Evidence map›Paper›PMID 39022300›Full record

ArticleMolecular genetics and metabolism reports2024

Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase.

Coleman Turgeon, Kari Casas, Ryan Flanagan, Amy White, Dawn Peck, Gisele Bentz Pino, April Studinski Jones, Dimitar Gavrilov, Devin Oglesbee, Matthew J Schultz and 3 more

Abstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

13 authors.

Coleman TurgeonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Kari CasasSanford Health, Fargo, ND, USA.
Ryan FlanaganDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Amy WhiteDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Dawn PeckDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Gisele Bentz PinoDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
April Studinski JonesDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Dimitar GavrilovDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Devin OglesbeeDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Matthew J SchultzDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Silvia TortorelliDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Dietrich MaternDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Patricia L HallDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of phenylketonuria (PKU) has evolved since the initial introduction of a phenylalanine (Phe) restricted diet. The most recent option for adults affected with PKU is treatment with an alternate enzyme, phenylalanine ammonia lyase (PAL), that metabolizes excess Phe. Proper management of all patients with PKU relies on accurate measurement of Phe levels in blood, to comply with guidance intended to minimize the neurological symptoms. Recently, our laboratory was notified of discrepant results for a patient with PKU who is treated with pegvaliase. Two specimens were collected at the same time but yielded unexpectedly different Phe concentrations. After exclusion of specimen mix-ups or analytical errors, we suspected that there was residual pegvaliase activity in the specimens continuing to degrade Phe after collection. To investigate this possibility, we performed spiking studies that showed the degradation of Phe over time at ambient temperatures. Sample preparation by protein crash appears to deactivate pegvaliase and prevents further Phe degradation. However, because pegvaliase deactivation would be required immediately following blood collection, appropriate mitigation measures must be implemented, including stringent pre-analytical requirements, alternate sample matrices such as dried blood spots, or point of care testing. Until then, health care professionals need to be cautious in their interpretation of Phe levels in their patients with PKU that are treated with pegvaliase.

Indexed as

PegvaliasePhenylalaninePhenylketonuriaPre-analytical error

Identifiers

PMID39022300
PMCPMC11252920

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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.