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Alopecia as an emerging adverse event to CGRP monoclonal antibodies: Cases Series, evaluation of FAERS, and literature review
Background Alopecia is associated with erenumab post-marketing, but no cases have been described. Methods We describe two patients that reported temporary hair loss and review the FDA Adverse Event Reporting System (FAERS). Results The first patient experienced alopecia within three months of starti...
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Published in: | Cephalalgia 2023-02, Vol.43 (2), p.3331024221143538-3331024221143538 |
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container_end_page | 3331024221143538 |
container_issue | 2 |
container_start_page | 3331024221143538 |
container_title | Cephalalgia |
container_volume | 43 |
creator | Ruiz, Miguel Cocores, Alexandra Tosti, Antonella Goadsby, Peter J Monteith, Teshamae S |
description | Background
Alopecia is associated with erenumab post-marketing, but no cases have been described.
Methods
We describe two patients that reported temporary hair loss and review the FDA Adverse Event Reporting System (FAERS).
Results
The first patient experienced alopecia within three months of starting erenumab, which did not improve with ongoing use or transition to fremanezumab. The second patient reported alopecia within two weeks of starting erenumab, which continued after transition to galcanezumab; months later, there was also recurrent hair loss within one month of starting fremanzeumab. According to FAERS (last accessed 18 August 2022), alopecia was reported most with erenumab (1158), followed by galcanezumab (554), fremanezumab (175), eptinezumab (23), rimegepant (26), ubrogepant (4), and atogepant (3).
Conclusion
Most events were reported in women and non-serious. The potential mechanism of alopecia with drugs targeting calcitonin gene-related peptide or its receptor possibly includes disruptions in the microvascular circulation and other homeostatic mechanisms. |
doi_str_mv | 10.1177/03331024221143538 |
format | article |
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Alopecia is associated with erenumab post-marketing, but no cases have been described.
Methods
We describe two patients that reported temporary hair loss and review the FDA Adverse Event Reporting System (FAERS).
Results
The first patient experienced alopecia within three months of starting erenumab, which did not improve with ongoing use or transition to fremanezumab. The second patient reported alopecia within two weeks of starting erenumab, which continued after transition to galcanezumab; months later, there was also recurrent hair loss within one month of starting fremanzeumab. According to FAERS (last accessed 18 August 2022), alopecia was reported most with erenumab (1158), followed by galcanezumab (554), fremanezumab (175), eptinezumab (23), rimegepant (26), ubrogepant (4), and atogepant (3).
Conclusion
Most events were reported in women and non-serious. The potential mechanism of alopecia with drugs targeting calcitonin gene-related peptide or its receptor possibly includes disruptions in the microvascular circulation and other homeostatic mechanisms.</description><identifier>ISSN: 0333-1024</identifier><identifier>EISSN: 1468-2982</identifier><identifier>DOI: 10.1177/03331024221143538</identifier><identifier>PMID: 36739513</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Antibodies, Monoclonal ; Calcitonin Gene-Related Peptide ; Calcitonin Gene-Related Peptide Receptor Antagonists ; Female ; Humans ; Male ; Migraine Disorders ; Receptors, Calcitonin Gene-Related Peptide</subject><ispartof>Cephalalgia, 2023-02, Vol.43 (2), p.3331024221143538-3331024221143538</ispartof><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-44d1a54009597fd52dcfb7c43639ed40f527a430d08323999e0934389acdc2b53</citedby><cites>FETCH-LOGICAL-c383t-44d1a54009597fd52dcfb7c43639ed40f527a430d08323999e0934389acdc2b53</cites><orcidid>0000-0003-3260-5904 ; 0000-0001-8912-252X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/03331024221143538$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/03331024221143538$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,21966,27853,27924,27925,44945,45333</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36739513$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ruiz, Miguel</creatorcontrib><creatorcontrib>Cocores, Alexandra</creatorcontrib><creatorcontrib>Tosti, Antonella</creatorcontrib><creatorcontrib>Goadsby, Peter J</creatorcontrib><creatorcontrib>Monteith, Teshamae S</creatorcontrib><title>Alopecia as an emerging adverse event to CGRP monoclonal antibodies: Cases Series, evaluation of FAERS, and literature review</title><title>Cephalalgia</title><addtitle>Cephalalgia</addtitle><description>Background
Alopecia is associated with erenumab post-marketing, but no cases have been described.
Methods
We describe two patients that reported temporary hair loss and review the FDA Adverse Event Reporting System (FAERS).
Results
The first patient experienced alopecia within three months of starting erenumab, which did not improve with ongoing use or transition to fremanezumab. The second patient reported alopecia within two weeks of starting erenumab, which continued after transition to galcanezumab; months later, there was also recurrent hair loss within one month of starting fremanzeumab. According to FAERS (last accessed 18 August 2022), alopecia was reported most with erenumab (1158), followed by galcanezumab (554), fremanezumab (175), eptinezumab (23), rimegepant (26), ubrogepant (4), and atogepant (3).
Conclusion
Most events were reported in women and non-serious. The potential mechanism of alopecia with drugs targeting calcitonin gene-related peptide or its receptor possibly includes disruptions in the microvascular circulation and other homeostatic mechanisms.</description><subject>Antibodies, Monoclonal</subject><subject>Calcitonin Gene-Related Peptide</subject><subject>Calcitonin Gene-Related Peptide Receptor Antagonists</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Migraine Disorders</subject><subject>Receptors, Calcitonin Gene-Related Peptide</subject><issn>0333-1024</issn><issn>1468-2982</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp9kEtLAzEUhYMoWqs_wI1k6aKjSW7mEXelWBUExcd6SJM7JTIzqclMxYX_3SlVN4Kry-F-5yw-Qk44O-c8zy8YAHAmpBCcS0ih2CEjLrMiEaoQu2S0-Scb4IAcxvjKGEszlu2TA8hyUCmHEfmc1n6FxmmqI9UtxQbD0rVLqu0aQ0SKa2w72nk6u358oI1vval9q-sB7tzCW4fxks50xEifMAxpMlR03evO-Zb6is6nV49PkwG3tHYdBt31AWnAtcP3I7JX6Tri8fcdk5f51fPsJrm7v76dTe8SAwV0iZSW61QyplKVVzYV1lSL3EjIQKGVrEpFriUwywoQoJRCpkBCobSxRixSGJOz7e4q-LceY1c2Lhqsa92i72Mp8hy4EIUsBpRvURN8jAGrchVco8NHyVm5sV7-sT50Tr_n-0WD9rfxo3kAzrdA1EssX30fBoPxn8Uv-7KI3w</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Ruiz, Miguel</creator><creator>Cocores, Alexandra</creator><creator>Tosti, Antonella</creator><creator>Goadsby, Peter J</creator><creator>Monteith, Teshamae S</creator><general>SAGE Publications</general><scope>AFRWT</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>7X8</scope><orcidid>https://orcid.org/0000-0003-3260-5904</orcidid><orcidid>https://orcid.org/0000-0001-8912-252X</orcidid></search><sort><creationdate>202302</creationdate><title>Alopecia as an emerging adverse event to CGRP monoclonal antibodies: Cases Series, evaluation of FAERS, and literature review</title><author>Ruiz, Miguel ; Cocores, Alexandra ; Tosti, Antonella ; Goadsby, Peter J ; Monteith, Teshamae S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-44d1a54009597fd52dcfb7c43639ed40f527a430d08323999e0934389acdc2b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibodies, Monoclonal</topic><topic>Calcitonin Gene-Related Peptide</topic><topic>Calcitonin Gene-Related Peptide Receptor Antagonists</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Migraine Disorders</topic><topic>Receptors, Calcitonin Gene-Related Peptide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruiz, Miguel</creatorcontrib><creatorcontrib>Cocores, Alexandra</creatorcontrib><creatorcontrib>Tosti, Antonella</creatorcontrib><creatorcontrib>Goadsby, Peter J</creatorcontrib><creatorcontrib>Monteith, Teshamae S</creatorcontrib><collection>SAGE Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cephalalgia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruiz, Miguel</au><au>Cocores, Alexandra</au><au>Tosti, Antonella</au><au>Goadsby, Peter J</au><au>Monteith, Teshamae S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alopecia as an emerging adverse event to CGRP monoclonal antibodies: Cases Series, evaluation of FAERS, and literature review</atitle><jtitle>Cephalalgia</jtitle><addtitle>Cephalalgia</addtitle><date>2023-02</date><risdate>2023</risdate><volume>43</volume><issue>2</issue><spage>3331024221143538</spage><epage>3331024221143538</epage><pages>3331024221143538-3331024221143538</pages><issn>0333-1024</issn><eissn>1468-2982</eissn><abstract>Background
Alopecia is associated with erenumab post-marketing, but no cases have been described.
Methods
We describe two patients that reported temporary hair loss and review the FDA Adverse Event Reporting System (FAERS).
Results
The first patient experienced alopecia within three months of starting erenumab, which did not improve with ongoing use or transition to fremanezumab. The second patient reported alopecia within two weeks of starting erenumab, which continued after transition to galcanezumab; months later, there was also recurrent hair loss within one month of starting fremanzeumab. According to FAERS (last accessed 18 August 2022), alopecia was reported most with erenumab (1158), followed by galcanezumab (554), fremanezumab (175), eptinezumab (23), rimegepant (26), ubrogepant (4), and atogepant (3).
Conclusion
Most events were reported in women and non-serious. The potential mechanism of alopecia with drugs targeting calcitonin gene-related peptide or its receptor possibly includes disruptions in the microvascular circulation and other homeostatic mechanisms.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>36739513</pmid><doi>10.1177/03331024221143538</doi><orcidid>https://orcid.org/0000-0003-3260-5904</orcidid><orcidid>https://orcid.org/0000-0001-8912-252X</orcidid><oa>free_for_read</oa></addata></record> |
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source | SAGE Open Access |
subjects | Antibodies, Monoclonal Calcitonin Gene-Related Peptide Calcitonin Gene-Related Peptide Receptor Antagonists Female Humans Male Migraine Disorders Receptors, Calcitonin Gene-Related Peptide |
title | Alopecia as an emerging adverse event to CGRP monoclonal antibodies: Cases Series, evaluation of FAERS, and literature review |
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