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Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy.
Gillingham, Melanie B; Choi, Dongseok; Gregor, Ashley; Wongchaisuwat, Nida; Black, Danielle; Scanga, Hannah L; Nischal, Ken K; Sahel, Jose-Alain; Arnold, Georgianne; Vockley, Jerry; Harding, Cary O; Pennesi, Mark E.
Afiliação
  • Gillingham MB; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, USA.
  • Choi D; OHSU-PSU School of Public Health, Biostatistics, Oregon Health & Science University, Portland, Oregon, USA.
  • Gregor A; Casey Eye Institute, Oregon Health & Science University, Portland, Oregon, USA.
  • Wongchaisuwat N; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, USA.
  • Black D; Casey Eye Institute, Oregon Health & Science University, Portland, Oregon, USA.
  • Scanga HL; Division of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Nischal KK; Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Sahel JA; Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Arnold G; Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Vockley J; Division of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Harding CO; Division of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Pennesi ME; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, USA.
J Inherit Metab Dis ; 47(4): 746-756, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38623632
ABSTRACT
Long chain 3-hydroxyacyl-CoA dehydrogenase (LCHADD) is the only fatty acid oxidation disorder to develop a progressive chorioretinopathy resulting in vision loss; newborn screening (NBS) for this disorder began in the United States around 2004. We compared visual outcomes among 40 participants with LCHADD or trifunctional protein deficiency diagnosed symptomatically to those who were diagnosed via NBS or a family history. Participants completed ophthalmologic testing including measures of visual acuity, electroretinograms (ERG), fundal imaging, contrast sensitivity, and visual fields. Records were reviewed to document medical and treatment history. Twelve participants presented symptomatically with hypoglycemia, failure to thrive, liver dysfunction, cardiac arrest, or rhabdomyolysis. Twenty eight were diagnosed by NBS or due to a family history of LCHADD. Participants diagnosed symptomatically were older but had similar percent males and genotypes as those diagnosed by NBS. Treatment consisted of fasting avoidance, dietary long-chain fat restriction, MCT, C7, and/or carnitine supplementation. Visual acuity, rod- and cone-driven amplitudes on ERG, contrast sensitivity scores, and visual fields were all significantly worse among participants diagnosed symptomatically compared to NBS. In mixed-effects models, both age and presentation (symptomatic vs. NBS) were significant independent factors associated with visual outcomes. This suggests that visual outcomes were improved by NBS, but there was still lower visual function with advancing age in both groups. Early diagnosis and treatment by NBS is associated with improved visual outcomes and retinal function compared to participants who presented symptomatically. Despite the impact of early intervention, chorioretinopathy was greater with advancing age, highlighting the need for novel treatments.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Acuidade Visual / Triagem Neonatal / Diagnóstico Precoce / Proteína Mitocondrial Trifuncional / Erros Inatos do Metabolismo Lipídico Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Acuidade Visual / Triagem Neonatal / Diagnóstico Precoce / Proteína Mitocondrial Trifuncional / Erros Inatos do Metabolismo Lipídico Idioma: En Revista: J Inherit Metab Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos