Evidence map›Paper›PMID 42644808›Full record

ReviewJournal of inherited metabolic disease2026

Cobalamin-Related Remethylation Disorders: Pregnancy Outcomes and Prenatal Treatment-New Cases and a Literature Study.

Karolina M Stepien, Jolanta Sykut-Cegielska, Jennifer Sloan, Flavia Piazzon, Sarah Bick, Juliette Bouchereau, Edwin C Ferren, Nina Gold, Apolline Imbard, Mirian C H Janssen and 13 more

Abstract readCase ReportsReview
In one paragraph

Review in Journal of inherited metabolic disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

23 authors.

Karolina M StepienSalford Royal Hospital, Northern Care Alliance NHS Foundation Trust, Salford, UK.ORCID https://orcid.org/0000-0003-0148-6332
Jolanta Sykut-CegielskaDepartment of Inborn Errors of Metabolism and Pediatrics, Institute of Mother and Child, Warsaw, Poland.ORCID https://orcid.org/0000-0003-0762-3721
Jennifer SloanNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-4520-0949
Flavia PiazzonCentre de référence maladies héréditaires du métabolisme, Hôpital Timone Enfants, APHM, Marseille, France.ORCID https://orcid.org/0000-0003-1685-2884
Sarah BickDivision of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-3868-5474
Juliette BouchereauReference Center for Inborn Error of Metabolism, Hôpital Necker-Enfants Malades, APHP and Université Paris Cité, Paris, France.
Edwin C FerrenWake Forest University School of Medicine, Atrium Health Pediatric Genetics, Charlotte, North Carolina, USA.ORCID https://orcid.org/0000-0002-4603-1430
Nina GoldDivision of Medical Genetics and Metabolism, Massachusetts General Hospital for Children, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-0867-722X
Apolline ImbardReference Center for Inborn Error of Metabolism, Hôpital Necker-Enfants Malades, APHP and Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0002-0420-8322
Mirian C H JanssenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID https://orcid.org/0000-0003-4668-9977
Pavel JesinaDepartment of Pediatrics and Inherited Metabolic Disorders, Charles University-First Faculty of Medicine and General University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0000-0002-8513-0976
Lisa A JosephNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-6862-3616
Amanda Krzywdzińska-RogowskaDepartment of Inborn Errors of Metabolism and Pediatrics, Institute of Mother and Child, Warsaw, Poland.ORCID https://orcid.org/0000-0002-7621-8378
Louise LapagesseMedical Genetics Service/Reference Center for Rare Disorders -Hospital Infantil Joana de Gusmão, Florianopolis, Brazil.
Fanny MochelReference Center for Adult Neurometabolic Diseases, Assistance Publique Hôpitaux de Paris; Sorbonne University, La Pitié-Salpêtrière University Hospital, Paris, France.ORCID https://orcid.org/0000-0003-3970-3486
Carol Van RyzinNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Manuel SchiffReference Center for Inborn Error of Metabolism, Hôpital Necker-Enfants Malades, APHP and Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0001-8272-232X
Ida Vanessa SchwartzHospital de Clínicas de Porto Alegre and Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-7933-6687
Audrey ThurmNational Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-0489-9485
Wadih M ZeinNational Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-3771-6120
Charles P VendittiNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-6599-1253
Martina HuemerDivision of Metabolism and Children's Research Center, University Children's Hospital, Zürich, Switzerland.ORCID https://orcid.org/0000-0002-0590-678X
Irini ManoliNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-1543-2941

Funding

Investigations of Methylmalonic Acidemia and Related DisordersZIAHG200318 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI VENDITTI, CHARLES P · 2009 to 2025
$29.7M
TRAINING GRANT IN GENETICST32GM007748 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Anne O'Donnell-Luria, Louise Wilkins-Haug · 1985 to 2026
$12.0M
Intramural NIH HHS ZIA HG200318NIGMS NIH HHS T32 GM007748NIH HHS 1ZIAHG200318NIH HHS BBMRI_CZ LM2023033NIH HHS NU23-07-00383
6 · The paper itself

Abstract

Cobalamin-related remethylation disorders (cbl-RD) are rare, heterogenous conditions with a wide phenotypic spectrum, including prenatal and early infantile manifestations. Data on pregnancy outcomes in affected women and the efficacy and safety of prenatal treatment of affected fetuses remain limited. Here we report (1) five women with cbl-RDs (3 cblC/epi-cblC, 1 cblD, 1 cblE) who had in total nine pregnancies and (2) eight fetuses with cbl-RD (7 cblC, 1 cblF) diagnosed and treated prenatally. All affected mothers were treated with hydroxocobalamin (OHCbl) during pregnancy and two also received betaine and carnitine. Complications included three preterm deliveries and nephrotic-range proteinuria in one previously undiagnosed mother with cblE. All offspring had favourable outcomes. In pregnancies with affected fetuses, OHCbl was administered to the mother between gestational weeks 5 and 32 at varying doses. Prenatally treated cblC cases exhibited attenuated phenotypes without microcephaly, epilepsy, or severe multisystemic disease. Notably, three of five infants harbouring severe MMACHC variants, who received high-dose pre- and postnatal OHCbl, exhibited normal neurodevelopment and no maculopathy up to age 2-3 years, though variability in genotype, treatment regimens, and duration of follow-up limit generalizability. A literature review identified nine additional pregnancies in women with cbl-RD and seven prenatally treated fetuses, with follow-up available for three. Collectively, our main findings support the safety of maternal and fetal OHCbl treatment during pregnancy. We recommend that when combined with preconception counselling, early standardized diagnosis, optimal monitoring and postnatal care, prenatal OHCbl therapy can improve pregnancy outcomes and mitigate neurodevelopmental and ophthalmic complications in cbl-RD.

Indexed as

Amino Acid Metabolism, Inborn ErrorsHomocystinuriaVitamin B 12Vitamin B 12 DeficiencyAdultBetaineCarnitineFemaleHumansHydroxocobalaminInfant, NewbornMethylationPregnancyPregnancy ComplicationsPregnancy OutcomeBetaineCarnitineHydroxocobalaminVitamin B 12cobalamin disorderfetushydroxocobalaminin uteropregnancyremethylation defecttreatment

Identifiers

PMID42644808
PMCPMC13510120

What OpenQuestion holds

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Registered trials

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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.