Evidence map›Paper›PMID 37465909›Full record

ArticlePediatrics2023

Evidence and Recommendation for Guanidinoacetate Methyltransferase Deficiency Newborn Screening.

Margie A Ream, Wendy K K Lam, Scott D Grosse, Jelili Ojodu, Elizabeth Jones, Lisa A Prosser, Angela M Rose, Anne Marie Comeau, Susan Tanksley, Cynthia M Powell and 1 more

Open access · greenAbstract read
In one paragraph

Article in Pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

11 authors at 8 institutions in 1 country.

Margie A ReamDivision of Child Neurology, Nationwide Children's Hospital, Columbus, Ohio.
Wendy K K LamDuke Clinical and Translational Science Institute, Duke University School of Medicine, Durham, North Carolina.
Scott D GrosseNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jelili OjoduAssociation of Public Health Laboratories, Silver Spring, Maryland.
Elizabeth JonesAssociation of Public Health Laboratories, Silver Spring, Maryland.
Lisa A ProsserSusan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Angela M RoseSusan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Anne Marie ComeauNew England Newborn Screening Program, Department of Pediatrics, UMass Chan School of Medicine, Worcester, Massachusetts.
Susan TanksleyTexas Department of State Health Services, Laboratory Services Section, Austin, Texas.
Cynthia M PowellDivision of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Alex R KemperDivision of Primary Care Pediatrics, Nationwide Children's Hospital, Columbus, Ohio.
Association of Public Health Laboratories · USNationwide Children's Hospital · USUniversity of Michigan–Ann Arbor · USCenters for Disease Control and Prevention · USDuke University · USTexas Department of State Health Services · USUniversity of Massachusetts Chan Medical School · USUniversity of North Carolina at Chapel Hill · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder of creatine biosynthesis due to pathogenic variants in the GAMT gene that lead to cerebral creatine deficiency and neurotoxic levels of guanidinoacetate. Untreated, GAMT deficiency is associated with hypotonia, significant intellectual disability, limited speech development, recurrent seizures, behavior problems, and involuntary movements. The birth prevalence of GAMT deficiency is likely between 0.5 and 2 per million live births. On the basis of small case series and sibling data, presymptomatic treatment with oral supplements of creatine, ornithine, and sodium benzoate, and a protein-restricted diet to reduce arginine intake, appear to substantially improve health and developmental outcomes. Without newborn screening, diagnosis typically happens after the development of significant impairment, when treatment has limited utility. GAMT deficiency newborn screening can be incorporated into the tandem-mass spectrometry screening that is already routinely used for newborn screening, with about 1 per 100 000 newborns screening positive. After a positive screen, diagnosis is established by finding an elevated guanidinoacetate concentration and low creatine concentration in the blood. Although GAMT deficiency is significantly more rare than other conditions included in newborn screening, the feasibility of screening, the low number of positive results, the relative ease of diagnosis, and the expected benefit of presymptomatic dietary therapy led to a recommendation from the Advisory Committee on Heritable Disorders in Newborns and Children to the Secretary of Health and Human Services that GAMT deficiency be added to the Recommended Uniform Screening Panel. This recommendation was accepted in January 2023.

Indexed as

Language Development DisordersMovement DisordersChildCreatineGuanidinoacetate N-MethyltransferaseHumansInfant, NewbornNeonatal ScreeningCreatineGuanidinoacetate N-Methyltransferase

Identifiers

PMID37465909
PMCPMC10527896
OpenAlexW4384664337

What OpenQuestion holds

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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.