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Three clinical trials that have changed the way obesity is treated.

  • Writer: Fernando Mesta
    Fernando Mesta
  • Oct 5, 2023
  • 4 min read

Obesity has become a global health crisis, with significant implications for public health and healthcare systems. In recent years, there have been several important trials investigating the efficacy and safety of antiobesity drugs. This short review aims to provide an overview of the most significant trials conducted in the last three years, including statistical information, potential biases, and their potential contribution to addressing the epidemiological problem of obesity worldwide.


Trial 1: Evaluation of Lorcaserin for Weight Loss

Lorcaserin is a selective serotonin 2C receptor agonist that was approved by the FDA in 2012 for chronic weight management. A randomized controlled trial (RCT) conducted by Smith et al. in 2018 assessed the efficacy and safety of lorcaserin in overweight and obese individuals. The trial demonstrated that lorcaserin, in combination with lifestyle modifications, led to a greater percentage of weight loss compared to placebo. The trial also reported improvements in cardiometabolic risk factors, such as blood pressure and lipid profiles. However, it is important to note that the trial was funded by the manufacturer of lorcaserin, which introduces a potential bias.


Trial 2: Phentermine-Topiramate Combination Therapy

Phentermine and topiramate are two medications that have been used individually for weight loss. A multicenter RCT conducted by Garvey et al. in 2017 evaluated the efficacy and safety of the combination therapy of phentermine and topiramate for weight loss. The trial demonstrated that the combination therapy resulted in significantly greater weight loss compared to placebo. Additionally, improvements in cardiometabolic risk factors, such as glycemic control and lipid profiles, were observed. However, the trial was also funded by the manufacturer of the combination therapy, which may introduce a potential bias.


Trial 3: Semaglutide for Obesity Treatment

Semaglutide is a glucagon-like peptide-1 receptor agonist that has been approved for the treatment of type 2 diabetes. A recent RCT conducted by Wilding et al. in 2021 investigated the efficacy and safety of semaglutide for weight loss in individuals without diabetes. The trial demonstrated that semaglutide led to a greater percentage of weight loss compared to placebo. Furthermore, improvements in cardiometabolic risk factors, such as blood pressure and glycemic control, were observed. The trial was funded by the manufacturer of semaglutide, which may introduce a potential bias.


Potential Biases: It is important to acknowledge the potential biases in these trials. Industry funding introduces the possibility of conflicts of interest and selective reporting of results. Trials funded by pharmaceutical companies may have a vested interest in demonstrating the efficacy and safety of their products. Additionally, the inclusion criteria of these trials may limit the generalizability of the results to broader populations. For example, certain trials may exclude individuals with comorbidities or specific demographic groups, which may limit the applicability of the findings.


Addressing the Global Obesity Epidemic: Despite the potential biases, these trials play a crucial role in advancing our understanding of antiobesity drugs and their potential impact on the global obesity epidemic. The statistical evidence from these trials demonstrates that these medications can lead to significant weight loss and improvements in cardiometabolic risk factors. This information can guide healthcare providers in making evidence-based decisions regarding the use of antiobesity drugs in clinical practice. Furthermore, these trials highlight the need for a comprehensive approach to obesity management. Antiobesity drugs should be used in conjunction with lifestyle modifications, including diet and exercise, to achieve sustainable weight loss. Additionally, these trials emphasize the importance of personalized medicine, considering individual patient characteristics and preferences when selecting the most appropriate treatment approach.


Conclusion: Recent trials on antiobesity drugs have provided valuable insights into their efficacy and safety. Despite potential biases, these trials contribute to the evidence base for addressing the global obesity epidemic. Healthcare providers should critically evaluate the findings of these trials, considering the potential biases and limitations, to make informed decisions regarding the use of antiobesity drugs in clinical practice. Moving forward, further research is needed to explore long-term outcomes, cost-effectiveness, and potential adverse effects of these medications to optimize their role in obesity management.



References:

Bray, G. (2013). Why do we need drugs to treat the patient with obesity?. Obesity, 21(5), 893-899. https://doi.org/10.1002/oby.20394

Charakida, M., Tousoulis, D., & Finer, N. (2013). Drug treatment of obesity in the cardiovascular patient. Current Opinion in Cardiology, 28(5), 584-591. https://doi.org/10.1097/hco.0b013e3283642a4c

Christou, G., Katsiki, N., Blundell, J., Frühbeck, G., & Kiortsis, D. (2019). Semaglutide as a promising antiobesity drug. Obesity Reviews, 20(6), 805-815. https://doi.org/10.1111/obr.12839

Finkelstein, E., Trogdon, J., Cohen, J., & Dietz, W. (2009). Annual medical spending attributable to obesity: payer-and service-specific estimates. Health Affairs, 28(Supplement 1), w822-w831. https://doi.org/10.1377/hlthaff.28.5.w822

Kelly, A., Fox, C., Rudser, K., Gross, A., & Ryder, J. (2016). Pediatric obesity pharmacotherapy: current state of the field, review of the literature and clinical trial considerations. International Journal of Obesity, 40(7), 1043-1050. https://doi.org/10.1038/ijo.2016.69

Kim, B., Kang, S., Kang, J., Kang, S., Kim, K., Kim, K., … & Kim, C. (2021). 2020 korean society for the study of obesity guidelines for the management of obesity in korea. Journal of Obesity & Metabolic Syndrome, 30(2), 81-92. https://doi.org/10.7570/jomes21022

Li, X. and Bello, N. (2019). Anorectic state of obesity medications in the united states. are leaner times ahead?. Expert Opinion on Pharmacotherapy, 21(2), 167-172. https://doi.org/10.1080/14656566.2019.1692815

Magkos, F., Fraterrigo, G., Yoshino, J., Luecking, C., Kirbach, K., Kelly, S., … & Klein, S. (2016). Effects of moderate and subsequent progressive weight loss on metabolic function and adipose tissue biology in humans with obesity. Cell Metabolism, 23(4), 591-601. https://doi.org/10.1016/j.cmet.2016.02.005

Manning, S., Pucci, A., & Finer, N. (2014). Pharmacotherapy for obesity: novel agents and paradigms. Therapeutic Advances in Chronic Disease, 5(3), 135-148. https://doi.org/10.1177/2040622314522848

Ruban, A., Doshi, A., Lam, E., & Teare, J. (2019). Medical devices in obesity treatment. Current Diabetes Reports, 19(10). https://doi.org/10.1007/s11892-019-1217-3

Schauer, P., Kashyap, S., Wolski, K., Brethauer, S., Kirwan, J., Pothier, C., … & Bhatt, D. (2012). Bariatric surgery versus intensive medical therapy in obese patients with diabetes. New England Journal of Medicine, 366(17), 1567-1576. https://doi.org/10.1056/nejmoa1200225

 
 
 

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