Congenital hypothyroidism: Long-term outcome

被引:95
作者
Rovet, JF
机构
[1] Hosp Sick Children, Brain & Behav Program, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Toronto, ON, Canada
关键词
D O I
10.1089/thy.1999.9.741
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although mental retardation associated with congenital hypothyroidism (CH) is prevented by newborn screening and early treatment, affected children still undergo a brief period of thyroid hormone deficiency reflecting etiology of thyroid disease, illness severity, and treatment factors. Because thyroid hormone is essential for normal brain development and because some processes require thyroid hormone in the period when thyroid hormone was lacking, children with CH treated early may still have subtle neurocognitive deficits. As the period when thyroid hormone is needed differs for different brain regions, there may be different types of deficits depending on when thyroid hormone levels were insufficient. Since 1980, we have been following a large cohort of Toronto-based children with congenital hypothyroidism identified by newborn screening from infancy to adolescence. Early findings revealed a 5-10-point decline in IQ, poorer visuomotor and visuospatial abilities, delayed speech and language development, selective neuromotor deficiencies, and poorer attention and memory skills, which were correlated with different disease and treatment factors. Now a comparison between 48 subjects at adolescence and matched controls indicates that deficits persist in visuospatial, memory, and attention domains and these are correlated with severity of early hypothyroidism. Negative relationships between attention indices and thyroxine (T-4) elevations at time of testing also suggest a role for thyroid hormone in the regulation of attention.
引用
收藏
页码:741 / 748
页数:8
相关论文
共 76 条
[1]  
[Anonymous], 1983, GROWTH EPIDEMIOL NEU, DOI [10.1016/b978-0-7236-7017-9.50018-1, DOI 10.1016/B978-0-7236-7017-9.50018-1]
[2]  
[Anonymous], 1972, PATHOLOGY MENTAL RET
[3]   UNUSUAL SCARCITY OF RESTRICTION SITE POLYMORPHISM IN THE HUMAN THYROGLOBULIN GENE - A LINKAGE STUDY SUGGESTING AUTOSOMAL DOMINANCE OF A DEFECTIVE THYROGLOBULIN ALLELE [J].
BAAS, F ;
BIKKER, H ;
VANOMMEN, GJB ;
DEVIJLDER, JJM .
HUMAN GENETICS, 1984, 67 (03) :301-305
[4]  
Bayley N., 1969, BAYLEY SCALES INFANT
[6]  
BINDER LI, 1985, J CELL BIOL, V101, P1371, DOI 10.1083/jcb.101.4.1371
[7]  
BODE HH, 1978, PEDIATRICS, V62, P13
[8]   DIFFERENTIAL EXPRESSION OF ALPHA-THYROID AND BETA-THYROID HORMONE RECEPTOR GENES IN RAT-BRAIN AND PITUITARY [J].
BRADLEY, DJ ;
YOUNG, WS ;
WEINBERGER, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :7250-7254
[9]   ALPHA-THYROID AND BETA-THYROID HORMONE-RECEPTOR (TR) GENE-EXPRESSION DURING AUDITORY NEUROGENESIS - EVIDENCE FOR TR ISOFORM-SPECIFIC TRANSCRIPTIONAL REGULATION IN-VIVO [J].
BRADLEY, DJ ;
TOWLE, HC ;
YOUNG, WS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :439-443
[10]  
BRADLEY DJ, 1992, J NEUROSCI, V12, P2288