Administration of Methionine in Patients With Pulmonary Alveolar Proteinosis by Mutation of the MARS Gene. (MetPAP)
Primary Purpose
Pulmonary Alveolar Proteinosis, Mutation Ala393Thr of the MARS Gene, mutationSer567Leu of the MARS Gene
Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
Methionine
Vitamin B12, B9, B6, C supplementation
Methionine/homocysteine Dosage
Thoracic CT scan
Abdominal and liver ultrasound.
Brain MRI
Sponsored by
About this trial
This is an interventional treatment trial for Pulmonary Alveolar Proteinosis focused on measuring Pulmonary alveolar proteinosis, MARS gene, methionine
Eligibility Criteria
Inclusion Criteria:
- Minor Patient with alveolar proteinosis by double mutation Ala393Thr and SER567LEU of the MARS gene, genetically proven.
- Patient in need of prolonged hospitalization in Necker for treatment of bronchial-alveolar washes in the context of care.
- Patient for which methionine can be administered orally or by enteral probe (Nasogastric or gastrostomy probe)
- Signed Informed consent form by parents / legal guardian
Exclusion Criteria:
- Patient with alveolar proteinosis by other mutations of the MARS gene
- Patient with alveolar proteinosis secondary to another etiology or without identified cause
- Refusal to participate in the study
- High blood pressure requiring drug treatment
- Heart failure
- Known hypersensitivity to one of the substances used or potentially used in the study: methionine, vitamins B6, B12, B9 and C
- Pre-Hypermethioninemia (Methioninemia > + 2 DS of normal for age) whatever the cause
Sites / Locations
- Hôpital Necker-Enfants Malades
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Methionine
Arm Description
Outcomes
Primary Outcome Measures
Tolerance Assessment
No adverse event from day 0 to day 75.
Secondary Outcome Measures
Respiratory rate (cycles /min)
number of cycles per minute
Oxygen need (L/min)
Flow in L/min
Respiratory signs of struggle
Presence or absence of signs
Lung lesions
Lesions appearance on thoracic CT scan, scored form 0 to 4
Lipo-proteinaceous material
Fluid examination
Weight
To evaluate Nutritional status
mid upper arm circumference / head circumference rapport
To evaluate Nutritional status
Hepatomegaly
liver damage evaluate by physician during clinical examination
cholestasis and hepatic cytolysis
liver damage evaluate by biological parameters : ASAT, ALAT, GGT, PAL, Bilirubin
Hepatomegaly
liver damage evaluate by echography
C reactive protein
Biological parameters to evaluate Systemic inflammation
sedimentation rate
Biological parameters to evaluate Systemic inflammation
Immunoglobulin G level
Biological parameters to evaluate Systemic inflammation
Haemoglobin level
Biological parameters to evaluate inflammatory anaemia
Plasma concentration of methionine
Variation of the concentration for each patient
Plasma concentration of homocysteine
Variation of the concentration for each patient
Full Information
NCT ID
NCT03887169
First Posted
March 12, 2019
Last Updated
November 6, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT03887169
Brief Title
Administration of Methionine in Patients With Pulmonary Alveolar Proteinosis by Mutation of the MARS Gene.
Acronym
MetPAP
Official Title
Oral or Enteral Administration of Methionine in Patients With Pulmonary Alveolar Proteinosis by Mutation of the MARS Gene.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
September 16, 2019 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
June 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine the safety and tolerance of an oral administration of methionine in the treatment of pulmonary alveolar proteinosis due to the double mutation Ala393Thr / Ser567Leu in the MARS gene. This disease is very severe and especially leads to chronic respiratory insufficiency. There is no curative treatment for this disease. The MARS gene encodes the methionine tRNA synthetase (MetRS). Mutations in this gene leads to a defect in MetRS function. In cultured mutated yeast, addition of methionine in culture medium restores MetRS function. Therefore, the investigators hypothesized that treatment of patients with methionine could have beneficial effects on the disease.
Detailed Description
Pulmonary alveolar proteinosis (PAP) is a rare respiratory disorder. Recently, a genetic cause has been identified for a specific form of PAP predominant on La Reunion Island. This form is characterized by a multisystem phenotype including PAP, failure to thrive, hepatic involvement and chronic inflammation. This is a severe disease without any specific treatment and a high rate of mortality related to end-stage respiratory insufficiency. Two recurrent mutations were isolated in the MARS gene that encodes the methionine tRNA synthetase (MetRS). This enzyme catalyzes the ligation of methionine to tRNA and is critical for protein biosynthesis. Functional studies on mutated yeast show an altered growth and protein synthesis as compared to control yeast. Addition of methionine in culture medium corrects these defects. Complementary experiments on human purified MetRS show altered enzymatic catalytic parameters in mutated forms. Increasing blood concentration of methionine in patients could correct these parameters and potentially improve patients' phenotype in this severe disorder where no curative treatment exists.
The main objective of this protocol is to determine the tolerance of a prolonged daily supplementation of methionine in patients presenting a MARS related PAP. The secondary objectives are to determine the efficiency of such treatment on respiratory, hepatic, inflammatory and growth status.
To meet the objectives of the study, enrolled patients will receive daily oral or enteral methionine administration at increasing doses, under surveillance of plasma levels of methionine and homocysteine, and possible clinical side effects, until determining the "ideal" dose for each patient.
Once daily dosage determined for each patient, this dosage will be continued for a total of 2 months with daily clinical monitoring of tolerance and bi-monthly plasma levels surveillance of methionine and homocysteine.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Alveolar Proteinosis, Mutation Ala393Thr of the MARS Gene, mutationSer567Leu of the MARS Gene
Keywords
Pulmonary alveolar proteinosis, MARS gene, methionine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Methionine
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Methionine
Intervention Description
Administration of methionine from D1 to D60
Intervention Type
Drug
Intervention Name(s)
Vitamin B12, B9, B6, C supplementation
Intervention Description
In case of hyperhomocysteinemia
Intervention Type
Diagnostic Test
Intervention Name(s)
Methionine/homocysteine Dosage
Intervention Description
Plasma concentration control of methionine and homocysteine from D0 to D75
Intervention Type
Diagnostic Test
Intervention Name(s)
Thoracic CT scan
Intervention Description
At D60
Intervention Type
Diagnostic Test
Intervention Name(s)
Abdominal and liver ultrasound.
Intervention Description
At D60
Intervention Type
Diagnostic Test
Intervention Name(s)
Brain MRI
Intervention Description
In case of abnormal neurological examination
Primary Outcome Measure Information:
Title
Tolerance Assessment
Description
No adverse event from day 0 to day 75.
Time Frame
From day 0 to day 75
Secondary Outcome Measure Information:
Title
Respiratory rate (cycles /min)
Description
number of cycles per minute
Time Frame
At day 0, day 15, day 30, day 45, day 60, day 75
Title
Oxygen need (L/min)
Description
Flow in L/min
Time Frame
At day 0, day 15, day 30, day 45, day 60, day 75
Title
Respiratory signs of struggle
Description
Presence or absence of signs
Time Frame
At day 0, day 15, day 30, day 45, day 60, day 75
Title
Lung lesions
Description
Lesions appearance on thoracic CT scan, scored form 0 to 4
Time Frame
At Day 60
Title
Lipo-proteinaceous material
Description
Fluid examination
Time Frame
At each bronchial-alveolar washes during the 2,5 months
Title
Weight
Description
To evaluate Nutritional status
Time Frame
At Day 15, Day 30, Day 45, Day 60, Day 75
Title
mid upper arm circumference / head circumference rapport
Description
To evaluate Nutritional status
Time Frame
At Day 15, Day 30, Day 45, Day 60, Day 75
Title
Hepatomegaly
Description
liver damage evaluate by physician during clinical examination
Time Frame
At Day 0, Day 15, Day 30, Day 45, Day 60, Day 75
Title
cholestasis and hepatic cytolysis
Description
liver damage evaluate by biological parameters : ASAT, ALAT, GGT, PAL, Bilirubin
Time Frame
At Day 0, Day 15, Day 30, Day 60, Day 75
Title
Hepatomegaly
Description
liver damage evaluate by echography
Time Frame
At Day 0 and Day 60
Title
C reactive protein
Description
Biological parameters to evaluate Systemic inflammation
Time Frame
At Day 0, Day 30, Day 60
Title
sedimentation rate
Description
Biological parameters to evaluate Systemic inflammation
Time Frame
At Day 0, Day 30, Day 60
Title
Immunoglobulin G level
Description
Biological parameters to evaluate Systemic inflammation
Time Frame
At Day 0, Day 30, Day 60
Title
Haemoglobin level
Description
Biological parameters to evaluate inflammatory anaemia
Time Frame
At Day 0, Day 30, Day 60
Title
Plasma concentration of methionine
Description
Variation of the concentration for each patient
Time Frame
From Day 0 to Day 75
Title
Plasma concentration of homocysteine
Description
Variation of the concentration for each patient
Time Frame
From Day 0 to Day 75
10. Eligibility
Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Minor Patient with alveolar proteinosis by double mutation Ala393Thr and SER567LEU of the MARS gene, genetically proven.
Patient in need of prolonged hospitalization in Necker for treatment of bronchial-alveolar washes in the context of care.
Patient for which methionine can be administered orally or by enteral probe (Nasogastric or gastrostomy probe)
Signed Informed consent form by parents / legal guardian
Exclusion Criteria:
Patient with alveolar proteinosis by other mutations of the MARS gene
Patient with alveolar proteinosis secondary to another etiology or without identified cause
Refusal to participate in the study
High blood pressure requiring drug treatment
Heart failure
Known hypersensitivity to one of the substances used or potentially used in the study: methionine, vitamins B6, B12, B9 and C
Pre-Hypermethioninemia (Methioninemia > + 2 DS of normal for age) whatever the cause
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alice HADCHOUEL, PhD
Organizational Affiliation
Hospital Necker Enfants Malades
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Necker-Enfants Malades
City
Paris
State/Province
Ile De France
ZIP/Postal Code
75015
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34503986
Citation
Hadchouel A, Drummond D, Pontoizeau C, Aoust L, Hurtado Nedelec MM, El Benna J, Gachelin E, Perisson C, Vigier C, Schiff M, Lacaille F, Molina TJ, Berteloot L, Renolleau S, Ottolenghi C, Treluyer JM, de Blic J, Delacourt C. Methionine supplementation for multi-organ dysfunction in MetRS-related pulmonary alveolar proteinosis. Eur Respir J. 2022 Apr 21;59(4):2101554. doi: 10.1183/13993003.01554-2021. Print 2022 Apr.
Results Reference
derived
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Administration of Methionine in Patients With Pulmonary Alveolar Proteinosis by Mutation of the MARS Gene.
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