Patient Area Gastroenterology, Dermatovenerology and Rheumatology, Inflammation and Infection Theme Karolinska University Hospital, Stockholm, Sweden.
Unit of Internal Medicine, Institute Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Am J Gastroenterol. 2019 Feb;114(2):291-304. doi: 10.14309/ajg.0000000000000062.
Most studies on fractures in inflammatory bowel disease (IBD) are based on patients from tertiary centers or patients followed up before the introduction of immunomodulators or biologics. In addition, the role of corticosteroids in fracture risk has rarely been examined.
We conducted a nationwide population-based cohort study of 83,435 patients with incident IBD (ulcerative colitis [UC]: n = 50,162, Crohn's disease [CD]: n = 26,763, and IBD unclassified: 6,510) and 825,817 reference individuals from 1964 to 2014. Using multivariable Cox regression, we estimated hazard ratios (HRs) for hip fracture and any fracture and the association with cumulative corticosteroid exposure.
During 1,225,415 person-years of follow-up in patients with IBD, there were 2,491 first-time hip fractures (203/100,000 person-years) compared with 20,583 hip fractures during 12,405,642 person-years in reference individuals (159/100,000 person-years). This corresponded to an HR of 1.42 (95% confidence interval [CI] = 1.36-1.48). The risk for hip fracture was higher in CD compared with UC (P < 0.001). Inflammatory bowel disease was also associated with any fracture (IBD: HR = 1.18; 95% CI = 1.15-1.20). Hazard ratios for hip fracture had not changed since the introduction of immunomodulators or biologics. Increasing exposure to corticosteroids was associated with hip fracture in both IBD and non-IBD individuals (P < 0.001), but only in elderly (>60 years) patients with IBD. The association between IBD and hip fracture was nonsignificant among individuals without corticosteroids (HR = 1.11; 95% CI = 0.86-1.44).
Inflammatory bowel disease (CD and UC) is associated with an increased risk of hip fracture and any fracture, but not in individuals without a history of corticosteroid treatment. The association between corticosteroids and hip fracture was restricted to elderly patients with IBD.
大多数关于炎症性肠病(IBD)骨折的研究都是基于三级中心的患者或在使用免疫调节剂或生物制剂之前接受随访的患者。此外,皮质类固醇在骨折风险中的作用很少被研究。
我们进行了一项全国范围内基于人群的队列研究,纳入了 83435 例新发 IBD 患者(溃疡性结肠炎[UC]:n=50162,克罗恩病[CD]:n=26763,未分类 IBD:n=6510)和 825817 名参考个体(1964 年至 2014 年)。我们使用多变量 Cox 回归估计了髋部骨折和任何骨折的风险比(HR),并评估了与累积皮质类固醇暴露的关系。
在 IBD 患者的 1225415 人年随访期间,有 2491 例首次髋部骨折(203/100000 人年),而在参考个体的 12405642 人年随访期间,有 20583 例髋部骨折(159/100000 人年)。这相当于 HR 为 1.42(95%置信区间[CI]:1.36-1.48)。与 UC 相比,CD 患者髋部骨折风险更高(P<0.001)。IBD 也与任何骨折相关(IBD:HR=1.18;95%CI:1.15-1.20)。自免疫调节剂或生物制剂问世以来,髋部骨折的风险比没有改变。在 IBD 和非 IBD 个体中,皮质类固醇暴露量的增加与髋部骨折相关(P<0.001),但仅在老年(>60 岁)IBD 患者中。在没有皮质类固醇治疗的个体中,IBD 与髋部骨折之间的关联无统计学意义(HR=1.11;95%CI:0.86-1.44)。
IBD(CD 和 UC)与髋部骨折和任何骨折的风险增加相关,但与无皮质类固醇治疗史的个体无关。皮质类固醇与髋部骨折的关联仅限于老年 IBD 患者。