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      Serial Plasma Levels of Angiogenic Factors in Patients With ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention

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      https://www.riss.kr/link?id=A104688438

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      다국어 초록 (Multilingual Abstract)

      Background and Objectives: Patients with acute myocardial infarction show varying degrees of collateral development. However, the relationships between angiogenic factors and degree of collaterals are not well known.
      Subjects and Methods: Fifty-nine patients (mean age, 59±10 years) with ST-segment elevation myocardial infarction (STEMI) under-went primary percutaneous coronary intervention (PCI). Patients were divided into one of 2 groups: group I (Rentrop collateral grade 0/1,n=34) or group II (grade 2/3, n=25). Plasma levels of vascular endothelial growth factor (VEGF), soluble VEGF receptor (sFlt-1), angiopoi-etin (Ang)-2, and soluble Tie-2 at baseline, 24 and 48 hours after PCI were measured.
      Results: There were fewer diabetic patients and higher incidence of previous angina and multi-vessel disease in group II. Group II had a lower left ventricular ejection fraction and a trend toward longer pain-to-balloon time. Plasma levels of Ang-2, sFlt-1 were elevated prior to primary PCI and decreased after PCI, whereas plasma level of VEGF was relatively low initially, however rose after PCI. sTie-2 levels showed no significant interval change in group I, but decreased over time in group II. VEGF, sFlt-1, and Tie-2 levels did not differ between the groups at each time point. However, plasma levels of Ang-2 were higher in group I than in group II at baseline and at 48 hours.
      Conclusion: Presence of collaterals in STEMI patients undergoing primary PCI was associated with lesser rise in Ang-2 plasma level. VEGF showed a delayed response to acute ischemia compared to Ang-2. Clinical implications of our findings need to be investigated in further studies.
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      Background and Objectives: Patients with acute myocardial infarction show varying degrees of collateral development. However, the relationships between angiogenic factors and degree of collaterals are not well known. Subjects and Methods: Fifty-nine ...

      Background and Objectives: Patients with acute myocardial infarction show varying degrees of collateral development. However, the relationships between angiogenic factors and degree of collaterals are not well known.
      Subjects and Methods: Fifty-nine patients (mean age, 59±10 years) with ST-segment elevation myocardial infarction (STEMI) under-went primary percutaneous coronary intervention (PCI). Patients were divided into one of 2 groups: group I (Rentrop collateral grade 0/1,n=34) or group II (grade 2/3, n=25). Plasma levels of vascular endothelial growth factor (VEGF), soluble VEGF receptor (sFlt-1), angiopoi-etin (Ang)-2, and soluble Tie-2 at baseline, 24 and 48 hours after PCI were measured.
      Results: There were fewer diabetic patients and higher incidence of previous angina and multi-vessel disease in group II. Group II had a lower left ventricular ejection fraction and a trend toward longer pain-to-balloon time. Plasma levels of Ang-2, sFlt-1 were elevated prior to primary PCI and decreased after PCI, whereas plasma level of VEGF was relatively low initially, however rose after PCI. sTie-2 levels showed no significant interval change in group I, but decreased over time in group II. VEGF, sFlt-1, and Tie-2 levels did not differ between the groups at each time point. However, plasma levels of Ang-2 were higher in group I than in group II at baseline and at 48 hours.
      Conclusion: Presence of collaterals in STEMI patients undergoing primary PCI was associated with lesser rise in Ang-2 plasma level. VEGF showed a delayed response to acute ischemia compared to Ang-2. Clinical implications of our findings need to be investigated in further studies.

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      참고문헌 (Reference)

      1 Ferrara N, "Vascular endothelial growth factor: basic science and clinical progress" 25 : 581-611, 2004

      2 Holmes K, "Vascular endothelial growth factor receptor-2: structure, function, intracellular signalling and therapeutic inhibition" 19 : 2003-2012, 2007

      3 Findley CM, "VEGF induces Tie2 shedding via a phosphoinositide 3-kinase/Akt dependent pathway to modulate Tie2 signaling" 27 : 2619-2626, 2007

      4 Siemeister G, "Two independent mechanisms essential for tumor angiogenesis: inhibition of human melanoma xenograft growth by interfering with either the vascular endothelial growth factor receptor pathway or the Tie-2 pathway" 59 : 3185-3191, 1999

      5 Thomas M, "The role of the Angiopoietins in vascular morphogenesis" 12 : 125-137, 2009

      6 Elsman P, "Role of collateral circulation in the acute phase of ST-segment-elevation myocardial infarction treated with primary coronary intervention" 25 : 854-858, 2004

      7 Lee KW, "Plasma angiopoietin-1, angiopoietin-2, angiopoietin receptor tie-2, and vascular endothelial growth factor levels in acute coronary syndromes" 110 : 2355-2360, 2004

      8 Visconti RP, "Orchestration of angiogenesis and arteriovenous contribution by angiopoietins and vascular endothelial growth factor (VEGF)" 99 : 8219-8224, 2002

      9 Beygui F, "Myocardial viability, coronary flow reserve, and in-hospital predictors of late recovery of contractility following successful primary stenting for acute myocardial infarction" 89 : 179-183, 2003

      10 Yamazaki Y, "Molecular and functional diversity of vascular endothelial growth factors" 10 : 515-527, 2006

      1 Ferrara N, "Vascular endothelial growth factor: basic science and clinical progress" 25 : 581-611, 2004

      2 Holmes K, "Vascular endothelial growth factor receptor-2: structure, function, intracellular signalling and therapeutic inhibition" 19 : 2003-2012, 2007

      3 Findley CM, "VEGF induces Tie2 shedding via a phosphoinositide 3-kinase/Akt dependent pathway to modulate Tie2 signaling" 27 : 2619-2626, 2007

      4 Siemeister G, "Two independent mechanisms essential for tumor angiogenesis: inhibition of human melanoma xenograft growth by interfering with either the vascular endothelial growth factor receptor pathway or the Tie-2 pathway" 59 : 3185-3191, 1999

      5 Thomas M, "The role of the Angiopoietins in vascular morphogenesis" 12 : 125-137, 2009

      6 Elsman P, "Role of collateral circulation in the acute phase of ST-segment-elevation myocardial infarction treated with primary coronary intervention" 25 : 854-858, 2004

      7 Lee KW, "Plasma angiopoietin-1, angiopoietin-2, angiopoietin receptor tie-2, and vascular endothelial growth factor levels in acute coronary syndromes" 110 : 2355-2360, 2004

      8 Visconti RP, "Orchestration of angiogenesis and arteriovenous contribution by angiopoietins and vascular endothelial growth factor (VEGF)" 99 : 8219-8224, 2002

      9 Beygui F, "Myocardial viability, coronary flow reserve, and in-hospital predictors of late recovery of contractility following successful primary stenting for acute myocardial infarction" 89 : 179-183, 2003

      10 Yamazaki Y, "Molecular and functional diversity of vascular endothelial growth factors" 10 : 515-527, 2006

      11 Carmeliet P, "Mechanisms of angiogenesis and arteriogenesis" 6 : 389-395, 2000

      12 Ogawa H, "Increased blood vascular endothelial growth factor levels in patients with acute myocardial infarction" 93 : 93-99, 2000

      13 Berry C, "Importance of collateral circulation in coronary heart disease" 28 : 278-291, 2007

      14 Kendall RL, "Identification of a natural soluble form of the vascular endothelial growth factor receptor, FLT-1, and its heterodimerization with KDR" 226 : 324-328, 1996

      15 Saharinen P, "How do angiopoietins Tie in with vascular endothelial growth factors?" 17 : 198-205, 2010

      16 Hojo Y, "Expression of vascular endothelial growth factor in patients with acute myocardial infarction" 35 : 968-973, 2000

      17 Matsunaga T, "Expression of VEGF and angiopoietins-1 and -2 during ischemiainduced coronary angiogenesis" 285 : H352-H358, 2003

      18 Lee SH, "Early expression of angiogenesis factors in acute myocardial ischemia and infarction" 342 : 626-633, 2000

      19 Rentrop KP, "Determinants and protective potential of coronary arterial collaterals as assessed by an angioplasty model" 61 : 677-684, 1988

      20 Iribarren C, "Circulating angiopoietins-1 and -2, angiopoietin receptor Tie-2 and vascular endothelial growth factor-A as biomarkers of acute myocardial infarction: a prospective nested case-control study" 11 : 31-, 2011

      21 Rentrop KP, "Changes in collateral channel filling immediately after controlled coronary artery occlusion by an angioplasty balloon in human subjects" 5 : 587-592, 1985

      22 Helisch A, "Arteriogenesis: the development and growth of collateral arteries" 10 : 83-97, 2003

      23 Tressel SL, "Angiopoietin-2 stimulates blood flow recovery after femoral artery occlusion by inducing inflammation and arteriogenesis" 28 : 1989-1995, 2008

      24 Lobov IB, "Angiopoietin-2 displays VEGF-dependent modulation of capillary structure and endothelial cell survival in vivo" 99 : 11205-11210, 2002

      25 Van Royen N, "A critical review of clinical arteriogenesis research" 55 : 17-25, 2009

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2008-05-15 학회명변경 한글명 : 대한순환기학회 -> 대한심장학회
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      2005-08-02 학술지등록 한글명 : Korean Circulation Journal
      외국어명 : Korean Circulation Journal
      KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.13 0.34 0.71
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