Daschner M, Tönshoff B, Blum W F, Englaro P, Wingen A M, Schaefer F, Wühl E, Rascher W, Mehls O
Division of Pediatric Nephrology, University Children's Hospital, Heidelberg, Germany.
J Am Soc Nephrol. 1998 Jun;9(6):1074-9. doi: 10.1681/ASN.V961074.
Decreased spontaneous nutrient intake is a frequent clinical problem in patients with chronic renal failure (CRF). Leptin, the recently characterized gene product of the obese gene, is produced by adipocytes and is thought to act as an afferent satiety signal on the appetite and satiety centers of the brain. Serum leptin levels were investigated in 134 pediatric patients in different stages of CRF to evaluate a possible relationship between leptin, GFR, and spontaneous energy intake. Serum leptin levels, measured by a specific RIA, were elevated above the 50th percentile of the normal range in 78% of CRF patients and above the 95th percentile in 45% of patients. Gel chromatography of CRF sera yielded only one single immunoreactive peak at 16 kD, indicating that the increase of immunoreactive leptin levels in CRF serum was not due to accumulation of leptin degradation products. Multiple stepwise regression analysis revealed the percentage of body fat as assessed from skinfold measurements (r = 0.79, P < 0.0001) and GFR (r = -0.17, P < 0.005) as independent predictors of serum leptin levels, accounting for 66% of total statistical variability. There was an inverse linear correlation between standardized leptin levels (leptin z-score) and the spontaneous energy intake quantified from written dietary diaries (r = -0.36, P < 0.001). These data suggest that the percentage of body fat remains the main determinant of serum leptin in CRF patients, but their levels increase with declining GFR, presumably by reduced renal clearance. Leptin levels in CRF serum that are inappropriately elevated in relation to the percentage of body fat might lead to a dysregulation of the normal peripheral-central leptin feedback loop, thereby contributing to decreased nutrient intake in uremia.
自发性营养摄入减少是慢性肾衰竭(CRF)患者常见的临床问题。瘦素是肥胖基因最近鉴定出的基因产物,由脂肪细胞产生,被认为是作用于大脑食欲和饱腹感中枢的传入饱腹感信号。对134例处于不同CRF阶段的儿科患者的血清瘦素水平进行了研究,以评估瘦素、肾小球滤过率(GFR)与自发性能量摄入之间的可能关系。通过特异性放射免疫分析(RIA)测量的血清瘦素水平,在78%的CRF患者中高于正常范围的第50百分位数,在45%的患者中高于第95百分位数。CRF血清的凝胶色谱分析仅在16 kD处产生一个单一的免疫反应峰,表明CRF血清中免疫反应性瘦素水平的升高不是由于瘦素降解产物的积累。多步逐步回归分析显示,根据皮褶测量评估的体脂百分比(r = 0.79,P < 0.0001)和GFR(r = -0.17,P < 0.005)是血清瘦素水平的独立预测因素,占总统计变异性的66%。标准化瘦素水平(瘦素z评分)与根据书面饮食日记量化的自发性能量摄入之间存在负线性相关(r = -0.36,P < 0.001)。这些数据表明,体脂百分比仍然是CRF患者血清瘦素的主要决定因素,但随着GFR下降其水平升高,可能是由于肾脏清除率降低。CRF血清中瘦素水平相对于体脂百分比不适当升高可能导致正常的外周 - 中枢瘦素反馈回路失调,从而导致尿毒症患者营养摄入减少。