1例59岁女性减肥手术后,Denosumab注射治疗骨质疏松导致严重维生素D缺乏和严重低钙血症

J. Beal, Soemiwati W Holland, Krishna Chalasani, M. A. Hossain
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引用次数: 0

摘要

Denosumab是一种人单克隆抗体,结合核因子κ b配体受体激活因子(RANKL),抑制RANKL与RANK在破骨细胞表面的相互作用,阻止破骨细胞形成,导致骨吸收减少,骨量增加[1]。骨质疏松症的特点是骨量低、微结构破坏和骨骼脆弱性增加。在Rouxen-Y胃旁路手术的患者中很常见,由于其主要吸收点在十二指肠和近空肠的相对旁路,导致足够钙吸收所需的胃酸水平降低,维生素D减少[2,3]。Denosumab是胃旁路手术患者治疗骨质疏松症的合理选择,因为口服双膦酸盐[4]存在肠道吸收不良和吻合口溃疡风险。denosumab的一种罕见但可能致命的不良反应是严重的低钙血症和维生素D缺乏症,由于其半衰期长,通常会延长,因此在许多情况下难以治疗。我们提出了一个病例地单抗诱导严重低钙血症患者的胃旁路史,也被发现有急性严重维生素缺乏症D,尽管治疗后补充维生素D。因此,我们假设denosumab与高风险患者急性严重维生素D缺乏症之间存在潜在的因果关系,特别是肠道吸收不良和由此导致的维生素D缺乏症。
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A 59-year-old Female Post Bariatric Surgery with Severe Vitamin D Deficiency and Severe Hypocalcemia Induced by Denosumab Injection for Osteoporosis
Denosumab is a human monoclonal antibody that binds receptor activator of nuclear factor kappa-B ligand (RANKL) and inhibits interaction between RANKL and RANK on the surface of osteoclasts, which prevents osteoclast formation and causes decreased bone resorption and increased bone mass [1]. Osteoporosis is characterized by low bone mass, microarchitectural disruption, and increased skeletal fragility. It is common in those who have undergone Rouxen-Y gastric bypass surgery, which causes reduced gastric acid levels necessary for adequate calcium absorption and decreased vitamin D due to relative bypass of its primary absorption points in the duodenum and proximal jejunum [2,3]. Denosumab is a reasonable option for osteoporosis treatment in patients with gastric bypass surgery due to intestinal malabsorption and risk of anastomotic ulceration with oral bisphosphonates [4]. A rare yet potentially fatal adverse effect of denosumab is severe hypocalcemia and Vitamin D deficiency, which is often prolonged secondary to its long half-life and therefore difficult to treat in many cases [5]. We present a case of denosumab-induced severe hypocalcemia in a patient with history of gastric bypass who also was found to have acute severe hypovitaminosis D despite post-treatment vitamin D supplementation. Thus we hypothesize a potentially causal relationship between denosumab and acute severe vitamin D deficiency in high-risk patients, specifically with intestinal malabsorption and resultant predisposition to becoming vitamin D deficient.
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