Down Syndrome Clinical Trial
Official title:
Levothyroxine Treatment and Cardiometabolic Outcomes in Adolescents With Down Syndrome
The purpose of this research study is to learn about the effects of treating subclinical hypothyroidism (SCH) with thyroid hormone replacement in children and adolescents with Down syndrome (DS). We hypothesize that treatment of SCH with thyroid hormone replacement will improve cardiometabolic health and quality of life.
The American Academy of Pediatrics (AAP) recommends yearly screening of thyroid studies in
DS. Clinical experience suggests that thyroid stimulating hormone (TSH) concentrations in the
subclinical hypothyroid range (5-10 milli international units(mIU/L)) are not uncommon in DS,
but the benefits and risks of treating SCH in the DS population are not known. In adults, SCH
has been associated with increased cardiometabolic risk (CMR) and individuals with DS may be
at increased cardiometabolic risk as well.
Data in children with SCH are limited. Despite the recommendations to screen for thyroid
dysfunction, evidence to guide management of elevated TSH in children with DS is equally
sparse. In non-DS children, TSH>4.65 mIU/L was associated with lower HDL. One year of
levothyroxine treatment in short children with subclinical hypothyroidism and short stature
improved growth velocity. Left ventricular (LV) function and LV mass (by echocardiography)
was not different in 16 children with DS and subclinical hypothyroidism (TSH>6.5 mIU/L; mean
TSH = 7.8 mIU/L) vs. 25 children with DS and normal TSH. However, these findings may be
limited by the small sample size. An intervention study of 7 subjects age 2-42 years with DS
and hypothyroidism, defined as low T4 and normal or elevated TSH (0.2-18.9 mIU/L) on 8 weeks
of levothyroxine treatment did not improve developmental or functional outcomes.
Anthropometrics and CMR factors were not examined. In contrast, increased TSH in the absence
of overt congenital hypothyroidism is common in neonates with DS and prompted a randomized
controlled trial (RCT) in 181 neonates with DS. TSH-directed levothyroxine treatment was
associated with better growth, weight gain, and motor development after 24 months compared to
placebo. These findings highlight that the "asymptomatic" component of subclinical
hypothyroidism may have medically-relevant effects. This study will provide potentially
clinically relevant preliminary evidence for the treatment of subclinical hypothyroidism in
DS.
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