Evidence map›Paper›PMID 38613540›Full record

GuidelineCytotherapy2024

Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States.

Laura A Adang, Joshua L Bonkowsky, Jaap Jan Boelens, Eric Mallack, Rebecca Ahrens-Nicklas, John A Bernat, Annette Bley, Barbara Burton, Alejandra Darling, Florian Eichler and 22 more

Open access · greenAbstract readPractice GuidelineReview
In one paragraph

Guideline in Cytotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Rigorous genetic diagnosis review in natural history studies.Orphanet journal of rare diseases · 2026
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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

32 authors at 20 institutions in 9 countries.

Laura A AdangChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA. Electronic address: adangl@chop.edu.
Joshua L BonkowskyUniversity of Utah, Salt Lake City, Utah, USA.
Jaap Jan BoelensDepartment of Pediatrics, Stem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College of Cornell University, New York, New York, USA.
Eric MallackKennedy Krieger Institute, Baltimore, Maryland, USA.
Rebecca Ahrens-NicklasChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
John A BernatUniversity of Iowa Stead Family Children's Hospital, Iowa City, Iowa, USA.
Annette BleyUniversity Children's Hospital, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Barbara BurtonLurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Alejandra DarlingHospital Sant Joan de Déu, Barcelona, Spain.
Florian EichlerMassachusetts General Hospital, Boston, Massachusetts, USA.
Erik EklundLund University, Lund, Sweden.
Lisa EmrickBaylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.
Maria EscolarDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA; Forge Biologics, Grove City, Ohio, USA.
Ali FatemiKennedy Krieger Institute, Baltimore, Maryland, USA.
Jamie L FraserChildren's National Hospital, Washington, District of Columbia, USA.
Amy GaviglioDivision of Laboratory Services, Newborn Screening and Molecular Biology Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA; Association of Public Health Laboratories, Silver Spring, Maryland, USA.
Stephanie KellerChildren's Healthcare of Atlanta, Atlanta, Georgia, USA.
Marc C PattersonDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota, USA; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA; Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Paul OrchardUniversity of Minnesota, Minneapolis, Minnesota, USA.
Jennifer Orthmann-MurphyDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Jonathan D SantoroUniversity of Southern California, Children's Hospital Los Angeles, Keck School of Medicine, Los Angeles, California, USA.
Ludger SchölsDepartment of Neurology and Hertie-Institute for Clinical Brain Research German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Caroline SevinUniversité Paris-Saclay, Hôpital Bicêtre, Paris, France.
Isha N SrivastavaDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Deepa RajanUniversity of Pittsburgh, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Jennifer P RubinLurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Keith Van HarenDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Melissa WassersteinDepartment of Pediatrics, Albert Einstein College of Medicine and the Children's Hospital at Montefiore, Bronx, New York, USA.
Ayelet ZeremDana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Francesca FumagalliOspedale San Raffaele, Milano, Italy.
Lucia LaugwitzDepartment of Pediatric Neurology and Developmental Medicine, University Children's Hospital Tübingen, Tübingen, Germany.
Adeline VanderverChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Children's Hospital of Philadelphia · USKennedy Krieger Institute · USLurie Children's Hospital · USStanford University · USUniversity of Pittsburgh · USAlbert Einstein College of Medicine · USBaylor College of Medicine · USCenters for Disease Control and Prevention · USChildren's Healthcare of Atlanta · USChildren's National · USHertie Institute for Clinical Brain Research · DEHospital Sant Joan de Déu Barcelona · ESIRCCS Ospedale San Raffaele · ITLund University · SEMassachusetts General Hospital · USMayo Clinic · USMemorial Sloan Kettering Cancer Center · USTel Aviv University · ILUniversität Hamburg · DEUniversité Paris-Saclay · FR

Funding

Child Neurologist Career Development Program (CNCDP)K12NS098482 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI SCHLAGGAR, BRADLEY L · 2016 to 2025
$26.2M
Validation of the GMFC-MLDU54NS115052 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI S. Ali Fatemi · 2019 to 2026
$14.3M
Mechanistic investigation of therapies for Down Syndrome Regression DisorderR61HD109748 · NICHD · UNIVERSITY OF COLORADO DENVER · PI ESPINOSA, JOAQUIN M., SANNAR, ELISE M · 2022 to 2023
$1.5M
Non-invasive biometric screening for cerebrovascular disorders in persons with Down syndrome.K23HL155898 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI SANTORO, JONATHAN DOUGLAS · 2021 to 2025
$1.3M
Clinical measures in Aicardi Goutieres SyndromeK23NS114113 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI ADANG, LAURA ANN · 2019 to 2023
$947k
NHLBI NIH HHS K23 HL155898NICHD NIH HHS R61 HD109748NINDS NIH HHS K12 NS098482NINDS NIH HHS K23 NS114113NINDS NIH HHS U54 NS115052
6 · The paper itself

Abstract

Metachromatic leukodystrophy (MLD) is a fatal, progressive neurodegenerative disorder caused by biallelic pathogenic mutations in the ARSA (Arylsulfatase A) gene. With the advent of presymptomatic diagnosis and the availability of therapies with a narrow window for intervention, it is critical to define a standardized approach to diagnosis, presymptomatic monitoring, and clinical care. To meet the needs of the MLD community, a panel of MLD experts was established to develop disease-specific guidelines based on healthcare resources in the United States. This group developed a consensus opinion for best-practice recommendations, as follows: (i) Diagnosis should include both genetic and biochemical testing; (ii) Early diagnosis and treatment for MLD is associated with improved clinical outcomes; (iii) The panel supported the development of newborn screening to accelerate the time to diagnosis and treatment; (iv) Clinical management of MLD should include specialists familiar with the disease who are able to follow patients longitudinally; (v) In early onset MLD, including late infantile and early juvenile subtypes, ex vivo gene therapy should be considered for presymptomatic patients where available; (vi) In late-onset MLD, including late juvenile and adult subtypes, hematopoietic cell transplant (HCT) should be considered for patients with no or minimal disease involvement. This document summarizes current guidance on the presymptomatic monitoring of children affected by MLD as well as the clinical management of symptomatic patients. Future data-driven evidence and evolution of these recommendations will be important to stratify clinical treatment options and improve clinical care.

Indexed as

Leukodystrophy, MetachromaticCerebroside-SulfataseConsensusGenetic TherapyHumansInfant, NewbornNeonatal ScreeningUnited StatesCerebroside-Sulfatasegene therapyleukodystrophymetachromatic leukodystrophynewborn screeningtransplant

Identifiers

PMID38613540
PMCPMC11348704
OpenAlexW4393384747

What OpenQuestion holds

Textmetadata
LicenceTDM
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.