Lung function in children with diabetes mellitus
A cross‐sectional study design was undertaken to assess pulmonary function in children with insulin‐dependent diabetes mellitus (IDDM), and to establish if there is any relationship with diabetic factors and complications. Thirty‐eight children (10 ± 1.8 years) with IDDM and without clinical or radi...
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description | A cross‐sectional study design was undertaken to assess pulmonary function in children with insulin‐dependent diabetes mellitus (IDDM), and to establish if there is any relationship with diabetic factors and complications. Thirty‐eight children (10 ± 1.8 years) with IDDM and without clinical or radiological evidence of lung involvement, and 41 healthy age‐matched reference subjects, underwent a pulmonary function study. Thirteen (34%) of 38 subjects with IDDM were studied at the onset of their disease. Adjusted values expressed as SD score of forced vital capacity (FVC), forced expiratory volume in 1 sec (FEV1), and the transfer factor for carbon monoxide (TLCO) were found to be significantly lower than in controls (−0.54 ± 0.87 vs. 0.40 ± 1.10, P = 0.0008; −0.11 ± 0.96 vs. 0.52 ± 1.07, P = 0.01; −1.60 ± 1.07 vs. −0.57 ± 1.28, P = 0.001, respectively). These differences also existed in the group investigated at onset of diabetes. Residual volume (RV) and RV/total lung capacity ratio (RV/TLC) were significantly higher in the whole group of patients with IDDM than in controls (−0.20 ± 0.83 vs. −0.80 ± 0.88, P = 0.003; and 26 ± 6.2 vs. 21 ± 5.0, P = 0.0002, respectively). Seventeen patients (45%) had abnormal pulmonary function (SD score, less than −1.64): 16 subjects had reduced TLCO, 4 had reduced FVC, and in 3 of the 17, both functional indices were abnormal. There was no significant relationship between pulmonary function indices and diabetic factors or complications. The only significant association was between abnormal TLCO and females (P = 0.03), suggesting that sex may be a predisposing factor for the development of pulmonary complications. This study supports the view that the lung is functionally involved in children with IDDM early on in the course of the disease. Pediatr Pulmonol. 2004; 37:17–23. © 2004 Wiley‐Liss, Inc. |
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Thirty‐eight children (10 ± 1.8 years) with IDDM and without clinical or radiological evidence of lung involvement, and 41 healthy age‐matched reference subjects, underwent a pulmonary function study. Thirteen (34%) of 38 subjects with IDDM were studied at the onset of their disease. Adjusted values expressed as SD score of forced vital capacity (FVC), forced expiratory volume in 1 sec (FEV1), and the transfer factor for carbon monoxide (TLCO) were found to be significantly lower than in controls (−0.54 ± 0.87 vs. 0.40 ± 1.10, P = 0.0008; −0.11 ± 0.96 vs. 0.52 ± 1.07, P = 0.01; −1.60 ± 1.07 vs. −0.57 ± 1.28, P = 0.001, respectively). These differences also existed in the group investigated at onset of diabetes. Residual volume (RV) and RV/total lung capacity ratio (RV/TLC) were significantly higher in the whole group of patients with IDDM than in controls (−0.20 ± 0.83 vs. −0.80 ± 0.88, P = 0.003; and 26 ± 6.2 vs. 21 ± 5.0, P = 0.0002, respectively). Seventeen patients (45%) had abnormal pulmonary function (SD score, less than −1.64): 16 subjects had reduced TLCO, 4 had reduced FVC, and in 3 of the 17, both functional indices were abnormal. There was no significant relationship between pulmonary function indices and diabetic factors or complications. The only significant association was between abnormal TLCO and females (P = 0.03), suggesting that sex may be a predisposing factor for the development of pulmonary complications. This study supports the view that the lung is functionally involved in children with IDDM early on in the course of the disease. Pediatr Pulmonol. 2004; 37:17–23. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.10399</identifier><identifier>PMID: 14679484</identifier><identifier>CODEN: PEPUES</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Child ; Cross-Sectional Studies ; diabetes mellitus ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - physiopathology ; Female ; Forced Expiratory Volume ; General aspects ; Humans ; insulin-dependent ; Italy ; Lung - physiopathology ; Lung Diseases - etiology ; Lung Diseases - physiopathology ; Male ; Medical sciences ; Pneumology ; pulmonary diffusing capacity ; Residual Volume ; Respiratory Function Tests ; spirometry ; Total Lung Capacity ; Vital Capacity</subject><ispartof>Pediatric pulmonology, 2004-01, Vol.37 (1), p.17-23</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3939-f2bccad3d6ccbae43e82efa96db0b67bd20b9a00c34212300991787c765746733</citedby><cites>FETCH-LOGICAL-c3939-f2bccad3d6ccbae43e82efa96db0b67bd20b9a00c34212300991787c765746733</cites></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.10399$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.10399$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15461400$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14679484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cazzato, Salvatore</creatorcontrib><creatorcontrib>Bernardi, Filippo</creatorcontrib><creatorcontrib>Salardi, Silvana</creatorcontrib><creatorcontrib>Tassinari, Davide</creatorcontrib><creatorcontrib>Corsini, Ilaria</creatorcontrib><creatorcontrib>Ragni, Luca</creatorcontrib><creatorcontrib>Cicognani, Alessandro</creatorcontrib><creatorcontrib>Cacciari, Emanuele</creatorcontrib><title>Lung function in children with diabetes mellitus</title><title>Pediatric pulmonology</title><addtitle>Pediatr. Pulmonol</addtitle><description>A cross‐sectional study design was undertaken to assess pulmonary function in children with insulin‐dependent diabetes mellitus (IDDM), and to establish if there is any relationship with diabetic factors and complications. Thirty‐eight children (10 ± 1.8 years) with IDDM and without clinical or radiological evidence of lung involvement, and 41 healthy age‐matched reference subjects, underwent a pulmonary function study. Thirteen (34%) of 38 subjects with IDDM were studied at the onset of their disease. Adjusted values expressed as SD score of forced vital capacity (FVC), forced expiratory volume in 1 sec (FEV1), and the transfer factor for carbon monoxide (TLCO) were found to be significantly lower than in controls (−0.54 ± 0.87 vs. 0.40 ± 1.10, P = 0.0008; −0.11 ± 0.96 vs. 0.52 ± 1.07, P = 0.01; −1.60 ± 1.07 vs. −0.57 ± 1.28, P = 0.001, respectively). These differences also existed in the group investigated at onset of diabetes. Residual volume (RV) and RV/total lung capacity ratio (RV/TLC) were significantly higher in the whole group of patients with IDDM than in controls (−0.20 ± 0.83 vs. −0.80 ± 0.88, P = 0.003; and 26 ± 6.2 vs. 21 ± 5.0, P = 0.0002, respectively). Seventeen patients (45%) had abnormal pulmonary function (SD score, less than −1.64): 16 subjects had reduced TLCO, 4 had reduced FVC, and in 3 of the 17, both functional indices were abnormal. There was no significant relationship between pulmonary function indices and diabetic factors or complications. The only significant association was between abnormal TLCO and females (P = 0.03), suggesting that sex may be a predisposing factor for the development of pulmonary complications. This study supports the view that the lung is functionally involved in children with IDDM early on in the course of the disease. Pediatr Pulmonol. 2004; 37:17–23. © 2004 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Cross-Sectional Studies</subject><subject>diabetes mellitus</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - physiopathology</subject><subject>Female</subject><subject>Forced Expiratory Volume</subject><subject>General aspects</subject><subject>Humans</subject><subject>insulin-dependent</subject><subject>Italy</subject><subject>Lung - physiopathology</subject><subject>Lung Diseases - etiology</subject><subject>Lung Diseases - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pneumology</subject><subject>pulmonary diffusing capacity</subject><subject>Residual Volume</subject><subject>Respiratory Function Tests</subject><subject>spirometry</subject><subject>Total Lung Capacity</subject><subject>Vital Capacity</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1OwzAQhC0EoqVw4QFQLnBACtixY8dH1EJBqkolWuBmOY5DDfkpcaLSt8clgd447Ur7ze7sAHCK4BWCMLherZrMdZjzPdBHkHMfEk73QT9iYejTiOIeOLL2HUI34-gQ9BChjJOI9AGcNMWblzaFqk1ZeKbw1NJkSaULb23qpZcYGetaWy_XWWbqxh6Dg1RmVp90dQAWd7fz4b0_eRw_DG8mvsIccz8NYqVkghOqVCw1wToKdCo5TWIYUxYnAYy5hFBhEqAAb50hFjHFaMicOYwH4KLdu6rKz0bbWuTGKmdCFrpsrGAopIhC4sDLFlRVaW2lU7GqTC6rjUBQbPMR23zETz4OPuu2NnGukx3aBeKA8w6QVsksrWShjN1xIaGIQOg41HJrk-nNPyfFbLaY_B73W42xtf7608jqQ7iPWShepmPxNHqeT8nrSFD8DYm5i9A</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Cazzato, Salvatore</creator><creator>Bernardi, Filippo</creator><creator>Salardi, Silvana</creator><creator>Tassinari, Davide</creator><creator>Corsini, Ilaria</creator><creator>Ragni, Luca</creator><creator>Cicognani, Alessandro</creator><creator>Cacciari, Emanuele</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>200401</creationdate><title>Lung function in children with diabetes mellitus</title><author>Cazzato, Salvatore ; Bernardi, Filippo ; Salardi, Silvana ; Tassinari, Davide ; Corsini, Ilaria ; Ragni, Luca ; Cicognani, Alessandro ; Cacciari, Emanuele</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3939-f2bccad3d6ccbae43e82efa96db0b67bd20b9a00c34212300991787c765746733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Cross-Sectional Studies</topic><topic>diabetes mellitus</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - physiopathology</topic><topic>Female</topic><topic>Forced Expiratory Volume</topic><topic>General aspects</topic><topic>Humans</topic><topic>insulin-dependent</topic><topic>Italy</topic><topic>Lung - physiopathology</topic><topic>Lung Diseases - etiology</topic><topic>Lung Diseases - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pneumology</topic><topic>pulmonary diffusing capacity</topic><topic>Residual Volume</topic><topic>Respiratory Function Tests</topic><topic>spirometry</topic><topic>Total Lung Capacity</topic><topic>Vital Capacity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cazzato, Salvatore</creatorcontrib><creatorcontrib>Bernardi, Filippo</creatorcontrib><creatorcontrib>Salardi, Silvana</creatorcontrib><creatorcontrib>Tassinari, Davide</creatorcontrib><creatorcontrib>Corsini, Ilaria</creatorcontrib><creatorcontrib>Ragni, Luca</creatorcontrib><creatorcontrib>Cicognani, Alessandro</creatorcontrib><creatorcontrib>Cacciari, Emanuele</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cazzato, Salvatore</au><au>Bernardi, Filippo</au><au>Salardi, Silvana</au><au>Tassinari, Davide</au><au>Corsini, Ilaria</au><au>Ragni, Luca</au><au>Cicognani, Alessandro</au><au>Cacciari, Emanuele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lung function in children with diabetes mellitus</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr. Pulmonol</addtitle><date>2004-01</date><risdate>2004</risdate><volume>37</volume><issue>1</issue><spage>17</spage><epage>23</epage><pages>17-23</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><coden>PEPUES</coden><abstract>A cross‐sectional study design was undertaken to assess pulmonary function in children with insulin‐dependent diabetes mellitus (IDDM), and to establish if there is any relationship with diabetic factors and complications. Thirty‐eight children (10 ± 1.8 years) with IDDM and without clinical or radiological evidence of lung involvement, and 41 healthy age‐matched reference subjects, underwent a pulmonary function study. Thirteen (34%) of 38 subjects with IDDM were studied at the onset of their disease. Adjusted values expressed as SD score of forced vital capacity (FVC), forced expiratory volume in 1 sec (FEV1), and the transfer factor for carbon monoxide (TLCO) were found to be significantly lower than in controls (−0.54 ± 0.87 vs. 0.40 ± 1.10, P = 0.0008; −0.11 ± 0.96 vs. 0.52 ± 1.07, P = 0.01; −1.60 ± 1.07 vs. −0.57 ± 1.28, P = 0.001, respectively). These differences also existed in the group investigated at onset of diabetes. Residual volume (RV) and RV/total lung capacity ratio (RV/TLC) were significantly higher in the whole group of patients with IDDM than in controls (−0.20 ± 0.83 vs. −0.80 ± 0.88, P = 0.003; and 26 ± 6.2 vs. 21 ± 5.0, P = 0.0002, respectively). Seventeen patients (45%) had abnormal pulmonary function (SD score, less than −1.64): 16 subjects had reduced TLCO, 4 had reduced FVC, and in 3 of the 17, both functional indices were abnormal. There was no significant relationship between pulmonary function indices and diabetic factors or complications. The only significant association was between abnormal TLCO and females (P = 0.03), suggesting that sex may be a predisposing factor for the development of pulmonary complications. This study supports the view that the lung is functionally involved in children with IDDM early on in the course of the disease. Pediatr Pulmonol. 2004; 37:17–23. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14679484</pmid><doi>10.1002/ppul.10399</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Child Cross-Sectional Studies diabetes mellitus Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - physiopathology Female Forced Expiratory Volume General aspects Humans insulin-dependent Italy Lung - physiopathology Lung Diseases - etiology Lung Diseases - physiopathology Male Medical sciences Pneumology pulmonary diffusing capacity Residual Volume Respiratory Function Tests spirometry Total Lung Capacity Vital Capacity |
title | Lung function in children with diabetes mellitus |
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