To determine 1) the differences in the effects of food stimuli on the activation of brain regions associated with energy homeostasis and reward between women with chronic AN, women recovered from AN and healthy normal-weight women, 2) theā¦
ID
Source
Brief title
Condition
- Appetite and general nutritional disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
1) The brain activation associated with viewing food stimuli. 2) Serum
concentrations of leptin, ghrelin and PYY. 3) Measures of cognitive
functioning, in particular the Wisconsin Card Sorting Test (set shifting
ability), and the Iowa Gambling Task (decision making performance).
Secondary outcome
1) Subjective ratings of the desire to eat, 2) Subjective ratings of anxiety,
3) Energy intake (kJ) from the test meal.
Background summary
Anorexia Nervosa (AN) is a psychiatric disease which has a poor outcome due to
lack of effective treatment. AN is characterized by obsessive fears and
behavior with regard to food, weight and shape, which are all under strong
cognitive control in patients. Although patients are constantly thinking of
food, they refuse to eat. The central regulation of food intake behaviour is
governed by different interacting brain systems. The homeostatic system
regulates the balance between energy intake and energy expenditure and is
affected by peripheral signals such as hormones. The hedonic system deals with
the reward value of (food) stimuli and has neural circuits which encode wanting
(incentive motivation) and liking (pleasantness). On top of these systems, the
cognitive control system can strongly modulate the decision to eat or to
refrain from eating. In contrast with the majority of people, patients with AN
are able to starve themselves by restricting their food intake and ignoring the
drive to eat.
The eating behavior of AN patients is usually studied by looking at 1 of these
systems. Since such studies have not been able to find a good explanation for
the ambivalence towards food seen in AN patients, in this study we will examine
the integration of these 3 systems.
Study objective
To determine 1) the differences in the effects of food stimuli on the
activation of brain regions associated with energy homeostasis and reward
between women with chronic AN, women recovered from AN and healthy
normal-weight women, 2) the correlation between hormone concentrations and
these brain responses and 3) how variation in these brain responses correlates
with measures of cognitive functioning.
Study design
A cross-sectional experimental study. In the morning, subjects will undergo a
20 minute MRI scan. First, a perfusion MRI scan will be made. Second, a 15-min
functional MRI scan will be made, during which subjects will be shown images of
foods (varying in palatability) and of non-foods. During the functional scan,
participants rate their level of anxiety and their liking for the foods they
have been shown.
Intervention
MRI during the presentation of food images.
Study burden and risks
The experiment is non-therapeutic to the subjects and will consist of one study
session. During screening, subjects will be asked to answer to questionnaires
on eating disorders, personality traits, depression and anxiety to rule out any
inflicting psychiatric morbidity. On the study day, length, weight and % body
fat will be measured by measuring height and weighing subjects on a TANITA (an
impedance measurement device). Furthermore, a single fasting blood sample will
be drawn to determine the concentrations of relevant hormones involved in food
intake regulation. After blood sampling, the subjects will be scanned once with
the use of an MRI scanner for 20 min, during which they will rate their anxiety
and desire to eat. The same functional MRI paradigm has been used with AN
patients in the Institute of Psychiatry in London and it poses no risk.
Functional MRI is a safe and non-invasive technique. The tasks used for
assessing cognitive functioning have been extensively used in AN patients and
are not considered to be a burden; they are even perceived as amusing to
perform. In summary, the risk associated with participation is assessed as
negligible and the burden as minimal.
Heidelberglaan 100
3584 CX Utrecht
Nederland
Heidelberglaan 100
3584 CX Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
- Right-handed
- Chronically ill AN patients should have suffered from the illness for at least two years (as defined by the DSM IV criteria) and have a BMI below 17.5 kg/m2.
- The women recovered from AN should be weight-recovered for at least 1 year (BMI > 17.5 kg/m2) and have a regular menstrual cycle
- Healthy control women should have a normal BMI, i.e. between 18.5 and 25 kg/m2 and a regular menstrual cycle.
Exclusion criteria
- Contra-indications to MRI scanning on the basis of the MRI screening form, including: Claustrophobia, pregnancy, metal objects in the body incompatible with MRI scanning.
- Having a history of or current excessive alcohol consumption (> 28 units per week)
- Having a drug dependency
- Smoking daily
- Having a history of medical or surgical events that may significantly affect the study outcome.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL28258.041.09 |