Legovini P, De Menis E, Breda F, Billeci D, Carteri A, Pavan P, Conte N
Divisione Medica, Ospedale Regionale, Treviso, Italy.
J Endocrinol Invest. 1997 Sep;20(8):434-8. doi: 10.1007/BF03347998.
The effects of octreotide on biochemical markers of bone turnover were evaluated in patients with active acromegaly. Serum GH, IGF-I and serum and urinary markers of bone metabolism were measured before and after 4 months of treatment in 27 patients (short-term treatment) and after 12 and 24 months of treatment in 15 patients (long-term treatment). In the short-term, octreotide significantly decreased the levels of serum GH, IGF-I, calcium, osteocalcin, carboxyterminal propeptide of type I collagen and alkaline phosphatase plus urinary excretion of calcium. Short-term treatment significantly increased serum parathormone levels (before treatment 30.1 +/- 9.57 and at 4 months 46.1 +/- 24.98 ng/L, p < 0.001) and urinary excretion of phosphate; urinary excretion of hydroxyproline was unchanged. The same results were observed during long-term treatment, except that there was no significant difference of serum calcium and alkaline phosphatase levels before and after treatment. Parathormone concentrations were still higher at 24 months compared with those prior to treatment (before treatment 31.9 +/- 9.74 and at 24 months 44.9 +/- 21.18 ng/L, p < 0.05). The changes of most bone markers during octreotide therapy can be explained by the decrease of serum GH and IGF-I concentrations. On the other hand, the rise of parathormone concentrations suggests that octreotide has ulterior and long-standing actions on calcium homeostasis: intestinal malabsorption of calcium due to the octreotide could contribute to this secondary hyperparathyroidism. The clinical consequences of these alterations of bone metabolism need to be further clarified.
在活动性肢端肥大症患者中评估了奥曲肽对骨转换生化标志物的影响。对27例患者进行了4个月治疗前和治疗后的血清GH、IGF-I以及血清和尿液骨代谢标志物测量(短期治疗),对15例患者进行了12个月和24个月治疗前和治疗后的测量(长期治疗)。在短期内,奥曲肽显著降低了血清GH、IGF-I、钙、骨钙素、I型胶原羧基末端前肽和碱性磷酸酶水平以及尿钙排泄。短期治疗显著提高了血清甲状旁腺激素水平(治疗前30.1±9.57,4个月时46.1±24.98 ng/L,p<0.001)和尿磷排泄;羟脯氨酸尿排泄未改变。长期治疗期间观察到相同结果,但治疗前后血清钙和碱性磷酸酶水平无显著差异。与治疗前相比,24个月时甲状旁腺激素浓度仍较高(治疗前31.9±9.74,24个月时44.9±21.18 ng/L,p<0.05)。奥曲肽治疗期间大多数骨标志物的变化可以用血清GH和IGF-I浓度降低来解释。另一方面,甲状旁腺激素浓度升高表明奥曲肽对钙稳态有潜在的长期作用:奥曲肽导致的肠道钙吸收不良可能导致这种继发性甲状旁腺功能亢进。这些骨代谢改变的临床后果需要进一步阐明。