Lymphatic Phenotype in Noonan Syndrome Spectrum Disorders

Lymphatic Diseases Clinical Trial

— LENS  

Official title:

Lymphatic Phenotype in Patients With Noonan Syndrome Without a Clinical History of Lymphatic Disease

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06267807
• Other study ID #: 114369
• Secondary ID: NL84520.091.23
• Status: Recruiting
• Phase: N/A
• Start date: March 27, 2024
• Est. completion date: June 1, 2025

Study information

• Verified date: January 2024
• Source: Radboud University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To get a better insight into the central conducting lymphatic system in adult volunteers with Noonan Syndrome (NS) without clinical symptoms or signs of lymphatic disease compared to NS and CardioFacioCutaan syndrome patients with severe lymphatic disease

Description:

Rationale: Noonan Syndrome Spectrum Disorders (NSSDs) are caused by pathogenic variants in genes of the Ras/MAPK signaling pathway, and belong to the RASopathy.

Lymphatic disease occur in 36% of patients with Noonan Syndrome (NS) during their lifetime, with different symptoms, severity, and onset. However, it is unknown how many patients with RASopathy are exactly impaired with lymph flow disorders, since many of these patients have unrecognized symptoms and go undiagnosed. For example, patients diagnosed with primary lymphedema (which implies being without known etiologic cause) may have an anatomic or functional abnormality of the central conducting lymph system that is not diagnosed as the causative lymph flow problem. With the diagnosis being based on the symptoms and not on the underlying pathophysiological mechanism, therapy will focus on diminishing symptoms and not on healing the pathophysiological cause. To eventually improve therapeutic intervention, a better understanding of the pathophysiology is necessary, and may be found by studying the central conducting lymphatic system of patients with NS and lymphatic disease, and adult volunteers with Noonan Syndrome without lymphatic disease. Objective: To get a better insight into the central conducting lymphatic system in adult volunteers with Noonan Syndrome (NS) without clinical symptoms or signs of lymphatic disease compared to NS and CardioFacioCutaan syndrome patients with severe lymphatic disease and healthy volunteers. (ongoing study: (Lymphomics; improving the understanding the anatomy of the lymphatic system and the direction and velocity of lymph flow; approved by the Medical Ethics Committee at Radboud University Medical Center Nijmegen file number 2021-7514) Study design: A single center, prospective collection of data Study population: Adult volunteers with Noonan Syndrome without (a history of) complaints or signs of lymphatic disease. Intervention: Three questionnaires (general health, lymphatic abnormalities and general MRI safety) will be taken prior to the dynamic MR lymphangiography. In addition to standard physical examination and electronic patient file screening, for inclusion and exclusion purposes. Subsequently, the MR lymphangiography will be performed. After 24 hours, the subject will be called for a follow-up by phone. Main study parameters/endpoints: the anatomy of the central lymph vessels, the velocity and direction of lymph flow, which can be compared with reference values. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Participation in this study places subjects at minimal risk. Subjects will undergo placement of a small needle in an inguinal lymph node on both sides, with very little risk of bleeding and/or infection, as with other minimal invasive procedures. The dynamic MR lymphangiography will take approximately two hours

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 15
• Est. completion date: June 1, 2025
• Est. primary completion date: March 13, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Noonan Syndrome confirmed by genetic test with a class 4 or 5 pathogenic variant according to ClinVar

• 18 years and older (no restriction for sex)

• Willing and able to have MR lymphangiography scanning in the Radboudumc

• Oral and written informed consent

• None of the exclusion criteria

Exclusion Criteria:

• unsuitable for MRI (e.g. metallic objects in the body, severe claustrophobia)

• A history of symptoms related to lymphatic disease

• pregnancy

• renal insufficiency

• liver cirrhosis

• History of surgery related to cardiovascular disease with hemodynamic consequence

• Other genetic diseases

Related Conditions & MeSH terms

• Lymphatic Disease
• Lymphatic Diseases
• Noonan Syndrome
• Syndrome

Intervention

Diagnostic Test:
• Dynamic contrast-enhanced lymphangiography
The subject is placed supine on a detachable MR imaging table, outside the scanning room. Both inguinal regions are prepared under sterile conditions. Using Ultrasound guidance, the thoracic duct outlet at the left venous angle is identified. Under US guidance, a small 25 gauge needle is placed at the corticomedullar junction of an inguinal lymph node on each side. The needle position is confirmed and checked that there is no extravasation at saline injection under US visualization. The subject is then transferred to the MR imaging machine. First, pre-contrast imaging is performed, this takes around 20 minutes.

Locations

Country	Name	City	State
Netherlands	Radboudumc	Nijmegen	Gelderland

Sponsors (1)

Lead Sponsor	Collaborator
Radboud University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Demographics age	Age (years)	Demographics will be assessed before the start of the scan
Other	Demographics gender	Gender	Demographics will be assessed before the start of the scan
Other	Demographics	body height (centimeters)	Demographics will be assessed before the start of the scan
Other	Demographics weight	Weight (Kg)	Demographics will be assessed before the start of the scan
Other	Demographics clinical history	Clinical histroy of lymphatic disease trough a questionnaire with yes/no questions	Demographics will be assessed before the start of the scan also used for inclusion
Other	Demographics genetic background	Genetic background of the participant will be assessed trough questionnaire, or if available trought the electronical patient record. Both the gene, as well as C-DNA changes will be noted.	Demographics will be assessed before the start of the scan also used for inclusion purposes
Primary	Central lymphatic system anatomy and flow descriptive parameters.	Categorical assessment of the anatomy and lymphatic flow in the central lymphatic system. Including the presence or absence of the central lymphatic vessels, edema and fluid collections.	Through study completion, an average of 1 year.
Primary	Diameter Thoracic duct	Measurements consist of the maximal diameter of the thoracic duct, the diameter at the level of the diaphragm, and the width and length of the cisterna chyli.	Through study completion, an average of 1 year.
Primary	Lymph flow velocity	Lymph flow velocity will be determined on the dynamic MR lymphangiography by measuring the distance of contrast movement covered over time in cm/min.	Through study completion, an average of 1 year.