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Adolescent development and energy expenditure in females with cystic fibrosis
Poor nutrition and growth status are common in people with cystic fibrosis (CF), and females often have a worse clinical course. Relationships between sexual maturity, nutrition, resting energy expenditure (REE), and pulmonary status in females with CF and pancreatic insufficiency (PI) were evaluate...
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Published in: | Clinical nutrition (Edinburgh, Scotland) Scotland), 2005-10, Vol.24 (5), p.737-745 |
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creator | Stallings, Virginia A. Tomezsko, Jean L. Schall, Joan I. Mascarenhas, Maria R. Stettler, Nicolas Scanlin, Thomas F. Zemel, Babette S. |
description | Poor nutrition and growth status are common in people with cystic fibrosis (CF), and females often have a worse clinical course. Relationships between sexual maturity, nutrition, resting energy expenditure (REE), and pulmonary status in females with CF and pancreatic insufficiency (PI) were evaluated.
Pre- and post-menarcheal females with CF and PI (8–29
yr) were compared to healthy females.
Z-scores for growth and body composition, anthropometry and DEXA were assessed. REE was measured in all subjects and pulmonary function in CF.
Compared to healthy females (
n
=
28
, 14.6±4.1
yr), females with CF (
n
=
16
, 14.7±4.4
yr) had lower height
Z (−0.1±0.9 versus −0.9±0.9,
P
=
0.009
) and muscle area
Z (0.8±1.3 versus –0.4±1.2,
P
=
0.007
), and higher REE (100±10 versus 110±11% predicted,
P
=
0.008
). Difference in REE was more pronounced for post-menarcheal girls. REE adjusted for fat and fat-free mass was significantly higher with CF (+110
calories/day), and declined with menarcheal age in all subjects. FEV
1 was positively associated with BMI
Z score, and negatively associated with age at menarche.
Height and muscle stores were reduced and REE elevated in subjects with CF compared to healthy controls. Poorer growth and nutritional status and delayed menarche were associated with poorer pulmonary function in CF and were likely related to the cumulative effect of energy imbalance on growth and body composition. |
doi_str_mv | 10.1016/j.clnu.2005.02.005 |
format | article |
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Pre- and post-menarcheal females with CF and PI (8–29
yr) were compared to healthy females.
Z-scores for growth and body composition, anthropometry and DEXA were assessed. REE was measured in all subjects and pulmonary function in CF.
Compared to healthy females (
n
=
28
, 14.6±4.1
yr), females with CF (
n
=
16
, 14.7±4.4
yr) had lower height
Z (−0.1±0.9 versus −0.9±0.9,
P
=
0.009
) and muscle area
Z (0.8±1.3 versus –0.4±1.2,
P
=
0.007
), and higher REE (100±10 versus 110±11% predicted,
P
=
0.008
). Difference in REE was more pronounced for post-menarcheal girls. REE adjusted for fat and fat-free mass was significantly higher with CF (+110
calories/day), and declined with menarcheal age in all subjects. FEV
1 was positively associated with BMI
Z score, and negatively associated with age at menarche.
Height and muscle stores were reduced and REE elevated in subjects with CF compared to healthy controls. Poorer growth and nutritional status and delayed menarche were associated with poorer pulmonary function in CF and were likely related to the cumulative effect of energy imbalance on growth and body composition.</description><identifier>ISSN: 0261-5614</identifier><identifier>EISSN: 1532-1983</identifier><identifier>DOI: 10.1016/j.clnu.2005.02.005</identifier><identifier>PMID: 16182037</identifier><identifier>CODEN: CLNUDP</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Basal Metabolism - physiology ; Biological and medical sciences ; Body Composition - physiology ; Body Height - physiology ; Body Weight - physiology ; Calorimetry, Indirect ; Case-Control Studies ; Child ; Cystic fibrosis ; Cystic Fibrosis - metabolism ; Cystic Fibrosis - physiopathology ; Energy expenditure ; Energy Metabolism - physiology ; Errors of metabolism ; Exocrine Pancreatic Insufficiency - physiopathology ; Female ; Gender ; Humans ; Intestinal Absorption ; Medical sciences ; Menarche - physiology ; Menarcheal status ; Metabolic diseases ; Miscellaneous hereditary metabolic disorders ; Nutritional Status ; Pancreatic insufficiency ; Pulmonary function ; Respiratory Function Tests ; Sexual Maturation - physiology</subject><ispartof>Clinical nutrition (Edinburgh, Scotland), 2005-10, Vol.24 (5), p.737-745</ispartof><rights>2005 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-404e4df795a8225c061ea0b12fe6c3d86bc8ba175018b11bf7aed82539c9ba4e3</citedby><cites>FETCH-LOGICAL-c384t-404e4df795a8225c061ea0b12fe6c3d86bc8ba175018b11bf7aed82539c9ba4e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17130329$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16182037$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stallings, Virginia A.</creatorcontrib><creatorcontrib>Tomezsko, Jean L.</creatorcontrib><creatorcontrib>Schall, Joan I.</creatorcontrib><creatorcontrib>Mascarenhas, Maria R.</creatorcontrib><creatorcontrib>Stettler, Nicolas</creatorcontrib><creatorcontrib>Scanlin, Thomas F.</creatorcontrib><creatorcontrib>Zemel, Babette S.</creatorcontrib><title>Adolescent development and energy expenditure in females with cystic fibrosis</title><title>Clinical nutrition (Edinburgh, Scotland)</title><addtitle>Clin Nutr</addtitle><description>Poor nutrition and growth status are common in people with cystic fibrosis (CF), and females often have a worse clinical course. Relationships between sexual maturity, nutrition, resting energy expenditure (REE), and pulmonary status in females with CF and pancreatic insufficiency (PI) were evaluated.
Pre- and post-menarcheal females with CF and PI (8–29
yr) were compared to healthy females.
Z-scores for growth and body composition, anthropometry and DEXA were assessed. REE was measured in all subjects and pulmonary function in CF.
Compared to healthy females (
n
=
28
, 14.6±4.1
yr), females with CF (
n
=
16
, 14.7±4.4
yr) had lower height
Z (−0.1±0.9 versus −0.9±0.9,
P
=
0.009
) and muscle area
Z (0.8±1.3 versus –0.4±1.2,
P
=
0.007
), and higher REE (100±10 versus 110±11% predicted,
P
=
0.008
). Difference in REE was more pronounced for post-menarcheal girls. REE adjusted for fat and fat-free mass was significantly higher with CF (+110
calories/day), and declined with menarcheal age in all subjects. FEV
1 was positively associated with BMI
Z score, and negatively associated with age at menarche.
Height and muscle stores were reduced and REE elevated in subjects with CF compared to healthy controls. Poorer growth and nutritional status and delayed menarche were associated with poorer pulmonary function in CF and were likely related to the cumulative effect of energy imbalance on growth and body composition.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Basal Metabolism - physiology</subject><subject>Biological and medical sciences</subject><subject>Body Composition - physiology</subject><subject>Body Height - physiology</subject><subject>Body Weight - physiology</subject><subject>Calorimetry, Indirect</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - metabolism</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Energy expenditure</subject><subject>Energy Metabolism - physiology</subject><subject>Errors of metabolism</subject><subject>Exocrine Pancreatic Insufficiency - physiopathology</subject><subject>Female</subject><subject>Gender</subject><subject>Humans</subject><subject>Intestinal Absorption</subject><subject>Medical sciences</subject><subject>Menarche - physiology</subject><subject>Menarcheal status</subject><subject>Metabolic diseases</subject><subject>Miscellaneous hereditary metabolic disorders</subject><subject>Nutritional Status</subject><subject>Pancreatic insufficiency</subject><subject>Pulmonary function</subject><subject>Respiratory Function Tests</subject><subject>Sexual Maturation - physiology</subject><issn>0261-5614</issn><issn>1532-1983</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kLFu2zAQhokiQe24fYEOhZZkk8IjJYoCugRB2hRIkCWdCYo8tTQkyiUlJ377UrABb53-G747_PcR8gVoARTE7bYwvZ8LRmlVUFak-EDWUHGWQyP5BVlTJiCvBJQrchXjliaC1_IjWYEAySiv1-T5zo49RoN-yizusR93wzJrbzP0GH4fMnzfobdumgNmzmcdDjptZG9u-pOZQ5ycyTrXhjG6-IlcdrqP-PmUG_Lr-8Pr_WP-9PLj5_3dU264LKe8pCWWtqubSkvGKkMFoKYtsA6F4VaK1shWQ11RkC1A29UarWQVb0zT6hL5htwc7-7C-HfGOKnBpR_6Xnsc56iEFKwUVZ1AdgRN6hcDdmoX3KDDQQFVi0S1VYtEtUhUlKlF0YZ8PV2f2wHteeVkLQHXJ0BHo_suaG9cPHM1cMpZk7hvRw6Ti73DoKJx6A1aF9BMyo7ufz3-AYllkN0</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Stallings, Virginia A.</creator><creator>Tomezsko, Jean L.</creator><creator>Schall, Joan I.</creator><creator>Mascarenhas, Maria R.</creator><creator>Stettler, Nicolas</creator><creator>Scanlin, Thomas F.</creator><creator>Zemel, Babette S.</creator><general>Elsevier Ltd</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>20051001</creationdate><title>Adolescent development and energy expenditure in females with cystic fibrosis</title><author>Stallings, Virginia A. ; Tomezsko, Jean L. ; Schall, Joan I. ; Mascarenhas, Maria R. ; Stettler, Nicolas ; Scanlin, Thomas F. ; Zemel, Babette S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-404e4df795a8225c061ea0b12fe6c3d86bc8ba175018b11bf7aed82539c9ba4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Basal Metabolism - physiology</topic><topic>Biological and medical sciences</topic><topic>Body Composition - physiology</topic><topic>Body Height - physiology</topic><topic>Body Weight - physiology</topic><topic>Calorimetry, Indirect</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - metabolism</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Energy expenditure</topic><topic>Energy Metabolism - physiology</topic><topic>Errors of metabolism</topic><topic>Exocrine Pancreatic Insufficiency - physiopathology</topic><topic>Female</topic><topic>Gender</topic><topic>Humans</topic><topic>Intestinal Absorption</topic><topic>Medical sciences</topic><topic>Menarche - physiology</topic><topic>Menarcheal status</topic><topic>Metabolic diseases</topic><topic>Miscellaneous hereditary metabolic disorders</topic><topic>Nutritional Status</topic><topic>Pancreatic insufficiency</topic><topic>Pulmonary function</topic><topic>Respiratory Function Tests</topic><topic>Sexual Maturation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stallings, Virginia A.</creatorcontrib><creatorcontrib>Tomezsko, Jean L.</creatorcontrib><creatorcontrib>Schall, Joan I.</creatorcontrib><creatorcontrib>Mascarenhas, Maria R.</creatorcontrib><creatorcontrib>Stettler, Nicolas</creatorcontrib><creatorcontrib>Scanlin, Thomas F.</creatorcontrib><creatorcontrib>Zemel, Babette S.</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>Clinical nutrition (Edinburgh, Scotland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stallings, Virginia A.</au><au>Tomezsko, Jean L.</au><au>Schall, Joan I.</au><au>Mascarenhas, Maria R.</au><au>Stettler, Nicolas</au><au>Scanlin, Thomas F.</au><au>Zemel, Babette S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adolescent development and energy expenditure in females with cystic fibrosis</atitle><jtitle>Clinical nutrition (Edinburgh, Scotland)</jtitle><addtitle>Clin Nutr</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>24</volume><issue>5</issue><spage>737</spage><epage>745</epage><pages>737-745</pages><issn>0261-5614</issn><eissn>1532-1983</eissn><coden>CLNUDP</coden><abstract>Poor nutrition and growth status are common in people with cystic fibrosis (CF), and females often have a worse clinical course. Relationships between sexual maturity, nutrition, resting energy expenditure (REE), and pulmonary status in females with CF and pancreatic insufficiency (PI) were evaluated.
Pre- and post-menarcheal females with CF and PI (8–29
yr) were compared to healthy females.
Z-scores for growth and body composition, anthropometry and DEXA were assessed. REE was measured in all subjects and pulmonary function in CF.
Compared to healthy females (
n
=
28
, 14.6±4.1
yr), females with CF (
n
=
16
, 14.7±4.4
yr) had lower height
Z (−0.1±0.9 versus −0.9±0.9,
P
=
0.009
) and muscle area
Z (0.8±1.3 versus –0.4±1.2,
P
=
0.007
), and higher REE (100±10 versus 110±11% predicted,
P
=
0.008
). Difference in REE was more pronounced for post-menarcheal girls. REE adjusted for fat and fat-free mass was significantly higher with CF (+110
calories/day), and declined with menarcheal age in all subjects. FEV
1 was positively associated with BMI
Z score, and negatively associated with age at menarche.
Height and muscle stores were reduced and REE elevated in subjects with CF compared to healthy controls. Poorer growth and nutritional status and delayed menarche were associated with poorer pulmonary function in CF and were likely related to the cumulative effect of energy imbalance on growth and body composition.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>16182037</pmid><doi>10.1016/j.clnu.2005.02.005</doi><tpages>9</tpages></addata></record> |
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source | ScienceDirect Freedom Collection |
subjects | Adolescent Adult Basal Metabolism - physiology Biological and medical sciences Body Composition - physiology Body Height - physiology Body Weight - physiology Calorimetry, Indirect Case-Control Studies Child Cystic fibrosis Cystic Fibrosis - metabolism Cystic Fibrosis - physiopathology Energy expenditure Energy Metabolism - physiology Errors of metabolism Exocrine Pancreatic Insufficiency - physiopathology Female Gender Humans Intestinal Absorption Medical sciences Menarche - physiology Menarcheal status Metabolic diseases Miscellaneous hereditary metabolic disorders Nutritional Status Pancreatic insufficiency Pulmonary function Respiratory Function Tests Sexual Maturation - physiology |
title | Adolescent development and energy expenditure in females with cystic fibrosis |
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