Risk factors for osteonecrosis of the jaw in patients with chronic kidney disease: a nested case-control study.

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Ken Iseri, Noriko Hida
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Abstract

Osteonecrosis of the jaw (ONJ) is a severe disease leading to decreased quality of life, but risk factors for ONJ in chronic kidney disease (CKD) patients remain unclear. We conducted a nested case-control study using a large Japanese administrative database to investigate. CKD patients were identified based on estimated glomerular filtration rate (eGFR) measurements, and ONJ cases were identified using ICD-10 codes and diagnostic terms. Controls were matched 1:4 by age and sex. Among 597 026 CKD patients, 75 ONJ cases were identified during a median follow-up of 2.9 yr (incidence rate: 3.27 per 100 000 patient-years). A total of 375 patients (250 males, 66.7%) with a median age of 72 yr (interquartile range (IQR), 64-78) were included after matching controls. The use of bisphosphonates and denosumab for tumor-related disorders in the case group was significantly higher compared to the control group. There was no significant association between kidney functions and the ONJ risk. Multivariate analysis revealed that anti-resorptive drugs for tumor-related disorders [odds ratio (OR): 74.74, 95% confidence interval (CI): 8.81-634.39, p<.001] and oral corticosteroids (OR: 13.23, 95% CI: 3.34-52.33, p<.001) were significantly associated with increased ONJ risk, while anti-resorptive drugs for osteoporosis and injectable corticosteroid use were not. Other relevant factors such as diabetes, liver disease, anabolic drugs, and radiation therapy did not have a significant association with ONJ risk. When stratified by indications for bisphosphonate use (known to be eliminated by renal excretion), bisphosphonate use for tumor-related disorders showed a significant association with ONJ risk (OR: 27.80, 95% CI: 2.47-313.29, p<.01), while bisphosphonates use for osteoporosis did not (OR: 0.74, 95% CI: 0.19-2.92, p=.67). These findings suggest that anti-resorptive drugs for tumor-related disorders and oral corticosteroids are associated with ONJ risk in CKD patients. Heightened surveillance may be necessary for CKD patients receiving these treatments to prevent or detect ONJ early.

慢性肾病患者颌骨坏死的风险因素:一项嵌套病例对照研究。
颌骨坏死(ONJ)是一种导致生活质量下降的严重疾病,但慢性肾脏病(CKD)患者颌骨坏死的风险因素仍不清楚。我们利用日本的大型行政数据库进行了一项巢式病例对照研究。我们根据估算的肾小球滤过率(eGFR)测量结果确定了 CKD 患者,并使用 ICD-10 编码和诊断术语确定了 ONJ 病例。对照组按年龄和性别1:4配对。在 597 026 名慢性肾脏病患者中,在中位 2.9 年的随访期间发现了 75 例 ONJ(发病率:每 10 万患者年 3.27 例)。在匹配对照组后,共纳入了 375 名患者(250 名男性,66.7%),中位年龄为 72 岁(IQR,64-78 岁)。与对照组相比,病例组患者因肿瘤相关疾病而使用双膦酸盐和地诺单抗的比例明显较高。肾功能与 ONJ 风险之间无明显关联。多变量分析显示,肿瘤相关疾病的抗骨质吸收药物(OR:74.74,95% CI:8.81-634.39,P
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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