Energy expenditure of patients with cystic fibrosis
Resting energy expenditure was measured by open-circuit indirect calorimetry in 71 patients, aged 8.9 to 35.5 years, with cystic fibrosis who had no recent history of acute lung infection. Pulmonary function and nutritional status were studied simultaneously. In most patients, resting energy expendi...
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| Veröffentlicht in: | The Journal of pediatrics 1987-10, Vol.111 (4), p.496-500 |
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| container_title | The Journal of pediatrics |
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| creator | Vaisman, Nachum Pencharz, Paul B. Corey, Mary Canny, Gerard J. Hahn, Elizabeth |
| description | Resting energy expenditure was measured by open-circuit indirect calorimetry in 71 patients, aged 8.9 to 35.5 years, with cystic fibrosis who had no recent history of acute lung infection. Pulmonary function and nutritional status were studied simultaneously. In most patients, resting energy expenditure was above normal (range 95% to 153% of predicted values for age, sex, and weight as derived from the Harris Benedict equations), and was negatively correlated with pulmonary function (P |
| doi_str_mv | 10.1016/S0022-3476(87)80107-5 |
| format | Article |
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Pulmonary function and nutritional status were studied simultaneously. In most patients, resting energy expenditure was above normal (range 95% to 153% of predicted values for age, sex, and weight as derived from the Harris Benedict equations), and was negatively correlated with pulmonary function (P<0.01) and nutritional status (P<0.01) when expressed as a percentage of body fat. Pulmonary status was positively correlated with nutritional status (P<0.01). We conclude that resting energy expenditure in patients with cystic fibrosis exceeds normal values and that the increase correlates with a deterioration in lung function and nutritional status.</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/S0022-3476(87)80107-5</identifier><identifier>PMID: 3655979</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Adult ; Animals ; Anthropometry ; Basal Metabolism ; Biological and medical sciences ; Body Composition ; Calorimetry, Indirect ; Child ; Cricetinae ; Cystic Fibrosis - metabolism ; Cystic Fibrosis - physiopathology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Nutritional Status ; Other diseases. Semiology ; Respiratory Function Tests</subject><ispartof>The Journal of pediatrics, 1987-10, Vol.111 (4), p.496-500</ispartof><rights>1987 The C. V. Mosby Company</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-721d9317fe4eb144d45e17c843ca0e92f3bfb597f439b1d589a88b49460346d03</citedby><cites>FETCH-LOGICAL-c389t-721d9317fe4eb144d45e17c843ca0e92f3bfb597f439b1d589a88b49460346d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-3476(87)80107-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7512031$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3655979$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vaisman, Nachum</creatorcontrib><creatorcontrib>Pencharz, Paul B.</creatorcontrib><creatorcontrib>Corey, Mary</creatorcontrib><creatorcontrib>Canny, Gerard J.</creatorcontrib><creatorcontrib>Hahn, Elizabeth</creatorcontrib><title>Energy expenditure of patients with cystic fibrosis</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><description>Resting energy expenditure was measured by open-circuit indirect calorimetry in 71 patients, aged 8.9 to 35.5 years, with cystic fibrosis who had no recent history of acute lung infection. Pulmonary function and nutritional status were studied simultaneously. In most patients, resting energy expenditure was above normal (range 95% to 153% of predicted values for age, sex, and weight as derived from the Harris Benedict equations), and was negatively correlated with pulmonary function (P<0.01) and nutritional status (P<0.01) when expressed as a percentage of body fat. Pulmonary status was positively correlated with nutritional status (P<0.01). We conclude that resting energy expenditure in patients with cystic fibrosis exceeds normal values and that the increase correlates with a deterioration in lung function and nutritional status.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Anthropometry</subject><subject>Basal Metabolism</subject><subject>Biological and medical sciences</subject><subject>Body Composition</subject><subject>Calorimetry, Indirect</subject><subject>Child</subject><subject>Cricetinae</subject><subject>Cystic Fibrosis - metabolism</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nutritional Status</subject><subject>Other diseases. Semiology</subject><subject>Respiratory Function Tests</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EgvL4BKQsEIJFYBw7sb1CqOIlVWIBrC3HGYNRmxQ7Afr3uA91y2oWc-7M1SHklMIVBVpdvwAURc64qC6kuJRAQeTlDhlRUCKvJGO7ZLRFDshhjJ8AoDjAPtlnVVkqoUaE3bUY3hcZ_s6xbXw_BMw6l81N77HtY_bj-4_MLmLvbeZ8Hbro4zHZc2Ya8WQzj8jb_d3r-DGfPD88jW8nuWVS9bkoaKMYFQ451pTzhpdIhZWcWQOoCsdqV6cWjjNV06aUykhZc8UrYLxqgB2R8_Xdeei-Boy9nvlocTo1LXZD1JIChxRLYLkGbeoXAzo9D35mwkJT0EtZeiVLL01oKfRKli5T7nTzYKhn2GxTGztpf7bZm2jN1AXTWh-3mChpAYwm7GaNYZLx7THoaJM9i40PaHvddP6fIn9kIYS8</recordid><startdate>19871001</startdate><enddate>19871001</enddate><creator>Vaisman, Nachum</creator><creator>Pencharz, Paul B.</creator><creator>Corey, Mary</creator><creator>Canny, Gerard J.</creator><creator>Hahn, Elizabeth</creator><general>Mosby, Inc</general><general>Elsevier</general><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>19871001</creationdate><title>Energy expenditure of patients with cystic fibrosis</title><author>Vaisman, Nachum ; Pencharz, Paul B. ; Corey, Mary ; Canny, Gerard J. ; Hahn, Elizabeth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-721d9317fe4eb144d45e17c843ca0e92f3bfb597f439b1d589a88b49460346d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Anthropometry</topic><topic>Basal Metabolism</topic><topic>Biological and medical sciences</topic><topic>Body Composition</topic><topic>Calorimetry, Indirect</topic><topic>Child</topic><topic>Cricetinae</topic><topic>Cystic Fibrosis - metabolism</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nutritional Status</topic><topic>Other diseases. Semiology</topic><topic>Respiratory Function Tests</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vaisman, Nachum</creatorcontrib><creatorcontrib>Pencharz, Paul B.</creatorcontrib><creatorcontrib>Corey, Mary</creatorcontrib><creatorcontrib>Canny, Gerard J.</creatorcontrib><creatorcontrib>Hahn, Elizabeth</creatorcontrib><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>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vaisman, Nachum</au><au>Pencharz, Paul B.</au><au>Corey, Mary</au><au>Canny, Gerard J.</au><au>Hahn, Elizabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Energy expenditure of patients with cystic fibrosis</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>1987-10-01</date><risdate>1987</risdate><volume>111</volume><issue>4</issue><spage>496</spage><epage>500</epage><pages>496-500</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>Resting energy expenditure was measured by open-circuit indirect calorimetry in 71 patients, aged 8.9 to 35.5 years, with cystic fibrosis who had no recent history of acute lung infection. Pulmonary function and nutritional status were studied simultaneously. In most patients, resting energy expenditure was above normal (range 95% to 153% of predicted values for age, sex, and weight as derived from the Harris Benedict equations), and was negatively correlated with pulmonary function (P<0.01) and nutritional status (P<0.01) when expressed as a percentage of body fat. Pulmonary status was positively correlated with nutritional status (P<0.01). We conclude that resting energy expenditure in patients with cystic fibrosis exceeds normal values and that the increase correlates with a deterioration in lung function and nutritional status.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>3655979</pmid><doi>10.1016/S0022-3476(87)80107-5</doi><tpages>5</tpages></addata></record> |
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| ispartof | The Journal of pediatrics, 1987-10, Vol.111 (4), p.496-500 |
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| source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
| subjects | Adolescent Adult Animals Anthropometry Basal Metabolism Biological and medical sciences Body Composition Calorimetry, Indirect Child Cricetinae Cystic Fibrosis - metabolism Cystic Fibrosis - physiopathology Female Gastroenterology. Liver. Pancreas. Abdomen Humans Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Nutritional Status Other diseases. Semiology Respiratory Function Tests |
| title | Energy expenditure of patients with cystic fibrosis |
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