Potential Osteocatabolic Effect Caused by Anti-CGRP mAbs in Migraine Patients Treated With Anti-CGRP mAbs - an Observational Pilot Project With Prospectively Collected Health Related Data

Background: To gain insight on the osteoanabolic activity of anti-CGRP mAbs in patients with migraine as this was not yet specifically investigated in registration or post-approval clinical studies, however, being pathophysiologically plausible. If a clinically relevant, osteocatabolic effect caused by anti-CGRP mAbs will be demonstrated by the present investigation monitoring and mitigating strategies might be required and addressed in dedicated future studies. Objectives: To investigate whether treatment with anti-CGRP mAbs over 6, 12, and 24 months is associated with changes in bone density, structure and/or metabolic turnover in migraine patients. Project Design and Procedures: Prospective collection of health-related clinical data, open label, controlled pilot study. Demographic (ethnicity, age, sex) and physical (age, height) data, data on medical and migraine history will be collected. Clinical procedures include bone mineral measurement (bone densitometry, dxa) performed according to clinical practice; venipunctures for laboratory assessments (haematology and blood chemistry; bone turnover biomarkers P1NP and CTX).

Migraine is a chronic and often lifelong disease defined by recurrent unprovoked headache episodes lasting over four hours with one or more disabling symptoms including nausea, vomiting, dizziness, and extreme sensitivity to sound and light. It directly affects more than 1 billion people worldwide, representing the most common neurological condition with an estimated 1-year prevalence of 15%. It is approximately twice as high in females compared to males. In individuals younger than 50 years, migraine represents the leading cause of years lived with disability worldwide, and a major public health concern, as it is insufficiently recognized leading to considerable individual and societal costs. The current migraine treatment armamentarium available includes acute and preventive medications, as well as non-pharmacological approaches. Preventive therapies used until recently were just non-specific medications such as beta-blockers, calcium channel antagonists, antidepressants, and antiepileptic drugs, which are often limited by insufficient efficacy and/or relevant short and long-term side effects. More recently, anti-calcitonin gene related peptide (CGRP) monoclonal antibodies (mAbs) have been approved as pharmacological preventive therapies for migraine and currently represent game changer in the field. CGRP, a 37-residue neuropeptide produced in specific neurons by alternative splicing of the calcitonin gene, acts as a potent vasodilator as well as a neurotransmitter. In humans, CGRP is present in two isoforms, α-CGRP and β-CGRP. α-CGRP is the principal isoform localized in the peripheral and central sensory nervous system, and plays a key role in the underlying mechanism of migraine, as illustrated by several lines of preclinical and human evidence. Intravenous infusion of this neuropeptide elicits vasodilatation and precipitates migraine attacks in subjects diagnosed with migraine. Additionally, an increase in plasma CGRP concentrations can be measured in the craniovascular circulation during migraine attacks. At the trigeminocervical complex, CGRP also plays a crucial role in central sensitization, a critical step in the development of migraine headache. Accordingly, blockade of the CGRPergic transmission has become attractive for the development of targeted and highly effective migraine treatment strategies. These include mAbs binding CGRP (galcanezumab, fremanezumab, eptinezumab), or its receptor (CGRPR; erenumab). When used as preventive therapies in patients with episodic or chronic migraine, these new antimigraine mAbs (anti-CGRP mAbs) showed effectiveness in reducing the frequency and intensity of attacks and as well as migraine associated symptoms. Anti- CGRP mAbs were well-tolerated and safe according to pivotal trials and their open label extensions up to 5 years. The most frequent adverse events reported in these studies were nasopharyngitis, upper respiratory tract infections, nausea, arthralgia, fatigue, and injection site pain, however these did not generally exceed rates observed in placebo treatment arms. However, patients included in registration clinical trials may differ from those treated in the clinical practice, since the former are typically limited in number, younger, and with a low burden of comorbidities and concomitant medications. Consequently, the adverse event profile of a given drug can significantly differ in these two contexts, underlining the importance of post-marketing surveillance and 'real world' observational studies. According to that, in clinical trials the administration of anti-CGRP mAbs did not produce significant cardiovascular side effects, which represented a concern since CGRP is a potent physiological vasodilator widely represented in the human body. Instead, the first-inclass mAb erenumab was recently found to be associated with an increased risk of new onset or worsening arterial hypertension, which has now been included among warnings in the the erenumab label by FDA. Based on the wide distribution of CGRP and its receptor in the body, additional off-target effects might be also expected when anti-CGRP mAbs are used extensively in the clinical practice. Besides the cardiovascular system, the CGRP/CGRP receptor system is actually present in the central and peripheral nervous system (particularly, the blood brain barrier, the anterior pituitary, the pineal gland, and the area postrema), gastrointestinal and vestibular system, the kidney and the skin, and has a role in the endocrinal system and bone metabolism. The objective of this study is to investigate whether treatment with anti-CGRP mAbs over 6, 12, and 24 months is associated with changes in bone density, structure and/or metabolic turnover in migraine patients. We hypothesize that the continuous use of anti-CGRP mAbs causes bone reabsorption, which in turn reflects in increased bone catabolic biomarkers, decreased bone anabolic biomarkers and ultimately in reduced bone density (BMD) and altered trabecular structure (TMS).