Evidence map›Paper›PMID 40176950›Full record

ArticleJBMR plus2025

Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2.

Carlos R Ferreira, Mary E Hackbarth, Yvonne Nitschke, Ulrike Botschen, Rachel I Gafni, M Zulf Mughal, Genevieve Baujat, Dirk Schnabel, I Manjula Schou, Gus Khursigara and 4 more

Abstract read
In one paragraph

Article in JBMR plus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

14 authors.

Carlos R FerreiraEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.
Mary E HackbarthNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID https://orcid.org/0000-0003-1325-3165
Yvonne NitschkeDepartment of General Pediatrics, Münster University Children's Hospital, 48149 Münster, Germany.
Ulrike BotschenDepartment of General Pediatrics, Münster University Children's Hospital, 48149 Münster, Germany.
Rachel I GafniNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, United States.
M Zulf MughalAl Jalila Children's Specialty Hospital, Dubai, UAE.
Genevieve BaujatDépartement de Génétique, Centre de Référence Maladies Osseuses Constitutionnelles (CR MOC) et Filière OSCAR, Hôpital Necker-Enfants Malades, 75015 Paris, France.
Dirk SchnabelCenter for Chronically Sick Children, Pediatric Endocrinology, Charitè, University Medicine Berlin, 10117 Berlin, Germany.
I Manjula SchouPulse Economics Pty Ltd., Macquarie Park, NSW 2113, Australia.
Gus KhursigaraInozyme Pharma, Inc., Boston, MA 02210, United States.
Oona ReardonPulse Economics Pty Ltd., Macquarie Park, NSW 2113, Australia.
Thomas R BurklowNIH Clinical Center, National Institutes of Health, Bethesda, MD 20892, United States.
Kathleen SwannerInozyme Pharma, Inc., Boston, MA 02210, United States.
Frank RutschDepartment of General Pediatrics, Münster University Children's Hospital, 48149 Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generalized arterial calcification of infancy (GACI) and autosomal recessive hypophosphatemic rickets type 2 (ARHR2) are age-related phenotypes of the rare genetic mineralization disorder, ENPP1 Deficiency, which evolve on a phenotypic continuum. To date, our understanding of the clinical spectrum of ENPP1 Deficiency is based on small studies or case reports, across which there is significant variability in clinical presentation, and limited duration of follow-up. From a previously published large retrospective natural history study, we performed a subgroup analysis to elucidate the most prevalent signs and symptoms of ENPP1 Deficiency diagnosed as GACI or ARHR2, to illustrate the onset and incidence of these complications over the lifetime, and to characterize the associated medical burden of disease. Of the 84 individuals with ENPP1 Deficiency analyzed, 51 had a recorded diagnosis of GACI, 11 were diagnosed with ARHR2, and 22 were diagnosed with both. We confirmed that those diagnosed with GACI presented predominantly with early-onset arterial calcification, respiratory distress, heart failure, and hypertension, necessitating acute inpatient care and leading to high (44%) infant mortality. Notably, we found that the majority (60.3%) of those with a history of GACI had prenatal ultrasound anomalies, including effusions, polyhydramnios, and hydrops fetalis. We estimated that 70% of individuals with ENPP1 Deficiency who survive to age 10 will have developed musculoskeletal complications, primarily rickets and/or osteomalacia. The clinical picture of ARHR2 in this study extended beyond skeletal deformities to include hearing impairment, joint involvement, and ongoing risk of cardiovascular problems. This study sheds light on the signs and symptoms of ENPP1 Deficiency in the real world, with implications for life-long patient monitoring.

Indexed as

diseases and disorders of/related to bonedisorders of calcium/phosphate metabolismepidemiologygeneticsosteomalacia and rickets

Identifiers

PMID40176950
PMCPMC11961066

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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.