Association between low levels of Mannan-binding lectin and markers of autoimmune thyroid disease in pregnancy
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu klinické zkoušky, časopisecké články, práce podpořená grantem
PubMed
24339961
PubMed Central
PMC3858249
DOI
10.1371/journal.pone.0081755
PII: PONE-D-13-31096
Knihovny.cz E-zdroje
- MeSH
- autoantigeny krev MeSH
- autoimunitní tyreoiditida krev MeSH
- autoprotilátky krev MeSH
- biologické markery krev MeSH
- dospělí MeSH
- jodidperoxidasa krev MeSH
- komplikace těhotenství krev MeSH
- lektin vázající mannosu krev MeSH
- lidé MeSH
- následné studie MeSH
- proteiny vázající železo krev MeSH
- první trimestr těhotenství krev MeSH
- retrospektivní studie MeSH
- těhotenství MeSH
- thyreotropin krev MeSH
- výsledek těhotenství * MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- autoantigeny MeSH
- autoprotilátky MeSH
- biologické markery MeSH
- jodidperoxidasa MeSH
- lektin vázající mannosu MeSH
- MBL2 protein, human MeSH Prohlížeč
- proteiny vázající železo MeSH
- thyreotropin MeSH
- TPO protein, human MeSH Prohlížeč
Functional deficiency of mannan-binding lectin (MBL) has been associated with adverse pregnancy outcome. Adverse events during pregnancy have also been described in women with autoimmune thyroid diseases (AITD), and thyroid hormones have been shown to influence serum levels of MBL. Therefore, the aim of this study was to analyse the impact of MBL-deficiency on the outcome of pregnancy in relation to the presence of AITD. Almost one year after delivery, we assessed serum MBL levels and MBL2-genotypes in 212 women positively screened for AITD in pregnancy. In 103 of these women, we could also measure MBL levels in frozen serum samples from the 9-12(th) gestational week, obtaining 96 pairs of MBL values (pregnancy vs. follow-up). As controls, 80 sera of pregnant women screened negatively for AITD were used. MBL2-genotyping was performed using multiplex PCR. Women with thyroid dysfunction and/or thyroid peroxidase antibodies (TPOAb) had lower MBL levels during pregnancy than controls, (3275 vs. 5000 ng/ml, p<0.05). The lowest levels were found in women with elevated thyroid-stimulating hormone (TSH) levels in the absence of TPOAb (2207 ng/ml; p<0.01 as compared to controls). MBL2 genotype distribution did not differ between subgroups. At a median follow-up period of 17 months (range: 3-78 months) after delivery, median MBL level had decreased further to 1923 ng/ml (p<0.0001) without significant changes in TSH. In an explorative survey, functional MBL-deficiency was neither linked to a history of spontaneous abortion, nor other obstetric complications, severe infections throughout life/pregnancy or antibiotics use in pregnancy. In conclusion, hypothyroidism during pregnancy is associated with decreased MBL levels, and the levels decreased further after delivery.
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