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Health and well-being of maturing adults with classic galactosemia.
Garrett, Olivia S; Druss, Jared J; Vos, E Naomi; Fu, Yu-Ting Debbie; Lucia, Stephanie; Greenstein, Patricia E; Bauer, Anna; Sykut-Cegielska, Jolanta; Stepien, Karolina M; Arbuckle, Cameron; Grafakou, Olga; Meyer, Uta; Vanhoutvin, Nele; Pané, Adriana; Bosch, Annet M; Rubio-Gozalbo, Estela; Berry, Gerard T; Fridovich-Keil, Judith L.
Afiliação
  • Garrett OS; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Druss JJ; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Vos EN; MosaKids Children's Hospital, Department of Pediatrics, Maastricht University Medical Center, Maastricht, Netherlands.
  • Fu YD; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Lucia S; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Greenstein PE; Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, USA.
  • Bauer A; Department of Inborn Errors of Metabolism and Pediatrics, Institute of Mother and Child, Warsaw, Poland.
  • Sykut-Cegielska J; Department of Inborn Errors of Metabolism and Pediatrics, Institute of Mother and Child, Warsaw, Poland.
  • Stepien KM; Adult Inherited Metabolic Disorders Department, Salford Royal Organization, Northern Care Alliance NHS Foundation Trust, Salford, UK.
  • Arbuckle C; Charles Dent Metabolic Unit, University College London Hospitals NHS Foundation Trust, London, UK.
  • Grafakou O; Clinical Genetics and Metabolic Disorders Clinic, Department of Pediatrics, Archbishop Makarios III Hospital, State Health Services Organization, Nicosia, Cyprus.
  • Meyer U; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
  • Vanhoutvin N; Department of Gastroenterology-Hepatology and Metabolic Center, University Hospitals Leuven, 3000 Leuven, Belgium.
  • Pané A; Endocrinology and Nutrition Department, Hospital Clinic de Barcelona, CIBEROBN, Instituto de Salud Carlos III, Madrid, Spain.
  • Bosch AM; Department of Pediatrics, Division of Metabolic Diseases, Amsterdam Gastroenterology Endocrinology and Metabolism, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
  • Rubio-Gozalbo E; MosaKids Children's Hospital, Department of Pediatrics, Maastricht University Medical Center, Maastricht, Netherlands.
  • Berry GT; Laboratory of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands.
  • Fridovich-Keil JL; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
J Inherit Metab Dis ; 2024 Aug 14.
Article em En | MEDLINE | ID: mdl-39143820
ABSTRACT
Long-term outcomes in classic galactosemia (CG) have been studied previously, but all prior studies have relied on cohorts of patients that were small in number, or heavily skewed toward children and young adults, or both. Here, we extend what is known about the health and well-being of maturing adults with CG by analyzing the results of anonymous custom surveys completed by 92 affected individuals, ages 30-78, and 38 unaffected sibling controls, ages 30-79. The median age for patients was 38.5 years and for controls was 41 years. These study participants hailed from 12 different countries predominantly representing Europe and North America. Participants reported on their general life experiences and outcomes in seven different domains including speech/voice/language, cognition, motor function, cataracts, bone health, psychosocial well-being, and gastrointestinal health. We also queried women about ovarian function. Our results indicated a prevalence of long-term complications across all outcome domains that aligned with levels previously reported in younger cohorts. Given the sample size and age range of participants in this study, these findings strongly suggest that the adverse developmental outcomes commonly linked to CG are not progressive with age for most patients. We also tested four candidate modifiers for possible association with each of the outcomes followed, including days of neonatal milk exposure, rigor of dietary galactose restriction in early childhood, current age, and home continent. We observed no associations that reached even nominal significance, except for the following cataracts with neonatal milk exposure (p = 2.347e-04), cataracts with age (p = 0.018), and bone health with home continent (p = 0.03).
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos