The aim of this study was to evaluate fracture risk after onset of myasthenia gravis using the UK General Practice Research Database. Overall fracture risk is not statistically increased compared with age- and gender-matched controls irrespective of glucocorticoid use, but was increased in those using antidepressants, anxiolytics or anticonvulsants. Myasthenia gravis (MG) is a neuromuscular disease which has been associated with an increased falls risk and glucocorticoid-induced osteoporosis, recognized determinants of increased fracture risk. The aim of this study was to evaluate the risk of fracture after onset of MG. We conducted a retrospective cohort study using the UK General Practice Research Database (1987-2009). Each MG patient was matched by age, sex, calendar time and practice to up to six patients without a history of MG and we identified all fractures and those associated with osteoporosis. Compared to the control cohort, there was no statistically significant increased risk observed in patients with MG for any fracture (adjusted hazard ratio [AHR] 1.11; 95 % confidence interval [CI], 0.84-1.47) or osteoporotic fractures (AHR 0.98 [95 % CI 0.67-1.41]). Further, use of oral glucocorticoids up to a cumulative dose exceeding 5 g prednisolone equivalents did not increase risk of osteoporotic fracture (AHR 0.99 [95 % CI, 0.31-3.14]) compared with MG patients without glucocorticoid exposure. However, fracture risk was higher in patients with MG prescribed antidepressants (AHR 3.27 [95 % CI, 1.63-6.55]), anxiolytics (AHR 2.18 [95 % CI, 1.04-4.57]) and anticonvulsants (AHR 6.88 [95 % CI, 2.91-16.27]). Overall risk of fracture in patients with MG is not statistically increased compared with age- and gender-matched controls irrespective of glucocorticoid use but was increased in those using antidepressants, anxiolytics or anticonvulsants. These findings have implications in strategies preserving bone health in patients with MG.
机构:
St Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Univ Toronto, Neurol Qual & Innovat Lab, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Kassardjian, Charles
Widdifield, Jessica
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Sunnybrook Res Inst, Sunnybrook Hlth Sci Ctr, Holland Bone & Joint Res Program, Toronto, ON, Canada
Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
ICES, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Widdifield, Jessica
Paterson, J. Michael
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Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
ICES, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Paterson, J. Michael
Kopp, Alexander
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ICES, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Kopp, Alexander
Nagamuthu, Chenthila
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ICES, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Nagamuthu, Chenthila
Barnett, Carolina
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Univ Hlth Network, Univ Toronto, Ellen & Martin Prosserman Ctr Neuromuscular Dis, Div Neurol,Dept Med, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Barnett, Carolina
Tu, Karen
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Univ Hlth Network, North York Gen Hosp, Dept Community & Family Med, Toronto, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada
Tu, Karen
Breiner, Ari
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Ottawa Hosp, Dept Med, Div Neurol, Ottawa, ON, Canada
Ottawa Hosp Res Inst, Ottawa, ON, CanadaSt Michaels Hosp, Div Neurol, Dept Med, Toronto, ON, Canada