Early maternal hypothyroxinemia alters histogenesis and cerebral cortex cytoarchitecture of the progeny

Lavado-Autric, R; Auso, E; Garcia-Velasco, JV; del Carmen Arufe, M; Escobar del Rey, F; Berbel, P; Morreale de Escobar, G

HERO ID

51030

Reference Type

Journal Article

Year

2003

Language

English

PMID

12671057

HERO ID 51030
In Press No
Year 2003
Title Early maternal hypothyroxinemia alters histogenesis and cerebral cortex cytoarchitecture of the progeny
Authors Lavado-Autric, R; Auso, E; Garcia-Velasco, JV; del Carmen Arufe, M; Escobar del Rey, F; Berbel, P; Morreale de Escobar, G
Journal Journal of Clinical Investigation
Volume 111
Issue 7
Page Numbers 1073-1082
Abstract Epidemiological studies from both iodine-sufficient and -deficient human populations strongly suggest that early maternal hypothyroxinemia (i.e., low circulating free thyroxine before onset of fetal thyroid function at midgestation) increases the risk of neurodevelopmental deficits of the fetus, whether or not the mother is clinically hypothyroid. Rat dams on a low iodine intake are hypothyroxinemic without being clinically hypothyroid because, as occurs in pregnant women, their circulating 3,5,3'-triiodothyronine level is usually normal. We studied cell migration and cytoarchitecture in the somatosensory cortex and hippocampus of the 40-day-old progeny of the iodine-deficient dams and found a significant proportion of cells at locations that were aberrant or inappropriate with respect to their birth date. Most of these cells were neurons, as assessed by single- and double-label immunostaining. The cytoarchitecture of the somatosensory cortex and hippocampus was also affected, layering was blurred, and, in the cortex, normal barrels were not formed. We believe that this is the first direct evidence of an alteration in fetal brain histogenesis and cytoarchitecture that could only be related to early maternal hypothyroxinemia. This condition may be 150-200 times more common than congenital hypothyroidism and ought to be prevented both by mass screening of free thyroxine in early pregnancy and by early iodine supplementation to avoid iodine deficiency, however mild.
Doi 10.1172/JCI16262
Pmid 12671057
Wosid WOS:000181970600019
Is Certified Translation No
Dupe Override No
Comments J. Clin. Invest. 111: 1073-1082.
Is Public Yes
Language Text English