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Proton pump inhibitors and fracture risk: true effect or residual confounding?

机译:质子泵抑制剂和骨折风险:真正的效果还是残留的混杂?

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摘要

Fracture is a major contributor to human morbidity and mortality, especially in the elderly. It has been discussed in the literature that conditions associated with decreased stomach acidity may lead to a decrease in intestinal calcium absorption and, consequently, to an increased fracture risk. In recent years, several observational studies reported a slightly increased fracture risk in association with the use of proton pump inhibitors (PPIs) and/or histamine H(2) receptor antagonists. It was the objective of this review to critically assess the available evidence linking PPI use to an increased fracture risk. A MEDLINE and EMBASE search from 1960 to June 2010 was performed to identify the relevant articles using predefined search terms. Because (i) there is no proven mechanism, (ii) the reported magnitude of the risk elevation associated with the use of PPIs was only weak, and (iii) the likelihood of residual confounding despite adjustment for known co-morbidities and drug use cannot be ruled out, we conclude that the currently available literature does not support the notion that the use of PPIs is causally related to a materially increased fracture risk in humans.
机译:骨折是人类发病率和死亡率的主要贡献者,尤其是在老年人中。在文献中已经讨论过,与胃酸度降低有关的病症可能导致肠内钙吸收的降低,并因此导致骨折风险增加。近年来,一些观察性研究报道与质子泵抑制剂(PPI)和/或组胺H(2)受体拮抗剂的使用有关的骨折风险略有增加。这篇综述的目的是严格评估将PPI的使用与骨折风险增加联系起来的现有证据。使用预定义的搜索词从1960年到2010年6月进行了MEDLINE和EMBASE搜索,以识别相关文章。因为(i)没有经过验证的机制,(ii)所报告的与使用PPI相关的风险升高幅度很小,并且(iii)尽管对已知的合并症和药物使用进行了调整,但残留混杂的可能性排除在外,我们得出结论,目前可用的文献不支持以下观点:PPI的使用与人类骨折风险的实质性增加有因果关系。

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