The leptin/adiponectin ratio: Potential implications for peritoneal dialysis

被引:42
作者
Teta, D. [1 ]
Maillard, M. [1 ]
Halabi, G. [1 ]
Burnier, M. [1 ]
机构
[1] CHU Vaudois, Dept Internal Med, Div Nephrol, CH-1011 Lausanne, Switzerland
关键词
adipokines; adiponectin; cardiovascular risk; leptin; peritoneal dialysis; plasma ratio;
D O I
10.1038/sj.ki.5002611
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
Leptin and adiponectin are adipokines with respective pro-atherogenic and anti-atherogenic properties, defining the plasma leptin/adiponectin ratio as a novel marker for atherosclerosis. In non-renal patients, both hyperleptinemia and hypoadiponectinemia are associated with cardiovascular complications. In peritoneal dialysis (PD) patients, the leptin/adiponectin ratio is markedly elevated, which is consistent with their increased cardiovascular risk. As glucose metabolism regulates adipokines, we hypothesized that glucose and/or other PD fluid components may affect adipokine production balance. This review summarizes the available data arising from research in this area. In 3T3-L1 adipocytes, glucose-based PD4 1.36% significantly increased leptin secretion vs amino-acid-based ( AA) and icodextrin (ICOD)-based PD fluids. In contrast, adiponectin secretion was significantly reduced by PD4 1.36% vs glucose-free dialysates. Glucose concentration in PD fluids was shown to determine leptin secretion. Preliminary data from PD patients showed that a single 6-h dwell with PD4 3.86% glucose acutely increased plasma leptin vs AA (P<0.05). The reduction in glucose load in a standard PD regimen was associated with an improvement in the plasma leptin/adiponectin ratio at 6 months. pH-neutral PD fluids increased leptin secretion in vitro vs acidic PD fluids, without effect on adiponectin. Whether this effect may have an impact on plasma leptin levels in PD patients is unknown. In conclusion, glucose-based PD fluids worsen the adipokine production balance in vitro while glucose-free solutions improve it. In PD patients, hypertonic glucose-based PD fluids may increase plasma leptin levels. Glucose-sparing PD regimens appear to improve the leptin/adiponectin ratio. However, their potential to reduce cardiovascular complications needs to be demonstrated.
引用
收藏
页码:S112 / S118
页数:7
相关论文
共 72 条
[1]   Decreased plasma adiponectin concentration in patients with essential hypertension [J].
Adamczak, M ;
Wiecek, A ;
Funahashi, T ;
Chudek, J ;
Kokot, F ;
Matsuzawa, Y .
AMERICAN JOURNAL OF HYPERTENSION, 2003, 16 (01) :72-75
[2]  
Agata J, 1997, AM J HYPERTENS, V10, P1171
[3]  
Aguilera Abelardo, 2002, Adv Perit Dial, V18, P212
[4]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[5]   Leptin [J].
Auwerx, J ;
Staels, B .
LANCET, 1998, 351 (9104) :737-742
[6]   Leptin induces oxidative stress in human endothelial cells [J].
Bouloumié, A ;
Marumo, T ;
Lafontan, M ;
Busse, R .
FASEB JOURNAL, 1999, 13 (10) :1231-1238
[7]   Regulation of ob gene expression and leptin secretion by insulin and dexamethasone in rat adipocytes [J].
Bradley, RL ;
Cheatham, B .
DIABETES, 1999, 48 (02) :272-278
[8]   Differential effects of local versus systemic angiotensin II in the regulation of leptin release from adipocytes [J].
Cassis, LA ;
English, VL ;
Bharawaj, K ;
Boustany, CM .
ENDOCRINOLOGY, 2004, 145 (01) :169-174
[9]   Expression of adiponectin receptors in human macrophages and regulation by agonists of the nuclear receptors PPARα, PPARγ, and LXR [J].
Chinetti, G ;
Zawadski, C ;
Fruchart, JC ;
Staels, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 314 (01) :151-158
[10]   Serum immunoreactive leptin concentrations in normal-weight and obese humans [J].
Considine, RV ;
Sinha, MK ;
Heiman, ML ;
Kriauciunas, A ;
Stephens, TW ;
Nyce, MR ;
Ohannesian, JP ;
Marco, CC ;
McKee, LJ ;
Bauer, TL ;
Caro, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (05) :292-295