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Occurrence of selected antiphospholipid antibodies in offspring born from mothers with autoimmunity
A. Mocková, Z. Ulčová-Gallová, J. Náhlovský, V. Lukášová, J. Dort, K. Bibková, Z. Micanová
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 1998-01-01 do 2015-12-31
SAGE Publications Journals
od 1999-01-01 do 2015-12-31
Medline Complete (EBSCOhost)
od 1998-01-01
Health & Medicine (ProQuest)
od 1998-01-01 do 2015-12-31
Family Health Database (ProQuest)
od 1998-01-01 do 2015-12-31
SAGE Journals
od 2012-01-01 do 2012-05-31
PubMed
22635236
DOI
10.1177/0961203312437808
Knihovny.cz E-zdroje
- MeSH
- antifosfolipidové protilátky krev MeSH
- autoimunitní nemoci krev imunologie MeSH
- dospělí MeSH
- kojenec MeSH
- komplikace těhotenství krev imunologie MeSH
- lidé MeSH
- mladý dospělý MeSH
- novorozenec krev imunologie MeSH
- prospektivní studie MeSH
- studie případů a kontrol MeSH
- těhotenství MeSH
- vývoj dítěte MeSH
- zdravotní stav MeSH
- Check Tag
- dospělí MeSH
- kojenec MeSH
- lidé MeSH
- mladý dospělý MeSH
- novorozenec krev imunologie MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Autoimmune diseases can be accompanied by presence of various antiphospholipid antibodies (aPL). The laboratory criteria of antiphospholipid syndrome are based on detection of anticardiolipin, lupus anticoagulant or to antiβ2- glycoprotein I but currently a significance of other multiple aPL is being discussed. Because of their vascular and neuroinflammatory effect aPL, if being transplacentally transferred, might inflict damage in developing organism. The aim of our study was to determine the occurrence of eight selected aPL in offspring of mothers with proven autoimmune disease with aPL positivity. The possible influence of aPL presence on clinical, ultrasound and laboratory outcome of children was observed as well. The prospective study included 38 women: 17 women with primary antiphospholipid syndrome and 21 women with other diagnosed autoimmune disease with detected aPL. Also included were 39 children born to the above mentioned mothers between January 2009 and April 2010 in Perinatology Centre in Pilsen, Czech Republic. The control group consisted of 30 mothers without AD and their 30 healthy singletons. Preliminary results of the study showed the presence of aPL in 42.1% neonates of aPL positive mothers with autoimmune disease, six month later aPL were present in only 37.5 % of these children. Observed occurrence of aPL positivity at 6 months of age in originally negative offspring could be attributed to vaccination or food exposure. Psychomotor development of children has proceeded without major deviations. The follow-up study continues and will evaluate both groups of children at two years of age.
Department of Gynaecology and Obstetrics Charles University Hospital Pilsen Czech Republic
Department of Neonatology Charles University Hospital Pilsen Czech Republic
Citace poskytuje Crossref.org
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- $a Autoimmune diseases can be accompanied by presence of various antiphospholipid antibodies (aPL). The laboratory criteria of antiphospholipid syndrome are based on detection of anticardiolipin, lupus anticoagulant or to antiβ2- glycoprotein I but currently a significance of other multiple aPL is being discussed. Because of their vascular and neuroinflammatory effect aPL, if being transplacentally transferred, might inflict damage in developing organism. The aim of our study was to determine the occurrence of eight selected aPL in offspring of mothers with proven autoimmune disease with aPL positivity. The possible influence of aPL presence on clinical, ultrasound and laboratory outcome of children was observed as well. The prospective study included 38 women: 17 women with primary antiphospholipid syndrome and 21 women with other diagnosed autoimmune disease with detected aPL. Also included were 39 children born to the above mentioned mothers between January 2009 and April 2010 in Perinatology Centre in Pilsen, Czech Republic. The control group consisted of 30 mothers without AD and their 30 healthy singletons. Preliminary results of the study showed the presence of aPL in 42.1% neonates of aPL positive mothers with autoimmune disease, six month later aPL were present in only 37.5 % of these children. Observed occurrence of aPL positivity at 6 months of age in originally negative offspring could be attributed to vaccination or food exposure. Psychomotor development of children has proceeded without major deviations. The follow-up study continues and will evaluate both groups of children at two years of age.
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