Creatine Metabolism in Rett Syndrome

Maastricht University Medical Centre (MUMC)

Status: Completed

Conditions: Rett Syndrome

Study type: Observational

Funder types: Other

Identifiers

NCT01198015

NL32481.068.10

MEC-10-2-038 (Other Identifier)

Details and patient eligibility

About

Rett syndrome (RTT) is an X-linked severe neurodevelopmental disorder. Despite their good appetite, many females with RTT meet the criteria for moderate to severe malnutrition. The pathological mechanism is barely understood. Although feeding difficulties may play a role in this, other constitutional factors as altered metabolic processes are suspected. Preliminary research showed elevated plasma creatine concentrations and increased urinary creatine/creatinine ratios in half of the RTT girls.

The aim of this study is to confirm previous findings and examine the functionality of the creatine transporter in RTT girls.

The investigators assume that previous findings will be confirmed, and are due to an altered functionality of the creatine transporter.

Enrollment: 13 estimated patients

Sex: Female

Ages: 3 to 20 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Clinical diagnosis of RTT (meeting consensus diagnostic criteria (Hagberg et al, 2002));
• MECP2-mutation;
• Complete neurophysiological work-up;
• Participant preliminary research (research protocol NL25356.068.08).

Exclusion criteria

• Male gender

Trial design

13 participants in 1 patient group

Rett syndrome girls

Description:

The study population (identical to the population in the preliminary research project) consists of a well-defined group of thirteen Dutch RTT girls with complete clinical, molecular, neurophysiological and metabolic work-up.