Bone Health · Bone Mineral Density

The relationship between proton pump inhibitor use and longitudinal change in bone mineral density: a population-based study [corrected] from the Canadian Multicentre Osteoporosis Study (CaMos)

Targownik LE, Leslie WD, Davison KS, Goltzman D, Jamal SA, Kreiger N, Josse RG, Kaiser SM, Kovacs CS, Prior JC, Zhou W, CaMos Research Group

Published September 2012 The American Journal of Gastroenterology, 107(9), 1361-1369
DOI 10.1038/ajg.2012.200 PMID 22777336 PMC PMC5104563

Abstract

Objectives

Proton pump inhibitor (PPI) use has been identified as a risk factor for hip and vertebral fractures. Evidence supporting a relationship between PPI use and osteoporosis remains scant. Demonstrating that PPIs are associated with accelerated bone mineral density (BMD) loss would provide supportive evidence for a mechanism through which PPIs could increase fracture risk.

Methods

We used the Canadian Multicentre Osteoporosis Study data set, which enrolled a population-based sample of Canadians who underwent BMD testing of the femoral neck, total hip, and lumbar spine (L1-L4) at baseline, and then again at 5 and 10 years. Participants also reported drug use and exposure to risk factors for osteoporosis and fracture. Multivariate linear regression was used to determine the independent association of PPI exposure and baseline BMD, and on change in BMD at 5 and 10 years.

Results

In all, 8,340 subjects were included in the baseline analysis, with 4,512 (55%) undergoing year 10 BMD testing. After adjusting for potential confounders, PPI use was associated with significantly lower baseline BMD at the femoral neck and total hip. PPI use was not associated with a significant acceleration in covariate-adjusted BMD loss at any measurement site after 5 and 10 years of follow-up.

Conclusions

PPI users had lower BMD at baseline than PPI non-users, but PPI use over 10 years did not appear to be associated with accelerated BMD loss. The reasons for discordant findings between PPI use at baseline and during follow-up require further study.

Topics

By this author

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Bone Health › Bone Mineral Density › Measurement · Therapeutics › Prescribing Safety › Drug Interactions
Laura E Targownik, William D Leslie, K Shawn Davison, David Goltzman, Sophie A Jamal, Nancy Kreiger, Robert G Josse, Stephanie M Kaiser, Christopher S Kovacs, Jerilynn C Prior, Wei Zhou
L Targownik, Bill Leslie, Will Leslie, Billy Leslie, W Leslie, Dave Goltzman, D Goltzman, S Jamal, N Kreiger, Bob Josse, Rob Josse, Bobby Josse, R Josse, S Kaiser, Chris Kovacs, C Kovacs, J Prior, W Zhou
PMID 22777336 22777336 DOI 10.1038/ajg.2012.200 10.1038/ajg.2012.200 Targownik et al. 2012, Targownik 2012