Inflammatory Response to Hydroxyurea Therapy in Sickle Cell Disease

Clinical Trial
Study Details
Enrollment
62
Interventions
Description

hydroxyurea 20-25 mg/kg/day since at least 3 months

Name
Hydroxycarbamide, Hydroxyurea (drug)
Type
Drug
Phase
N/A
Status
COMPLETED
Study ID #
NCT00784082
Study Type
Observational
Summary

In sickle cell disease (SCD), polymerisation of haemoglobin S and the resulting shape change of the red blood cells (RBC) lead to vascular occlusion and severe painful crises. Permanent inflammatory state and abnormal RBC adhesion to the endothelium trigger these phenomenon. Hydroxyurea (HU) is the only drug that has been shown to reduce clinical severity of SCD, and this was initially attributed to the stimulation of foetal haemoglobin (HbF). However, the clinical response does not correlate consistently with the degree and time of HbF increment, suggesting that HU clinical benefits may involve other mechanisms such as the induction of natural anti-inflammatory response via the hypothalami-pituitary-adrenal axis.

Study Overview
Conditions
Description

Plasmatic proinflammatory molecules (C-reactive protein, orosomucoid, RANTES, IL-6, IL-8, MCP-1, IL-1A, IL-1B, ET-1, IL-4, IL-10, TNFalpha, IFNgamma), hormones from the hypothalami-pituitary-adrenal axis (cortisol, ACTH), and hypothalamic peptids (arginine vasopressin, corticotrophin-releasing hormone) will be measured from SCD children treated or not with HU (20 treated children, 20 untreated children with a history of vaso-occlusive events, 20 asymptomatic children, and 20 healthy African controls).

Contacts and Locations
Locations
Facility

Hopital Louis Mourier
92701 Colombes
France

GeoPoint
48.91882, 2.25404