Vitamin D Clinical Trial
— VITADOSOfficial title:
Are Bone, Nutritional and Cardiovascular Status of French Children and Adolescents, Correlated With Their Vitamin D Status?
Verified date | February 2017 |
Source | Hospices Civils de Lyon |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Vitamin D is not seen anymore only as a phosphocalcic hormone, but also as having an effect
on global health (anti-infective, anti-inflammatory, anti-tumour roles and cardiovascular
protection).
The link between vitamin D deficiency and osteomalacia lesions is well-known. In paediatrics,
systematic vitamin D supplementation of infants and toddlers, associated with milk
enrichment, has allowed an almost total disappearance of rickets. Vitamin D repletion was
defined as the minimal concentration that enables the prevention of rickets in children and
osteomalacia in adults, that is approximately 8 ng/mL (20 nmol/L). However, in 2010, most of
the international experts agreed to set minimal threshold of 25 OH vitamin D serum
concentration, higher than the one previously admitted, with a limit of 20 ng/mL (50 nmol/L)
to define a vitamin D deficiency and a limit of 30 ng/mL (75 nmol/L) to define vitamin D
insufficiency in adults. In the paediatric population, the consensus is less obvious and we
consider that a serum concentration of minimum 20 ng/mL is necessary.
A study on more than 200 children from Lyon, followed in the paediatric nephrology unit and
having a renal function normal or sub-normal, demonstrated an important prevalence of vitamin
D deficiency (75%) in adolescents and pre-adolescents.
Concurrently, the appearance of new bone imaging techniques (especially high-resolution
peripheral quantitative computed tomography HR-pQCT) improved bone status evaluation in a
non-invasive manner.
Given the new pathophysiological data on pleiotropic role of vitamin D (bone, cardiovascular
system, adipose tissue) and given the proportion of French children possibly suffering from
vitamin D deficiency, it seems urgent to actualize current recommendations regarding
systematic supplementation in vitamin D. This transversal study on 200 healthy children and
adolescents will allow to have an overview of vitamin D status in French healthy children and
adolescents, studying with non-invasive, safe, reliable and innovative tools, the theoretical
targets of vitamin D (bones, cardiovascular system and nutritional status); and then to lay
the foundations of therapeutic trials aiming to evaluate the mode of vitamin D
supplementation for healthy children and adolescents; while having a cohort for HR-pQCT
measurements, that will allow us to have French reference range in a 10-17 year-old
population, for this innovative, non-invasive and low radiation exposure technique.
Status | Completed |
Enrollment | 100 |
Est. completion date | July 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 10 Years to 17 Years |
Eligibility |
Inclusion Criteria: - 10 year-old <or= Age < 18 year-old - Without mobility handicap (medical walker, crutch, wheelchair…) - Written informed consent (signed by parents) Exclusion Criteria: - History of treatment with growth hormone - History of treatment with oral corticoids, taken over more than 3 consecutive months - Current treatment with growth hormone, corticoids or anti-calcineurin - Treatment with aspirin or nonsteroidal anti-inflammatory drug within the last three weeks - Treatment with paracetamol within the last week - Chronic pathology with an impact on growth: - Parenteral nutrition - Chronic inflammatory disease (rheumatologic or digestive notably) - System diseases (lupus, granulomatosis, vascularitis) - Renal failure - Diabetes - Serious intercurrent disease (infection, neoplasia) - Ongoing pregnancy - Patient unaffiliated with the French universal healthcare system. |
Country | Name | City | State |
---|---|---|---|
France | Hôpital Femme Mère Enfant | Lyon |
Lead Sponsor | Collaborator |
---|---|
Hospices Civils de Lyon |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To study the correlation between the results of bone microarchitecture obtained by high-resolution peripheral quantitative computed tomography (HR-pQCT) and vitamin D serum concentration. | The HR-pQCT evaluates bones down to the level of the tiny individual elements that nature configures in a way that makes bones as strong as possible. HR-pQCT measures bone density and quantifies the three dimensional geometry, strength and microarchitecture of bone at the lower arm (radius) and lower leg (tibia). | up to 3 months | |
Secondary | Values and standard deviation of 25-OH vitamin D3 plasma concentration concentration in the population studied. | Blood intake. | Once. At inclusion (V1). | |
Secondary | To study the correlation between vitamin D plasma concentration and nutritional and pubertal status, cardiovascular status, inflammatory status . | Nutritional and pubertal status will be assessed thanks to: Body Mass Index, Dual-energy X-ray Absorptiometry, adipokines level. Cardiovascular status will be assessed thanks to arterial pressure, Intima-media Thickness (IMT), Extra-media Thickness (EMT), lipid profile, endothelial function. IMT and EMT will be obtained using carotid ultrasound. Endothelial function will be evaluated following a protocol of iontophoresis of acetylcholine and sodium nitroprusside. Inflammatory status will be measured looking at C-reactive protein plasma level. |
up to 3 months | |
Secondary | To evaluate the relation between bone parameters (HR-pQCT) and adipokines; and the relation between bone parameters and cardio-vascular data (blood pressure, IMT, EMT, lipid profile, endothelial function). | up to 3 months |
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