PittsburghV1, PubMed, Curation, bibRecord, 000A94

Overweight and obesity in patients with cystic fibrosis: a center-based analysis.

Identifieur interne : 000A94 ( PubMed/Curation ); précédent : 000A93; suivant : 000A95

Overweight and obesity in patients with cystic fibrosis: a center-based analysis.

Auteurs : Reem M. Hanna [États-Unis] ; Daniel J. Weiner

Source :

Pediatric pulmonology [ 1099-0496 ] ; 2015.

RBID : pubmed:24757043

Descripteurs français

KwdFr :
- Adolescent, Diabète (étiologie), Enfant, Enregistrements, Femelle, Humains, Insuffisance pancréatique exocrine (), Intolérance au glucose, Mucoviscidose (), Mâle, Nourrisson, Obésité (), Surpoids (), État nutritionnel.
MESH :
- étiologie : Diabète.
- Adolescent, Enfant, Enregistrements, Femelle, Humains, Insuffisance pancréatique exocrine, Intolérance au glucose, Mucoviscidose, Mâle, Nourrisson, Obésité, Surpoids, État nutritionnel.

English descriptors

KwdEn :
- Adolescent, Child, Cystic Fibrosis (complications), Diabetes Mellitus (etiology), Exocrine Pancreatic Insufficiency (complications), Female, Glucose Intolerance, Humans, Infant, Male, Nutritional Status, Obesity (complications), Overweight (complications), Registries.
MESH :
- complications : Cystic Fibrosis, Exocrine Pancreatic Insufficiency, Obesity, Overweight.
- etiology : Diabetes Mellitus.
- Adolescent, Child, Female, Glucose Intolerance, Humans, Infant, Male, Nutritional Status, Registries.

Abstract

Cystic fibrosis (CF) has long been associated with malnutrition. However, due to early diagnosis, nutritional supplements, and increased prevalence of obesity in the general population, overweight, and obesity in the CF patient population is becoming a concern. The aim of this study was to determine the prevalence of obesity and overweight in patients with CF seen at our center, to analyze factors associated with nutritional status, to evaluate the relation between nutritional status and lung function, and to document any adverse health outcomes.

DOI: 10.1002/ppul.23033
PubMed: 24757043

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: Pour aller vers cette notice dans l'étape Curation :000A94

Links to Exploration step

pubmed:24757043

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Overweight and obesity in patients with cystic fibrosis: a center-based analysis.</title>
<author><name sortKey="Hanna, Reem M" sort="Hanna, Reem M" uniqKey="Hanna R" first="Reem M" last="Hanna">Reem M. Hanna</name>
<affiliation wicri:level="2"><nlm:affiliation>Division of Pulmonary Medicine, Allergy, and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
<wicri:cityArea>Division of Pulmonary Medicine, Allergy, and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh</wicri:cityArea>
</affiliation>
</author>
<author><name sortKey="Weiner, Daniel J" sort="Weiner, Daniel J" uniqKey="Weiner D" first="Daniel J" last="Weiner">Daniel J. Weiner</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2015">2015</date>
<idno type="RBID">pubmed:24757043</idno>
<idno type="pmid">24757043</idno>
<idno type="doi">10.1002/ppul.23033</idno>
<idno type="wicri:Area/PubMed/Corpus">000A94</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000A94</idno>
<idno type="wicri:Area/PubMed/Curation">000A94</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000A94</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Overweight and obesity in patients with cystic fibrosis: a center-based analysis.</title>
<author><name sortKey="Hanna, Reem M" sort="Hanna, Reem M" uniqKey="Hanna R" first="Reem M" last="Hanna">Reem M. Hanna</name>
<affiliation wicri:level="2"><nlm:affiliation>Division of Pulmonary Medicine, Allergy, and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName><region type="state">Pennsylvanie</region>
</placeName>
<wicri:cityArea>Division of Pulmonary Medicine, Allergy, and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh</wicri:cityArea>
</affiliation>
</author>
<author><name sortKey="Weiner, Daniel J" sort="Weiner, Daniel J" uniqKey="Weiner D" first="Daniel J" last="Weiner">Daniel J. Weiner</name>
</author>
</analytic>
<series><title level="j">Pediatric pulmonology</title>
<idno type="eISSN">1099-0496</idno>
<imprint><date when="2015" type="published">2015</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Child</term>
<term>Cystic Fibrosis (complications)</term>
<term>Diabetes Mellitus (etiology)</term>
<term>Exocrine Pancreatic Insufficiency (complications)</term>
<term>Female</term>
<term>Glucose Intolerance</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Nutritional Status</term>
<term>Obesity (complications)</term>
<term>Overweight (complications)</term>
<term>Registries</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Diabète (étiologie)</term>
<term>Enfant</term>
<term>Enregistrements</term>
<term>Femelle</term>
<term>Humains</term>
<term>Insuffisance pancréatique exocrine ()</term>
<term>Intolérance au glucose</term>
<term>Mucoviscidose ()</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Obésité ()</term>
<term>Surpoids ()</term>
<term>État nutritionnel</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Cystic Fibrosis</term>
<term>Exocrine Pancreatic Insufficiency</term>
<term>Obesity</term>
<term>Overweight</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Diabetes Mellitus</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Diabète</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Child</term>
<term>Female</term>
<term>Glucose Intolerance</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Nutritional Status</term>
<term>Registries</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Enfant</term>
<term>Enregistrements</term>
<term>Femelle</term>
<term>Humains</term>
<term>Insuffisance pancréatique exocrine</term>
<term>Intolérance au glucose</term>
<term>Mucoviscidose</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Obésité</term>
<term>Surpoids</term>
<term>État nutritionnel</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Cystic fibrosis (CF) has long been associated with malnutrition. However, due to early diagnosis, nutritional supplements, and increased prevalence of obesity in the general population, overweight, and obesity in the CF patient population is becoming a concern. The aim of this study was to determine the prevalence of obesity and overweight in patients with CF seen at our center, to analyze factors associated with nutritional status, to evaluate the relation between nutritional status and lung function, and to document any adverse health outcomes.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24757043</PMID>
<DateCreated><Year>2014</Year>
<Month>12</Month>
<Day>24</Day>
</DateCreated>
<DateCompleted><Year>2016</Year>
<Month>03</Month>
<Day>31</Day>
</DateCompleted>
<DateRevised><Year>2014</Year>
<Month>12</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1099-0496</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>50</Volume>
<Issue>1</Issue>
<PubDate><Year>2015</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Pediatric pulmonology</Title>
<ISOAbbreviation>Pediatr. Pulmonol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Overweight and obesity in patients with cystic fibrosis: a center-based analysis.</ArticleTitle>
<Pagination><MedlinePgn>35-41</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/ppul.23033</ELocationID>
<Abstract><AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">Cystic fibrosis (CF) has long been associated with malnutrition. However, due to early diagnosis, nutritional supplements, and increased prevalence of obesity in the general population, overweight, and obesity in the CF patient population is becoming a concern. The aim of this study was to determine the prevalence of obesity and overweight in patients with CF seen at our center, to analyze factors associated with nutritional status, to evaluate the relation between nutritional status and lung function, and to document any adverse health outcomes.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The CF Patient Registry was queried for patients aged 2-18 who were seen at our center between June 2011 and June 2012. Nutritional statuses of patients were classified in accordance with the CF Foundation guidelines. Analysis of variance was utilized to analyze the differences in lung function between the five weight status groups.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Of the 226 patients with CF aged 2-18 years, 129 (57%) had a BMI percentile consistent with a healthy weight status, 16 (7%) were in nutritional failure, 28 (12%) were at risk of nutritional failure, 35 (15%) were overweight, and 18 (8%) were obese. Based on fecal elastase levels, 50% of the overweight patients and 20% of the obese patients were pancreatic insufficient. FEV1 % predicted was lowest in patients with nutritional failure (P = 0.005). No significant differences were noted between the other four weight groups. In our obese and overweight population, three patients have impaired glucose tolerance, one has CF-related diabetes (CFRD) with fasting hyperglycemia, three have hypertension, and one has obstructive sleep apnea (OSA).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The prevalence of overweight and obesity in our CF center is noteworthy, and a significant number of the patients were pancreatic insufficient. In our patient population, overweight, and obesity were not associated with further improvement of lung function. Nutritional approaches need to address the adverse outcomes of overweight and obesity.</AbstractText>
<CopyrightInformation>© 2014 Wiley Periodicals, Inc.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hanna</LastName>
<ForeName>Reem M</ForeName>
<Initials>RM</Initials>
<AffiliationInfo><Affiliation>Division of Pulmonary Medicine, Allergy, and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Weiner</LastName>
<ForeName>Daniel J</ForeName>
<Initials>DJ</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2014</Year>
<Month>04</Month>
<Day>23</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Pediatr Pulmonol</MedlineTA>
<NlmUniqueID>8510590</NlmUniqueID>
<ISSNLinking>1099-0496</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003550" MajorTopicYN="N">Cystic Fibrosis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003920" MajorTopicYN="N">Diabetes Mellitus</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010188" MajorTopicYN="N">Exocrine Pancreatic Insufficiency</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018149" MajorTopicYN="N">Glucose Intolerance</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007223" MajorTopicYN="N">Infant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009752" MajorTopicYN="N">Nutritional Status</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009765" MajorTopicYN="N">Obesity</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D050177" MajorTopicYN="N">Overweight</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012042" MajorTopicYN="N">Registries</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">cystic fibrosis</Keyword>
<Keyword MajorTopicYN="N">lung function</Keyword>
<Keyword MajorTopicYN="N">nutritional status</Keyword>
<Keyword MajorTopicYN="N">pancreatic insufficiency</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2013</Year>
<Month>03</Month>
<Day>27</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2014</Year>
<Month>02</Month>
<Day>06</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2014</Year>
<Month>4</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2014</Year>
<Month>4</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2016</Year>
<Month>4</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">24757043</ArticleId>
<ArticleId IdType="doi">10.1002/ppul.23033</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Amérique/explor/PittsburghV1/Data/PubMed/Curation

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000A94 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Curation/biblio.hfd -nk 000A94 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Amérique
   |area=    PittsburghV1
   |flux=    PubMed
   |étape=   Curation
   |type=    RBID
   |clé=     pubmed:24757043
   |texte=   Overweight and obesity in patients with cystic fibrosis: a center-based analysis.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Curation/RBID.i   -Sk "pubmed:24757043" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Curation/biblio.hfd   \
       | NlmPubMed2Wicri -a PittsburghV1

This area was generated with Dilib version V0.6.38.
Data generation: Fri Jun 18 17:37:45 2021. Site generation: Fri Jun 18 18:15:47 2021

	Serveur d'exploration sur Pittsburgh
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Serveur d'exploration sur Pittsburgh

Overweight and obesity in patients with cystic fibrosis: a center-based analysis.

Overweight and obesity in patients with cystic fibrosis: a center-based analysis.

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki