2020
DOI: 10.1016/j.ebiom.2020.103025
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No pain, no gain: Will migraine therapies increase bone loss and impair fracture healing?

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Cited by 8 publications
(3 citation statements)
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“…CGRP is spontaneously released by cultured trigeminal ganglion cells [9], and CGRP is expressed in the perivascular afferents of cranial arteries [10]. Other functions of the CGRP signaling pathway include glucose-insulin regulation, gastrointestinal motility, systemic vasodilation, skin immunity, airway homeostasis, osteoblast, and adipocyte regulations [11,12].…”
Section: Calcitonin Gene-related Peptidementioning
confidence: 99%
“…CGRP is spontaneously released by cultured trigeminal ganglion cells [9], and CGRP is expressed in the perivascular afferents of cranial arteries [10]. Other functions of the CGRP signaling pathway include glucose-insulin regulation, gastrointestinal motility, systemic vasodilation, skin immunity, airway homeostasis, osteoblast, and adipocyte regulations [11,12].…”
Section: Calcitonin Gene-related Peptidementioning
confidence: 99%
“…PNS function can also modify the immune response. In addition, changes in peripheral nerve function can alter muscle, behavior, and movement, resulting in local adaptation of the bone due to altered biomechanical loading [ 3 ]. Though complex, these broad potential relationships between the PNS and bone present a unique opportunity for discovery.…”
Section: Introductionmentioning
confidence: 99%
“…Future studies should attempt to clarify the association between bone turnover and migraine, and further evaluate the possible effect of vitamin D treatment for patients affected by migraine, even if it does not yet have a clear impact on migraine attacks. Moreover, clinicians should consider possible consequences from prophylaxis therapies with topiramate 9 and anti-CGRP 10 in regulating the bone mass.…”
mentioning
confidence: 99%