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Study of Metabolic Modifications in Children With Noonan Syndrome

Study of Metabolic Modifications in Children With Noonan Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02383316
Acronym
MetabNoonan
Enrollment
20
Registered
2015-03-09
Start date
2015-01-31
Completion date
2016-06-30
Last updated
2025-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Syndrome

Keywords

Insulin sensitivity, Metabolism, Noonan syndrome, Shp2

Brief summary

Noonan syndrome (NS) is a rare genetic disease (incidence 1/2500 live births) characterized by the association of craniofacial manifestations, cardiopathies, short stature, and tumor predisposition. The genetic causes of Noonan Syndrome are mutations of genes involved in the Ras/Mitogen-Activated Protein Kinases (MAPK) pathway, mainly the gene encoding the tyrosine phosphatase Shp2 (50% of patients).Shp2 appears to be involved in many facets of energy metabolism control (glucose homeostasis, adipose tissue function…), through mechanisms that are poorly understood. Several metabolic anomalies (reduced adiposity, improved glucose tolerance) have been recently identified in an original mouse model carrying Shp2 mutation. Moreover, recent clinical survey has shown that adult Noonan Syndrome patients are protected from developping overweight and obesity when compared to the general population. However, the metabolic status associated with Noonan Syndrome condition has not been explored to date.

Detailed description

Differential hormone sensitivity is associated with Noonan Syndrome and participates in the development of some symptoms. The investigators have demonstrated that MAPK upregulation in Noonan Syndrome is responsible for partial growth hormone (GH) insensitivity, and subsequent growth retardation. Clinical traits evocative of energy metabolism dysfunctions have been recently reported in Noonan Syndrome patients, although the origins and consequences of these metabolic changes have not been documented to date. The aim of this study is to explore the metabolic status of children with Noonan Syndrome. Children with Noonan Syndrome will be compared with age- and sex-matched healthy children. The investigators hypothesize than Noonan Syndrome children have an increased insulin sensitivity compared to GHD children. Study parameters will be collected including: clinical measurements (height, weight, body mass index, waist circumference, and blood pressure), glucose and insulin levels at baseline and after an oral glucose tolerance test (OGTT), body composition measured by dual-energy x-ray absorptiometry (DXA). The study will include only one visit.

Interventions

OTHEROral Glucose tolerance test

Oral glucose tolerance test (OGTT): glucose and insulin levels will be measured at time points 0, 90 and 120 min or 30, 60, 90 and 120 after 1.75 g/Kg (max 75 g) glucose administration depending of the patient weight.

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Noonan syndrome genetically confirmed * Informed consent obtained from children and parents

Exclusion criteria

* Chronic disease associated with variation of insulin sensitivity: body mass * Treatment associated with variation of insulin sensitivity: corticoid treatment \> 5 days preceding the study inclusion * Tumoral disease (leukemia) in treatment

Design outcomes

Primary

MeasureTime frameDescription
Insulin sensitivity determined from the calculation of the Quantitative insulin sensitivity check index (QUICKI).T0 on an empty stomachMeasured at the patient's arrival (TO) from the blood levels of glucose and fasting insulin

Secondary

MeasureTime frameDescription
Blood pressureT0These tests will be done on arrival in hospital before the oral glucose tolerance test. Blood pressure is measured after 10 minutes of rest in the elongated child.
Blood level of hemoglobin A1c and ghrelinT0 on an empty stomachBlood sample realised at T0 before the oral glucose tolerance test.
Body composition as fat mass and muscle mass measured by dual-energy x-ray absorptiometry (DXA)T0This test will be realised during hospitalisation day, except if it has been done up to 6 months prior to enrollment.
Insulin sensitivity determined with HOMA indexT30, T60, T90 and T120 minutes after oral glucose tolerance testGlucose and insulin levels will be measured at time points 0, 90 and 120 min (children weigh 17-25kg) or 30, 60, 90 and 120 min (children weigh \>25kg) after 1.75g/kg glucose administration (oral glucose tolerance test)
Waist circumferenceT0This test will be realised during hospitalisation day, at patient arrival.
Blood level of leptinT0 on an empty stomachBlood sample realised at T0 before the oral glucose tolerance test.
Blood level of ghrelinT0 on an empty stomachBlood sample realised at T0 before the oral glucose tolerance test.
Body mass indexT0This test will be realised during hospitalisation day, at patient arrival.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026