Hostname: page-component-745bb68f8f-d8cs5 Total loading time: 0 Render date: 2025-02-06T06:10:18.982Z Has data issue: false hasContentIssue false

Prevalence and predictors of coronary artery disease in adults with Kawasaki disease

Published online by Cambridge University Press:  23 October 2014

Jalaj Garg
Affiliation:
Department of Internal Medicine, Division of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, New York, United States of America
Parasuram Krishnamoorthy
Affiliation:
Department of Internal Medicine, Mount Sinai Englewood Hospital and Medical Center, Englewood, New Jersey, United States of America
Chandrasekar Palaniswamy
Affiliation:
Department of Internal Medicine, Division of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, New York, United States of America
Rajiv Paudel
Affiliation:
Department of Internal Medicine, Division of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, New York, United States of America
Saurav Chatterjee*
Affiliation:
Division of Cardiology, St. Luke’s Roosevelt Hospital, Mount Sinai Medical Center, New York, New York, United States of America
Hasan Ahmad
Affiliation:
Department of Internal Medicine, Division of Cardiology, Westchester Medical Center, New York Medical College, Valhalla, New York, United States of America
Christopher Snyder
Affiliation:
Department of Pediatrics, Division of Cardiology, Case Western Reserve School of Medicine, Rainbow Babies and Children’s Hospital, Cleveland, Ohio, United States of America
*
Correspondence to: S. Chatterjee, MD, Division of Cardiology St. Luke’s Roosevelt Hospital Centre, Mount Sinai Medical Center, New York, NY 10025, United States of America. Tel: 418 988 0084; Fax: 347 244 7148; Email: sauravchatterjeemd@gmail.com
Rights & Permissions [Opens in a new window]

Abstract

Background: Accelerated coronary atherosclerosis in patients with Kawasaki disease, in conjunction with coronary artery aneurysm and stenosis that characterise this disease, are potential risk factors for developing coronary artery disease in young adults. We aimed to determine the prevalence and predictors of coronary artery disease in adult patients with Kawasaki disease. Methods: All patients aged 18−55 years of age diagnosed with Kawasaki disease were sampled from Nationwide Inpatient Sample database using International Classification of Diseases 9th revision (ICD 9 code 446.1) from 2009 to 2010. Demographics, prevalence of coronary artery disease, and other traditional risk factors in adult patients with Kawasaki disease were analysed using ICD 9 codes. Results: The prevalence of Kawasaki disease among adults was 0.0005% (n=215) of all in-hospital admissions in United States. The mean age was 27.3 years with women (27.6 years) older than men (27.1 years). Traditional risk factors were hypertension (21%), hyperlipidaemia (15.6%), diabetes (11.5%), tobacco use (8.8%), and obesity (8.8%), with no significant difference between men and women. Coronary artery disease (32.4%), however, was more prevalent in men (44.7%) than in women (12.1%; p=0.03). In multivariate regression analysis, after adjusting for demographics and traditional risk factors, hypertension (OR=13.2, p=0.03) was an independent risk factor of coronary artery disease. Conclusion: There was increased preponderance of coronary artery disease in men with Kawasaki disease. On multivariate analysis, hypertension was found to be the only independent predictor of coronary artery disease in this population after adjusting for other risk factors.

Type
Original Articles
Copyright
© Cambridge University Press 2014 

Kawasaki disease, or mucocutanoeus lymph-node syndrome, first described by Tomisaku Kawasaki in 1967, is a vasculitis of the small- and medium-sized arteries.Reference Kawasaki 1 Kawasaki disease is characterised by persistent fever for at least 5 days, accompanied by other clinical features such as erythematous rash, bilateral non-exudative conjunctivitis, erythema of the lips, tongue, and oropharynx, and cervical lymphadenopathy.Reference Newburger, Takahashi and Gerber 2 Other less common clinical features include diarrhoea, hepatitis, pancreatitis, jaundice, aseptic meningitis, anterior uveitis, arthralgia, or arthritis. In the United States, Kawasaki disease is the leading cause of acquired heart disease in children.Reference Taubert, Rowley and Shulman 3

The most common long-term complication of Kawasaki disease is coronary artery vasculitis, leading to coronary artery aneurysm or ectasia in 15−25% of untreated patients.Reference Kato, Inoue and Kawasaki 4 , Reference Burns, Shike and Gordon 5 The overall size of the coronary artery aneurysm has been proven as an important prognostic factor.Reference Newburger, Takahashi and Gerber 2 , Reference Akagi, Rose and Benson 6 Other cardiac complications of Kawasaki disease include arrhythmias, myopericarditis, pericardial effusion, and/or sudden cardiac death. As children with Kawasaki disease grow older, it is thought that they are at increased risk for developing myocardial ischaemia, heart failure, and other adverse events.Reference Burns, Shike and Gordon 5 , Reference Gordon, Kahn and Burns 7 Persistent remodelling,Reference Fukazawa, Ikegam and Watanabe 8 intimal proliferation, and calcificationReference Sugimura, Kato and Inoue 9 , Reference Mitani, Ohashi and Sawada 10 often result in stenosis adjacent to the aneurysm or occlusion of the coronaries, resulting in ischaemic heart disease.Reference Kato, Inoue and Kawasaki 4

Administration of intravenous immunoglobulin and high-dose aspirin has been considered as the most effective therapeutic regimen in reducing the likelihood of coronary artery complications in patients with Kawasaki disease.Reference Rosenfeld, Corydon and Shulman 11 , Reference Terai and Shulman 12 Of the patients, 10−20%, however, are unresponsive to intravenous immunoglobulin,Reference de Magalhaes, Alves and de Melo 13 and this is associated with an increased risk for coronary artery complications.Reference Tremoulet, Pancoast and Franco 14 , Reference Uehara, Belay and Maddox 15 The American Heart Association recommends a single dose of intravenous immunoglobulin (2 g/kg) to be infused over 12 hoursReference Newburger, Takahashi and Gerber 2 and 80–100 mg/kg/day of aspirin in four divided doses,Reference Newburger, Takahashi and Gerber 2 followed by 3–5 mg/kg/day for at least 6−8 weeks. For patients with coronary artery aneurysm, low-dose aspirin is recommended to be continued indefinitely. With prompt diagnosis and early treatment (intravenous immunoglobulin and/or aspirin) coupled with recent advances in long-term management, most patients diagnosed with Kawasaki disease are now adult survivors. However, arterial wall inflammation during acute illness leading to accelerated atherosclerosis and long-term cardiovascular sequelae is not well studied and remains controversial. As little is known regarding the prevalence of Kawasaki disease in adults, the purpose of this study was to determine the prevalence and predictors of coronary artery disease in adult patients with a history of Kawasaki disease.

Materials and methods

The analysis included all patients aged 18–55 years of age with a diagnosis of Kawasaki disease (ICD-9 code 446.1) from the Nationwide Inpatient Sample (NIS) Database for the years 2009–2010. This is the largest all-payer hospitalisation database that includes all non-federal US hospitals representing up to 8 million hospital stays per year. Each hospitalisation is coded with one primary diagnosis and up to 24 secondary diagnoses associated with that stay. Patient information, regardless of the type of hospital, rural or urban, teaching or non-teaching, is included in the NIS database. Hospital and discharge weights are provided to project national estimates.

Primary outcome was to determine predictors of coronary artery disease in adult patients diagnosed with Kawasaki disease. Demographic and traditional risk factors for coronary artery disease in patients with Kawasaki disease were analysed. Traditional risk factors included in the analysis were diabetes, hypertension, obesity, hyperlipidaemia, and smoking. Other chronic conditions were heart failure, ventricular arrhythmias, and alcohol use. Long-term complications including coronary artery aneurysm and coronary artery disease were studied in patients with Kawasaki disease.

Statistical analysis

Categorical variables were presented as percentage (%), while continuous variables were presented as mean±SD. Multivariate regression analysis was performed to identify the predictors of coronary artery disease in adult Kawasaki disease patients, after adjusting for patient’s demographics and traditional cardiovascular risk factors. A p-value of <0.05 was considered statistically significant. All statistical analyses were performed using STATA IC 10.0 (Statacorp, College Station, Texas, United States of America).

Results

Characteristics of the study population

We identified a total of 215 adult patients with Kawasaki disease hospitalised during 2009–2010 (0.0005% of all inpatient admissions), of which 62.33% were men and 37.67% women. The mean age was 27.3 years, with no significant difference between men and women (27.1 years versus 27.6 years; p=0.81). The mean length of hospitalisation was 3.05±0.4 days, and 77% of the population was white. Traditional risk factors prevalent in the study group were hypertension (21%), hyperlipidaemia (15.6%), diabetes (11.5%), tobacco use (8.8%), and obesity (8.8%), with no significant differences noted between men and women. In addition, coronary artery aneurysm was prevalent in 11.16% of the study population, with no statistical significant difference between men and women (14.09% versus 6.31%; p=0.44). Coronary artery disease was seen in 32% of the patients, with a higher prevalence in men (44.7% in men versus 12.1% in women; p=0.03). Interestingly, we found that ST-segment elevation myocardial infarction was prevalent in 8.09% patients, non–ST-segment elevation myocardial infarction in 2.39% patients, and unstable angina in 11.93% patients, with no statistical significant difference between men and women. Baseline demographic characteristics of this study population are presented in Table 1.

Table 1 Baseline demographics of adult patients with Kawasaki disease.

IQR=interquartile range

* Continuous variables are expressed as median (IQR). Categorical variables are expressed as %

** Pearson’s χ2 for categorical; linear regression for continuous variables

Outcomes

Of the 215 patients diagnosed with Kawasaki disease admitted to hospital, there was no in-hospital mortality. In unadjusted analysis, age (OR 1.13, 95% CI 1.04−1.25, p=0.007), diabetes mellitus (OR 12.16, 95% CI 1.09–135.20, p=0.04), and hypertension (OR 7.91, 95% CI 1.20–52.17, p=0.03) were independent predictors of coronary artery disease, whereas female sex (OR 0.17, 95% CI 0.03–0.98, p=0.048) predicted less coronary artery disease risk in adult patients with Kawasaki disease (Table 2). In multivariate logistic regression analysis adjusted for demographic and traditional risk factors, however, hypertension (OR 14.26, 95% CI 1.49−136.45, p=0.022) was the only predictor of coronary artery disease in adult patients with Kawasaki disease (Table 3).

Table 2 Unadjusted analysis for predictors of coronary artery disease in adult patients with Kawasaki disease.

Table 3 Multimodal logistic regression analysis for predictors of coronary artery disease in adult patients with Kawasaki disease.

* Model adjusted for age, sex, diabetes, obesity, hyperlipidaemia, and smoking

Discussion

There has been increase in the incidence of Kawasaki diseaseReference Nakamura, Yashiro and Uehara 16 , Reference Nakamura, Yashiro and Uehara 17 since the description of the first case. The inflammatory insult as a result of Kawasaki disease in childhood has the potential to affect all components of cardiovascular system. As children with Kawasaki disease age, they may be at increased risk for developing coronary artery aneurysm and, subsequently, coronary artery disease, acute myocardial infarction, and other adverse events.Reference Burns, Shike and Gordon 5

Currently, very little is known regarding the long-term risk factors of Kawasaki disease vasculopathy. To the best of our knowledge, this is the largest study in the United States to determine the prevalence and predictors of coronary artery disease in adults previously affected with Kawasaki disease. Principal findings of our study are as follows: (1) the prevalence of Kawasaki disease in hospitalised adults was 215/39,053,810 (0.0005%) with no in-hospital mortality; (2) the prevalence of coronary artery disease in our population was 32%, with increased prevalence in men as compared with women (45% versus 12%); and (3) hypertension was an independent predictor of coronary artery disease in adult Kawasaki disease patients.

In our analysis, adult patients with Kawasaki disease were predominantly men (62%). The results are consistent with a previous study from Taiwan, where men had a higher prevalence of Kawasaki disease.Reference Wu, Chen and Yeh 18 In our study, the prevalence of coronary artery disease was also high among adult male Kawasaki disease patients as compared with female patients. This parallels the higher incidence of coronary artery disease in adult men as compared with women in general population. It is quite possible that sex-related difference in hormone-mediated glucose and lipid metabolism observed in general population might also contribute to differences in progression of coronary artery disease in patients with Kawasaki disease.Reference Samaan and Crawford 19 , Reference Rossouw 20 Tsuda et alReference Tsuda, Abe and Tamaki 21 demonstrated that smoking was associated with an increased incidence of acute myocardial infarction in adult Kawasaki disease patients. Our study failed to demonstrate any statistical significance (OR 2.02, p=ns), however. This may be explained by a smaller percentage of smokers (9%) in our study as compared with the former (47%).

Pathophysiology of coronary artery disease in Kawasaki disease is different from patients with classic coronary atherosclerosis. Autopsy reports of patients who died as a result of cardiovascular sequelae of Kawasaki disease demonstrated myointimal proliferation, calcified aneurysms, and organised thrombus burden in the coronary vasculature with scanty deposits of lipid-laden macrophages, and cholesterol crystals, which are the hallmarks of atherosclerotic disease.Reference Muneuchi, Joo and Morihana 22

In the acute inflammatory phase of Kawasaki disease, there is disruption and disassociation of the internal elastic lamina and oedematous dissociation of the tunica media. In the sub-acute phase, the inflamed tunica intima and thinned media/adventitia are replaced by the fibrous connective tissue.Reference Takahashi, Oharaseki and Naoe 23 The normal coronary vasculature is destroyed by inflammatory cell infiltrate with necrosis of the smooth muscle cell associated with fibrosis and calcification and, in turn, loss of elasticity of the vessel wall, with subsequent increase in the arterial stiffness, thereby demonstrating that this was not the aim of this study. There has been increasing evidence demonstrating that arterial stiffness is an independent risk factor for the development of coronary artery disease.Reference Vlachopoulos, Aznaouridis and Stefanadis 24 Various indices have also been studied to assess arterial stiffness – aortic pulse-wave velocity and the augmentation index.Reference Laurent, Cockcroft and Bortel 25 , Reference Oishi, Miyoshi and Mizuguchi 26 Studies have shown that augmentation index is associated with increased cardiovascular risk and is an independent predictor of adverse cardiovascular events.Reference Nurnberger, Keflioglu-Scheiber and Opazo Saez 27 Tobayama et alReference Tobayama, Takahashi and Fukunaga 28 demonstrated that adults with a history of Kawasaki disease have increased arterial stiffness as assessed by augmentation index as compared with age- and gender-matched control group.

Endothelial function is regarded as a marker of integrative index of cardiovascular risk factors and vasculoprotective factors.Reference Vogel and Corretti 29 Mechanical forces and fluid shear stress elicit a large number of humoral and structural responses in the endothelial cells, and modulate the endothelial cell function and vascular function in both healthy and diseased states.Reference Chatzizisis, Coskun and Jonas 30 Endothelium-derived nitric oxide is a potent endogenous vasodilator and plays a pivotal role in flow-mediated dilatation.Reference Forstermann, Closs and Pollock 31 Reactive oxygen species produced as result of haemodynamic stress react with nitric oxide and reduce its vascular bioavailability and enhance cellular damage resulting in endothelial dysfunction.Reference Cai and Harrison 32 , Reference Tomasian, Keaney and Vita 33 The reduced anti-inflammatory effect of dysfunctional endothelial results in creation of raised plaque, plaque destabilisation, and eventually results in progressive atherosclerosis.

Measurement of flow-mediated dilatation – arterial response to reactive hyperaemia – is a non-invasive index to assess endothelial cell function.Reference Ikemoto, Ogino and Teraguchi 34 , Reference Kadono, Sugiyama and Hoshiai 35 Studies have demonstrated that endothelial cell dysfunction is one of the long-term sequelae of Kawasaki disease and even occurs late after resolution of the acute phase.Reference Dhillon, Clarkson and Donald 36 Noto et alReference Noto, Okada and Karasawa 37 also demonstrated that persistence of vascular endothelial dysfunction in addition to advancing age resulted in accelerated premature atherosclerosis in adults with a history of Kawasaki disease as compared with healthy controls.

We demonstrated that hypertension was an independent predictor of coronary artery disease in adult patients with a history of Kawasaki disease. The association between hypertension and coronary artery disease has been well documented. The Framingham risk model has been widely used to predict a 10-year risk for coronary heart disease in the presence of risk factors.Reference Wilson, D’Agostino and Levy 38 Zhang et alReference Zhang, Lelong and Kretz 39 has also demonstrated that uncontrolled hypertension at young age is associated with increased cardiovascular risk as compared with age-matched healthy individuals.

As endothelial dysfunction is one of the earliest manifestations of atherosclerosis,Reference Ross 40 we propose that endothelial dysfunction and arterial stiffness as a result of vasculitis in Kawasaki disease along with hypertension may result in synergistic effect and, in turn, result in accelerated atherosclerosis and coronary artery disease. We also found that hypertension as an additional risk factor for accelerated premature atherosclerosis and coronary artery disease in patients with Kawasaki disease, which has never been established before. Adult patients with Kawasaki disease should be screened for hypertension at periodic intervals. When appropriate, additional screening strategies such as ambulatory blood pressure monitoring should be considered. Optimal blood pressure control with lifestyle measures and anti-hypertensive agents may be an effective strategy to improve endothelial function and reduce the incidence of coronary artery disease in this population.

The strength of this study is its large sample size and inclusion of patients from all geographical regions in the country. There are several limitations to our study that deserve special mention. We only included hospitalised Kawasaki disease patients, thereby excluding patients admitted to the hospital under observational status, owing to the absence of information recorded in the NIS database, or who were discharged from the emergency room directly. Patients admitted to any federal hospital are excluded from this database. Thus, it is quite possible that the actual estimate of patients with Kawasaki disease was way more than recorded in the database, thereby underestimating the power of the study. Moreover, diagnostic codes are subject to misclassification and there is no way to determine whether secondary diagnosis represented an active problem versus past medical history. In addition, ICD 9 446.1 code does not distinguish between the complete Kawasaki disease and incomplete or atypical forms of Kawasaki disease. We also could not differentiate whether any patient had essential hypertension or hypertension secondary to vasculitis, renovascular disease, etc. Information on prior treatment of Kawasaki disease, if any, is not available from this registry. The retrospective observational design of the study can only demonstrate association, and hence causation between the predictors of coronary artery disease cannot be determined. Relevant information such as echocardiogram, coronary angiogram findings, cardiac biomarkers, and dates is not available from NIS database.

In conclusion, coronary artery disease was widely prevalent in adult patients with Kawasaki disease. Hypertension was found to be the only independent predictor of coronary artery disease in this population. As more patients with Kawasaki disease survive into adulthood, the adult cardiologists need to be familiar with the sub-acute and chronic coronary and non-coronary sequelae of Kawasaki disease. Further prospective studies with long-term follow-up are needed to investigate the extent of cardiovascular disease and appropriate target for blood pressure control in adult patients with Kawasaki disease.

Acknowledgements

None.

Financial Support

This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.

Conflicts of Interest

None.

References

1. Kawasaki, T. Acute febrile mucocutaneous syndrome with lymphoid involvement with specific desquamation of the fingers and toes in children. Arerugi 1967; 16: 178222.Google Scholar
2. Newburger, JW, Takahashi, M, Gerber, MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation 2004; 110: 27472771.Google Scholar
3. Taubert, KA, Rowley, AH, Shulman, ST. Nationwide survey of Kawasaki disease and acute rheumatic fever. J Pediatr 1991; 119: 279282.Google Scholar
4. Kato, H, Inoue, O, Kawasaki, T, et al. Long-term consequences of Kawasaki disease. A 10- to 21-year follow-up study of 594 patients. Circulation 1996; 94: 13791385.Google Scholar
5. Burns, JC, Shike, H, Gordon, JB, et al. Sequelae of Kawasaki disease in adolescents and young adults. J Am Coll Cardiol 1996; 28: 253257.Google Scholar
6. Akagi, T, Rose, V, Benson, LN, et al. Outcome of coronary artery aneurysms after Kawasaki disease. J Pediatr 1992; 121: 689694.CrossRefGoogle ScholarPubMed
7. Gordon, JB, Kahn, AM, Burns, JC. When children with Kawasaki disease grow up: myocardial and vascular complications in adulthood. J Am Coll Cardiol 2009; 54: 19111920.Google Scholar
8. Fukazawa, R, Ikegam, E, Watanabe, M, et al. Coronary artery aneurysm induced by Kawasaki disease in children show features typical senescence. Circ J 2007; 71: 709715.CrossRefGoogle ScholarPubMed
9. Sugimura, T, Kato, H, Inoue, O, et al. Intravascular ultrasound of coronary arteries in children. Assessment of the wall morphology and the lumen after Kawasaki disease. Circulation 1994; 89: 258265.Google Scholar
10. Mitani, Y, Ohashi, H, Sawada, H, et al. In vivo plaque composition and morphology in coronary artery lesions in adolescents and young adults long after Kawasaki disease: a virtual histology-intravascular ultrasound study. Circulation 2009; 119: 28292836.CrossRefGoogle Scholar
11. Rosenfeld, EA, Corydon, KE, Shulman, ST. Kawasaki disease in infants less than one year of age. J Pediatr 1995; 126: 524529.Google Scholar
12. Terai, M, Shulman, ST. Prevalence of coronary artery abnormalities in Kawasaki disease is highly dependent on gamma globulin dose but independent of salicylate dose. J Pediatr 1997; 131: 888893.Google Scholar
13. de Magalhaes, CM, Alves, NR, de Melo, AV, et al. Catastrophic Kawasaki disease unresponsive to IVIG in a 3-month-old infant: a diagnostic and therapeutic challenge. Pediatr Rheumatol Online J 2012; 10: 28. doi:10.1186/1546-0096-10-28.CrossRefGoogle Scholar
14. Tremoulet, AH, Pancoast, P, Franco, A, et al. Calcineurin inhibitor treatment of intravenous immunoglobulin-resistant Kawasaki disease. J Pediatr 2012; 161: 506512.Google Scholar
15. Uehara, R, Belay, ED, Maddox, RA, et al. Analysis of potential risk factors associated with nonresponse to initial intravenous immunoglobulin treatment among Kawasaki disease patients in Japan. Pediatr Infect Dis J 2008; 27: 155160.CrossRefGoogle ScholarPubMed
16. Nakamura, Y, Yashiro, M, Uehara, R, et al. Increasing incidence of Kawasaki disease in Japan: nationwide survey. Pediatr Int 2008; 50: 287290.CrossRefGoogle ScholarPubMed
17. Nakamura, Y, Yashiro, M, Uehara, R, et al. Epidemiologic features of Kawasaki disease in Japan: results of the 2007–2008 nationwide survey. J Epidemiol 2010; 20: 302307.Google Scholar
18. Wu, MH, Chen, HC, Yeh, SJ, et al. Prevalence and the long-term coronary risks of patients with Kawasaki disease in a general population <40 years: a national database study. Circ Cardiovasc Qual Outcomes 2012; 5: 566570.CrossRefGoogle Scholar
19. Samaan, SA, Crawford, MH. Estrogen and cardiovascular function after menopause. J Am Coll Cardiol 1995; 26: 14031410.Google Scholar
20. Rossouw, JE. Estrogens for prevention of coronary heart disease. putting the brakes on the bandwagon. Circulation 1996; 94: 29822985.Google Scholar
21. Tsuda, E, Abe, T, Tamaki, W. Acute coronary syndrome in adult patients with coronary artery lesions caused by Kawasaki disease: review of case reports. Cardiol Young 2011; 21: 7482.CrossRefGoogle ScholarPubMed
22. Muneuchi, J, Joo, K, Morihana, E, et al. Detectable silent calcification in a regressed coronary artery aneurysm of a young adult with a history of Kawasaki disease. Pediatr Cardiol 2008; 29: 195197.Google Scholar
23. Takahashi, K, Oharaseki, T, Naoe, S, et al. Neutrophilic involvement in the damage to coronary arteries in acute stage of Kawasaki disease. Pediatr Int 2005; 47: 305310.Google Scholar
24. Vlachopoulos, C, Aznaouridis, K, Stefanadis, C. Prediction of cardiovascular events and all-cause mortality with arterial stiffness: a systematic review and meta-analysis. J Am Coll Cardiol 2010; 55: 13181327.Google Scholar
25. Laurent, S, Cockcroft, J, Bortel, LV, et al. Expert consensus document on arterial stiffness: methodological issues and clinical applications. Eur Heart J 2006; 27: 25882605.CrossRefGoogle ScholarPubMed
26. Oishi, Y, Miyoshi, H, Mizuguchi, Y, et al. Aortic stiffness is strikingly increased with age >/= 50 years in clinically normal individuals and preclinical patients with cardiovascular risk factors: assessment by the new technique of 2D strain echocardiography. J Cardiol 2011; 57: 354359.CrossRefGoogle ScholarPubMed
27. Nurnberger, J, Keflioglu-Scheiber, A, Opazo Saez, AM, et al. Augmentation index is associated with cardiovascular risk. J Hypertens 2002; 20: 24072414.CrossRefGoogle ScholarPubMed
28. Tobayama, H, Takahashi, K, Fukunaga, H, et al. Analysis of arterial function in adults with a history of Kawasaki disease. J Cardiol 2013; 61: 330335.Google Scholar
29. Vogel, RA, Corretti, MC. Estrogens, progestins, and heart disease: can endothelial function divine the benefit? Circulation 1998; 97: 12231226.Google Scholar
30. Chatzizisis, YS, Coskun, AU, Jonas, M, et al. Role of endothelial shear stress in the natural history of coronary atherosclerosis and vascular remodeling: molecular, cellular, and vascular behavior. J Am Coll Cardiol 2007; 49: 23792393.CrossRefGoogle ScholarPubMed
31. Forstermann, U, Closs, EI, Pollock, JS, et al. Nitric oxide synthase isozymes. Characterization, purification, molecular cloning, and functions. Hypertension 1994; 23: 11211131.Google Scholar
32. Cai, H, Harrison, DG. Endothelial dysfunction in cardiovascular diseases: the role of oxidant stress. Circ Res 2000; 87: 840844.Google Scholar
33. Tomasian, D, Keaney, JF, Vita, JA. Antioxidants and the bioactivity of endothelium-derived nitric oxide. Cardiovasc Res 2000; 47: 426435.CrossRefGoogle ScholarPubMed
34. Ikemoto, Y, Ogino, H, Teraguchi, M, et al. Evaluation of preclinical atherosclerosis by flow-mediated dilatation of the brachial artery and carotid artery analysis in patients with a history of Kawasaki disease. Pediatr Cardiol 2005; 26: 782786.CrossRefGoogle ScholarPubMed
35. Kadono, T, Sugiyama, H, Hoshiai, M, et al. Endothelial function evaluated by flow-mediated dilatation in pediatric vascular disease. Pediatr Cardiol 2005; 26: 385390.Google Scholar
36. Dhillon, R, Clarkson, P, Donald, AE, et al. Endothelial dysfunction late after Kawasaki disease. Circulation 1996; 94: 21032106.Google Scholar
37. Noto, N, Okada, T, Karasawa, K, et al. Age-related acceleration of endothelial dysfunction and subclinical atherosclerosis in subjects with coronary artery lesions after Kawasaki disease. Pediatr Cardiol 2009; 30: 262268.Google Scholar
38. Wilson, PW, D’Agostino, RB, Levy, D, et al. Prediction of coronary heart disease using risk factor categories. Circulation 1998; 97: 18371847.Google Scholar
39. Zhang, Y, Lelong, H, Kretz, S, et al. Characteristics and future cardiovascular risk of patients with not-at-goal hypertension in general practice in France: the AVANT’AGE study. J Clin Hypertens (Greenwich) 2013; 15: 291295.CrossRefGoogle ScholarPubMed
40. Ross, R. The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature 1993; 362: 801809.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Baseline demographics of adult patients with Kawasaki disease.

Figure 1

Table 2 Unadjusted analysis for predictors of coronary artery disease in adult patients with Kawasaki disease.

Figure 2

Table 3 Multimodal logistic regression analysis for predictors of coronary artery disease in adult patients with Kawasaki disease.