Di Somma C, Colao A, Pivonello R, Klain M, Faggiano A, Tripodi F S, Merola B, Salvatore M, Lombardi G
Department of Molecular and Clinical Endocrinology, Federico II University of Naples, Italy.
Clin Endocrinol (Oxf). 1998 May;48(5):655-62. doi: 10.1046/j.1365-2265.1998.00486.x.
Osteoporosis is common in patients with Cushing's disease and is likely due to an imbalance between bone formation and resorption. Alendronate is an aminobisphosphonate that is able to increase bone mass mainly by inhibiting bone resorption.
We have evaluated the effect of chronic treatment with alendronate on bone mineral density (BMD) in patients with Cushing's disease.
39 patients with Cushing's disease entered this study. 39 age-, sex- and BMI-matched normals served as controls for baseline evaluation. The 39 patients were divided into four groups: 1) 10 patients with active disease treated with alendronate and ketoconazole; 2) 11 patients with inactive disease treated with alendronate; 3) 8 patients with active disease treated with ketoconazole alone, 4) 10 patients with inactive disease received no treatment.
Alendronate was given for 12 months in a dose of 10 mg orally once daily after fasting at 0800 h in the morning. Ketoconazole was given in a dose of 200-600 mg orally daily, when pituitary surgery was unsuccessful.
Lumbar spine (L1-L4) and femoral neck BMD, serum osteocalcin (OC), urinary cross-linked N-telopeptides of type I collagen (Ntx) levels were evaluated at study entry, in patients and controls, and were repeated after 6 and 12 months in the 39 patients.
BMD values were lower in patients with Cushing's disease than in controls at both L1-L4 (0.72 +/- 0.4 vs. 1.01 +/- 0.6 g/cm2, P < 0.05) and femoral neck (0.69 +/- 0.3 vs. 0.96 +/- 0.6 g/cm2, P < 0.05). In the 39 patients with Cushing's disease considered as a whole, serum OC levels were lower (1.1 +/- 0.1 vs 1.5 +/- 0.1 nmol/l, P < 0.01), while Ntx values were higher than in controls (168 +/- 25 vs. 61 +/- 31 nmol BCE/mmol creatinine, P < 0.01). In the alendronate-treated groups, serum OC levels increased, while Ntx levels significantly decreased after 6 and 12 months of treatment without any significant difference between the two groups. BMD values measured at L1-L4 and femoral neck significantly increased after 12 months of therapy. In patients of group 4, a significant increase of serum OC levels and a significant decrease of Ntx levels were observed together with a slight increase of BMD values after 12 months. No significant change in either biochemical markers or BMD values was found in patients of group 3.
Patients with Cushing's disease have osteoporosis which needs to be rapidly reversed to limit the risk of fracture. The results of the present study show that a 12 month treatment period with alendronate induced an improvement in bone mineral density greater than in untreated patients.
骨质疏松症在库欣病患者中很常见,可能是由于骨形成与骨吸收之间的失衡所致。阿仑膦酸钠是一种氨基双膦酸盐,主要通过抑制骨吸收来增加骨量。
我们评估了阿仑膦酸钠长期治疗对库欣病患者骨密度(BMD)的影响。
39例库欣病患者进入本研究。39名年龄、性别和体重指数相匹配的正常人作为基线评估的对照。39例患者分为四组:1)10例活动性疾病患者接受阿仑膦酸钠和酮康唑治疗;2)11例非活动性疾病患者接受阿仑膦酸钠治疗;3)8例活动性疾病患者仅接受酮康唑治疗;4)10例非活动性疾病患者未接受治疗。
阿仑膦酸钠以10mg的剂量口服,每天一次,于早上8点空腹后服用,持续12个月。当垂体手术不成功时,酮康唑以200 - 600mg的剂量口服,每日一次。
在研究开始时,对患者和对照评估腰椎(L1 - L4)和股骨颈的骨密度、血清骨钙素(OC)、尿I型胶原交联N - 端肽(Ntx)水平,并在39例患者中于6个月和12个月后重复评估。
库欣病患者在L1 - L4(0.72±0.4 vs. 1.01±0.6g/cm²,P < 0.05)和股骨颈(0.69±0.3 vs. 0.96±0.6g/cm²,P < 0.05)的骨密度值均低于对照组。总体而言,39例库欣病患者的血清OC水平较低(1.1±0.1 vs 1.5±0.1nmol/l,P < 0.01),而Ntx值高于对照组(168±25 vs. 61±31nmol BCE/mmol肌酐,P < 0.01)。在阿仑膦酸钠治疗组中,血清OC水平升高,而治疗6个月和12个月后Ntx水平显著降低,两组之间无显著差异。治疗12个月后,L1 - L4和股骨颈处测量的骨密度值显著增加。在第4组患者中,12个月后观察到血清OC水平显著升高、Ntx水平显著降低以及骨密度值略有增加。第3组患者的生化标志物或骨密度值均未发现显著变化。
库欣病患者患有骨质疏松症,需要迅速纠正以降低骨折风险。本研究结果表明,阿仑膦酸钠12个月的治疗期可使骨密度改善程度大于未治疗患者。