Skip to main content

Association between plasma leptin/adiponectin ratios with the extent and severity of coronary artery disease



Leptin can have a direct effect on endothelial and vascular smooth muscle cells and high level of leptin is involved in the pathogenesis of atherosclerosis. This study aimed to determine the relationship between leptin/adiponectin (L/A) ratio and the extent and severity of coronary artery disease (CAD).


This case-control study was conducted in an educational hospital in Ilam, Iran from June 2014 to September 2015. Totally 300 participants including 150 patients with CAD (case group) and 150 healthy individuals (control group) were selected and their plasma leptin, adiponectin and leptin/adiponectin ratio was measured. The extent and severity of coronary artery disease were assayed based on the number of involved vessels and Gensini score (GS) and the relation between scores and L/A findings were compared between cases and controls.


Totally, 300 participants including 150 (42.7% male), mean age 59.5 ± 11.4 years as cases and 150 (50.7% male), mean age 59.8 ± 10.7 as controls were analyzed. Plasma level of leptin and L/A ratio were higher in cases compared to controls, but level of adiponectin was significantly lower in CAD patients than the control group. More number of involved coronary vessels was significantly correlated to higher level of plasma leptin, L/A ratio and lower level of adiponectin among case group. Moreover, adiponectin was negatively and leptin or L/A ratio were positively correlated with number of involved vessels. 7.3% of cases had only one involved vessel, 42.7% had two involved vessels, and 50% of total patients had involved vessels and the mean ± SD of GS in the case group was 23.6 ± 6.9.


Plasma levels of leptin, and adiponectin can indicate the extent of coronary artery diseases but leptin may be a better marker of extent of CAD than either L/A ratio or adiponectin separately.

Peer Review reports


Coronary artery disease is one of the most common causes of mortality and morbidity worldwide [1]. Despite the high prevalence of this disease, the exact mechanisms associated with the development of atherosclerosis remain unclear [2]. Several risk factors associated with the progression of coronary artery disease including obesity, smoking, hypertension, hyperlipidemia and other chronic inflammatory conditions have been identified [3]. Studies suggest that obesity is the one of the most important risk factors for CAD and one of the important factors underlying the link between obesity and CAD is the leptin and adiponectin levels secreted by adipose tissue [4]. Although the main role of leptin is human energy homeostasis and body weight regulation by the brain [5], it also has a variety of functions, such as participation in inflammatory processes, immune function [6], angiogenesis and vascular functions [7]. In addition, leptin can have a direct effect on endothelial and vascular smooth muscle cells [8] and a high level of leptin is involved in the pathogenesis of atherosclerosis [9]. Some reports have shown a significant independent association between leptin and coronary artery calcification (CAC) [10] and the intima-media thickness of common carotid artery in patients with type 2 diabetes mellitus [11]. Though some studies have shown that leptin is an independent risk factor for CHD [12]; however, studies on leptin and CAD have also reported conflicting results [13]. Adiponectin is known as a cardioprotective and anti-atherogenic mediator [14] and its plasma levels are reduced in obese and dyslipidemic individuals [15]. Some studies have reported correlations between hypoadiponectinemia and an increased risk of CAD [16]. Despite extensive studies, the pro-atherogenic effects of leptin and the anti-atherogenic effects of adiponectin in atherosclerotic patients have not been fully defined. The plasma L/A ratio may be a more appropriate indicator for predicting the risk of CAD compared to leptin or adiponectin serum level alone [17, 18]. However, the relationship between L/A ratio and the extent and severity of coronary artery disease is not clear. The aim of this study was to investigate the relationship between the leptin and L/A ratio indices and the severity and extent of coronary artery disease using angiography and GS.


Study design

This case-control study was conducted in patients referred to Mustafa Khomeini Hospital, an educational hospital and major referral medical center, in Ilam, Iran between June 2014 and September 2015. During the mentioned period, all patients with inclusion criteria were selected as cases and for each case a healthy individual at the same date was randomly selected as control. A total of 150 CAD patients underwent coronary angiography in Cardiology Department (case group) and 150 healthy individuals from the same center (control group) were selected as the study subjects. Controls did not show any coronary involvements based on angiographic results. Inclusion criteria for participants were as follow: typical chest pain, coronary involvement after non-invasive evaluations such as physical exam or scan, and post-myocardial infarction (MI), and exclusion criteria were as follow: heart failure (left ventricular ejection fraction < 40%), history of acute myocardial infarction, history of coronary artery diseases by coronary angioplasty, acute or chronic renal failure, hepatic diseases such as nonalcoholic fatty liver disease (NAFLD) or cirrhosis, chronic infection, malignancy, any autoimmune diseases or hematological disorders and any inflammatory or metabolic diseases. To eliminate the effect of glucose and lipid metabolism, patients with diabetes were excluded from the study. Using a standardized questionnaire, the demographic characteristics of participants, including age, sex, cardiovascular risk factors such as smoking, family history of heart diseases, and hypertension (HTN), were obtained. A complete physical examination was performed, and blood pressure (BP) was taken from each patient’s right arm, after 10 min resting in a quiet room, in a seating position. Two successive BP readings were obtained, at 5 min intervals, and their average was considered as patient’s blood pressure. Hypertension was defined as systolic blood pressure (SBP) ≥ 140 mmHg or a diastolic blood pressure (DBP) ≥ 90 mmHg or the use of antihypertensive drugs [19]. The weight and height of participants were measured using a digital scale and tapeline by the same individual. Body mass index (BMI, kg /m2) was calculated as the weight (kg) divided by height (m2). Waist circumference (WC) was measured at the end of expiration at the narrowest point of the abdomen, approximately 5.2 cm between the umbilicus and hip. This measurement was performed at the maximum bulge point in a standing position, with closed feet.

Coronary angiography

Coronary angiography was carried out using the standard Judkins technique and a semi-quantitative coronary angiographic system [20]. The angiographic results were collected by two cardiologists, and based on the different findings, the patients were divided into 3 categories. The first category was determined according to the number of involved vessels indicating 1, 2, or 3 involved vessels groups; the second category was determined according to the type of involved vessels indicating the place of involved vessels such as left anterior descending artery (LAD), right coronary artery (RCA), left circumflex artery (LCX), and the diagonal or marginal artery; and the third category was determined according to the rate of stenosis of the vessels indicating a percentage of stenosis such as less than 50%, 50–75% and more than 75%. In this study, coronary artery stenosis was assayed using Gensini scores, which represents both the severity and the extent of coronary atherosclerosis [21]. Gensini score is a widely used mean of quantifying angiographic atherosclerosis, where a zero score indicates absence of atherosclerotic disease. The Gensini score accounts for the degree of artery narrowing as well as locations of narrowing. The severity of stenosis is indicated by the reduction in lumen diameter, and a nonlinear score is assigned to each lesion based upon it.

The studied patients were divided into the following six groups according to the American Heart Association protocols: Score 1—stenosis < 25%; Score 2—stenosis 26–50%; Score 4—stenosis 51–75%; Score 8—stenosis 76–90%; Score 16—stenosis 91–99%; and Score 32—stenosis 100%.

Another grouping of patients was based on the severity of coronary artery lesions using GS as normal coronary artery (Score 0–1), mild lesions (Score 2–20), moderate lesions (Score 20–40), and severe lesions (Score > 40).

Biochemical assay

After a 12-h fasting, 10 ml/l of vein blood sample was obtained from each patient and after centrifuging by 1000 g for 10 min, and the samples were stored at − 70 °C. Lipid profiles, including triglycerides (TGs), cholesterol (Chol), low density lipoprotein cholesterol (LDL-C) and high density lipoprotein cholesterol (HDL-C), and plasma glucose were measured using routine laboratory techniques (Pars Azmoon kit, Catalog No 1500017, Tehran, Iran for TG and Chol and Zist Shimi kit, Serial No D00749, Tehran, Iran for HDL-C respectively). LDL-C was estimated based on direct measurement with autoanalyzer. ELISA kits were used to assay the ratios of serum adiponectin (R&D Systems, USA) and serum leptin (D&G Diagnostics, Germany), and the assays were conducted according to the manufacturer’s protocol.

Statistical analysis

Data were expressed as the mean ± SD for quantitative variables and/or frequencies for qualitative variables. The normality of data was assessed using the Kolmogorov-Smirnov test. Student’s t-test and the chi-square tests were applied appropriately. Pearson correlation coefficient method was applied for the correlation between plasma leptin, adiponectin or the L/A ratios and the demographic or clinical characteristics of participants. In addition, Spearman correlation coefficient method was applied for variables without normal distribution. Logistic regression and multivariate analysis were applied for testing the predicting value of some plasma factors for CAD extension and severity. P value equal or less than 0.05 was considered statistically significant for all variables. The data analysis was performed via IBM SPSS Statistics for Windows, version 2019 (IBM Corp., Armonk, N.Y., USA). The Epanechnikov Kernel Smoothing was applied to show a non- linear association between adiponectin or leptin and Gensini score.


All demographic, laboratory, anthropometric and angiographic findings of participants are indicated in Table 1. The male percentage and mean ± SD for age among control and case groups were 50.7%; 59.8 ± 10.7 and 42.7%; 59.5 ± 11.4 years respectively and there were no significant differences for gender or age between groups (p = 0.101 and p = 0.802, respectively). The angiographic evaluations of patients showed that 7.3% of cases had only one involved vessel, 42.7% had two involved vessels, and 50% of total patients had involved vessels and the mean ± SD of Gensini score in the case group was 23.6 ± 6.9.

Table 1 Demographic and clinical characteristics of study participants

Logistic regression and multivariate analysis were applied for testing the predicting value of some plasma factors for CAD extension and severity. Since the difference between mean plasma leptin among cases and controls was high (85.87 ± 10.69 vs. 9.84 ± 5.36) with a significant difference (p = 0.0001), at the first step, the logistic identified only this factor as a powerful variable and other factors could not enter the equation. After deleting this variable three other factors were identified significantly (adiponectin, L/A ratio and waist circumference). Therefore, four most associated predictors for CAD extension were as follows: leptin, adiponectin, L/A ratio and waist circumference and the best predictor value for CAD extension in the current study was LEPTIN (Table 2).

Table 2 Bivariate relationship between different variables and serum leptin, adiponectin and L/A ratio in participants

The mean ± SD for the serum leptin level, based on the number of involved coronary vessels, is shown by Fig. 1. Based on the findings of this study, the mean serum leptin level in patients with one, two and three involved coronary vessels were 27.34 ± 10.32 ng/ml, 47.46 ± 15.43 ng/ml and 54.35 ± 15.43 ng/ml respectively and a positive and significant correlation between serum leptin levels and the number of coronary involved vessels was revealed (p = 0.008).

Also, logistic regression and t-test was applied for CAD extension and the results showed that those with 2 and 3 vessels involvement have 3.6 and 5.6 times higher chance of CAD than those with one vessel involvement respectively.

Fig. 1
figure 1

Mean ± SD of serum leptin level, based on the number of involved vessels (VD) in participants

The mean ± SD for the serum adiponectin level, based on the number of coronary involved vessels, is shown by Fig. 2. The mean ± SD serum adiponectin levels for one, two and three involved vessels were 24.24 ± 4.53 IU/ml, 20.78 ± 6.52 IU/ml, and 18.60 ± 7.54 IU/ml respectively and the correlation between the serum adiponectin levels and the number of involved coronary vessels was significant (p = 0.000).

Fig. 2
figure 2

Mean ± SD of serum adiponectin level, based on the number of involved vessels (VD) in participants

The mean and standard deviation of L/A ratio, based on the number of involved coronary vessels is shown by Fig. 3. The mean serum L/A ratio among one, two and three involved coronary vessels were 1.84 ± 0.54, 3.90 ± 1.12 and 4.13 ± 0.98 respectively. There was also a significant correlation between the serum L/A ratio and the number of involved vessels (p = 0.001).

Fig. 3
figure 3

Mean ± SD of leptin/adiponectin ratio, based on the number of involved vessels (VD) in partcipants

The relationship between serum levels of adiponectin and the GS is shown by Fig. 4. According to the findings of this study, as the levels of adiponectin was increased, the GS was decreased, indicating an inverse association between serum adiponectin levels and the GS but this relationship was not significant.

Fig. 4
figure 4

Correlations between serum adiponectin levels and Ginsini score in participants

The relationship between serum leptin levels and the GS is shown by Fig. 5 and based on the findings, the GS increased with increasing the serum levels of leptin, indicating a direct relationship between the serum leptin levels and GS insignificantly.

Fig. 5
figure 5

Correlations between serum leptin levels and Ginsini score in participants

Comparison between the serum L/A ratio and the GS also revealed an insignificant positive association and as the serum L/A ratio increased, the GS increased too (Fig. 6).

Fig. 6
figure 6

Correlations between leptin/adiponectin ratio and Gensini score in participants


The current study investigated any relationship between the leptin, adiponectin and L/A ratio and the extent or severity of coronary artery disease based on the number of involved vessels and GS, and this was the first study in this field. In fact, several studies have reported the association between leptin or adiponectin and CAD separately; however, there is no study to show any correlation between the L/A ratio and angiographic findings. Our study findings showed that the serum adiponectin level among case group was significantly lower than that among healthy individuals. Additionally, a significant and inverse relationship between serum adiponectin levels and the extent of CAD, according to number of involved vessels, was revealed among patients. According to this finding, hypoadiponectinemia was identified as an independent risk factor for the extent of CAD and this finding was in accordance with previous reports [22]. Some studies have shown that hypoadiponectinemia was associated with CAD, particularly in the content of obesity, hyperinsulinemia, diabetes type 2, and dyslipidemia [23, 24]. Another study reported that hypoadiponectinemia could increase the risk of atherosclerosis and acute coronary syndrome [25]. Different mechanisms exist regarding the protective role of adiponectin in the control of atherosclerosis, but its anti-atherogenic role is not clear [25]; nevertheless, some studies reported that the anti-atherogenic effect of adiponectin was mediated through the inhibition of neointimal formation [26]. In vitro studies have shown a progressive neointimal damage and proliferation of smooth muscle in damaged arteries among mice without adiponectin [27, 28]. Furthermore, some studies have shown that the accumulation of adiponectin in the sub-endothelial spaces of damaged arteries causes an inhibition of genes related to inflammation, such as tumor necrosis factor-α (TNF-α), and markers related to endothelial malfunction, such as VCAM-1 and ICAM-1. With these effects, adiponectin may inhibit the adhesion of monocytes to the endothelial of cells, which is the first step in arteriogenesis, and their migration to the sub-endothelial spaces, as well as impose anti-atherogenic effects. The adiponectin-based inhibition of lipid accumulation in macrophages and increasing blood flow, resulted from vasodilator effects through nitric oxide (NO) production, are other beneficial effects of adiponectin in the inhibition of atherosclerosis [29, 30]. Our study showed that adiponectin has an inverse but insignificant relationship with the GS, namely an increase in the GS was associated to a reduction of adiponectin level among CAD patients. A study by Fukuta et al. reported that lower level of adiponectin was associated with LV diastolic dysfunction, among patients with CAD [31]. Another study reported that leptin was associated with increased atherogenic processes [32]. The results of our study indicated that serum levels of leptin were significantly higher among CAD patients than in healthy control subjects and leptin was also directly related to the extent of coronary artery disease, based on number of involved vessels. Unlike adiponectin, leptin significantly increased with increasing the numbers of involved vessels in CAD patients. Previous studies have shown a harmful effect of leptin in the pathogenesis of atherosclerosis and demonstrated that leptin was an independent risk factor for CAD [33]. It has been shown that leptin can increase the risk of CAD more than other risk factors for cardiovascular diseases such as sex, race, smoking, and body mass index [34]. A study reported that after excluding other risk factors, the odds ratio for increased disease severity among patients with high leptin levels was preserved [31]. The atherogenic mechanisms of leptin have not been clearly identified but its beneficial effects, such as increasing NO production, improving coronary blood flow [35] and its role in the process of angiogenesis have been reported [36]. On the other hand, some adverse effects of leptin have such as direct contact with the components of metabolic syndrome and impaired fibrinolysis have been reported [37]. Based on different reports, leptin can have other effects, such as obesity-related hypertension as well as pro-thrombotic properties, in the cardiovascular system [38,39,40]. Though the current study showed an higher significant serum level of Leptin among CAD patients than the healthy individuals, but it’s correlation with GS and CAD severity was not significant. The difference between our findings about relationship between leptin and severity of CAD with other reports is not clear but it may bay associated with the performance of coronary angiography and its interpretation by interventional cardiologists and score estimation or even a lower number of evaluated patients in the current study.

Based on the possible atherogenic, thrombotic and angiogenic effects of leptin, and existence of its receptors in the endothelial cells, rising of this factor in the blood may predict restenosis after some vascular accidents [41,42,43]. There is a controversy in the effects of leptin on CAD patients and though several study have reported a modest relationship between higher level of plasma leptin and risk of CAD incident [13] other have shown a protective effect for leptin [44, 45].

An important result of the current study was a significantly higher L/A ratio in patients with CAD in comparison with healthy individuals. This study also revealed that the L/A ratio was directly correlated with the extent but not severity of coronary artery disease. Additionally, the L/A ratio showed a direct correlation with the number of involved coronary vessels, indicating that patients with three-vessel coronary artery involvement had a higher serum L/A ratio than patients with two or one coronary artery involvement. A few studies have investigated the effects of serum L/A ratio on CAD. Kappelle and colleagues showed that the serum L/A ratio could be a useful marker for predicting the risk of the first cardiovascular event in men [46]. The advantage of our study was the investigation of serum L/A ratio in CAD patients compared with healthy subjects and its association with the numbers of involved coronary arteries and GS. Though the predictor effects of either serum leptin or adiponectin for the severity and extent of coronary artery disease has been reported previously [13], and our findings were almost in consistence with these reports; however, the current study revealed that the serum L/A ratio was another predictor rather than either leptin or adiponectin for CAD separately. This study was limited to compare the factors related to endothelial dysfunction or cardiac anatomic findings with the serum leptin, or adiponectin levels and/or the serum L/A ratio. A future cohort study, examining the relationship between the serum L/A ratio and patient’s prognosis would be helpful.

In the current study, serum levels of leptin were associated with incident of CAD and it was also directly related to the extent of coronary artery disease. As the number of involved vessels was higher, the serum level of leptin was higher too and this association could be shown as an increasing trend, so that leptin values in patients with one involved vessel compared to controls and those with two involved vessels compared to one and those with three involved vessels compared to two involved vessels were higher. A similar trend was revealed for the L/A ratio and the number of involved vessels in CAD patients but with an insignificant difference between 3 vessels compared to two vessels; however, in case of serum level of adiponectin, a negative relationship with involved vessels was appeared. Based on these results two concepts could be considered. Firstly, the serum level of both leption and L/A ratio are related to the increase in coronary atherosclerotic load. Secondly, at the start and during the progression of coronary atherosclerosis, the release of proaterogenic adipocytokines is increased, may be due to increased inflammatory process, and after a primary inflammation, this phenomenon declines and the serum level of leptin does not increase as markedly.


As a conclusion, the effects of serum level of leptin or adiponectin were higher among CAD patients than healthy individuals and associated with the extent of coronary artery disease and our findings were in consistence with other previously reports. Also, the current study revealed that the serum level of leptin was a better predictor than either L/A ratio or adiponectin separately.

Availability of data and materials

Data are kept by the first authors and in case of need they are available by the corresponding author.



Body mass index


Blood pressure


Coronary artery disease


Coronary artery calcification




Diastolic blood pressure


Fasting blood sugar


Gensini score


High density lipoprotein,






Left anterior descending artery


Low density lipoprotein,


Left circumflex artery


Myocardial infarction


Nonalcoholic fatty liver disease


Nitric oxide


Right coronary artery


Systolic blood pressure


Standard deviation




Tumor necrosis factor-α


Vessel disease


Waist circumference


  1. Shu W, Lei W, Peng S. Recent development of ischemic heart disease in sex difference. Postgrad Med J. 2007;83:240–3.

    Article  Google Scholar 

  2. Arita Y, Kihara S, Ouchi N, Maeda K, Kuriyama H, Okamoto Y, et al. Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB–binding protein and regulates growth factor–induced common post receptor signal in vascular smooth muscle cell. Circulation. 2002;105(24):2893–8.

    Article  CAS  Google Scholar 

  3. Yusuf S, Reddy S, Ôunpuu S, Anand S. Global burden of cardio-vascular diseases part I: general considerations, the epidemiologic transition, risk factors, and impact of urbanization. Circulation. 2001;104(22):2746–53.

    Article  CAS  Google Scholar 

  4. Yu YH, Ginsberg HN. Adipocyte signaling and lipid homeostasis: sequel of insulin-resistant adipose tissue. Circ Res. 2005;96(10):1042–52.

    Article  CAS  Google Scholar 

  5. Finucane FM, Luan J, Wareham NJ, Sharp SJ, O'Rahilly S, Balkau B, et al. Correlation of the leptin: adiponectin ratio with measures of insulin resistance in non-diabetic individuals. Diabetologia. 2009;52(11):2345–9.

    Article  CAS  Google Scholar 

  6. Jenne DE, Tschopp J. Clusterin: the intriguing guises of a widely-expressed glycoprotein. Trends Biochem Sci. 1992;17(4):154–9.

    Article  CAS  Google Scholar 

  7. Vecchione C, Maffei A, Colella S, Aretini A, Poulet R, Frati G, et al. Leptin effect on endothelial nitric oxide is mediated through Akt-endothelial nitric oxide syntheses’ phosphorylation pathway. Diabetes. 2002;51(1):168–73.

    Article  CAS  Google Scholar 

  8. Campbell M, Allen WE, Silversides JA, Trimble ER. Glucose-induced phosphatidylinositol 3-kinase and mitogen-activated protein kinase-dependent up regulation of the platelet-derived growth factor-beta receptor potentiates vascular smooth muscle cell chemotaxis. Diabetes. 2003;52(2):519–26.

    Article  CAS  Google Scholar 

  9. Dubey Laxman and Zeng Hesong. Leptin and atherosclerosis. Exp Clin Cardiol. 2006;11(4):269–75.

  10. Yudkin JS, Yajnik CS, Mohamed-Ali V, Bulmer K. High levels of circulating proinflammatory cytokines and leptin, but not rural, Indians. A potential explanation for increased risk of diabetes and coronary heart disease. Diabetes Care. 1999;22:363–4.

    Article  CAS  Google Scholar 

  11. Catalán V, Gómez-Ambrosi J, Rodríguez A, Silva C, Rotellar F, Gil MJ, et al. Expression of caveolin-1 in human adipose tissue is unregulated in obesity and obesity-associated type 2 diabetes mellitus and related to inflammation. Clin Endocrinol. 2008;68(2):213–9.

    Google Scholar 

  12. Wallace AM, McMahon AD, Packard CJ, Kelly A, Shepherd J, Gaw A, et al. Plasma leptin and the risk of cardiovascular disease in the west of Scotland coronary prevention study (WOSCOPS). Circulation. 2001;104(25):3052–6.

    Article  CAS  Google Scholar 

  13. Sattar N, Wannamethee G, Sarwar N, Chernova J, Lawlor DA, Kelly A, et al. Leptin and coronary heart disease: prospective study and systematic review. J Am Coll Cardiol. 2009;53(2):167–75.

    Article  CAS  Google Scholar 

  14. Bełtowski J, Jamroz Wiśniewska A, Widomska S. Adiponectin and its role in cardiovascular diseases. Cardiovascular Hematol Disord Drug Targets. 2008;8:7–46.

    Article  Google Scholar 

  15. Cao JJ. Effects of obesity on bone metabolism. J Orthop Surg Res. 2011;6:30.

    Article  Google Scholar 

  16. Nakamura Y, Shimada K, Fukuda D, Shimada Y, Ehara S, Hirose M, et al. Implications of plasma concentrations of adiponectin in patients with coronary artery disease. Heart. 2004;90:528–33.

    Article  CAS  Google Scholar 

  17. Agatston AS, Janowitz WR, Hildner FJ, Zusmer NR, Viamonte M Jr, Detrano R. Quantification of coronary artery calcium using ultrafast computed tomography. J Am Coll Cardiol. 1990;15:827–32.

    Article  CAS  Google Scholar 

  18. Reilly MP, Wolfe ML, Localio AR, Rader DJ. Coronary artery calcification and cardiovascular risk factors: impact of the analytic approach. Atherosclerosis. 2004;173:69–78.

    Article  CAS  Google Scholar 

  19. Havel PJ, Kasim-Karakas S, Mueller W, Johnson PR, Gingerich RL, Stern JS. Relationship of plasma leptin to plasma insulin and adiposity in normal weight and overweight women: effects of dietary fat content and sustained weight loss. J Clin Endocrinol Metab. 1996;81:4406–13.

    CAS  Google Scholar 

  20. Kappelle PJ, Dullaart RP, van Beek AP, Hillege HL, Wolffenbuttel BH. The plasma leptin/adiponectin ratio predicts first cardiovascular event in men: a prospective nested case-control study. Eur J Intern Med. 2012;23(8):755–9.

    Article  CAS  Google Scholar 

  21. Austen WG, Edwards JE, Frye RL, Gensini GG, Gott VL, Griffith LS, et al. A reporting system on patients evaluated for coronary artery disease. Report of the ad hoc Committee for Grading of coronary artery disease, council on cardiovascular surgery, American Heart Association. Circulation. 1975;51:5–40.

    Article  CAS  Google Scholar 

  22. Gensini GG. A more meaningful scoring system for determining the severity of coronary heart disease. Am J Cardiol. 1983;51:606.

    Article  CAS  Google Scholar 

  23. von Eynatten M, Schneider JG, Humpert PM, Kreuzer J, Kuecherer H, Katus HA, et al. Serum adiponectin levels are an independent predictor of the extent of coronary artery disease in men. J Am Coll Cardiol. 2006;47:2124–6.

    Article  CAS  Google Scholar 

  24. Saltevo J, Laakso M, Jokelainen J, Keinanen-Kiukaanniemi S, Kumpusalo E, Vanhala M. Levels of adiponectin, C-reactive protein and interleukin-1 receptor antagonist are associated with insulin sensitivity: a population based study. Diabetes Metab Res Rev. 2008;24:378–83.

    Article  CAS  Google Scholar 

  25. Ley SH, Harris SB, Connelly PW, Mamakeesick M, Gittelsohn J, Hegele RA, et al. Adipokines and incident type 2diabetes in an aboriginal Canadian population: the Sandy Lake health and diabetes project. Diabetes Care. 2008;31:1410–5.

    Article  CAS  Google Scholar 

  26. Hasan-Ali H, Abd El-Mottaleb NA, Hamed HB, Abd-Elsayed A. Serum adiponectin and leptin as predictors of the presence and degree of coronary atherosclerosis. Coronary Artery Dis. 2011;22(4):264–9.

    Article  Google Scholar 

  27. Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, et al. Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem. 2002;277:25863–6.

    Article  CAS  Google Scholar 

  28. Asadollahi K, Abassi N, Afshar N, Alipour M, Asadollahi P. Investigation of the effects of Prosopis farcta plant extract on Rat’s aorta. J Med Plants Res. 2010;4(2):142–7.

    Google Scholar 

  29. Matsuda M, Shimomura I, Sata M, Arita Y, Nishida M, Maeda N, et al. Role of adiponectin in preventing vascular stenosis: the missing link of adipovascular axis. J Biol Chem. 2002;277:37487–91.

    Article  CAS  Google Scholar 

  30. Qiaoqing Z, Shuiping Z, Bilian Y, Xing W, Robina M, Yunping L, et al. High-density lipoprotein increases the uptake ofOxidized low density lipoprotein via PPARγ/CD36 pathway in inflammatory adipocytes. Int J Biol Sci. 2015;11(3):256–65.

    Article  CAS  Google Scholar 

  31. Fukuta H, Ohte N, Wakami K, Goto T, Tani T, Kimura G. Relation of plasma levels of adiponectin to left ventricular diastolic dysfunction in patients undergoing cardiac catheterization for coronary artery disease. Am J Cardiol. 2011;108(8):1081–5.

    Article  CAS  Google Scholar 

  32. Khafaji HARH, Bener AB, Nasser M, Al Suwaid J. Elevated serum leptin levels in patients with acute myocardial infarction; correlation with coronary angiographic and echocardiography findings. BMC Res Notes. 2012;5:262.

    Article  Google Scholar 

  33. Katsiki N, Mikhailidis DP, Banach M. Leptin, cardiovascular diseases and type 2 diabetes mellitus. Acta Pharmacol Sin. 2018;39(7):1176–88.

    Article  CAS  Google Scholar 

  34. Chai S, Sun F, Nie X-L, Wang J. Leptin and coronary heart disease: A systematic review and meta-analysis. Atherosclerosis. 2014;233:3–10.

    Article  CAS  Google Scholar 

  35. Zhang T, Yang P, Li T, Gao J, Zhang Y. Leptin expression in human Epicardial adipose tissue is associated with local coronary atherosclerosis. Med Sci Monit. 2019;24(25):9913–22.

    Article  Google Scholar 

  36. Frühbeck G, Gómez-Ambrosi J. Modulation of the leptin-induced white adipose tissue lipolysis by nitric oxide. Cell Signal. 2001;13(11):827–33.

    Article  Google Scholar 

  37. Werner N, Nickenig G. From fat fighter to risk factor: the zigzag trek of leptin. Arterioscler Thromb Vasc Biol. 2004;24:7–9.

    Article  CAS  Google Scholar 

  38. Eriksson MA, Rask E, Johnson O, Carlström K, Ahrén B, Eliasson M, et al. Sex-related differences in the associations between hyperleptinemia, insulin resistance and dysfibrinolysis. Blood Coagul Fibrinolysis. 2008;19(7):625–32.

    Article  CAS  Google Scholar 

  39. Kshatriya S, Reams GP, Spear RM, Freeman RH, Dietz JR, Villarreal D. Obesity hypertension: the emerging role of leptin in renal and cardiovascular dyshomeostasis. Curr Opin Nephrol Hypertens. 2010;19(1):72–8.

    Article  CAS  Google Scholar 

  40. Schäfer K, Halle M, Goeschen C, Dellas C, Pynn M, Loskutoff DJ, et al. Leptin promotes vascular remodeling and neointimal growth in mice. Arterioscler Thromb Vasc Biol. 2004;24(1):112–7.

    Article  CAS  Google Scholar 

  41. Koh KK. Leptin and cardiovascular disease: response to therapeutic interventions. Circulation. 2008;117(25):3238–49.

    Article  Google Scholar 

  42. Beltowski J. Leptin and atherosclerosis. Atherosclerosis. 2006;189(1):47–60.

    Article  CAS  Google Scholar 

  43. Beltowski J. Role of leptin in blood pressure regulation and arterial hypertension. J Hypertens. 2006;24(5):789–801.

    Article  CAS  Google Scholar 

  44. Vida-Simiti LA, Stoia MA. Better prognosis in overweight/obese coronary heart disease patients with high plasma levels of leptin. Clujul Med. 2016.

  45. Ku IA, et al. Association of low leptin with cardiovascular events and mortality in patients with stable coronary artery disease: The Heart and Soul Study. Atherosclerosis. 2011;217(2):503–8.

    Article  CAS  Google Scholar 

  46. Lekva T, Michelsen EA, Aukrust P, Henriksen T, Bollerslev J, UelandLeptin T. Leption and adiponectin as predictors of cardiovascular risk after gestational diabetes mellitus. Cardiovasc Diabetol. 2017;16:5.

    Article  CAS  Google Scholar 

Download references


We gratefully thank the Faculty of Medicine, Ilam University of Medical Sciences, and the Vice Chancellor of Researches and Technology for their assistance in this study.


This work was financially supported by the Ilam University of Medical Sciences, Ilam, Iran by code number: 9654/0334. The funding body did not have any role in the design, collection, analysis, interpretation of data or in writing the manuscript.

Author information

Authors and Affiliations



RA and H R contributed in the study design and interpretation of the results. T Y and M Y drafted the manuscript, participated in the laboratory working, and data collection. A K and SK revised critically the paper and interpreted the data based on the study aims and statistical analysis. All authors read and approved this article for publication.

Corresponding author

Correspondence to Khairollah Asadollahi.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Ethics Committee of Ilam University of Medical Sciences, and informed consent was taken from all participants. The clinical purpose of this study was explained for the participants at the start and a written consent was obtained. All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments.

Consent for publication

Not applicable.

Competing interests

Authors declare that they have no conflict of interest.

Additional information

Publisher’s Note

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

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Rahmani, A., Toloueitabar, Y., Mohsenzadeh, Y. et al. Association between plasma leptin/adiponectin ratios with the extent and severity of coronary artery disease. BMC Cardiovasc Disord 20, 474 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Coronary artery disease
  • Leptin
  • Adiponectin
  • Leptin/adiponectin ratio
  • Gensini score