Ente Ospedaliero Cantonale, Regional Hospital of Lugano, Department of Neurology, Neurocenter of Southern Switzerland, 6900, Lugano, Switzerland.
Ente Ospedaliero Cantonale, Regional Hospital of Lugano, Clinic for Endocrinology and Diabetology, Lugano, Switzerland.
CNS Drugs. 2024 Oct;38(10):819-825. doi: 10.1007/s40263-024-01104-0. Epub 2024 Aug 22.
Calcitonin gene-related peptide (CGRP), implicated in migraine pain, also possesses bone anabolic properties, which leads to the possibility that monoclonal antibodies targeting CGRP (anti-CGRPs) might increase the risk of bone density abnormalities.
The objective of this study was to explore bone mineral density abnormalities in a cohort of migraine patients treated with anti-CGRPs.
This was a single-center, cross-sectional, cohort study including migraine patients who underwent a densitometry assessment during anti-CGRP treatment. We assessed the frequency of osteopenia or osteoporosis (OSTEO+ status), defined as a bone mineral density T-score of -1 to -2.5, and <-2.5 standard deviations from the young female adult mean, respectively. Additionally, the association of OSTEO+ status with anti-CGRP treatment duration and primary osteoporosis' risk factors was investigated using logistic regression models.
Data from 51 patients (43 female, mean age 46 ± 13.9 years) were evaluated. The mean duration of anti-CGRP treatment was 15.7 (±11.8) months. Twenty-seven patients (53%) were OSTEO+ (n = 22 osteopenia; n = 5 osteoporosis). In the final model, menopause [odds ratio 11.641 (95% confidence interval 1.486-91.197), p = 0.019] and anti-seizure drug use [odds ratio 12.825 (95% confidence interval 1.162-141.569), p = 0.037] were associated with OSTEO+ status.
In our cohort of migraine patients, no evidence of an association between anti-CGRP treatment duration and an increasing risk of bone mineral density abnormalities was found. However, these findings are preliminary and necessitate further longitudinal research with larger cohorts and extended follow-up to be validated.
降钙素基因相关肽(CGRP)与偏头痛疼痛有关,它还具有骨合成代谢的特性,这使得靶向 CGRP 的单克隆抗体(抗 CGRP)有可能增加骨密度异常的风险。
本研究旨在探讨接受抗 CGRP 治疗的偏头痛患者的骨密度异常情况。
这是一项单中心、横断面、队列研究,纳入了在接受抗 CGRP 治疗期间接受骨密度评估的偏头痛患者。我们评估了骨质疏松症或骨质疏松症的发生率(OSTEO+状态),定义为骨矿物质密度 T 评分在-1 至-2.5 之间,分别为年轻女性成年人平均值的-1 至-2.5 标准差。此外,还使用逻辑回归模型研究了 OSTEO+状态与抗 CGRP 治疗持续时间和原发性骨质疏松症危险因素的相关性。
共评估了 51 例患者(43 例女性,平均年龄 46 ± 13.9 岁)的数据。抗 CGRP 治疗的平均持续时间为 15.7(±11.8)个月。27 例患者(53%)为 OSTEO+(n = 22 例骨质疏松症;n = 5 例骨质疏松症)。在最终模型中,绝经[比值比 11.641(95%置信区间 1.486-91.197),p = 0.019]和抗癫痫药物的使用[比值比 12.825(95%置信区间 1.162-141.569),p = 0.037]与 OSTEO+状态相关。
在我们的偏头痛患者队列中,没有发现抗 CGRP 治疗持续时间与骨矿物质密度异常风险增加之间存在关联的证据。然而,这些发现是初步的,需要进一步进行有更大队列和更长随访时间的纵向研究来验证。