Optimal management of hypothyroidism, hypothyroxinaemia and euthyroid TPO antibody positivity preconception and in pregnancy

被引:95
作者
Chan, Shiao [1 ,2 ]
Boelaert, Kristien [2 ]
机构
[1] Univ Birmingham, Coll Med & Dent Sci, Sch Clin & Expt Med, Ctr Womens & Childrens Hlth, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Coll Med & Dent Sci, Sch Clin & Expt Med, Ctr Endocrinol Diabet & Metab, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会;
关键词
MATERNAL THYROID-FUNCTION; FREE-THYROXINE CONCENTRATIONS; 5-YEAR FOLLOW-UP; SUBCLINICAL HYPOTHYROIDISM; 1ST TRIMESTER; CHILDREN BORN; RISK-FACTOR; TSH LEVELS; LEVOTHYROXINE REQUIREMENTS; NEUROCOGNITIVE DEVELOPMENT;
D O I
10.1111/cen.12605
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Normal physiological changes of pregnancy warrant the need to employ gestation specific reference ranges for the interpretation of thyroid function tests. Thyroid hormones play crucial roles in foetal growth and neurodevelopment which are dependent on adequate supply of maternal thyroid hormones from early gestation onwards. The prevention of significant adverse obstetric and neurodevelopmental outcomes from hypothyroidism requires a strategy of empirical levothyroxine dose increases and predictive dose adjustments in pregnancy combined with regular thyroid function testing, starting before pregnancy and until the postpartum period. Subclinical hypothyroidism has been associated with an increased risk of pregnancy loss and neurocognitive deficits in children, especially when diagnosed before or during early pregnancy. Whilst trials of levothyroxine replacement for mild hypothyroidism in pregnancy have not indicated definite evidence of improvements in these outcomes, professional guidelines recommend treatment, especially if evidence of underlying thyroid autoimmunity is present. Studies of isolated hypothyroxinaemia in pregnancy have shown conflicting evidence with regards to adverse obstetric and neurodevelopmental outcomes and no causative relationships have been determined. Treatment of this condition in pregnancy may be considered in those with underlying thyroid autoimmunity. Whilst the evidence for a link between the presence of anti-TPO antibodies and increased risks of pregnancy loss and infertility is compelling, the results of ongoing randomized trials of levothyroxine in euthyroid women with underlying autoimmunity are currently awaited. Further studies to define the selection of women who require levothyroxine replacement and to determine the benefits of a predictive dose adjustment strategy are required.
引用
收藏
页码:313 / 326
页数:14
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