Anorexia Nervosa Clinical Trial
Official title:
How do Glutathione Levels Affect Compulsivity? A Double-blind, Placebo-controlled Study
The investigators will examine whether compulsivity in those who score above-average (but below clinical cut-off) on an eating disorder questionnaire can be altered by 9 days of N-acetyl cysteine (NAC). N-acetyl cysteine has been shown to be of some benefit in individuals with other compulsive disorders, such as trichotillomania and addiction, so this research investigates whether a short period of time taking N-acetyl cysteine changes compulsivity, measured using cognitive tasks and questionnaires.
Anorexia nervosa is a psychiatric disorder with a high mortality rate and for which there is
very little evidence for pharmacological interventions of value. The picture is similar in
bulimia nervosa, with a high mortality rate and with mixed outcomes from studies testing
Selective Serotonin Reuptake Inhibitors (SSRIs). It is possible to conceptualise eating
disorders as akin to compulsive disorders, especially noting that repetitive weighing,
calorie counting and compulsive exercise and compensatory mechanisms might fit into a
hypothetic obsessive-compulsive spectrum (OC spectrum). Some disorders on this OC spectrum
are associated with oxidative stress. This may also be true in eating disorders: it has
recently been found in a meta-analysis that there is evidence of increased oxidative stress
markers in AN.
Glutathione is the main cellular anti-oxidant in mammals and it is possible to increase
glutathione levels (and thus potentially combat oxidative stress) with a dietary supplement
called N-Acetyl Cysteine (NAC). NAC is an acetylated form of the naturally occurring amino
acid cysteine, and is converted to cysteine in the body. Cysteine is a key precursor of
glutathione. Oral administration of cysteine itself does not increase brain glutathione
levels because cysteine is poorly absorbed from the gastro-intestinal tract. However NAC is
bioavailable and thus administration of it does increase glutathione in the brain.
Using NAC to increase glutathione levels has been shown to be beneficial in some compulsive
disorders such as addictions, Obsessive-Compulsive Disorder (OCD) and related disorders such
as trichotillomania in preliminary studies. There have been positive indications for use and
evidence in pathological gambling, trichotillomania, OCD and cocaine addiction. However, NAC
has not to our knowledge ever been considered for the treatment of eating disorders. This
research therefore aims to investigate whether increasing glutathione can reduce
neuropsychological markers of compulsivity in a group at risk for eating disorders.
The researchers have chosen to use a female non-patient group which is thought to be highly
compulsive, but which will also be without the possible confounds of medication (as in OCD or
addiction disorders) and without malnutrition (as in clinical eating disorders). Those
recruited will be females, because there is evidence that there may be different risk factors
and thus mechanisms underlying the development of eating disorders in males and females, such
that recruiting both might produce a confound. The investigators have also chosen to use a
short duration of NAC administration. This not only allows the use of a cross-over design
without fears of high attrition rates and non-compliance, but it also will allow the
detection of subtle and early changes in compulsivity. The hypothesis is thus that
improvements will be seen in tasks measuring compulsivity, and also potentially in tasks
which measure related constructs such as impulsivity, habit-based learning, and delay
discounting. The researchers do not expect improvement in self-report symptom questionnaires.
However, a possible future study would be a randomized clinical trial looking at increasing
glutathione in a clinical group over time and how it affects clinical symptomatology.
The questionnaires chosen will identify eating disorder symptom levels (the Eating Attitudes
Test - 26 (EAT-26) is a validated way of doing this) and look at compulsive starvation using
the self-starvation scale (Godier & Park 2015). The Structured Clinical Interview for the
Diagnostic and Statistical Manual of Mental Disorders-IV (SCID) will be used to rule out
those with a current Axis I diagnosis including an eating disorder, to prevent the
complications of starvation and medication in this initial pilot study. The Eysenck
Personality Questionnaire (EPQ) will be used to ascertain personality traits, and the
National Adult Reading Test (NART) will be used to estimate Intelligence Quotient (IQ).
The rationale for choosing the tasks was based on the hypothesis that compulsivity may be
improved by increasing glutathione levels. Thus, the tasks chosen are designed to pick up
differences in different facets of compulsivity. The Wisconsin Card Sorting Task (WCST) is
able to quantitatively measure set shifting, which is known to be impaired in eating
disorders (Roberts et al. 2007) and is a facet of compulsivity. The Affective Go/No go picks
up on attention bias within the umbrella of compulsivity; and the Attention Switching task
picks up the ability to switch attention between different task demands, within the same
compulsivity umbrella. The Cambridge Gambling Task is a good measure of disadvantageous
decision making within the umbrella of impulsivity (which is thought to be orthogonally
related to, rather than opposite to, compulsivity) (Fineberg et al. 2014). The sequential
learning task has been used in OCD, where it is able to disentangle goal-directed learning
from habitual learning based on two computational algorithms. The hypothesis is that
compulsivity is related to a disturbance in goal-directed learning, with habit learning
preferred leading to rigid behaviours (Gillan & Robbins 2014) (Voon et al. 2015). Thus it
will be useful to see if more goal-directed and less habit learning occurs after increases in
glutathione levels. The delay discount task measures the ability to ignore delays in time
when considering reward value, which is relevant in eating disorders as often delay
discounting is reduced so performance is better (Steinglass et al. 2012). This has an
interesting interaction with impulsivity as it seems almost to be opposite to it, yet
anorexic patients have shown a better performance. Thus this task might be useful as an
exploratory measure. The Facial Expression Recognition Task (FERT) is very sensitive to early
changes in emotional biases after only small pharmacological changes, and as the profile of
individuals high eating disorder symptoms is different in this task compared to healthy
controls (Jones et al. 2008) - it can operate as a positive control to identify if increased
glutathione is having any effect on general emotional biases, even if it is not on
compulsivity.
Because the aim of the study is to see whether NAC may lower compulsivity by increasing
glutathione levels, a researcher will take a small venous blood sample (5mls) and a saliva
sample prior to testing in both arms of the study to check to what to what extent NAC
treatment elevates glutathione levels over placebo. Participants who do not wish to give
blood will not be excluded but asked to provide a saliva sample only. Blood and saliva will
be rendered acellular by centrifugation and stored until assay in the University Departments
of Chemistry and Pharmacology. Once assayed any remaining sample will be discarded according
to Standard Operating Procedures for sample disposal.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05531604 -
Appetitive Conditioning in Anorexia Nervosa
|
||
Enrolling by invitation |
NCT04174703 -
Preparing for Eating Disorders Treatment Through Compassionate Letter-Writing
|
N/A | |
Active, not recruiting |
NCT04883554 -
Impact of an Olfactory Sensory Therapeutic Group for Adolescent Patients With Restrictive Anorexia Nervosa , Pilot Study
|
N/A | |
Recruiting |
NCT04213820 -
TMS and Body Image Treatment for Anorexia Nervosa
|
N/A | |
Completed |
NCT03414112 -
The Impact of Oxytocin on the Neurobiology of Anorexia Nervosa
|
Early Phase 1 | |
Recruiting |
NCT06144905 -
Norwegian Microbiota Study in Anorexia Nervosa
|
||
Recruiting |
NCT05803707 -
Home-based Adapted Physical Activity in Anorexia Nervosa: a Feasibility Pilot Study
|
N/A | |
Recruiting |
NCT05682417 -
Impact of Body Schema Distortion on Remission and Weight Regain in Anorexia Nervosa
|
N/A | |
Not yet recruiting |
NCT06380257 -
Anorexia Nervosa and Brain in Adolescence
|
||
Not yet recruiting |
NCT04804800 -
Virtual Reality Place in the Management of Body Dysmorphia Disorders in Anorexia Nervosa
|
N/A | |
Not yet recruiting |
NCT03600610 -
Evaluation of CARdiac Abnormalities by Echocardiography and MRI in Malnourished Patients Suffering From Anorexia Nervosa
|
N/A | |
Completed |
NCT02745067 -
Effectiveness of Enhanced Cognitive Behavioral Therapy (CBT-E) in the Treatment of Anorexia Nervosa
|
N/A | |
Completed |
NCT02382055 -
Changing Habits in Anorexia Nervosa: Novel Treatment Development
|
N/A | |
Terminated |
NCT02240797 -
Kappa Opioid Receptor Imaging in Anorexia
|
N/A | |
Completed |
NCT03075371 -
Homeostatic and Non-homeostatic Processing of Food Cues in Anorexia Nervosa
|
N/A | |
Completed |
NCT03144986 -
Insula-coil Deep TMS for Treatment Resistant Anorexia Nervosa
|
N/A | |
Unknown status |
NCT01761942 -
Fatty Acids Omega -3 Diet Supplementation Efficiency and Safety Evaluation in Anorexia Nervosa
|
Phase 2 | |
Completed |
NCT02551445 -
A fMRI Pilot Study of the Effects of Meal-support in Eating Disorders.
|
N/A | |
Completed |
NCT01579682 -
Adaptive Family Treatment for Adolescent Anorexia Nervosa
|
N/A | |
Completed |
NCT00946816 -
The Effects of Dietary Intervention on Gastrointestinal Function in Patients With Anorexia Nervosa and Obesity
|
N/A |