• Medientyp: E-Artikel
  • Titel: Longitudinal Assessment of Intellectual Achievement in Patients With Classical Galactosemia
  • Beteiligte: Schadewaldt, Peter; Hoffmann, Björn; Hammen, Hans-Werner; Kamp, Gudrun; Schweitzer-Krantz, Susanne; Wendel, Udo
  • Erschienen: American Academy of Pediatrics (AAP), 2010
  • Erschienen in: Pediatrics, 125 (2010) 2, Seite e374-e381
  • Sprache: Englisch
  • DOI: 10.1542/peds.2008-3325
  • ISSN: 0031-4005; 1098-4275
  • Schlagwörter: Pediatrics, Perinatology and Child Health
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  • Beschreibung: OBJECTIVE:To conduct a longitudinal assessment of long-term cognitive outcome in patients with classical galactosemia.METHODS:Inclusion criteria were (1) previous assessment of IQ dating back >10 years with tests being comparable with the recent German tests HAWIK-III and HAWIE-R, (2) absence of illnesses other than galactosemia, (3) absence of foreign language problems, (4) enzymatic-metabolic proof of classical galactosemia, (5) compliance with dietary therapy, and (6) written informed consent. Twenty-three patients who fulfilled these criteria were found. They underwent the first IQ test at a mean age of 11 ± 5 years and the second 13.6 to 15.5 years later at a mean age of 26 ± 5 years. Results were corrected for the obsolescence of test norms (Flynn effect).RESULTS:Mean total IQ scores on the first and second tests were 78 ± 14 and 73 ± 15, respectively, and not significantly different. IQ scores in the average range were observed for 7 patients on the first test and for 5 patients on the second test. For 17 patients, the intraindividual IQ scores remained essentially unchanged. Five patients showed a decrease and 1 an increase of the IQ score over time. No consistent pattern of change was found with respect to performance or verbal IQ subscores or in achievements in the individual subtest.CONCLUSIONS:The results confirm the presence of reduced cognitive ability in classical galactosemia and present evidence for an absence of substantial galactosemia-induced aggravation of this impairment with increasing age, at least in patients from 4 to 40 years of age. It remains to be clarified whether a reduction of cognitive function in galactosemia may be initiated by an in utero toxicity of endogenously formed galactose and which role such a process may play in the development of intellectual deficiencies that are later maintained throughout life.