Evidence map›Paper›PMID 41989430›Full record

Observational studyJournal of inherited metabolic disease2026

Real-Life Application of a Point-of-Care Biosensor for Phenylalanine in Patients With Phenylketonuria.

Corentin Gondrand, Anna T Reischl-Hajiabadi, Estelle Bonedeau, Nicolas Weiß, Gerd Schneider, Maurice Fahn, Frederic Myers, Philipp Minel Städle, Kathrin Jeltsch, Georg F Hoffmann and 5 more

2 registry-linked trialsAbstract readObservational Study
In one paragraph

Observational study 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. It is linked to 2 registered trials, which are not on this 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.

NCT05998109 completednot on this map

PheCheck Feasibility Study

TypeobservationalSponsorLumos DiagnosticsRan2023 to 2024Enrolled30ConditionsPhenylketonuriasArmsPheCheck™, HPLC Amino Acid Analyzer, Dried Blood Spot Cards
NCT06940193 enrolling by invitationnot on this map

Egoo Phe System - A Blood Phenylalanine Self-Test Measuring System

Typeobservational_patient_registrySponsorEgoo Health ApsRan2025 to 2025Enrolled20ConditionsPhenylketonuria (PKU)
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Observational
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

15 authors.

Corentin GondrandDepartment of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany.
Anna T Reischl-HajiabadiMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-7766-4847
Estelle BonedeauDepartment of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany.
Nicolas WeißPhellow Seven GmbH, Heidelberg, Germany.
Gerd SchneiderPhellow Seven GmbH, Heidelberg, Germany.
Maurice FahnPhellow Seven GmbH, Heidelberg, Germany.
Frederic MyersFrederic Myers Consulting (JERY), Reutlingen, Germany.
Philipp Minel StädleFrederic Myers Consulting (JERY), Reutlingen, Germany.
Kathrin JeltschMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Georg F HoffmannMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Jürgen G OkunMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Dorothea HaasMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.
Sven F GarbadeMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-7420-4757
Kai JohnssonDepartment of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany.
Thomas OpladenMedical Faculty of Heidelberg, Department of Pediatrics, Division of Pediatric Neurology and Metabolic Medicine, Heidelberg University, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-4349-7662

Funding

Fraunhofer-Max Planck Cooperation ProgramMarie Skłodowska-Curie grant agreement (H2020-MSCAITN-CONSENSE) 955623M. Lomtadze
6 · The paper itself

Abstract

Phenylketonuria (PKU) is a rare metabolic disorder causing elevated phenylalanine (PHE) levels requiring lifelong dietary or pharmacological management and regular monitoring. Current PHE monitoring methods, such as tandem mass spectrometry (FIA-MS/MS), are laboratory and sample transport-dependent, leading to delays in obtaining results. This highlights the need for accessible point-of-care (PoC) solutions. Building on a previously developed bioluminescence-based PHE quantification method, we created a PoC PHE sensor integrated with a smartphone app (phenyx app) for real-time monitoring and data sharing. In a clinical study with PKU patients, we evaluated the reliability of the sensor and the app by comparing at-home PHE measurements with dried blood samples (DBS) analyzed using the gold standard FIA-MS/MS. We also assessed time differences between sampling and results, sensor practicality, and user experience. Forty-seven PKU patients (median age 10.0 years, range 0.7-53.4) performed one supervised and four at-home measurements using the PHE sensor, alongside DBS sampling for FIA-MS/MS. The sensor showed higher PHE values than FIA-MS/MS, with a mean difference of 84.8 μmol/L (p = 0.0017). Variability was influenced by test supervision (clinic vs. home) and test kit age (greater difference in older batches, p = 0.001). Usability of the PHE sensor and phenyx app was rated favorably; all patients preferred the PHE sensor over laboratory testing. PoC measurement using the PHE sensor and phenyx app is feasible, reliable, and provides rapid results comparable to FIA-MS/MS, representing a key step toward patient self-testing. Trial Registration: NCT05998109, NCT06940193, DRKS00031972.

Indexed as

Biosensing TechniquesPhenylalaninePhenylketonuriasPoint-of-Care SystemsAdolescentAdultChildChild, PreschoolDried Blood Spot TestingFemaleHumansInfantMaleMiddle AgedRapid Diagnostic TestsReproducibility of ResultsPhenylalanineat‐home testbiosensorphenylalanine hydroxylase deficiencyPhenylketonuriaPKUpoint‐of‐care testing

Identifiers

PMID41989430
PMCPMC13086054

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.