Drug treatments for obesity: Difference between revisions
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<ref>Tziomalos K ''et al.'' | <ref>Tziomalos K ''et al.'' The use of sibutramine in the management of obesity and related disorders: An update. ''Vascular Health and Risk Management'' 5:1 pp. (2009) 441-452.</ref> | ||
<ref>"Part 2," Appetite and obesity. 2006. Retrieved July 21, 2009 from [http://www.appetiteandobesity.org/part2.html http://www.appetiteandobesity.org/part2.html]</ref> | <ref>"Part 2," Appetite and obesity. 2006. Retrieved July 21, 2009 from [http://www.appetiteandobesity.org/part2.html http://www.appetiteandobesity.org/part2.html]</ref> |
Revision as of 08:53, 9 October 2009
This page was started in the framework of an Eduzendium course and needs to be assessed for quality. If this is done, this {{EZnotice}} can be removed.
A brief overview of your interest group (be sure to put its name in bold in the first sentence) and the scope of the article goes here.[1]
The following list of sections should serve as a loose guideline for developing the body of your article. The works cited in references 2-5 are all fake; their purpose is to serve as a formatting model for your own citations.
Introduction
History
In here you could write about various informations linked to various references for example from journals. [2] [3]
Limited Efficacy
You can also insert diagram.
Serotonin & Noradrenaline Related Drugs
By Bruce McLintock
Endocannabinoids
By Neil R. J. Watson [6]
One method of pharmaceutically tackling obesity is to give cannabinoid receptor type 1 (CB1 receptor) antagonists such as rimonabant. Mice genetically engineered to be deficient in CB-1 receptors have been shown to be resistant to diet induced obesity. Numerous clinical trials have demonstrated weight loss in obese subjects, as well as improving the ratio of good (HDL) to bad (LDL) cholesterol. However, a major issue in using CB1 antagonists is the incidence of psychiatric problems, in particular, depression (unfortunately several suicides occured during trials). As a result, the FDA has not approved the use of rimonabant in the United States. The European Medicines Agency (EMEA) has recommended the marketing authorisation of rimonabant be suspended across the EU, and consequently NICE has withdrawn its guidance for the use of the drug.
http://eurheartj.oxfordjournals.org/cgi/reprint/ehn255v1.pdf
http://www.nice.org.uk/TA144
Peripheral Drugs
By Rachael Kirkbride
[REMINDER TO SELF: NEED BIT MORE ON METHOD OF ACTION, AND OTHER PERIPHERAL DRUGS]
‘Peripherally acting anti-obesity drugs’ are another class of medication aimed at causing weight loss in overweight and obese individuals. These work by reducing the calorie intake from food, or altering the metabolism of it in the gastrointestinal system (gut). There is currently only one drug of this kind that is approved for use globally - Orlistat (Xenicol) - and it works by inhibiting the enzyme lipase that breaks down fat in the gut, meaning that the fat cannot be absorbed from food, and instead it is excreted out of the body.[R3]. Studies have shown that is can reduce the amount of fat absorbed from the gut by 30%, causing a decreased calorie intake and therefore weight loss. The weight loss from taking this medication is found to be between 5-10% on average.[R2][R6]. As well as weight loss, Orlistat has been shown to improve several other cardiovascular risk-factors. Low-density lipoproteins (LDL) and triglyceride levels were shown to be reduced by 10% more than expected for the weight loss, as well as blood pressure, waist circumference and lipids being reduced.[R2][R5]. Some research also suggests that Orlistat reduces fasting glucose and HbA1c levels in type 2 diabetics by more than predicted for the weight loss, with suggested methods including increased insulin sensitivity and glucagon-like peptide-1 secretion in the small intestine. Orlistat also helps to reduce the risk of type 2 diabetes in obese subjects by 37.3%. [R2].
However, this drug does not come without some side-effects. Oily-spotting, flatulence, abdominal cramps, faecal urgency/incontinence and liquid stools are the common adverse effects of Orlistat, due to an increase of fat in the gut and stools.[R3]. These side-effects are reported to only be experienced during the early stages, “but they subside as patients learn to use the drug”.[R4]. Orlistat also prevents some absorption of fat-soluble vitamins (A,E,D,K), and so patients are recommended to take supplements.[R3]. The drug does not have any systemic side-effects as it is contained in the gut, however it does affect the absorption of acyclovir, and they shouldn’t be used at the same time. [R4].
In 2001 the NHS National Institute for Health and Clinical Excellence (NICE) issued a press release on guidance for Orlistat use, and it states that it is cost effective to the NHS.[R8]. Studies have also shown that Orlistat is a cost-effective drug in obese adults.[R2].
Other Drug Therapies
Off Label Uses of Prescribed Medication
Anti-Diabetic Medication
M1 - Reference: Review: Role of metformin for weight management in patients without type 2 diabetes [Desilets A. R.]
M2 - Reference: Review: Is there a role for metformin or acarbose as a weight-loss agent in the absence of diabetes? [Siraj E. S.]
Diuretics
M3 - Reference: Review: Effects of Antihypertensive Therapy on insulin Resistance [Kaplan N. M.]
Thyroid Hormones
M4 - Reference: Review: Thyroid hormones in the pathogenesis and treatment of obesity [Krotkiewski M.]
M5 - Reference: Review: New Targets for Obesity Pharmacotherapy [Aronne L. J.]
Caffeine
M6 - Reference: Review: The safety and efficacy of pharmaceutical and herbal caffeine and ephedrine use as a weight loss agent [Greenway et Al.]
M7 - Reference: Review: Obesity and thermogenesis related to the consumption of caffeine, ephedrine, capsaicin, and green tea [Diepvens et Al.]
Amphetamines & Cocaine
M8 - Article: Paper: Hypothalamic CART is a new anorectic peptide regulated by leptin [Kristensen et Al.]
Ephedrine
M9 - Reference: Review: Obesity and thermogenesis related to the consumption of caffeine, ephedrine, capsaicin, and green tea [Diepvens et Al.]
Conclusion
References
- ↑ See the "Writing an Encyclopedia Article" handout for more details.
- ↑ First Author and Second Author, "The perfect reference for Subpart 1," Fake Journal of Neuroendocrinology 36:2 (2015) pp. 36-52.
- ↑ First Author and Second Author, "Another perfect reference for Subpart 1," Fake Journal of Neuroendocrinology 25:2 (2009) pp. 62-99.
- ↑ Tziomalos K et al. The use of sibutramine in the management of obesity and related disorders: An update. Vascular Health and Risk Management 5:1 pp. (2009) 441-452.
- ↑ "Part 2," Appetite and obesity. 2006. Retrieved July 21, 2009 from http://www.appetiteandobesity.org/part2.html
- ↑ Authors names, "The perfect review for part 3," Publishers City (2009)