Leptin administration does not prevent the bone mineral metabolism changes induced by weight loss

被引:24
作者
Conroy, Rushika [2 ]
Girotra, Monica [1 ]
Shane, Elizabeth [1 ]
McMahon, Donald J. [1 ]
Pavlovich, Katherine H. [2 ]
Leibel, Rudolph L. [2 ]
Rosenbaum, Michael [2 ]
Korner, Judith [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Pediat, New York, NY 10032 USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2011年 / 60卷 / 09期
基金
美国国家卫生研究院;
关键词
BODY-WEIGHT; HYPOTHALAMIC AMENORRHEA; RECOMBINANT LEPTIN; ENERGY-EXPENDITURE; OB/OB MICE; THERAPY; OBESE; MASS; RESTRICTION; DEFICIENCY;
D O I
10.1016/j.metabol.2011.02.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective was to examine the effects of weight loss and leptin administration following weight loss on calciotropic hormones and bone turnover. This was a prospective, single-blinded study of 12 subjects (8 women, 4 men; 2 nonobese, 10 obese; age range, 19-46 years) who were studied on an inpatient basis while maintaining their usual weight [Wt(initial)] and during maintenance of 10% weight loss while receiving twice-daily injections of either a placebo [Wt(-10%P)] or replacement doses of leptin [Wt(-10%L)]. The main outcome measures were markers of bone formation (bone alkaline phosphatase and procollagen type 1 amino terminal propeptide) and resorption (N-telopeptide) as well as parathyroid hormone, calcium, and 25-hydroxy vitamin D measured from fasting morning serum. As expected, serum leptin declined with weight loss. Bone alkaline phosphatase decreased by 12.3% +/- 3.9% between Wt(initial) and Wt(-10%P) and remained suppressed after leptin administration (both P < .01 compared with baseline). N-telopeptides increased by 37.2% +/- 11.3% from Wt(initial) to Wt(-10%L) (P < .01). Procollagen type 1 amino terminal propeptide, parathyroid hormone, calcium, and 25-hydroxy vitamin D did not change. These results suggest that both decreased bone formation and increased bone resorption underlie bone loss associated with weight loss. Leptin administration did not prevent the uncoupling of bone remodeling that accompanies weight loss. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1222 / 1226
页数:5
相关论文
共 30 条
[21]  
Rosenbaum M, 2000, AM J CLIN NUTR, V71, P1421
[22]   Long-term persistence of adaptive thermogenesis in subjects who have maintained a reduced body weight [J].
Rosenbaum, Michael ;
Hirsch, Jules ;
Gallagher, Dympna A. ;
Leibel, Rudolph L. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 88 (04) :906-912
[23]   Effect of subcutaneous leptin replacement therapy on bone metabolism in patients with generalized lipodystrophy [J].
Simha, V ;
Zerwekh, JE ;
Sakhaee, K ;
Garg, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (11) :4942-4945
[24]   Leptin is a potent stimulator of bone growth in ob/ob mice [J].
Steppan, CM ;
Crawford, DT ;
Chidsey-Frink, KL ;
Ke, HZ ;
Swick, AG .
REGULATORY PEPTIDES, 2000, 92 (1-3) :73-78
[25]   The complex effects of leptin on bone metabolism through multiple pathways [J].
Thomas, T .
CURRENT OPINION IN PHARMACOLOGY, 2004, 4 (03) :295-300
[26]  
UNUSIRASI K, 2009, J MUSCULOSKEL NEURON, V9, P72
[27]   Recombinant human leptin in women with hypothalamic amenorrhea [J].
Welt, CK ;
Chan, JL ;
Bullen, J ;
Murphy, R ;
Smith, P ;
DePaoli, AM ;
Karalis, A ;
Mantzoros, CS .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (10) :987-997
[28]  
Westerterp-Plantenga MS, 2001, AM J CLIN NUTR, V74, P426
[29]  
Weyer C, 2000, AM J CLIN NUTR, V72, P946
[30]  
2002, AM J PHYSL REGUL INT, V283, pR281