Back to Search
Start Over
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.
- Source :
-
Journal of inherited metabolic disease [J Inherit Metab Dis] 2024 Jul; Vol. 47 (4), pp. 746-756. Date of Electronic Publication: 2024 Apr 16. - Publication Year :
- 2024
-
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.<br /> (© 2024 SSIEM.)
- Subjects :
- Humans
Male
Female
Infant, Newborn
Child
Adult
Infant
Child, Preschool
Adolescent
Muscular Diseases diagnosis
Muscular Diseases genetics
Young Adult
Carnitine analogs & derivatives
Carnitine therapeutic use
Electroretinography
Mitochondrial Myopathies diagnosis
Mitochondrial Myopathies genetics
3-Hydroxyacyl CoA Dehydrogenases deficiency
3-Hydroxyacyl CoA Dehydrogenases genetics
Cardiomyopathies diagnosis
Cardiomyopathies genetics
Treatment Outcome
Rhabdomyolysis diagnosis
Rhabdomyolysis genetics
Nervous System Diseases
Neonatal Screening
Early Diagnosis
Visual Acuity
Lipid Metabolism, Inborn Errors diagnosis
Lipid Metabolism, Inborn Errors genetics
Lipid Metabolism, Inborn Errors therapy
Retinal Diseases diagnosis
Retinal Diseases genetics
Mitochondrial Trifunctional Protein deficiency
Subjects
Details
- Language :
- English
- ISSN :
- 1573-2665
- Volume :
- 47
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of inherited metabolic disease
- Publication Type :
- Academic Journal
- Accession number :
- 38623632
- Full Text :
- https://doi.org/10.1002/jimd.12738