Anti-acid therapy in SSc-associated interstitial lung disease: long-term outcomes from the German Network for Systemic Sclerosis

Abstract Objectives Gastroesophageal reflux disease (GERD) occurs frequently in patients with SSc. We investigated whether the presence of GERD and/or the use of anti-acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-term outcomes, especially in SSc-associated inters...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2023-09, Vol.62 (9), p.3067-3074
Hauptverfasser: Kreuter, Michael, Bonella, Francesco, Blank, Norbert, Riemekasten, Gabriela, Müller-Ladner, Ulf, Henes, Jörg, Siegert, Elise, Günther, Claudia, Kötter, Ina, Pfeiffer, Christiane, Schmalzing, Marc, Zeidler, Gabriele, Korsten, Peter, Susok, Laura, Juche, Aaron, Worm, Margitta, Jandova, Ilona, Ehrchen, Jan, Sunderkötter, Cord, Keyßer, Gernot, Ramming, Andreas, Schmeiser, Tim, Kreuter, Alexander, Kuhr, Kathrin, Lorenz, Hanns-Martin, Moinzadeh, Pia, Hunzelmann, Nicolas
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container_issue 9
container_start_page 3067
container_title Rheumatology (Oxford, England)
container_volume 62
creator Kreuter, Michael
Bonella, Francesco
Blank, Norbert
Riemekasten, Gabriela
Müller-Ladner, Ulf
Henes, Jörg
Siegert, Elise
Günther, Claudia
Kötter, Ina
Pfeiffer, Christiane
Schmalzing, Marc
Zeidler, Gabriele
Korsten, Peter
Susok, Laura
Juche, Aaron
Worm, Margitta
Jandova, Ilona
Ehrchen, Jan
Sunderkötter, Cord
Keyßer, Gernot
Ramming, Andreas
Schmeiser, Tim
Kreuter, Alexander
Kuhr, Kathrin
Lorenz, Hanns-Martin
Moinzadeh, Pia
Hunzelmann, Nicolas
description Abstract Objectives Gastroesophageal reflux disease (GERD) occurs frequently in patients with SSc. We investigated whether the presence of GERD and/or the use of anti-acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-term outcomes, especially in SSc-associated interstitial lung disease (SSc-ILD). Methods We retrospectively analysed patients with SSc and SSc-ILD from the German Network for Systemic Sclerosis (DNSS) database (2003 onwards). Kaplan–Meier analysis compared overall survival (OS) and progression-free survival (PFS) in patients with GERD vs without GERD (SSc and SSc-ILD), and PPI vs no PPI use (SSc-ILD only). Progression was defined as a decrease in either percentage predicted forced vital capacity of ≥10% or single-breath diffusing capacity for carbon monoxide of ≥15%, or death. Results It was found that 2693/4306 (63%) registered patients with SSc and 1204/1931 (62%) with SSc-ILD had GERD. GERD was not associated with decreased OS or decreased PFS in patients in either cohort. In SSc-ILD, PPI use was associated with improved OS vs no PPI use after 1 year [98.4% (95% CI: 97.6, 99.3); n = 760 vs 90.8% (87.9–93.8); n = 290] and after 5 years [91.4% (89.2–93.8); n = 357 vs 70.9% (65.2–77.1); n = 106; P 
doi_str_mv 10.1093/rheumatology/kead023
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We investigated whether the presence of GERD and/or the use of anti-acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-term outcomes, especially in SSc-associated interstitial lung disease (SSc-ILD). Methods We retrospectively analysed patients with SSc and SSc-ILD from the German Network for Systemic Sclerosis (DNSS) database (2003 onwards). Kaplan–Meier analysis compared overall survival (OS) and progression-free survival (PFS) in patients with GERD vs without GERD (SSc and SSc-ILD), and PPI vs no PPI use (SSc-ILD only). Progression was defined as a decrease in either percentage predicted forced vital capacity of ≥10% or single-breath diffusing capacity for carbon monoxide of ≥15%, or death. Results It was found that 2693/4306 (63%) registered patients with SSc and 1204/1931 (62%) with SSc-ILD had GERD. GERD was not associated with decreased OS or decreased PFS in patients in either cohort. In SSc-ILD, PPI use was associated with improved OS vs no PPI use after 1 year [98.4% (95% CI: 97.6, 99.3); n = 760 vs 90.8% (87.9–93.8); n = 290] and after 5 years [91.4% (89.2–93.8); n = 357 vs 70.9% (65.2–77.1); n = 106; P &lt; 0.0001]. PPI use was also associated with improved PFS vs no PPI use after 1 year [95.9% (94.6–97.3); n = 745 vs 86.4% (82.9–90.1); n = 278] and after 5 years [66.8% (63.0–70.8); n = 286 vs 45.9% (39.6–53.2); n = 69; P &lt; 0.0001]. Conclusion GERD had no effect on survival in SSc or SSc-ILD. PPIs improved survival in patients with SSc-ILD. Controlled, prospective trials are needed to confirm this finding.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/kead023</identifier><identifier>PMID: 36708008</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Clinical Science</subject><ispartof>Rheumatology (Oxford, England), 2023-09, Vol.62 (9), p.3067-3074</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-821aa54d95a942f1385d662ec7f698fdd323ca3181c19b8e48a2bc7783efafc43</citedby><cites>FETCH-LOGICAL-c449t-821aa54d95a942f1385d662ec7f698fdd323ca3181c19b8e48a2bc7783efafc43</cites><orcidid>0000-0001-6065-5680 ; 0000-0003-4402-2159 ; 0000-0001-7680-9971 ; 0000-0002-9419-1690 ; 0000-0001-5940-3195</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36708008$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kreuter, Michael</creatorcontrib><creatorcontrib>Bonella, Francesco</creatorcontrib><creatorcontrib>Blank, Norbert</creatorcontrib><creatorcontrib>Riemekasten, Gabriela</creatorcontrib><creatorcontrib>Müller-Ladner, Ulf</creatorcontrib><creatorcontrib>Henes, Jörg</creatorcontrib><creatorcontrib>Siegert, Elise</creatorcontrib><creatorcontrib>Günther, Claudia</creatorcontrib><creatorcontrib>Kötter, Ina</creatorcontrib><creatorcontrib>Pfeiffer, Christiane</creatorcontrib><creatorcontrib>Schmalzing, Marc</creatorcontrib><creatorcontrib>Zeidler, Gabriele</creatorcontrib><creatorcontrib>Korsten, Peter</creatorcontrib><creatorcontrib>Susok, Laura</creatorcontrib><creatorcontrib>Juche, Aaron</creatorcontrib><creatorcontrib>Worm, Margitta</creatorcontrib><creatorcontrib>Jandova, Ilona</creatorcontrib><creatorcontrib>Ehrchen, Jan</creatorcontrib><creatorcontrib>Sunderkötter, Cord</creatorcontrib><creatorcontrib>Keyßer, Gernot</creatorcontrib><creatorcontrib>Ramming, Andreas</creatorcontrib><creatorcontrib>Schmeiser, Tim</creatorcontrib><creatorcontrib>Kreuter, Alexander</creatorcontrib><creatorcontrib>Kuhr, Kathrin</creatorcontrib><creatorcontrib>Lorenz, Hanns-Martin</creatorcontrib><creatorcontrib>Moinzadeh, Pia</creatorcontrib><creatorcontrib>Hunzelmann, Nicolas</creatorcontrib><title>Anti-acid therapy in SSc-associated interstitial lung disease: long-term outcomes from the German Network for Systemic Sclerosis</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Abstract Objectives Gastroesophageal reflux disease (GERD) occurs frequently in patients with SSc. We investigated whether the presence of GERD and/or the use of anti-acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-term outcomes, especially in SSc-associated interstitial lung disease (SSc-ILD). Methods We retrospectively analysed patients with SSc and SSc-ILD from the German Network for Systemic Sclerosis (DNSS) database (2003 onwards). Kaplan–Meier analysis compared overall survival (OS) and progression-free survival (PFS) in patients with GERD vs without GERD (SSc and SSc-ILD), and PPI vs no PPI use (SSc-ILD only). Progression was defined as a decrease in either percentage predicted forced vital capacity of ≥10% or single-breath diffusing capacity for carbon monoxide of ≥15%, or death. Results It was found that 2693/4306 (63%) registered patients with SSc and 1204/1931 (62%) with SSc-ILD had GERD. GERD was not associated with decreased OS or decreased PFS in patients in either cohort. In SSc-ILD, PPI use was associated with improved OS vs no PPI use after 1 year [98.4% (95% CI: 97.6, 99.3); n = 760 vs 90.8% (87.9–93.8); n = 290] and after 5 years [91.4% (89.2–93.8); n = 357 vs 70.9% (65.2–77.1); n = 106; P &lt; 0.0001]. PPI use was also associated with improved PFS vs no PPI use after 1 year [95.9% (94.6–97.3); n = 745 vs 86.4% (82.9–90.1); n = 278] and after 5 years [66.8% (63.0–70.8); n = 286 vs 45.9% (39.6–53.2); n = 69; P &lt; 0.0001]. Conclusion GERD had no effect on survival in SSc or SSc-ILD. PPIs improved survival in patients with SSc-ILD. Controlled, prospective trials are needed to confirm this finding.</description><subject>Clinical Science</subject><issn>1462-0324</issn><issn>1462-0332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkU1v1DAQhiMEoqXwDxDykUu6_kpic0FV1RakqhwWztasPdk1TeLFdkB746fX1S6rcuvJ1swzjz16q-o9o-eMarGIG5xHyGEI693iHsFRLl5Up0y2vKZC8JfHO5cn1ZuUflJKGybU6-pEtB1VlKrT6u_FlH0N1juSNxhhuyN-IsulrSGlYD1kdKWSMabss4eBDPO0Js4nhISfyBCmdV26IwlztmHERPoYxkcZuSllmMgd5j8h3pM-RLLcpYyjt2RpB4wh-fS2etXDkPDd4Tyrflxffb_8Ut9-u_l6eXFbWyl1rhVnAI10ugEteV_WaFzbcrRd32rVOye4sCCYYpbplUKpgK9s1ymBPfRWirPq8967nVcjOotTjjCYbfQjxJ0J4M3_nclvzDr8NozKTjDdFMPHgyGGXzOmbEafLA4DTBjmZHjXFVRLpgsq96gtO6aI_fEdRs1jeuZpeuaQXhn78PSPx6F_cRVgsQfCvH2e8gHalbAF</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Kreuter, Michael</creator><creator>Bonella, Francesco</creator><creator>Blank, Norbert</creator><creator>Riemekasten, Gabriela</creator><creator>Müller-Ladner, Ulf</creator><creator>Henes, Jörg</creator><creator>Siegert, Elise</creator><creator>Günther, Claudia</creator><creator>Kötter, Ina</creator><creator>Pfeiffer, Christiane</creator><creator>Schmalzing, Marc</creator><creator>Zeidler, Gabriele</creator><creator>Korsten, Peter</creator><creator>Susok, Laura</creator><creator>Juche, Aaron</creator><creator>Worm, Margitta</creator><creator>Jandova, Ilona</creator><creator>Ehrchen, Jan</creator><creator>Sunderkötter, Cord</creator><creator>Keyßer, Gernot</creator><creator>Ramming, Andreas</creator><creator>Schmeiser, Tim</creator><creator>Kreuter, Alexander</creator><creator>Kuhr, Kathrin</creator><creator>Lorenz, Hanns-Martin</creator><creator>Moinzadeh, Pia</creator><creator>Hunzelmann, Nicolas</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6065-5680</orcidid><orcidid>https://orcid.org/0000-0003-4402-2159</orcidid><orcidid>https://orcid.org/0000-0001-7680-9971</orcidid><orcidid>https://orcid.org/0000-0002-9419-1690</orcidid><orcidid>https://orcid.org/0000-0001-5940-3195</orcidid></search><sort><creationdate>20230901</creationdate><title>Anti-acid therapy in SSc-associated interstitial lung disease: long-term outcomes from the German Network for Systemic Sclerosis</title><author>Kreuter, Michael ; Bonella, Francesco ; Blank, Norbert ; Riemekasten, Gabriela ; Müller-Ladner, Ulf ; Henes, Jörg ; Siegert, Elise ; Günther, Claudia ; Kötter, Ina ; Pfeiffer, Christiane ; Schmalzing, Marc ; Zeidler, Gabriele ; Korsten, Peter ; Susok, Laura ; Juche, Aaron ; Worm, Margitta ; Jandova, Ilona ; Ehrchen, Jan ; Sunderkötter, Cord ; Keyßer, Gernot ; Ramming, Andreas ; Schmeiser, Tim ; Kreuter, Alexander ; Kuhr, Kathrin ; Lorenz, Hanns-Martin ; Moinzadeh, Pia ; Hunzelmann, Nicolas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-821aa54d95a942f1385d662ec7f698fdd323ca3181c19b8e48a2bc7783efafc43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Clinical Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kreuter, Michael</creatorcontrib><creatorcontrib>Bonella, Francesco</creatorcontrib><creatorcontrib>Blank, Norbert</creatorcontrib><creatorcontrib>Riemekasten, Gabriela</creatorcontrib><creatorcontrib>Müller-Ladner, Ulf</creatorcontrib><creatorcontrib>Henes, Jörg</creatorcontrib><creatorcontrib>Siegert, Elise</creatorcontrib><creatorcontrib>Günther, Claudia</creatorcontrib><creatorcontrib>Kötter, Ina</creatorcontrib><creatorcontrib>Pfeiffer, Christiane</creatorcontrib><creatorcontrib>Schmalzing, Marc</creatorcontrib><creatorcontrib>Zeidler, Gabriele</creatorcontrib><creatorcontrib>Korsten, Peter</creatorcontrib><creatorcontrib>Susok, Laura</creatorcontrib><creatorcontrib>Juche, Aaron</creatorcontrib><creatorcontrib>Worm, Margitta</creatorcontrib><creatorcontrib>Jandova, Ilona</creatorcontrib><creatorcontrib>Ehrchen, Jan</creatorcontrib><creatorcontrib>Sunderkötter, Cord</creatorcontrib><creatorcontrib>Keyßer, Gernot</creatorcontrib><creatorcontrib>Ramming, Andreas</creatorcontrib><creatorcontrib>Schmeiser, Tim</creatorcontrib><creatorcontrib>Kreuter, Alexander</creatorcontrib><creatorcontrib>Kuhr, Kathrin</creatorcontrib><creatorcontrib>Lorenz, Hanns-Martin</creatorcontrib><creatorcontrib>Moinzadeh, Pia</creatorcontrib><creatorcontrib>Hunzelmann, Nicolas</creatorcontrib><collection>Oxford Academic Journals (Open Access)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kreuter, Michael</au><au>Bonella, Francesco</au><au>Blank, Norbert</au><au>Riemekasten, Gabriela</au><au>Müller-Ladner, Ulf</au><au>Henes, Jörg</au><au>Siegert, Elise</au><au>Günther, Claudia</au><au>Kötter, Ina</au><au>Pfeiffer, Christiane</au><au>Schmalzing, Marc</au><au>Zeidler, Gabriele</au><au>Korsten, Peter</au><au>Susok, Laura</au><au>Juche, Aaron</au><au>Worm, Margitta</au><au>Jandova, Ilona</au><au>Ehrchen, Jan</au><au>Sunderkötter, Cord</au><au>Keyßer, Gernot</au><au>Ramming, Andreas</au><au>Schmeiser, Tim</au><au>Kreuter, Alexander</au><au>Kuhr, Kathrin</au><au>Lorenz, Hanns-Martin</au><au>Moinzadeh, Pia</au><au>Hunzelmann, Nicolas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-acid therapy in SSc-associated interstitial lung disease: long-term outcomes from the German Network for Systemic Sclerosis</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>62</volume><issue>9</issue><spage>3067</spage><epage>3074</epage><pages>3067-3074</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><abstract>Abstract Objectives Gastroesophageal reflux disease (GERD) occurs frequently in patients with SSc. We investigated whether the presence of GERD and/or the use of anti-acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-term outcomes, especially in SSc-associated interstitial lung disease (SSc-ILD). Methods We retrospectively analysed patients with SSc and SSc-ILD from the German Network for Systemic Sclerosis (DNSS) database (2003 onwards). Kaplan–Meier analysis compared overall survival (OS) and progression-free survival (PFS) in patients with GERD vs without GERD (SSc and SSc-ILD), and PPI vs no PPI use (SSc-ILD only). Progression was defined as a decrease in either percentage predicted forced vital capacity of ≥10% or single-breath diffusing capacity for carbon monoxide of ≥15%, or death. Results It was found that 2693/4306 (63%) registered patients with SSc and 1204/1931 (62%) with SSc-ILD had GERD. GERD was not associated with decreased OS or decreased PFS in patients in either cohort. In SSc-ILD, PPI use was associated with improved OS vs no PPI use after 1 year [98.4% (95% CI: 97.6, 99.3); n = 760 vs 90.8% (87.9–93.8); n = 290] and after 5 years [91.4% (89.2–93.8); n = 357 vs 70.9% (65.2–77.1); n = 106; P &lt; 0.0001]. PPI use was also associated with improved PFS vs no PPI use after 1 year [95.9% (94.6–97.3); n = 745 vs 86.4% (82.9–90.1); n = 278] and after 5 years [66.8% (63.0–70.8); n = 286 vs 45.9% (39.6–53.2); n = 69; P &lt; 0.0001]. Conclusion GERD had no effect on survival in SSc or SSc-ILD. PPIs improved survival in patients with SSc-ILD. Controlled, prospective trials are needed to confirm this finding.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36708008</pmid><doi>10.1093/rheumatology/kead023</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6065-5680</orcidid><orcidid>https://orcid.org/0000-0003-4402-2159</orcidid><orcidid>https://orcid.org/0000-0001-7680-9971</orcidid><orcidid>https://orcid.org/0000-0002-9419-1690</orcidid><orcidid>https://orcid.org/0000-0001-5940-3195</orcidid><oa>free_for_read</oa></addata></record>
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title Anti-acid therapy in SSc-associated interstitial lung disease: long-term outcomes from the German Network for Systemic Sclerosis
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