Obesity Clinical Trial
Official title:
Bariatric Embolization Trial for the Obese Nonsurgical
The purpose of this study is to assess the safety profile of bariatric embolizations and confirm published reports of sustained post-procedural weight loss, and pathologically assess post-procedural metabolic effects.
Since 2003, the proportion of Canadians who were obese has increased 17.5%. Obesity is ranked
as the fifth leading risk for mortality globally. Obesity has been strongly linked to
numerous comorbidities, including type II diabetes, hyperlipidemia, hypertension, obstructive
sleep apnea, heart disease, stroke, asthma, cancer, and depression.
The pathophysiology of obesity is complex and inadequately understood. Nevertheless, an
energy imbalance is fundamentally at fault. As recently as 1996, ghrelin, the hormonal
stimulus for hunger was identified. Further research has revealed that ghrelin, predominantly
produced in the fundus of the stomach, stimulates appetite and increases serum concentrations
of growth hormone, adrenocorticotropic hormone, cortisol, prolactin, and glucose.
Congruously, the complexity of obesity is reflected in the efficacy of modern therapy.
Treatment for obesity lies along a spectrum of available modalities beginning with diet
modification, exercise therapy, pharmacotherapy, and surgery. Despite initial positive
results, diet and exercise frequently prove futile for long-term management of weight loss.
Likewise, it is uncommon for diabetic remission to be achieved through pharmaco-therapeutic
agents, most of the medications designed to stabilize and improve diabetic control. This has
led to the advent of interventional treatment for these conditions.
Bariatric surgery is the current gold-standard in the treatment of morbid obesity with recent
evidence revealing that bariatric surgery is more effective than medical treatment for the
long-term control of obese patients with type 2 diabetes. It is postulated that in addition
to the restrictive effects associated with bariatric surgery, resection or disruption of the
ghrelin producing regions of the stomach may play a significant role in eventual weight loss.
The primary source of blood flow to the fundus of the stomach, where the majority of
ghrelin-producing cells are found, is the left gastric artery. This artery is commonly
accessed percutaneously for the management of refractory upper gastrointestinal bleeding.
Embolizations are typically well tolerated, therefore, it has been purported that selective
embolization of this artery could induce adequate ischemia to the fundus resulting in a rapid
decrease in ghrelin-producing cells along with its neurological and metabolic effects.
In 2007, Arepally et al reported a minimally-invasive method of destroying ghrelin-producing
cells in a porcine model. With mixed success, Arepally was able to demonstrate a correlation
between left gastric artery embolizations, weight loss, and fluctuations in ghrelin levels.
Propagation of his efforts was performed by Bawudun et al, utilizing a liquid sclerosant and
500-700-mm polyvinyl alcohol (PVA) particles as embolic agents, Bawudun was able to
demonstrate significant decreases in ghrelin and body weight measurements in the experimental
arms in a canine model. Subsequently, Paxton, et al. demonstrated lowered ghrelin levels and
reduced weight gain utilizing 40-micron microsphere particle embolizations in a similar
porcine model no duodenal upregulation for ghrelin was found. These studies also revealed
potential complications including non-target embolization, frank gastric ulcerations, and
gastritis.
Following these preclinical animal studies, Gunn and Oklu performed a small retrospective
study of patients who underwent a left gastric artery embolization for upper gastrointestinal
bleeds. The results, although limited, revealed significant weight loss amongst the
experimental group as compared with the control (patients who underwent embolization for
upper gastrointestinal bleeds without left gastric artery selection). Kipshidze et al
reported significant weight loss amongst all five patients who underwent the first-in-human
prospective left gastric artery embolization trial utilizing 300-500 µm microspheres. Human
trials have resulted in few reported complications, namely minor pyrosis and indigestion. The
safety profile of the procedure is well reported given that elective left gastric artery
embolizations are offered to stable patients with refractory non-variceal bleeds. Case
reports have reported on the uncommon instances of hepatic infarction, gastric infarction,
gastric volvulus, and arterial rupture.
The momentum behind this procedure has led to the design and implementation of two phase I
clinical trials [Gastric Artery Embolization Trial for the Lessening of Appetite
Nonsurgically (GET LEAN) and Bariatric Embolization of Arteries for the Treatment of Obesity
(BEAT Obesity)] which sought to demonstrate the safety profile of left gastric artery
embolizations and demonstrate post-procedural weight loss.
Results have been promising with weight loss and safety demonstrated in both trials.
Minor complications included post-procedural nausea, vomiting, and mild epigastric discomfort
which was treated with oral proton pump inhibitors (PPIs) following administration of one
course of intravenous (IV) PPIs. 3 asymptomatic gastric ulcers were identified on
post-procedural endoscopy however these resolved within 1 month (a 1-month endoscopy was
performed).
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