Abstract

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 9-12th 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.

Highlights

  • Functional deficiency of mannan-binding lectin (MBL) has been associated with adverse pregnancy outcome

  • As we have previously shown, serum MBL levels are linked to thyroid hormones in patients with autoimmune thyroid diseases (AITD) [18] and they correlate with thyroid function in patients with sepsis [19]

  • We present an analysis of the relationship between serum MBL levels/MBL2 genotypes and a number of clinical characteristics in a well-described cohort of pregnant women screened positive for thyroid disorders in the first trimester of pregnancy

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Summary

Introduction

Functional deficiency of mannan-binding lectin (MBL) has been associated with adverse pregnancy outcome. Mannan-binding lectin (MBL) is a central component of the lectin pathway of complement, which contributes to the defense against microbial organisms. In the Czech population, 36.2% of individuals have variant MBL2 genotypes associated with decreased blood levels of MBL [1]. In childhood, decreased MBL levels may lead to recurrent respiratory tract infections [3]. MBL deficiency seems to be clinically relevant only in immunocompromized or severely ill patients [2]. Functional MBL deficiency has been associated with the occurrence of a number of non-infectious disorders, especially autoimmune diseases such as systemic lupus erythematosus (SLE) or inflammatory bowel disease. Functional MBL deficiency seems to be protective in ischemiareperfusion injury [3]

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