LDL-C, TG and TC, respectively. These were expressed as standard deviations, calculated from follow-up results obtained in 1 year for patients who have undergone PCI. The value of NLR was the mean of the follow-up results. Lipid control was defined as LDL-C<1.8 mmol/L at each follow-up measurement. A total of 3118 patients had their blood lipids controlled. Smoking was defined as currently smoking or stopping less than one month ago. Heart failure was defined by EF < 40% or NT-pro BNP > 2000 pg/ml.
Statistical analysis was performed using SPSS software version 22.0 (SPSS Inc., Chicago, IL, USA). Continuous variables were non-normally distributed and presented as medians (25–75%). Categorical variables were represented as n (%). Univariate analysis and multivariate regression analysis for each factor were performed by linear regression analysis. In the subgroup analysis, multivariate linear regressions were performed on patients with or without diabetes mellitus, with controlled or uncontrolled blood lipid, who were taking statin with ezetimibe or not, and who were taking rosuvastatin or atorvastatin. All reported P-values were two-sided, and P-values of < 0.05 were considered statistically significant.
In present study, 4445 patients who had undergone elective PCI at the Sir Run Run Shaw Hospital between January 2009 and April 2019 were included, according to the inclusion and exclusion criteria. Participants’ median age was 64 (58–71), 71.9% were men, 63.4% had hypertension and 25.6% had diabetes mellitus. Demographic information, laboratory examination and baseline medication can be seen in Table 1.
Results of univariate and multivariate linear regression for the mean of NLR
The univariate analysis suggested that age, gender, diabetes, hypertension, types of statins, HDL-C (STDEV), CRP (mean), LDL-C (mean), creatinine and uric acid were all risk factors for the mean value of NLR during follow-up. In contrast, ezetimibe, baseline TC, baseline HDL-C and HDL-C (mean) were protective factors for the mean value of NLR (see Table 2).
Once the univariate analysis was corrected to allow for confounding factors, results from the multivariable logistic regression analysis showed that age, gender, types of statins, HDL-C (STDEV), LDL-C (STDEV), LDL-C (mean), CRP (mean) and creatinine were all risk factors for the mean value of NLR. Baseline TC and HDL-C (mean) were protective factors for the mean value of NLR (see Table 2).
For HDL-C (STDEV), multivariate linear regression analysis results for each subgroup are stable, showing that HDL-C (STDEV) is a risk factor for the mean value of NLR during the follow-up (see Fig. 1).
In contrast, the relationship between LDL-C (STDEV) and the mean value of NLR was consistent across patients with blood lipid controlled (regression coefficients [β] 0.603, [95% CI] 0.204–1.001, P-value = 0.003), diabetes ([β] 0.913, [95% CI] 0.295–1.532, P-value = 0.004), those who were taking statins ([β] 0.0.619, [95% CI] 0.275–0.963, P-value< 0.001) and those taking atorvastatin ([β] 0.499, [95% CI] 0.103–0.895, P-value = 0.014) (see Fig. 2).
Results of univariate and multivariate linear regression for the variability in NLR
The univariate analysis suggested that age, gender, types of statins, HDL-C (STDEV), CRP (mean) and creatinine were all risk factors for NLR variability during follow-up. In contrast, baseline TC, HDL-C (mean) and baseline HDL-C were protective factors for NLR variability (see Table 3).
After correction for the confounding factors screened from the univariate analysis, the multivariable linear regression analysis revealed that age, gender, types of statins, HDL-C (STDEV), LDL-C (STDEV), CRP (mean) and creatinine were risk factors for NLR variability. Baseline TC, HDL-C (mean) and baseline HDL-C were protective factors for the variability in NLR (see Table 3).
For HDL-C (STDEV), multivariate linear regression analysis results for each subgroup are stable, suggesting that HDL-C (STDEV) is a risk factor for NLR variability during the follow-up (see Fig. 3).
On the other hand, the relationship between LDL-C (STDEV) and NLR variability was consistent across the patients with controlled blood lipid ([β] 0.613, [95% CI] 0.159–1.067, P-value = 0.008), diabetes ([β] 0.725, [95% CI] 0.040–1.410, P-value = 0.0038), those with no diabetes ([β] 0.470, [95% CI] 0.053–0.887, P-value = 0.027), those taking statins ([β] 0.765, [95% CI] 0.382–1.149, P-value< 0.001), and those taking atorvastatin ([β] 0.634, [95% CI] 0.178–1.090, P-value = 0.006) (see Fig. 4).
The main findings of the current study are as follows: (1) variability of HDL-C and LDL-C were risk factors for the value and variability in NLR; (2) the relationship between variability of HDL-C and NLR was consistent for each subgroup analysis (those with or without diabetes mellitus, controlled or uncontrolled blood lipid, taking statin with ezetimibe or not, and taking rosuvastatin or atorvastatin). The relationship between variability of LDL-C and NLR was also confirmed in patients with controlled blood lipid, diabetes, those taking statin and those taking atorvastatin. Subgroup analysis results suggest that the linear relationship between HDL-C and NLR is more stable than for LDL-C.
Blood lipid levels play a crucial role in the process of atherosclerosis [1, 17]. HDL-C is an independent predictor of coronary heart disease risk . Authors of four large studies have concluded that each increase of 1 mg per deciliter (0.03 mmol per liter) in HDL-C is associated with a decrease of 2 to 3% in future coronary heart disease risk . Low-density lipoprotein has important physiological effects as a carrier for transporting cholesterol to peripheral tissues, although its elevated level is associated with an increased risk of cardiovascular disease [1, 20, 21]. NLR can be easily calculated from differential WBC counts, which are widely available and routinely performed. These counts provide physicians with important information regarding not only the prognosis of mUC  and CAP  patients, but also with additional risk stratification beyond conventional risk scores such as predicting mortality in cardiovascular diseases . Increased NLR values may indicate subclinical inflammation . In addition, NLR is associated with pro-inflammatory mediators (high sensitive CRP, tumor necrosis factor-α) and progressive subclinical atherogenesis . A high NLR is a predictor of atherosclerosis progression [10, 24, 25] and long-term prognosis in patients after PCI . As a protective factor for blood vessels, HDL-C has been observed in both healthy people  and CAD patients  as associated with NLR levels at lower levels. However, few authors have focused on the relationship between variability in blood lipids and NLR.
Visit-to-visit LDL-C variability was found to be an independent predictor of cardiovascular events for patients with stable coronary artery disease in the TNT trial , while Boey et al. confirmed that visit-to-visit LDL-C and HDL-C variability are associated with occurrence of a MACE at 5 year follow-up following STEMI . Results of the current study further support the clinical relevance of LDL-C and HDL-C variability by showing that LDL-C and HDL-C variability are risk factors for NLR. In contrast to Boey et al., the focus of this study is on NLR rather than clinical outcomes. The current study sample was Asian rather than Caucasian patients who were followed-up for 1 year following PCI. In addition, by confirming the variability in HDL-C and LDL-C can affect NLR variability, the clinical connection between blood lipid and NLR was further explored. The results of the current study may have certain reference significance for lipid-lowering therapy in patients at this time.
The exact mechanism for increased variability in LDL-C, HDL-C and an increased risk of NLR remains unknown. However, several hypotheses have been suggested. Statins primarily (although not exclusively) stabilize plaque  through a cholesterol-dependent mechanism, thereby reducing plaque cholesterol levels . In turn, lipid reduction inhibits inflammation as well as reducing collagen hydrolyzing activity and thrombotic potential. LDL-C variability may result in instability of the vessel wall due to damage to cholesterol-dependent plaque stabilization mechanisms , thus increasing the likelihood of plaque vulnerability and rupture, although most ruptures do not cause clinic events. Conversely, high HDL-C variability may lead to plaque instability by impairing cholesterol outflows in surrounding tissues and macrophages, thus increasing the risk of damage to the vessel wall and inducing inflammation . Additionally, LDL particles in circulation can penetrate the endothelium of the arterial wall and be oxidized, promoting inflammation and causing endothelial damage . Neutrophils indicate systemic inflammatory states, while lymphocytes suggest fibrotic hyperplasia and homeostasis of overall inflammation. Both of these respond to inflammation caused by arterial plaque [2, 32, 33]. Further to this, vasculogenesis, a process involved in cardiovascular injury, initiates various chronic adaptive processes including elevation of circulating neutrophils, which will further damage vascular endothelial cells through processes such as inflammatory reactions and oxidative stress , partially explaining this study’s results. Interestingly, the use of subgroup analysis in this study showed that the relationship between the variability of HDL-C and NLR is more stable than the variability of LDL-C, which deserves further investigation. In clinical practice, there is no effective treatment method for controlling NLR. It was found that blood lipid variability is an independent risk factor for NLR, suggesting that the control of blood lipid variability can affect NLR, thereby improving the prognosis of patients undergoing PCI.
First, as a single center, retrospective observational study, residual confounding or selection bias cannot be excluded, which is inherent to any retrospective study. Second, patients’ statin dose was not taken as a factor of inquiry, which may affect blood lipid variability. Third, factors that may affect NLR, such as hypertension and diabetes, were not ruled out, but instead were used as corrective factors in the multivariate regression. Last but not least, information on patients’ interleukin-6, which can reflect the inflammatory status in vivo, was not collected. Additionally, there was no focus on the relationship of CRP, another indicator of inflammation, with blood lipid variability, but this was included in multivariate regression.
The variability of HDL-C and LDL-C are risk factors for NLR in patients who have undergone elective percutaneous coronary intervention, while the relationship between the variability of HDL-C and NLR is more stable than the variability of LDL-C.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Neutrophil to lymphocyte ratio
Low-density lipoprotein cholesterol
High-density lipoprotein cholesterol
Coronary artery disease
Percutaneous coronary intervention
White blood cell count
Very low-density lipoprotein
Glass CK, Witztum JL. Atherosclerosis. The road ahead. Cell. 2001;104:503–16..
Rezende AB, Neto NN, Fernandes LR, Ribeiro AC, Alvarez-Leite JI, Teixeira HC. Splenectomy increases atherosclerotic lesions in apolipoprotein E deficient mice. J Surg Res. 2011;171:e231–6.
Afari ME, Bhat T. Neutrophil to lymphocyte ratio (NLR) and cardiovascular diseases: an update. Expert Rev Cardiovasc Ther. 2016;14:573–7.
Petroianu A, Veloso DF, Alberti LR, de Souza Vasconcellos L. Plasma lipid alterations after total splenectomy, subtotal splenectomy and splenic auto-implants in rats. J Gastroenterol Hepatol. 2008;23:e221–4.
Libby P, Theroux P. Pathophysiology of coronary artery disease. Circulation. 2005;111:3481–8.
Balta S, Celik T, Mikhailidis DP, Ozturk C, Demirkol S, Aparci M, Iyisoy A. The relation between atherosclerosis and the neutrophil-lymphocyte ratio. Clin Appl Thromb Hemost. 2016;22:405–11.
Banna GL, Di Quattro R, Malatino L, Fornarini G, Addeo A, Maruzzo M, Urzia V, Rundo F, Lipari H, De Giorgi U, Basso U. Neutrophil-to-lymphocyte ratio and lactate dehydrogenase as biomarkers for urothelial cancer treated with immunotherapy. Clin Transl Oncol. 2020;1:1–6.
Cataudella E, Giraffa CM, Di Marca S, Pulvirenti A, Alaimo S, Pisano M, Terranova V, Corriere T, Ronsisvalle ML, Di Quattro R, et al. Neutrophil-to-lymphocyte ratio: an emerging marker predicting prognosis in elderly adults with community-acquired pneumonia. J Am Geriatr Soc. 2017;65:1796–801.
Kaya MG, Akpek M, Lam YY, Yarlioglues M, Celik T, Gunebakmaz O, Duran M, Ulucan S, Keser A, Oguzhan A, Gibson MC. Prognostic value of neutrophil/lymphocyte ratio in patients with ST-elevated myocardial infarction undergoing primary coronary intervention: a prospective, multicenter study. Int J Cardiol. 2013;168:1154–9.
Kalay N, Dogdu O, Koc F, Yarlioglues M, Ardic I, Akpek M, Cicek D, Oguzhan A, Ergin A, Kaya MG. Hematologic parameters and angiographic progression of coronary atherosclerosis. Angiology. 2012;63:213–7.
Machado GP, Araujo GN, Carpes CK, Lech M, Mariani S, Valle FH, Bergoli LCC, Goncalves SC, Wainstein RV, Wainstein MV. Comparison of neutrophil-to-lymphocyte ratio and mean platelet volume in the prediction of adverse events after primary percutaneous coronary intervention in patients with ST-elevation myocardial infarction. Atherosclerosis. 2018;274:212–7.
Zhang S, Diao J, Qi C, Jin J, Li L, Gao X, Gong L, Wu W. Predictive value of neutrophil to lymphocyte ratio in patients with acute ST segment elevation myocardial infarction after percutaneous coronary intervention: a meta-analysis. BMC Cardiovasc Disord. 2018;18:75.
Horne BD, Anderson JL, John JM, Weaver A, Bair TL, Jensen KR, Renlund DG, Muhlestein JB. Intermountain heart collaborative study G: which white blood cell subtypes predict increased cardiovascular risk? J Am Coll Cardiol. 2005;45:1638–43.
Tok D, Iscen S, Ozenc S. Neutrophil-lymphocyte ratio is associated with low high-density lipoprotein cholesterol in healthy young men. SAGE Open Med. 2014;2:2050312114532079.
Prajapati JH, Sahoo S, Nikam T, Shah KH, Maheriya B, Parmar M. Association of high density lipoprotein with platelet to lymphocyte and neutrophil to lymphocyte ratios in coronary artery disease patients. J Lipids. 2014;2014:686791.
Levine GN, Bates ER, Blankenship JC, Bailey SR, Bittl JA, Cercek B, Chambers CE, Ellis SG, Guyton RA, Hollenberg SM, et al. ACCF/AHA/SCAI guideline for percutaneous coronary intervention: executive summary: a report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines and the Society for Cardiovascular Angiography and Interventions. Circulation. 2011(124):2574–609.
Carr SS, Hooper AJ, Sullivan DR, Burnett JR. Non-HDL-cholesterol and apolipoprotein B compared with LDL-cholesterol in atherosclerotic cardiovascular disease risk assessment. Pathology. 2019;51:148–54.
Barter P, Gotto AM, LaRosa JC, Maroni J, Szarek M, Grundy SM, Kastelein JJ, Bittner V, Fruchart JC. Treating to new targets I: HDL cholesterol, very low levels of LDL cholesterol, and cardiovascular events. N Engl J Med. 2007;357:1301–10.
Gordon DJ, Probstfield JL, Garrison RJ, Neaton JD, Castelli WP, Knoke JD, Jacobs DR Jr, Bangdiwala S, Tyroler HA. High-density lipoprotein cholesterol and cardiovascular disease. Four prospective American studies. Circulation. 1989;79:8–15.
Qamar A, Libby P. Low-density lipoprotein cholesterol after an acute coronary syndrome: how low to go? Curr Cardiol Rep. 2019;21:77.
Katzmann JL, Laufs U. New insights in the control of low-density lipoprotein cholesterol to prevent cardiovascular disease. Curr Cardiol Rep. 2019;21:69.
Balta S, Demirkol S, Unlu M, Arslan Z, Celik T. Neutrophil to lymphocyte ratio may be predict of mortality in all conditions. Br J Cancer. 2013;109:3125–6.
Suarez-Cuenca JA, Ruiz-Hernandez AS, Mendoza-Castaneda AA, Dominguez-Perez GA, Hernandez-Patricio A, Vera-Gomez E, De la Pena-Sosa G, Banderas-Lares DZ, Montoya-Ramirez J, Blas-Azotla R, et al. Neutrophil-to-lymphocyte ratio and its relation with pro-inflammatory mediators, visceral adiposity and carotid intima-media thickness in population with obesity. Eur J Clin Investig. 2019;49:e13085.
Nam KW, Kwon HM, Jeong HY, Park JH, Kim SH, Jeong SM. High neutrophil to lymphocyte ratios predict intracranial atherosclerosis in a healthy population. Atherosclerosis. 2018;269:117–21.
Corriere T, Di Marca S, Cataudella E, Pulvirenti A, Alaimo S, Stancanelli B, Malatino L. Neutrophil-to-lymphocyte ratio is a strong predictor of atherosclerotic carotid plaques in older adults. Nutr Metab Cardiovasc Dis. 2018;28:23–7.
Bangalore S, Breazna A, DeMicco DA, Wun CC, Messerli FH, Committee TNTS. Investigators: visit-to-visit low-density lipoprotein cholesterol variability and risk of cardiovascular outcomes: insights from the TNT trial. J Am Coll Cardiol. 2015;65:1539–48.
Boey E, Gay GM, Poh KK, Yeo TC, Tan HC, Lee CH. Visit-to-visit variability in LDL- and HDL-cholesterol is associated with adverse events after ST-segment elevation myocardial infarction: a 5-year follow-up study. Atherosclerosis. 2016;244:86–92.
Thondapu V, Kurihara O, Yonetsu T, Russo M, Kim HO, Lee H, Soeda T, Minami Y, Jang IK. Comparison of Rosuvastatin versus atorvastatin for coronary plaque stabilization. Am J Cardiol. 2019;123:1565–71.
Crisby M, Nordin-Fredriksson G, Shah PK, Yano J, Zhu J, Nilsson J. Pravastatin treatment increases collagen content and decreases lipid content, inflammation, metalloproteinases, and cell death in human carotid plaques: implications for plaque stabilization. Circulation. 2001;103:926–33.
Navab M, Reddy ST, Van Lenten BJ, Fogelman AM. HDL and cardiovascular disease: atherogenic and atheroprotective mechanisms. Nat Rev Cardiol. 2011;8:222–32.
Sloop GD. Atherosclerosis--an inflammatory disease. N Engl J Med. 1999;340:1928 author reply 1929.
Pillay J, Kamp VM, van Hoffen E, Visser T, Tak T, Lammers JW, Ulfman LH, Leenen LP, Pickkers P, Koenderman L. A subset of neutrophils in human systemic inflammation inhibits T cell responses through mac-1. J Clin Invest. 2012;122:327–36.
Drew AF, Tipping PG. T helper cell infiltration and foam cell proliferation are early events in the development of atherosclerosis in cholesterol-fed rabbits. Arterioscler Thromb Vasc Biol. 1995;15:1563–8.
Siminiak T, Flores NA, Sheridan DJ. Neutrophil interactions with endothelium and platelets: possible role in the development of cardiovascular injury. Eur Heart J. 1995;16:160–70.
We are grateful for the language polish service provided by EditSprings.
This work was supported by the Zhejiang Natural Science Fund (LY18H020007), National Natural Science Foundation of China (81700213) and Chinese Cardiovascular Association-V.G fund (2017-CCA-VG-030).
Ethics approval and consent to participate
The study was given approval by the Ethics Committee of Sir Run Run Shaw Hospital of Zhejiang University.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhao, L., Xu, T., Li, Y. et al. Variability in blood lipids affects the neutrophil to lymphocyte ratio in patients undergoing elective percutaneous coronary intervention: a retrospective study. Lipids Health Dis 19, 124 (2020). https://doi.org/10.1186/s12944-020-01304-9
- High-density lipoprotein cholesterol
- Low-density lipoprotein cholesterol
- Neutrophil to lymphocyte ratio
- Percutaneous coronary intervention