Impact of medications on salivary flow rate in patients with xerostomia: a retrospective study by the Xeromeds Consortium

Objectives This study evaluates the impact of systemic medications and polypharmacy on unstimulated (UWS) and chewing-stimulated whole saliva (SWS) flow rates in patients with xerostomia. Material and methods This cross-sectional multicenter study is based on data of patients referred to five oral m...

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Veröffentlicht in:Clinical oral investigations 2023-01, Vol.27 (1), p.235-248
Hauptverfasser: Fortuna, Giulio, Whitmire, Sarah, Sullivan, Kathleen, Alajbeg, Ivan, Andabak-Rogulj, Ana, Pedersen, Anne Marie Lynge, Vissink, Arjan, di Fede, Olga, Aria, Massimo, Jager, Derk Jan, Noll, Jenene, Jensen, Siri Beier, Wolff, Andy, Brennan, Michael T.
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container_end_page 248
container_issue 1
container_start_page 235
container_title Clinical oral investigations
container_volume 27
creator Fortuna, Giulio
Whitmire, Sarah
Sullivan, Kathleen
Alajbeg, Ivan
Andabak-Rogulj, Ana
Pedersen, Anne Marie Lynge
Vissink, Arjan
di Fede, Olga
Aria, Massimo
Jager, Derk Jan
Noll, Jenene
Jensen, Siri Beier
Wolff, Andy
Brennan, Michael T.
description Objectives This study evaluates the impact of systemic medications and polypharmacy on unstimulated (UWS) and chewing-stimulated whole saliva (SWS) flow rates in patients with xerostomia. Material and methods This cross-sectional multicenter study is based on data of patients referred to five oral medicine outpatient practices in Europe and USA from January 2000 and April 2014. Relevant demographic, social, medical history and current medications were collected. Results The study included 1144 patients, 972 (85%) females, with a mean (SD) age of 59 (14.1) years. In unmatched patients, the UWS flow rate was lower in patients taking a medication (vs. not taking a medication) from the following drug categories: opioid analgesics, anticonvulsants, antidepressants, antihypertensives, benzodiazepines, corticosteroids, diuretics, disease-modifying antirheumatic drugs (DMARDs) and hormones. There was a greater negative effect on SWS flow rate in patients taking (vs. not taking) anticonvulsants, antidepressants, benzodiazepines, corticosteroids, and DMARDs. In matched patients, both UWS (0.22 vs. 0.19 ml/min; p  = 0.03) and SWS (0.97 vs. 0.85 ml/min; p  = .017) flow rates were higher in patients on non-opioid analgesics (vs. not taking). The UWS flow rate was lower in patients taking antidepressants (vs. not taking) (0.16 vs. 0.22 ml/min p  = .002) and higher (and within normal range) in patients taking sex hormones (vs. not taking) (0.25 vs. 0.16 ml/min; p  = .005). On the other hand, SWS was lower in patients taking corticosteroid (vs. not taking) (0.76 vs. 1.07 ml/min;  p  = .002), and in patients taking DMARDs (vs. not taking) (0.71 vs. 0.98 ml/min;  p  = .021). Finally, differences in medians of both UWS and SWS were statistically significant in patients taking 1 or more than 1 opioid analgesic (vs. not taking, p  ≤ .0001 and p  = .031, respectively), 1 or more than 1 anticonvulsants (vs. not taking, p  = .008 and p  = .007), 1 or more than 1 antidepressants (vs. not taking, p  
doi_str_mv 10.1007/s00784-022-04717-1
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Material and methods This cross-sectional multicenter study is based on data of patients referred to five oral medicine outpatient practices in Europe and USA from January 2000 and April 2014. Relevant demographic, social, medical history and current medications were collected. Results The study included 1144 patients, 972 (85%) females, with a mean (SD) age of 59 (14.1) years. In unmatched patients, the UWS flow rate was lower in patients taking a medication (vs. not taking a medication) from the following drug categories: opioid analgesics, anticonvulsants, antidepressants, antihypertensives, benzodiazepines, corticosteroids, diuretics, disease-modifying antirheumatic drugs (DMARDs) and hormones. There was a greater negative effect on SWS flow rate in patients taking (vs. not taking) anticonvulsants, antidepressants, benzodiazepines, corticosteroids, and DMARDs. In matched patients, both UWS (0.22 vs. 0.19 ml/min; p  = 0.03) and SWS (0.97 vs. 0.85 ml/min; p  = .017) flow rates were higher in patients on non-opioid analgesics (vs. not taking). The UWS flow rate was lower in patients taking antidepressants (vs. not taking) (0.16 vs. 0.22 ml/min p  = .002) and higher (and within normal range) in patients taking sex hormones (vs. not taking) (0.25 vs. 0.16 ml/min; p  = .005). On the other hand, SWS was lower in patients taking corticosteroid (vs. not taking) (0.76 vs. 1.07 ml/min;  p  = .002), and in patients taking DMARDs (vs. not taking) (0.71 vs. 0.98 ml/min;  p  = .021). Finally, differences in medians of both UWS and SWS were statistically significant in patients taking 1 or more than 1 opioid analgesic (vs. not taking, p  ≤ .0001 and p  = .031, respectively), 1 or more than 1 anticonvulsants (vs. not taking, p  = .008 and p  = .007), 1 or more than 1 antidepressants (vs. not taking, p  &lt; .0001 for both), 1 or more than 1 DMARDs (vs. not taking, p  = .042, and p  = .003). Conclusions A greater negative impact on UWS and SWS flow rates was seen in patients taking more than one medication from the same drug class. Intake of antidepressants, corticosteroids and DMARDs is associated with lower whole saliva flow rates. Clinical relevance Salivary flow rate can be modified by some specific medications, mostly by polypharmacy.</description><identifier>ISSN: 1436-3771</identifier><identifier>ISSN: 1432-6981</identifier><identifier>EISSN: 1436-3771</identifier><identifier>DOI: 10.1007/s00784-022-04717-1</identifier><identifier>PMID: 36269468</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analgesics ; Anticonvulsants ; Antidepressants ; Antidepressive Agents - therapeutic use ; Antihypertensives ; Antirheumatic Agents ; Benzodiazepines ; Corticosteroids ; Cross-Sectional Studies ; Dentistry ; Diuretics ; Female ; Humans ; Male ; Medicine ; Middle Aged ; Narcotics ; Opioids ; Original Article ; Patients ; Polypharmacy ; Retrospective Studies ; Saliva ; Sex hormones ; Statistical analysis ; Steroids ; Xerostomia</subject><ispartof>Clinical oral investigations, 2023-01, Vol.27 (1), p.235-248</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. 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The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-eddf351f62bf197783d1c2119667378241cf983178f3832ae62e459508ad35673</citedby><cites>FETCH-LOGICAL-c419t-eddf351f62bf197783d1c2119667378241cf983178f3832ae62e459508ad35673</cites><orcidid>0000-0003-0638-4335</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/s00784-022-04717-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00784-022-04717-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36269468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fortuna, Giulio</creatorcontrib><creatorcontrib>Whitmire, Sarah</creatorcontrib><creatorcontrib>Sullivan, Kathleen</creatorcontrib><creatorcontrib>Alajbeg, Ivan</creatorcontrib><creatorcontrib>Andabak-Rogulj, Ana</creatorcontrib><creatorcontrib>Pedersen, Anne Marie Lynge</creatorcontrib><creatorcontrib>Vissink, Arjan</creatorcontrib><creatorcontrib>di Fede, Olga</creatorcontrib><creatorcontrib>Aria, Massimo</creatorcontrib><creatorcontrib>Jager, Derk Jan</creatorcontrib><creatorcontrib>Noll, Jenene</creatorcontrib><creatorcontrib>Jensen, Siri Beier</creatorcontrib><creatorcontrib>Wolff, Andy</creatorcontrib><creatorcontrib>Brennan, Michael T.</creatorcontrib><title>Impact of medications on salivary flow rate in patients with xerostomia: a retrospective study by the Xeromeds Consortium</title><title>Clinical oral investigations</title><addtitle>Clin Oral Invest</addtitle><addtitle>Clin Oral Investig</addtitle><description>Objectives This study evaluates the impact of systemic medications and polypharmacy on unstimulated (UWS) and chewing-stimulated whole saliva (SWS) flow rates in patients with xerostomia. Material and methods This cross-sectional multicenter study is based on data of patients referred to five oral medicine outpatient practices in Europe and USA from January 2000 and April 2014. Relevant demographic, social, medical history and current medications were collected. Results The study included 1144 patients, 972 (85%) females, with a mean (SD) age of 59 (14.1) years. In unmatched patients, the UWS flow rate was lower in patients taking a medication (vs. not taking a medication) from the following drug categories: opioid analgesics, anticonvulsants, antidepressants, antihypertensives, benzodiazepines, corticosteroids, diuretics, disease-modifying antirheumatic drugs (DMARDs) and hormones. There was a greater negative effect on SWS flow rate in patients taking (vs. not taking) anticonvulsants, antidepressants, benzodiazepines, corticosteroids, and DMARDs. In matched patients, both UWS (0.22 vs. 0.19 ml/min; p  = 0.03) and SWS (0.97 vs. 0.85 ml/min; p  = .017) flow rates were higher in patients on non-opioid analgesics (vs. not taking). The UWS flow rate was lower in patients taking antidepressants (vs. not taking) (0.16 vs. 0.22 ml/min p  = .002) and higher (and within normal range) in patients taking sex hormones (vs. not taking) (0.25 vs. 0.16 ml/min; p  = .005). On the other hand, SWS was lower in patients taking corticosteroid (vs. not taking) (0.76 vs. 1.07 ml/min;  p  = .002), and in patients taking DMARDs (vs. not taking) (0.71 vs. 0.98 ml/min;  p  = .021). Finally, differences in medians of both UWS and SWS were statistically significant in patients taking 1 or more than 1 opioid analgesic (vs. not taking, p  ≤ .0001 and p  = .031, respectively), 1 or more than 1 anticonvulsants (vs. not taking, p  = .008 and p  = .007), 1 or more than 1 antidepressants (vs. not taking, p  &lt; .0001 for both), 1 or more than 1 DMARDs (vs. not taking, p  = .042, and p  = .003). Conclusions A greater negative impact on UWS and SWS flow rates was seen in patients taking more than one medication from the same drug class. Intake of antidepressants, corticosteroids and DMARDs is associated with lower whole saliva flow rates. Clinical relevance Salivary flow rate can be modified by some specific medications, mostly by polypharmacy.</description><subject>Analgesics</subject><subject>Anticonvulsants</subject><subject>Antidepressants</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Antihypertensives</subject><subject>Antirheumatic Agents</subject><subject>Benzodiazepines</subject><subject>Corticosteroids</subject><subject>Cross-Sectional Studies</subject><subject>Dentistry</subject><subject>Diuretics</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Middle Aged</subject><subject>Narcotics</subject><subject>Opioids</subject><subject>Original Article</subject><subject>Patients</subject><subject>Polypharmacy</subject><subject>Retrospective Studies</subject><subject>Saliva</subject><subject>Sex hormones</subject><subject>Statistical analysis</subject><subject>Steroids</subject><subject>Xerostomia</subject><issn>1436-3771</issn><issn>1432-6981</issn><issn>1436-3771</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kctu1TAQhi0Eohd4ARbIEptuAh7bsZ3u0FFvUiU2ILGzfBKbukri1HZaztsz9JSLWLDx2Jpv_vHMT8gbYO-BMf2h4GFkwzhvmNSgG3hGDkEK1Qit4flf9wNyVMotYyCVFi_JgVBcdVKZQ7K7mhbXV5oCnfwQe1djmgtNMy1ujPcu72gY0wPNrnoaZ7og4Oda6EOsN_S7z6nUNEV3Sh3NvuJz8X2N956Wug47ut3ReuPpVwRRv9ANqqdc4zq9Ii-CG4t__RSPyZfzs8-by-b608XV5uN100voauOHIYgWguLbAJ3WRgzQc4BO4SjacAl96IwAbYIwgjuvuJdt1zLjBtEic0xO9rpLTnerL9VOsfR-HN3s01os11wryQy0iL77B71Na57xd0gpg206LZDie6rHaUv2wS45TrgpC8z-NMbujbFojH00xgIWvX2SXre4iN8lv5xAQOyBgqn5m89_ev9H9ge1ZJkd</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Fortuna, Giulio</creator><creator>Whitmire, Sarah</creator><creator>Sullivan, Kathleen</creator><creator>Alajbeg, Ivan</creator><creator>Andabak-Rogulj, Ana</creator><creator>Pedersen, Anne Marie Lynge</creator><creator>Vissink, Arjan</creator><creator>di Fede, Olga</creator><creator>Aria, Massimo</creator><creator>Jager, Derk Jan</creator><creator>Noll, Jenene</creator><creator>Jensen, Siri Beier</creator><creator>Wolff, Andy</creator><creator>Brennan, Michael T.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0638-4335</orcidid></search><sort><creationdate>20230101</creationdate><title>Impact of medications on salivary flow rate in patients with xerostomia: a retrospective study by the Xeromeds Consortium</title><author>Fortuna, Giulio ; Whitmire, Sarah ; Sullivan, Kathleen ; Alajbeg, Ivan ; Andabak-Rogulj, Ana ; Pedersen, Anne Marie Lynge ; Vissink, Arjan ; di Fede, Olga ; Aria, Massimo ; Jager, Derk Jan ; Noll, Jenene ; Jensen, Siri Beier ; Wolff, Andy ; Brennan, Michael T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-eddf351f62bf197783d1c2119667378241cf983178f3832ae62e459508ad35673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analgesics</topic><topic>Anticonvulsants</topic><topic>Antidepressants</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Antihypertensives</topic><topic>Antirheumatic Agents</topic><topic>Benzodiazepines</topic><topic>Corticosteroids</topic><topic>Cross-Sectional Studies</topic><topic>Dentistry</topic><topic>Diuretics</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Middle Aged</topic><topic>Narcotics</topic><topic>Opioids</topic><topic>Original Article</topic><topic>Patients</topic><topic>Polypharmacy</topic><topic>Retrospective Studies</topic><topic>Saliva</topic><topic>Sex hormones</topic><topic>Statistical analysis</topic><topic>Steroids</topic><topic>Xerostomia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fortuna, Giulio</creatorcontrib><creatorcontrib>Whitmire, Sarah</creatorcontrib><creatorcontrib>Sullivan, Kathleen</creatorcontrib><creatorcontrib>Alajbeg, Ivan</creatorcontrib><creatorcontrib>Andabak-Rogulj, Ana</creatorcontrib><creatorcontrib>Pedersen, Anne Marie Lynge</creatorcontrib><creatorcontrib>Vissink, Arjan</creatorcontrib><creatorcontrib>di Fede, Olga</creatorcontrib><creatorcontrib>Aria, Massimo</creatorcontrib><creatorcontrib>Jager, Derk Jan</creatorcontrib><creatorcontrib>Noll, Jenene</creatorcontrib><creatorcontrib>Jensen, Siri Beier</creatorcontrib><creatorcontrib>Wolff, Andy</creatorcontrib><creatorcontrib>Brennan, Michael T.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Material and methods This cross-sectional multicenter study is based on data of patients referred to five oral medicine outpatient practices in Europe and USA from January 2000 and April 2014. Relevant demographic, social, medical history and current medications were collected. Results The study included 1144 patients, 972 (85%) females, with a mean (SD) age of 59 (14.1) years. In unmatched patients, the UWS flow rate was lower in patients taking a medication (vs. not taking a medication) from the following drug categories: opioid analgesics, anticonvulsants, antidepressants, antihypertensives, benzodiazepines, corticosteroids, diuretics, disease-modifying antirheumatic drugs (DMARDs) and hormones. There was a greater negative effect on SWS flow rate in patients taking (vs. not taking) anticonvulsants, antidepressants, benzodiazepines, corticosteroids, and DMARDs. In matched patients, both UWS (0.22 vs. 0.19 ml/min; p  = 0.03) and SWS (0.97 vs. 0.85 ml/min; p  = .017) flow rates were higher in patients on non-opioid analgesics (vs. not taking). The UWS flow rate was lower in patients taking antidepressants (vs. not taking) (0.16 vs. 0.22 ml/min p  = .002) and higher (and within normal range) in patients taking sex hormones (vs. not taking) (0.25 vs. 0.16 ml/min; p  = .005). On the other hand, SWS was lower in patients taking corticosteroid (vs. not taking) (0.76 vs. 1.07 ml/min;  p  = .002), and in patients taking DMARDs (vs. not taking) (0.71 vs. 0.98 ml/min;  p  = .021). Finally, differences in medians of both UWS and SWS were statistically significant in patients taking 1 or more than 1 opioid analgesic (vs. not taking, p  ≤ .0001 and p  = .031, respectively), 1 or more than 1 anticonvulsants (vs. not taking, p  = .008 and p  = .007), 1 or more than 1 antidepressants (vs. not taking, p  &lt; .0001 for both), 1 or more than 1 DMARDs (vs. not taking, p  = .042, and p  = .003). Conclusions A greater negative impact on UWS and SWS flow rates was seen in patients taking more than one medication from the same drug class. Intake of antidepressants, corticosteroids and DMARDs is associated with lower whole saliva flow rates. Clinical relevance Salivary flow rate can be modified by some specific medications, mostly by polypharmacy.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36269468</pmid><doi>10.1007/s00784-022-04717-1</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-0638-4335</orcidid><oa>free_for_read</oa></addata></record>
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subjects Analgesics
Anticonvulsants
Antidepressants
Antidepressive Agents - therapeutic use
Antihypertensives
Antirheumatic Agents
Benzodiazepines
Corticosteroids
Cross-Sectional Studies
Dentistry
Diuretics
Female
Humans
Male
Medicine
Middle Aged
Narcotics
Opioids
Original Article
Patients
Polypharmacy
Retrospective Studies
Saliva
Sex hormones
Statistical analysis
Steroids
Xerostomia
title Impact of medications on salivary flow rate in patients with xerostomia: a retrospective study by the Xeromeds Consortium
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