Tubular and glomerular injury in diabetes and the impact of ACE inhibition

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Standard

Tubular and glomerular injury in diabetes and the impact of ACE inhibition. / Nielsen, Stine E; Sugaya, Takeshi; Tarnow, Lise; Lajer, Maria; Schjoedt, Katrine J; Astrup, Anne Sofie; Baba, Tsuneharu; Parving, Hans-Henrik; Rossing, Peter.

I: Diabetes Care, Bind 32, Nr. 9, 2009, s. 1684-1688.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Nielsen, SE, Sugaya, T, Tarnow, L, Lajer, M, Schjoedt, KJ, Astrup, AS, Baba, T, Parving, H-H & Rossing, P 2009, 'Tubular and glomerular injury in diabetes and the impact of ACE inhibition', Diabetes Care, bind 32, nr. 9, s. 1684-1688. https://doi.org/10.2337/dc09-0429

APA

Nielsen, S. E., Sugaya, T., Tarnow, L., Lajer, M., Schjoedt, K. J., Astrup, A. S., Baba, T., Parving, H-H., & Rossing, P. (2009). Tubular and glomerular injury in diabetes and the impact of ACE inhibition. Diabetes Care, 32(9), 1684-1688. https://doi.org/10.2337/dc09-0429

Vancouver

Nielsen SE, Sugaya T, Tarnow L, Lajer M, Schjoedt KJ, Astrup AS o.a. Tubular and glomerular injury in diabetes and the impact of ACE inhibition. Diabetes Care. 2009;32(9):1684-1688. https://doi.org/10.2337/dc09-0429

Author

Nielsen, Stine E ; Sugaya, Takeshi ; Tarnow, Lise ; Lajer, Maria ; Schjoedt, Katrine J ; Astrup, Anne Sofie ; Baba, Tsuneharu ; Parving, Hans-Henrik ; Rossing, Peter. / Tubular and glomerular injury in diabetes and the impact of ACE inhibition. I: Diabetes Care. 2009 ; Bind 32, Nr. 9. s. 1684-1688.

Bibtex

@article{21287b006a3b11df928f000ea68e967b,
title = "Tubular and glomerular injury in diabetes and the impact of ACE inhibition",
abstract = "OBJECTIVE: We studied tubular and glomerular damage in type 1 diabetic patients by measuring urinary-liver fatty acid binding protein (U-LFABP) and albuminuria. Subsequently, we evaluated the effect of ACE inhibition on U-LFABP in patients with diabetic nephropathy. RESEARCH DESIGN AND METHODS: We studied Caucasians with type 1 diabetes: 58 with normoalbuminuria (urinary albumin <30 mg/24 h), 45 with persistent microalbuminuria (30-300 mg/24 h), and 45 with persistent macroalbuminuria (> or =300 mg/24 h). A control group consisted of 57 healthy individuals. The groups were matched by sex and duration of diabetes. In addition, U-LFABP was measured in 48 type 1 diabetic patients with diabetic nephropathy in a randomized crossover trial consisting of 2 months of treatment with 20, 40, and 60 mg lisinopril once daily in random order. RESULTS: In the cross-sectional study, levels of U-LFABP were significantly higher in normoalbuminuric patients versus those in the control group (median 2.6 [interquartile range 1.3-4.1] vs. 19 [0.8-3.0] microg/g creatinine, P = 0.02) and increased with increasing levels of albuminuria (microalbuminuric group 4.2 [1.8-8.3] microg/g creatinine and nephropathy group 71.2 [8.1-123.4], P < 0.05 for all comparisons). U-LFABP correlates with the urinary albumin-to-creatinine ratio (R(2) = 0.54, P < 0.001). In the intervention study, all doses of lisinopril significantly reduced urinary albumin excretion rate and U-LFABP from baseline. The reductions in U-LFABP were 43, 46, and 40% with increasing doses of lisinopril (NS). CONCLUSIONS: An early and progressive increase in tubulointerstitial damage as reflected by increased U-LFABP levels occurs in type 1 diabetic patients and is associated with albuminuria. Furthermore, ACE inhibition reduces the tubular and glomerular damage and dysfunction.",
author = "Nielsen, {Stine E} and Takeshi Sugaya and Lise Tarnow and Maria Lajer and Schjoedt, {Katrine J} and Astrup, {Anne Sofie} and Tsuneharu Baba and Hans-Henrik Parving and Peter Rossing",
note = "Keywords: Adult; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Case-Control Studies; Creatinine; Cross-Sectional Studies; Diabetes Mellitus, Type 1; Diabetic Nephropathies; Fatty Acid-Binding Proteins; Female; Humans; Lisinopril; Male; Middle Aged",
year = "2009",
doi = "10.2337/dc09-0429",
language = "English",
volume = "32",
pages = "1684--1688",
journal = "Diabetes Care",
issn = "0149-5992",
publisher = "American Diabetes Association",
number = "9",

}

RIS

TY - JOUR

T1 - Tubular and glomerular injury in diabetes and the impact of ACE inhibition

AU - Nielsen, Stine E

AU - Sugaya, Takeshi

AU - Tarnow, Lise

AU - Lajer, Maria

AU - Schjoedt, Katrine J

AU - Astrup, Anne Sofie

AU - Baba, Tsuneharu

AU - Parving, Hans-Henrik

AU - Rossing, Peter

N1 - Keywords: Adult; Albuminuria; Angiotensin-Converting Enzyme Inhibitors; Case-Control Studies; Creatinine; Cross-Sectional Studies; Diabetes Mellitus, Type 1; Diabetic Nephropathies; Fatty Acid-Binding Proteins; Female; Humans; Lisinopril; Male; Middle Aged

PY - 2009

Y1 - 2009

N2 - OBJECTIVE: We studied tubular and glomerular damage in type 1 diabetic patients by measuring urinary-liver fatty acid binding protein (U-LFABP) and albuminuria. Subsequently, we evaluated the effect of ACE inhibition on U-LFABP in patients with diabetic nephropathy. RESEARCH DESIGN AND METHODS: We studied Caucasians with type 1 diabetes: 58 with normoalbuminuria (urinary albumin <30 mg/24 h), 45 with persistent microalbuminuria (30-300 mg/24 h), and 45 with persistent macroalbuminuria (> or =300 mg/24 h). A control group consisted of 57 healthy individuals. The groups were matched by sex and duration of diabetes. In addition, U-LFABP was measured in 48 type 1 diabetic patients with diabetic nephropathy in a randomized crossover trial consisting of 2 months of treatment with 20, 40, and 60 mg lisinopril once daily in random order. RESULTS: In the cross-sectional study, levels of U-LFABP were significantly higher in normoalbuminuric patients versus those in the control group (median 2.6 [interquartile range 1.3-4.1] vs. 19 [0.8-3.0] microg/g creatinine, P = 0.02) and increased with increasing levels of albuminuria (microalbuminuric group 4.2 [1.8-8.3] microg/g creatinine and nephropathy group 71.2 [8.1-123.4], P < 0.05 for all comparisons). U-LFABP correlates with the urinary albumin-to-creatinine ratio (R(2) = 0.54, P < 0.001). In the intervention study, all doses of lisinopril significantly reduced urinary albumin excretion rate and U-LFABP from baseline. The reductions in U-LFABP were 43, 46, and 40% with increasing doses of lisinopril (NS). CONCLUSIONS: An early and progressive increase in tubulointerstitial damage as reflected by increased U-LFABP levels occurs in type 1 diabetic patients and is associated with albuminuria. Furthermore, ACE inhibition reduces the tubular and glomerular damage and dysfunction.

AB - OBJECTIVE: We studied tubular and glomerular damage in type 1 diabetic patients by measuring urinary-liver fatty acid binding protein (U-LFABP) and albuminuria. Subsequently, we evaluated the effect of ACE inhibition on U-LFABP in patients with diabetic nephropathy. RESEARCH DESIGN AND METHODS: We studied Caucasians with type 1 diabetes: 58 with normoalbuminuria (urinary albumin <30 mg/24 h), 45 with persistent microalbuminuria (30-300 mg/24 h), and 45 with persistent macroalbuminuria (> or =300 mg/24 h). A control group consisted of 57 healthy individuals. The groups were matched by sex and duration of diabetes. In addition, U-LFABP was measured in 48 type 1 diabetic patients with diabetic nephropathy in a randomized crossover trial consisting of 2 months of treatment with 20, 40, and 60 mg lisinopril once daily in random order. RESULTS: In the cross-sectional study, levels of U-LFABP were significantly higher in normoalbuminuric patients versus those in the control group (median 2.6 [interquartile range 1.3-4.1] vs. 19 [0.8-3.0] microg/g creatinine, P = 0.02) and increased with increasing levels of albuminuria (microalbuminuric group 4.2 [1.8-8.3] microg/g creatinine and nephropathy group 71.2 [8.1-123.4], P < 0.05 for all comparisons). U-LFABP correlates with the urinary albumin-to-creatinine ratio (R(2) = 0.54, P < 0.001). In the intervention study, all doses of lisinopril significantly reduced urinary albumin excretion rate and U-LFABP from baseline. The reductions in U-LFABP were 43, 46, and 40% with increasing doses of lisinopril (NS). CONCLUSIONS: An early and progressive increase in tubulointerstitial damage as reflected by increased U-LFABP levels occurs in type 1 diabetic patients and is associated with albuminuria. Furthermore, ACE inhibition reduces the tubular and glomerular damage and dysfunction.

U2 - 10.2337/dc09-0429

DO - 10.2337/dc09-0429

M3 - Journal article

C2 - 19502542

VL - 32

SP - 1684

EP - 1688

JO - Diabetes Care

JF - Diabetes Care

SN - 0149-5992

IS - 9

ER -

ID: 20009228