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Autosomal Dominant Resistance to Thyrotropin as a Distinct Entity in Five Multigenerational Kindreds: Clinical Characterization and Exclusion of Candidate Loci

Departments of Medicine (H.G., N.H.S., R.E.W., S.R.) and Pediatrics (S.R.) and Committee on Genetics (S.R.), The University of Chicago, Chicago, Illinois 60637; Schneider Children’s Medical Center (A.M.-B., M.M.), Sackler School of Medicine, Petah-Tiqva 49202 Israel; Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (C.R., M.A., J.v.S., G.V.) and Department of Genetics (G.V.), Campus Erasme, Universite Libre de Bruxelles, 1070 Brussels, Belgium; Clinic Marc Linquette (M.-C.V.), Lille University Hospital, 59000 Lille, France; Sainte-Justine Hospital (G.v.V.), University of Montreal, Montreal, Quebec, Canada H3T 1C5; Endocrinology and Diabetes Unit (D.L.M.), British Columbia’s Children’s Hospital, Vancouver, British Columbia, Canada V6H 3V4; Department of Pediatrics (H.A.), University of Alabama at Birmingham, Birmingham, Alabama 35203; and Universita degli Studi di Napoli (P.E.M.), Federico II, 80131 Naples, Italy

Address all correspondence and requests for reprints to: Samuel Refetoff, The University of Chicago, MC3090, 5841 South Maryland Avenue, Chicago, Illinois 60637. E-mail: refetoff{at}uchicago.edu.

Context: Resistance to TSH (RTSH) is an inherited disorder of variable hyposensitivity to TSH. The metabolic consequences can range from euthyroid hyperthyrotropinemia to severe congenital hypothyroidism with thyroid hypoplasia. Although subclinical and mild hypothyroidism fitting the RTSH phenotype is common in the population, the role of genetic factors is far from being understood. Only in rare cases has RTSH been attributed to TSHR or PAX8 gene mutations.

Objective, Setting, and Participants: Toward the identification of novel RTSH genes, we studied five large, unrelated families comprising 102 individuals, 56 of whom were affected.

Results: Inheritance of RTSH in these families followed an autosomal dominant pattern without evidence for incomplete penetrance, yet expressivity was variable. Considering only fully phenotyped generations, 64% of the progeny was affected, with a 1:1.4 male-to-female ratio. Of 18 affected individuals tested in the neonatal period, two were undetected because of borderline results. The thyroid phenotype was indistinguishable from that observed with PAX8 and TSHR defects. In four families, untreated affected subjects of all ages had elevated serum thyroglobulin levels, consistent with a defect in the thyroid follicle cells. Linkage of RTSH to TSHR and PAX8 was excluded in all five families. For the largest families, we likewise excluded a contribution of genes previously only associated with syndromic forms of RTSH, namely TITF1, GNAS, and FOXE1.

Conclusions: These kindreds represent a distinct etiological entity of autosomal dominant RTSH. According to the clinical presentation of these families, genetic causes of mild hyperthyrotropinemia in the general population may be more common than currently appreciated.

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				H. Grasberger, J. Van Sande, A. Hag-Dahood Mahameed, Y. Tenenbaum-Rakover, and S. Refetoff A Familial Thyrotropin (TSH) Receptor Mutation Provides in Vivo Evidence that the Inositol Phosphates/Ca2+ Cascade Mediates TSH Action on Thyroid Hormone Synthesis J. Clin. Endocrinol. Metab., July 1, 2007; 92(7): 2816 - 2820. [Abstract] [Full Text] [PDF]