Journals / The Anatolian Journal of Cardiology / 2017 / Cilt: 17 - Sayı: 5

Impact of serum erythropoietin level on collateral vessel development in patients with coronary artery disease

Pages
386–391
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

The present study, with the largest patient population studying this topic, suggests that presence of anemia, but not serum EPO level, is associated with good collateral development.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Experimental data have shown that Erythropoietin (EPO) stimulates angiogenesis and neovascularization which may result in improved collateral development.
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Key Findings & Data:Patient characteristics possibly related with coronary collaterals were also sought.Methods: A total of 256 patients with high grade coronary stenosis or occlusion were evaluated for the extent of coronary collaterals using Rentrop classification.
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Conclusion & Impact:The present study, with the largest patient population studying this topic, suggests that presence of anemia, but not serum EPO level, is associated with good collateral development.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: Experimental data have shown that Erythropoietin (EPO) stimulates angiogenesis and neovascularization which may result in improved collateral development. The aim of this study was to investigate the association between serum EPO levels and the extent of coronary collaterals. Patient characteristics possibly related with coronary collaterals were also sought.Methods: A total of 256 patients with high grade coronary stenosis or occlusion were evaluated for the extent of coronary collaterals using Rentrop classification. Patients with grade 0 or 1 collaterals were grouped as poor collaterals, while grade 2 or 3 collaterals were grouped as good collaterals.Results: Mean age of the study population was 63 years, 77% were males. Subjects with good collaterals were significantly more likely to have anemia (p=0.038) and stable angina pectoris as clinical presentation (p=0.40). Serum EPO levels were not different among good and poor collateral groups (10.4±9.4 mU/mL vs. 9.7±11 mU/mL, p=0.397). The prevalence of all other cardiovascular risk factors, medications, and angiographic characteristics were similar between the two groups. After adjusting for age, gender, and clinical presentation with stable angina pectoris, presence of anemia persisted to be a significant correlate of the good collateral formation (OR: 1.95; 95%; CI: 1.07-3.54, p=0.029).Conclusion: There has been conflicting results from trials studying the effects of serum EPO on coronary collateral development. The present study, with the largest patient population studying this topic, suggests that presence of anemia, but not serum EPO level, is associated with good collateral development.

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Cite This Article

ÖZYÜNCÜ, N., GÜLEÇ, H. S., ÖZDÖL, Ç., CANDEMİR, B., ONGUN, A., KAYA, C. T., EROL, Ç. (2017). Impact of serum erythropoietin level on collateral vessel development in patients with coronary artery disease. The Anatolian Journal of Cardiology, Cilt: 17 - Sayı: 5, 386–391. https://ajindex.com/articles/365351

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References (12)

  1. Cohen M, Rentrop KP. Limitation of myocardial ischemia by collateral circulation during sudden controlled coronary artery occlusion in hu- man subjects: a prospective study. Circulation 1986; 74: 469-76.
  2. Kodama K, Kusuoka H, Sakai A, Adachi T, Hasegawa S, Ueda Y, et al. Collateral channels that develop after an acute myocardial infarction prevent subsequent left ventricular dilation. J Am Coll Cardiol 1996; 27: 1133-9.
  3. Hirai T, Fujita M, Nakajima H, Asanoi H, Yamanishi K, Ohno A, et al. Importance of collateral circulation for prevention of left ventricular aneurysm formation in acute myocardial infarction. Circulation 1989; 79: 791-6. Korselman J, van der Graaf Y, de Jaegere PPT, Grobbee DE. Coronary collaterals, an important and underexposed aspect of coronary artery disease. Circulation 2003; 107: 2507-11.
  4. Kilian JG, Keech A, Adams MR, Celermajer DS. Coronary collateraliza- tion: determinants of adequate distal vessel filling after arterial occlu- sion. Coron Artery Dis 2002; 13: 155-9.
  5. Pourati I, Kimmelstiel C, Rand W, Karas RH. Statin use is associated with enhanced collateralization of severely diseased coronary arter- ies. Am Heart J 2003; 146: 876-81.
  6. Güleç S, Özdemir AO, Maradit-Kremers H, Dinçer I, Atmaca Y, Erol C. Elevated levels of C-reactive protein are associated with impaired coronary collateral development. Eur J Clin Invest 2006; 36: 369-75.
  7. Güleç S, Karabulut H, Özdemir AO, Özdöl C, Turhan S, Altın A, et al. Glu- 298Asp polymorphism of the eNOS gene is associated with coronary collateral development. Atherosclerosis 2008; 198: 354-9.
  8. Westenbrink BD, Lipsic E, van der Meer P, van der HP, Oeseburg H, Du Marchie Sarvaas GJ, et al. Erythropoietin improves cardiac function through endothelial progenitor cell and vascular endothelial growth factormediated neovascularization. Eur Heart J 2007; 28: 2018-27.
  9. Heeschen C, Aicher A, Lehmann R, Fichtlscherer S, Vasa M, Urbich C, et al. Erythropoietin is a potent physiologic stimulus for endothelial pro- genitor cell mobilization. Blood 2003; 102: 1340-6.
  10. Scholz D, Schaper W. Enhanced arteriogenesis in mice overexpressing erythropoietin. Cell Tissue Res 2006; 324: 395-401.
  11. Elliott S, Busse L, Swift S, McCaffery I, Rossi J, Kassner P, et al. Lack of expression and function of erythropoietin receptors in the kidney. Nephrol Dial Transplant 2012; 27: 2733-45.
  12. Sinclair AM, Coxon A, McCaffery I, Kaufman S, Paweletz K, Liu L, et al. Functional erythropoietin receptor is undetectable in endothelial, car- dia