Intrauterine Ureaplasma is associated with small airway obstruction in extremely preterm infants

Background The long‐term follow‐up of lung function (LF) in extremely preterm (EP) infants with bronchopulmonary dysplasia (BPD) has shown a worldwide increase in small airway obstructions (SAO). Objectives We investigated the relationships between intrauterine Ureplasma infection in EP infants and...

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Veröffentlicht in:Pediatric pulmonology 2022-11, Vol.57 (11), p.2763-2773
Hauptverfasser: Kitajima, Hiroyuki, Fujimura, Masanori, Takeuchi, Makoto, Kawamoto, Yutaka, Sumi, Kiyoaki, Matsunami, Katsura, Shiraishi, Jun, Hirano, Shinya, Nakura, Yukiko, Yanagihara, Itaru
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container_end_page 2773
container_issue 11
container_start_page 2763
container_title Pediatric pulmonology
container_volume 57
creator Kitajima, Hiroyuki
Fujimura, Masanori
Takeuchi, Makoto
Kawamoto, Yutaka
Sumi, Kiyoaki
Matsunami, Katsura
Shiraishi, Jun
Hirano, Shinya
Nakura, Yukiko
Yanagihara, Itaru
description Background The long‐term follow‐up of lung function (LF) in extremely preterm (EP) infants with bronchopulmonary dysplasia (BPD) has shown a worldwide increase in small airway obstructions (SAO). Objectives We investigated the relationships between intrauterine Ureplasma infection in EP infants and bubbly/cystic lung, BPD, and SAO at school age. Methods Placental pathology, placental Ureaplasma DNA (pU‐DNA), and cord blood immunoglobulin M (IgM) (C‐IgM) were investigated in 360 EP infants born from 1981 to 2004. Maternal amniotic inflammatory response (M‐AIR) scores and hemosiderin deposition (HD) were estimated in the chorioamnion. The study subjects were divided into groups based on their M‐AIR scores. Their LF at school age was compared with those of 33 healthy siblings. Findings pU‐DNA and C‐IgM were significantly related to SAO at school age (p 1000 units had an odds ratio (OR) of 35 (95% confidence interval: 10–172) and 18 (5.6–67) for bubbly/cystic lung, and 11 (3.1 − 43) and 31 (4.5–349) for severe BPD, and 5.3 (2.1–11) and 12 (2.4–74) for SAO, respectively. The ORs of surfactant treatment, BPD grade III, O2 at 40 weeks, HD, and C‐IgM >30 mg/dl for SAO were 0.21 (0.075–0.58), 5.3 (2.1–15), 2.5 (1.4–4.6), 3.6 (1.5–9.1) and 2.5 (1.0–5.2). 84% (90/107) SAO infants showed no or mild BPD in infancy, and 61% of infants had no severe CAM. Conclusion Our long‐term cohort study of LF in EP infants revealed that intrauterine Ureaplasma was associated with bubbly/cystic lung, severe BPD, and SAO at school age.
doi_str_mv 10.1002/ppul.26098
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Objectives We investigated the relationships between intrauterine Ureplasma infection in EP infants and bubbly/cystic lung, BPD, and SAO at school age. Methods Placental pathology, placental Ureaplasma DNA (pU‐DNA), and cord blood immunoglobulin M (IgM) (C‐IgM) were investigated in 360 EP infants born from 1981 to 2004. Maternal amniotic inflammatory response (M‐AIR) scores and hemosiderin deposition (HD) were estimated in the chorioamnion. The study subjects were divided into groups based on their M‐AIR scores. Their LF at school age was compared with those of 33 healthy siblings. Findings pU‐DNA and C‐IgM were significantly related to SAO at school age (p &lt; 0.012). M‐AIR score 3 and pU‐DNA &gt;1000 units had an odds ratio (OR) of 35 (95% confidence interval: 10–172) and 18 (5.6–67) for bubbly/cystic lung, and 11 (3.1 − 43) and 31 (4.5–349) for severe BPD, and 5.3 (2.1–11) and 12 (2.4–74) for SAO, respectively. The ORs of surfactant treatment, BPD grade III, O2 at 40 weeks, HD, and C‐IgM &gt;30 mg/dl for SAO were 0.21 (0.075–0.58), 5.3 (2.1–15), 2.5 (1.4–4.6), 3.6 (1.5–9.1) and 2.5 (1.0–5.2). 84% (90/107) SAO infants showed no or mild BPD in infancy, and 61% of infants had no severe CAM. Conclusion Our long‐term cohort study of LF in EP infants revealed that intrauterine Ureaplasma was associated with bubbly/cystic lung, severe BPD, and SAO at school age.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.26098</identifier><identifier>PMID: 35931924</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Airway management ; Airway Obstruction ; bronchopulmonary dysplasia ; Bronchopulmonary Dysplasia - complications ; bubbly/cystic lung ; Cohort Studies ; extremely preterm infant ; Female ; Gestational Age ; Hemosiderin ; Humans ; Immunoglobulin M ; Infant ; Infant, Extremely Premature ; Infant, Newborn ; Placenta ; Pregnancy ; small airway obstruction ; Surface-Active Agents ; Ureaplasma</subject><ispartof>Pediatric pulmonology, 2022-11, Vol.57 (11), p.2763-2773</ispartof><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3578-9c505131d9fcf908173a32e627168bfdcb11fd8082644b6f730ecf8e1ef6e65d3</citedby><cites>FETCH-LOGICAL-c3578-9c505131d9fcf908173a32e627168bfdcb11fd8082644b6f730ecf8e1ef6e65d3</cites><orcidid>0000-0001-9882-8196</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fppul.26098$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.26098$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35931924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kitajima, Hiroyuki</creatorcontrib><creatorcontrib>Fujimura, Masanori</creatorcontrib><creatorcontrib>Takeuchi, Makoto</creatorcontrib><creatorcontrib>Kawamoto, Yutaka</creatorcontrib><creatorcontrib>Sumi, Kiyoaki</creatorcontrib><creatorcontrib>Matsunami, Katsura</creatorcontrib><creatorcontrib>Shiraishi, Jun</creatorcontrib><creatorcontrib>Hirano, Shinya</creatorcontrib><creatorcontrib>Nakura, Yukiko</creatorcontrib><creatorcontrib>Yanagihara, Itaru</creatorcontrib><title>Intrauterine Ureaplasma is associated with small airway obstruction in extremely preterm infants</title><title>Pediatric pulmonology</title><addtitle>Pediatr Pulmonol</addtitle><description>Background The long‐term follow‐up of lung function (LF) in extremely preterm (EP) infants with bronchopulmonary dysplasia (BPD) has shown a worldwide increase in small airway obstructions (SAO). Objectives We investigated the relationships between intrauterine Ureplasma infection in EP infants and bubbly/cystic lung, BPD, and SAO at school age. Methods Placental pathology, placental Ureaplasma DNA (pU‐DNA), and cord blood immunoglobulin M (IgM) (C‐IgM) were investigated in 360 EP infants born from 1981 to 2004. Maternal amniotic inflammatory response (M‐AIR) scores and hemosiderin deposition (HD) were estimated in the chorioamnion. The study subjects were divided into groups based on their M‐AIR scores. Their LF at school age was compared with those of 33 healthy siblings. Findings pU‐DNA and C‐IgM were significantly related to SAO at school age (p &lt; 0.012). M‐AIR score 3 and pU‐DNA &gt;1000 units had an odds ratio (OR) of 35 (95% confidence interval: 10–172) and 18 (5.6–67) for bubbly/cystic lung, and 11 (3.1 − 43) and 31 (4.5–349) for severe BPD, and 5.3 (2.1–11) and 12 (2.4–74) for SAO, respectively. The ORs of surfactant treatment, BPD grade III, O2 at 40 weeks, HD, and C‐IgM &gt;30 mg/dl for SAO were 0.21 (0.075–0.58), 5.3 (2.1–15), 2.5 (1.4–4.6), 3.6 (1.5–9.1) and 2.5 (1.0–5.2). 84% (90/107) SAO infants showed no or mild BPD in infancy, and 61% of infants had no severe CAM. Conclusion Our long‐term cohort study of LF in EP infants revealed that intrauterine Ureaplasma was associated with bubbly/cystic lung, severe BPD, and SAO at school age.</description><subject>Airway management</subject><subject>Airway Obstruction</subject><subject>bronchopulmonary dysplasia</subject><subject>Bronchopulmonary Dysplasia - complications</subject><subject>bubbly/cystic lung</subject><subject>Cohort Studies</subject><subject>extremely preterm infant</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Hemosiderin</subject><subject>Humans</subject><subject>Immunoglobulin M</subject><subject>Infant</subject><subject>Infant, Extremely Premature</subject><subject>Infant, Newborn</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>small airway obstruction</subject><subject>Surface-Active Agents</subject><subject>Ureaplasma</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtqGzEUQEVJaBy3m3xAEGQTCpPo4dFIyxKaJmCIF_Fa1WiuqILmUUmD67-PXKdddBG4ILg6HC4HoQtKbigh7Haa5nDDBFHyA1pQolRFVkqcoIVs6roSUvAzdJ7SCyHlT9GP6IzXilPFVgv043HI0cwZoh8AbyOYKZjUG-wTNimN1psMHd75_BOXdQjY-Lgzezy2KcfZZj8O2A8YfucIPYQ9niIUW1-Wzgw5fUKnzoQEn9_eJdref3u-e6jWT98f776uK8vrRlbK1qSmnHbKWaeIpA03nIFgDRWydZ1tKXWdJJKJ1aoVruEErJNAwQkQdceX6ProneL4a4aUde-ThRDMAOOcNBNKNUTwMkt09R_6Ms5xKNdp1rCalmpKFerLkbJxTCmC01P0vYl7TYk-dNeH7vpP9wJfvinntofuH_o3dAHoEdj5APt3VHqz2a6P0ldqg48V</recordid><startdate>202211</startdate><enddate>202211</enddate><creator>Kitajima, Hiroyuki</creator><creator>Fujimura, Masanori</creator><creator>Takeuchi, Makoto</creator><creator>Kawamoto, Yutaka</creator><creator>Sumi, Kiyoaki</creator><creator>Matsunami, Katsura</creator><creator>Shiraishi, Jun</creator><creator>Hirano, Shinya</creator><creator>Nakura, Yukiko</creator><creator>Yanagihara, Itaru</creator><general>Wiley Subscription Services, Inc</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>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9882-8196</orcidid></search><sort><creationdate>202211</creationdate><title>Intrauterine Ureaplasma is associated with small airway obstruction in extremely preterm infants</title><author>Kitajima, Hiroyuki ; Fujimura, Masanori ; Takeuchi, Makoto ; Kawamoto, Yutaka ; Sumi, Kiyoaki ; Matsunami, Katsura ; Shiraishi, Jun ; Hirano, Shinya ; Nakura, Yukiko ; Yanagihara, Itaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3578-9c505131d9fcf908173a32e627168bfdcb11fd8082644b6f730ecf8e1ef6e65d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Airway management</topic><topic>Airway Obstruction</topic><topic>bronchopulmonary dysplasia</topic><topic>Bronchopulmonary Dysplasia - complications</topic><topic>bubbly/cystic lung</topic><topic>Cohort Studies</topic><topic>extremely preterm infant</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Hemosiderin</topic><topic>Humans</topic><topic>Immunoglobulin M</topic><topic>Infant</topic><topic>Infant, Extremely Premature</topic><topic>Infant, Newborn</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>small airway obstruction</topic><topic>Surface-Active Agents</topic><topic>Ureaplasma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kitajima, Hiroyuki</creatorcontrib><creatorcontrib>Fujimura, Masanori</creatorcontrib><creatorcontrib>Takeuchi, Makoto</creatorcontrib><creatorcontrib>Kawamoto, Yutaka</creatorcontrib><creatorcontrib>Sumi, Kiyoaki</creatorcontrib><creatorcontrib>Matsunami, Katsura</creatorcontrib><creatorcontrib>Shiraishi, Jun</creatorcontrib><creatorcontrib>Hirano, Shinya</creatorcontrib><creatorcontrib>Nakura, Yukiko</creatorcontrib><creatorcontrib>Yanagihara, Itaru</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 Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitajima, Hiroyuki</au><au>Fujimura, Masanori</au><au>Takeuchi, Makoto</au><au>Kawamoto, Yutaka</au><au>Sumi, Kiyoaki</au><au>Matsunami, Katsura</au><au>Shiraishi, Jun</au><au>Hirano, Shinya</au><au>Nakura, Yukiko</au><au>Yanagihara, Itaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrauterine Ureaplasma is associated with small airway obstruction in extremely preterm infants</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr Pulmonol</addtitle><date>2022-11</date><risdate>2022</risdate><volume>57</volume><issue>11</issue><spage>2763</spage><epage>2773</epage><pages>2763-2773</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>Background The long‐term follow‐up of lung function (LF) in extremely preterm (EP) infants with bronchopulmonary dysplasia (BPD) has shown a worldwide increase in small airway obstructions (SAO). Objectives We investigated the relationships between intrauterine Ureplasma infection in EP infants and bubbly/cystic lung, BPD, and SAO at school age. Methods Placental pathology, placental Ureaplasma DNA (pU‐DNA), and cord blood immunoglobulin M (IgM) (C‐IgM) were investigated in 360 EP infants born from 1981 to 2004. Maternal amniotic inflammatory response (M‐AIR) scores and hemosiderin deposition (HD) were estimated in the chorioamnion. The study subjects were divided into groups based on their M‐AIR scores. Their LF at school age was compared with those of 33 healthy siblings. Findings pU‐DNA and C‐IgM were significantly related to SAO at school age (p &lt; 0.012). M‐AIR score 3 and pU‐DNA &gt;1000 units had an odds ratio (OR) of 35 (95% confidence interval: 10–172) and 18 (5.6–67) for bubbly/cystic lung, and 11 (3.1 − 43) and 31 (4.5–349) for severe BPD, and 5.3 (2.1–11) and 12 (2.4–74) for SAO, respectively. The ORs of surfactant treatment, BPD grade III, O2 at 40 weeks, HD, and C‐IgM &gt;30 mg/dl for SAO were 0.21 (0.075–0.58), 5.3 (2.1–15), 2.5 (1.4–4.6), 3.6 (1.5–9.1) and 2.5 (1.0–5.2). 84% (90/107) SAO infants showed no or mild BPD in infancy, and 61% of infants had no severe CAM. Conclusion Our long‐term cohort study of LF in EP infants revealed that intrauterine Ureaplasma was associated with bubbly/cystic lung, severe BPD, and SAO at school age.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35931924</pmid><doi>10.1002/ppul.26098</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9882-8196</orcidid></addata></record>
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subjects Airway management
Airway Obstruction
bronchopulmonary dysplasia
Bronchopulmonary Dysplasia - complications
bubbly/cystic lung
Cohort Studies
extremely preterm infant
Female
Gestational Age
Hemosiderin
Humans
Immunoglobulin M
Infant
Infant, Extremely Premature
Infant, Newborn
Placenta
Pregnancy
small airway obstruction
Surface-Active Agents
Ureaplasma
title Intrauterine Ureaplasma is associated with small airway obstruction in extremely preterm infants
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