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Risk factor assessment for the development of osteoradionecrosis.放射性骨坏死发生的危险因素评估。
J Oral Maxillofac Surg. 2007 Nov;65(11):2311-6. doi: 10.1016/j.joms.2007.05.021.
2
Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis.每年一次唑来膦酸用于治疗绝经后骨质疏松症。
N Engl J Med. 2007 May 3;356(18):1809-22. doi: 10.1056/NEJMoa067312.
3
Smoking and oral health status.吸烟与口腔健康状况。
J Can Dent Assoc. 2007 Mar;73(2):155.
4
Incidence, risk factors and management of osteonecrosis of the jaw in patients with multiple myeloma: a single-centre experience in 303 patients.多发性骨髓瘤患者颌骨骨坏死的发病率、危险因素及管理:303例患者的单中心经验
Br J Haematol. 2006 Sep;134(6):620-3. doi: 10.1111/j.1365-2141.2006.06230.x. Epub 2006 Aug 1.
5
Bisphosphonates are associated with increased risk for jaw surgery in medical claims data: is it osteonecrosis?在医疗理赔数据中,双膦酸盐类药物与颌骨手术风险增加相关:这是骨坏死吗?
J Oral Maxillofac Surg. 2006 Jun;64(6):917-23. doi: 10.1016/j.joms.2006.02.011.
6
Bisphosphonate-induced avascular osteonecrosis of the jaws: a clinical report of 11 cases.双膦酸盐所致颌骨无血管性骨坏死:11例临床报告
Int J Oral Maxillofac Surg. 2006 Jul;35(7):588-93. doi: 10.1016/j.ijom.2006.02.022. Epub 2006 May 9.
7
Osteonecrosis of the jaw in multiple myeloma patients: clinical features and risk factors.多发性骨髓瘤患者颌骨骨坏死:临床特征与危险因素
J Clin Oncol. 2006 Feb 20;24(6):945-52. doi: 10.1200/JCO.2005.04.2465.
8
Osteonecrosis of the jaw in cancer after treatment with bisphosphonates: incidence and risk factors.双膦酸盐治疗后癌症患者颌骨骨坏死:发病率及危险因素
J Clin Oncol. 2005 Dec 1;23(34):8580-7. doi: 10.1200/JCO.2005.02.8670.
9
Zoledronic-acid-induced circulating level modifications of angiogenic factors, metalloproteinases and proinflammatory cytokines in metastatic breast cancer patients.唑来膦酸对转移性乳腺癌患者血管生成因子、金属蛋白酶和促炎细胞因子循环水平的影响
Oncology. 2005;69(1):35-43. doi: 10.1159/000087286. Epub 2005 Aug 2.
10
Osteonecrosis: death of bone cells.
Orthop Nurs. 2005 Jul-Aug;24(4):295-301; quiz 302-3. doi: 10.1097/00006416-200507000-00012.

唑来膦酸、吸烟和肥胖是颌骨坏死的强烈危险因素:一项病例对照研究。

Zoledronate, smoking, and obesity are strong risk factors for osteonecrosis of the jaw: a case-control study.

作者信息

Wessel John H, Dodson Thomas B, Zavras Athanasios I

机构信息

Harvard School of Dental Medicine, Boston, MA 02115, USA.

出版信息

J Oral Maxillofac Surg. 2008 Apr;66(4):625-31. doi: 10.1016/j.joms.2007.11.032.

DOI:10.1016/j.joms.2007.11.032
PMID:18355585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2435366/
Abstract

PURPOSE

Bisphosphonates (BPs) effectively treat metastatic bone disease, hypercalcemia, and osteoporosis. BP exposure, however, may be associated with osteonecrosis of the jaw (ONJ). The aim of the present study was to estimate the magnitude of the association between intravenous (IV) BP exposure and ONJ, and to identify potential confounders.

MATERIALS AND METHODS

Using a case-control study design, the investigators identified and adjudicated a sample of cases with ONJ and matched them randomly with 5 controls per case. The controls were matched to cases on age, gender, cancer type, and date of cancer diagnosis. The medical records were abstracted and data on BP exposure, cancer therapy, and comorbidities were recorded. Statistical analyses were carried out using conditional logistic regression in Stata 9.0 (Stata Corp, College Station, TX).

RESULTS

Thirty cases of ONJ were identified at Massachusetts General Hospital from February 2003 through February 2007. Zoledronate was found to confer significant risk toward development of ONJ (adjusted odds ratio = 31.8, P < .05). Although a trend toward increased risk was noted for pamidronate, this association was not significant after controlling for zoledronate. Obesity and smoking were associated significantly with ONJ development, whereas oral BPs had no effect.

CONCLUSION

In this study, cancer patients who had received zoledronate exhibited a significant 30-fold increase in their risk to develop ONJ. More studies are needed to elucidate the exact role of obesity and smoking in the development of ONJ, and the complex interactions of IV BPs with other chemotherapies during cancer treatment.

摘要

目的

双膦酸盐(BPs)可有效治疗转移性骨病、高钙血症和骨质疏松症。然而,接触双膦酸盐可能与颌骨坏死(ONJ)有关。本研究的目的是评估静脉注射(IV)双膦酸盐暴露与颌骨坏死之间关联的程度,并确定潜在的混杂因素。

材料与方法

采用病例对照研究设计,研究人员识别并判定了一组颌骨坏死病例样本,并为每个病例随机匹配5名对照。对照在年龄、性别、癌症类型和癌症诊断日期方面与病例进行匹配。提取病历并记录有关双膦酸盐暴露、癌症治疗和合并症的数据。使用Stata 9.0(Stata公司,德克萨斯州大学城)中的条件逻辑回归进行统计分析。

结果

2003年2月至2007年2月期间,在马萨诸塞州总医院共识别出30例颌骨坏死病例。发现唑来膦酸会显著增加发生颌骨坏死的风险(调整后的优势比 = 31.8,P < 0.05)。尽管帕米膦酸有增加风险的趋势,但在控制唑来膦酸后,这种关联并不显著。肥胖和吸烟与颌骨坏死的发生显著相关,而口服双膦酸盐则无影响。

结论

在本研究中,接受唑来膦酸治疗的癌症患者发生颌骨坏死的风险显著增加了30倍。需要更多研究来阐明肥胖和吸烟在颌骨坏死发生中的确切作用,以及静脉注射双膦酸盐在癌症治疗期间与其他化疗药物的复杂相互作用。