Evidence map›Paper›PMID 39267130›Full record

SynthesisOrphanet journal of rare diseases2024

Meta-analysis of bone mineral density in adults with phenylketonuria.

Júlio C Rocha, Álvaro Hermida, Cheryl J Jones, Yunchou Wu, Gillian E Clague, Sarah Rose, Kaleigh B Whitehall, Kirsten K Ahring, André L S Pessoa, Cary O Harding and 6 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

16 authors.

Júlio C RochaNOVA Medical School/Faculdade de Ciências Médicas (NMS/FCM), Universidade NOVA de Lisboa, Lisboa, Portugal. rochajc@nms.unl.pt.ORCID 0000-0002-4977-8345
Álvaro HermidaUniversity of Santiago de Compostela, Santiago de Compostela, Spain.
Cheryl J JonesHCD Economics, Knutsford, UK.
Yunchou WuHCD Economics, Knutsford, UK.
Gillian E ClagueBioMarin Pharmaceutical Inc, Novato, CA, USA.
Sarah RoseBioMarin Pharmaceutical Inc, Novato, CA, USA.
Kaleigh B WhitehallBioMarin Pharmaceutical Inc, Novato, CA, USA.
Kirsten K AhringClinic for PKU, Copenhagen University Hospital, Copenhagen, Denmark.
André L S PessoaFederal University of Ceará - UFC, Fortaleza, CE, Brazil.
Cary O HardingOregon Health & Science University, Portland, OR, USA.
Fran RohrMet Ed Consultants, Boulder, CO, USA.
Anita InwoodQueensland Lifespan Metabolic Medicine Service, Queensland Children's Hospital, South Brisbane, QLD, Australia.
Nicola LongoUniversity of Utah School of Medicine, Salt Lake City, UT, USA.
Ania C MuntauUniversity Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Serap SivriHacettepe University, Ankara, Turkey.
François MaillotInternal Medicine Department and Reference Center for Inherited Metabolic Disease, University of Tours, Tours, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLifelong management of phenylketonuria (PKU) centers on medical nutrition therapy, including dietary phenylalanine (Phe) restriction in addition to Phe-free or low-Phe medical foods/protein substitutes. Studies have reported low bone mineral density (BMD) in mixed-age PKU populations, possibly related to long-term Phe restriction. Therefore, a meta-analysis investigating BMD specifically in adults with PKU was conducted.

methodsStudies reporting BMD-related outcomes were identified from a systematic literature review evaluating somatic comorbidities experienced by adults with PKU on a Phe-restricted diet (searched February 1, 2022, updated November 1, 2023). Risk of study bias was assessed (Scottish Intercollegiate Guidelines Network checklists). The primary outcome of the meta-analysis was pooled mean BMD Z-scores of different bones. Secondary outcomes were the prevalence of low BMD Z-scores at pre-specified thresholds. Subgroup analyses of mean BMD Z-scores (decade of study publication, controlled versus uncontrolled blood Phe levels, gender) were conducted.

resultsBMD-related data from 4097 individuals across 10 studies rated as at least acceptable quality were included. Mean BMD Z-scores were statistically significantly lower compared with an age-matched control or reference (non-PKU) population, across bones, but still within the expected range for age (> -2.0): lumbar spine (seven studies, n = 304), -0.63 (95% confidence interval (CI): -0.74, -0.52); femoral neck (four studies, n = 170), -0.74 (95% CI: -1.25, -0.22); radius (three studies, n = 114), -0.77 (95% CI: -1.21, -0.32); total body (four studies, n = 157), -0.61 (95% CI: -0.77, -0.45). The small number of observations in the subgroup analyses resulted in a high degree of uncertainty, limiting interpretation. Estimated prevalence of BMD Z-scores ≤ -2.0 was 8% (95% CI: 5%, 13%; four studies, n = 221) and < -1.0 was 42% (95% CI: 35%, 51%; five studies, n = 144).

conclusionsAdults with PKU had lower BMD Z-scores than the reference (non-PKU) population but < 1 in 10 were below the expected range for age. The low number of studies prevents identification of which population characteristics are most impacting BMD. This meta-analysis was supported by BioMarin Pharmaceutical Inc., Novato, CA and is registered with the Research Registry (reviewregistry1476).

Indexed as

Bone DensityPhenylketonuriasAdultFemaleHumansMalePhenylalanineSystematic Reviews as TopicPhenylalanineBoneBone mineral densityDietDiet adherenceMeta-analysisOsteopeniaOsteoporosisPhenylalaninePhenylketonuriaZ-score

Identifiers

PMID39267130
PMCPMC11391789

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.