Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients
Author(s) -
Marit ME van Bakel,
Gert Printzen,
Bendicht Wermuth,
Ulrich Wiesmann
Publication year - 2000
Publication title -
american journal of clinical nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.608
H-Index - 336
eISSN - 1938-3207
pISSN - 0002-9165
DOI - 10.1093/ajcn/72.4.976
Subject(s) - glutathione peroxidase , medicine , endocrinology , selenium , antioxidant , selenium deficiency , hormone , triiodothyronine , chemistry , thyroid , uric acid , superoxide dismutase , biochemistry , organic chemistry
Subjects consuming protein-restricted diets, such as patients with phenylketonuria (PKU) or milder hyperphenylalaninemias (HPAs) are at risk of selenium deficiency. Selenium is a cofactor of the antioxidant enzyme glutathione peroxidase and of the thyroid hormone converting enzyme thyroxine deiodinase.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom