Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Osteoporos Int. 2013 May;24(5):1741-9. doi: 10.1007/s00198-012-2170-z. Epub 2013 Jan 29.
Antidepressants are associated with bone loss and fractures in older adults. We treated depressed older adults with an antidepressant and examined its effects on bone turnover by comparing blood samples before and after treatment. Bone resorption increased after antidepressant treatment, which may increase fracture risk.
Antidepressants have been associated with increased bone loss and fractures in older adults in observational studies, but the mechanism is unclear. We examined the effects of a serotonin-norepinephrine reuptake inhibitor, venlafaxine, on biomarkers of bone turnover in a prospective treatment study of late-life depression.
Seventy-six individuals aged 60 years and older with current major depressive disorder received a 12-week course of venlafaxine XR 150-300 mg daily. We measured serum C-terminal cross-linking telopeptide of type I collagen (β-CTX) and N-terminal propeptide of type I procollagen (P1NP), measures of bone resorption and formation, respectively, before and after treatment. We then analyzed the change in β-CTX and P1NP within each participant. Venlafaxine levels were measured at the end of the study. We assessed depression severity at baseline and remission status after treatment.
After 12 weeks of venlafaxine, β-CTX increased significantly, whereas P1NP did not significantly change. The increase in β-CTX was significant only in participants whose depression did not remit (increase by 10 % in non-remitters vs. 4 % in remitters). Change in β-CTX was not correlated with serum levels of venlafaxine or norvenlafaxine.
Our findings suggest that the primary effect of serotonergic antidepressants is to increase bone resorption. However, such an increase in bone resorption seemed to depend on whether or not participants' depression remitted. Our results are in agreement with prior observational studies reporting increased bone loss in older adults taking serotonergic antidepressants. These negative effects on bone homeostasis could potentially contribute to increased fracture risk in older adults.
抗抑郁药与老年人的骨质流失和骨折有关。我们用抗抑郁药治疗老年抑郁症患者,并通过比较治疗前后的血液样本来观察其对骨转换的影响。抗抑郁药治疗后骨吸收增加,这可能会增加骨折风险。
观察性研究表明,抗抑郁药与老年人的骨质流失和骨折有关,但具体机制尚不清楚。我们在一项针对老年抑郁症的前瞻性治疗研究中,研究了一种 5-羟色胺-去甲肾上腺素再摄取抑制剂文拉法辛对骨转换生物标志物的影响。
76 名年龄在 60 岁及以上、目前患有重度抑郁症的患者接受了为期 12 周的文拉法辛 XR 治疗,每日剂量为 150-300mg。我们在治疗前后分别测量了血清 I 型胶原 C 端交联肽(β-CTX)和 I 型前胶原 N 端前肽(P1NP),分别作为骨吸收和形成的标志物。然后,我们分析了每个参与者的β-CTX 和 P1NP 的变化。在研究结束时测量文拉法辛的水平。我们在基线时评估抑郁严重程度和治疗后的缓解状态。
文拉法辛治疗 12 周后,β-CTX 显著增加,而 P1NP 无明显变化。β-CTX 的增加仅在抑郁未缓解的患者中显著(未缓解者增加 10%,缓解者增加 4%)。β-CTX 的变化与血清文拉法辛或去甲文拉法辛水平无关。
我们的研究结果表明,5-羟色胺能抗抑郁药的主要作用是增加骨吸收。然而,这种骨吸收的增加似乎取决于患者的抑郁是否缓解。我们的结果与先前的观察性研究结果一致,即服用 5-羟色胺能抗抑郁药的老年人骨丢失增加。这些对骨稳态的负面影响可能会导致老年人骨折风险增加。