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Serum leptin levels are independently related to the incidence of ischemic heart disease in a prospective study of patients with type 2 diabetes

Cardiovascular Diabetology volume 14, Article number: 62 (2015) Cite this article

Abstract

Background

New and clinically useful markers of cardiovascular risk are of essence in type 2 diabetes since ischemic heart disease is a major cause of death in these patients.

Methods

We analyzed baseline data from 476 men and 244 women who participated in “Cardiovascular Risk factors in Patients with Diabetes -a Prospective study in Primary care” study. All participants had type 2 diabetes and were 55-66 years old at recruitment during year 2005 to 2008. Except for established traditional risk markers for vascular disease, we also estimated vascular complications non-invasively by performance of carotid-femoral pulse-wave velocity (PWV, with applanation-tonometry) and intima-media thickness of carotid arteries (IMT, with B-mode ultrasound). Patients were followed for incidence of ischemic heart disease mortality and morbidity until end of the year 2012, using the national Swedish Cause of Death and Hospitalization Registries.

Results

During the follow-up period of a median of 6 years 47 men and 10 women died or were hospitalized for ischemic heart disease including myocardial infarction. Leptin levels were positively related to the hazard ratio (HR) in men (HR for each log 10 unit 4.9, CI 1.99 to 11.8) and women (HR 11.5, CI 1.47 to 89.7). Leptin predicted ischemic heart disease independently of age, HbA1c, BMI, systolic blood pressure and LDL-cholesterol/HDL-cholesterol ratio (men: HR 12.9 CI 3.2-53, women: HR 19.9, CI 1.2-327) This finding of increased risk related to high leptin levels was also statistically significant when carotid-femoral PWV and IMT were both added to the equations in men (hazard ratio 9.2 CI 2.1-41).

Conclusions

Our data support the use of serum leptin in type 2 diabetes to add independent prognostic information in terms of ischemic heart disease when compared with traditional cardiovascular risk factors. In the men of the cohort this prognostic information was in addition also to data on IMT and PWV, two non-invasive measurements of the extent of vascular disease. The power to detect a similar relationship in women was less strong due to lower incidence of cardiovascular disease.

Trial registration

ClinicalTrials.gov: NCT01049737.

Background

New and clinically useful markers of risk are of essence in high risk states such as type 2 diabetes mellitus. The major cause of death in type 2 diabetes mellitus is cardiovascular disease. One of the strongest predictors of such manifestations of arteriosclerosis is the pulse wave velocity in aorta, which is a non-invasive measure of the degree of arterial calcification [1]. Yet another non-invasive estimation of the degree of vascular disease can be done by evaluating the thickness of the intima and media of carotid arteries by ultrasound [2]. Both these clinical physiological examinations are non-invasive and hence risk-free to perform. However, both these measures of risk require skilled personnel and the equipment needed also carries a considerable cost. Leptin is a hormone that is secreted by adipose tissue that regulates metabolism and reduces appetite. Levels of leptin in humans are log-linearly increased in relation to obesity [3] and lack of leptin induces severe obesity, demonstrating that leptin signaling is necessary for normal feedback control of body weight [4]. The feedback information to the central nervous system regarding adipose tissue size by leptin is influenced by so called leptin resistance [5] which likely is a reason for poor effect to reduce body weight with recombinant leptin in humans [6]. Potential adverse effects of this hormone includes increased activity of the sympathetic nervous system and of the adrenal glands to secrete corticosteroids [7] and leptin thus not only increases metabolic rate but it also elevates blood pressure according to experimental studies [8-11]. Leptin also has immune-modulatory effects and it has been suggested that this hormone links obesity with inflammation and hence with cardiovascular disease by such mechanisms [12-14].

Since leptin apparently interact with many of the features of cardiovascular risk, such as blood pressure and inflammation, it might be a useful marker of prognosis that gives information that is independent of a cluster of classical clinical risk factors. Thus we prospectively studied leptin levels in relation to ischemic heart disease in middle aged patients with type 2 diabetes mellitus. In summary we found that levels of leptin were positively related to the hazard ratio (HR) of ischemic heart disease in both men and women and this was independently of age, HbA1c, BMI, systolic blood pressure and LDL-cholesterol/HDL-cholesterol ratio.

Methods

We analyzed baseline data from 244 women and 476 men who participated in a community-based cohort, CArdiovascular Risk factors in patients with DIabetes – a Prospective study in Primary care, acronym CARDIPP, in which serum leptin was measured at the baseline investigation. This prospective observational study was launched in November 2005 and recruitment of the participants was completed in 2008. The patients all had type 2 diabetes mellitus and were between 55–66 years old when they were consecutively recruited from 22 different primary health care centers in the counties of Östergötland and Jönköping, Sweden. Detailed information about the structure and results from CARDIPP has been described previously [15]. The centres were located in different demographic areas and differed in size. However, the model of treatment and care of diabetes was organized similarly and all the primary care centres adhered to the same national guidelines of diabetes care. The size of the cohort and age of participants was chosen to allow collection of endpoint data within 6 years, when assuming similar incidence of cardiovascular disease as in other cohorts of diabetes in Sweden [16].

Anthropometric measurements

Nurses dedicated to treatment of diabetes at the primary health care centers measured height to the nearest cm and weight to the nearest 0.1 kg with the patients wearing light indoor clothing. Waist circumference was measured according to WHO’s recommendations with the patient standing, after a regular expiration, to the nearest cm, midway between the lowest rib and the iliac crest. A standardized medical history was taken that included medication, previous cardiovascular diseases and smoking habits.

Laboratory analyses

Blood was drawn in the morning after a 10 hour over-night fast. Standard tests such as HbA1c, plasma glucose and serum lipids were analyzed according to routines at the primary health care centers. The laboratory analyses were performed at Department of Clinical Chemistry at the Linköping University Hospital. Levels of cholesterol, HDL and triglycerides were measured with enzymatic methodology and spectrophotometry, (Selectra E, Vital Scientific, Dieren, Netherlands). LDL was calculated by Friedewalds formula: LDL = cholesterol - HDL - 0.45 × fS/P-triglycerides. HbA1c was analyzed according to the Swedish Mono-S HPLC, all HbA1c values were converted to DCCT standard values using the formula: HbA1c DCCT = 0.923 × HbA1c (Mono-S) + 1.345 (R2 = 0.998).

The Milliplex® MAP Gut Hormone Panel (Merck Millipore, Billerica, MA, USA) designed for analysis with Luminex®-technique (Luminex, Austin, TX, USA) was used for analysis of leptin, in concordance with accompanying instructions. Total coefficient of variation (intra + inter assay) for leptin was 11%. The leptin levels were corrected for the inter-batch difference of control samples in the 10 batches in total used in the Luminex based analysis of the total cohort.

Clinical physiological investigations

Determination of pulse PWV was done at the Department of Physiology, Linköping University Hospital, Linköping and at the County Hospital Ryhov, Jönköping. Aortic PWV was measured with applanation tonometry (SphygmoCor® system, model MM3, AtCor Medical, Sydney, Australia) over the carotid and femoral arteries. The aortic pulse wave transit times were measured by electrocardiogram-guided readings of the femoral arterial pulse waves, using the carotid arterial pulse wave as the reference site. The surface distances were estimated from the suprasternal notch to the carotid and femoral measurement sites, respectively. PWV was calculated by dividing the surface distance with the pulse wave transit time yielding m × s-1.

Intima-media thickness of the carotid arteries (IMT) were evaluated using B-mode ultrasound. A digital ultrasound system (ATL HDI 5000, Bothell, WA, USA) equipped with a broadband linear transducer (L12-5) was used for scanning the carotid artery in the longitudinal section. A 10 mm long section of the common carotid artery in the proximity of the carotid bulb was selected to obtain mean lumen diameter and far wall IMT. Three consecutive frozen images with focus on lumen-intima echo and media-adventitia echo of the far arterial wall were used. The digital B-mode images were subsequently transferred to a computer with dedicated software for off-line measurement of IMT (Artery Measurement System II, Image and Data Analysis, Gothenburg, Sweden). Calibration and subsequent measurement was performed by manually tracing a cursor along the leading edge of the intima-lumen echo of the near wall, leading edge of the lumen- intima echo and media-adventitia echo of the far wall. During analysis, the measurement window was hidden for the reader and values were saved in a text file. Mean values of IMT from both the right and the left sides were used in all analyses.

Ischemic heart disease during follow-up

The participants were followed for occurrence of death or hospitalization for myocardial infarction or ischemic heart disease until December 31, 2012, by linkage with the Swedish Cause of Death and Inpatient registries (The National Board of Health and Welfare, Stockholm, Sweden) using their unique personal identification numbers.

Ethics

All participants gave written informed consent prior to participating in the study. The study, which complied with the declaration of Helsinki, was approved by the Regional Ethical Review Board in Linköping, Sweden.

Statistics

IBM SPSS statistics 21 and 22 (IBM corporation, Somers, NY, USA) were used for statistics. In the main statistical analyses, Cox regression (Proportional Hazard Model) was used. Pearson correlation coefficients were also calculated and statistical significance was defined as p < 0.05. Leptin levels were log-transformed in calculations since the distribution is skewed. Data were analyzed separately in men and women since relationship between leptin and obesity differs in genders [3]. The power of the study regarding an association between leptin and ischemic heart disease was greater than 99%, both for males and females.

Results

Data on leptin in serum were successfully obtained in 246 women and 474 men in the cohort. There was strong a positive linear relationship between leptin levels and BMI (men: r = 0.631, women: r = 0.667, both p < 0.0001). Women had higher leptin levels (p < 0.0001) also when the comparison was corrected for BMI (p < 0.0001). Table 1 shows baseline characteristics in men and women analyzed separately. There were no statistically significant correlations between leptin and age, duration of diabetes or HbA1c levels in either gender (all p > 0.19 in men or women). In univariate analyses leptin levels correlated positively with PWV in men (r = 0.181, p < 0.0001) but not with IMT (r = 0.06, p = 0.2), and these findings were also apparent in women (leptin with PWV: r = 0.32, p = 0.049, leptin with IMT: r = -0.10, p = 0.10). Leptin levels were positively correlated with CRP (levels above 5 mg/l excluded, considered to be outliers) in men (r = 0.248, p < 0.0001, 72 excluded) and women (r = 0.187. p = 0.017, 69 excluded).

Table 1 Baseline characteristics of the final cohort
Full size table

Cox regression analyses were performed separately in men and women. No patients were lost to follow-up. During the follow-up period of a median of 6 years 47 men and 10 women died or were hospitalized for ischemic heart disease including myocardial infarction. Of these 57 incidents, 30 were due to angina, 21 of myocardial infarction and the remaining 6 were deaths due to ischemic heart disease. Serum leptin levels (crude) were positively related to the composite endpoint in men (hazard ratio for each log 10 unit of leptin 4.851, CI 1.987 to 11.84) and women (hazard ratio of 11.5 for each log 10 leptin unit, CI 1.468 to 89.73). When entering major known cardiovascular risk factors to the Cox regression leptin levels were positively related to ischemic heart disease in men, independently of age, HbA1c, BMI, systolic blood pressure and LDL-cholesterol/HDL-cholesterol ratio, smoking, and known duration of diabetes (Table 2a). This finding of increased risk for ischemic heart disease related to leptin levels was also statistically significant when carotid-femoral PWV and IMT of the carotid arteries were added to these equations in men (Table 2b), while in women the relationship was significantly related with the LDL/HDL ratio (Table 2d).

Table 2 a-d Hazard ratios for ischemic heart disease during follow up
Full size table

Figure 1a and b show Cox regression analyses of levels of leptin in the lowest and highest tertiles in men and women, after correction for the risk factors as in Table 2b and d, respectively. When CRP was added to the analyses in Table 2b and d leptin levels were still significantly related to ischemic heart disease in men while CRP was not (leptin: p = 0.005, CRP: p = 0.96), however, neither of these markers were independently related with ischemic heart disease incidence in the corresponding analyses in women (leptin: p = 0.68, CRP: p = 0.25).

Figure 1
figure 1

Cox regression analyses of event free survival in relation to leptin levels. The dashed line represents the lower tertile and solid line the higher tertile of leptin levels in men (a) hazard ratio 9.219, confidence interval from 2.088 to 40.705, p = 0.003 and women (b) hazard ratio 26.8 confidence interval from 0.432 to 1662, p = 0.118. Data are adjusted for age, known duration of diabetes, HbA1c, systolic blood pressure, smoking, LDL/HDL- ratio, BMI, carotid-femoral PWV and carotid IMT.

Full size image

Discussion

We found that high levels of leptin were related to increased risks of ischemic heart disease independently of traditional risk factors in men and that this prognostic information also remained significant when carotid IMT and aortic PWV were both included in the Cox regression. Importantly these analyses included BMI as a measure of obesity and this implies that leptin gave additional information independently of the degree of adiposity. This is in line with the idea that leptin resistance, an insensitivity to feedback signaling of adipose stores to the CNS, is linked with increased risk for ischemic heart disease in patients [17]. However, since our study did not include an intervention aimed to affect leptin levels, this does not provide definite proof of causality. Elevated levels of CRP have been suggested to participate in induction of leptin resistance by direct interaction with the leptin molecule [18]. The positive correlation between leptin and CRP in both men and in women in our study is in line with such a theory. Also leptin is a regulator of the sympathetic nervous system with effects that, according to experimental studies, include increases of metabolic rate, angiogenesis and arterial tone [9]. This could theoretically have impact on ischemic heart disease incidence that goes beyond many traditional markers of cardiovascular risk, including BMI [19] which is in line with our findings in men with type 2 diabetes mellitus. High circulating leptin levels have earlier been reported to be associated with diabetes incidence and also with development of other components of the metabolic syndrome [20]. However, leptin levels were not found to be related to cardiovascular morbidity and mortality in a study of non-diabetic elderly people [21].

In a study of patients with type 2 diabetes mellitus by Brennan et al. leptin levels were reported not to be related to cardiovascular disease in 1194 women that were followed for 12 years [22]. This finding was in contrast to our data which do support prognostic use of leptin in serum when added to traditionally used risk factors, to estimate risk for ischemic heart disease in women. However, statistical significance was lost in the women in our trial when IMT and PWV were included in the equations. It is possible that less efficient treatment of complications in diabetes might have obscured specific actions of leptin, not acting through traditional risk factors, in the study by Brennan et al., since data were analyzed during 12 years up to the year 2002 [22], i.e. ending 3 years before we made our baseline investigation. In line with this LDL-cholesterol levels were 3.4-3.7 mmol/l across quintiles of leptin in the study by Brennan et al. while corresponding mean value was 2.77 in the women in the study presented herein. This is suggestive of more efficient lipid lowering therapy in our study which has been a trend in treatment of type 2 diabetes mellitus in general during the last decade [23]. It is also possible that age of participants is crucial in analyses of the risks related to leptin since at higher age obesity is not strongly linked with morbidity and mortality. Indeed, the term “obesity paradox” has been applied to the phenomenon that moderate obesity might even be beneficial in older age [24]. Indeed, better prognosis in obese as compared with leaner subjects in patients with diabetes > 65 years of age has been demonstrated [25] and patients in the study by Brennan et al. became older during follow up [22] than those in our cohort.

In males the relationship between leptin and IHD was independent of traditional risk factors which was in line with earlier trials in men with high risk but not necessarily restricted to type 2 diabetes [26-29]. However, a study of patients which also included a large proportion of patients with diabetes and renal impairment did not find an independent relationship with cardiovascular events of leptin when analyzed among many other cytokines [30]. We acknowledge that we had no information about cytokines such as adiponectin or macrophage migration inhibitory factor as in the paper by Schöttker et al. [30] but we did find leptin to be independently related to ischemic heart disease also in combination with two specific measures of arteriosclerosis, IMT and PWV. This might seem contradictory if leptin indeed mainly relates to arteriosclerotic disease per se. Potential explanation could be that PWV and IMT do not capture all information about true burden of arteriosclerosis. Another potential explanation is that although IMT and PWV together carry much information about arteriosclerosis in large vessels, we do not gain much knowledge from these measures of risk for plaque rupture which is the main cause of acute ischemic heart disease and which is to a large extent dependent on whether a plaque is vulnerable or stable [31]. Indeed, leptin has been found to be related to endothelial dysfunction in diabetes [32].

Strengths in our study include use of registry data with high quality and in terms of mortality and morbidity incidence no lost to follow-up. Weaknesses include a rather short follow-up time and consequently low rates of mortality and morbidity. However the relatively short follow-up period suggests clinical relevance insofar that patients were indeed being cared for in a manner that is in accordance with current standards. This was confirmed by frequent treatment with statins and antihypertensive medications, and levels of HbA1c and blood pressures were also generally close to targets recommended by guidelines. Indeed, it is possible that our finding of an association between circulating leptin and risk for ischemic heart disease was statistically significant after correction for traditional risk factors in men and women was made possible by reasonably good control of glycaemia, blood pressure and cholesterol that increased the chance to detect the risk related leptin, that might act through other mechanisms than mediated by the traditional risk factors that are known to the provider of care. The positive relationship between serum leptin levels and CRP, confirmed in our study, is an example of such a risk factor that is not targeted in routine clinic care, as of yet.

Conclusions

This prospective observational data support the use of serum leptin for estimation of risk for ischemic heart disease independently of traditional risk factors. In the men serum leptin also provided information about risk that was independent of two strong non-invasive markers of cardiovascular disease, carotid IMT and carotid-femoral PWV. The results of our study support further assessment in larger cohorts of the role of measuring leptin levels as a predictive marker if ischemic heart disease in the care of patients with type 2 diabetes.

Abbreviations

BMI:

Body-mass index

BP:

Blood pressure

CARDIPP:

CArdiovascular Risk factors in patients with DIabetes – a Prospective study in Primary care

CRP:

C-reactive protein

IHD:

Ischemic heart disease

HR:

Hazard ratio

IMT:

Intima-media thickness

OAD:

Oral antidiabetic drug

PWV:

Pulse-wave velocity

WHO:

World Health Organization

References

  1. Cruickshank K, Riste L, Anderson SG, Wright JS, Dunn G, Gosling RG. Aortic pulse-wave velocity and its relationship to mortality in diabetes and glucose intolerance: an integrated index of vascular function? Circulation. 2002;106(16):2085–90.

    Article  PubMed  Google Scholar 

  2. Djaberi R, Beishuizen ED, Pereira AM, Rabelink TJ, Smit JW, Tamsma JT, et al. Non-invasive cardiac imaging techniques and vascular tools for the assessment of cardiovascular disease in type 2 diabetes mellitus. Diabetologia. 2008;51(9):1581–93.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  3. Nystrom F, Ekman B, Osterlund M, Lindstrom T, Ohman KP, Arnqvist HJ. Serum leptin concentrations in a normal population and in GH deficiency: negative correlation with testosterone in men and effects of GH treatment. Clin Endocrinol (Oxf). 1997;47(2):191–8.

    Article  CAS  Google Scholar 

  4. Zhou Y, Rui L. Leptin signaling and leptin resistance. Front Med. 2013;7(2):207–22.

    Article  PubMed Central  PubMed  Google Scholar 

  5. Jung CH, Kim MS. Molecular mechanisms of central leptin resistance in obesity. Arch Pharm Res. 2013;36(2):201–7.

    Article  CAS  PubMed  Google Scholar 

  6. Heymsfield SB, Greenberg AS, Fujioka K, Dixon RM, Kushner R, Hunt T, et al. Recombinant leptin for weight loss in obese and lean adults: a randomized, controlled, dose-escalation trial. JAMA. 1999;282(16):1568–75.

    Article  CAS  PubMed  Google Scholar 

  7. van Dijk G, Donahey JC, Thiele TE, Scheurink AJ, Steffens AB, Wilkinson CW, et al. Central leptin stimulates corticosterone secretion at the onset of the dark phase. Diabetes. 1997;46(11):1911–4.

    Article  PubMed  Google Scholar 

  8. Hall JE, Hildebrandt DA, Kuo J. Obesity hypertension: role of leptin and sympathetic nervous system. Am J Hypertens. 2001;14(6 Pt 2):103S–15.

    Article  CAS  PubMed  Google Scholar 

  9. Haynes WG. Interaction between leptin and sympathetic nervous system in hypertension. Curr Hypertens Rep. 2000;2(3):311–8.

    Article  CAS  PubMed  Google Scholar 

  10. Haynes WG, Morgan DA, Walsh SA, Mark AL, Sivitz WI. Receptor-mediated regional sympathetic nerve activation by leptin. J Clin Invest. 1997;100(2):270–8.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Simonds SE, Pryor JT, Ravussin E, Greenway FL, Dileone R, Allen AM, et al. Leptin mediates the increase in blood pressure associated with obesity. Cell. 2014;159(6):1404–16.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  12. Harle P, Straub RH. Leptin is a link between adipose tissue and inflammation. Ann N Y Acad Sci. 2006;1069:454–62.

    Article  PubMed  Google Scholar 

  13. Stofkova A. Leptin and adiponectin: from energy and metabolic dysbalance to inflammation and autoimmunity. Endocr Regul. 2009;43(4):157–68.

    CAS  PubMed  Google Scholar 

  14. Viikari LA, Huupponen RK, Viikari JS, Marniemi J, Eklund C, Hurme M, et al. Relationship between leptin and C-reactive protein in young Finnish adults. J Clin Endocrinol Metab. 2007;92(12):4753–8.

    Article  CAS  PubMed  Google Scholar 

  15. Wijkman M, Lanne T, Engvall J, Lindstrom T, Ostgren CJ, Nystrom FH. Masked nocturnal hypertension–a novel marker of risk in type 2 diabetes. Diabetologia. 2009;52(7):1258–64.

    Article  CAS  PubMed  Google Scholar 

  16. Fharm E, Cederholm J, Eliasson B, Gudbjornsdottir S, Rolandsson O. Time trends in absolute and modifiable coronary heart disease risk in patients with Type 2 diabetes in the Swedish National Diabetes Register (NDR) 2003-2008. Diabet Med. 2012;29(2):198–206.

    Article  CAS  PubMed  Google Scholar 

  17. Martin SS, Qasim A, Reilly MP. Leptin resistance: a possible interface of inflammation and metabolism in obesity-related cardiovascular disease. J Am Coll Cardiol. 2008;52(15):1201–10.

    Article  CAS  PubMed  Google Scholar 

  18. Chen K, Li F, Li J, Cai H, Strom S, Bisello A, et al. Induction of leptin resistance through direct interaction of C-reactive protein with leptin. Nat Med. 2006;12(4):425–32.

    Article  CAS  PubMed  Google Scholar 

  19. Lukich A, Gavish D, Shargorodsky M. Normal weight diabetic patients versus obese diabetics: relation of overall and abdominal adiposity to vascular health. Cardiovasc Diabetol. 2014;13(1):141.

    Article  PubMed Central  PubMed  Google Scholar 

  20. Franks PW, Brage S, Luan J, Ekelund U, Rahman M, Farooqi IS, et al. Leptin predicts a worsening of the features of the metabolic syndrome independently of obesity. Obes Res. 2005;13(8):1476–84.

    Article  CAS  PubMed  Google Scholar 

  21. Welsh P, Murray HM, Buckley BM, de Craen AJ, Ford I, Jukema JW, et al. Leptin predicts diabetes but not cardiovascular disease: results from a large prospective study in an elderly population. Diabetes Care. 2009;32(2):308–10.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Brennan AM, Li TY, Kelesidis I, Gavrila A, Hu FB, Mantzoros CS. Circulating leptin levels are not associated with cardiovascular morbidity and mortality in women with diabetes: a prospective cohort study. Diabetologia. 2007;50(6):1178–85.

    Article  CAS  PubMed  Google Scholar 

  23. Wing RR, Bolin P, Brancati FL, Bray GA, Clark JM, Coday M, et al. Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. N Engl J Med. 2013;369(2):145–54.

    Article  CAS  PubMed  Google Scholar 

  24. Lavie CJ, McAuley PA, Church TS, Milani RV, Blair SN. Obesity and cardiovascular diseases: implications regarding fitness, fatness, and severity in the obesity paradox. J Am Coll Cardiol. 2014;63(14):1345–54.

    Article  PubMed  Google Scholar 

  25. Carnethon MR, Rasmussen-Torvik LJ, Palaniappan L. The obesity paradox in diabetes. Curr Cardiol Rep. 2014;16(2):446.

    Article  PubMed  Google Scholar 

  26. Shanker J, Rao VS, Ravindran V, Dhanalakshmi B, Hebbagodi S, Kakkar VV. Relationship of adiponectin and leptin to coronary artery disease, classical cardiovascular risk factors and atherothrombotic biomarkers in the IARS cohort. Thromb Haemost. 2012;108(4):769–80.

    Article  CAS  PubMed  Google Scholar 

  27. 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  PubMed  Google Scholar 

  28. Soderberg S, Ahren B, Jansson JH, Johnson O, Hallmans G, Asplund K, et al. Leptin is associated with increased risk of myocardial infarction. J Intern Med. 1999;246(4):409–18.

    Article  CAS  PubMed  Google Scholar 

  29. 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  PubMed  Google Scholar 

  30. Schottker B, Herder C, Rothenbacher D, Roden M, Kolb H, Muller H, et al. Proinflammatory cytokines, adiponectin, and increased risk of primary cardiovascular events in diabetic patients with or without renal dysfunction: results from the ESTHER study. Diabetes Care. 2013;36(6):1703–11.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  31. Cardoso L, Weinbaum S. Changing views of the biomechanics of vulnerable plaque rupture: a review. Ann Biomed Eng. 2014;42(2):415–31.

    Article  PubMed Central  PubMed  Google Scholar 

  32. Morioka T, Emoto M, Yamazaki Y, Kawano N, Imamura S, Numaguchi R, et al. Leptin is associated with vascular endothelial function in overweight patients with type 2 diabetes. Cardiovasc Diabetol. 2014;13:10.

    Article  PubMed Central  PubMed  Google Scholar 

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Acknowledgements

The study was supported by grants from the Medical Research Council of Southeast Sweden, Futurum, King Gustaf V and Queen Victoria Freemason Foundation, GE Healthcare and the Swedish Heart-Lung Foundation and the Swedish Research Council Grant 12661. The County Council of Östergötland and Linköping University, Department of Medical and Health Sciences, also supported the trial with grants and other resources.

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Authors and Affiliations

  1. Department of Medical and Health Sciences, Linköping University, SE 581 85, Linköping, Sweden

    Camilla Vavruch, Toste Länne, Torbjörn Lindström, Carl Johan Östgren & Fredrik H Nystrom

  2. Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden

    Mats Fredrikson

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Correspondence to Fredrik H Nystrom.

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The authors declare that they have no competing interests with regard to the study.

Authors’ contributions

CJÖ, FN and TLä designed and lead the initial CARDIPP study. CV collected and researched data with MF and TLi. All authors contributed in analyzing data, writing the manuscript and all authors read and approved the final version of the manuscript.

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Vavruch, C., Länne, T., Fredrikson, M. et al. Serum leptin levels are independently related to the incidence of ischemic heart disease in a prospective study of patients with type 2 diabetes. Cardiovasc Diabetol 14, 62 (2015). https://doi.org/10.1186/s12933-015-0208-1

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Keywords

Cardiovascular Diabetology

ISSN: 1475-2840