Murphy M G, Bach M A, Plotkin D, Bolognese J, Ng J, Krupa D, Cerchio K, Gertz B J
Merck Research Laboratories, Rahway, New Jersey, USA.
J Bone Miner Res. 1999 Jul;14(7):1182-8. doi: 10.1359/jbmr.1999.14.7.1182.
Growth hormone (GH) stimulates osteoblasts in vitro and increases bone turnover and stimulates osteoblast activity when given to elderly subjects. Probably a major effect of GH on bone is mediated through stimulation of either circulating or locally produced insulin-like growth factor I (IGF-I). We determined the effect of chronic administration of the GH secretagogue, MK-677, on serum IGF-I and markers of bone turnover in 187 elderly adults (65 years or older) enrolled in three randomized, double-blind, placebo-controlled clinical studies lasting 2-9 weeks. Urine was collected for determination of N-telopeptide cross-links (NTXs), a marker of bone resorption, and blood was collected for determination of serum osteocalcin and bone-specific alkaline phosphatase (BSAP), as bone formation markers, and serum IGF-I levels pre- and post-treatment. Dose response data were initially obtained in healthy elderly subjects who received oral doses of 10 mg or 25 mg of MK-677 or placebo for 2 weeks (n = 10-12/group). Treatment with 10 mg and 25 mg of MK-677 for 2 weeks increased mean urine NTXs 10% and 17%, respectively (p < 0.05 vs. placebo). Additionally, 50 healthy elderly subjects received either placebo (n = 20) for 4 weeks or 25 mg of MK-677 (n = 30) daily for 2 weeks followed by 50 mg daily for 2 weeks. MK-677 increased mean serum osteocalcin by 8% (p < 0.05 vs. placebo). In both studies, MK-677 increased serum IGF-I levels significantly (55-94%). Subsequently, the biological effects of MK-677 were studied in 105 elderly subjects who met objective criteria for functional impairment. Subjects were randomized to receive oral doses of placebo for 9 weeks or either 5, 10, or 25 mg of MK-677 daily for an initial 2 weeks followed by 25 mg of MK-677 daily for the next 7 weeks(n = 63 on MK-677 and n = 28 on placebo completed 9 weeks of therapy). Treatment with MK-677 (all MK-677 groups combined) for 9 weeks increased mean serum osteocalcin by 29.4% and BSAP by 10.4% (p < 0.001 vs. placebo) and mean urinary NTX excretion by 22.6% (p < 0.05 vs. placebo). The change from baseline serum osteocalcin correlated with the change from baseline serum IGF-I in the MK-677 group (r = 0.37; p < 0.01). In conclusion, once daily dosing with MK-677, an orally active GH secretagogue, stimulates bone turnover in elderly subjects based on elevations in biochemical markers of bone resorption and formation.
生长激素(GH)在体外可刺激成骨细胞,增加骨转换,并在给予老年受试者时刺激成骨细胞活性。GH对骨骼的主要作用可能是通过刺激循环中的或局部产生的胰岛素样生长因子I(IGF-I)介导的。我们在187名65岁及以上的老年人中,进行了三项为期2 - 9周的随机、双盲、安慰剂对照临床研究,以确定长期给予生长激素促分泌剂MK-677对血清IGF-I和骨转换标志物的影响。收集尿液以测定骨吸收标志物N-端肽交联物(NTXs),收集血液以测定血清骨钙素和骨特异性碱性磷酸酶(BSAP)作为骨形成标志物,以及治疗前后的血清IGF-I水平。剂量反应数据最初是在健康老年受试者中获得的,他们口服10毫克或25毫克MK-677或安慰剂,为期2周(每组n = 10 - 12)。用10毫克和25毫克MK-677治疗2周,平均尿NTXs分别增加了10%和17%(与安慰剂相比,p < 0.05)。此外,50名健康老年受试者接受了4周的安慰剂治疗(n = 20),或每天25毫克MK-677治疗2周,随后每天50毫克治疗2周(n = 30)。MK-677使平均血清骨钙素增加了8%(与安慰剂相比,p < 0.05)。在两项研究中,MK-677均显著提高了血清IGF-I水平(55 - 94%)。随后,在105名符合功能障碍客观标准的老年受试者中研究了MK-677的生物学效应。受试者被随机分为接受9周口服安慰剂,或最初2周每天口服5、10或25毫克MK-677,随后7周每天25毫克MK-677(MK-677组n = 63,安慰剂组n = 28完成了9周治疗)。用MK-677治疗(所有MK-677组合并)9周,平均血清骨钙素增加了29.4%,BSAP增加了10.4%(与安慰剂相比,p < 0.001),平均尿NTX排泄增加了2 : 6%(与安慰剂相比,p < 0.05)。MK-677组中,血清骨钙素相对于基线的变化与血清IGF-I相对于基线的变化相关(r = 0.37;p < 0.01)。总之,口服活性生长激素促分泌剂MK-677每日一次给药,基于骨吸收和形成的生化标志物升高,刺激老年受试者的骨转换。