Lansoprazole Increases Inorganic Pyrophosphate in Patients with Pseudoxanthoma Elasticum: A Double-Blind, Randomized, Placebo-Controlled Crossover Trial

Author:

Murcia Casas Belén1,Carrillo Linares Juan Luis12,Baquero Aranda Isabel3,Rioja Villodres José24ORCID,Merino Bohórquez Vicente5ORCID,González Jiménez Andrés2ORCID,Rico Corral Miguel Ángel6,Bosch Ricardo7,Sánchez Chaparro Miguel Ángel128,García Fernández María29ORCID,Valdivielso Pedro1248ORCID

Affiliation:

1. Internal Medicine Unit, Hospital Universitario Virgen de la Victoria, 29010 Málaga, Spain

2. Instituto de Investigación Biomédica de Málaga (IBIMA), 29010 Málaga, Spain

3. Ophtalmology Unit, Hospital Universitario Virgen de la Victoria, 29010 Málaga, Spain

4. Centro de Investigaciones Médico-Sanitarias (CIMES), Universidad de Málaga, 29071 Málaga, Spain

5. Pharmacy Unit, Hospital Universitario Virgen Macarena, 41009 Sevilla, Spain

6. Internal Medicine Unit, Hospital Universitario Virgen Macarena, 41009 Sevilla, Spain

7. Dermatology Unit, Hospital Universitario Virgen de la Victoria, 29010 Málaga, Spain

8. Department of Medicine and Dermatology, University of Málaga, 29016 Málaga, Spain

9. Department of Phisiology, Universidad de Málaga, 29016 Málaga, Spain

Abstract

Pseudoxanthoma elasticum (PXE) is characterized by low levels of inorganic pyrophosphate (PPi) and a high activity of tissue-nonspecific alkaline phosphatase (TNAP). Lansoprazole is a partial inhibitor of TNAP. The aim was to investigate whether lansoprazole increases plasma PPi levels in subjects with PXE. We conducted a 2 × 2 randomized, double-blind, placebo-controlled crossover trial in patients with PXE. Patients were allocated 30 mg/day of lansoprazole or a placebo in two sequences of 8 weeks. The primary outcome was the differences in plasma PPi levels between the placebo and lansoprazole phases. 29 patients were included in the study. There were eight drop-outs due to the pandemic lockdown after the first visit and one due to gastric intolerance, so twenty patients completed the trial. A generalized linear mixed model was used to evaluate the effect of lansoprazole. Overall, lansoprazole increased plasma PPi levels from 0.34 ± 0.10 µM to 0.41 ± 0.16 µM (p = 0.0302), with no statistically significant changes in TNAP activity. There were no important adverse events. 30 mg/day of lansoprazole was able to significantly increase plasma PPi in patients with PXE; despite this, the study should be replicated with a large number of participants in a multicenter trial, with a clinical end point as the primary outcome.

Funder

Spanish Association of Persons Affected by PXE

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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