Treating
antenatal patients with levothyroxine who have hypothyroidism or hypothyroxinemia
between 8 to 20 weeks of pregnancy did not result in better cognitive outcome
and IQ in children through 5 years of age as compared to women who received
placebo.
The study
was published online on March 2, 2017 in the New England Journal of Medicine.
Earlier
studies have shown that the fetus requires thyroxine for normal neurocognitive
development specially in first half of pregnancy. Subclinical hypothyroidism is
associated with numerous adverse pregnancy outcomes like miscarriage, preterm
delivery, low birth weight, and lower-than-normal IQ in offspring.
The debate
to treat subclinical hypothyroidism in pregnancy continues as different
societies recommend different guidelines for routine screening of all pregnant
women for hypothyroidism.
ACOG advises
against routine screening of all pregnant women for hypothyroidism at this stage
because of lack of clear cut benefits in absence of robust clinical trials
evidence.
While American
Thyroid Association (ATA), advises for treating subclinical hypothyroidism in
pregnancy despite lack of clear cut benefits. In fact, ATA recently released
new guidelines on thyroid disease in pregnancy. The article can be accessed here.
The current
multicenter study by Casey et al. screened all study participants for subclinical
hypothyroidism (TSH = 4mIU per liter or more and normal free thyroxine (T4)
level (0.86 to 1.90 ng per deciliter) and hypothyroxinemia (normal thyrotropin
level (0.08 to 3.99 mU per liter) and a low free T4 level (<0.86 ng per
deciliter)
Women in
either groups were randomized to receive thyroxine or placebo. Thyroid function
was done monthly and the children were followed up for 5 years for cognitive
development and IQ tested at 5 years.
There was no
significant difference between IQ levels of children in subclinical
hypothyroidism (97) and placebo (94) and hypothyroxinemia (94) and placebo
(91) at 5 years of age.
No
significant differences in maternal pregnancy outcome and neonatal morbidity
were observed between the groups.
David
Cooper, MD, Johns Hopkins University School of Medicine, Baltimore, Maryland,
and Elizabeth Pearce, MD, Boston University School of Medicine, Massachusetts
wrote an editorial accompanying the article in which they compared the study findings
with several other earlier trials which also failed to show much maternal and neonatal
benefits.
They
concluded that starting the treatment for subclinical hypothyroidism and hypothyroxinemia
is not much beneficial if done well into second trimester, but it is
inexpensive and will do no harm. It could be beneficial if the screening and
initiation of treatment is done well in first trimester.
Does concomitant Metformin therapy alters serum TSH level anyway? Should we routinely insist on TPO Ab screening in Indian context those who can afford particularly to supplement L-TX in preg and or to avert Postpartum thyroid its? Your opinion please?
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