Identifying Variants in MC4R Pathway-Associated Obesity With Novel Hyperphagia Questionnaires

Overview

Información sobre este estudio

The purpose of this study is to assess the ability of the hyperphagia questionnaires to identify children and young adults with early-onset obesity for genetic testing to identify variants in 36 genes of interest associated with MC4R pathway genetic obesity

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Patients who are or will be included in POWER registry.
  • Patients aged 6 to 26 years at time of recruitment for the current study.
  • Patients who satisfy the criteria for early-onset obesity:
    • Criteria to identify early-onset obesity among patients aged 6 to 26 years will be consistent with the criteria used for the Uncovering Rare Obesity® Program, as follows:
      • For patients aged 6 to 18 years at study recruitment::
      • The patient’s body mass index (BMI) is ≥ 97th percentile at recruitment based on the Centers for Disease Control (CDC) charts, and;
      • The patient has early-onset obesity.
      • Early-onset obesity will be determined based on historical records of weight, height, age, and gender in the electronic medical record or patient chart using the following definitions:
      • Historical measurements from age < 2 years: sex-specific weight for recumbent length is ≥ 97.7th percentile on the World Health Organization (WHO) charts.
      • Historical measurements from age 2-5 years: BMI ≥97th percentile based on the CDC charts.
      • Only patients with verified weight and height information before the age of 6 years and who meet the criteria of early-onset obesity will be included in the study. For new patients without available measurements to confirm early-onset obesity (electronic medical record, patient chart and/or POWER data), at least 1 weight and height measurement prior to the age of 6 years will be obtained by the study investigator at each participating site (either from the electronic medical record or from the patient’s primary care provider).
      • For patients aged ≥ 18 years at study recruitment:
      • The patient’s BMI is ≥ 40 kg/m^2 at recruitment AND
      • The patient has early-onset obesity (as defined above), as documented in the electronic medical record or patient chart.

Exclusion Criteria: 

  • Patients with prior testing for variants in the 36 genes of interest.
  • Patients who have any of the following potential causes of secondary obesity:
    • Endocrine diagnoses (e.g., hypothyroidism, Cushing syndrome, growth hormone [GH] deficiency);
    • Neurologic diagnoses.;
    • Intracranial injury (including, but not limited to: tumor, trauma, surgery, pituitary resection, irradiation);
    • Hypothalamic obesity;
    • Medication-induced weight gain, as determined by the Investigator.

Eligibility last updated 8/31/22. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Seema Kumar, M.D.

Cerrado para la inscripción

Contact information:

Katrina Olson CCRP

(507) 266-1078

Pierce.Katrina@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20544094

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