Usefulness of Monocyte To HDL-cholesterol Ratio To Predict High SYNTAX Score in Patients With Stable Coronary Artery Disease

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Research Article

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Usefulness of monocyte to HDL-cholesterol


ratio to predict high SYNTAX score in
patients with stable coronary artery
disease

Aim: We aimed to investigate whether baseline monocyte to high-density lipoprotein Mehmet Kadri Akboga*,1,
cholesterol ratio (MHR), an easily available inflammatory and oxidative stress marker, Kevser Gulcihan Balci1, Orhan
is associated with SYNTAX score. Patients & methods: In this cross-sectional study, Maden1, Ahmet Goktug
n = 1229 consecutive patients with coronary artery disease were classified into two Ertem1, Ozgur Kirbas1, Cagri
groups, low SYNTAX score (≤22) and high SYNTAX score (≥23). Results: MHRs were Yayla1, Burak Acar1, Dursun
Aras1, Halil Kisacik1 & Sinan
significantly higher in patients with high SYNTAX score (p < 0.05). In multivariate
Aydogdu1
regression analysis, MHR remained as independent predictor of high SYNTAX 1
Turkiye Yuksek Ihtisas Training &
score together with C-reactive protein (CRP), hypertension and diabetes mellitus. Research Hospital, Department of
In correlation analysis, MHR showed significant positive correlations with SYNTAX Cardiology, Ankara, Turkey
score (r = 0.371, p < 0.001) and CRP level (r = 0.336, p < 0.001). Conclusion: This study *Author for correspondence:
Tel.: +90 312 3061134
suggests MHR is independently associated with burden of coronary atherosclerosis.
mkakboga@ yahoo.com

First draft submitted: 15 December 2015; Accepted for publication: 9 February 2016;
Published online: 21 March 2016

Keywords:  high SYNTAX score • inflammation/oxidative stress • monocyte/HDL-cholesterol


ratio

The SYNTAX score is an angiographic scor- their ­ predictive and prognostic value in
ing system that was developed during the cardiovascular diseases has been studied
SYNTAX trial and used to quantify the well  [10,11] . Macrophages and monocytes are
properties of lesion including complexity, the most important cell types for secretion
morphology and location in the coronary of proinflammatory and prooxidant cyto-
tree [1] . The usefulness of the SYNTAX score kines at the site of inflammation [12] . On
while making revascularization decisions and the contrary, high-density lipoprotein cho-
in predicting adverse events in patients with lesterol (HDL-C) defends endothelial cells
coronary artery disease has been appreciated via aiding vasorelaxation, interfering low-
in several studies [2–5] . In addition to predict- density lipoprotein cholesterol oxidation
ing possible peri-procedural difficulties, the and increasing endothelial nitric oxide syn-
SYNTAX score also reflects the pattern of thase expression [13,14] . Recently, monocyte
atheroma incorporating length, calcification to HDL-C ratio (MHR), combining the
and thrombosis of the lesion [6] . predictive and prognostic value of both eas-
It was known that inflammation, endo- ily available laboratory markers into a single
thelial dysfunction, oxidative stress and fraction  [15] , has emerged as a new marker
platelet activation play a significant role in cardiovascular diseases [16,17] . Thus, in
in the formation and progression of ath- this study, we aimed to investigate the rela-
erosclerosis  [7–9] . Alteration in white blood tion between MHR and the SYNTAX score
cell counts and differentials were a­ ssociated among patients with stable coronary artery
part of
with the inflammatory condition, and disease (CAD) and if this simple laboratory

10.2217/bmm-2015-0050 © 2016 Future Medicine Ltd Biomark. Med. (Epub ahead of print) ISSN 1752-0363
Research Article  Akboga, Balci, Maden et al.

Table 1. Baseline clinical and angiographic characteristics of the study patients (1229).
 Parameters SYNTAX score p-value
Low group High group
(≤22; n = 821) (≥23; n = 408)
Age, years 59.8 ± 10.8 62.4 ± 10.5 <0.001
Male sex, n (%) 499 (60.8) 292 (71.6) <0.001
Hypertension, n (%) 377 (45.9) 219 (53.7) 0.010
Diabetes mellitus, n (%) 181 (22.0) 114 (27.9) 0.023
Active smoker, n (%) 294 (35.8) 162 (39.7) 0.183
Family history of CAD, n (%) 151 (18.4) 88 (21.6) 0.185
LVEF (%) 61.1 ± 8.2 54.6 ± 11.6 <0.001
Prior medical therapy, n (%):
 - RAS blocker 244 (29.7) 141 (34.6) 0.085
 - Diuretic 86 (10.5) 53 (13.0) 0.190
 - Calcium channel blocker 111 (13.5) 62 (15.2) 0.426
 - β-blocker 103 (12.5) 59 (14.5) 0.350
 - Statin 89 (10.8) 51 (12.5) 0.388
 - Antiaggregant 104 (12.7) 65 (15.9) 0.118
 - Oral antidiabetic drug, n (%) 147 (17.9) 86 (21.1) 0.181
Multivessel disease 320 (39.0) 290 (71.1) <0.001
Chronic total occlusion 124 (15.1) 230 (56.4) <0.001
Location of coronary lesions:
 - LMCA 46 (5.6) 60 (14.7) <0.001
 - LAD 359 (43.7) 270 (66.2) <0.001
 - LCx 310 (37.8) 177 (43.4) 0.160
 - RCA 469 (57.1) 237 (58.1) 0.827
Management of CAD:     <0.001
 - Stenting 604 (73.5)  174 (42.6)  
 - CABG 152 (18.5) 196 (48.0)  
 - Conservative 67 (8.1) 39 (9.5)  
Data were given as mean ± standard deviation or %.
CABG: Coronary artery bypass grafting; CAD: Coronary artery disease; LAD: Left anterior descending artery; LCx: Left circumflex artery;
LMCA: Left main coronary artery; LVEF: Left ventricular ejection fraction; RAS: Renin–angiotensin system; RCA: Right coronary artery.

marker could reflect the severity and the complexity severe coronary artery stenosis. The angiographic data
of the CAD. of all patients were retrospectively retrieved and ana-
lyzed at our tertiary center angiography units. Stable
Pateints & methods angina pectoriswas diagnosed according to the criteria
Study population recommended by the current guidelines [18] .
In this retrospective cross-sectional study, in between Patients enrolled in present study underwent
July 2012 and November 2014, 4870 patients with detailed clinical examination for the assessment of the
CAD who were referred to the catheter laboratory for baseline clinical characteristics of the study popula-
coronary angiogram with an initial diagnosis of stable tion including history of hypertension, diabetes mel-
angina pectoris or angina equivalents were evaluated. litus, smoking, family history of CAD were recorded.
According to the exclusion criteria, the final study Arterial hypertension was considered in patients with
group consisted of 1229 patients. The decision for cor- repeated blood pressure measurements ≥140/90 mm
onary angiography was made according to a positive Hg or active use of antihypertensive drugs. Diabetes
noninvasive stress test or high clinical suspicion for a mellitus was defined as fasting plasma glucose levels

10.2217/bmm-2015-0050 Biomark. Med. (Epub ahead of print) future science group


Association of MHR with SYNTAX score  Research Article

more than 126 mg/dL in multiple measurements or liver disease (with liver function parameters >3x upper
glucose level over 200 mg/dL at any measurement normal value), chronic obstructive pulmonary disease,
or active use of antidiabetic medications. Smoking and any hematologic or malignant disease. The ethical
was defined as current smoking. The family his- implications regarding the study were approved by the
tory of CAD was defined as presence of a history of local Ethics Committee
CAD or sudden cardiac death in a first-degree rela-
tive before the age of 55 years for men and before the Coronary angiography
age of 65 years for women. The estimated glomerular Standard Judkins technique was used for coronary
filtration rate was calculated by applying the Modifi- artery visualization. Selective cine-angiographic
cation of Diet in Renal Disease formula to the serum images of the coronaries were recorded using a digi-
­creatinine concentration. tal angiographic system (AXIOM Artis, Siemens AG,
Exclusion criteria were as following: recent acute Munich, Germany). At least two orthogonal plane
coronary syndrome either with or without ST-seg- images were taken for each coronary artery. Accord-
ment elevation (≤6 months before enrollment), previ- ing to the baseline coronary angiograms, the SYNTAX
ous revascularization history (coronary artery bypass score was calculated in all patients by two independent
grafting or percutaneous coronary intervention), experienced interventional cardiologists who were
decompensated heart failure, nonischemic dilated car- blinded to the identities and clinical information of
diomyopathy, significant valvular heart disease, symp- the patients from baseline diagnostic coronary angio-
tomatic peripheral vascular disease, evidence of acute grams. The SYNTAX score was determined for all
or chronic infection, systemic inflammatory or auto- coronary lesions with >50% diameter stenosis in a ves-
immune disease, chronic kidney disease (­glomerular sel >1.5 mm, based on the SYNTAX score calculator
filtration rate <60 ml/min/1.73 m2), history of any 2.1 [19] . The patients were divided into two groups as

Table 2. Laboratory parameters of the study patients.


Parameters SYNTAX Score p-value
Low group High group
(≤22; n = 821) (≥23; n = 408)
Hemoglobin, g/dL 14.2 ± 1.2 14.3 ± 1.2 0.392
RDW (%) 13.8 ± 1.6 14.0 ± 1.6 0.153
Platelet, 10³/mm³ 251 ± 49 261 ± 58 0.028
Mean platelet volume, fL 8.5 ± 1.3 8.7 ± 1.4 0.056
White blood cell, μL 7566 ± 1694 7881 ± 1601 0.002
Neutrophil, μL 4555 ± 1410 4846 ± 1424 0.001
Lymphocyte, μL 2296 ± 680 2246 ± 747 0.239
Monocyte, μL† 510 (400–700) 600 (420–740) 0.001
Creatinine, mg/dL 0.84 ± 0.17 0.85 ± 0.18 0.304
eGFR, mL/min/1.73 m2  94.5 ± 23.9 92.2 ± 21.6 0.296
Uric acid, mg/dL† 5.0 (4.2–6.9) 5.6 (4.9–6.3) 0.118
ALT, U/l 22.6 ± 6.4 22.7 ± 6.7 0.973
AST, U/l 22.4 ± 7.9 23.2 ± 8.7 0.132
C-reactive protein, mg/L †
6.2 (3.5–11.1) 10.0 (5.1–18.4) <0.001
Total cholesterol, mg/dL 198 ± 43 196 ± 48 0.491
HDL-cholesterol, mg/dL †
43.0 (37.0–52.0) 38.5 (33.0–45.0) <0.001
LDL-cholesterol, mg/dL 122 ± 37 126 ± 43 0.117
Triglyceride, mg/dL† 137 (102–197) 143 (99–205) 0.709
Monocyte/HDL-C ratio †
12.1 (8.5–16.9) 14.6 (11.1–20.4) <0.001
Data are given as mean ± standard deviation, or %.

Median (interquartile range).
ALT: Alanine aminotransferase; AST: Aspartate aminotransferase; eGFR: estimated glomerular filtration rate; HDL-C: High-density lipoprotein
cholesterol; LDL-C: Low-density lipoprotein cholesterol; RDW: Red cell distribution width.

future science group www.futuremedicine.com10.2217/bmm-2015-0050


Research Article  Akboga, Balci, Maden et al.

Table 3. Baseline characteristics and laboratory parameters of the study groups according to SYNTAX score tertiles.
Parameters SYNTAX score p-value
Low group Intermediate group High group
(≤22; n = 821) (23–32; n = 226) (≥33; n = 182)
Age, years 59.8 ± 10.8 61.6 ± 10.9 63.4 ± 10.3 <0.001
Male sex, n (%) 499 (60.8) 154 (68.1) 138 (75.8) <0.001
Hypertension, n (%) 377 (45.9) 115 (50.9) 104 (57.1) 0.017
Diabetes mellitus, n (%) 181 (22.0) 56 (24.8) 58 (31.9) 0.019
LVEF (%) 61.1 ± 8.2 55.3 ± 11.2 53.6 ± 12.1 <0.001
Hemoglobin, g/dL 14.2 ± 1.2 14.2 ± 1.3 14.3 ± 1.5 0.894
RDW (%) 13.8 ± 1.6 13.9 ± 1.5 14.1 ± 1.8 0.299
Platelet, 10³/mm³ 251 ± 49 257 ± 51 266 ± 62 0.030
Mean platelet volume, fL 8.5 ± 1.3 8.7 ± 1.4 8.8 ± 1.4 0.096
White blood cell, μL 7566 ± 1694 7728 ± 1538 8071 ± 1660 0.001
Neutrophil, μL 4555 ± 1410 4754 ± 1312 4960 ± 1549 0.001
Monocyte, μL† 510 (400–700) 545 (400–742) 600 (477–725) 0.001
eGFR, mL/min/1.73 m2  94.5 ± 23.9 92.9 ± 21.1 91.1 ± 22.4 0.515
C-reactive protein, mg/L †
6.2 (3.5–11.1) 8.4 (4.4–16.1) 12.1 (6.1–20.1) <0.001
Total cholesterol, mg/dL 198 ± 43 197 ± 47 195 ± 50 0.712
HDL-cholesterol, mg/dL† 43.0 (37.0–52.0) 40.0 (34.0–47.3) 37.0 (31.0–44.0) <0.001
LDL-cholesterol, mg/dL 122 ± 37 124 ± 40 128 ± 45 0.167
Triglyceride, mg/dL †
137 (102–197) 143 (104–205) 142 (94–203) 0.633
Monocyte/HDL-C ratio† 12.1 (8.5–16.9) 13.9 (10.5–18.9) 16.1 (11.6–21.3) <0.001

Data were given as mean ± standard deviation or %.
Median (interquartile range).
eGFR: Estimated glomerular filtration rate; HDL-C: High-density lipoprotein cholesterol; LDL-C: Low-density lipoprotein cholesterol; LVEF: Left ventricular ejection
fraction; RDW: Red cell distribution width.

low SYNTAX score group (≤22) and high SYNTAX HDL-C levels were measured using a Beckman
score group (≥23) [20] . Transthoracic echocardiography Coulter AU680 (Beckman Coulter Inc, CA, USA).
was performed in all patients, and left ventricular ejec-
tion fraction (LVEF) was calculated using ­modified Statistical analysis
Simpson method. In all statistical analysis SPSS 20.0 Statistical Pack-
age Program for Windows (SPSS Inc., IL, USA) was
Laboratory analysis used. Kolmogorov–Smirnov test was used to test nor-
Blood samples were collected from the antecubital mality of distribution. Quantitative variables with a
vein before the index coronary angiography after normal distribution were specified as the mean ± stan-
an overnight fast. Laboratory parameters (includ- dard deviation, and those with non-normal distri-
ing complete blood count, SA, biochemistry panel bution were specified with median (minimum and
and lipid panel that were taken before the index maximum); categorical variables were specified with
coronary angiography) of all the participants were number and percentage values. To compare paramet-
recorded. Samples for the complete blood count ric continuous variables, Student’s t test or analysis of
(CBC) analysis (with differential analysis) were col- variance (ANOVA) was used; to compare nonpara-
lected in EDTA anticoagulated Monovette tubes metric continuous variables, Mann–Whitney U test
(Sarstedt, Leicester, UK). Monocyte count was cal- or ­K ruskal–Wallis test was used as appropriate. Cat-
culated using data obtained from the CBC differen- egorical variables were compared with Chi-square test.
tial analysis (using an automated blood cell counter). Spearman’s correlation coefficient was computed to
The reference value for monocyte in our laboratory is examine the relationship between MHR and SYN-
0.2–1.2 × 103 /dL and for HDL-C is 40–60 mg/dL. TAX score and C-reactive protein (CRP). Multiple

10.2217/bmm-2015-0050 Biomark. Med. (Epub ahead of print) future science group


Association of MHR with SYNTAX score  Research Article

logistic regression analysis was used to determine the stent implantation for the coronary lesions was sig-
independent predictors of high SYNTAX score (≥23). nificantly higher in the low SYNTAX score group
Possible confounding factors for which the unadjusted (Table 1) . The laboratory data of the study groups
p-value was <0.10 in univariate regression analysis were demonstrated in Table 2. Platelet, white blood
(age, male sex, hypertension, diabetes mellitus, LVEF, cell (WBC), neutrophil, monocyte, MHR and CRP
platelet, mean platelet volume, white blood cell, neu- values were significantly higher in the high SYNTAX
trophil, CRP and MHR) were identified as potential score group whereas HDL-C level was significantly
risk markers and included in multivariate logistic lower in the high SYNTAX score group as compared
regression model. A p-value of <0.05 was considered with the low SYNTAX score group (p < 0.05). We
statistically ­significant. also presented the baseline clinical characteristics and
laboratory findings of the study population accord-
Results ing to SYNTAX score tertiles in Table 3. In addition,
Baseline clinical and angiographic characteristics of demographic and clinical characteristics of the study
the study patients were presented in Table 1. There population based on MHR tertiles were given in
were 408 (33.1%) patients with high (≥23) SYN- Table 4. From tertile 1 (with the lowest MHR) to ter-
TAX score (mean age was 62.4 ± 10.5 years, 71.6% tile 3 (with the highest MHR), direct i­nflammatory
males), and 821 (66.9%) patients low (≤22) SYN- markers including CRP, WBC and neutrophil values
TAX score (mean age was 59.8 ± 10.9 years, 60.8% showed a significant increase whereas LVEF showed a
males). Patients with high SYNTAX score were older, significant decrease (p < 0.05).
more likely to be male and more often had hyperten- Univariate regression analysis showed that age,
sion and diabetes mellitus. There were no significant male sex, hypertension, diabetes mellitus, LVEF,
differences between two groups with respect to num- platelet, mean platelet volume, WBC, neutrophil,
ber of current smokers and prehospital treatments. CRP and MHR were possible confounding factors
However, LVEF was significantly lower in the high for the high SYNTAX score. After multi­variate logis-
SYNTAX score group than in the low SYNTAX score tic regression analysis, MHR (odds ratio [OR]: 1.083
group (p < 0.05). ­Multivessel disease, chronic total [1.060–1.108]; p < 0.001) remained as indepen-
occlusions, the left main coronary artery lesions and dent predictor of high SYNTAX score as well as
the left anterior descending coronary artery lesions CRP (OR: 1.062 [1.043–1.080]; p < 0.001), LVEF
were more often present in the high SYNTAX score (OR: 0.942 [0.929–0.954]; p < 0.001), hyper­tension
group. The rate of patients who underwent coronary (OR: 1.397 [1.056–1.847]; p = 0.019) and ­diabetes
artery bypass grafting was also significantly higher in mellitus (OR: 1.464 [1.062–2.019]; p = 0.020)
the high SYNTAX score group, whereas the rate of (Table 5) . Namely, one unit increment in both MHR

40.0 40.0
Monocyte/HDL-C ratio
Monocyte/HDL-C ratio

30.0 30.0

20.0 20.0

10.0 10.0

r = 0.371 r = 0.336
0 p < 0.001 0 p < 0.001

1.0 10.0 20.0 30.0 40.0 1.0 10.0 20.0 30.0 40.0
SYNTAX score C-reactive protein (mg/l)

Figure 1. Correlation analysis showing statistically significant positive correlation between monocyte/HDL-C ratio with SYNTAX
score and C-reactive protein.
HDL-C: High-density lipoprotein cholesterol.

future science group www.futuremedicine.com10.2217/bmm-2015-0050


Research Article  Akboga, Balci, Maden et al.

and CRP was associated with an 8.3% and 6.2% Lately, Kanbay et al. described a novel ­inflammatory
increased the risk of high SYNTAX score, whereas one marker that combined the predictive values of the
unit d
­ ecrement in LVEF was associated 5.8% increased ­circulating monocyte count and serum HDL ­cholesterol
the risk of high SYNTAX score. Finally, in correlation into a single proportion [15] . They showed that MHR
analysis, MHR showed significant positive correlations was associated cardiovascular prognosis in patients with
with SYNTAX score (r = 0.371; p < 0.001) and CRP chronic kidney disease. In addition to that, another
(r = 0.336; p < 0.001) (Figure 1A & B) . study showed that higher MHR was associated with
the presence and severity of isolated coronary artery
Discussion ectasia [17] . In our study, we observed higher MHRs in
In the present study, we showed that baseline MHR patients with SYNTAX score ≥23, also high MHRs
is significantly associated with the extent and com- and CRP levels were independently related to higher
plexity of coronary artery disease, as estimated by the SYNTAX score. When patients were classified accord-
SYNTAX score in patients with stable coronary artery ing to the MHR tertiles, CRP levels were significantly
disease. Also, MHR is correlated positively with high higher, and the LVEF was significantly lower in the
SYNTAX score and CRP level. highest tertile. Previously, Canpolat et al. reported that
Atherosclerosis is a maladaptive, nonresolving MHR correlated positively with high-sensitivity CRP
chronic inflammatory disease occurring at sites of in slow coronary flow [16] . ­Similarly, we also observed
blood flow disturbance [21,22] . The subendothelial a positive correlation between MHR and CRP that
retention of cholesterol-containing plasma lipoproteins MHR may indirectly reflect the underlying inflamma-
at these sites and flow-mediated inflammatory changes tory condition. Higher MHRs in patients with stable
in endothelial cells are thought to trigger the athero- coronary artery disease and higher SYNTAX scores
genic process [23,24] . In the center of this atheroscle- (≥23) support that increased MHR may be a predictor
rotic plaque, macrophages derived from monocytes for atherosclerosis development and progression, and
take an active role by ingesting oxidized LDL and resultant cardiovascular events.
forming the dangerous foamy cells. It has been shown SYNTAX score is an anatomic scoring system that
that monocyte count was an independent and signifi- reflects both the lesion characteristics and cardiovascu-
cant predictor of plaque formation and progression in lar morbidity and mortality [1–3] . In different clinical
atherosclerosis  [25] . Contrary to monocytes, HDL-C conditions, irrespective of the disease severity, higher
interferes LDL oxidation and has anti-inflammatory, SYNTAX score predicts early and late mortality and
antioxidant, antithrombotic and beneficial vascular morbidity including major adverse cardiac events,
effects  [13,14] . These activities are exerted by both the all-cause death, cardiac death, myocardial infarction,
quality and quantity of HDL-C [17] . and target vessel revascularization [1–6] . The SYN-

Table 4. Demographic and clinical characteristics of the study groups according to monocyte/high-
density lipoprotein cholesterol ratio tertiles.
Parameters Monocyte/HDL-C ratio tertiles p-value
Tertile 1 (n = 410) Tertile 2 (n = 410) Tertile 3 (n = 409)
Age, years 60.3 ± 10.8 60.7 ± 10.5 61.1 ± 11.1 0.560
Male sex, n (%) 255 (62.2) 263 (64.1) 273 (66.7) 0.394
Hypertension, n (%) 184 (44.9) 199 (48.5) 213 (52.1) 0.119
Diabetes mellitus, n (%) 86 (21.0) 96 (23.4) 113 (27.6) 0.079
LVEF (%) 60.3 ± 8.5 58.8 ± 10.3 57.5 ± 10.7 <0.001
RDW (%) 13.8 ± 1.4 13.9 ± 1.7 13.9 ± 1.6 0.905
Platelet, 10³/mm³ 251.6 ± 47 254.3 ± 55 258.5 ± 56 0.394
Mean platelet volume, fL 8.6 ± 1.2 8.6 ± 1.4 8.7 ± 1.4 0.655
White blood cell, μL 7.1 ± 1.5 7.5 ± 1.6 8.3 ± 1.6 <0.001
Neutrophil, μL 4.2 ± 1.2 4.6 ± 1.4 5.1 ± 1.4 <0.001
C-reactive protein, mg/L †
5.6 (3.2–9.6) 7.1 (3.8–13.2) 9.5 (5.4–18.2) <0.001
Data were given as mean ± standard deviation or %.

Median (interquartile range).
HDL-C: High-density lipoprotein cholesterol; LVEF: Left ventricular ejection fraction; RDW: Red cell distribution width.

10.2217/bmm-2015-0050 Biomark. Med. (Epub ahead of print) future science group


Association of MHR with SYNTAX score  Research Article

Table 5. Univariate and multivariate logistic regression analysis for assessment of independent
predictors of high SYNTAX score.
Variables Univariate Multivariate
OR (95% CI) p-value OR (95% CI) p-value
Age 1.022 (1.011–1.034) <0.001 – –
Male sex 1.624 (1.257–2.100) <0.001 – – 
Hypertension 1.365 (1.075–1.732) 0.011 1.397 (1.056–1.847) 0.019
Diabetes mellitus 1.381 (1.052–1.813) 0.020 1.464 (1.062–2.019) 0.020
LVEF 0.937 (0.925–0.949) <0.001 0.942 (0.929–0.954) <0.001
Platelet 1.002 (1.000–1.003) 0.022 – –
Mean platelet volume 1.086 (0.998–1.183) 0.056 – –
White blood cell 1.119 (1.042–1.202) 0.002 – –
Neutrophil 1.154 (1.061–1.254) 0.001 – –
C-reactive protein 1.075 (1.059–1.091) <0.001 1.062 (1.043–1.080) <0.001
Monocyte/HDL-C ratio 1.085 (1.065–1.105) <0.001 1.083 (1.060–1.108) <0.001
HDL-C: High-density lipoprotein cholesterol; LVEF: Left ventricular ejection fraction; OR: Odds ratio.

TAX score not only reflects the technical difficulty simply and indirectly show underlying inflammatory
of ­percutaneous coronary intervention and also gives status. Furthermore, adding ­inflammatory markers to
information about the pattern of atheroma [6] . The a scoring system may be useful in predicting adverse
association between SYNTAX score and MHR sup- events by improving its predictive ability.
ports that the patients having high levels of circulating
monocytes and devoid of HDL beneficial effects may Future perspective
have more severe and complex coronary artery disease. MHR combining the predictive and prognostic value
However, none of the inflammatory markers includ- of both readily available inflammatory and oxidative
ing high sensitivity-CRP have been involved in any stress markers has emerged a new marker in cardio-
clinical and angiographic scoring system incorporating vascular diseases. In our study higher MHR values in
GRACE, SYNTAX, TIMI, STS, Euroscore [26–28] . In patients with higher SYNTAX scores supported that
this context adding inflammatory markers into a scor- increased MHR may be a predictor for atherosclerosis
ing system may improve the predictive and prognostic development and progression, and resultant cardio­
value of the applied score. vascular events. In order to understand this ­relationship
in detail, further studies are needed.
Limitations
The first limitation of this study is inherent to its retro- Financial & competing interests disclosure
spective design and absence of follow-up data about the The authors have no relevant affiliations or financial in-
patient group. Second, coronary angiogram assessment volvement with any organization or entity with a financial
was limited to visual interpretation. Third, rather than interest in or financial conflict with the subject matter or
follow-up values only a single measurement of MHR materials discussed in the manuscript. This includes employ-
was used. At last, only white blood cell counts with ment, consultancies, honoraria, stock ownership or options,
differentials and CRP were used to assess inflamma- expert testimony, grants or patents received or pending, or
tory condition because the other markers were not used ­royalties.
routinely in clinical practice. No writing assistance was utilized in the production of this
manuscript.
Conclusion
Our study showed that higher MHR levels were signifi- Ethical conduct of research
cantly and independently associated with higher SYN- The authors state that they have obtained appropriate institu-
TAX score in patient with stable CAD. Add to this, tional review board approval or have followed the principles
according to the MHR tertiles, we observed higher outlined in the Declaration of Helsinki for all human or animal
CRP levels in the highest tertile, and there was a posi- experimental investigations. In addition, for investigations in-
tive correlation between CRP and MHR. MHR that volving human subjects, informed consent has been obtained
can be easily derived from routine laboratory tests may from the participants involved.

future science group www.futuremedicine.com10.2217/bmm-2015-0050


Research Article  Akboga, Balci, Maden et al.

Executive summary
Background
• It was known that inflammation, endothelial dysfunction, oxidative stress and platelet activation play a
significant role in the formation and progression of atherosclerosis.
• Recently, monocyte to high-density lipoprotein-C ratio (MHR), combining the predictive and prognostic value
of both easily available laboratory markers into a single fraction has emerged a new marker in cardiovascular
diseases.
Results
• Inflammation, endothelial dysfunction and oxidative stress play a significant role in the formation and
progression of atherosclerosis.
• MHR an easily available inflammatory and oxidative stress marker.
• SYNTAX score is an anatomic scoring system that reflects both the lesion characteristics and cardiovascular
morbidity and mortality.
• MHR were significantly higher in patients with high SYNTAX score.
• MHR showed significant positive correlations with SYNTAX score and C-reactive protein level.
• MHR was independently associated with burden of coronary atherosclerosis assessed by SYNTAX score.
Conclusion
• Our study showed that higher MHR levels as readily available inflammatory and oxidative stress markers were
significantly and independently associated with higher SYNTAX score in patient with stable coronary artery
disease.
• Furthermore, adding inflammatory markers to a scoring system may be useful in predicting adverse events by
improving its predictive ability.

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future science group www.futuremedicine.com10.2217/bmm-2015-0050

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