Evidence map›Paper›PMID 35242576›Full record

ArticleMolecular genetics and metabolism reports2022

Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair.

Nathan Grant, Young Bae Sohn, N Matthew Ellinwood, Ericka Okenfuss, Bryce A Mendelsohn, Leslie E Lynch, Elizabeth A Braunlin, Paul R Harmatz, Julie B Eisengart

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Evidence and recommendation for mucopolysaccharidosis type II newborn screening in the United States.Genetics in medicine : official journal of the American College of Medical Genetics · 2023
    Review
  10. Article
  11. Article
  12. 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

9 authors at 5 institutions in 2 countries.

Nathan GrantDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Young Bae SohnDepartment of Medical Genetics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Republic of Korea.
N Matthew EllinwoodNational MPS Society, Durham, NC, USA.
Ericka OkenfussKaiser Permanente, Oakland, CA, USA.
Bryce A MendelsohnKaiser Permanente, Oakland, CA, USA.
Leslie E LynchUCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.
Elizabeth A BraunlinDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Paul R HarmatzUCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.
Julie B EisengartDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USKaiser Permanente · USUCSF Benioff Children's Hospital · USAjou University · KRNational MPS Society · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hunter syndrome, or mucopolysaccharidosis (MPS) II, is a rare lysosomal disorder characterized by progressive, multi-system disease. As most symptoms cannot be reversed once established, early detection and treatment prior to the onset of clinical symptoms are critical. However, it is difficult to identify affected individuals early in disease, and therefore the long-term outcomes of initiating treatment during this optimal time period are incompletely described. We report long-term clinical outcomes of treatment when initiated prior to obvious clinical signs by comparing the courses of two siblings with neuronopathic Hunter syndrome (c.1504 T > G[p.W502G]), one who was diagnosed due to clinical disease (Sibling-O, age 3.7 years) and the other who was diagnosed before disease was evident (Sibling-Y, age 12 months), due to his older sibling's findings. The brothers began enzyme replacement therapy within a month of diagnosis. Around the age of 5 years, Sibling-O had a cognitive measurement score in the impaired range of <55 (average range 85-115), whereas Sibling-Y at this age received a score of 91. Sibling-O has never achieved toilet training and needs direct assistance with toileting, dressing, and washing, while Sibling-Y is fully toilet-trained and requires less assistance with daily activities. Both siblings have demonstrated sensory-seeking behaviors, hyperactivity, impulsivity, and sleep difficulties; however, Sibling-O demonstrates physical behaviors that his brother does not, namely biting, pushing, and frequent elopement. Since the time of diagnosis, Sibling-O has had significant joint contractures and a steady deterioration in mobility leading to the need for an adaptive stroller at age 11, while Sibling-Y at age 10.5 could hike more than 6 miles without assistance. After nearly a decade of therapy, there were more severe and life-limiting disease manifestations for Sibling-O; data from caregiver interview indicated substantial differences in Quality of Life for the child and the family, dependent on timing of ERT. The findings from this sibling pair provide evidence of superior somatic and neurocognitive outcomes associated with presymptomatic treatment of Hunter syndrome, aligned with current considerations for newborn screening.

Indexed as

ABR, Auditory brainstem responseCNS, central nervous system;DAS-II, Differential Ability Scales, Second Edition;Early interventionEnzyme replacement therapyERT, enzyme replacement therapy;GAG, glycosaminoglycan;HCT, hematopoietic cell transplantation;Hunter syndromeIDS, iduronate-2-sulphatase;IT, intrathecal;MPS II, mucopolysaccharidosis type II, Hunter syndrome;MPS, mucopolysaccharidosis;MRI, magnetic resonance imaging;Mucopolysaccharidosis type IINBS, newborn screening;Newborn screeningRUSP, Recommended Uniform Screening PanelSibling study

Identifiers

PMID35242576
PMCPMC8856919
OpenAlexW4220874979

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.