2016
DOI: 10.1007/s00198-016-3509-7
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Proton pump inhibitors and fracture: they impair bone quality and increase fall risk?

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Cited by 10 publications
(6 citation statements)
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“…[ 46 ] Bone fragility depends not only on areal BMD but also on other factors including bone quality, which may be affected by other factors such as vitamin B12 levels and modulated skeletal fragility due to collagen cross-linking independent of areal BMD. [ 47 ]…”
Section: Discussionmentioning
confidence: 99%
“…[ 46 ] Bone fragility depends not only on areal BMD but also on other factors including bone quality, which may be affected by other factors such as vitamin B12 levels and modulated skeletal fragility due to collagen cross-linking independent of areal BMD. [ 47 ]…”
Section: Discussionmentioning
confidence: 99%
“…Vitamin B12 deficiency can lead to an increase in osteoclastic activity, a decrease in osteoblastic activity, and homocysteinemia causing abnormal collagen cross-linking [ 11 ]. The deficiency of vitamin B12 can affect bone fragility through modulation of collagen cross-linking independently of areal BMD [ 41 , 42 ]. This increased bone fragility, along with increased fall risk in elderly patients with PPI use due to peripheral neuropathy caused by vitamin B12 deficiency, can contribute to increased fracture rates [ 42 , 43 ].…”
Section: Reviewmentioning
confidence: 99%
“…The deficiency of vitamin B12 can affect bone fragility through modulation of collagen cross-linking independently of areal BMD [ 41 , 42 ]. This increased bone fragility, along with increased fall risk in elderly patients with PPI use due to peripheral neuropathy caused by vitamin B12 deficiency, can contribute to increased fracture rates [ 42 , 43 ].…”
Section: Reviewmentioning
confidence: 99%
“…Proposed mechanisms include chronic PPI use leading to decreased intestinal absorption of calcium resulting in an increase in bone fracture rate; PPI-induced inhibitory effects on the vacuolar type of H + K + ATPase of osteoclasts leading to an increase in their activity; PPI-induced hypochlorhydria leading to hypergastrinemia, which in turn stimulates the development of parathyroid hyperplasia; PP-induced hypomagnesemia, which can contribute to altered bone metabolism and increased risk of bone fractures; and the hypergastrinemic stimulation of ECL hyperplasia resulting in an increased in histamine production, which can stimulate proliferation of osteoclasts resulting in increased bone absorption [18,292,293,294,330]. More recently, it has been proposed that low VB 12 levels, which can be associated with PPI treatment [297], affects skeletal fragility through the modulation of collagen cross-linking independently of areal bone mineral density [343]. This increased bone fragility coupled with recently evidence reporting an increased risk of falling in elderly patients with PPIs use may be contributing to increasing bone fracture rates [343,344,345,346].…”
Section: Insights Of Effects Of Chronic Hypergastrinemia In Patienmentioning
confidence: 99%
“…More recently, it has been proposed that low VB 12 levels, which can be associated with PPI treatment [297], affects skeletal fragility through the modulation of collagen cross-linking independently of areal bone mineral density [343]. This increased bone fragility coupled with recently evidence reporting an increased risk of falling in elderly patients with PPIs use may be contributing to increasing bone fracture rates [343,344,345,346]. Although a placebo controlled, double-blind trial in postmenopausal females found decreased calcium absorption with PPI treatment, the results suggesting PPI causes osteoporosis are largely negative [18,334,347,348], as are studies reporting PPI treatment does not cause changes in bone mineral density or bone structure that would predispose to fracture [348].…”
Section: Insights Of Effects Of Chronic Hypergastrinemia In Patienmentioning
confidence: 99%