Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM)
Purpose Although computed tomography (CT) has been used previously to assess disease severity in lymphangioleiomyomatosis (LAM), the associations between the extent of pulmonary cysts on CT and six-minute walk test (6MWT), matrix metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF...
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Veröffentlicht in: | Lung 2014-12, Vol.192 (6), p.967-974 |
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creator | Baldi, Bruno Guedes Araujo, Mariana Sponholz Freitas, Carolina Salim Gonçalves da Silva Teles, Gustavo Borges Kairalla, Ronaldo Adib Dias, Olívia Meira Pereira, Daniel Antunes Silva Pimenta, Suzana Pinheiro Carvalho, Carlos Roberto Ribeiro |
description | Purpose
Although computed tomography (CT) has been used previously to assess disease severity in lymphangioleiomyomatosis (LAM), the associations between the extent of pulmonary cysts on CT and six-minute walk test (6MWT), matrix metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF-D) are not well established. We performed a cross-sectional study to quantify the extent of pulmonary cysts in CT and to establish their correlations with pulmonary function tests (PFTs), 6MWT results, including a composite index (desaturation–distance ratio, DDR), and levels of VEGF-D and MMPs in LAM.
Methods
Twenty-three LAM patients underwent CT scanning to automatically quantify the extent of pulmonary cysts and performed PFTs and 6MWT. Serum levels of MMP-2, MMP-9, and VEGF-D were also measured.
Results
The severity of pulmonary cystic involvement was mild (the extent of cysts was 6.8 %) and correlated best with FEV
1
/FVC (
r
= −0.84), residual volume (
r
= 0.66), DL
CO
(
r
= −0.82), the DDR index (
r
= 0.77), and desaturation during the 6MWT (
r
= −0.81). There was a weak correlation with VEGF-D (
r
= 0.45), but no association was found with MMP-2 and MMP-9.
Conclusions
The severity of pulmonary cystic involvement was mild in this sample of LAM patients and correlated best with airway obstruction, air trapping, reduced DL
CO
, the DDR index, and desaturation during the 6MWT. Serum VEGF-D cannot be completely defined as a valuable marker of disease severity and there may be a mechanism independent of MMPs to explain the formation of pulmonary cysts. |
doi_str_mv | 10.1007/s00408-014-9641-2 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1627077239</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A426081625</galeid><sourcerecordid>A426081625</sourcerecordid><originalsourceid>FETCH-LOGICAL-c644t-b3505fcf134bba0ab0612ad289f580a4b27f2315cb9d0ae59af174346feb4c8f3</originalsourceid><addsrcrecordid>eNqNk89u1DAQxiMEoqXwAFyQJSRUDim24_w7rlZbQNoKJApXy8mONy6OvbUdYJ-CV8YhBaVoqSofrBn_vm9kzUySPCf4jGBcvvEYM1ylmLC0LhhJ6YPkmLCMpqTM8cPkGGdjMjJHyRPvrzAmZUHyx8kRzSkmuCqPk5-rb0IPIihrkJUodIBWPwKYMEYfB91bI9weLfc-eCTMBl12oBxaeG9bNcm-q9Ch88G0YyQ0-iKcEo2Gif8EbujRhXBfwXmkDFrv-10nzFZZDcr2e9uLYL3y6HS9uHj9NHkkhfbw7OY-ST6fry6X79L1h7fvl4t12haMhbTJcpzLVpKMNY3AosEFoWJDq1rmFRasoaWkGcnbpt5gAXktJClZxgoJDWsrmZ0kp5PvztnrAXzgvfItaC0M2MFzUtASlyXN6oi-_Ae9soOLP_1NFYTUZT2jtkIDV0ba4EQ7mvIFowWuIpvfSWU1KUmd0yxS6QFqCwac0NaAVDF9y_U-_Nz_7AAfzwZ61R4scC_BvMKrmaADoUPnrR7GEfG3ne8E545kAltnvXcg-c6pPs4mJ5iP28CnbeBxG_i4DZxGzYubzg1ND5u_ij_jHwE6AT4-mS24WWv_6_oLD0IQGg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1626119799</pqid></control><display><type>article</type><title>Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM)</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Baldi, Bruno Guedes ; Araujo, Mariana Sponholz ; Freitas, Carolina Salim Gonçalves ; da Silva Teles, Gustavo Borges ; Kairalla, Ronaldo Adib ; Dias, Olívia Meira ; Pereira, Daniel Antunes Silva ; Pimenta, Suzana Pinheiro ; Carvalho, Carlos Roberto Ribeiro</creator><creatorcontrib>Baldi, Bruno Guedes ; Araujo, Mariana Sponholz ; Freitas, Carolina Salim Gonçalves ; da Silva Teles, Gustavo Borges ; Kairalla, Ronaldo Adib ; Dias, Olívia Meira ; Pereira, Daniel Antunes Silva ; Pimenta, Suzana Pinheiro ; Carvalho, Carlos Roberto Ribeiro</creatorcontrib><description>Purpose
Although computed tomography (CT) has been used previously to assess disease severity in lymphangioleiomyomatosis (LAM), the associations between the extent of pulmonary cysts on CT and six-minute walk test (6MWT), matrix metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF-D) are not well established. We performed a cross-sectional study to quantify the extent of pulmonary cysts in CT and to establish their correlations with pulmonary function tests (PFTs), 6MWT results, including a composite index (desaturation–distance ratio, DDR), and levels of VEGF-D and MMPs in LAM.
Methods
Twenty-three LAM patients underwent CT scanning to automatically quantify the extent of pulmonary cysts and performed PFTs and 6MWT. Serum levels of MMP-2, MMP-9, and VEGF-D were also measured.
Results
The severity of pulmonary cystic involvement was mild (the extent of cysts was 6.8 %) and correlated best with FEV
1
/FVC (
r
= −0.84), residual volume (
r
= 0.66), DL
CO
(
r
= −0.82), the DDR index (
r
= 0.77), and desaturation during the 6MWT (
r
= −0.81). There was a weak correlation with VEGF-D (
r
= 0.45), but no association was found with MMP-2 and MMP-9.
Conclusions
The severity of pulmonary cystic involvement was mild in this sample of LAM patients and correlated best with airway obstruction, air trapping, reduced DL
CO
, the DDR index, and desaturation during the 6MWT. Serum VEGF-D cannot be completely defined as a valuable marker of disease severity and there may be a mechanism independent of MMPs to explain the formation of pulmonary cysts.</description><identifier>ISSN: 0341-2040</identifier><identifier>EISSN: 1432-1750</identifier><identifier>DOI: 10.1007/s00408-014-9641-2</identifier><identifier>PMID: 25201087</identifier><identifier>CODEN: LUNGD9</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Biomarkers - analysis ; Carbon monoxide ; Complications and side effects ; Cross-Sectional Studies ; Cysts ; Cysts - blood ; Cysts - diagnostic imaging ; Cysts - epidemiology ; Development and progression ; Disease Progression ; Exercise ; Exercise Test - methods ; Female ; Follow-Up Studies ; Genetic aspects ; Health aspects ; Humans ; Lung diseases ; Lung Diseases - blood ; Lung Diseases - diagnostic imaging ; Lung Diseases - epidemiology ; Lung Neoplasms - blood ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - epidemiology ; Lymphangioleiomyomatosis - blood ; Lymphangioleiomyomatosis - diagnostic imaging ; Lymphangioleiomyomatosis - epidemiology ; Matrix Metalloproteinase 2 - blood ; Matrix Metalloproteinase 9 - blood ; Medicine ; Medicine & Public Health ; Middle Aged ; Patient outcomes ; Physiological aspects ; Pneumology/Respiratory System ; Proteases ; Respiratory Function Tests ; Risk Assessment ; Risk factors ; Severity of Illness Index ; Tomography ; Tomography, X-Ray Computed - methods ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - blood</subject><ispartof>Lung, 2014-12, Vol.192 (6), p.967-974</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>COPYRIGHT 2014 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c644t-b3505fcf134bba0ab0612ad289f580a4b27f2315cb9d0ae59af174346feb4c8f3</citedby><cites>FETCH-LOGICAL-c644t-b3505fcf134bba0ab0612ad289f580a4b27f2315cb9d0ae59af174346feb4c8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00408-014-9641-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00408-014-9641-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25201087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baldi, Bruno Guedes</creatorcontrib><creatorcontrib>Araujo, Mariana Sponholz</creatorcontrib><creatorcontrib>Freitas, Carolina Salim Gonçalves</creatorcontrib><creatorcontrib>da Silva Teles, Gustavo Borges</creatorcontrib><creatorcontrib>Kairalla, Ronaldo Adib</creatorcontrib><creatorcontrib>Dias, Olívia Meira</creatorcontrib><creatorcontrib>Pereira, Daniel Antunes Silva</creatorcontrib><creatorcontrib>Pimenta, Suzana Pinheiro</creatorcontrib><creatorcontrib>Carvalho, Carlos Roberto Ribeiro</creatorcontrib><title>Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM)</title><title>Lung</title><addtitle>Lung</addtitle><addtitle>Lung</addtitle><description>Purpose
Although computed tomography (CT) has been used previously to assess disease severity in lymphangioleiomyomatosis (LAM), the associations between the extent of pulmonary cysts on CT and six-minute walk test (6MWT), matrix metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF-D) are not well established. We performed a cross-sectional study to quantify the extent of pulmonary cysts in CT and to establish their correlations with pulmonary function tests (PFTs), 6MWT results, including a composite index (desaturation–distance ratio, DDR), and levels of VEGF-D and MMPs in LAM.
Methods
Twenty-three LAM patients underwent CT scanning to automatically quantify the extent of pulmonary cysts and performed PFTs and 6MWT. Serum levels of MMP-2, MMP-9, and VEGF-D were also measured.
Results
The severity of pulmonary cystic involvement was mild (the extent of cysts was 6.8 %) and correlated best with FEV
1
/FVC (
r
= −0.84), residual volume (
r
= 0.66), DL
CO
(
r
= −0.82), the DDR index (
r
= 0.77), and desaturation during the 6MWT (
r
= −0.81). There was a weak correlation with VEGF-D (
r
= 0.45), but no association was found with MMP-2 and MMP-9.
Conclusions
The severity of pulmonary cystic involvement was mild in this sample of LAM patients and correlated best with airway obstruction, air trapping, reduced DL
CO
, the DDR index, and desaturation during the 6MWT. Serum VEGF-D cannot be completely defined as a valuable marker of disease severity and there may be a mechanism independent of MMPs to explain the formation of pulmonary cysts.</description><subject>Adult</subject><subject>Biomarkers - analysis</subject><subject>Carbon monoxide</subject><subject>Complications and side effects</subject><subject>Cross-Sectional Studies</subject><subject>Cysts</subject><subject>Cysts - blood</subject><subject>Cysts - diagnostic imaging</subject><subject>Cysts - epidemiology</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>Exercise</subject><subject>Exercise Test - methods</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lung diseases</subject><subject>Lung Diseases - blood</subject><subject>Lung Diseases - diagnostic imaging</subject><subject>Lung Diseases - epidemiology</subject><subject>Lung Neoplasms - blood</subject><subject>Lung Neoplasms - diagnostic imaging</subject><subject>Lung Neoplasms - epidemiology</subject><subject>Lymphangioleiomyomatosis - blood</subject><subject>Lymphangioleiomyomatosis - diagnostic imaging</subject><subject>Lymphangioleiomyomatosis - epidemiology</subject><subject>Matrix Metalloproteinase 2 - blood</subject><subject>Matrix Metalloproteinase 9 - blood</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Patient outcomes</subject><subject>Physiological aspects</subject><subject>Pneumology/Respiratory System</subject><subject>Proteases</subject><subject>Respiratory Function Tests</subject><subject>Risk Assessment</subject><subject>Risk factors</subject><subject>Severity of Illness Index</subject><subject>Tomography</subject><subject>Tomography, X-Ray Computed - methods</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - blood</subject><issn>0341-2040</issn><issn>1432-1750</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNk89u1DAQxiMEoqXwAFyQJSRUDim24_w7rlZbQNoKJApXy8mONy6OvbUdYJ-CV8YhBaVoqSofrBn_vm9kzUySPCf4jGBcvvEYM1ylmLC0LhhJ6YPkmLCMpqTM8cPkGGdjMjJHyRPvrzAmZUHyx8kRzSkmuCqPk5-rb0IPIihrkJUodIBWPwKYMEYfB91bI9weLfc-eCTMBl12oBxaeG9bNcm-q9Ch88G0YyQ0-iKcEo2Gif8EbujRhXBfwXmkDFrv-10nzFZZDcr2e9uLYL3y6HS9uHj9NHkkhfbw7OY-ST6fry6X79L1h7fvl4t12haMhbTJcpzLVpKMNY3AosEFoWJDq1rmFRasoaWkGcnbpt5gAXktJClZxgoJDWsrmZ0kp5PvztnrAXzgvfItaC0M2MFzUtASlyXN6oi-_Ae9soOLP_1NFYTUZT2jtkIDV0ba4EQ7mvIFowWuIpvfSWU1KUmd0yxS6QFqCwac0NaAVDF9y_U-_Nz_7AAfzwZ61R4scC_BvMKrmaADoUPnrR7GEfG3ne8E545kAltnvXcg-c6pPs4mJ5iP28CnbeBxG_i4DZxGzYubzg1ND5u_ij_jHwE6AT4-mS24WWv_6_oLD0IQGg</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Baldi, Bruno Guedes</creator><creator>Araujo, Mariana Sponholz</creator><creator>Freitas, Carolina Salim Gonçalves</creator><creator>da Silva Teles, Gustavo Borges</creator><creator>Kairalla, Ronaldo Adib</creator><creator>Dias, Olívia Meira</creator><creator>Pereira, Daniel Antunes Silva</creator><creator>Pimenta, Suzana Pinheiro</creator><creator>Carvalho, Carlos Roberto Ribeiro</creator><general>Springer US</general><general>Springer</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>7QL</scope><scope>7RV</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM)</title><author>Baldi, Bruno Guedes ; Araujo, Mariana Sponholz ; Freitas, Carolina Salim Gonçalves ; da Silva Teles, Gustavo Borges ; Kairalla, Ronaldo Adib ; Dias, Olívia Meira ; Pereira, Daniel Antunes Silva ; Pimenta, Suzana Pinheiro ; Carvalho, Carlos Roberto Ribeiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c644t-b3505fcf134bba0ab0612ad289f580a4b27f2315cb9d0ae59af174346feb4c8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Biomarkers - analysis</topic><topic>Carbon monoxide</topic><topic>Complications and side effects</topic><topic>Cross-Sectional Studies</topic><topic>Cysts</topic><topic>Cysts - blood</topic><topic>Cysts - diagnostic imaging</topic><topic>Cysts - epidemiology</topic><topic>Development and progression</topic><topic>Disease Progression</topic><topic>Exercise</topic><topic>Exercise Test - methods</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Lung diseases</topic><topic>Lung Diseases - blood</topic><topic>Lung Diseases - diagnostic imaging</topic><topic>Lung Diseases - epidemiology</topic><topic>Lung Neoplasms - blood</topic><topic>Lung Neoplasms - diagnostic imaging</topic><topic>Lung Neoplasms - epidemiology</topic><topic>Lymphangioleiomyomatosis - blood</topic><topic>Lymphangioleiomyomatosis - diagnostic imaging</topic><topic>Lymphangioleiomyomatosis - epidemiology</topic><topic>Matrix Metalloproteinase 2 - blood</topic><topic>Matrix Metalloproteinase 9 - blood</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Patient outcomes</topic><topic>Physiological aspects</topic><topic>Pneumology/Respiratory System</topic><topic>Proteases</topic><topic>Respiratory Function Tests</topic><topic>Risk Assessment</topic><topic>Risk factors</topic><topic>Severity of Illness Index</topic><topic>Tomography</topic><topic>Tomography, X-Ray Computed - methods</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baldi, Bruno Guedes</creatorcontrib><creatorcontrib>Araujo, Mariana Sponholz</creatorcontrib><creatorcontrib>Freitas, Carolina Salim Gonçalves</creatorcontrib><creatorcontrib>da Silva Teles, Gustavo Borges</creatorcontrib><creatorcontrib>Kairalla, Ronaldo Adib</creatorcontrib><creatorcontrib>Dias, Olívia Meira</creatorcontrib><creatorcontrib>Pereira, Daniel Antunes Silva</creatorcontrib><creatorcontrib>Pimenta, Suzana Pinheiro</creatorcontrib><creatorcontrib>Carvalho, Carlos Roberto Ribeiro</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Lung</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baldi, Bruno Guedes</au><au>Araujo, Mariana Sponholz</au><au>Freitas, Carolina Salim Gonçalves</au><au>da Silva Teles, Gustavo Borges</au><au>Kairalla, Ronaldo Adib</au><au>Dias, Olívia Meira</au><au>Pereira, Daniel Antunes Silva</au><au>Pimenta, Suzana Pinheiro</au><au>Carvalho, Carlos Roberto Ribeiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM)</atitle><jtitle>Lung</jtitle><stitle>Lung</stitle><addtitle>Lung</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>192</volume><issue>6</issue><spage>967</spage><epage>974</epage><pages>967-974</pages><issn>0341-2040</issn><eissn>1432-1750</eissn><coden>LUNGD9</coden><abstract>Purpose
Although computed tomography (CT) has been used previously to assess disease severity in lymphangioleiomyomatosis (LAM), the associations between the extent of pulmonary cysts on CT and six-minute walk test (6MWT), matrix metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF-D) are not well established. We performed a cross-sectional study to quantify the extent of pulmonary cysts in CT and to establish their correlations with pulmonary function tests (PFTs), 6MWT results, including a composite index (desaturation–distance ratio, DDR), and levels of VEGF-D and MMPs in LAM.
Methods
Twenty-three LAM patients underwent CT scanning to automatically quantify the extent of pulmonary cysts and performed PFTs and 6MWT. Serum levels of MMP-2, MMP-9, and VEGF-D were also measured.
Results
The severity of pulmonary cystic involvement was mild (the extent of cysts was 6.8 %) and correlated best with FEV
1
/FVC (
r
= −0.84), residual volume (
r
= 0.66), DL
CO
(
r
= −0.82), the DDR index (
r
= 0.77), and desaturation during the 6MWT (
r
= −0.81). There was a weak correlation with VEGF-D (
r
= 0.45), but no association was found with MMP-2 and MMP-9.
Conclusions
The severity of pulmonary cystic involvement was mild in this sample of LAM patients and correlated best with airway obstruction, air trapping, reduced DL
CO
, the DDR index, and desaturation during the 6MWT. Serum VEGF-D cannot be completely defined as a valuable marker of disease severity and there may be a mechanism independent of MMPs to explain the formation of pulmonary cysts.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>25201087</pmid><doi>10.1007/s00408-014-9641-2</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
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ispartof | Lung, 2014-12, Vol.192 (6), p.967-974 |
issn | 0341-2040 1432-1750 |
language | eng |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Adult Biomarkers - analysis Carbon monoxide Complications and side effects Cross-Sectional Studies Cysts Cysts - blood Cysts - diagnostic imaging Cysts - epidemiology Development and progression Disease Progression Exercise Exercise Test - methods Female Follow-Up Studies Genetic aspects Health aspects Humans Lung diseases Lung Diseases - blood Lung Diseases - diagnostic imaging Lung Diseases - epidemiology Lung Neoplasms - blood Lung Neoplasms - diagnostic imaging Lung Neoplasms - epidemiology Lymphangioleiomyomatosis - blood Lymphangioleiomyomatosis - diagnostic imaging Lymphangioleiomyomatosis - epidemiology Matrix Metalloproteinase 2 - blood Matrix Metalloproteinase 9 - blood Medicine Medicine & Public Health Middle Aged Patient outcomes Physiological aspects Pneumology/Respiratory System Proteases Respiratory Function Tests Risk Assessment Risk factors Severity of Illness Index Tomography Tomography, X-Ray Computed - methods Vascular endothelial growth factor Vascular Endothelial Growth Factor A - blood |
title | Evaluation of the Extent of Pulmonary Cysts and Their Association with Functional Variables and Serum Markers in Lymphangioleiomyomatosis (LAM) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T05%3A27%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evaluation%20of%20the%20Extent%20of%20Pulmonary%20Cysts%20and%20Their%20Association%20with%20Functional%20Variables%20and%20Serum%20Markers%20in%20Lymphangioleiomyomatosis%20(LAM)&rft.jtitle=Lung&rft.au=Baldi,%20Bruno%20Guedes&rft.date=2014-12-01&rft.volume=192&rft.issue=6&rft.spage=967&rft.epage=974&rft.pages=967-974&rft.issn=0341-2040&rft.eissn=1432-1750&rft.coden=LUNGD9&rft_id=info:doi/10.1007/s00408-014-9641-2&rft_dat=%3Cgale_proqu%3EA426081625%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1626119799&rft_id=info:pmid/25201087&rft_galeid=A426081625&rfr_iscdi=true |