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      급성 심근경색증 환자에서 순환 내피전구세포에 대한 조기 스타틴 치료의 효과

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      https://www.riss.kr/link?id=A104686608

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      다국어 초록 (Multilingual Abstract)

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent
      a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy
      before reperfusion therapy on the circulating EPCs during the acute phase in patients with acute myocardial infarction
      (AMI). Subjects and Methods: A total of 84 consecutive AMI patients undergoing primary percutaneous
      coronary intervention (PCI) within 24 hours of pain onset were included in this study. We randomly divided the
      patients into 3 groups according to rosuvastatin therapy before PCI: the control group (n:27, 19 males and 8
      females, 58±2 years of age), the rosuvastatin 10 mg group (n: 28, 21 males and 7 females, 58±3 years of age)
      and the 40 mg group (n: 29, 23 males and 6 females, 59±2 years of age). The circulating EPCs and high
      sensitivity C-reactive protein (hs-CRP) levels were analyzed on admission and at 1, 3, 5, 7 and 30 days after PCI.
      The circulating EPCs were measured by flow cytometry as the CD45lowCD34+VEGFR2+ cells. Results: The circulating
      EPCs peaked on day 3 after PCI, whereas the increment of circulating EPCs was significantly suppressed
      in the rosuvastatin 10 mg and 40 mg groups compared with the control group on day 3 (control vs rosuvastatin 10
      mg vs rosuvastatin 40 mg: 0.072% vs 0.067% vs 0.061%, respectively, p=0.002) and day 5 (0.068% vs 0.060% vs
      0.058%, respectively, p=0.029). The level of hs-CRP markedly increased from day 1 and this peaked on day 3 after
      PCI. Early statin therapy significantly suppressed the elevation of hs-CRP compared with the control group
      on day 1 (24.36 mg/L vs 17.88 mg/L vs 13.08 mg/L, respectively, p=0.035) and on day 3 (30.15 mg/L vs 22.78 mg/L
      vs 17.16 mg/L, respectively, p=0.034). There was a statistically significant correlation between the circulating
      EPCs and the hs-CRP (r=0.349, p=0.007). Conclusion: In the AMI patients, the early stain therapy before reperfusion
      therapy didn’t increase the mobilization of circulating EPCs, but it suppressed the elevation of hs-CRP.
      This data suggests that the mobilization of circulating EPCs may be related to systemic inflammation during the
      acute phase in patients with AMI.
      번역하기

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy before reperfusion ther...

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent
      a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy
      before reperfusion therapy on the circulating EPCs during the acute phase in patients with acute myocardial infarction
      (AMI). Subjects and Methods: A total of 84 consecutive AMI patients undergoing primary percutaneous
      coronary intervention (PCI) within 24 hours of pain onset were included in this study. We randomly divided the
      patients into 3 groups according to rosuvastatin therapy before PCI: the control group (n:27, 19 males and 8
      females, 58±2 years of age), the rosuvastatin 10 mg group (n: 28, 21 males and 7 females, 58±3 years of age)
      and the 40 mg group (n: 29, 23 males and 6 females, 59±2 years of age). The circulating EPCs and high
      sensitivity C-reactive protein (hs-CRP) levels were analyzed on admission and at 1, 3, 5, 7 and 30 days after PCI.
      The circulating EPCs were measured by flow cytometry as the CD45lowCD34+VEGFR2+ cells. Results: The circulating
      EPCs peaked on day 3 after PCI, whereas the increment of circulating EPCs was significantly suppressed
      in the rosuvastatin 10 mg and 40 mg groups compared with the control group on day 3 (control vs rosuvastatin 10
      mg vs rosuvastatin 40 mg: 0.072% vs 0.067% vs 0.061%, respectively, p=0.002) and day 5 (0.068% vs 0.060% vs
      0.058%, respectively, p=0.029). The level of hs-CRP markedly increased from day 1 and this peaked on day 3 after
      PCI. Early statin therapy significantly suppressed the elevation of hs-CRP compared with the control group
      on day 1 (24.36 mg/L vs 17.88 mg/L vs 13.08 mg/L, respectively, p=0.035) and on day 3 (30.15 mg/L vs 22.78 mg/L
      vs 17.16 mg/L, respectively, p=0.034). There was a statistically significant correlation between the circulating
      EPCs and the hs-CRP (r=0.349, p=0.007). Conclusion: In the AMI patients, the early stain therapy before reperfusion
      therapy didn’t increase the mobilization of circulating EPCs, but it suppressed the elevation of hs-CRP.
      This data suggests that the mobilization of circulating EPCs may be related to systemic inflammation during the
      acute phase in patients with AMI.

      더보기

      다국어 초록 (Multilingual Abstract)

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent
      a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy
      before reperfusion therapy on the circulating EPCs during the acute phase in patients with acute myocardial infarction
      (AMI). Subjects and Methods: A total of 84 consecutive AMI patients undergoing primary percutaneous
      coronary intervention (PCI) within 24 hours of pain onset were included in this study. We randomly divided the
      patients into 3 groups according to rosuvastatin therapy before PCI: the control group (n:27, 19 males and 8
      females, 58±2 years of age), the rosuvastatin 10 mg group (n: 28, 21 males and 7 females, 58±3 years of age)
      and the 40 mg group (n: 29, 23 males and 6 females, 59±2 years of age). The circulating EPCs and high
      sensitivity C-reactive protein (hs-CRP) levels were analyzed on admission and at 1, 3, 5, 7 and 30 days after PCI.
      The circulating EPCs were measured by flow cytometry as the CD45lowCD34+VEGFR2+ cells. Results: The circulating
      EPCs peaked on day 3 after PCI, whereas the increment of circulating EPCs was significantly suppressed
      in the rosuvastatin 10 mg and 40 mg groups compared with the control group on day 3 (control vs rosuvastatin 10
      mg vs rosuvastatin 40 mg: 0.072% vs 0.067% vs 0.061%, respectively, p=0.002) and day 5 (0.068% vs 0.060% vs
      0.058%, respectively, p=0.029). The level of hs-CRP markedly increased from day 1 and this peaked on day 3 after
      PCI. Early statin therapy significantly suppressed the elevation of hs-CRP compared with the control group
      on day 1 (24.36 mg/L vs 17.88 mg/L vs 13.08 mg/L, respectively, p=0.035) and on day 3 (30.15 mg/L vs 22.78 mg/L
      vs 17.16 mg/L, respectively, p=0.034). There was a statistically significant correlation between the circulating
      EPCs and the hs-CRP (r=0.349, p=0.007). Conclusion: In the AMI patients, the early stain therapy before reperfusion
      therapy didn’t increase the mobilization of circulating EPCs, but it suppressed the elevation of hs-CRP.
      This data suggests that the mobilization of circulating EPCs may be related to systemic inflammation during the
      acute phase in patients with AMI.
      번역하기

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy before reperfusion th...

      Background and Objectives: The mobilization of circulating endothelial progenitor cells (EPCs) might represent
      a useful strategy for the clinical therapy of ischemic heart disease. We examined the effect of early statin therapy
      before reperfusion therapy on the circulating EPCs during the acute phase in patients with acute myocardial infarction
      (AMI). Subjects and Methods: A total of 84 consecutive AMI patients undergoing primary percutaneous
      coronary intervention (PCI) within 24 hours of pain onset were included in this study. We randomly divided the
      patients into 3 groups according to rosuvastatin therapy before PCI: the control group (n:27, 19 males and 8
      females, 58±2 years of age), the rosuvastatin 10 mg group (n: 28, 21 males and 7 females, 58±3 years of age)
      and the 40 mg group (n: 29, 23 males and 6 females, 59±2 years of age). The circulating EPCs and high
      sensitivity C-reactive protein (hs-CRP) levels were analyzed on admission and at 1, 3, 5, 7 and 30 days after PCI.
      The circulating EPCs were measured by flow cytometry as the CD45lowCD34+VEGFR2+ cells. Results: The circulating
      EPCs peaked on day 3 after PCI, whereas the increment of circulating EPCs was significantly suppressed
      in the rosuvastatin 10 mg and 40 mg groups compared with the control group on day 3 (control vs rosuvastatin 10
      mg vs rosuvastatin 40 mg: 0.072% vs 0.067% vs 0.061%, respectively, p=0.002) and day 5 (0.068% vs 0.060% vs
      0.058%, respectively, p=0.029). The level of hs-CRP markedly increased from day 1 and this peaked on day 3 after
      PCI. Early statin therapy significantly suppressed the elevation of hs-CRP compared with the control group
      on day 1 (24.36 mg/L vs 17.88 mg/L vs 13.08 mg/L, respectively, p=0.035) and on day 3 (30.15 mg/L vs 22.78 mg/L
      vs 17.16 mg/L, respectively, p=0.034). There was a statistically significant correlation between the circulating
      EPCs and the hs-CRP (r=0.349, p=0.007). Conclusion: In the AMI patients, the early stain therapy before reperfusion
      therapy didn’t increase the mobilization of circulating EPCs, but it suppressed the elevation of hs-CRP.
      This data suggests that the mobilization of circulating EPCs may be related to systemic inflammation during the
      acute phase in patients with AMI.

      더보기

      참고문헌 (Reference)

      1 최진호, "심혈관 질환에서 혈관신생치료(Angiogenesis):현재와 미래" 대한심장학회 33 (33): 739-745, 2003

      2 임도선, "심장혈관 질환과 줄기세포" 대한심장학회 34 (34): 435-440, 2004

      3 Guven H, "The number of endothelial progenitor cell colonies in the blood is increased in patients with angiographically significant coronary artery disease" 48 : 1579-1587, 2006

      4 Landmesser U, "Statin-induced improvement of endothelial progenitor cell mobilization, myocardial neovascularization, left ventricular function, and survival after experimental myocardial infarction requires endothelial nitric oxide synthase" 110 : 1933-1939, 2004

      5 Rupp S, "Statin therapy in patients with coronary artery disease improves the impaired endothelial progenitor cell differentiation into cardiomyogenic cells" 99 : 61-68, 2004

      6 Kondo T, "Smoking cessation rapidly increases circulating progenitor cell in peripheral blood in chronic smokers" 24 : 1442-1447, 2004

      7 Laufs U, "Physical training increases endothelial progenitor cells, inhibits neointima formation, and enhances angiogenesis" 109 : 220-226, 2004

      8 Aicher A, "Mobilizing endothelial progenitor cells" 45 : 321-325, 2005

      9 Shintani S, "Mobilization of endothelial progenitor cells in patients with acute myocardial infarction" 103 : 2776-2779, 2001

      10 Leonel AM, "Mobilization of bone marrow-derived stem cells after myocardial infarction and left ventricular function" 26 : 1196-1204, 2005

      1 최진호, "심혈관 질환에서 혈관신생치료(Angiogenesis):현재와 미래" 대한심장학회 33 (33): 739-745, 2003

      2 임도선, "심장혈관 질환과 줄기세포" 대한심장학회 34 (34): 435-440, 2004

      3 Guven H, "The number of endothelial progenitor cell colonies in the blood is increased in patients with angiographically significant coronary artery disease" 48 : 1579-1587, 2006

      4 Landmesser U, "Statin-induced improvement of endothelial progenitor cell mobilization, myocardial neovascularization, left ventricular function, and survival after experimental myocardial infarction requires endothelial nitric oxide synthase" 110 : 1933-1939, 2004

      5 Rupp S, "Statin therapy in patients with coronary artery disease improves the impaired endothelial progenitor cell differentiation into cardiomyogenic cells" 99 : 61-68, 2004

      6 Kondo T, "Smoking cessation rapidly increases circulating progenitor cell in peripheral blood in chronic smokers" 24 : 1442-1447, 2004

      7 Laufs U, "Physical training increases endothelial progenitor cells, inhibits neointima formation, and enhances angiogenesis" 109 : 220-226, 2004

      8 Aicher A, "Mobilizing endothelial progenitor cells" 45 : 321-325, 2005

      9 Shintani S, "Mobilization of endothelial progenitor cells in patients with acute myocardial infarction" 103 : 2776-2779, 2001

      10 Leonel AM, "Mobilization of bone marrow-derived stem cells after myocardial infarction and left ventricular function" 26 : 1196-1204, 2005

      11 Asahara T, "Isolation of putative progenitor endothelial cells for angiogenesis" 275 : 964-967, 1997

      12 Ray KK, "Intensive statin therapy in acute coronary syndromes: clinical benefits and vascular biology" 15 : 637-643, 2004

      13 Massa M, "Increased circulating hematopoietic and endothelial progenitor cells in the early phase of acute myocardial infarction" 105 : 199-206, 2005

      14 Vasa M, "Increase in circulating endothelial progenitor cells by statin therapy in patients with stable coronary artery disease" 103 : 2885-2890, 2001

      15 Dimmeler S, "HMG-CoA reductase inhibitors (statin) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway" 108 : 391-397, 2001

      16 Libby P, "Effects of statins in reducing thrombotic risk and modulating plaque vulnerability" 26 : I11-I14, 2003

      17 Strandberg TE, "Effect of statins on C-reactive protein in patients with coronary artery disease" 353 : 118-119, 1999

      18 Kim W, "Effect of green tea consumption on endothelial function and circulating endothelial progenitor cells in chronic smokers" 70 : 1052-1057, 2006

      19 Ray KK, "Early time to benefit with intensive statin treatment: could it be the pleiotropic effects?" 96 : 54F-60F, 2005

      20 George J, "Comparative analysis of methods for assessment of circulating endothelial progenitor cells" 12 : 331-335, 2006

      21 George J, "Circulating endothelial progenitor cells in patients with unstable angina: association with systemic inflammation" 25 : 1003-1008, 2004

      22 Dupuis J, "Cholesterol reduction rapidly improves endothelial function after acute coronary syndromes" 99 : 3227-3233, 1999

      23 Suh W, "C-reactive protein impairs angiogenic functions and decreases the secretion of arteriogenic chemo-cytokines in human endothelial progenitor cells" 321 : 65-71, 2004

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-05-15 학회명변경 한글명 : 대한순환기학회 -> 대한심장학회
      영문명 : The Korean Society Of Circulation -> The Korean Society of Cardiology
      KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      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
      2001-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.13 0.34 0.71
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.45 0.36 0.52 0.12
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