Intestinal Microbiota and Vitamin K Levels in PXE Patients (IMPROVE Study)

NCT ID: NCT03813550

Last Updated: 2019-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-01-21

Study Completion Date

2020-01-30

Brief Summary

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This study aims to demonstrate a potential association between gut microbiota composition, plasma levels of various forms of vitamin K, and severity of clinical manifestations of Pseudoxanthoma Elasticum (PXE).

Detailed Description

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Vitamin K deficiency contributes to pathological calcification which underlies the clinical picture of pseudoxanthoma elasticum (PXE), an inherited autosomal recessive disease. A substantial proportion of vitamin K, namely the K2 form (menaquinones), is produced by gut microbiota. In healthy volunteers fecal levels of the major menaquinone producers, Escherichia coli and Bacteroides species, are approximately 5 and 9 log10 CFU/g dry weight respectively. There is however a lack of data on gut microbiota in PXE patients. The objective of our project is to demonstrate a potential association between gut microbiota composition, plasma levels of various forms of vitamin K and severity of clinical manifestations in PXE patients.

This study will be performed as Research surrounding bio collection "Clinical and biological exploration of PXE patients" kept at the Center of Biological Resources of Angers University Hospital (bio collection n° DC 20116-14-67, authorization to transfer n° 2016-27-99). Fecal samples, plasma samples and clinical data will be collected from patients diagnosed with PXE who will be monitored at the Angers University Hospital Referral Center (France) in 2019-2020. Clinical severity of PXE will be assessed using modified Phenodex score. Gut microbiota will be analyzed using metagenomic sequencing. Plasma Vitamin K species and fecal excretion of menaquinones will be assessed using HPLC. Plasma dp-ucMGP (circulating biomarker of vitamin K status) and serum PIVKA-II (protein induced by vitamin K absence-II) will be assessed using immunoassay. Results will be compared to healthy age- and gender-matched controls from the pre-existing Biofortis database.

Conditions

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Pseudoxanthoma Elasticum

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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PXE cohort 2019-2020

PXE patient cohort monitored at referral centre from 2019 to 2020: fecal and blood samples

Group Type OTHER

Fecal and blood samples

Intervention Type DIAGNOSTIC_TEST

Fecal samples for intestinal microbiota analysis; Blood and fecal samples for assessment of various forms of vitamin K

Interventions

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Fecal and blood samples

Fecal samples for intestinal microbiota analysis; Blood and fecal samples for assessment of various forms of vitamin K

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients with phenotypically and genetically (ABCC6) proven PXE
* Aged over 18 years
* Written consent obtained for Angers University Hospital (France) PXE bio-collection

Exclusion Criteria

* Patients under the age of 18
* Patients unwilling to participate in the study, or unable to sign the bio-collection consent form
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Maastricht University

OTHER

Sponsor Role collaborator

Biofortis Mérieux NutriSciences

OTHER

Sponsor Role collaborator

University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ludovic MARTIN, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Dermatology, University Hospital of Angers

Locations

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Biofortis Mérieux NutriSciences

Saint-Herblain, Pays de la Loire Region, France

Site Status ACTIVE_NOT_RECRUITING

Department of Dermatology, University Hospital of Angers

Angers, Pays de Loire, France

Site Status RECRUITING

Department of Biochemistry, University Maastricht

Maastricht, , Netherlands

Site Status ACTIVE_NOT_RECRUITING

Countries

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France Netherlands

Central Contacts

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Ludovic MARTIN, MD, PhD

Role: CONTACT

+332.41.35.55.76

Facility Contacts

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Ludovic Martin, MD, PhD

Role: primary

+332.41.35.55.76

References

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Other Identifiers

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2018/79

Identifier Type: -

Identifier Source: org_study_id

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