Skip to main content

Etiopathogenesis of Obesity

  • Reference work entry
  • First Online:
Obesity, Bariatric and Metabolic Surgery

Abstract

Obesity develops in an individual when energy intake exceeds energy expenditure over a prolonged period and the excess is stored as triglyceride, predominantly in adipose tissue. The rising prevalence of obesity worldwide is a major contributor to poor health, including diabetes, heart disease, and cancer. To understand the pathogenesis of obesity, it is important to understand the regulation of energy balance, which, although very tightly regulated, is subject to biological variation and easily overwhelmed by societal pressures and marketing influences. Control pathways for food intake and energy expenditure during as well as between meals include short-term mechanisms that operate from gastrointestinal tract to the central nervous system, as well as long-term signals that regulate the “set point” for body weight, which are dominated by leptin, an adipocyte-derived hormone. These pathways converge in the central nervous system, notably the hypothalamus, which plays a vital role in controlling food intake, energy expenditure, and other aspects of metabolism. Various genetic and environmental factors can influence these energy homeostasis mechanisms. Foods that are high in sugars and fat are potent rewards that promote eating even in the absence of absolute energy requirement, particularly in modern societies where food is available in abundance, and contribute to the obesity epidemic. Single gene disorders that result in obesity such as leptin deficiency and mutations in the pro-opiomelanocortin gene are rare but demonstrate the biological importance of these systems. Other etiological factors in some people may include drugs that increase appetite through central or peripheral mechanisms and structural damage to the hypothalamic areas involved in control of appetite. However, the recent increase in the prevalence of obesity is predominantly due to adverse environmental factors that are able to override these regulatory systems. These include widespread availability of high-energy foods, coupled with an unprecedented decline in levels of physical activity.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 599.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 1,099.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

References

  1. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K. Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature. 1999;402(6762):656–60.

    Article  CAS  Google Scholar 

  2. Weltens N, Iven J, Van Oudenhove L, Kano M. The gut-brain axis in health neuroscience: implications for functional gastrointestinal disorders and appetite regulation. Ann N Y Acad Sci. 2018;1428(1):129–50.

    Article  Google Scholar 

  3. Zhang YY, Proenca R, Maffei M, Barone M, Leopold L, Friedman JM. Positional cloning of the mouse obese gene and its human homolog. Nature. 1994;372:425–32.

    Article  CAS  Google Scholar 

  4. Tartaglia LA, Dembski M, Weng X, Deng NH, Culpepper J, Devos R, et al. Identification and expression cloning of a leptin receptor, Ob-r. Cell. 1995;83:1263–71.

    Article  CAS  Google Scholar 

  5. Schwartz MW, Seeley RJ, Campfield LA, Burn P, Baskin DG. Identification of targets of leptin action in rat hypothalamus. J Clin Investig. 1996;98:1101–6.

    Article  CAS  Google Scholar 

  6. Farooqi IS, Bullmore E, Keogh J, Gillard J, O'Rahilly S, Fletcher PC. Leptin regulates striatal regions and human eating behavior. Science. 2007;317(5843):1355.

    Article  CAS  Google Scholar 

  7. Schwartz MW, Figlewicz DP, Baskin DG, Woods SC, Porte D. Insulin in the brain: a hormonal regulator of energy balance. Endocr Rev. 1992;13:387–413.

    CAS  Google Scholar 

  8. Turton MD, O'Shea D, Gunn I, Beak SA, Edwards CMB, Meeran K, et al. A role for glucagon-like peptide-1 in the central control of feeding. Nature. 1996;379:69–72.

    Article  CAS  Google Scholar 

  9. Pi-Sunyer X, Astrup A, Fujioka K, Greenway F, Halpern A, Krempf M, et al. A randomized, controlled trial of 3.0 mg of liraglutide in weight management. N Engl J Med. 2015;373(1):11–22.

    Article  Google Scholar 

  10. Batterham RL, Cohen MA, Ellis SM, Le Roux CW, Withers DJ, Frost GS, et al. Inhibition of food intake in obese subjects by peptide YY3-36. N Engl J Med. 2003;349(10):941–8.

    Article  CAS  Google Scholar 

  11. Rodgers RJ, Tschop MH, Wilding JPH. Anti-obesity drugs: past, present and future. Dis Model Mech. 2012;5(5):621–6.

    Article  CAS  Google Scholar 

  12. Hall KD, Obesity Energetics GJ. Body weight regulation and the effects of diet composition. Gastroenterology. 2017;152(7):1718-27.e3.

    Article  Google Scholar 

  13. Dulloo AG. Translational issues in targeting brown adipose tissue thermogenesis for human obesity management. Ann N Y Acad Sci. 2013;1302(1):1–10.

    Article  CAS  Google Scholar 

  14. von Loeffelholz C BA. The role of non-exercise activity thermogenesis in human Obesity: Endotext (internet); 2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK279077/?report=reader#_NBK279077_pubdet_

    Google Scholar 

  15. Melanson EL, Keadle SK, Donnelly JE, Braun B, King NA. Resistance to exercise-induced weight loss: compensatory behavioral adaptations. Med Sci Sports Exerc. 2013;45(8):1600–9.

    Article  Google Scholar 

  16. Bray GA, Kim KK, Wilding JPH, World Obesity F. Obesity: a chronic relapsing progressive disease process. A position statement of the World Obesity federation. Obes Rev. 2017;18(7):715–23.

    Article  CAS  Google Scholar 

  17. Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015;518(7538):197–206.

    Article  CAS  Google Scholar 

  18. Farooqi SI. Genetic, molecular and physiological mechanisms involved in human obesity: Society for Endocrinology medal lecture 2012. Clin Endocrinol. 2015;82(1):23–8.

    Article  Google Scholar 

  19. Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science. 2007;316(5826):889–94.

    Article  CAS  Google Scholar 

  20. Khera AV, Chaffin M, Wade KH, Zahid S, Brancale J, Xia R, et al. Polygenic prediction of weight and Obesity trajectories from birth to adulthood. Cell. 2019;177(3):587-96.e9.

    Article  Google Scholar 

  21. Clément K, Mosbah H, Poitou C. Rare genetic forms of obesity: from gene to therapy. Physiol Behav. 2020;227:113134.

    Article  Google Scholar 

  22. Celis-Morales CA, Lyall DM, Gray SR, Steell L, Anderson J, Iliodromiti S, et al. Dietary fat and total energy intake modifies the association of genetic profile risk score on obesity: evidence from 48 170 UK biobank participants. Int J Obes. 2017;41(12):1761–8.

    Article  CAS  Google Scholar 

  23. Hu FB. Television watching and other sedentary behaviors in relation to risk of Obesity and type 2 diabetes mellitus in women. JAMA. 2003;289(14):1785.

    Article  Google Scholar 

  24. Ogilvie RP, Patel SR. The epidemiology of sleep and obesity. Sleep Health. 2017;3(5):383–8.

    Article  Google Scholar 

  25. Wen CP, David Cheng TY, Tsai SP, Chan HT, Hsu HL, Hsu CC, et al. Are Asians at greater mortality risks for being overweight than Caucasians? Redefining obesity for Asians. Public Health Nutr. 2009;12(4):497–506.

    Article  Google Scholar 

  26. Ralston J, Brinsden H, Buse K, Candeias V, Caterson I, Hassell T, et al. Time for a new obesity narrative. Lancet. 2018;392(10156):1384–6.

    Article  Google Scholar 

  27. Seetho IW, Wilding JPH. How to approach endocrine assessment in severe obesity? Clin Endocrinol. 2013;79(2):163–7.

    Article  Google Scholar 

  28. Wells JCK, Marphatia AA, Cole TJ, McCoy D. Associations of economic and gender inequality with global obesity prevalence: understanding the female excess. Soc Sci Med. 2012;75(3):482–90.

    Article  Google Scholar 

  29. Zellner DA, Loaiza S, Gonzalez Z, Pita J, Morales J, Pecora D, et al. Food selection changes under stress. Physiol Behav. 2006;87(4):789–93.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to John P. H. Wilding .

Editor information

Editors and Affiliations

Section Editor information

Rights and permissions

Reprints and permissions

Copyright information

© 2023 Springer Nature Switzerland AG

About this entry

Check for updates. Verify currency and authenticity via CrossMark

Cite this entry

Rajeev, S.P., Wilding, J.P.H. (2023). Etiopathogenesis of Obesity. In: Agrawal, S. (eds) Obesity, Bariatric and Metabolic Surgery. Springer, Cham. https://doi.org/10.1007/978-3-030-60596-4_2

Download citation

  • DOI: https://doi.org/10.1007/978-3-030-60596-4_2

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-60595-7

  • Online ISBN: 978-3-030-60596-4

  • eBook Packages: MedicineReference Module Medicine

Publish with us

Policies and ethics