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Drug clustering to anticipate new aspects of drug safety profile: application to gabapentinoids and other voltage-gated calcium channel ligand drugs: Drug clustering to anticipate drug safety profile
Aims : Gabapentin and pregabalin bind to α2‐δ subunit of voltage‐gated calcium channels (Cav). Other drugs targeting Cav include cardiovascular calcium channel blockers (CCBs) and anticonvulsants (levetiracetam, ethosuximide and zonisamide). In addition to pharmacodynamics, the safety profile of gab...
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Published in: | British journal of clinical pharmacology 2024-02, Vol.90 (2), p.475-482 |
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creator | Viguier, Thibault Agier, Marie‐sara Jonville-Béra, Annie‐pierre Giraudeau, Bruno Largeau, Bérenger |
description | Aims : Gabapentin and pregabalin bind to α2‐δ subunit of voltage‐gated calcium channels (Cav). Other drugs targeting Cav include cardiovascular calcium channel blockers (CCBs) and anticonvulsants (levetiracetam, ethosuximide and zonisamide). In addition to pharmacodynamics, the safety profile of gabapentinoids seems to overlap with the one of cardiovascular CCBs (oedema) and Cav‐blocking anticonvulsants (suicide and ataxia). The objective of this study was to cluster the safety profile of different Cav‐ligand drugs by focusing on whether gabapentinoids present a distinct adverse drug reaction (ADR) signature from cardiovascular CCBs and anticonvulsants. Methods: We extracted all ADRs with at least one significant disproportionate reporting (reporting odds ratio) related to gabapentinoids, CCBs or anticonvulsants in VigiBase. After principal component analysis preprocessing, a hierarchical ascendent classification was performed to cluster gabapentinoids and other Cav‐ligand drugs that share a similar ADR signature. The robustness of the results was determined through four sensitivity analyses, varying on the dataset or the clustering method. Results: A total of 16 drugs and 65 ADRs were included. Gabapentinoids were in Cluster #1, which included eight other drugs (isradipine, nicardipine, lacidipine, lercanidipine, ethosuximide, levetiracetam, zonisamide and nimodipine). Cluster #2 contained two drugs (diltiazem and verapamil) and Cluster #3 contained four drugs (amlodipine, felodipine, nifedipine and nitrendipine). The clustering results were consistent in all sensitivity analyses.Conclusions: The safety profile of gabapentinoids overlaps with those of some dihydropyridine CCBs and Cav‐blocking anticonvulsants. These results could be used to anticipate some unidentified ADRs of gabapentinoids from information accumulated with older drugs and sharing a common molecular target and ADR signature. |
doi_str_mv | 10.1111/bcp.15931 |
format | article |
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Other drugs targeting Cav include cardiovascular calcium channel blockers (CCBs) and anticonvulsants (levetiracetam, ethosuximide and zonisamide). In addition to pharmacodynamics, the safety profile of gabapentinoids seems to overlap with the one of cardiovascular CCBs (oedema) and Cav‐blocking anticonvulsants (suicide and ataxia). The objective of this study was to cluster the safety profile of different Cav‐ligand drugs by focusing on whether gabapentinoids present a distinct adverse drug reaction (ADR) signature from cardiovascular CCBs and anticonvulsants. Methods: We extracted all ADRs with at least one significant disproportionate reporting (reporting odds ratio) related to gabapentinoids, CCBs or anticonvulsants in VigiBase. After principal component analysis preprocessing, a hierarchical ascendent classification was performed to cluster gabapentinoids and other Cav‐ligand drugs that share a similar ADR signature. The robustness of the results was determined through four sensitivity analyses, varying on the dataset or the clustering method. Results: A total of 16 drugs and 65 ADRs were included. Gabapentinoids were in Cluster #1, which included eight other drugs (isradipine, nicardipine, lacidipine, lercanidipine, ethosuximide, levetiracetam, zonisamide and nimodipine). Cluster #2 contained two drugs (diltiazem and verapamil) and Cluster #3 contained four drugs (amlodipine, felodipine, nifedipine and nitrendipine). The clustering results were consistent in all sensitivity analyses.Conclusions: The safety profile of gabapentinoids overlaps with those of some dihydropyridine CCBs and Cav‐blocking anticonvulsants. These results could be used to anticipate some unidentified ADRs of gabapentinoids from information accumulated with older drugs and sharing a common molecular target and ADR signature.</description><identifier>ISSN: 0306-5251</identifier><identifier>EISSN: 1365-2125</identifier><identifier>DOI: 10.1111/bcp.15931</identifier><identifier>PMID: 37872105</identifier><language>eng</language><publisher>Wiley</publisher><subject>Life Sciences ; Pharmaceutical sciences ; Pharmacology</subject><ispartof>British journal of clinical pharmacology, 2024-02, Vol.90 (2), p.475-482</ispartof><rights>Attribution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-6824-7283 ; 0000-0003-3031-8258 ; 0000-0003-3031-8258 ; 0000-0002-6824-7283</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04674979$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Viguier, Thibault</creatorcontrib><creatorcontrib>Agier, Marie‐sara</creatorcontrib><creatorcontrib>Jonville-Béra, Annie‐pierre</creatorcontrib><creatorcontrib>Giraudeau, Bruno</creatorcontrib><creatorcontrib>Largeau, Bérenger</creatorcontrib><title>Drug clustering to anticipate new aspects of drug safety profile: application to gabapentinoids and other voltage-gated calcium channel ligand drugs: Drug clustering to anticipate drug safety profile</title><title>British journal of clinical pharmacology</title><description>Aims : Gabapentin and pregabalin bind to α2‐δ subunit of voltage‐gated calcium channels (Cav). Other drugs targeting Cav include cardiovascular calcium channel blockers (CCBs) and anticonvulsants (levetiracetam, ethosuximide and zonisamide). In addition to pharmacodynamics, the safety profile of gabapentinoids seems to overlap with the one of cardiovascular CCBs (oedema) and Cav‐blocking anticonvulsants (suicide and ataxia). The objective of this study was to cluster the safety profile of different Cav‐ligand drugs by focusing on whether gabapentinoids present a distinct adverse drug reaction (ADR) signature from cardiovascular CCBs and anticonvulsants. Methods: We extracted all ADRs with at least one significant disproportionate reporting (reporting odds ratio) related to gabapentinoids, CCBs or anticonvulsants in VigiBase. After principal component analysis preprocessing, a hierarchical ascendent classification was performed to cluster gabapentinoids and other Cav‐ligand drugs that share a similar ADR signature. The robustness of the results was determined through four sensitivity analyses, varying on the dataset or the clustering method. Results: A total of 16 drugs and 65 ADRs were included. Gabapentinoids were in Cluster #1, which included eight other drugs (isradipine, nicardipine, lacidipine, lercanidipine, ethosuximide, levetiracetam, zonisamide and nimodipine). Cluster #2 contained two drugs (diltiazem and verapamil) and Cluster #3 contained four drugs (amlodipine, felodipine, nifedipine and nitrendipine). The clustering results were consistent in all sensitivity analyses.Conclusions: The safety profile of gabapentinoids overlaps with those of some dihydropyridine CCBs and Cav‐blocking anticonvulsants. These results could be used to anticipate some unidentified ADRs of gabapentinoids from information accumulated with older drugs and sharing a common molecular target and ADR signature.</description><subject>Life Sciences</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacology</subject><issn>0306-5251</issn><issn>1365-2125</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqVjU1OwzAQhS0Eoimw4AazZZFix3VC2CF-1AXL7qOp4zhGrm3ZTlHvwYFJJC7AbJ709L1vCLlndMPmezzIsGGi5eyCFIzXoqxYJS5JQTmtS1EJtiLrlL4oZZzV4pqsePPUVIyKgvy8xUmDtFPKKhqnIXtAl400AbMCp74BU1AyJ_AD9AuccFD5DCH6wVj1DBiCNRKz8W5ZazxgULPCedOnWdaDz6OKcPI2o1alnsU9SLTSTEeQIzqnLFijF3T5kG7J1YA2qbu_vCEPH-_71105ou1CNEeM586j6XYvn93S0W3dbNumPTH-H_YXY5xj7A</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Viguier, Thibault</creator><creator>Agier, Marie‐sara</creator><creator>Jonville-Béra, Annie‐pierre</creator><creator>Giraudeau, Bruno</creator><creator>Largeau, Bérenger</creator><general>Wiley</general><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-6824-7283</orcidid><orcidid>https://orcid.org/0000-0003-3031-8258</orcidid><orcidid>https://orcid.org/0000-0003-3031-8258</orcidid><orcidid>https://orcid.org/0000-0002-6824-7283</orcidid></search><sort><creationdate>202402</creationdate><title>Drug clustering to anticipate new aspects of drug safety profile: application to gabapentinoids and other voltage-gated calcium channel ligand drugs</title><author>Viguier, Thibault ; Agier, Marie‐sara ; Jonville-Béra, Annie‐pierre ; Giraudeau, Bruno ; Largeau, Bérenger</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_04674979v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Life Sciences</topic><topic>Pharmaceutical sciences</topic><topic>Pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Viguier, Thibault</creatorcontrib><creatorcontrib>Agier, Marie‐sara</creatorcontrib><creatorcontrib>Jonville-Béra, Annie‐pierre</creatorcontrib><creatorcontrib>Giraudeau, Bruno</creatorcontrib><creatorcontrib>Largeau, Bérenger</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>British journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Viguier, Thibault</au><au>Agier, Marie‐sara</au><au>Jonville-Béra, Annie‐pierre</au><au>Giraudeau, Bruno</au><au>Largeau, Bérenger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug clustering to anticipate new aspects of drug safety profile: application to gabapentinoids and other voltage-gated calcium channel ligand drugs: Drug clustering to anticipate drug safety profile</atitle><jtitle>British journal of clinical pharmacology</jtitle><date>2024-02</date><risdate>2024</risdate><volume>90</volume><issue>2</issue><spage>475</spage><epage>482</epage><pages>475-482</pages><issn>0306-5251</issn><eissn>1365-2125</eissn><abstract>Aims : Gabapentin and pregabalin bind to α2‐δ subunit of voltage‐gated calcium channels (Cav). Other drugs targeting Cav include cardiovascular calcium channel blockers (CCBs) and anticonvulsants (levetiracetam, ethosuximide and zonisamide). In addition to pharmacodynamics, the safety profile of gabapentinoids seems to overlap with the one of cardiovascular CCBs (oedema) and Cav‐blocking anticonvulsants (suicide and ataxia). The objective of this study was to cluster the safety profile of different Cav‐ligand drugs by focusing on whether gabapentinoids present a distinct adverse drug reaction (ADR) signature from cardiovascular CCBs and anticonvulsants. Methods: We extracted all ADRs with at least one significant disproportionate reporting (reporting odds ratio) related to gabapentinoids, CCBs or anticonvulsants in VigiBase. After principal component analysis preprocessing, a hierarchical ascendent classification was performed to cluster gabapentinoids and other Cav‐ligand drugs that share a similar ADR signature. The robustness of the results was determined through four sensitivity analyses, varying on the dataset or the clustering method. Results: A total of 16 drugs and 65 ADRs were included. Gabapentinoids were in Cluster #1, which included eight other drugs (isradipine, nicardipine, lacidipine, lercanidipine, ethosuximide, levetiracetam, zonisamide and nimodipine). Cluster #2 contained two drugs (diltiazem and verapamil) and Cluster #3 contained four drugs (amlodipine, felodipine, nifedipine and nitrendipine). The clustering results were consistent in all sensitivity analyses.Conclusions: The safety profile of gabapentinoids overlaps with those of some dihydropyridine CCBs and Cav‐blocking anticonvulsants. These results could be used to anticipate some unidentified ADRs of gabapentinoids from information accumulated with older drugs and sharing a common molecular target and ADR signature.</abstract><pub>Wiley</pub><pmid>37872105</pmid><doi>10.1111/bcp.15931</doi><orcidid>https://orcid.org/0000-0002-6824-7283</orcidid><orcidid>https://orcid.org/0000-0003-3031-8258</orcidid><orcidid>https://orcid.org/0000-0003-3031-8258</orcidid><orcidid>https://orcid.org/0000-0002-6824-7283</orcidid><oa>free_for_read</oa></addata></record> |
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source | Wiley-Blackwell Read & Publish Collection |
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title | Drug clustering to anticipate new aspects of drug safety profile: application to gabapentinoids and other voltage-gated calcium channel ligand drugs: Drug clustering to anticipate drug safety profile |
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