Reduction of urinary connective tissue growth factor by Losartan in type 1 patients with diabetic nephropathy

被引:39
作者
Andersen, S
van Nieuwenhoven, FA
Tarnow, L
Rossing, P
Rossing, K
Wieten, L
Goldschmeding, R
Parving, HH
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Univ Med Ctr, Dept Pathol, Utrecht, Netherlands
[3] Univ Aarhus, Fac Hlth Sci, DK-8000 Aarhus, Denmark
关键词
CTGF; diabetic nephropathy; angiotensin II receptor blockade;
D O I
10.1111/j.1523-1755.2005.00337.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Connective tissue growth factor (CTGF) is an important profibrotic cytokine implicated in development of diabetic glomerulosclerosis. Urinary CTGF is reported to be significantly increased in patients with diabetic nephropathy. The present study aimed to investigate the short- and long term effects of angiotensin II receptor blockade by Losartan on urinary CTGF levels in hypertensive type I diabetic patients with diabetic nephropathy. Methods. Seventy-one hypertensive type I diabetic patients with diabetic nephropathy were included in the study. After a washout period of 4 weeks, the patients received Losartan 50 mg, 100 mg, and 150 mg once daily in treatment periods each lasting 2 months. Thereafter, patients were followed prospectively during treatment with Losartan 100 mg o.d. with a total mean follow-up time of 36 months. At baseline, after 2, 4, and 6 months and then biannually, urinary and plasma CTGF levels [enzyme linked immunosorbent assay (ELISA) fibroGen], albuminuria (Turbidimetry), glomerular filtration rate (GFR) [51-creatinine ethylenediaminetetraacetic acid (Cr-51-EDTA plasma clearance)] and 24 hours blood pressure (TM2420)) were determined. Results. Baseline levels of urinary and plasma CTGF were 7076 (5708 to 8770) ng/24 hours [geometric mean (95% CI)] and 12.7 (7.3) ng/mL [mean (SD)], respectively. Albuminuria, GFR, and arterial blood pressure at baseline were 1152 (937 to 1416) mg/24 hours, 88 (24) mL/min/1.73 m(2), and 153/80 (17/9) mm Hg, respectively. Losartan significantly reduced urinary CTGF by 21% (9 to 31) (95% CI) initially (P < 0.05 vs. baseline), with no further reduction after increasing dose. The sustained reduction in urinary CTGF was 22% (12 to 32) (P < 0.05 vs. baseline). Rate of decline in GFR during the study was 3.2 (-1.6 to 15.9) mL/min/year [median (range)]. Reduction in urinary CTGF was correlated with a lower rate of decline in GFR (r = 0.23, P = 0.05). Plasma CTGF remained unchanged throughout the study. Conclusion. Our 3-year study demonstrates that Losartan persistently reduces urinary CTGF excretion, which is associated with a slower rate of decline in GFR.
引用
收藏
页码:2325 / 2329
页数:5
相关论文
共 29 条
[11]   Urinary transforming growth factoro-β excretion in patients with hypertension, type 2 diabetes, and elevated albumin excretion rate -: Effects of angiotensin receptor blockade and sodium restriction [J].
Houlihan, CA ;
Akdeniz, A ;
Tsalamandris, C ;
Cooper, ME ;
Jerums, G ;
Gilbert, RE .
DIABETES CARE, 2002, 25 (06) :1072-1077
[12]   Expression of connective tissue growth factor in human renal fibrosis [J].
Ito, Y ;
Aten, J ;
Bende, RJ ;
Oemar, BS ;
Rabelink, TJ ;
Weening, JJ ;
Goldschmeding, R .
KIDNEY INTERNATIONAL, 1998, 53 (04) :853-861
[13]  
JONG PE, 1999, LANCET, V354, P352
[14]   Effects of endothelin or angiotensin II receptor blockade on diabetes in the transgenic (mRen-2)27 rat [J].
Kelly, DJ ;
Skinner, SL ;
Gilbert, RE ;
Cox, AJ ;
Cooper, ME ;
Wilkinson-Berka, JL .
KIDNEY INTERNATIONAL, 2000, 57 (05) :1882-1894
[15]   Connective tissue growth factor and IGF-I are produced by human renal fibroblasts and cooperate in the induction of collagen production by high glucose [J].
Lam, S ;
van der Geest, RN ;
Verhagen, NAM ;
van Nieuwenhoven, FA ;
Blom, IE ;
Aten, J ;
Goldschmeding, R ;
Daha, MR ;
van Kooten, C .
DIABETES, 2003, 52 (12) :2975-2983
[16]   Enhancing learners' cognitive skills through multimedia design [J].
Liu, M .
INTERACTIVE LEARNING ENVIRONMENTS, 2003, 11 (01) :23-39
[17]  
PARVING HH, 1983, LANCET, V1, P1175
[18]   Targeting TGF-β overexpression in renal disease:: Maximizing the antifibrotic action of angiotensin II blockade [J].
Peters, H ;
Border, WA ;
Noble, NA .
KIDNEY INTERNATIONAL, 1998, 54 (05) :1570-1580
[19]   Urinary CCN2 (CTGF) as a possible predictor of diabetic nephropathy: Preliminary report [J].
Riser, BL ;
Cortes, P ;
Denichilo, M ;
Deshmukh, PV ;
Chahal, PS ;
Mohammed, AK ;
Yee, J ;
Kahkonen, D .
KIDNEY INTERNATIONAL, 2003, 64 (02) :451-458
[20]   Connective tissue growth factor and its regulation: A new element in diabetic glomerulosclerosis [J].
Riser, BL ;
Cortes, P .
RENAL FAILURE, 2001, 23 (3-4) :459-470