Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS
The goal of this study was to determine the changes that occur in surfactant-associated proteins in bronchoalveolar lavage fluid (BAL) and serum of patients at risk for ARDS and during the course of ARDS. We found that the concentrations of SP-A and SP-B were low in the BAL of patients at risk for A...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 1999-12, Vol.160 (6), p.1843-1850 |
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creator | GREENE, K. E WRIGHT, J. R NAGAE, H HUDSON, L. D MARTIN, T. R STEINBERG, K. P RUZINSKI, J. T CALDWELL, E WONG, W. B HULL, W WHITSETT, J. A AKINO, T KUROKI, Y |
description | The goal of this study was to determine the changes that occur in surfactant-associated proteins in bronchoalveolar lavage fluid (BAL) and serum of patients at risk for ARDS and during the course of ARDS. We found that the concentrations of SP-A and SP-B were low in the BAL of patients at risk for ARDS before the onset of clinically defined lung injury, whereas the concentration of SP-D was normal. In patients with established ARDS, BAL SP-A and SP-B concentrations were low during the entire 14-d observation period, but the median SP-D concentrations remained in the normal range. Immunoreactive SP-A and SP-D were not increased in the serum of patients at risk for ARDS, but both increased after the onset of ARDS to a maximum on Day 3 and remained elevated for as long as 14 d. The BAL SP-A concentrations were significantly lower in at-risk patients who developed ARDS, and no patient with a BAL SP-A concentration greater than 1.2 microg/ml developed ARDS. On Days 1 and 3 of ARDS, the BAL SP-D concentration was significantly lower in patients who died, and the BAL SP-D concentration was significantly related to the PI(O(2))/FI(O(2)) ratio. Thus, surfactant protein abnormalities occur before and after the onset of ARDS, and the responses of SP-A, SP-B, and SP-D differ in important ways. The BAL SP-A and SP-D measurements can be used to classify patients as high or low risk for progression to ARDS and/or death after the onset of ARDS. Strategies to increase these surfactant proteins in the lungs of patients with ARDS could be useful to modify the onset or the course of ARDS. |
doi_str_mv | 10.1164/ajrccm.160.6.9901117 |
format | Article |
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E ; WRIGHT, J. R ; NAGAE, H ; HUDSON, L. D ; MARTIN, T. R ; STEINBERG, K. P ; RUZINSKI, J. T ; CALDWELL, E ; WONG, W. B ; HULL, W ; WHITSETT, J. A ; AKINO, T ; KUROKI, Y</creator><creatorcontrib>GREENE, K. E ; WRIGHT, J. R ; NAGAE, H ; HUDSON, L. D ; MARTIN, T. R ; STEINBERG, K. P ; RUZINSKI, J. T ; CALDWELL, E ; WONG, W. B ; HULL, W ; WHITSETT, J. A ; AKINO, T ; KUROKI, Y</creatorcontrib><description>The goal of this study was to determine the changes that occur in surfactant-associated proteins in bronchoalveolar lavage fluid (BAL) and serum of patients at risk for ARDS and during the course of ARDS. We found that the concentrations of SP-A and SP-B were low in the BAL of patients at risk for ARDS before the onset of clinically defined lung injury, whereas the concentration of SP-D was normal. In patients with established ARDS, BAL SP-A and SP-B concentrations were low during the entire 14-d observation period, but the median SP-D concentrations remained in the normal range. Immunoreactive SP-A and SP-D were not increased in the serum of patients at risk for ARDS, but both increased after the onset of ARDS to a maximum on Day 3 and remained elevated for as long as 14 d. The BAL SP-A concentrations were significantly lower in at-risk patients who developed ARDS, and no patient with a BAL SP-A concentration greater than 1.2 microg/ml developed ARDS. On Days 1 and 3 of ARDS, the BAL SP-D concentration was significantly lower in patients who died, and the BAL SP-D concentration was significantly related to the PI(O(2))/FI(O(2)) ratio. Thus, surfactant protein abnormalities occur before and after the onset of ARDS, and the responses of SP-A, SP-B, and SP-D differ in important ways. The BAL SP-A and SP-D measurements can be used to classify patients as high or low risk for progression to ARDS and/or death after the onset of ARDS. Strategies to increase these surfactant proteins in the lungs of patients with ARDS could be useful to modify the onset or the course of ARDS.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/ajrccm.160.6.9901117</identifier><identifier>PMID: 10588595</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>Adolescent ; Adult ; Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; APACHE ; Biological and medical sciences ; Bronchoalveolar Lavage Fluid - chemistry ; Emergency and intensive respiratory care ; Glycoproteins - metabolism ; Humans ; Intensive care medicine ; Lung - metabolism ; Medical sciences ; Middle Aged ; Proteolipids - metabolism ; Pulmonary Surfactant-Associated Protein A ; Pulmonary Surfactant-Associated Protein D ; Pulmonary Surfactant-Associated Proteins ; Pulmonary Surfactants - blood ; Pulmonary Surfactants - metabolism ; Respiratory Distress Syndrome, Adult - etiology ; Respiratory Distress Syndrome, Adult - metabolism ; Risk Factors ; ROC Curve ; Sepsis - complications ; Wounds and Injuries - complications</subject><ispartof>American journal of respiratory and critical care medicine, 1999-12, Vol.160 (6), p.1843-1850</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-9f519730c77c6cb8492da30420cff12dc2a7b3d39833976b2f58c6477ffd05603</citedby><cites>FETCH-LOGICAL-c400t-9f519730c77c6cb8492da30420cff12dc2a7b3d39833976b2f58c6477ffd05603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1213394$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10588595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GREENE, K. E</creatorcontrib><creatorcontrib>WRIGHT, J. R</creatorcontrib><creatorcontrib>NAGAE, H</creatorcontrib><creatorcontrib>HUDSON, L. D</creatorcontrib><creatorcontrib>MARTIN, T. R</creatorcontrib><creatorcontrib>STEINBERG, K. P</creatorcontrib><creatorcontrib>RUZINSKI, J. T</creatorcontrib><creatorcontrib>CALDWELL, E</creatorcontrib><creatorcontrib>WONG, W. B</creatorcontrib><creatorcontrib>HULL, W</creatorcontrib><creatorcontrib>WHITSETT, J. A</creatorcontrib><creatorcontrib>AKINO, T</creatorcontrib><creatorcontrib>KUROKI, Y</creatorcontrib><title>Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>The goal of this study was to determine the changes that occur in surfactant-associated proteins in bronchoalveolar lavage fluid (BAL) and serum of patients at risk for ARDS and during the course of ARDS. We found that the concentrations of SP-A and SP-B were low in the BAL of patients at risk for ARDS before the onset of clinically defined lung injury, whereas the concentration of SP-D was normal. In patients with established ARDS, BAL SP-A and SP-B concentrations were low during the entire 14-d observation period, but the median SP-D concentrations remained in the normal range. Immunoreactive SP-A and SP-D were not increased in the serum of patients at risk for ARDS, but both increased after the onset of ARDS to a maximum on Day 3 and remained elevated for as long as 14 d. The BAL SP-A concentrations were significantly lower in at-risk patients who developed ARDS, and no patient with a BAL SP-A concentration greater than 1.2 microg/ml developed ARDS. On Days 1 and 3 of ARDS, the BAL SP-D concentration was significantly lower in patients who died, and the BAL SP-D concentration was significantly related to the PI(O(2))/FI(O(2)) ratio. Thus, surfactant protein abnormalities occur before and after the onset of ARDS, and the responses of SP-A, SP-B, and SP-D differ in important ways. The BAL SP-A and SP-D measurements can be used to classify patients as high or low risk for progression to ARDS and/or death after the onset of ARDS. Strategies to increase these surfactant proteins in the lungs of patients with ARDS could be useful to modify the onset or the course of ARDS.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>APACHE</subject><subject>Biological and medical sciences</subject><subject>Bronchoalveolar Lavage Fluid - chemistry</subject><subject>Emergency and intensive respiratory care</subject><subject>Glycoproteins - metabolism</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Lung - metabolism</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Proteolipids - metabolism</subject><subject>Pulmonary Surfactant-Associated Protein A</subject><subject>Pulmonary Surfactant-Associated Protein D</subject><subject>Pulmonary Surfactant-Associated Proteins</subject><subject>Pulmonary Surfactants - blood</subject><subject>Pulmonary Surfactants - metabolism</subject><subject>Respiratory Distress Syndrome, Adult - etiology</subject><subject>Respiratory Distress Syndrome, Adult - metabolism</subject><subject>Risk Factors</subject><subject>ROC Curve</subject><subject>Sepsis - complications</subject><subject>Wounds and Injuries - complications</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1LxDAQhoMoun78A5EcxFvXSZMmzXFZP0EQ_ABvYZomWmnTNWkP_nvr7oKeZhie92V4CDllMGdMikv8jNZ2cyZhLudaA2NM7ZAZK3iRCa1gd9pB8UwI_XZADlP6BGB5yWCfHDAoyrLQxYzgs4sNttR-YHh3iTaBpjF6tAOGIcOUetvg4Gq6iv3gmrAm2jG8Uww1TS6OHa2c76NbH9APLtI-JDfQ3tPF09XzMdnz2CZ3sp1H5PXm-mV5lz083t4vFw-ZFQBDpn3BtOJglbLSVqXQeY0cRA7We5bXNkdV8ZrrknOtZJX7orRSKOV9DYUEfkQuNr3Tp1-jS4PpmmRd22Jw_ZiM1FNQcjWBYgPa2KcUnTer2HQYvw0D86vWbNSaSa2RZqt2ip1t-8eqc_W_0MblBJxvAUwWWx8x2Cb9cTmbHhD8B6n7guo</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>GREENE, K. 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Cell therapy and gene therapy</topic><topic>APACHE</topic><topic>Biological and medical sciences</topic><topic>Bronchoalveolar Lavage Fluid - chemistry</topic><topic>Emergency and intensive respiratory care</topic><topic>Glycoproteins - metabolism</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Lung - metabolism</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Proteolipids - metabolism</topic><topic>Pulmonary Surfactant-Associated Protein A</topic><topic>Pulmonary Surfactant-Associated Protein D</topic><topic>Pulmonary Surfactant-Associated Proteins</topic><topic>Pulmonary Surfactants - blood</topic><topic>Pulmonary Surfactants - metabolism</topic><topic>Respiratory Distress Syndrome, Adult - etiology</topic><topic>Respiratory Distress Syndrome, Adult - metabolism</topic><topic>Risk Factors</topic><topic>ROC Curve</topic><topic>Sepsis - complications</topic><topic>Wounds and Injuries - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GREENE, K. 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A</au><au>AKINO, T</au><au>KUROKI, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>1999-12-01</date><risdate>1999</risdate><volume>160</volume><issue>6</issue><spage>1843</spage><epage>1850</epage><pages>1843-1850</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>The goal of this study was to determine the changes that occur in surfactant-associated proteins in bronchoalveolar lavage fluid (BAL) and serum of patients at risk for ARDS and during the course of ARDS. We found that the concentrations of SP-A and SP-B were low in the BAL of patients at risk for ARDS before the onset of clinically defined lung injury, whereas the concentration of SP-D was normal. In patients with established ARDS, BAL SP-A and SP-B concentrations were low during the entire 14-d observation period, but the median SP-D concentrations remained in the normal range. Immunoreactive SP-A and SP-D were not increased in the serum of patients at risk for ARDS, but both increased after the onset of ARDS to a maximum on Day 3 and remained elevated for as long as 14 d. The BAL SP-A concentrations were significantly lower in at-risk patients who developed ARDS, and no patient with a BAL SP-A concentration greater than 1.2 microg/ml developed ARDS. On Days 1 and 3 of ARDS, the BAL SP-D concentration was significantly lower in patients who died, and the BAL SP-D concentration was significantly related to the PI(O(2))/FI(O(2)) ratio. Thus, surfactant protein abnormalities occur before and after the onset of ARDS, and the responses of SP-A, SP-B, and SP-D differ in important ways. The BAL SP-A and SP-D measurements can be used to classify patients as high or low risk for progression to ARDS and/or death after the onset of ARDS. Strategies to increase these surfactant proteins in the lungs of patients with ARDS could be useful to modify the onset or the course of ARDS.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>10588595</pmid><doi>10.1164/ajrccm.160.6.9901117</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Journals@Ovid Complete; American Thoracic Society (ATS) Journals Online; EZB-FREE-00999 freely available EZB journals |
subjects | Adolescent Adult Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy APACHE Biological and medical sciences Bronchoalveolar Lavage Fluid - chemistry Emergency and intensive respiratory care Glycoproteins - metabolism Humans Intensive care medicine Lung - metabolism Medical sciences Middle Aged Proteolipids - metabolism Pulmonary Surfactant-Associated Protein A Pulmonary Surfactant-Associated Protein D Pulmonary Surfactant-Associated Proteins Pulmonary Surfactants - blood Pulmonary Surfactants - metabolism Respiratory Distress Syndrome, Adult - etiology Respiratory Distress Syndrome, Adult - metabolism Risk Factors ROC Curve Sepsis - complications Wounds and Injuries - complications |
title | Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS |
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