Role of the kidney in the metabolism of apolipoprotein A-IV:: influence of the type of proteinuria

被引:27
作者
Lingenhel, Arno
Lhotta, Karl
Neyer, Ulrich
Heid, Iris M.
Rantner, Barbara
Kronenberg, Martina F.
Koenig, Paul
von Eckardstein, Arnold
Schober, Maria
Dieplinger, Hans
Kronenberg, Florian [1 ]
机构
[1] Innsbruck Med Univ, Div Genet Epidemiol, Dept Med Genet Mol & Clin Pharmacol, Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Clin Nephrol, Innsbruck, Austria
[3] Acad Teaching Hosp, Dept Nephrol & Dialysis, Feldkirch, Austria
[4] GSF, Natl Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
[5] Univ Munich, Inst Biostat & Epidemiol, Munich, Germany
[6] Univ Zurich, Inst Clin Chem, CH-8006 Zurich, Switzerland
[7] Univ Zurich Hosp, Inst Clin Chem, CH-8091 Zurich, Switzerland
[8] Innsbruck Med Univ, Univ Clin, Cent Lab, Innsbruck, Austria
关键词
nephrotic syndrome; tubular proteinuria; atherosclerosis; Dent's disease;
D O I
10.1194/jlr.M600178-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increased plasma concentrations of apolipoprotein A-IV (apoA-IV) in chronic renal disease suggest a metabolic role of the kidney for this antiatherogenic protein. Therefore, we investigated patients with various forms of proteinuria and found increased serum concentrations of apoA-IV in 124 nephrotic patients compared with 274 controls (mean 21.9 +/- 9.6 vs. 14.4 +/- 4.0 mg/dl; P < 0.001). Decreasing creatinine clearance showed a strong association with increasing apoA-IV levels. However, serum albumin levels significantly modulated apoA-IV levels in patients with low creatinine clearance, resulting in lower levels of apoA-IV in patients with low compared with high albumin levels (21.4 +/- 8.6 vs. 29.2 +/- 8.4 mg/dl; P = 0.0007). Furthermore, we investigated urinary apoA-IV levels in an additional 66 patients with a wide variety of proteinuria and 30 controls. Especially patients with a tubular type of proteinuria had significantly higher amounts of apoA-IV in urine than those with a pure glomerular type of proteinuria and controls (median 45, 14, and 0.6 ng/mg creatinine, respectively). We confirmed these results in affected members of a family with Dent's disease, who are characterized by an inherited protein reabsorption defect of the proximal tubular system. In summary, our data demonstrate that the increase of apoA-IV caused by renal impairment is significantly modulated by low levels of serum albumin as a measure for the severity of the nephrotic syndrome. From this investigation of apoA-IV in urine as well as earlier immunohistochemical studies, we conclude that apoA-IV is filtered through the normal glomerulus and is subsequently reabsorbed mainly by proximal tubular cells.
引用
收藏
页码:2071 / 2079
页数:9
相关论文
共 46 条
[1]   Renal albumin absorption in physiology and pathology [J].
Birn, H ;
Christensen, E .
KIDNEY INTERNATIONAL, 2006, 69 (03) :440-449
[2]   Apolipoprotein A-IV predicts progression of chronic kidney disease:: The mild to moderate kidney disease study [J].
Boes, Eva ;
Fliser, Danilo ;
Ritz, Eberhard ;
Koenig, Paul ;
Lhotta, Karl ;
Mann, Johannes F. E. ;
Mueller, Gerhard A. ;
Neyer, Ulrich ;
Riegel, Werner ;
Riegler, Peter ;
Kronenberg, Florian .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (02) :528-536
[3]  
Brenner BM, 2004, BRENNER RECTORS KIDN, V7th
[4]  
CHEN CH, 2005, BIOCHIM BIOPHYS ACTA, V836, P279
[5]  
Christensen EI, 1999, J AM SOC NEPHROL, V10, P2224
[6]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[7]   The urinary proteome in Fanconi syndrome implies specificity in the reabsorption of proteins by renal proximal tubule cells [J].
Cutillas, PR ;
Chalkley, RJ ;
Hansen, KC ;
Cramer, R ;
Norden, AGW ;
Waterfield, MD ;
Burlingame, AL ;
Unwin, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 287 (03) :F353-F364
[8]   TISSUE SITES OF DEGRADATION OF HIGH-DENSITY-LIPOPROTEIN APOLIPOPROTEIN A-IV IN RATS [J].
DALLINGATHIE, GM ;
VANTHOOFT, FM ;
VANTOL, A .
ARTERIOSCLEROSIS, 1986, 6 (03) :277-284
[9]   Increased VLDL in nephrotic patients results from a decreased catabolism while increased LDL results from increased synthesis [J].
de Sain-van der Velden, M ;
Kaysen, GA ;
Barrett, HA ;
Stellaard, F ;
Gadellaa, MM ;
Voorbij, HA ;
Reijngoud, DJ ;
Rabelink, TJ .
KIDNEY INTERNATIONAL, 1998, 53 (04) :994-1001
[10]  
De Sain-Van der Velden MGM, 1998, J AM SOC NEPHROL, V9, P1474