Gonnelli S, Cepollaro C, Montomoli M, Gennari L, Montagnani A, Palmieri R, Gennari C
Institute of Internal Medicine, University of Siena, Italy.
Clin Endocrinol (Oxf). 1997 Jan;46(1):55-61. doi: 10.1046/j.1365-2265.1997.d01-1750.x.
The usefulness of GH in the treatment of post-menopausal osteoporosis (PMO) is still debated. We have studied the effects of recombinant human GH (rhGH) given alone or in combination with salmon calcitonin (sCT) in the treatment of PMO.
Thirty women with established PMO (aged 61.1 +/- 4.4 years) were divided into 3 groups of 10 and randomly assigned to 3 treatment sequences: rhGH (12IU/day) s.c. for 7 days, followed by sCT (50 IU/day) s.c. for 21 days and by 61 days without treatment (group 1); placebo for 7 days, followed by sCT for 21 days and by 61 days without treatment (group 2); rhGH for 7 days, followed by placebo for 21 days, and by 61 days without treatment (group 3). Each cycle was repeated 8 times (24 months).
At days 0, 8, 29 and 90 of each cycle, serum IGF-I, calcium, phosphate, osteocalcin, alkaline phosphatase and urinary excretion of calcium, hydroxyproline and pyridinoline cross-links (Pyr) were measured. At months 0, 6, 12, 18 and 24, bone mineral density (BMD) was measured by dualphoton absorptiometry (DPA), at lumbar spine (LS), femoral shaft (F) and distal radius (DR).
A significant increase in serum osteocalcin and urinary calcium, hydroxyproline and Pyr was detected after each rhGH period. In group 1, BMD at lumbar spine increased by 2.5% at year 2; in contrast, significant (P < 0.05) decreases in BMD-LS values were found in patients treated with CT and placebo (group 2) and with GH and placebo (group 3). BMD-F did not show any significant change in patients of group 2, but a significant (P < 0.05) decrease was found in groups 1 and 3. BMD-DR did not show any significant change with respect to baseline in any of the three groups. No significant difference between the three groups was found in bone mass at the three different regions.
Our study demonstrates that treatment with rhGH increases bone turnover in postmenopausal osteoporotic women. Combined treatment with rhGH and CT over a period of 24 months is able to maintain bone mass at lumbar spine and distal radius, but induces a decline at femoral shaft; therefore, it does not seem particularly useful in the therapy of post-menopausal osteoporosis.
生长激素(GH)在绝经后骨质疏松症(PMO)治疗中的有效性仍存在争议。我们研究了重组人生长激素(rhGH)单独使用或与鲑鱼降钙素(sCT)联合使用在PMO治疗中的效果。
30名确诊为PMO的女性(年龄61.1±4.4岁)被分为3组,每组10人,并随机分配至3种治疗顺序:皮下注射rhGH(12IU/天)7天,随后皮下注射sCT(50IU/天)21天,然后61天不治疗(第1组);皮下注射安慰剂7天,随后皮下注射sCT 21天,然后61天不治疗(第2组);皮下注射rhGH 7天,随后皮下注射安慰剂21天,然后61天不治疗(第3组)。每个周期重复8次(24个月)。
在每个周期的第0、8、29和90天,测量血清胰岛素样生长因子-I(IGF-I)、钙、磷、骨钙素、碱性磷酸酶以及尿钙、羟脯氨酸和吡啶啉交联物(Pyr)的排泄量。在第0、6、12、18和24个月,采用双能光子吸收法(DPA)测量腰椎(LS)、股骨干(F)和桡骨远端(DR)的骨密度(BMD)。
在每个rhGH治疗期后,血清骨钙素以及尿钙、羟脯氨酸和Pyr均显著增加。在第1组中,第2年腰椎BMD增加了2.5%;相比之下,接受CT和安慰剂治疗的患者(第2组)以及接受GH和安慰剂治疗的患者(第3组),其LS的BMD值显著下降(P<0.05)。第2组患者的F处BMD未显示任何显著变化,但第1组和第3组出现了显著下降(P<0.05)。三组中任何一组的DR处BMD与基线相比均未显示任何显著变化。在三个不同区域的骨量方面,三组之间未发现显著差异。
我们的研究表明,rhGH治疗可增加绝经后骨质疏松症女性的骨转换。rhGH与CT联合治疗24个月能够维持腰椎和桡骨远端的骨量,但会导致股骨干骨量下降;因此,它在绝经后骨质疏松症的治疗中似乎并非特别有效。