=======Obesity Powerpoint=======
{{:life-sci-4m03-group-1-obesity.pptx|}}
====== Obesity ======
Obesity is a common and preventable disease that is characterized by abnormal or excessive fat accumulation in adipose tissue.[1] The excess accumulation of fat leads to the impairment of health and is subsequently a major risk factor for the development of various non-communicable diseases such as diabetes, as well as premature death.[2]
{{:the_evolution_of_man.jpg?nolink|}}
===== Body Mass Index & Limitations =====
There are various methods which can be used to measure excessive adipose tissue in the body.[3] This includes skinfold thickness measurements, underwater weighing and bioelectrical impedance. The drawbacks of these methods is that they are not always readily available, the are either expensive or require highly trained personal to be conducted. In addition, many of these methods can be difficult to standardize, making it difficult for comparisons across studies and time periods.[3] Anthropometric measurements such as weight and height are the most basic methods of assessing body composition.[4] Specifically, body weight is the most frequently used measure of obesity.[4] Body mass index (BMI) is a metric that is used to assess body weight.[3] It is measured by dividing an individuals weight in kilograms by their height in meters squared. BMI is widely used as a risk factor for the development and prevalence of disease.[3]
{{ :obesity_scale.png |}}
The advantages of BMI are that it is useful for measuring obesity in a population.[4] It is a general measure of obesity that can be used for most individuals.[3] In addition, changes in BMI levels allow researchers to get a good idea of changes of obesity levels in a population.[3] Despite its strengths, BMI has many limitations when used to assess body weight.[4] For instance, it does not differentiate between lean and fat body mass. An individual may have a healthy weight according to their BMI, but still face health risks due to excessive body fat. Another limitation of BMI is that it overestimates health risks for individuals with increased muscle mass.[4]
===== Epidemiology =====
=== World Wide Prevalence ===
{{ ::prevalence.png?nolink|}}
Undoubtedly, obesity is a disease that continues to sweep the globe. Over the past 3 and a half decades alone, the obesity prevalence has nearly doubled.[5] In 2016, 650 million adults and 340 million children qualified as obese. Additionally, amongst children, 41 million under the age of 5 were considered overweight or obese.[6] This constitutes a worldwide count of 990 million obese individuals. From a statistical point of view, nearly 30% of the world’s population are overweight or obese.[7] Obesity tends to be more prevalent in women than in men, with 14% of women worldwide and 10% of men worldwide affected by the disease.[8,9]
=== Ethnic Prevalence ===
Majority of the world’s population live in countries where obesity and/or being overweight kills more people than from being underweight.[6] Obesity rates are greater in certain ethnic subpopulations. The rates range from lower than 6% in Korea and Japan to greater than 30% in the United States, Mexico, New Zealand, and Hungary. Canada, Australia, United Kingdom, Chile, and South Africa are a close second, with greater than 25% of adults categorized as obese in each of these countries. In Canada, the United States, Mexico, England, France, and Switzerland, obesity rates have been on a steady incline since the 1990s. It is believed that some countries have had stabilized prevalence of obesity, however, there is no definitive indication of reduction of the epidemic anywhere.[10]
=== Canadian prevalence ===
In Canada, an estimated 14 million adults and 470,000 youth are characterized as obese.[11] Approximately 25% of Canadians are obese. Two provinces, British Columbia and Quebec, have the lowest levels of obesity. The greatest prevalence is observed in the Northwest Territories and Newfoundland and Labrador. City-wise, the lowest levels of obesity are seen in Canada’s three largest cities: Toronto, Montreal and Vancouver.[12]
=== Ontario (local) prevalence ===
Ontario has been reported to have a province-wide obesity prevalence of about 25%, which is the same as the national average. However, some Ontario cities ranked in the higher end, with Sudbury, Brantford, Hamilton, and Thunder Bay being the second, fourth, fifth and seventh most obese cities, respectively, in the country.[12]
===== Evolutionary Basis of Obesity =====
===Human babies and the need for fat ===
Human babies have the highest percent fat at birth for mammals.[13] They have 15% body fat at birth. The second highest mammal for body fat % is the guinea pig, with 10.8. Adipose tissue is used as insulation to prevent heat from escaping the body. Human beings are hairless mammals, and therefore, are exposed to environmental stressors more directly then say a polar bear. The fur a polar bear has allows it to survive at temperatures as low as -69 degrees Celsius, even though they have a lower fat percentage than humans. Another reason humans require a high fat percentage at birth is because of the size of their brains. It is estimated that the infant brain consumes 50-60% of its total metabolic expenditure.[14] The brain is not only an expensive organ, but it is also a sensitive one. It requires lots of fat to maintain itself and grow, as well as insulation to keep it at a steady temperature of around 38 degrees Celsius. This explains our natural tendency to store fat more effectively than other mammals.
An important question remains: If obesity is such a detrimental condition to the human population, then why is it so evident today?
=== Theory One ===
Evolutionarily speaking, the ability to store fat is quite the effective adaptation. Food supplies could be abundant one day, and depleted the next. This is why it is believed that another major reason for fat storage in humans is in fact an energy reserve.[15] Although obesity is quite the pandemic in many developed nations today, it was rare throughout our evolutionary history within primitive populations. In fact, there is evidence to suggest no obesity within traditional hunting and gathering populations.[15] Regardless, those with genes that promoted greater storage of fat had a higher likelihood to survive when resources became scarce. This has led to evolutionary pressures to select for genes doing just that. In the next section concerning gender and obesity, this is elaborated in more detail.
=== Theory Two ===
Obesity was often perceived as a status of wealth and power.[15] This is because only those who had access to high energy foods on a year round basis were able to actually become overweight. This would have lead it to be a desirable trait of the opposite sex over evolutionary time.
===== Obesity and Gender =====
Obesity is seen primarily in females versus males.[16] Figure 1 shows the distribution of obesity by gender for differential income as well as geographic location. It is clear that regardless of social status or ethnic location the overwhelming majority of obese and overweight individuals are in fact female.In fact, 15% body fat is average for males and 25% is average for females.16 This is the case for several reasons. Firstly, woman (evolutionarily speaking) were not required to engage in as many physically demanding activities as males were. Males, having to hunt, build etc were exposed to greater stressors on their bodies compared to their female counterparts.[15] This lead to a higher percentage of muscle mass, and a lower percentage of fat for males. The second (and perhaps more pressing reason) is the fact that females are tasked with giving birth. Child bearing is very costly to a mother, and requires a large amount of energy to facilitate a very fragile fetus. Further, following childbirth breast milk is excreted that is full of nutrients and fat. This high fat milk is crucial to the development of a healthy child.[17]
{{ :gender.png?550|}}
===== Pathophysiology =====
=== Macronutrients Vs Micronutrients ===
Macronutrients Vs Micronutrients
Macronutrients are the energy providing nutrients and are thus needed in larger amounts. These include carbohydrates, proteins and fats.[18] Carbohydrates are they body’s main energy source, whereas proteins provide the amino acids important for the cell structure and the cell membrane.[18] On the other hand, fats are used for making steroid and hormones in the body.[18] Furthermore, fats have the highest caloric content with approximately 9 calories per gram of fat, and when burned, they provide the largest amount of energy compared to carbohydrates and proteins.[18] It has been reported that a high-fat diet induces the development of obesity.[19] There is a direct correlation between the amount of dietary fat and overconsumption, thus leading to weight gain.[19] It is speculated that this may be due to dietary fat’s weak satiety properties, leading to the feeling of not being satisfied or full after a meal.[19]
Micronutrients on the other hand are needed in smaller quantities and are essential for various chemical reactions in the body.[18] These include vitamins and minerals.[18] Vitamins allow for normal growth and metabolism as well as cellular functions.[18] These may be fat-soluble vitamins which are stored in the fatty tissues such as Vitamins A, D, E and K.[18] They may also be water-soluble which are excreted in the urine and must be taken daily such as Vitamins B and C.[18] Minerals are ionized in the body, for instance iron, sodium and potassium.[18]
=== Types of Adipocytes ===
{{ :fattissue.png?300|}}
Body fat or adipose tissue is composed of loose connective tissue which mostly consists of adipocytes or fat cells.[20] White adipose tissue (WAT) and brown adipose tissue (BAT) are the two types of adipocytes which make up the majority of adipose tissue.[20] Beige adipocytes are a third type of adipocyte, which have recently been identified, however their function and origin is not well understood.[21]
White adipocytes are the main cell type found in human adipose tissue.[20] Their main function is to store energy and they provide most of the total body fat. WAT cells have receptors for insulin, sex hormones, norepinephrine and glucocorticoids.[20] They secrete proteins such as leptin, adiponectin as well as other adipokines.[21] Furthermore, WAT is involved in controlling metabolism by acting as a thermal insulator to help maintain energy homeostasis.[20]
Brown adipocytes are found in almost in all mammals and they function to dissipate energy through thermogenesis.[22] Their characteristic brown appearance is due to a high number of iron-containing mitochondria.[22] BAT develop from the middle embryonic layer, the mesoderm, which is also the source of muscle cells and adipocytes.[20] It is abundant in newborns as well as metabolically active adult humans, however, its prevalence decreases in humans as they age.[20] Furthermore, brown adipocytes also contain more capillaries than white fat, which allows for tissue to be supplied with more oxygen and nutrients.[22] In this way, produced heat can easily be distributed throughout the body.[22]
=== Normal Function of Adipose Tissue & Adipose Tissue Development ===
Adipose tissue is an endocrine organ which is mainly responsible for energy storage as well as the synthesis and secretion of several hormones.[23] Adipose tissue is a major source of free fatty acids. Free fatty acids (FFA) are liberated from lipoproteins by lipoprotein lipase, allowing it to enter the adipocyte where it is reassembled into triglycerides by esterifying it onto glycerol. Adipocytes have an important physiological role in maintaining triglyceride and FFA levels.[23]
In conditions of obesity, hyperplasia and hypertrophy lead to the expansion of adipose tissue, which results in the development of adipocytes that are metabolically unhealthy.[24] The activation of biological pathways that favour the differentiation of adipocytes as well as the formation of adipocytes from precursor cells produces an increase in the number of adipocytes.[24] There are certain proteins and transcriptional factors involved in inhibiting or promoting the development of adipocytes.[23] Adipogenesis, the development of adipose tissue, involves the differentiation of preadipocytes into mature fat cells. Changes in transcription factor expression and activity is what results in the differentiation of these pre-adipocytes into mature fat cells.Transcription factors involved in promoting adipogenesis include the AP-1 family, PPARy, STATs, members of the KLF family, SREBP-1 and members C/EBP family. Conversely, Pref-1, GATA and Wnt family transcription factors are involved in inhibiting adipogenesis.[23]
Pre-adipocytes within adipose tissue can differentiate into mature adipocytes throughout their lifetime.[24] This allows for the expansion of adipose tissue when increased storage requirements are needed. Furthermore, mature adipocytes have the ability to accommodate increased storage needs, and in cases of overnutrition, these cells can become hypertrophic.[24]
Adipose tissue undergoes a continuous process of remodelling.[25] This normally maintains tissue health, however, this process is accelerated in obesity which can lead to the death of adipocytes along with the recruitment and activation of immune cells. Increased activation of the immune system leads to inflammation, which is the hallmark of obesity. Overall, an increase in the death of adipocytes, coupled with an increase in immune cell activation leads to many of the pathophysiological consequences of obesity.[25]
===== Hormones =====
=== Endorphin release when you eat ===
When energy-dense or high calorie food is consumed, endorphins and enkephalins are released in the brain, which are the brain’s natural opioids. Consuming fats and sugars essentially triggers shifts in the brain that are associated with addictive drugs such as heroin. This then stimulates dopamine release into the nucleus accumbens in the midbrain. Subsequently, this creates a feeling of reward.[26] Fast food meals can be extremely high in calories and can contain almost all of the recommended caloric daily intake for a person in a single sitting. This can cause physiological changes which may mute or alter the hormones responsible for satiety.[26]
=== Leptin ===
{{ :leptin.png?300|}}
Leptin is produced and secreted by adipose tissue in the body.[27] To signal satiety, the fat cells release leptin into the bloodstream, which then provides a signal in the hypothalamus, promoting a feeling of fullness.3 When leptin levels fall in response to lack of food or fasting, a signal is sent back to the body by the brain to promote food intake and a decrease in energy expenditure.[28] Because leptin is produced in fat cells, leptin levels are higher in obese people. However, people who are obese are not as sensitive to leptin and are thought to have a resistance to the hormone.[27]
=== Insulin ===
Insulin is a hormone produced by the beta-cells of the pancreas.[27,29] It plays a large role in the metabolism of carbohydrates and fat. Insulin maintains energy levels and ensures the body has the available energy it requires. It does this by stimulating glucose uptake in the blood from surrounding tissues.[27] When the body has the energy it needs, there is no need to consume more energy through food. In obesity, insulin signals are lost or become insensitive, therefore glucose uptake is low, and appetite suppression does not occur since there is not adequate signalling indicating the body has enough energy.[29] This can lead to the development of type II diabetes.[27] These defects may occur due to impaired insulin signalling in fat and muscle tissue, and a downregulation of the major insulin-responsive glucose receptor in fat cells, GLUT4.[29]
=== Sex Hormones ===
{{ :insulin.png?300|}}
Estrogens, the female sex hormones, and androgens, the male sex hormones, play a role in regulation of body fat distribution.[27] As women age and become postmenopausal, they produce lower levels of estrogen in their ovaries. Most of their estrogen is actually produced in their body fat, however this is not nearly the same amount that is produced by premenopausal ovaries. This plays a role in accumulation of fat around the abdomen, and animal studies have exhibited excessive weight gain associated with lack of estrogen.[27] As men age, the level of androgens produced by the testes also decreases.[27] Low levels of androgens have been associated with abdominal fat and obesity as well.[30]
=== Ghrelin ===
Ghrelin is a fast-acting hormone that plays a role in stimulating appetite and reducing fat utilization.[31] It is secreted by the stomach.[32] Ghrelin sends a signal to the hypothalamus, which then stimulates appetite. Although it is expected that ghrelin levels would be higher in obese individuals since it is the hunger hormone, it has been seen that ghrelin levels are actually decreased in obese humans.[31]
===== Environment =====
Many environmental factors are at play in the development of obesity, namely high-fat diets and low levels of physical activity.[33] The WHO reports that worldwide, 23 percent of adults and 81 percent of adolescents do not get enough physical activity to prevent chronic diseases such as obesity.[33] Furthermore, in developed nations, there has been an increase in food availability, large portion sizes or “super-sizing” of commercially available foods as well as the rise of fast-food restaurants, which can all lead to overconsumption.[34] There is also an indication that people living in poverty have a higher risk of weight gain.[34] This may be because impoverished areas, often called “food deserts”, have poor access to fresh foods.[34] Additionally, the low cost of fast-food restaurants is a much more affordable option for many people of lower socioeconomic status.[34]
===== Genetics =====
Family history is a known risk factor of obesity and is an important predictor of obesity in children.[35] However, the heritability component of obesity is still not well understood.
Non-syndromic monogenic obesity is an extreme form of the disease that results from a single gene mutation.[35] One such mutation that leads to this type of obesity is a frameshift homozygous mutation in the leptin (LEP) gene.[35] This results in a truncated version of leptin, in turn leading to a leptin deficiency.[35] Clinical manifestations of the LEP mutation include rapid weight gain in early childhood, excessive hunger and intolerant behaviour when presented with food.[35] These symptoms can be reversed through leptin therapy.[35]
Much of obesity’s genetic component is said to be attributed to multiple genetic variations contributing a small part, otherwise known as polygenic obesity.[35] One gene that has been associated with polygenic obesity is the fat mass and obesity-associated (FTO) gene.[35] There is evidence that suggests that there is a relationship between common single-nucleotide polymorphisms in the FTO gene and developing Type 2 diabetes, mediated by an increase in the BMI.[35] Furthermore, FTO is strongly associated with increased hip circumference, weight and risk of childhood obesity.[35]
====== Fad Diets ======
A fad diet is defined as a promise of quick weight loss through unconventional techniques.[36] The problem with these diets is they are generally very unhealthy, and have no scientific backing to support them. One of the earlier studies done that examined fad diets was conducted by Mirkin and Shore and examined “The Beverly Hills Diet.”[37] This diet was based around three principle claims. Firstly, “As long as food is fully digested, fully processed through the body, you will not gain weight. It’s only undigested food, food that is “stuck” in your body, for whatever reason, that accumulates and becomes fat.” Secondly, “Most enzymes do not work simultaneously… Many cancel one another out in our digestive systems.” And finally “Enzymes presented in certain fruits make hard to digest foods less fattening.” This along with many other absubities were sold to consumers by, in the case of the Beverly Hills Diet, an individual who is not a doctor nor a dietitian.[37] All these claims are to any medical professional or dietitian quite obscure-- of course fat must be digested into the body to accumulate, enzymes do not cancel each other out, and certain enzymes cannot take away the fat content of another food. Regardless, the promise of a “quick-fix” for an individual who is hoping to lose weight is extremely palatable as it appears to require less work than the alternative, proven weight loss techniques-- consume less calories than you burn and exercise.
**Gwyneth Paltrow and GOOP**
Celebrities are given a great deal of viability when promoting diets, even if they have no idea what is going on. One of the more recent cases of this is seen within GOOP-- a company created by actress Gwyneth Paltrow that gives health and lifestyle advice to other individuals.
Dr. Timothy Caulfield is a professor and public health at the University of Alberta. He is also the director of their Health Law Institute. Dr. Caulfield set out to examine the diets and their discrepancies set out by Paltrow in his book called “Is Gwyneth Paltrow wrong about everything?” The diet Paltrow promotes the most is called “The Clean Cleanse.” The program claims the human body accumulates toxins from the air around us and the food we eat over time, and therefore we need to rid our body of these toxins in some ways. Although quite the appealing idea, this concept of toxin build up in our bodies is not scientifically proven.[36] Our bodies are constantly detoxifying through sweating and urinating, and no diet can somehow change this process. Another avid point made by the cleanse team is that these toxins lead to “fatigue” of our adrenal gland, which leads to “sky high adrenals” which stress our bodies and cause us to put on weight. Once again, there is no scientific basis to this claim. Studies do show that eating healthier is associated with better effect and lower depression (ie. higher fruit and vegetable diets). There is no tie however to our adrenal glands being stressed and that causing us to gain weight. The program generally lasts 21 days, and from experience Dr. Caulfield has claimed he did, in fact, lose weight, but not from “detoxification” but more simply from a lack of calories being consumed over the period of time, not from a magical diet that cuts out wheat and sugars (as the Clean Cleanse does).
http://blog.cleanprogram.com/elimination-diet
This is a link to the program diet. There is no rhyme or reason to any of these foods being validated on the program list, but people lose weight and therefore the program continues to grow.
The unfortunate reality of these crash diets is that only 5% of individuals will actually keep the weight off for an extended period of time. This is why a continuation of healthy eating and living is the truly only effective way to lose weight and maintain it.
===== Treatments =====
When undergoing treatment options for obesity, the combination therapy involving exercise, behavioural and dietary modifications are recommended by physicians due to their proven effectiveness and least amount of side effects. When undergoing weight loss therapy a maximum of 10% of total body weight should be lost within a 6 month period.
=== Diet ===
{{ :diet.png?200|}}
The main component to the treatment of obesity is to have healthier modifications to the individual's diet. The goal for dietary therapy as well as each of the other lifestyle changes is to have the energy intake be lower than the energy expenditure, essentially having a negative energy balance.[38]
There are many types of diets prescribed to obese individuals, the main ones that are studied are the low-fat diet, very low-fat diet, high protein diet and low carbohydrate diet. The low-fat diet restricts individuals to consume 20-35% of their dietary calories in fats.[38] These diets are the most studied of all dietary approaches to weight loss and have shown a significant weight decrease in individuals following this diet. The very low-fat diet restricts individuals to consume less than or equal to 20% of their dietary calories from fats.[38] These diets are primarily plant-based, studies have shown that participants following the Ornish diet (a very low-fat diet) experienced significant weight loss and improvements in CVD risk factors.[38]
The high protein diet is when the intake of dietary protein is higher than 25% of the individuals daily calories. Studies have proven the efficacy of both weight loss and improvements in body composition with this diet.[38] Individuals following a high protein diet, decrease their waist circumference, waist to hip ratio and intra-abdominal adipose tissue.[38] This diet is of great interest due to the fact that certain chronic diseases are associated with these body composition.[38]
=== Exercise ===
The first component to the weight loss therapy is to treat obesity by increasing the levels of the obese individual’s physical activity.[39] The goal for any weight loss program is to have a negative energy balance at the end of the day, so the individual should aim to increase their energy expenditure and physical activity is an excellent way to do so.[39] Physical activity is linked to increased weight loss and weight management.[39]
It is important to take note that not every exercise routine responds the same way to each individual, one type may be more effective at reducing weight for some individuals than others. There are a variety of different exercise routines which can involve running, walking, rowing, free weights or a combination of any of these.[39] It is very difficult for obese individuals to lose weight due to all of the variables associated with their weight gain and because of this it can be just as much of a mental battle as a physical one, so it is recommended that the individuals acquire a trainer that can help them with their exercise regime as well as help set realistic goals throughout the process. A meta-analysis was done by Shaw et al., 2006 showed that exercise is an excellent weight loss intervention and the effects are improved with the combination of dietary modifications as well.[39] They also found that exercise was able to alleviate secondary symptoms associated with obesity like cardiovascular disease, blood pressure.[39]
=== Behavioural Modifications ===
{{ :screen_shot_2018-02-02_at_6.26.10_pm.png?200|}}
Behavioural therapy has recently started to become added into the therapies alongside the exercise and dietary modifications. This is because obesity is thought to be a result of maladaptive eating patterns and exercise habits and that these behaviours can be modified with specific interventions which will lead to weight loss.[40] The main goal for behavioural therapy is to help individuals with obesity develop skills that can help them achieve and maintain a healthier body weight. Cognitive behavioural therapy has become popular over the past two decades.[40]
A few of the common components used in behavioural therapy are:[40]
· Self-monitoring: this includes keeping a daily food log of all of the meals the individual has had throughout the day.
· Stimulus control: the purpose for this component is to alter the environment for the individual in order to avoid overeating. This is to basically eliminate energy-dense foods from the home and replace it with nutrient-dense foods.
· Goal setting: setting realistic goals for both the short and long term.
· Behavioural contracting: reinforcing of good behaviours.
· Social support: it has been shown that behavioural modifications have become more sustainable in the long term with social support. Receiving encouragement from family and friends can be effective in losing more weight.
=== Pharmaceuticals ===
Another line of treatment for obesity is to use medication in combination with the lifestyle changes mentioned above. Two popular obesity medications are in the classes of lipase inhibitors and appetite suppressants.
Lipase inhibitors function to prevent the absorption of fats from the individual's diet, therefore, reducing caloric intake. Orlistat is a common lipase inhibitor used to combat obesity, it is a derivative of lipstatin which is a natural inhibitor of pancreatic lipases.[41] Orlistat has been proven with definitive results to work with weight loss. A study showed that when prescribed orlistat combined with lifestyle changes individuals lost been 3% and 9% of their initial weight within one year compared to a control group who only underwent lifestyle changes.[42]
Appetite suppressants are also used to help with weight loss in combination with lifestyle changes. Phentermine is the most widely prescribed obesity medication in adults, it is a psychostimulant drug which is used as an appetite suppressant by affecting the central nervous system.[42] This drug is only permitted to be used for 3 months at a time alongside exercise and nutritional therapy or it may cause side effects in the cardiovascular system, gastrointestinal system and the central nervous system.[42]
A retrospective study wanted to test the efficacy of the drug with adolescents. They had 25 individuals who were medicated with phentermine and they matched them with a control individual who was receiving only the standard of care.[43] They found at each measurement date 1,3 and 6 months that there was a significant difference in weight loss between groups and there was no difference in blood pressure between groups.[43]
=== Bariatric Surgery ===
Bariatric surgery is a weight loss procedure which aims to decrease the size of the obese individual's stomach by either a gastric band or the removal of a portion of the stomach.[44] It is not recommended for individuals below a BMI of 40 to undergo bariatric surgery. Post-surgery patients are only able to have a clear liquid diet which is continued until the gastrointestinal tract is healed.[44] Once that stage is complete a blended diet where foods high in protein are recommended alongside soft meals. Finally, once recovery is complete the patient is able to eat all types of foods again, but they are restricted from overeating due to the surgery. If they over eat they will reach the capacity of their stomach which will cause discomfort.[44]
{{ :bariatric_surgery.png?500|}}
Studies have proven the effectiveness of this procedure in causing significant weight loss in the long term as well as secondary effects like recovery from diabetes, CVD and reduction in mortality.[45] There is great debate at the moment whether individuals with type 2 diabetes should be given bariatric surgery because of the success it has with diabetes remission; more research needs to be done on the topic with the focus group as well as the proper timing for the most effective treatment.[45]
=== Gene therapy – Leptin deficiency ===
{{ :gene.png?250|}}
Gene therapy is a hot topic in the science community at the moment, and advances in this technology and the understanding of the molecular basis for obesity have allowed for researchers to design therapies to tackle this disease. The main goal for gene therapy is to increase gene products in favour of fat loss and energy expenditure.[46]
The most studied gene directly linked to obesity is leptin, which plays a role in appetite and energy expenditure. It is thought that obese individuals have a mutation within this gene. A defect in the ob gene coding for leptin has been linked to severe obesity.[46] It was found that mice who homozygous for this defect in the leptin gene ate excessively and developed obesity. Researchers found that the delivery of leptin into the brain through a recombinant virus into mice was able to generate long-term beneficial effects with body weight.[46] Another study aimed to show that leptin sensitivity was also crucial with the weight loss with mice because HFD mice were unresponsive with the treatment but when they were delivered leptin receptor gene reduction in body weight was seen.[46]
===== References =====
1. Ofei, F. (2005). Obesity-a preventable disease. Ghana medical journal, 39(3), 98.
2. Webber, L., Kilpi, F., Marsh, T., Rtveladze, K., Brown, M., & McPherson, K. (2012). High rates of obesity and non-communicable diseases predicted across Latin America. PloS one, 7(8), e39589.
3. Healthy Weight. (2017, August 29). Retrieved February 01, 2018, from https://www.cdc.gov/healthyweight/assessing/bmi/adult_bmi/index.html
4. Nuttall, F. Q. (2015). Body mass index: obesity, BMI, and health: a critical review. Nutrition today, 50(3), 117.
5. Arroyo-Johnson, C., & Mincey, K. D. (2016). Obesity Epidemiology Worldwide. Obesity and Gastroenterology, 45(4), 571–579. https://doi.org/10.1016/j.gtc.2016.07.012
6. World Health Organization. (2017, October). Obesity and Overweight Fact Sheet. Retrieved from http://www.who.int/mediacentre/factsheets/fs311/en/
7. Institute for Health Metrics and Evaluation. (2014). Nearly one-third of the world’s population is obese or overweight, new data show. Retrieved from http://www.healthdata.org/news-release/nearly-one-third-world%E2%80%99s-population-obese-or-overweight-new-data-show
8. The GBD 2013 Obesity Collaboration, Ng, M., Fleming, T., Robinson, M., Thomson, B., Graetz, N., … Gakidou, E. (2014). Global, regional and national prevalence of overweight and obesity in children and adults 1980-2013: A systematic analysis. Lancet (London, England), 384(9945), 766–781. https://doi.org/10.1016/S0140-6736(14)60460-8
9. Seidell, J. C., & Halberstadt, J. (2015). The Global Burden of Obesity and the Challenges of Prevention. Annals of Nutrition and Metabolism, 66(suppl 2)(Suppl. 2), 7–12.
10. Organisation for Economic Cooperation and Development. (2017). OECD Obesity Update 2017. Retrieved from http://www.oecd.org/health/obesity-update.htm
11. Statistics Canada. (2017, September 19). Obesity. Retrieved from https://www.statcan.gc.ca/eng/help/bb/info/obesity
12. Statistics Canada (2015, October 27). Adjusting the scales: Obesity in the Canadian population after correcting for respondent bias. Retrieved from https://www.statcan.gc.ca/pub/82-624-x/2014001/article/11922-eng.htm
13. Kuzawa, C. W. (1998). Adipose tissue in human infancy and childhood: an evolutionary perspective. American journal of physical anthropology, 107(S27), 177-209.
14. Holliday M (1986) Body composition and energy needs during growth. In F Falkner and JM Tanner (eds.): Human Growth: A Comprehensive Treatise. New York:Plenum Press, pp. 117–139.
15. Brown, P. J., & Konner, M. (1987). An anthropological perspective on obesity. Annals of the New York Academy of Sciences, 499(1), 29-46.
16. Kanter, R., & Caballero, B. (2012). Global gender disparities in obesity: a review. Advances in nutrition, 3(4), 491-498.
17. Gunderson, E. P. (2009). Childbearing and obesity in women: weight before, during, and after pregnancy. Obstetrics and gynecology clinics of North America, 36(2), 317-332.
18. FAO. (n.d.). Macronutrients and Micronutrients. Retrieved January 31, 2018, from http://www.fao.org/elearning/Course/NFSLBC/en/story_content/external_files/Essential_Nutrients.pdf
19. Golay, A., & Bobbioni, E. (1997). The role of dietary fat in obesity. International journal of obesity and related metabolic disorders: journal of the International Association for the Study of Obesity, 21, S2-11.
20. Heymsfield, S. B., & Wadden, T. A. (2017). Mechanisms, pathophysiology, and management of obesity. New England Journal of Medicine, 376(3), 254-266.
21. Ofei, F. (2005). Obesity-a preventable disease. Ghana medical journal, 39(3), 98.
22. Balistreri, C. R., Caruso, C., & Candore, G. (2010). The role of adipose tissue and adipokines in obesity-related inflammatory diseases. Mediators of inflammation, 2010.
23. Stephens, J. M. (2012). The fat controller: adipocyte development. PLoS biology, 10(11), e1001436.
24. Ravussin, E., & Swinburn, B. A. (1992). Pathophysiology of obesity. The Lancet (USA).
25. Lee, M. J., Wu, Y., & Fried, S. K. (2010). Adipose tissue remodeling in pathophysiology of obesity. Current opinion in clinical nutrition and metabolic care, 13(4), 371.
26. Martindale, Diane. (2003, February 1). Burgers on the Brain. Retrieved from http://scholar.googleusercontent.com/scholar?q=cache:djUYPHLDAgIJ:scholar.google.com/+burgers+on+the+brain&hl=en&as_sdt=0,5
27. Victoria State Government. (2010). Obesity and Hormones. Retrieved from https://www.betterhealth.vic.gov.au/health/healthyliving/obesity-and-hormones
28. Ahima, R. S. (2008). Revisiting leptin’s role in obesity and weight loss. The Journal of Clinical Investigation, 118(7), 2380–2383. http://doi.org/10.1172/JCI36284.
29. Kahn, B. B., & Flier, J. S. (2000). Obesity and insulin resistance. Journal of Clinical Investigation, 106(4), 473–481.
30. Wang, C., Jackson, G., Jones, T. H., Matsumoto, A. M., Nehra, A., Perelman, M. A., … Cunningham, G. (2011). Low Testosterone Associated With Obesity and the Metabolic Syndrome Contributes to Sexual Dysfunction and Cardiovascular Disease Risk in Men With Type 2 Diabetes. Diabetes Care, 34(7), 1669–1675. http://doi.org/10.2337/dc10-2339
31. Tschöp, M., Weyer, C., Tataranni, P. A., Devanarayan, V., Ravussin, E., & Heiman, M. L. (2001). Circulating Ghrelin Levels Are Decreased in Human Obesity. Diabetes, 50(4), 707. https://doi.org/10.2337/diabetes.50.4.707
32. Heiman, M.L., Witcher, D.R. (2006). Ghrelin in Obesity. Metabolic Syndrome and Related Disorders, 4(1), 37-42. https://doi.org/10.1089/met.2006.4.37
33. Faith, M. S., & Kral, T. V. (2006). Social environmental and genetic influences on obesity and obesity-promoting behaviors: fostering research integration.
34. Obesity and overweight. (n.d.). Retrieved January 31, 2018, from http://www.who.int/mediacentre/factsheets/fs311/en/
35. Pigeyre, M., Yazdi, F. T., Kaur, Y., & Meyre, D. (2016). Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity. Clinical science, 130(12), 943-986.
36. Caulfield, T. (2015). Is Gwyneth Paltrow Wrong about Everything?: when celebrity culture and science clash. Penguin Canada.
37. Mirkin, G. B., & Shore, R. N. (1981). The Beverly Hills diet: Dangers of the newest weight loss fad. JAMA, 246(19), 2235-2237.
38. Makris, A., & Foster, G. D. (2011). Dietary approaches to the treatment of obesity. The Psychiatric Clinics of North America, 34(4), 813–27. http://doi.org/10.1016/j.psc.2011.08.004
39. Ka, S., Hc, G., Rourke, O. P., & C, D. M. (2009). Exercise for overweight or obesity (Review). Library, 18(1), CD003817. http://doi.org/10.1002/14651858.CD003817.pub3
40. Jacob, J. J., & Isaac, R. (2012). Behavioral therapy for management of obesity. Indian Journal of Endocrinology and Metabolism, 16(1), 28–32. http://doi.org/10.4103/2230-8210.91180
41. Guerciolini, R. (1997). Mode of action of orlistat. International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity, 21 Suppl 3, S12-23. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/9225172
42. Yanovski, S. Z., & Yanovski, J. a. (2014). Long-term drug treatment for obesity: a systematic and clinical review. JAMA : The Journal of the American Medical Association, 311(1), 74–86. http://doi.org/10.1001/jama.2013.281361
43. Ryder, J. R., Kaizer, A., Rudser, K. D., Gross, A., Kelly, A. S., & Fox, C. K. (2017). Effect of phentermine on weight reduction in a pediatric weight management clinic. International Journal of Obesity, 41(1), 90–93. http://doi.org/10.1038/ijo.2016.185
44. Tucker, O. N., Szomstein, S., & Rosenthal, R. J. (2018). Nutritional Consequences of Weight-Loss Surgery. Medical Clinics, 91(3), 499–514. http://doi.org/10.1016/j.mcna.2007.01.006
45. Robinson, M. K. (2009). Surgical Treatment of Obesity - Weighing the Facts. New England Journal of Medicine, 361(5), 520–521. http://doi.org/10.1056/NEJMe0904837
46. Gao, M., Liu, D., & Medicine, D. (2014). Gene therapy for obesity: progress and prospects. Discovery Medicine, 17(96), 319-28. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/24979252