Division of Endocrinology and Centre for Research in Anabolic Skeletal Targets in Health and Illness (ASTHI), CSIR-Central Drug Research Institute, Lucknow, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Front Endocrinol (Lausanne). 2023 Feb 2;14:1098841. doi: 10.3389/fendo.2023.1098841. eCollection 2023.
Primary hyperparathyroidism (PHPT) is characterized by increased bone remodeling and hypercalcemia. Parathyroidectomy (PTX), the current standard of care, is recommended in all symptomatic and some groups of asymptomatic patients. Anti-resorptive therapies (bisphosphonates and denosumab) have been used in patients where PTX is refused or contraindicated. In this meta-analysis, we investigated the effectiveness of anti-resorptives in preventing/treating PHPT-induced bone loss and mitigating hypercalcemia.
PubMed, Scopus, and Cochrane Library databases were searched for articles with keywords containing PHPT, bisphosphonates, and denosumab in various combinations. We extracted and tabulated areal BMD (aBMD), serum mineral, and bone turnover parameters from the qualified studies and used comprehensive meta-analysis software for analysis.
Of the 1,914 articles screened, 13 were eligible for meta-analysis. In the pooled analysis, 12 months of anti-resoptives (bisphosphonates and denosumab) therapy significantly increased aBMD at the lumbar spine (Standard difference in means (SDM)=0.447, 95% CI=0.230 to 0.664, p=0.0001), femoral neck (SDM=0.270, 95% CI=0.049 to 0.491, p=0.017) and increased serum PTH (SDM=0.489, 95% CI=0.139 to 0.839, p=0.006), and decreased serum calcium (SDM=-0.545, 95% CI=-0.937 to -0.154, p=0.006) compared with baseline. 12 months of bisphosphonate use significantly increased aBMD only at the lumbar spine (SDM=0.330, 95% CI=0.088 to 0.571, p=0.007) with a significant increased in serum PTH levels (SDM=0.546, 95% CI= 0.162 to 0.930, p=0.005), and a decreased in serum calcium (SDM=-0.608, 95% CI=-1.048 to -0.169, p=0.007) and bone-turnover markers (BTMs) compared with baseline. Denosumab use for 12 months significantly increased aBMD at both the lumbar spine (SDM=0.828, 95% CI=0.378 to 1.278, p=0.0001) and femur neck (SDM=0.575, 95% CI=0.135 to 1.015, p=0.010) compared with baseline. Mean lumbar spine aBMD (SDM=0.350, 95% CI=0.041 to 0.659, p=0.027) and serum PTH (SDM=0.602, 95% CI= 0.145 to 1.059, p=0.010) were significantly increased after 12 months of alendronate use compared with placebo. When compared with baseline, alendronate significantly decreased BTMs after 12 months and increased aBMD without altering the PTH and calcium levels after 24 months.
Anti-resorptives are effective in mitigating bone loss and hypercalcemia in PHPT while maintaining or increasing aBMD. PTX reversed all changes in PHPT and normalized PTH levels.
甲状旁腺功能亢进症(PHPT)的特征是骨重塑和高钙血症增加。甲状旁腺切除术(PTX)是目前所有有症状和部分无症状患者的标准治疗方法。在拒绝或禁忌 PTX 的情况下,抗吸收疗法(双膦酸盐和地舒单抗)已被用于治疗。在这项荟萃分析中,我们研究了抗吸收剂在预防/治疗 PHPT 引起的骨丢失和缓解高钙血症方面的有效性。
通过关键词搜索 PubMed、Scopus 和 Cochrane Library 数据库,搜索包含 PHPT、双膦酸盐和地舒单抗的文章。我们从合格的研究中提取和列出了面积骨密度(aBMD)、血清矿物质和骨转换参数,并使用综合荟萃分析软件进行分析。
在筛选出的 1914 篇文章中,有 13 篇符合荟萃分析的条件。在荟萃分析中,12 个月的抗吸收剂(双膦酸盐和地舒单抗)治疗显著增加了腰椎(标准均数差(SDM)=0.447,95%置信区间(CI)=0.230 至 0.664,p=0.0001)、股骨颈(SDM=0.270,95%CI=0.049 至 0.491,p=0.017)的 aBMD,血清甲状旁腺激素(PTH)水平(SDM=0.489,95%CI=0.139 至 0.839,p=0.006),并降低了血清钙(SDM=-0.545,95%CI=-0.937 至-0.154,p=0.006)与基线相比。使用双膦酸盐 12 个月显著增加了腰椎的 aBMD(SDM=0.330,95%CI=0.088 至 0.571,p=0.007),同时显著增加了血清 PTH 水平(SDM=0.546,95%CI=0.162 至 0.930,p=0.005),并降低了血清钙(SDM=-0.608,95%CI=-1.048 至-0.169,p=0.007)和骨转换标志物(BTMs)与基线相比。使用地舒单抗 12 个月显著增加了腰椎(SDM=0.828,95%CI=0.378 至 1.278,p=0.0001)和股骨颈(SDM=0.575,95%CI=0.135 至 1.015,p=0.010)的 aBMD与基线相比。与安慰剂相比,使用阿伦膦酸钠 12 个月后,腰椎的平均 aBMD(SDM=0.350,95%CI=0.041 至 0.659,p=0.027)和血清 PTH(SDM=0.602,95%CI=0.145 至 1.059,p=0.010)显著增加。与基线相比,阿伦膦酸钠在 12 个月后显著降低了 BTMs,增加了 aBMD,而在 24 个月后没有改变 PTH 和钙水平。
抗吸收剂在缓解 PHPT 引起的骨丢失和高钙血症的同时,维持或增加 aBMD。PTX 逆转了 PHPT 的所有变化,并使 PTH 水平正常化。