Mitochondrial Diseases Clinical Trial
Official title:
Phase II Feasibility Study of the Efficacy and Acceptability of a Low Residue Diet in Adult Patients With Mitochondrial Disease
Slow movement of patients guts is referred to as intestinal dysmotility, and is increasingly
recognised as a debilitating manifestation of mitochondrial disease both in adults and
children.
To date, symptoms of slow gut movements have been managed with laxatives and drugs that
increase movement of the guts with variable results. A low residue diet is a form of low
fibre diet (<10g fibre per day) that is used to minimise symptoms of poor movement of the
guts. This reduces fecal volume and bulk, and hence gut workload, ensuring limited bowel
activity and colonic rest. It has been shown to be well accepted in other conditions
associated with slow gut movements. However, its role in patients with mitochondrial disease
is unknown. The investigators are particularly interested in:
- Does a low residue diet (low fibre) cause a change in the number of stools per week and
stool consistency?
- Is a low residue diet tolerated well and easy to comply with?
- Does a low residue diet reduce gut symptoms of abdominal pain, bloating, and
constipation?
- Does a low residue diet improve quality of life and disease burden?
- Does a low residue diet affect the bacteria in the gut?
- Can we prove by X-ray that movement of food through the gut is slowed in patients with
mitochondrial disease, and whether a low residue diet alters the speed of movement of
food through the gut?
- Can a low residue diet change patients physical activity levels?
- Does a low reside diet change dietary patterns and food intake?
- Does a low residue diet alter anthropometrics, such as weight, body mass index and waist
to hit ratio?
- Can a low residue diet improve kidney and liver function and lipid profile in blood
samples?
The investigators hope that by looking at these areas that a low residue diet may be able to
improve patients slow gut movements, health, quality of life and disease burden.
Intestinal dysmotility is increasingly recognised as a debilitating manifestation of
mitochondrial disease both in adults and children (1). It is a frequent symptom of other
neurological conditions including Cerebral Palsy, Multiple Sclerosis and Parkinson's Disease.
Symptoms of intestinal dysmotility are often overlooked and frequently under-diagnosed in its
early stages.
Indeed, in its most severe form, intestinal dysmotility may manifest as intestinal pseudo
obstruction (IPO), characterised by a clinical picture suggestive of mechanical obstruction,
exemplifying the need for early detection and management. To date, symptoms of intestinal
dysmotility in slow transit time constipation, limited fluid and calorie intake, weight loss,
and small intestinal bacterial overgrowth and in severe cases intestinal pseudo obstruction
(2, 3). Moreover, the bacteria that reside within the gastrointestinal (GI) tract compete for
nutrients, contributing to weight loss due to malabsorption of fat (4), protein and
carbohydrates (5, 6), vitamin (7-11) and iron deficiency (12) are often evident. Further
problems include poor digestion and absorption food, an impaired immune system, and an
impaired drug absorption ability, all of which influence patient health, quality of life and
increases National Health Service (NHS) costs.
A low residue diet is a form of low fibre diet (<10g fibre per day) that is used to minimise
symptoms of intestinal dysmotility by reducing faecal volume and bulk and hence bowel
workload, ensuring limited bowel activity and colonic rest. It has been shown to be both
tolerable and efficacious in other conditions associated with intestinal dysmotility;
however, its role in patients with mitochondrial disease and intestinal dysmotility, is
unknown.
This feasibility study proposes to systematically gather data on whether a low residue diet
is tolerable and has an effect on intestinal dysmotility and health-related quality of life
in in patients with mitochondrial disease.
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