Human Reproduction Update, Vol.9, No.2 pp.149-161, 2003
© European Society of Human Reproduction and Embryology 2003; all rights reserved
Thyroid autoimmunity and hypothyroidism before and during pregnancy
1 Academisch Ziekenhuis, Department of Endocrinology, Laarbeeklaan, Brussels and 2 University Hospital Saint-Pierre, Department of Internal Medicine; Thyroid Investigation Clinic, Brussels, Belgium
To whom correspondence should be addressed at: Daniel Glinoer, University Hospital Saint-Pierre, Department of Internal Medicine; Thyroid Investigation Clinic, Rue Haute, 322, B-1000 Brussels, Belgium. e-mail: dglinoer{at}ulb.ac.be
Abstract
In the present review, an attempt was made to describe current knowledge and concepts concerning the complex relationships that link thyroid autoimmunity (TAI) and hypothyroidism with female and male infertility, as well as abnormalities occurring during pregnancy, such as pregnancy loss and maternal and fetal repercussions associated with hypothyroidism. In the case of infertility, although the clinical relevance of TAI is somewhat controversial, when all available information is considered the results strongly suggest that when infertility is due to well-defined female causes, autoimmunity is involved and TAI constitutes a useful marker of the underlying immune abnormality, independently of thyroid function disorders. In the case of pregnancy loss, the vast majority of available studies clearly establish that TAI (even with no overt thyroid dysfunction) is associated with a significant increase in miscarriage risk. To find an association, however, does not imply a causal relationship, and the aetiology of increased pregnancy loss associated with TAI remains presently not completely understood. With regard to maternal repercussions during gestation, the main risk associated with TAI is the occurrence of hypothyroidism and obstetric complications (premature birth, pre-eclampsia, etc.). Thus, systematic screening of TAI and hypothyroidism during early pregnancy, monitoring of thyroid function with/without L-thyroxine treatment and follow-up during post-partum have proved helpful and important in order to manage these patients adequately. Finally, with regard to potential repercussions affecting the offspring, recent evidence suggests that thyroid maternal underfunction, even when considered mild (or subclinical), may be associated with an impairment of fetal brain development. When present only during the first half of gestation, maternal hypothyroxinaemia is a risk factor for impaired fetal brain development, due to insufficient transfer of maternal thyroid hormones to the feto-placental unit. When hypothyroidism is not restricted to the first trimester and worsens as gestation progresses (as in untreated hypothyroidism), the fetus may also be deprived of adequate amounts of thyroid hormones during later neurological maturation and development, leading to poorer school performance and lower IQ.
Key words: hypothyroidism / infertility / pregnancy and pregnancy loss (miscarriage) / systematic screening / thyroid autoimmunity or autoimmune thyroid disorders
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