Evidence map›Paper›PMID 38816490›Full record

ArticleEuropean journal of human genetics : EJHG2024

Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy.

Lisa G Riley, Subrata Sabui, Hamid M Said, Aram Niaz, Katta M Girisha, Periyasamy Radhakrishnan, Sheela Nampoothiri, Dhanya Yesodharan, Tatjana Kilo, Janine Smith and 5 more

Abstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Looking back at 2024 in the European Journal of Human Genetics.European journal of human genetics : EJHG · 2025
    Article
  5. Summer reading in EJHG.European journal of human genetics : EJHG · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Lisa G RileyRare Diseases Functional Genomics, Kids Research, The Children's Hospital at Westmead and The Children's Medical Research Institute, Sydney, NSW, Australia. lisa.riley@health.nsw.gov.au.
Subrata SabuiDepartment of Physiology/Biophysics, University of California, Irvine, CA, USA.
Hamid M SaidDepartment of Physiology/Biophysics, University of California, Irvine, CA, USA.
Aram NiazRare Diseases Functional Genomics, Kids Research, The Children's Hospital at Westmead and The Children's Medical Research Institute, Sydney, NSW, Australia.ORCID 0000-0001-6636-2555
Katta M GirishaDepartment of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India.ORCID 0000-0002-0139-8239
Periyasamy RadhakrishnanSuma Genomics Private Limited and Manipal Center for Biotherapeutics Research, Manipal Academy of Higher Education, Manipal, India.
Sheela NampoothiriDepartment of Pediatric Genetics, Amrita Institute of Medical Sciences and Research Centre, Cochin, Kerala, India.ORCID 0000-0002-9575-0722
Dhanya YesodharanDepartment of Pediatric Genetics, Amrita Institute of Medical Sciences and Research Centre, Cochin, Kerala, India.
Tatjana KiloHaematology Department, Children's Hospital at Westmead, Westmead, NSW, Australia.
Janine SmithDepartment of Clinical Genetics, The Children's Hospital at Westmead, Sydney, NSW, 2145, Australia.
Rachel S H WongTY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Manoj P MenezesSpecialty of Child & Adolescent Health, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
Sachin GuptaSpecialty of Child & Adolescent Health, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
Sandra T CooperSpecialty of Child & Adolescent Health, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.ORCID 0000-0002-7314-5097
Shanti BalasubramaniamWestern Sydney Genetics Program, The Children's Hospital at Westmead, Westmead, NSW, Australia.

Funding

Physiology/Pathophysiology of Vitamin B1 Transport in Pancreatic Acinar CellsR01AA018071 · NIAAA · UNIVERSITY OF CALIFORNIA-IRVINE · PI SAID, HAMID M · 2009 to 2023
$6.3M
BLRD Research Career Scientist Award ApplicationIK6BX006189 · VA · VETERANS HEALTH ADMINISTRATION · PI HAMID M SAID · 2023 to 2026
–
BLRD VA I01 BX001142BLRD VA IK6 BX006189NIAAA NIH HHS R01 AA018071U.S. Department of Health & Human Services | National Institutes of Health (NIH) AA018071U.S. Department of Health & Human Services | NIH | Office of Extramural Research, National Institutes of Health (OER) AA018071U.S. Department of Veterans Affairs (Department of Veterans Affairs) I01BX001142U.S. Department of Veterans Affairs (Department of Veterans Affairs) IK6BX006189
6 · The paper itself

Abstract

The sodium-dependent multivitamin transporter encoded by SLC5A6 is responsible for uptake of biotin, pantothenic acid, and α-lipoic acid. Thirteen individuals from eight families are reported with pathogenic biallelic SLC5A6 variants. Phenotype ranges from multisystem metabolic disorder to childhood-onset peripheral motor neuropathy. We report three additional affected individuals with biallelic SLC5A6 variants. In Family A, a male proband (AII:1) presenting in early childhood with gross motor regression, motor axonal neuropathy, recurrent cytopenia and infections, and failure to thrive was diagnosed at 12 years of age via genome sequencing (GS) with a paternal NM_021095.4:c.393+2T>C variant and a maternal c.1285A>G p.(Ser429Gly) variant. An uncle with recurrent cytopenia and peripheral neuropathy was subsequently found to have the same genotype. We also report an unrelated female with peripheral neuropathy homozygous for the c.1285A>G p.(Ser429Gly) recurrent variant identified in seven reported cases, including this study. RT-PCR studies on blood mRNA from AII:1 showed c.393+2T>C caused mis-splicing with all canonically spliced transcripts in AII:1 containing the c.1285A>G variant. SLC5A6 mRNA expression in AII:1 fibroblasts was ~50% of control levels, indicative of nonsense-mediated decay of mis-spliced transcripts. Biotin uptake studies on AII:1 fibroblasts, expressing the p.(Ser429Gly) variant, showed an ~90% reduction in uptake compared to controls. Targeted treatment of AII:1 with biotin, pantothenic acid, and lipoic acid resulted in clinical improvement. Health Economic analyses showed implementation of GS as an early investigation could have saved $ AUD 105,988 and shortened diagnostic odyssey and initiation of treatment by up to 7 years.

Indexed as

SymportersBasal Ganglia DiseasesBiotinChildFemaleHumansMaleMutationOrganic Anion Transporters, Sodium-DependentPedigreePeripheral Nervous System DiseasesThioctic AcidWhole Genome SequencingBiotinbiotin transporterOrganic Anion Transporters, Sodium-DependentSymportersThioctic Acid

Identifiers

PMID38816490
PMCPMC11291669

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.