J Korean Med Sci.  2015 Apr;30(4):470-474. 10.3346/jkms.2015.30.4.470.

Coronary Heart Disease in Moyamoya Disease: Are They Concomitant or Coincidence?

Affiliations
  • 1Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. jsns.kim@samsung.com

Abstract

The purpose of this study was to determine the prevalence and characteristics of symptomatic coronary heart disease (CHD) in patients with moyamoya disease (MMD). This retrospective study evaluated 456 patients who received examination for MMD between 1995 and 2012. We reviewed the patients' medical history and coronary imaging, including conventional coronary angiography and coronary computed tomography angiogram (CTA). Among 456 patients with MMD, 21 (4.6%) patients were found to have symptomatic CHD. Ten patients were treated with coronary artery bypass graft or percutaneous coronary intervention for unstable angina or myocardial infarction. Eleven were treated with medication for stable angina (n = 6) and variant angina with mild degree of stenosis (n = 5).The median age of these patients was 44 yr (range, 27-59). The median Framingham score at diagnosing MMD was < 1% (range, < 1%-16%). The old age was associated with CHD in uni- and multivariate analyses (P = 0.021, OR, 1.053; 95% CI, 1.008-1.110). Considering low age of onset and low stroke risk factor, CHD might be a systemic manifestation that is clinically relevant to MMD.

Keyword

Moyamoya Disease; Coronary Disease; Prevalence; Characteristics

MeSH Terms

Adult
Age Factors
Aged
Coronary Angiography
Coronary Artery Disease/*etiology
Female
Humans
Logistic Models
Male
Middle Aged
Moyamoya Disease/*complications
Retrospective Studies

Figure

  • Fig. 1 Angiographic findings of coronary heart disease in moyamoya disease. (A) and (B) show coronary stenosis (arrows) without calcification. (C) shows calcified plaque (arrow) on a non-contrast coronary computed tomography, and (D) shows aneurysmal dilatation and focal stenosis (arrow). Nitroglycerin (NG) was administered to the patient.


Cited by  1 articles

Moyamoya Disease: Cardiologist's Perspectives
Duk-Kyung Kim, Sung-A Chang, Taek Kyu Park
J Lipid Atheroscler. 2016;5(2):115-120.    doi: 10.12997/jla.2016.5.2.115.


Reference

1. Suzuki J, Takaku A. Cerebrovascular "moyamoya" disease. Disease show ing abnormal net-like vessels in base of brain. Arch Neurol. 1969; 20:288–299.
2. Ahn IM, Park DH, Hann HJ, Kim KH, Kim HJ, Ahn HS. Incidence, prevalence, and survival of moyamoya disease in Korea: a nationwide, population-based study. Stroke. 2014; 45:1090–1095.
3. Ikeda E. Systemic vascular changes in spontaneous occlusion of the circle of Willis. Stroke. 1991; 22:1358–1362.
4. Yamada I, Himeno Y, Matsushima Y, Shibuya H. Renal artery lesions in patients with moyamoya disease: angiographic findings. Stroke. 2000; 31:733–737.
5. Guo DC, Papke CL, Tran-Fadulu V, Regalado ES, Avidan N, Johnson RJ, Kim DH, Pannu H, Willing MC, Sparks E, et al. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Am J Hum Genet. 2009; 84:617–627.
6. von Bary C, Liebig T, Gaa J, von Beckerath N. Ischaemic stroke and myocardial infarction in a Caucasian patient with Moya-Moya disease. Eur Heart J. 2008; 29:842.
7. St Goar FG, Gominak SC, Potkin BN. Bilateral aortoostial coronary artery disease: moyamoya of the heart? Am J Cardiol. 1999; 83:1296–1299. a10.
8. Kim DK, Yoo KJ. Off-pump coronary artery bypass grafting in moyamoya disease. Yonsei Med J. 2007; 48:876–878.
9. Komiyama M, Ishikawa T, Takanashi S, Shimizu Y. Minimal invasive direct coronary artery bypass in moyamoya disease. Interact Cardiovasc Thorac Surg. 2003; 2:65–67.
10. Komiyama M, Nishikawa M, Yasui T, Otsuka M, Haze K. Moyamoya disease and coronary artery disease--case report. Neurol Med Chir (Tokyo). 2001; 41:37–41.
11. Murakami T, Ueno M, Takeda A, Yakuwa S, Kuroda S. Image in cardiovascular medicine. Multiple coronary stenosis in infantile Moyamoya disease. Circulation. 2009; 119:1689.
12. Wang N, Kuluz J, Barron M, Perryman R. Cardiopulmonary bypass in a patient with moyamoya disease. Anesth Analg. 1997; 84:1160–1163.
13. Akasaki T, Kagiyama S, Omae T, Ohya Y, Ibayashi S, Abe I, Fujishima M. Asymptomatic moyamoya disease associated with coronary and renal artery stenoses--a case report. Jpn Circ J. 1998; 62:136–138.
14. Ahn YK, Jeong MH, Bom HS, Park JC, Kim JK, Chung DJ, Chung MY, Cho JG, Kang JC. Myocardial infarction with Moyamoya disease and pituitary gigantism in a young female patient. Jpn Circ J. 1999; 63:644–648.
15. Wilson PW, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation. 1998; 97:1837–1847.
16. Lee JH, Youn TJ, Yoon YE, Park JJ, Hong SJ, Chun EJ, Choi SI, Cho YS, Cho GY, Chae IH, et al. Coronary artery stenosis in moyamoya disease: tissue characterization by 256-slice multi-detector CT and virtual histology. Circulation. 2013; 127:2063–2065.
17. Roder C, Peters V, Kasuya H, Nishizawa T, Takehara Y, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B. Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans. Childs Nerv Syst. 2011; 27:245–252.
18. Achrol AS, Guzman R, Lee M, Steinberg GK. Pathophysiology and genetic factors in moyamoya disease. Neurosurg Focus. 2009; 26:E4.
19. Sata M, Saiura A, Kunisato A, Tojo A, Okada S, Tokuhisa T, Hirai H, Makuuchi M, Hirata Y, Nagai R. Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. Nat Med. 2002; 8:403–409.
20. Davies MJ, Woolf N, Rowles PM, Pepper J. Morphology of the endothelium over atherosclerotic plaques in human coronary arteries. Br Heart J. 1988; 60:459–464.
21. Asia Pacific Cohort Studies Collaboration. The impact of cardiovascular risk factors on the age-related excess risk of coronary heart disease. Int J Epidemiol. 2006; 35:1025–1033.
22. Greenland P, LaBree L, Azen SP, Doherty TM, Detrano RC. Coronary artery calcium score combined with Framingham score for risk prediction in asymptomatic individuals. JAMA. 2004; 291:210–215.
23. Ikeda U, Fujikawa H, Shimada K. Variant angina pectoris associated with moyamoya disease. Lancet. 1998; 351:183–184.
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