质子泵抑制剂的使用与骨质疏松或骨密度加速丢失无关。

Proton-pump inhibitor use is not associated with osteoporosis or accelerated bone mineral density loss.

机构信息

Section of Gastroenterology, Division of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Gastroenterology. 2010 Mar;138(3):896-904. doi: 10.1053/j.gastro.2009.11.014. Epub 2009 Nov 18.

Abstract

BACKGROUNDS & AIMS: Recent studies have shown an association between proton-pump inhibitor use (PPI) and hip fracture. The mechanism by which PPI use promotes the development of hip fracture is uncharacterized. Therefore, we sought to determine whether PPI use is associated with osteoporosis or accelerated bone mineral density (BMD) loss.

METHODS

We used the Manitoba Bone Mineral Density Database to determine the relationship between chronic PPI use and osteoporosis on an initial assessment of BMD and on BMD loss between successive assessments of BMD. In the cross-sectional study, cases with osteoporosis at the hip or lumbar vertebrae (T-score < or =-2.5) were matched to 3 controls with normal BMD (T-score > or =-1.0). In the longitudinal analysis, the change in BMD among PPI users and nonusers between successive BMD assessments was assessed. Conditional logistic regression and multivariate linear regression were used to obtain estimates of the association between PPI use and osteoporosis and of the annualized change in BMD associated with PPI use.

RESULTS

PPI use was not associated with having osteoporosis at either the hip (OR, 0.84; 95% CI, 0.55-1.34) or the lumbar spine (OR, 0.79; 95% CI, 0.59-1.06) for PPI use >1500 doses over the previous 5 years. In the longitudinal study no significant decrease was observed in BMD at either site attributable to PPI use.

CONCLUSIONS

PPI use does not appear to be associated with either the presence of osteoporosis or accelerated BMD loss. The association between PPI use and hip fracture is probably related to factors independent of osteoporosis.

摘要

背景与目的

最近的研究表明质子泵抑制剂(PPI)的使用与髋部骨折之间存在关联。PPI 使用促进髋部骨折发展的机制尚不清楚。因此,我们试图确定 PPI 使用是否与骨质疏松症或骨密度(BMD)丢失加速有关。

方法

我们使用马尼托巴省骨密度数据库,在 BMD 的初始评估以及在连续 BMD 评估之间的 BMD 丢失上,确定慢性 PPI 使用与骨质疏松症之间的关系。在横断面研究中,将髋部或腰椎(T 评分≤-2.5)骨质疏松症的病例与 3 名 BMD 正常的对照(T 评分≥-1.0)进行匹配。在纵向分析中,评估了 PPI 使用者和非使用者之间在连续 BMD 评估之间的 BMD 变化。使用条件逻辑回归和多元线性回归来获得 PPI 使用与骨质疏松症之间的关联以及与 PPI 使用相关的 BMD 年化变化的估计值。

结果

在过去 5 年中使用 PPI >1500 剂时,PPI 使用与髋部(OR,0.84;95%CI,0.55-1.34)或腰椎(OR,0.79;95%CI,0.59-1.06)的骨质疏松症无关。在纵向研究中,未观察到与 PPI 使用相关的任何部位的 BMD 明显下降。

结论

PPI 使用似乎与骨质疏松症或 BMD 丢失加速无关。PPI 使用与髋部骨折之间的关联可能与骨质疏松症无关的因素有关。

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