Assessment of Bone Mineral Density Over 1 Year in a Cross-Sectional Cohort of Migraine Patients Receiving Anti-CGRP Monoclonal Antibodies

Background 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. Objective The objective of this study...

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Veröffentlicht in:CNS drugs 2024-10, Vol.38 (10), p.819-825
Hauptverfasser: Para, Davide, Camponovo, Chiara, Riccitelli, Gianna Carla, Mallucci, Giulia, Maino, Paolo, Mondini Trissino da Lodi, Camilla, Saudina, Demurtas, Trimboli, Pierpaolo, Gobbi, Claudio, Zecca, Chiara
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container_issue 10
container_start_page 819
container_title CNS drugs
container_volume 38
creator Para, Davide
Camponovo, Chiara
Riccitelli, Gianna Carla
Mallucci, Giulia
Maino, Paolo
Mondini Trissino da Lodi, Camilla
Saudina, Demurtas
Trimboli, Pierpaolo
Gobbi, Claudio
Zecca, Chiara
description Background 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. Objective The objective of this study was to explore bone mineral density abnormalities in a cohort of migraine patients treated with anti-CGRPs. Methods 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
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Objective The objective of this study was to explore bone mineral density abnormalities in a cohort of migraine patients treated with anti-CGRPs. Methods 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 &lt;−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. Results 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. Conclusions 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.</description><identifier>ISSN: 1172-7047</identifier><identifier>ISSN: 1179-1934</identifier><identifier>EISSN: 1179-1934</identifier><identifier>DOI: 10.1007/s40263-024-01104-0</identifier><identifier>PMID: 39174745</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult ; Antibodies, Monoclonal - administration &amp; dosage ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - pharmacology ; Antibodies, Monoclonal - therapeutic use ; Body mass index ; Bone density ; Bone Density - drug effects ; Bone Diseases, Metabolic - epidemiology ; Bone mineral density ; Calcitonin ; Calcitonin gene-related peptide ; Calcitonin Gene-Related Peptide - immunology ; Cohort analysis ; Cohort Studies ; Convulsions &amp; seizures ; Cross-Sectional Studies ; Densitometry ; Drugs ; Female ; Females ; Fractures ; Headache ; Humans ; Male ; Medicine ; Medicine &amp; Public Health ; Menopause ; Metabolic disorders ; Middle Aged ; Migraine ; Migraine Disorders - drug therapy ; Monoclonal antibodies ; Neurology ; Neurosciences ; Original Research Article ; Osteopenia ; Osteoporosis ; Osteoporosis - drug therapy ; Patients ; Peptides ; Pharmacotherapy ; Prevention ; Psychiatry ; Psychopharmacology ; Regression analysis ; Risk Factors ; Seizures ; Side effects ; Software ; Standard deviation</subject><ispartof>CNS drugs, 2024-10, Vol.38 (10), p.819-825</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>Copyright Springer Nature B.V. Oct 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c300t-b88dd29e0e7311b056eb45613dad44b0fc338e88f86c2528c2f2046fb488bf1d3</cites><orcidid>0000-0002-9990-3431 ; 0000-0002-7554-0664 ; 0000-0002-0678-3240 ; 0000-0002-1202-5534 ; 0000-0002-2125-4937 ; 0000-0002-0031-9594 ; 0000-0002-5898-145X ; 0000-0001-8586-9925</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40263-024-01104-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40263-024-01104-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39174745$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Para, Davide</creatorcontrib><creatorcontrib>Camponovo, Chiara</creatorcontrib><creatorcontrib>Riccitelli, Gianna Carla</creatorcontrib><creatorcontrib>Mallucci, Giulia</creatorcontrib><creatorcontrib>Maino, Paolo</creatorcontrib><creatorcontrib>Mondini Trissino da Lodi, Camilla</creatorcontrib><creatorcontrib>Saudina, Demurtas</creatorcontrib><creatorcontrib>Trimboli, Pierpaolo</creatorcontrib><creatorcontrib>Gobbi, Claudio</creatorcontrib><creatorcontrib>Zecca, Chiara</creatorcontrib><title>Assessment of Bone Mineral Density Over 1 Year in a Cross-Sectional Cohort of Migraine Patients Receiving Anti-CGRP Monoclonal Antibodies</title><title>CNS drugs</title><addtitle>CNS Drugs</addtitle><addtitle>CNS Drugs</addtitle><description>Background 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. Objective The objective of this study was to explore bone mineral density abnormalities in a cohort of migraine patients treated with anti-CGRPs. Methods 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 &lt;−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. Results 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. Conclusions 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.</description><subject>Adult</subject><subject>Antibodies, Monoclonal - administration &amp; dosage</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Body mass index</subject><subject>Bone density</subject><subject>Bone Density - drug effects</subject><subject>Bone Diseases, Metabolic - epidemiology</subject><subject>Bone mineral density</subject><subject>Calcitonin</subject><subject>Calcitonin gene-related peptide</subject><subject>Calcitonin Gene-Related Peptide - immunology</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Convulsions &amp; seizures</subject><subject>Cross-Sectional Studies</subject><subject>Densitometry</subject><subject>Drugs</subject><subject>Female</subject><subject>Females</subject><subject>Fractures</subject><subject>Headache</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Menopause</subject><subject>Metabolic disorders</subject><subject>Middle Aged</subject><subject>Migraine</subject><subject>Migraine Disorders - drug therapy</subject><subject>Monoclonal antibodies</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Original Research Article</subject><subject>Osteopenia</subject><subject>Osteoporosis</subject><subject>Osteoporosis - drug therapy</subject><subject>Patients</subject><subject>Peptides</subject><subject>Pharmacotherapy</subject><subject>Prevention</subject><subject>Psychiatry</subject><subject>Psychopharmacology</subject><subject>Regression analysis</subject><subject>Risk Factors</subject><subject>Seizures</subject><subject>Side effects</subject><subject>Software</subject><subject>Standard deviation</subject><issn>1172-7047</issn><issn>1179-1934</issn><issn>1179-1934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU9vFCEYh4mxsbX1C3gwJF68UF_-DMMc11Fbk27aVD14mjDMOyvNLFSYbdKP4LeW3a2a9NALEHh-PwgPIa85nHKA-n1WILRkIBQDzqGMz8gR53XDeCPV891asBpUfUhe5nwDAEpq_YIcyobXqlbVEfm9yBlzXmOYaRzphxiQLn3AZCf6EUP28z29vMNEOf2BNlEfqKVtijmzr-hmH0MB2_gzpl1-6VfJlji9srMvnZleo0N_58OKLsLsWXt2fUWXMUQ37aLbzT4OHvMJORjtlPHVw3xMvn_-9K09ZxeXZ1_axQVzEmBmvTHDIBoErCXnPVQae1VpLgc7KNXD6KQ0aMxotBOVME6MApQee2VMP_JBHpN3-97bFH9tMM_d2meH02QDxk3uJDRaGKhAFvTtI_QmblJ5dqE4aFlxrraU2FNu-y0Jx-42-bVN9x2Hbiuq24vqiqhuJ6qDEnrzUL3p1zj8i_w1UwC5B3I5CitM_-9-ovYPDlOdSA</recordid><startdate>20241001</startdate><enddate>20241001</enddate><creator>Para, Davide</creator><creator>Camponovo, Chiara</creator><creator>Riccitelli, Gianna Carla</creator><creator>Mallucci, Giulia</creator><creator>Maino, Paolo</creator><creator>Mondini Trissino da Lodi, Camilla</creator><creator>Saudina, Demurtas</creator><creator>Trimboli, Pierpaolo</creator><creator>Gobbi, Claudio</creator><creator>Zecca, Chiara</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9990-3431</orcidid><orcidid>https://orcid.org/0000-0002-7554-0664</orcidid><orcidid>https://orcid.org/0000-0002-0678-3240</orcidid><orcidid>https://orcid.org/0000-0002-1202-5534</orcidid><orcidid>https://orcid.org/0000-0002-2125-4937</orcidid><orcidid>https://orcid.org/0000-0002-0031-9594</orcidid><orcidid>https://orcid.org/0000-0002-5898-145X</orcidid><orcidid>https://orcid.org/0000-0001-8586-9925</orcidid></search><sort><creationdate>20241001</creationdate><title>Assessment of Bone Mineral Density Over 1 Year in a Cross-Sectional Cohort of Migraine Patients Receiving Anti-CGRP Monoclonal Antibodies</title><author>Para, Davide ; Camponovo, Chiara ; Riccitelli, Gianna Carla ; Mallucci, Giulia ; Maino, Paolo ; Mondini Trissino da Lodi, Camilla ; Saudina, Demurtas ; Trimboli, Pierpaolo ; Gobbi, Claudio ; Zecca, Chiara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c300t-b88dd29e0e7311b056eb45613dad44b0fc338e88f86c2528c2f2046fb488bf1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Antibodies, Monoclonal - administration &amp; dosage</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Body mass index</topic><topic>Bone density</topic><topic>Bone Density - drug effects</topic><topic>Bone Diseases, Metabolic - epidemiology</topic><topic>Bone mineral density</topic><topic>Calcitonin</topic><topic>Calcitonin gene-related peptide</topic><topic>Calcitonin Gene-Related Peptide - immunology</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Convulsions &amp; seizures</topic><topic>Cross-Sectional Studies</topic><topic>Densitometry</topic><topic>Drugs</topic><topic>Female</topic><topic>Females</topic><topic>Fractures</topic><topic>Headache</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Menopause</topic><topic>Metabolic disorders</topic><topic>Middle Aged</topic><topic>Migraine</topic><topic>Migraine Disorders - drug therapy</topic><topic>Monoclonal antibodies</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Original Research Article</topic><topic>Osteopenia</topic><topic>Osteoporosis</topic><topic>Osteoporosis - drug therapy</topic><topic>Patients</topic><topic>Peptides</topic><topic>Pharmacotherapy</topic><topic>Prevention</topic><topic>Psychiatry</topic><topic>Psychopharmacology</topic><topic>Regression analysis</topic><topic>Risk Factors</topic><topic>Seizures</topic><topic>Side effects</topic><topic>Software</topic><topic>Standard deviation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Para, Davide</creatorcontrib><creatorcontrib>Camponovo, Chiara</creatorcontrib><creatorcontrib>Riccitelli, Gianna Carla</creatorcontrib><creatorcontrib>Mallucci, Giulia</creatorcontrib><creatorcontrib>Maino, Paolo</creatorcontrib><creatorcontrib>Mondini Trissino da Lodi, Camilla</creatorcontrib><creatorcontrib>Saudina, Demurtas</creatorcontrib><creatorcontrib>Trimboli, Pierpaolo</creatorcontrib><creatorcontrib>Gobbi, Claudio</creatorcontrib><creatorcontrib>Zecca, Chiara</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>CNS drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Para, Davide</au><au>Camponovo, Chiara</au><au>Riccitelli, Gianna Carla</au><au>Mallucci, Giulia</au><au>Maino, Paolo</au><au>Mondini Trissino da Lodi, Camilla</au><au>Saudina, Demurtas</au><au>Trimboli, Pierpaolo</au><au>Gobbi, Claudio</au><au>Zecca, Chiara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of Bone Mineral Density Over 1 Year in a Cross-Sectional Cohort of Migraine Patients Receiving Anti-CGRP Monoclonal Antibodies</atitle><jtitle>CNS drugs</jtitle><stitle>CNS Drugs</stitle><addtitle>CNS Drugs</addtitle><date>2024-10-01</date><risdate>2024</risdate><volume>38</volume><issue>10</issue><spage>819</spage><epage>825</epage><pages>819-825</pages><issn>1172-7047</issn><issn>1179-1934</issn><eissn>1179-1934</eissn><abstract>Background 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. Objective The objective of this study was to explore bone mineral density abnormalities in a cohort of migraine patients treated with anti-CGRPs. Methods 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 &lt;−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. Results 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. Conclusions 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.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>39174745</pmid><doi>10.1007/s40263-024-01104-0</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9990-3431</orcidid><orcidid>https://orcid.org/0000-0002-7554-0664</orcidid><orcidid>https://orcid.org/0000-0002-0678-3240</orcidid><orcidid>https://orcid.org/0000-0002-1202-5534</orcidid><orcidid>https://orcid.org/0000-0002-2125-4937</orcidid><orcidid>https://orcid.org/0000-0002-0031-9594</orcidid><orcidid>https://orcid.org/0000-0002-5898-145X</orcidid><orcidid>https://orcid.org/0000-0001-8586-9925</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Antibodies, Monoclonal - administration & dosage
Antibodies, Monoclonal - adverse effects
Antibodies, Monoclonal - pharmacology
Antibodies, Monoclonal - therapeutic use
Body mass index
Bone density
Bone Density - drug effects
Bone Diseases, Metabolic - epidemiology
Bone mineral density
Calcitonin
Calcitonin gene-related peptide
Calcitonin Gene-Related Peptide - immunology
Cohort analysis
Cohort Studies
Convulsions & seizures
Cross-Sectional Studies
Densitometry
Drugs
Female
Females
Fractures
Headache
Humans
Male
Medicine
Medicine & Public Health
Menopause
Metabolic disorders
Middle Aged
Migraine
Migraine Disorders - drug therapy
Monoclonal antibodies
Neurology
Neurosciences
Original Research Article
Osteopenia
Osteoporosis
Osteoporosis - drug therapy
Patients
Peptides
Pharmacotherapy
Prevention
Psychiatry
Psychopharmacology
Regression analysis
Risk Factors
Seizures
Side effects
Software
Standard deviation
title Assessment of Bone Mineral Density Over 1 Year in a Cross-Sectional Cohort of Migraine Patients Receiving Anti-CGRP Monoclonal Antibodies
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