Rizzoli R, Thiébaud D, Bundred N, Pecherstorfer M, Herrmann Z, Huss H J, Rückert F, Manegold C, Tubiana-Hulin M, Steinhauer E U, Degardin M, Thürlimann B, Clemens M R, Eghbali H, Body J J
World Health Organization Collaborating Center for Osteoporosis and Bone Diseases, Department of Internal Medicine, University Hospital, Geneva, Switzerland.
J Clin Endocrinol Metab. 1999 Oct;84(10):3545-50. doi: 10.1210/jcem.84.10.6026.
The pathogenesis of hypercalcemia of malignancy comprises increased net bone resorption and enhanced renal tubular reabsorption of calcium (Ca). To evaluate the prevalence of an increased renal tubular reabsorption of Ca index [tubular reabsorption of calcium index (TRCaI)] in cancer patients with hypercalcemia and of elevated circulating levels of PTH-related protein (PTHrP), which is recognized as a major mediator of this syndrome, we investigated 315 well rehydrated patients, aged 58.1 +/- 0.7 yr (mean +/- SEM), with hypercalcemia [albumin-corrected plasma Ca (pCa), >2.7 mmol/L] secondary to histologically proven malignancy. Changes in pCa and, therefore, various Ca filtered loads were obtained by different degrees of bone resorption inhibition achieved with a single infusion of the bisphosphonate ibandronate, given at various doses on a randomized, double blind basis. PTHrP was determined at baseline in 147 of the patients and 7 days after bisphosphonate therapy in 73. Before ibandronate therapy, pCa was 3.36 +/- 0.02 mmol/L, mean TRCaI was increased at 3.09 +/- 0.03 mmol/L glomerular filtration rate (GFR; normal, 2.40-2.90), and 65% of patients had TRCaI above 2.90 mmol/L GFR. Mean serum PTHrP levels were 4.9 +/- 0.5 pmol/L (normal, <2.5) and values above the normal range were found in 53% of the patients (76% in lung and upper respiratory tract malignancies). By 7 days after the infusion of ibandronate, a decrease in pCa of 0.69 +/- 0.03 mmol/L (20.0 +/- 0.7%; P < 0.001) and in bone resorption [mean change in fasting urinary Ca, 0.09 +/- 0.04 mmol/L GFR (47.6 +/- 8.6%; P < 0.001) and 14.4 +/- 1.7 nmol/mmol (27.6 +/- 10.6%; P < 0.01) in deoxypyridinoline] was observed. TRCaI was slightly lowered by 0.30 +/- 0.09 mmol/L GFR. Mean changes in PTHrP, 1,25-dihydroxyvitamin D3, and PTH were +0.7 +/- 0.4 (P = NS), +27.6 +/- 3.0 (P < 0.001), and +2.9 +/- 0.8 (P < 0.005) pmol/L, respectively. After ibandronate treatment, the relative risk of relapsing hypercalcemia was particularly increased (3.43-fold) in lung and upper respiratory tract malignancies. These results obtained in a large cohort of patients indicate a significant prevalence of an increased renal tubular reabsorption of calcium index in hypercalcemia of malignancy and a substantial proportion of patients with detectable PTHrP.
恶性肿瘤高钙血症的发病机制包括净骨吸收增加和肾小管对钙(Ca)的重吸收增强。为评估高钙血症癌症患者中肾小管钙重吸收指数[肾小管钙重吸收指数(TRCaI)]升高以及循环中甲状旁腺激素相关蛋白(PTHrP)水平升高(该蛋白被认为是此综合征的主要介质)的发生率,我们研究了315例水化良好、年龄为58.1±0.7岁(均值±标准误)、因组织学证实的恶性肿瘤继发高钙血症[白蛋白校正血浆钙(pCa),>2.7 mmol/L]的患者。通过单次静脉输注不同剂量的双膦酸盐伊班膦酸钠,以随机、双盲方式实现不同程度的骨吸收抑制,从而获得pCa的变化以及相应的各种钙滤过负荷。在147例患者中于基线时测定PTHrP,73例患者在双膦酸盐治疗7天后测定。在伊班膦酸钠治疗前,pCa为3.36±0.02 mmol/L,平均TRCaI在肾小球滤过率(GFR;正常范围为2.40 - 2.90)为3.09±0.03 mmol/L时升高,65%的患者TRCaI高于2.90 mmol/L GFR。血清PTHrP平均水平为4.9±0.5 pmol/L(正常范围,<2.5),53%的患者值高于正常范围(肺和上呼吸道恶性肿瘤患者中为76%)。在输注伊班膦酸钠7天后,pCa降低了0.69±0.03 mmol/L(20.0±0.7%;P<0.001),骨吸收降低[空腹尿钙平均变化,在脱氧吡啶啉中为0.09±0.04 mmol/L GFR(47.6±8.6%;P<0.001)和14.4±1.7 nmol/mmol(27.6±10.6%;P<0.01)]。TRCaI略有降低,降低了0.30±0.09 mmol/L GFR。PTHrP、1,25 - 二羟维生素D3和PTH的平均变化分别为+0.7±0.4(P = 无显著性差异)、+27.6±3.0(P<0.001)和+2.9±0.8(P<0.005)pmol/L。伊班膦酸钠治疗后,肺和上呼吸道恶性肿瘤患者复发高钙血症的相对风险尤其增加(3.43倍)。在一大群患者中获得的这些结果表明,恶性肿瘤高钙血症患者中肾小管钙重吸收指数升高的发生率很高,且相当比例的患者可检测到PTHrP。