Quantification of Urine and Plasma Porphyrin Precursors Using LC–MS in Acute Hepatic Porphyrias: Improvement in Routine Diagnosis and in the Monitoring of Kidney Failure Patients

Author:

Poli Antoine1234,Manceau Hana135,Nguyen Anvi Laetitia4,Moulouel Boualem2,Dessendier Nathalie2,Talbi Neila123,Puy Hervé123,Junot Christophe4,Gouya Laurent123,Schmitt Caroline123,Lefebvre Thibaud1234

Affiliation:

1. Université de Paris Cité, INSERM U1149, Centre de Recherche sur l’Inflammation , HIROS Team, F-75018 Paris , France

2. Assistance Publique-Hôpitaux de Paris, Centre Français des Porphyries, Hôpital Louis Mourier , F-92700 Colombes , France

3. Laboratory of Excellence, Gr-Ex , Paris , France

4. Département Médicaments et Technologies pour La Santé (DMTS), Université Paris-Saclay, CEA, INRAE, MetaboHUB , F-91191 Gif-sur-Yvette , France

5. Assistance Publique-Hôpitaux de Paris, Laboratoire de Biochimie, Hôpital Beaujon , F-92110 Clichy la Garenne , France

Abstract

Abstract Background The quantification of delta-aminolevulinic acid (ALA) and porphobilinogen (PBG) in urine are the first-line tests for diagnosis and monitoring of acute hepatic porphyrias (AHP). Ion-exchange chromatography (IEC), which is time- and staff-consuming and limited to urine, is still the preferred method in many specialized laboratories, despite the development of mass spectrometry-based methods. Methods We describe a new LC-MS method that allows for rapid and simple quantification of ALA and PBG in urine and plasma with an affordable instrument that was used to analyze 2260 urine samples and 309 blood samples collected in 2 years of routine activity. The results were compared to those obtained with IEC, and urine reference ranges and concentrations in asymptomatic carriers were determined. Plasma concentrations were measured in healthy subjects and subgroups of symptomatic and asymptomatic AHP carriers. Results In urine, the clinical decision limits were not impacted by the change of method despite discrepancies in low absolute concentrations, leading to lower normal values. Two-thirds of asymptomatic AHP carriers (with the exception of coproporphyria carriers) showed an increased urine PBG concentration. Urine and plasma levels showed a good correlation except in patients with kidney disease in whom the urine/plasma ratio was relatively low. Conclusion We described an LC-MS based method for the routine diagnosis and monitoring of AHP that allows for the detection of more asymptomatic carriers than the historical method. Blood analysis appears to be particularly relevant for patients with kidney disease, where urine measurement underestimates the increase in ALA and PBG levels.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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