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      단백뇨를 동반한 IgA 신병증 환자들에서 데플라자코트의 신기능 보존 효과 = Renoprotective effect of deflazacort in IgA nephropathy with proteinuria

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      https://www.riss.kr/link?id=A76562361

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      다국어 초록 (Multilingual Abstract)

      Background/Aims: Steroid therapy is reported to improve the clinical outcome of IgA nephropathy. In addition, recent studies have revealed that deflazacort has fewer side effects than prednisolone. This study examined the effect of steroids and compared the clinical efficacy of deflazacort and prednisolone in patients with IgA nephropathy. Methods: We retrospectively reviewed 136 patients with biopsy-proven IgA nephropathy who received deflazacort (n=50), prednisolone (n=29), or neither (n=59), and in whom blood pressure was controlled with angiotensin converting enzyme inhibitors or angiotensin receptor blockers. The mean duration of steroid administration was 9.5±9.1 months. The initial clinical status and change in the amount of protein in the 24-hour urine were compared among the three groups. Results: The baseline characteristics (age, blood pressure, serum creatinine level, initial protein in the 24-hour urine, and creatinine clearance) did not differ significantly among the groups. The decrement of protein in the 24-hour urine was higher in the deflazacort and prednisolone groups, as compared with the control group (4.4±5.4, 4.2±1.5, and 2.1±3.1 g/day, respectively, p=0.013). The increment in the creatinine clearance was higher in the deflazacort and prednisolone groups, as compared with the control group (11.5±16.4, 12.3±26.2, and 4.8±14.91.3±0.9, respectively, p=0.009). There were no significant differences in the above parameters between the deflazacort and prednisolone groups. Conclusions: Steroid therapy reduces urinary protein excretion in IgA nephropathy, and the clinical efficacy of deflazacort and prednisolone was found to be similar. (Korean J Med 77:593-600, 2009)
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      Background/Aims: Steroid therapy is reported to improve the clinical outcome of IgA nephropathy. In addition, recent studies have revealed that deflazacort has fewer side effects than prednisolone. This study examined the effect of steroids and compar...

      Background/Aims: Steroid therapy is reported to improve the clinical outcome of IgA nephropathy. In addition, recent studies have revealed that deflazacort has fewer side effects than prednisolone. This study examined the effect of steroids and compared the clinical efficacy of deflazacort and prednisolone in patients with IgA nephropathy. Methods: We retrospectively reviewed 136 patients with biopsy-proven IgA nephropathy who received deflazacort (n=50), prednisolone (n=29), or neither (n=59), and in whom blood pressure was controlled with angiotensin converting enzyme inhibitors or angiotensin receptor blockers. The mean duration of steroid administration was 9.5±9.1 months. The initial clinical status and change in the amount of protein in the 24-hour urine were compared among the three groups. Results: The baseline characteristics (age, blood pressure, serum creatinine level, initial protein in the 24-hour urine, and creatinine clearance) did not differ significantly among the groups. The decrement of protein in the 24-hour urine was higher in the deflazacort and prednisolone groups, as compared with the control group (4.4±5.4, 4.2±1.5, and 2.1±3.1 g/day, respectively, p=0.013). The increment in the creatinine clearance was higher in the deflazacort and prednisolone groups, as compared with the control group (11.5±16.4, 12.3±26.2, and 4.8±14.91.3±0.9, respectively, p=0.009). There were no significant differences in the above parameters between the deflazacort and prednisolone groups. Conclusions: Steroid therapy reduces urinary protein excretion in IgA nephropathy, and the clinical efficacy of deflazacort and prednisolone was found to be similar. (Korean J Med 77:593-600, 2009)

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      참고문헌 (Reference)

      1 이강욱, "신장질환에서 Angiotensinsin converting enzyme inhibitor 및 angiotensin II AT1 receptor antagonist" 57 : 489-494, 1999

      2 Laville M, "Treatment options for IgA nephropathy in adults: a proposal for evidence‐based strategy" 19 : 1947-1951, 2004

      3 Praga M, "Treatment of IgA nephropathy with ACE inhibitors: a randomized and controlled trial" 14 : 1578-1583, 2003

      4 Barratt J, "Treatment of IgA nephropathy" 69 : 1934-1938, 200

      5 Katafuchi R, "The improvement of renal survival with steroid pulse therapy in IgA nephropathy" 23 : 3915-3920, 2008

      6 Eitner F, "Supportive Versus Immunosuppressive Therapy of Progressive IgA nephropathy (STOP) IgAN trial: rationale and study protocol" 21 : 284-289, 2008

      7 Markham LW, "Steroid therapy and cardiac function in Duchenne muscular dystrophy" 26 : 768-771, 2005

      8 Hotta O, "Regression of IgA nephropathy: a repeat biopsy study" 39 : 493-502, 2002

      9 Ballardie FW, "Quantitative appraisal of treatment options for IgA nephropathy" 18 : 2806-2809, 2007

      10 Floege J, "Present and future therapy options in IgAnephropathy" 18 : 354-361, 2005

      1 이강욱, "신장질환에서 Angiotensinsin converting enzyme inhibitor 및 angiotensin II AT1 receptor antagonist" 57 : 489-494, 1999

      2 Laville M, "Treatment options for IgA nephropathy in adults: a proposal for evidence‐based strategy" 19 : 1947-1951, 2004

      3 Praga M, "Treatment of IgA nephropathy with ACE inhibitors: a randomized and controlled trial" 14 : 1578-1583, 2003

      4 Barratt J, "Treatment of IgA nephropathy" 69 : 1934-1938, 200

      5 Katafuchi R, "The improvement of renal survival with steroid pulse therapy in IgA nephropathy" 23 : 3915-3920, 2008

      6 Eitner F, "Supportive Versus Immunosuppressive Therapy of Progressive IgA nephropathy (STOP) IgAN trial: rationale and study protocol" 21 : 284-289, 2008

      7 Markham LW, "Steroid therapy and cardiac function in Duchenne muscular dystrophy" 26 : 768-771, 2005

      8 Hotta O, "Regression of IgA nephropathy: a repeat biopsy study" 39 : 493-502, 2002

      9 Ballardie FW, "Quantitative appraisal of treatment options for IgA nephropathy" 18 : 2806-2809, 2007

      10 Floege J, "Present and future therapy options in IgAnephropathy" 18 : 354-361, 2005

      11 Cockcroft DW, "Prediction of creatinine clearance from serum creatinine" 16 : 31-41, 1976

      12 D’Amico G, "Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome" 24 : 179-196, 2004

      13 Rasche FM, "Mycophenolic acid therapy after cyclophosphamide pulses in progressive IgA nephropathy" 19 : 465-472, 2006

      14 박미나, "IgA 신병증 환자에게 있어 ACE 유전자 다형성에 따른 Angiotensin receptor blocker의 치료 효과" 대한신장학회 27 (27): 13-19, 2008

      15 Ferraris JR, "Effects of deflazacort vs. methylprednisone: a randomized study in kidney transplant patients" 22 : 734-741, 2007

      16 Ferraris JR, "Effect of deflazacort versus methylprednisone on growth, body composition, lipid profile, and bone mass after renal transplantation" 14 : 682-688, 2000

      17 Shoji T, "Early treatment with corticosteroids ameliorates proteinuria, proliferative lesions, and mesangial phenotypic modulation in adult diffuse proliferative IgA nephropathy" 35 : 194-201, 2000

      18 Woo KT, "Disease progression, response to ACEI/ATRA therapy and influence of ACE gene in IgA nephritis" 4 : 227-232, 2007

      19 Lv J, "Delayed severe pneumonia in mycophenolate mofetil‐treated patients with IgA nephropathy" 23 : 2868-2872, 2008

      20 Gonzalez‐Perez O, "Deflazacort: a glucocorticoid with few metabolic adverse effects but important immunosuppressive activity" 24 : 1052-1060, 2007

      21 Houde S, "Deflazacort use in Duchenne muscular dystrophy: an 8‐year follow‐up" 38 : 200-206, 2008

      22 Pozzi C, "Corticosteroids in IgA nephropathy: a randomised controlled trial" 353 : 883-887, 1999

      23 Katafuchi R, "Controlled, prospective trial of steroid treatment in IgA nephropathy: a limitation of low‐dose prednisolone therapy" 41 : 972-983, 2003

      24 Ballardie FW, "Controlled prospective trial of prednisolone and cytotoxics in progressive IgA nephropathy" 13 : 142-148, 2002

      25 Saviola G, "Compared clinical efficacy and bone metabolic effects of low‐dose deflazacort and methyl prednisolone in male inflammatory arthropathies: a 12‐month open randomized pilot study" 46 : 994-998, 2007

      26 Di Munno O, "Clinical equivalence between deflazacort oral drops and tablets in active rheumatoid arthritis" 18 : 140-144, 1999

      27 Nakamura T, "Beneficial effects of olmesartan and temocapril on urinary liver‐type fatty acid‐binding protein levels in normo tensive patients with immunoglobin A nephropathy" 20 : 1195-1201, 2007

      28 Strippoli GF, "An “evidence‐based” survey of therapeutic options for IgA nephropathy: assessment and criticism" 41 : 1129-1139, 2003

      29 Grosso S, "A comparative study of hydrocortisone versus deflazacort in drug‐resistant epilepsy of childhood" 81 : 80-85, 2008

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 계속평가 신청대상 (계속평가)
      2021-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2018-12-01 평가 등재후보 탈락 (계속평가)
      2017-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2013-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-05-15 학술지명변경 외국어명 : Korean Journal of Medicine -> The Korean Journal of Medicine KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2003-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2002-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.1 0.1 0.1
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.11 0.1 0.259 0.02
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