Freedberg D E, Haynes K, Denburg M R, Zemel B S, Leonard M B, Abrams J A, Yang Y-X
Division of Digestive and Liver Diseases, Columbia University Medical Center, 630 West 168th Street, PH-7, New York, NY, 10032, USA.
Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Osteoporos Int. 2015 Oct;26(10):2501-7. doi: 10.1007/s00198-015-3168-0. Epub 2015 May 19.
Proton pump inhibitors (PPIs) are associated with risk for fracture in osteoporotic adults. In this population-based study, we found a significant association between PPIs and fracture in young adults, with evidence of a dose-response effect. Young adults who use PPIs should be cautioned regarding risk for fracture.
Proton pump inhibitors (PPIs) are associated with fracture in adults with osteoporosis. Because PPI therapy may interfere with bone accrual and attainment of peak bone mineral density, we studied the association between use of PPIs and fracture in children and young adults.
We conducted a population-based, case-control study nested within records from general medical practices from 1994 to 2013. Participants were 4-29 years old with ≥ 1 year of follow-up who lacked chronic conditions associated with use of long-term acid suppression. Cases of fracture were defined as the first incident fracture at any site. Using incidence density sampling, cases were matched with up to five controls by age, sex, medical practice, and start of follow-up. PPI exposure was defined as 180 or more cumulative doses of PPIs. Conditional logistic regression was used to estimate the odds ratio and confidence interval for use of PPIs and fracture.
We identified 124,799 cases and 605,643 controls. The adjusted odds ratio for the risk of fracture associated with PPI exposure was 1.13 (95% CI 0.92 to 1.39) among children aged < 18 years old and 1.39 (95% CI 1.26 to 1.53) among young adults aged 18-29 years old. In young adults but not children, we observed a dose-response effect with increased total exposure to PPIs (p for trend <0.001).
PPI use was associated with fracture in young adults, but overall evidence did not support a PPI-fracture relationship in children. Young adults who use PPIs should be cautioned regarding potentially increased risk for fracture, even if they lack traditional fracture risk factors.
质子泵抑制剂(PPIs)与骨质疏松成年人的骨折风险相关。在这项基于人群的研究中,我们发现PPIs与年轻人骨折之间存在显著关联,并有剂量反应效应的证据。使用PPIs的年轻人应被告知骨折风险。
质子泵抑制剂(PPIs)与骨质疏松成年人的骨折相关。由于PPI治疗可能会干扰骨量积累和峰值骨密度的获得,我们研究了PPIs使用与儿童和年轻人骨折之间的关联。
我们在1994年至2013年普通医疗实践记录中进行了一项基于人群的病例对照研究。参与者年龄在4至29岁之间,随访时间≥1年,且无与长期使用抑酸药物相关的慢性病。骨折病例定义为任何部位的首次骨折事件。采用发病密度抽样,病例按年龄、性别、医疗实践和随访开始时间与最多5名对照进行匹配。PPI暴露定义为累积使用180剂或更多的PPIs。采用条件逻辑回归估计PPIs使用与骨折的比值比和置信区间。
我们确定了124,799例病例和605,643名对照。年龄<18岁儿童中,与PPI暴露相关的骨折风险调整后比值比为1.13(95%CI 0.92至1.39),18至29岁年轻人中为1.39(95%CI 1.26至1.53)。在年轻人而非儿童中,我们观察到随着PPIs总暴露量增加的剂量反应效应(趋势p<0.001)。
使用PPIs与年轻人骨折相关,但总体证据不支持PPIs与儿童骨折之间的关系。使用PPIs的年轻人应被告知骨折风险可能增加,即使他们缺乏传统的骨折风险因素。