Effect of selective serotonin reuptake inhibitors on the risk of fracture

被引:284
作者
Richards, J. Brent
Papaioannou, Alexandra
Adachi, Jonathan D.
Joseph, Lawrence
Whitson, Heather E.
Prior, Jerilynn C.
Goltzman, David
机构
[1] Royal Victoria Hosp, Bone & Calcium Res Labs, Montreal, PQ H3Y 2W3, Canada
[2] McGill Univ, Dept Med, Div Endocrinol & Metab, Montreal, PQ, Canada
[3] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ, Canada
[4] McMaster Univ, Div Geriatr Med, Dept Med, Hamilton, ON, Canada
[5] McMaster Univ, St Josephs Healthcare, Dept Med, Hamilton, ON, Canada
[6] Univ British Columbia, Dept Endocrinol & Med, Vancouver, BC V5Z 1M9, Canada
[7] Duke Univ, Sch Med, Dept Med, Div Geriatr, Durham, NC 27706 USA
关键词
D O I
10.1001/archinte.167.2.188
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Depression and osteoporotic fractures are common ailments among elderly persons. Selective serotonin reuptake inhibitors (SSRIs) are frequently used in the treatment of depression in this population, and the association between daily SSRI use and fragility fractures is unclear. Our objective was to examine the effect of daily SSRI use on the risk of incident clinical fragility fracture. Methods: A population-based, randomly selected, prospective cohort study of 5008 community-dwelling adults 50 years and older, followed up over 5 years for incident fractures. Clinical fragility fractures were classified as minimal trauma fractures that were clinically reported and radiographically confirmed. The risk of fragility fracture associated with daily SSRI use was determined while controlling for relevant covariates. Results: Daily SSRI use was reported by 137 subjects. After adjustment for many potential covariates, daily SSRI use was associated with substantially increased risk of incident clinical fragility fracture (hazard rate, 2.1; 95% confidence interval, 1.3-3.4). Daily SSRI use was also associated with increased odds of falling (odds ratio, 2.2; 95% confidence interval, 1.4-3.5), lower bone mineral density at the hip, and a trend toward lower bone mineral density at the spine. These effects were dose dependent and were similar for those who reported taking SSRIs at baseline and at 5 years' follow-up. Conclusions: Daily SSRI use in adults 50 years and older remained associated with a 2-fold increased risk of clinical fragility fracture after adjustment for potential covariates. Depression and fragility fractures are common in this age group, and the elevated risk attributed to daily SSRI use may have important public health consequences.
引用
收藏
页码:188 / 194
页数:7
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