Sphingolipidomic Profile in Anorexia Nervosa

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorIstituto Auxologico Italiano

About this trial

: The objective of this research project will be to determine the sphingolipidomic profile in a group of women (\> 18 years) affected by Anorexia Nervosa (AN), phenotypically characterized (restricting \[AN-R\] vs binge-eating purging \[AN-BP\]). Specific questionnaires will be administered for the definition of the severity of the eating disorder and depressive state (suicidality), to which will be added the evaluation of gonadal function (i.e., plasma levels of estradiol/progesterone and use of oral contraceptives).

Based on the specific lipidomic profile, which the present research project hopes to characterize, it will be possible to appropriately modify the diet of rehabilitation programs and, in the future, improve the effectiveness of the treatment itself, especially in the long term.

Eligibility criteria

Qualifiers

Female sex

Age: 18 years or older

Diagnosis of Anorexia Nervosa in the acute phase

Hospitalized at the Division of Eating and Nutrition Disorders (END), San Giuseppe Hospital, Istituto Auxologico Italiano, IRCCS, Piancavallo (VB), Italy

Disqualifiers

Absence of signed Informed Consent

Female sex

Age: 18 years or older

BMI between 18.5 and 24.9 kg/m2

Trial design

Treatments tested in this trial

  • Determination of sphingolipidomic profile

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators