Anastasilakis A D, Goulis D G, Polyzos S A, Gerou S, Koukoulis G N, Efstathiadou Z, Kita M, Avramidis A
Department of Endocrinology, Hippocration General Hospital, Thessaloniki, Greece.
Int J Clin Pract. 2008 Jun;62(6):919-24. doi: 10.1111/j.1742-1241.2008.01768.x. Epub 2008 Apr 17.
We aimed to compare the effect of risedronate (RIS) and teriparatide (TPTD) (recombinant human parathyroid hormone 1-34) on bone turnover markers in women with postmenopausal osteoporosis.
Forty-four Caucasian women (age 65.1 +/- 1.6 years) with postmenopausal osteoporosis were randomly assigned to receive either RIS 35 mg once weekly (n = 22) or TPTD 20 microg once daily (n = 22) for 12 months. Serum N-terminal propeptide of type 1 collagen (P1NP), C-terminal telopeptide of type 1 collagen (CTx), total alkaline phosphatase (ALP) and intact parathyroid hormone (iPTH) were obtained from all women before, 3 and 6 months after treatment initiation. Lumbar spine bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry before and 12 months after treatment initiation.
P1NP, CTx and total ALP levels decreased in RIS group (p < 0.001) and increased in TPTD group (p < 0.001) throughout the treatment. iPTH increased significantly in RIS group (p < 0.05) and decreased in TPTD group (p < 0.001). Finally, lumbar spine BMD increased significantly in both RIS (p = 0.003) and TPTD groups (p < 0.001) without significant differences between them.
Our data suggest that both serum P1NP and CTx are reliable markers of RIS and TPTD action in women with postmenopausal osteoporosis. In a similar way, serum total ALP can be used as an alternative marker for monitoring both RIS and TPTD action, while iPTH can be used only for TPTD-treated women. The increase in P1NP and CTx after 3 months of treatment with RIS or TPTD can predict the increase in BMD after 12 months of treatment.
我们旨在比较利塞膦酸盐(RIS)和特立帕肽(TPTD)(重组人甲状旁腺激素1 - 34)对绝经后骨质疏松症女性骨转换标志物的影响。
44名绝经后骨质疏松症的白种女性(年龄65.1±1.6岁)被随机分配,分别接受每周一次35毫克的RIS(n = 22)或每日一次20微克的TPTD(n = 22),为期12个月。在所有女性开始治疗前、治疗开始后3个月和6个月时,检测血清1型胶原N端前肽(P1NP)、1型胶原C端末肽(CTx)、总碱性磷酸酶(ALP)和完整甲状旁腺激素(iPTH)。在治疗开始前和治疗开始后12个月,通过双能X线吸收法测量腰椎骨密度(BMD)。
在整个治疗过程中,RIS组的P1NP、CTx和总ALP水平下降(p < 0.001),而TPTD组升高(p < 0.001)。RIS组的iPTH显著升高(p < 0.05),TPTD组降低(p < 0.001)。最后,RIS组(p = 0.003)和TPTD组(p < 0.001)的腰椎BMD均显著增加,且两组之间无显著差异。
我们的数据表明,血清P1NP和CTx都是绝经后骨质疏松症女性中RIS和TPTD作用的可靠标志物。同样,血清总ALP可作为监测RIS和TPTD作用的替代标志物,而iPTH仅可用于接受TPTD治疗的女性。用RIS或TPTD治疗3个月后P1NP和CTx的升高可预测治疗12个月后BMD的增加。