N-Terminal Propeptide of Type III Procollagen as a Biomarker of Anabolic Response to Recombinant Human GH and Testosterone

被引:58
作者
Bhasin, Shalender [1 ]
He, E. Jiaxiu [3 ]
Kawakubo, Miwa [5 ]
Schroeder, E. Todd [4 ]
Yarasheski, Kevin [7 ]
Opiteck, Gregory J. [6 ]
Reicin, Alise [6 ]
Chen, Fabian [6 ]
Lam, Raymond [6 ]
Tsou, Jeffrey A. [6 ]
Castaneda-Sceppa, Carmen [8 ]
Binder, Ellen F. [7 ]
Azen, Stanley P. [5 ]
Sattler, Fred R. [2 ]
机构
[1] Boston Univ, Sch Med, Boston Med Ctr, Sect Endocrinol Diabet & Nutr,Boston Claude D Pep, Boston, MA 02118 USA
[2] Univ So Calif, Dept Med, Los Angeles, CA 90089 USA
[3] Univ So Calif, Sch Dent, Los Angeles, CA 90089 USA
[4] Univ So Calif, Div Biokinesiol, Los Angeles, CA 90089 USA
[5] Univ So Calif, Dept Prevent Med, Los Angeles, CA 90089 USA
[6] Merck Res Labs, Rahway, NJ 07065 USA
[7] Washington Univ, Sch Med, St Louis, MO 63110 USA
[8] Tufts Univ, Human Nutr Res Ctr Aging, Jean Mayer US Dept Agr, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
GROWTH-HORMONE ABUSE; ANDROGEN RECEPTOR MODULATORS; COLLAGEN TURNOVER; DOUBLE-BLIND; FACTOR-I; EXERCISE; MARKERS; MUSCLE; ADULTS; SERUM;
D O I
10.1210/jc.2009-1434
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Biomarkers that predict musculoskeletal response to anabolic therapies should expedite drug development. During collagen synthesis in soft lean tissue, N-terminal propeptide of type III procollagen (P3NP) is released into circulation. We investigated P3NP as a biomarker of lean body mass (LBM) and muscle strength gains in response to testosterone and GH. Design: Community-dwelling older men received GnRH agonist plus 5 or 10 g testosterone gel plus 0, 3, or 5 mu g recombinant human GH daily. P3NP levels were measured at baseline and wk 4, 8, 12, and 16. LBM and appendicular skeletal muscle mass(ASM) were measured by dual-energy x-ray absorptiometry. Results: One hundred twelve men completed treatment; 106 underwent serum P3NP measurements. P3NP levels were higher at wk 4 than baseline (6.61 +/- 2.14 vs. 4.51 +/- 1.05, P < 0.0001) and reached plateau by wk 4 in men receiving testosterone alone. However, wk 8 P3NP levels were higher than wk 4 levels in men receiving testosterone plus recombinant human GH. Increases in P3NP from baseline to wk 4 and 16 were significantly associated with gains in LBM (r = 0.26, P = 0.007; r = 0.53, P < 0.001) and ASM (r = 0.17, P = 0.07; r = 0.40, P < 0.0001). Importantly, for participants receiving only testosterone, P3NP increases at wk 4 and 16 were related to muscle strength gains (r = 0.20, P = 0.056 and r = 0.36, P = 0.04). In stepwise regression, change in P3NP explained 28 and 30% of the change in ASM and LBM, respectively, whereas change in testosterone but not IGF-I and age provided only small improvements in the models. Conclusion: Early changes in serum P3NP levels are associated with subsequent changes in LBM and ASM during testosterone and GH administration. Serum P3NP may be a useful early predictive biomarker of anabolic response to GH and testosterone. (J Clin Endocrinol Metab 94: 4224-4233, 2009)
引用
收藏
页码:4224 / 4233
页数:10
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