Card T, West J, Hubbard R, Logan R F A
Division of Epidemiology and Public Health, Queen's Medical Centre, University of Nottingham, Nottingham NG7 2UH, UK.
Gut. 2004 Feb;53(2):251-5. doi: 10.1136/gut.2003.026799.
Inflammatory bowel disease (IBD) is known to be associated with reduced bone density but the extent to which this results in an increased risk of fracture and the contribution of corticosteroid therapy are unclear. We have conducted a large cohort study to address these issues.
We selected subjects within the General Practice Research Database (GPRD) with a diagnosis of IBD and up to five matched controls for each patient. We derived dates of recorded hip fractures and also information on smoking, use of corticosteroids, and a number of other drugs. We calculated the absolute risk of fracture and the relative risk as a hazard ratio corrected for available confounders by Cox regression.
Seventy two hip fractures were recorded in 16 550 IBD cases and 223 in 82 917 controls. Cox modelling gave an unadjusted relative risk of hip fracture of 1.62 (95% confidence interval (CI) 1.24-2.11) for all IBD, 1.49 (1.04-2.15) for ulcerative colitis (UC) and 2.08 (1.36-3.18) for Crohn's disease (CD). Multivariate modelling showed that both current and cumulative use of corticosteroids and use of opioid analgesics confounded this relationship. After adjusting for confounding, the relative risk was 1.41 (0.94-2.11) for UC and 1.68 (1.01-2.78) for CD.
The risk of hip fracture is increased approximately 60% in IBD patients. Corticosteroid use is a contributor to this, both in the long term as previously recognised and also in an acute reversible manner. The majority of hip fracture risk in IBD patients however cannot be attributed to steroid use.
已知炎症性肠病(IBD)与骨密度降低有关,但这在多大程度上导致骨折风险增加以及皮质类固醇治疗的作用尚不清楚。我们进行了一项大型队列研究以解决这些问题。
我们在全科医学研究数据库(GPRD)中选择了诊断为IBD的受试者,并为每位患者匹配多达5名对照。我们获取了记录的髋部骨折日期以及吸烟、使用皮质类固醇和其他一些药物的信息。我们计算了骨折的绝对风险和相对风险,作为通过Cox回归校正了可用混杂因素的风险比。
在16550例IBD病例中记录了72例髋部骨折,在82917例对照中记录了223例。Cox模型显示,所有IBD患者髋部骨折的未调整相对风险为1.62(95%置信区间(CI)1.24 - 2.11),溃疡性结肠炎(UC)为1.49(1.04 - 2.15),克罗恩病(CD)为2.08(1.36 - 3.18)。多变量模型显示,当前和累积使用皮质类固醇以及使用阿片类镇痛药混淆了这种关系。调整混杂因素后,UC的相对风险为1.41(0.94 - 2.11),CD为1.68(1.01 - 2.78)。
IBD患者髋部骨折风险增加约60%。使用皮质类固醇是导致这一情况的一个因素,长期来看如之前所认识到的那样,并且在短期内也以一种急性可逆的方式起作用。然而,IBD患者髋部骨折的大部分风险不能归因于类固醇的使用。