Literature
首页医源资料库在线期刊美国临床营养学杂志2005年82卷第1期

Solutions in weight control: lessons from gastric surgery

来源:《美国临床营养学杂志》
摘要:GeorgeLBlackburn1FromtheBethIsraelDeaconessMedicalCenter,HarvardMedicalSchool,Boston2Presentedatthesymposium“Science-BasedSolutionstoObesity:WhatAretheRolesofAcademia,Government,Industry,andHealthCare。ABSTRACTSurgicaltherapyiscurrentlytheonlyprovenwayto......

点击显示 收起

George L Blackburn

1 From the Beth Israel Deaconess Medical Center, Harvard Medical School, Boston

2 Presented at the symposium "Science-Based Solutions to Obesity: What Are the Roles of Academia, Government, Industry, and Health Care?", held in Boston, MA, March 10–11, 2004 and Anaheim, CA, October 2, 2004.

3 Supported by the S. Daniel Abraham Chair in Nutrition Medicine at Harvard Medical School and the Harvard Center for Healthy Living.

4 Address reprint requests and correspondence to GL Blackburn, Beth Israel Deaconess Medical Center, Feldberg 880, East Campus, 330 Brookline Avenue, Boston, MA 02215. E-mail: gblackbu{at}bidmc.harvard.edu.

ABSTRACT

Surgical therapy is currently the only proven way to achieve significant long-term weight loss, improve obesity-related comorbidities, reduce the risk of premature death, and improve quality of life in a large proportion of treated individuals. Roux-en-Y gastric bypass, the most widely performed procedure in the United States, is known to achieve permanent (>14 y of follow-up) and significant (>50% of excess body weight) weight loss in >90% of patients who undergo the operation. Gastric bypass procedures induce physiologic and neuroendocrine changes that appear to affect the weight regulatory centers in the brain. Researchers have begun to explore the molecular pathways responsible for these outcomes. Identifying the differences between surgical and nonsurgical treatments will eventually lead to new therapeutic options.

Key Words: Weight loss surgery • WLS • bariatric surgery • gastric bypass • gastroplasty • laparoscopic adjustable gastric banding

INTRODUCTION

Available weight loss treatments for obesity range from diet, exercise, behavioral modification, and pharmacotherapy to surgery, with varying risks and efficacies. Nonsurgical modalities, although less invasive, typically achieve only relatively short-term and limited weight loss in most patients. However, these therapies are very useful in the preoperative period to reduce risks related to surgical treatment of severe (class III) obesity (1).

Weight loss surgery is an appropriate treatment for patients with class III obesity or class II obesity and major comorbidities (2). Data indicate that weight loss surgery is safe and effective, with well-defined risks (1, 3-10), that it is the most effective modality in terms of extent and duration of weight reduction in selected patients with acceptable operative risks (11). A recent study of >1000 gastric bypass surgery (GBP) patients showed that, after 5 y, there was an 89% reduction in mortality in severely obese patients who had weight loss surgery compared with those who did not (3). A new meta-analysis indicates that weight loss surgery is one of the most effective treatments for diabetes, hypertension, obstructive sleep apnea, and high cholesterol in severely obese patients (12).

The rapid spread of severe obesity, combined with lack of adequately effective dietary and pharmacologic treatments, has led to growing demand for weight loss surgery. Between the early 1990s and 2003, the number of procedures performed nationwide rose from around 16 000 to more than 100 000 per year. Continued growth is expected, with >140 000 procedures anticipated for 2004 (Figure 1) (5). However, fast growth in an unregulated environment has raised concerns that obesity surgery is being performed by those who have inadequate training and experience or are practicing in hospitals and clinics with inadequate facilities and personnel. Those concerns are being addressed (13).


View larger version (27K):
FIGURE 1.. Increased US demand for weight loss surgery operations performed in 1992–2003 (5). Reprinted with permission from reference 5.

 
MAJOR MECHANISMS

Surgical treatment produces weight loss via two major mechanisms: gastric restriction and intestinal malabsorption (Table 1). Restrictive operations involve creation of a small neogastric pouch and gastric outlet to decrease food intake. Examples include vertical banded gastroplasty (VBG) (Figure 2A) and laparoscopic adjustable gastric banding (LAGB) (Figure 2B).


View this table:
TABLE 1. Types of bariatric procedures1

 

View larger version (17K):
FIGURE 2.. Restrictive procedures. Restrictive bariatric operations. A, Vertical banded gastroplasty; B, adjustable gastric banding; C, Roux-en-Y gastric bypass. Drawings were rendered by Dr. Alejandro Heffess and generously provided by Edward C. Mun (1). Reprinted with permission from reference 1.

 
Malabsorptive procedures involve rearrangement of the small intestine to decrease the functional length or efficiency of the intestinal mucosa for nutrient absorption. Examples include jejunoileal bypass (Figure 3A), biliopancreatic diversion (Figure 3B), and duodenal switch (Figure 3C). Malabsorptive surgeries produce more rapid and profound weight loss than restrictive procedures but put patients at risk for such metabolic complications as vitamin deficiencies and protein energy malnutrition. Restrictive procedures are considered simpler and safer than their malabsorptive counterparts but tend to result in inferior long-term weight loss.


View larger version (24K):
FIGURE 3.. Malabsorptive bariatric procedures. Malabsorptive bariatric operations. A, Jejunoileal bypass; B, biliopancreatic diversion; C, duodenal switch. Drawings were rendered by Dr. Alejandro Heffess and generously provided by Edward C. Mun (1). Reprinted with permission from reference 1.

 
TYPES OF SURGERIES

Accrued clinical experience and advances in technology have shaped and changed the field of weight loss surgery. Some procedures have evolved, whereas others have become obsolete. Over the past decade, VBG has been displaced by Roux-en-Y gastric bypass (RYGB) and newer laparoscopic approaches. The LAGB, introduced to the US market in 2001, has become increasingly popular.

Surgeries currently being performed include gastric bypass, malabsorptive procedures (eg, biliopancreatic diversions), and restrictive operations (gastroplasties with the use of adjustable gastric bands). RYGB and LAGB are the most common weight loss surgeries in the United States. Each can be performed either laparoscopically or in an open manner. Biliopancreatic diversion with duodenal switch, although effective in producing weight loss, is still considered investigational by many surgeons because of limited data on long-term safety and metabolic side effects. Others, who have developed particular expertise with the procedure, consider it an important approach to management of extreme obesity.

ROUX-EN-Y GASTRIC BYPASS

RYGB is the gold standard procedure for weight loss surgery in the United States today and the most frequently performed operation. It produces greater long-term weight loss than gastric partitioning alone or VBG. It is also substantially safer than jejunoileal bypass. The most important feature of RYGB (Figure 2C) is a small neogastric pouch and a tight stoma that limits oral intake, making restriction the primary mechanism for weight loss.

The procedure involves creating the small stomach pouch and rerouting a portion of the alimentary tract to bypass the distal stomach and proximal small bowel. This process leads to significant long-term weight loss and improvement or resolution of obesity-related comorbidities (12). Long limb (>150 cm) RYGB may produce superior short-term weight loss in patients who are >200 lb/91 kg overweight or have body mass index 50. Optimal limb length is unknown, but long-term follow-up indicates that the benefit of longer limb length decreases over time and may disappear completely.

RYGB is not without risks. These include the following: infrequent but serious surgical complications, eg, pulmonary embolism, intestinal leak, wound infection, and staple line failure; long-term deficiencies of iron, calcium, vitamin B12, and vitamin D; and the possibility of weight regain. Benefits have been found to outweigh these risks (12).

LAPAROSCOPIC WEIGHT LOSS SURGERY

Weight loss surgeons have developed laparoscopic approaches to gastric bypass and other weight loss surgery procedures. Like open procedures, laparoscopic weight loss surgery has proven effective at producing significant and sustained weight loss, along with improvements in comorbid conditions and quality of life. Because it is less invasive than open surgery, it shortens recovery time (14). Additional benefits include decreased rates of wound infection and incisional hernia (14-16).

Laparoscopic surgeons gain access to the abdomen via several small incisions. They insert a tiny video camera through one of the incisions and surgical instruments through the others. They operate by watching their work on a large-screen monitor. Laparoscopic techniques for weight loss surgery are difficult and associated with a longer and steeper learning curve than equivalent open procedures.

Open and laparoscopic RYGB produce similar short-term weight loss and improvements in comorbid medical conditions. The laparoscopic approach improves short-term recovery from surgery and has a lower incidence of incisional hernias than the open RYGB; long-term data are not yet available. Laparoscopic RYGB, although increasingly common, needs to be performed by appropriately trained and qualified laparoscopic weight loss surgeons.

LAPAROSCOPIC ADJUSTABLE GASTRIC BANDING

In LAGB, an adjustable silicone band is placed around the upper stomach to create a small pouch and a restricted outlet. The diameter of the outlet can be changed by injecting or removing saline through a portal under the skin. If the device is ineffective, or if serious complications develop, the band can be removed.

Although a large body of evidence, especially from European studies, suggests that LAGB is effective and safe for weight loss, long-term data from US patients are still limited. Studies indicate variation in benefits, the source of which remains unclear. Complications from gastric banding include band migration or erosion, gastroesophageal reflux disease, esophagitis, and problems with the subcutaneous port or tubing.

LAGB produces variable short-term weight loss and improvements in obesity-related comorbidities, with lower average mortality rates than RYGB or malabsorptive procedures. Placement of the LABG in the pars flaccida path rather than the retrogastric position appears to reduce the incidence of postoperative complications.

EFFICACY OF WEIGHT LOSS SURGERY

GBP has the most profound effect on reward-based eating, suggesting alteration of the CNS "reward pathways." It decreases the intensity of hunger and enhances the effectiveness of satiety to decrease food intake. GBP also dramatically alters food preferences and selection independent of specific cravings or aversions. The exact mechanisms for these outcomes have yet to be identified.

Neuroendocrine changes are thought to be key factors in producing weight loss. Gastrointestinal regulators of energy balance include those that promote energy storage [ie, ghrelin, glucose-dependent insulinotropic polypeptide (GIP), galanin, bombesin, and glucagon] and those that promote energy dissipation (ie, peptide YY 3-36, glucagon-like peptide-1, oxyntomodulin, pancreatic polypeptide, urocortins, cholecystokinin, and insulin). Ghrelin, the 28 amino acid neuroendocrine peptide secreted by the stomach, is the most potent endocrine stimulator of appetite and food intake. Ghrelin has been identified as the natural endogenous ligand for the growth hormone secretagogue receptor (17). It is thought that there may be ghrelin receptors on hypothalamic neurons central to weight regulation.

Weight loss through nonsurgical means increases circulating ghrelin. Plasma ghrelin levels are low after gastric bypass (18-21), although not all studies agree (22, 23). GIP secreted from the duodenum and jejunum is thought to promote fat synthesis and deposition. Whereas absence of GIP signaling appears to protect against obesity, secretion has been found to be acutely stimulated by food intake. GIP response to a meal increases after diet-induced weight loss. Surgery is fundamentally different from dieting. It changes the physiology to reset energy equilibrium, it affects the complex weight regulatory system at multiple levels, and it inhibits environmental influences on weight regulation and defeats powerful mechanisms that are inappropriately active in obesity.

Cummings et al. (24) suggest that the RYGB mediates weight loss and improved glucose tolerance via mechanisms that include following: 1) gastric restriction, which limits energy intake; 2) bypass of the foregut, which impairs ghrelin secretion in the long-limb variants of RYGB; and 3) expedited delivery of nutrients to the hindgut, which enhances the ileal brake and stimulates the release of peptide YY and glucagon-like peptide-1. In some patients, a dumping reaction to ingestion of concentrated carbohydrates may contribute to weight loss.

In addition to promoting weight loss, weight loss surgery is known to improve or resolve hyperlipidemia, diabetes, obstructive sleep apnea, and hypertension (12). Resolution of diabetes has often been found to occur within days of weight loss surgery, before marked weight loss (25). This effect was more prevalent after the predominantly malabsorptive procedures (bileopancreatic diversion or duodenal switch) and the mixed malabsorptive/restrictive gastric bypass compared with the purely restrictive gastroplasty and gastric banding procedures (12).

The putative extent and time relations of the different operative procedures to diabetes resolution may be related to some of the changes in the gut-related hormones. The hormonal milieu, or the relative balance of foregut mediators, is differently affected when the distal stomach is bypassed or a partial gastrectomy is performed, and the enteric contents are separated from the biliopancreatic stream in the upper small intestinal tract (12).

Current metabolic studies of patients with diabetes undergoing weight loss surgery have shown the following: a recovery of acute insulin response (26); significant decreases of inflammatory indicators (C-reactive protein and interleukin) (27); improvement in insulin sensitivity correlated with increases in plasma adiponectin (28, 29); significant changes in the enteroglucagon response to glucose (30); significant reduction in ghrelin levels after gastric bypass (19) but not gastric banding (31); and significant improvement in ß cell function after gastric banding (32).

CONCLUSIONS

Surgical therapy is the most effective modality for treatment of severe obesity (1, 3, 4, 12). The most commonly performed procedure, gastric bypass, causes changes in circulating ghrelin and GIP levels that promote weight loss observed after gastric bypass surgery. The reduction in ghrelin and GIP levels are opposite to the increases caused by diet-induced weight loss. These changes are thought to contribute to the greater efficacy of gastric bypass. Other neuroendocrine mechanisms are likely to be involved as well.

Changes in gut-related hormones are believed to be involved in both weight loss and improvement or resolution of obesity-related comorbidities. Improvement or resolution of diabetes has been found to occur within days of weight loss surgery, before marked weight loss (12). The study of the impact of the various weight loss surgical procedures on leptin, ghrelin, resistin, acylation-stimulating protein, adiponectin, entroglucagon, cholecystokinin, and other gastrointestinal satiety mediators is receiving increasing attention (22, 28, 33, 34).

The field of weight loss surgery is changing at an accelerating rate, one that makes it incumbent on leaders in the field to establish best practice standards for weight loss surgery. Patients will be well served by the development of standards and systems that will make it easier to track high incidences of complications or mortality. The field of weight loss surgery will be well served by future research that focuses on standardizing the technical aspects of weight loss surgery and comparing the efficacy and safety of malabsorptive and restrictive procedures (13).

ACKNOWLEDGMENTS

I thank Rita Buckley for assistance with medical editing. The author had no conflicts of interest.

REFERENCES

  1. Mun EC, Blackburn GL, Matthews JB. Current status of medical and surgical therapy for obesity. Gastroenterology 2001;120:669–81.
  2. Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults: the evidence report. National Institutes of Health. Obes Res 1998;6(suppl 2):51S–209S. (Published erratum appears in Obes Res 1998;6:464).
  3. Christou NV, Sampalis JS, Liberman M, et al. Surgery decreases long-term mortality, morbidity, and health care use in morbidly obese patients. Ann Surg 2004;240:416–23.
  4. Brolin RE. Bariatric surgery and long-term control of morbid obesity. JAMA 2002;288:2793–6.
  5. Steinbrook R. Surgery for severe obesity. N Engl J Med 2004;350:1075–9.
  6. Christou NV, Jarand J, Sylvestre JL, McLean AP. Analysis of the incidence and risk factors for wound infections in open bariatric surgery. Obes Surg 2004;14:16–22.
  7. Sampalis JS, Liberman M, Auger S, Christou NV. The impact of weight reduction surgery on health-care costs in morbidly obese patients. Obes Surg 2004;14:939–47.
  8. Flum DR, Dellinger E. Impact of gastric bypass on survival: a population-based analysis. J Am Coll Surg 2004;199:543–51.
  9. Special report: the relationship between weight loss and changes in morbidity following bariatric surgery for morbid obesity. Blue Cross and Blue Shield Association Technology Evaluation Center. Internet: www.bcbs.com/tec/vol18/18_09.html (accessed 12 November 2004).
  10. Colquitt J, Clegg A, Sidhu M, Royle P. Surgery for morbid obesity (Cochrane review). In: The Cochrane Library, Issue 1. Chichester, UK: Wiley & Sons, 2004.
  11. U.S. Preventive Services Task Force. Guide to clinical preventive services. 2nd ed. Baltimore: Williams & Wilkins, 1996.
  12. Buchwald H, Avidor Y, Braunwald E, Jensen MD, Pories W, Fahrbach K, Schoelles K. Bariatric surgery: a systematic review and meta-analysis. JAMA 2004;292:1724–37.
  13. Commonwealth of Massachusetts Betsy Lehman Center for Patient Safety and Medical Error Reduction Expert Panel on Weight Loss Surgery: executive report. Lehman Center Weight Loss Surgery Expert Panel. Obes Res 2005;13:205–26.
  14. Nguyen NT, Ho HS, Palmer LS, Wolfe BM. A comparison study of laparoscopic versus open gastric bypass for morbid obesity. J Am Coll Surg 2000;191:149–55; discussion 155–7.
  15. Schauer PR, Ikramuddin S, Gourash W, Ramanathan R, Luketich J. Outcomes after laparoscopic Roux-en-Y gastric bypass for morbid obesity. Ann Surg 2000;232:515–29.
  16. Schauer P, Ikramuddin S, Hamad G, Gourash W. The learning curve for laparoscopic Roux-en-Y gastric bypass is 100 cases. Surg Endosc 2003;17:212–5.
  17. Kojima M, Hosoda H, Matsuo H, Kangawa K. Ghrelin: discovery of the natural endogenous ligand for growth hormone secretagogue receptor. Trends Endocrinol Metab 2001;12:118–22.
  18. Morinigo R, Casamitjana R, Moize V, et al. Short-term effects of gastric bypass surgery on circulating ghrelin levels. Obes Res 2004;12:1108–16.
  19. Cummings DE, Weigle DS, Frayo RS, et al. Plasma ghrelin levels after diet-induced weight loss or gastric bypass surgery. N Engl J Med 2002;346:1623–30.
  20. Geloneze B, Tambascia MA, Pilla VF, Geloneze SR, Repetto EM, Pareja JC. Ghrelin: a gut-brain hormone: effect of gastric bypass surgery. Obes Surg 2003;13:17–22.
  21. Tritos NA, Mun E, Bertkau A, Grayson R, Maratos-Flier E, Goldfine A. Serum ghrelin levels in response to glucose load in obese subjects post-gastric bypass surgery. Obes Res 2003;11:919–24.
  22. Faraj M, Havel PJ, Phelis S, Bank D, Sniderman AD, Cianflone K. Plasma acylation-stimulating protein, adiponectin, leptin, and ghrelin before and after weight loss induced by gastric bypass surgery in morbidly obese subjects. J Clin Endocrinol Metab 2003;88:1594–602.
  23. Holdstock C, Engstrom BE, Ohrvall M, Lind L, Sundbom M, Karlsson FA. Ghrelin and adipose tissue regulatory peptides: effect of gastric bypass surgery in obese humans. J Clin Endocrinol Metab 2003;88:3177–83.
  24. Cummings DE, Overduin J, Foster-Schubert KE. Gastric bypass for obesity: mechanisms of weight loss and diabetes resolution. J Clin Endocrinol Metab 2004;89:2608–15.
  25. Pories WJ, Swanson MS, MacDonald KG, et al. Who would have thought it? An operation proves to be the most effective therapy for adult-onset diabetes mellitus. Ann Surg 1995;222:339–50.
  26. Polyzogopoulou EV, Kalfarentzos F, Vagenakis AG, Alexandrides TK. Restoration of euglycemia and normal acute insulin response to glucose in obese subjects with type 2 diabetes following bariatric surgery. Diabetes. 2003;52:1098–103.
  27. Kopp HP, Kopp CW, Festa A, et al. Impact of weight loss on inflammatory proteins and their association with the insulin resistance syndrome in morbidly obese patients. Arterioscler Thromb Vasc Biol 2003;23:1042–7.
  28. Yannakoulia M, Yiannakouris N, Bluher S, Matalas AL, Klimis-Zacas D, Mantzoros CS. Body fat mass and macronutrient intake in relation to circulating soluble leptin receptor, free leptin index, adiponectin, and resistin concentrations in healthy humans. J Clin Endocrinol Metab 2003;88:1730–6.
  29. Geloneze B, Pereira JA, Parajea JC, Aglecio S, Marcos T, Elza M. Circulating concentrations of adiponectin increase parallel with enhancement of insulin sensitivity during weight loss in humans. Alexandria, VA: American Diabetes Association, 2003.
  30. Kellum JM, Kuemmerle JF, O'Dorisio TM, et al. Gastrointestinal hormone responses to meals before and after gastric bypass and vertical banded gastroplasty. Ann Surg 1990;211:763–70; discussion 770–1.
  31. Hanusch-Enserer U, Brabant G, Roden M. Ghrelin concentrations in morbidly obese patients after adjustable gastric banding. N Engl J Med 2003;348:2159–60.
  32. Dixon JB, Dixon AF, O'Brien PE. Improvements in insulin sensitivity and beta-cell function (HOMA) with weight loss in the severely obese. Homeostatic model assessment. Diabet Med 2003;20:127–34.
  33. Badman MK, Flier JS. The gut and energy balance: visceral allies in the obesity wars. Science. 2005;307:1909–14.
  34. Rubino F, Marescaux J. Effect of duodenal-jejunal exclusion in a non-obese animal model of type 2 diabetes: a new perspective for an old disease. Ann Surg 2004;239:1–11.
  35. Blackburn GL, Mun EC. Hepatic impact of surgery for weight loss. In: Kaplan LM, Berk PD, eds. Seminars in liver disease. New York: Thieme Medical Publishers, 2005, in press.

作者: George L Blackburn
医学百科App—中西医基础知识学习工具
  • 相关内容
  • 近期更新
  • 热文榜
  • 医学百科App—健康测试工具