The interaction between sickle cell disease and HIV infection: a systematic review.
Identifieur interne : 000708 ( Ncbi/Merge ); précédent : 000707; suivant : 000709The interaction between sickle cell disease and HIV infection: a systematic review.
Auteurs : Ewurama D A. Owusu [Pays-Bas] ; Benjamin J. Visser [Allemagne] ; Ingeborg M. Nagel [Pays-Bas] ; Petra F. Mens [Pays-Bas] ; Martin P. Grobusch [Allemagne]Source :
- Clinical infectious diseases : an official publication of the Infectious Diseases Society of America [ 1537-6591 ] ; 2015.
Descripteurs français
- KwdFr :
- Accident vasculaire cérébral (étiologie), Afrique (épidémiologie), Drépanocytose (), Drépanocytose (épidémiologie), Facteurs de risque, Humains, Hypertension pulmonaire, Infections à VIH (), Infections à VIH (traitement médicamenteux), Infections à VIH (épidémiologie), Ostéonécrose (étiologie), Prévalence, Sepsie (étiologie), Thérapie antirétrovirale hautement active, Études de cohortes, Évolution de la maladie.
- MESH :
- traitement médicamenteux : Infections à VIH.
- épidémiologie : Afrique, Drépanocytose, Infections à VIH.
- étiologie : Accident vasculaire cérébral, Ostéonécrose, Sepsie.
- Drépanocytose, Facteurs de risque, Humains, Hypertension pulmonaire, Infections à VIH, Prévalence, Thérapie antirétrovirale hautement active, Études de cohortes, Évolution de la maladie.
English descriptors
- KwdEn :
- Africa (epidemiology), Anemia, Sickle Cell (complications), Anemia, Sickle Cell (epidemiology), Antiretroviral Therapy, Highly Active, Cohort Studies, Disease Progression, HIV Infections (complications), HIV Infections (drug therapy), HIV Infections (epidemiology), Humans, Hypertension, Pulmonary, Osteonecrosis (etiology), Prevalence, Risk Factors, Sepsis (etiology), Stroke (etiology).
- MESH :
- geographic , epidemiology : Africa.
- complications : Anemia, Sickle Cell, HIV Infections.
- drug therapy : HIV Infections.
- epidemiology : Anemia, Sickle Cell, HIV Infections.
- etiology : Osteonecrosis, Sepsis, Stroke.
- Antiretroviral Therapy, Highly Active, Cohort Studies, Disease Progression, Humans, Hypertension, Pulmonary, Prevalence, Risk Factors.
Abstract
Human immunodeficiency virus (HIV) and sickle cell disease (SCD) are regarded as endemic in overlapping geographic areas; however, for most countries only scarce data on the interaction between HIV and SCD and disease burden exist. HIV prevalence in SCD patients varies between 0% and 11.5% in published studies. SCD has been suggested to reduce disease progression of HIV into AIDS. Various interactions of antiretroviral therapy with SCD exist. Both SCD and HIV act as common risk factors for stroke, avascular necrosis, severe splenic dysfunction, pulmonary arterial hypertension, and sepsis, which may result in synergistic increase in risk of developing these diseases. No treatment guidelines regarding SCD with HIV coinfection were identified. Available evidence is mainly based on small clinical studies, thus making strong recommendations difficult. An increased effort to elucidate the precise interactions is warranted to better understand both diseases and effect more adequate treatment approaches, especially in view of their geographical coprevalence.
DOI: 10.1093/cid/ciu832
PubMed: 25344542
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HIV prevalence in SCD patients varies between 0% and 11.5% in published studies. SCD has been suggested to reduce disease progression of HIV into AIDS. Various interactions of antiretroviral therapy with SCD exist. Both SCD and HIV act as common risk factors for stroke, avascular necrosis, severe splenic dysfunction, pulmonary arterial hypertension, and sepsis, which may result in synergistic increase in risk of developing these diseases. No treatment guidelines regarding SCD with HIV coinfection were identified. Available evidence is mainly based on small clinical studies, thus making strong recommendations difficult. An increased effort to elucidate the precise interactions is warranted to better understand both diseases and effect more adequate treatment approaches, especially in view of their geographical coprevalence.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25344542</PMID><DateCreated><Year>2015</Year><Month>01</Month><Day>24</Day></DateCreated><DateCompleted><Year>2015</Year><Month>09</Month><Day>03</Day></DateCompleted><DateRevised><Year>2015</Year><Month>01</Month><Day>24</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1537-6591</ISSN><JournalIssue CitedMedium="Internet"><Volume>60</Volume><Issue>4</Issue><PubDate><Year>2015</Year><Month>Feb</Month><Day>15</Day></PubDate></JournalIssue><Title>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</Title><ISOAbbreviation>Clin. Infect. Dis.</ISOAbbreviation></Journal><ArticleTitle>The interaction between sickle cell disease and HIV infection: a systematic review.</ArticleTitle><Pagination><MedlinePgn>612-26</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1093/cid/ciu832</ELocationID><Abstract><AbstractText>Human immunodeficiency virus (HIV) and sickle cell disease (SCD) are regarded as endemic in overlapping geographic areas; however, for most countries only scarce data on the interaction between HIV and SCD and disease burden exist. HIV prevalence in SCD patients varies between 0% and 11.5% in published studies. SCD has been suggested to reduce disease progression of HIV into AIDS. Various interactions of antiretroviral therapy with SCD exist. Both SCD and HIV act as common risk factors for stroke, avascular necrosis, severe splenic dysfunction, pulmonary arterial hypertension, and sepsis, which may result in synergistic increase in risk of developing these diseases. No treatment guidelines regarding SCD with HIV coinfection were identified. Available evidence is mainly based on small clinical studies, thus making strong recommendations difficult. An increased effort to elucidate the precise interactions is warranted to better understand both diseases and effect more adequate treatment approaches, especially in view of their geographical coprevalence.</AbstractText><CopyrightInformation>© The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Owusu</LastName><ForeName>Ewurama D A</ForeName><Initials>ED</Initials><AffiliationInfo><Affiliation>Department of Medical Laboratory Sciences, School of Allied Health Sciences, College of Health Sciences, University of Ghana, Accra Center of Tropical Medicine and Travel Medicine, Academic Medical Center, University of Amsterdam KIT Biomedical Research, Department of Parasitology, Amsterdam, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Visser</LastName><ForeName>Benjamin J</ForeName><Initials>BJ</Initials><AffiliationInfo><Affiliation>Center of Tropical Medicine and Travel Medicine, Academic Medical Center, University of Amsterdam Centre de Recherches Médicales de Lambaréné, Albert Schweitzer Hôpital, Lambaréné, Gabon Institute of Tropical Medicine, University of Tübingen, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Nagel</LastName><ForeName>Ingeborg M</ForeName><Initials>IM</Initials><AffiliationInfo><Affiliation>Medical Library, Academic Medical Center, University of Amsterdam, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mens</LastName><ForeName>Petra F</ForeName><Initials>PF</Initials><AffiliationInfo><Affiliation>Center of Tropical Medicine and Travel Medicine, Academic Medical Center, University of Amsterdam KIT Biomedical Research, Department of Parasitology, Amsterdam, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Grobusch</LastName><ForeName>Martin P</ForeName><Initials>MP</Initials><AffiliationInfo><Affiliation>Center of Tropical Medicine and Travel Medicine, Academic Medical Center, University of Amsterdam Centre de Recherches Médicales de Lambaréné, Albert Schweitzer Hôpital, Lambaréné, Gabon Institute of Tropical Medicine, University of Tübingen, Germany.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>10</Month><Day>23</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Clin Infect Dis</MedlineTA><NlmUniqueID>9203213</NlmUniqueID><ISSNLinking>1058-4838</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000349" MajorTopicYN="N" Type="Geographic">Africa</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000755" MajorTopicYN="N">Anemia, Sickle Cell</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D023241" MajorTopicYN="N">Antiretroviral Therapy, Highly Active</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015331" MajorTopicYN="N">Cohort Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018450" MajorTopicYN="N">Disease Progression</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015658" MajorTopicYN="N">HIV Infections</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006976" MajorTopicYN="N">Hypertension, Pulmonary</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010020" MajorTopicYN="N">Osteonecrosis</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015995" MajorTopicYN="N">Prevalence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012307" MajorTopicYN="N">Risk Factors</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018805" MajorTopicYN="N">Sepsis</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020521" MajorTopicYN="N">Stroke</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">HIV</Keyword><Keyword MajorTopicYN="N">disease interaction</Keyword><Keyword MajorTopicYN="N">sickle cell disease</Keyword><Keyword MajorTopicYN="N">sickle cell trait</Keyword><Keyword MajorTopicYN="N">systematic 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name="Hollande-Septentrionale"><name sortKey="Owusu, Ewurama D A" sort="Owusu, Ewurama D A" uniqKey="Owusu E" first="Ewurama D A" last="Owusu">Ewurama D A. Owusu</name></region><name sortKey="Mens, Petra F" sort="Mens, Petra F" uniqKey="Mens P" first="Petra F" last="Mens">Petra F. Mens</name><name sortKey="Nagel, Ingeborg M" sort="Nagel, Ingeborg M" uniqKey="Nagel I" first="Ingeborg M" last="Nagel">Ingeborg M. Nagel</name></country><country name="Allemagne"><noRegion><name sortKey="Visser, Benjamin J" sort="Visser, Benjamin J" uniqKey="Visser B" first="Benjamin J" last="Visser">Benjamin J. Visser</name></noRegion><name sortKey="Grobusch, Martin P" sort="Grobusch, Martin P" uniqKey="Grobusch M" first="Martin P" last="Grobusch">Martin P. Grobusch</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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