Southeast Louisiana Veterans Health Care System, Section of Gastroenterology and Hepatology, Tulane University Health Sciences Center, New Orleans, Louisiana 70112, USA.
J Clin Endocrinol Metab. 2013 Jun;98(6):2368-75. doi: 10.1210/jc.2013-1332. Epub 2013 Apr 17.
Low bone mineral density (BMD) is common in patients with inflammatory bowel diseases.
The objective of the study was to assess the prevalence and the predictors of low BMD (osteoporosis or osteopenia) and fragility fractures among men with ulcerative colitis.
This was a retrospective database analysis.
The study was conducted at a nationwide Veterans Affairs health care system.
Male ulcerative colitis patients who were followed up in the Veterans Affairs system between 2001 and 2011 were identified using the International Classification of Diseases, ninth revision (ICD-9).
We identified patients with low BMD and fragility fractures using ICD-9 codes. Steroid exposure was assessed using pharmacy data. A multivariate analysis was used to identify the independent effect of systemic steroids on the risk of low BMD and fragility fractures.
We identified 34 665 patients. Among them, 31% used steroids. The prevalence of low BMD was 15.8% and 7.1% among those who used and did not use steroids, respectively (P < .001). Prevalence of fragility fractures was 7.9%, 4.4%, and 1.1% for those with osteoporosis and osteopenia and those without low BMD, respectively (P < .001). Steroid exposure showed a dose-response pattern, patients who had cumulative prednisone exposure of greater than 11 136 mg (10th decile) were more likely to develop low BMD (odds ratio 8.9, P < .001) and fragility fractures (odds ratio 1.8, P < .001) as compared with non-steroid users after controlling for other possible predictors.
In this nationwide cohort, the prevalence of low BMD was higher than what was reported for the general male population. There was a strong correlation between the cumulative steroid use and the risk of low BMD. Both steroids and low BMD were independent risk factors for fragility fractures.
患有炎症性肠病的患者通常存在低骨密度(BMD)。
本研究旨在评估溃疡性结肠炎男性患者中低 BMD(骨质疏松症或骨量减少)和脆性骨折的患病率和预测因素。
这是一项回顾性数据库分析。
本研究在全国退伍军人事务部医疗保健系统中进行。
通过使用国际疾病分类第 9 版(ICD-9),确定了 2001 年至 2011 年期间在退伍军人事务系统中接受随访的溃疡性结肠炎男性患者。
我们使用 ICD-9 代码确定低 BMD 和脆性骨折患者。使用药房数据评估类固醇暴露情况。使用多元分析确定全身类固醇对低 BMD 和脆性骨折风险的独立影响。
我们确定了 34665 名患者。其中,31%的患者使用了类固醇。使用和未使用类固醇的患者中低 BMD 的患病率分别为 15.8%和 7.1%(P <.001)。骨质疏松症和骨量减少以及无低 BMD 的患者中脆性骨折的患病率分别为 7.9%、4.4%和 1.1%(P <.001)。类固醇暴露呈剂量反应模式,与未使用类固醇的患者相比,累积泼尼松暴露量大于 11136mg(第 10 百分位数)的患者更有可能发生低 BMD(比值比 8.9,P <.001)和脆性骨折(比值比 1.8,P <.001),在控制其他可能的预测因素后。
在这项全国性队列研究中,低 BMD 的患病率高于一般男性人群的报告。累积类固醇使用与低 BMD 风险之间存在很强的相关性。类固醇和低 BMD 都是脆性骨折的独立危险因素。