Published online Jul 15, 2021. doi: 10.4239/wjd.v12.i7.1093
Peer-review started: January 28, 2021
First decision: May 3, 2021
Revised: May 10, 2021
Accepted: June 25, 2021
Article in press: June 25, 2021
Published online: July 15, 2021
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Over the last decade, obesity rates have continued to rise in the United States as well as worldwide and are showing no signs of slowing down. This rise is in parallel with the increasing rates of type 2 diabetes mellitus (T2DM). Given the association between obesity and T2DM and their strong correlation with increased morbidity and mortality in addition to healthcare expenditure, it is important to recognize the most effective ways to combat them. Thus, we performed a review of literature that focused on assessing the outcomes of T2DM following bariatric surgery. Available evidence suggests that bariatric surgery provides better T2DM resolution in obese patients when compared to best medical management alone. Additionally, Biliopancreatic diversion with duodenal switch as well as Roux-en-Y gastric bypass have demonstrated higher rates of T2DM resolution when compared with other bariatric procedures.
Core Tip: Bariatric surgery is a safe and effective way to achieve diabetes remission in those with obesity via a variety of mechanisms, the majority of which are independent of weight loss. Available evidence suggests that bariatric surgery provides better type 2 diabetes mellitus resolution in obese patients when compared to best medical manage
- Citation: Chumakova-Orin M, Vanetta C, Moris DP, Guerron AD. Diabetes remission after bariatric surgery. World J Diabetes 2021; 12(7): 1093-1101
- URL: https://www.wjgnet.com/1948-9358/full/v12/i7/1093.htm
- DOI: https://dx.doi.org/10.4239/wjd.v12.i7.1093
Obesity rates continue to rise in the United States as well as worldwide. In fact, obesity prevalence doubled from 15% to 33% between 1980s and 2004 and was estimated to be 37.7% from 2013 to 2014[1,2]. Interestingly, some of the recent reports project that nearly 1 in 2 United States adults will have obesity [defined as body mass index (BMI) ≥ 30 kg/m2] by 2030 and nearly 1 in 4 adults will have severe obesity (defined as BMI ≥ 35 kg/m2) by then[3]. These numbers are alarming as obesity has been linked to developing type 2 diabetes mellitus (T2DM), coronary artery disease, non-alcoholic fatty liver disease, malignancy, amongst others, as well as lower life expectancy. Obesity was also attributable to 365000 deaths in 2000, second to only tobacco smoking[4]. Insulin resistance has been described as the main culprit for the development of T2DM in obese patients[5]. In fact, there is a > 6-fold increase in risk of developing T2DM in those with morbid obesity or BMI ≥ 40 kg/m2[6]. Diabetes remains one of the most prevalent chronic diseases in the United States affecting about 9% of the population in 2011, with rates continuing to grow in parallel with obesity[6].
This association between obesity and diabetes has detrimental effects on morbidity and mortality and creates a significant economic burden as a result. The cost of diabetes in 2012 was reported to be 45 billion dollars, with 69 billion dollars attributed to reduced productivity and 176 billion dollars attributed to direct medical costs[7]. Additionally, the cost of diabetes is projected to reach nearly 500 dollars billion by 2030[8]. This has led to an increased interest in finding ways to successfully treat diabetes and maintain remission.
While lifestyle modifications such as diet and exercise along with pharmacotherapy can be successful in treating both obesity and T2DM, few achieve sustained weight loss and only 10% of those with T2DM achieve favorable disease control in order to minimize and prevent long-term complications[9]. This article will thus focus on reviewing the most current data on diabetes remission following bariatric surgery.
Obesity has been linked to the development of T2DM via insulin resistance. Several mechanisms have been described. One of such proposed mechanisms involves increased release of a variety of factors including non-esterified fatty acids (NEFAs), glycerol, leptin, adiponectin, proinflammatory cytokines among others from adipose tissue which in turn leads to insulin resistance[10]. This occurs via reduced phosphorylation of phosphatidylinositol-3-OH kinase in muscle and increased gluconeogenic enzyme expression in the liver[9]. While this leads to insulin resistance, not all obese patients will go on to develop T2DM as they are able to overcome this by increased insulin release from pancreatic β cells to correct for decreased insulin sensitivity[9]. Thus, those with β cell dysfunction are at the highest risk of developing T2DM via increased release of NEFAs as they not only reduce insulin sensitivity but also decrease pancreatic β cell function[9].
Standard treatment of T2DM focuses on achieving good glycemic control in order to minimize cardiovascular and other risks and is mainly achieved via medical management. However, this treatment modality can become challenging in patients with obesity as a variety of pharmacotherapy agents can in fact cause weight gain and thus further worsen insulin resistance[11]. This is when bariatric surgery comes into play. Though initially described as surgical treatment for weight loss, bariatric surgery has demonstrated significant effects on reducing rates of T2DM in addition to improving cardiovascular health and thus reducing morbidity and mortality[12]. These beneficial effects are achieved via a multitude of mechanisms beyond weight loss.
While the exact mechanism for T2DM remission following bariatric surgery is not fully understood, several have been proposed. One such mechanism involves reduced caloric intake which in turn leads to significant weight loss and subsequently improved glucose sensitivity. This was thought to be achieved via restrictive and/or malabsorptive properties of bariatric surgery. However, this does not explain some of the drastic effects seen on glucose control immediately following surgery, and thus the majority of glucose-lowering is achieved prior to weight loss[13]. Additionally, scintigraphy studies demonstrate that nutrient delivery through gastric pouch is actually increased rather than restricted following Roux-en-Y gastric bypass (RYGB)[14].
One of the most important factors contributing to improved glucose tolerance is a significant decrease in insulin resistance fairly early following bariatric surgery. In fact, insulin resistance decreases about 50% in 1 wk following surgery and into the normal range seen in glucose tolerant patients when measured homeostatic model assessment of insulin resistance[15-17]. In addition to improved liver insulin sensitivity, insulin clearance also increases and is thought to be due to decreased caloric intake which in turn leads to decreased liver fat content. This has been demonstrated using post-operative magnetic resonance imaging of the liver following RYGB[14]. These combined effects in turn lead to decreased basal glucose concentration and are thought to improve pancreatic β cell function by decreasing the toxic effect of glucose[18].
According to the foregut-hindgut hypothesis, there is an increased amount of incompletely digested food delivered to the distal intestine due to bypassed foregut. This in turn stimulates specialized L cells which facilitate the release of glucagon-like-peptide-1 (GLP-1) and peptide YY, both of which have been implicated in achieving weight loss. Additionally, both provide a favorable effect on pancreatic β cells leading to increased insulin sensitivity[18,19]. Interestingly, GLP-1 Levels rise dramatically within days of bariatric surgery stimulating pancreatic β cells. This effect of β cell stimulation is further amplified by a temporary early increase in plasma glucose levels eventually leading to increased insulin release[17]. While this hypothesis may explain the benefits seen following RYGB and biliopancreatic diversion with duodenal switch (BPD-DS), it does not explain the beneficial effects on glucose metabolism seen following sleeve gastrectomy (SG) as the intestinal tract remains in continuity[16].
Circulating bile acids (BA) levels also increase following bariatric surgery and are correlated with improved glucose sensitivity. This is thought to occur following reduced mixture of partially digested nutrients with BAs following surgery thus leading to higher concentration of free circulating BAs. This, in turn, leads to reduction in hepatic glucose production as well as glucogeogenesis within gut segments that are devoid of BAs[20].
A comprehensive search of the published literature in PubMed, PubMed Central (PMC), EMBASE, Medline, and the Cochrane Register of Controlled Trials databases was conducted until January 2021. We used the guidelines of 2015 Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P). Randomised controlled trials with at least 12 mo of follow-up and prediction models of diabetes remission after bariatric surgery were included. Keywords containing “obesity”, “metabolic [or] bariatric surgery”, “type 2 diabetes”, “diabetes remission”, “predict”, “prediction models” and “score” were constructed for inclusion. Only studies in english language were included.
Mingrone et al[12] designed a randomized clinical trial (RCT) looking at 60 patients who were randomly assigned to one of the 3 groups: Conventional medical therapy, RYGB or BPD-DS. Their primary endpoint included diabetes remission which was defined as fasting glucose level < 100 mg/dL and glycosylated hemoglobin (HbA1c) < 6.5mmol/L without the use of pharmacotherapy. Fifty-six patients completed their 2 year follow up and at that time no patients in the medical group achieved remission while 75% in the RYGB and 95% in the BPD-DS were able to achieve remission (P < 0.05). Additionally, while the HbA1c levels did decrease significantly in all 3 groups from average baseline of 8.65% ± 1.45%, the 2 surgical groups had greater degree of lowering with average numbers at 2-year follow up being the following: 7.69% ± 0.57% for the medical group, 6.35% ± 1.42% in the RYGB group and 4.95% ± 0.49% in the BPD-DS group. The authors of this study concluded that bariatric surgery was able to achieve higher rates of remission in patients with severe obesity (BMI ≥ 35 kg/m2), and HbA1c < 6.5 mmol/L without the use of pharmacotherapy[12].
Calorie reduction or surgery: Seeking to Reduce Obesity and Diabetes Study was an RCT that assigned patients with obesity (BMI ≥ 30 kg/m2) and T2DM to either RYGB (n = 23) or intensive lifestyle and medical management (n = 20). Patients were followed for 1 year with primary outcome measured being T2DM resolution (defined as HbA1c <6% and being off medications). During this follow up, 60% of patients following RYGB achieved remission while nearly 6% of the medical group were able to do so (P < 0.05). This study reported no life-threatening complications in the surgical group. The authors concluded that RYGB yielded higher rates of T2DM remission at 1 year when compared to medical therapy alone[21].
Surgical Treatment and Medications Potentially Eradicate Diabetes Efficiently (STAMPEDE) RCT published by Schauer et al[22] in 2017 provides some of the longer-term data shedding light on the effectiveness of bariatric surgery on T2DM resolution. The study randomized 150 patients with obesity and T2DM to intensive medical therapy alone vs medical therapy and either RYGB or SG.One hundred and thirty-four patients completed 5 year follow up with primary endpoint being achievement of HbA1c level of ≤ 6%. Of those who underwent intense medical therapy alone, 5% were able to achieve this endpoint vs 29% of those who also underwent RYGB (adjusted P < 0.05) and 23% of those who underwent SG (adjusted P = 0.07). In the surgical group, this endpoint was achieved without the need for hypoglycemic medications in the majority of patients, whereas none of the patients in the medical group were able to achieve that endpoint without pharmacotherapy. Additionally, 89% of patients in the surgical group were off insulin during a 5 year follow up compared to 61% of patients in the medical group[22].
Hofsø et al[23] designed a triple blind RCT that was conducted in Norway comparing 109 patients with morbid obesity and presence of T2DM who were randomly assigned to SG (55/109) or RYGB (54/109). The primary outcome measured during their 1 year follow up was diabetes remission defined as having HbA1c ≤ 6% while being off pharmacotherapy. 107/109 patients completed 1 year follow up demonstrating that 47% of SG patients had diabetes remission and 74% of RYGB patients had diabetes remission (P < 0.05). This study also reported 57 adverse reactions during a follow up period with 1 patient returning back to the operating room following an intra-abdominal bleed following SG, 1 patient needing blood transfusions 10 days following RYGB. No deaths were observed in this study. Thus, the authors concluded that even though pancreatic β cell function improved after both types of surgery, RYGB was found to have greater effect on T2DM resolution when compared to SG at 1 year[23].
Another recent 3-arm RCT assigned 61 patients with obesity and T2DM to one of the 3 groups: RYGB, adjustable gastric banding (AGB) or intense medical therapy and were followed for 1 year initially. After 1 year follow up, the patients were assessed for additional 4 years following introduction of lower-level lifestyle interventions. Primary endpoint of this study was T2DM remission rates (partial: Fasting plasma glucose (FPG) ≤ 125 mg/dL, HbA1c < 6.5% and off medications and complete: FPG ≤ 100 mg/dL, HbA1c < 5.7% and off medications). At 5 years, partial or complete T2DM remission was achieved in 30% of RYGB group, 19% of AGB group and 0% of medical management group (P < 0.05). Additionally, 56% of RYGB patients were off medications at 5 years as compared to 45% of AGB group and 0% of medical management group (P < 0.05). Thus, the authors concluded that their surgical management was more effective in T2DM resolution than best medical management alone[11].
More recently, a study by Mingrone et al[24] published their 10 year follow up results comparing metabolic surgery and medical management for T2DM at a single center in Italy. This RCT included 3 treatment arms: BPD-DS, RYGB and medical management. They had 20 patients in each arm group with 60 patients total, 57 of which completed follow up. Remission was defined as FPG ≤ 100 mg/dL, HbA1c ≤ 6.5% and being off medications. Ten-year remission rates in the intention-to-treat analysis demonstrated that 5.5% [95% confidence interval (CI) 1.0-25.7] of medical group achieved remission when compared to 50% in BPD-DS [95%CI 29.9-70.1] group and 25% in RYGB [95%CI 11.2-49.9] group (P < 0.05)[24] (Table 1).
Ref. | Pts w/ follow up/enrolled pts | Study duration, years | Medical management T2DM resolution % | RYGB T2DM resolution % | SG T2DM resolution % | BPD-DS T2DM resolution % | AGB T2DM resolution % | T2DM resolution definition | P value |
Mingrone et al[12], 2012 | 56/60 | 2 | 0 | 75 | N/A | 95 | N/A | FPG < 100 mg/dL + HbA1c < 6.5 mmol/L + no pharmacotherapy | < 0.05 |
Cummings et al[21], 2016 | 43/43 | 1 | 6 | 60 | N/A | N/A | N/A | HbA1c < 6% + no pharmacotherapy | < 0.05 |
Schauer et al[22], 2017 | 134/150 | 5 | 5 | 29 | 23 | N/A | N/A | < 0.05 | |
Hofsø et al[23], 2019 | 107/109 | 1 | N/A | 74 | 47 | N/A | N/A | < 0.05 | |
Courcoulas et al[11], 2020 | 50/61 | 5 | 0 | 30 | N/A | N/A | 19 | < 0.05 | |
Mingrone et al[24], 2021 | 57/60 | 10 | 5 | 25 | N/A | 50 | N/A | < 0.05 |
Several prediction models have been developed in order to assess diabetes remission following bariatric surgery. The models used are either scoring systems, in which each variable is given a specific score and the addition of scores gives the probability of diabetes remission; or a logistic regression model in which higher odds means a higher probability of diabetes remission[25]. Relevant scoring systems include the DiaRem, age, bmi, c-peptide level and duration of diabetes score (ABCD), and individualized metabolic surgery scores (IMSS).
This model described by Still et al[26] in 2014 is based on a retrospective study of 690 diabetic obese patients who underwent RYGB. The preoperative factors which demonstrated to be independent predictive factors of diabetes remission were: Age, insulin use, HbA1c measurement, and type of antidiabetic medications. Preoperative insulin use was associated with the higher severity of diabetes and lower percentage of remission and was given the highest score of 10 points. The score range goes from 0 to 22, and the patients fall into one of five groups. The higher the score, the lowest the probability of diabetes remission.
Additionally, in 2019, the DiaRem2 score incorporated the duration of diabetes to the already validated DiaRem[27]. The association between “early remission” (defined as remission within the first 2 mo after surgery) and duration of diabetes, as well as early remission and score was analyzed. Patients were allocated into one of three remission groups according to their score: High (0-5), Intermediate (6-12) or Low (13-25). A highest score was associated with a decreased percentage of early remission.
In this score proposed by Lee et al[28] in 2013, a first cohort of 63 patients who underwent either RYGB or mini-gastric bypass in Asia was analyzed. The four preoperative factors identified as independent risk factors for remission were: Age, baseline BMI, C-peptide level, and duration of diabetes. Patients with higher scores had higher remission rates. A modified scoring system was then tested in 510 patients, including SG patients. It showed lower remission levels after SG than those correlated to RYGB. One of the limitations of this score was that insulin and other antidiabetic medications used were not taken into account.
IMSS was designed by Aminian et al[29] with the objective to guide procedure selection based on long-term diabetes remission. A sample of 659 patients who underwent RYGB or SG was analyzed. Duration of diabetes, number of diabetes medications, insulin use, and HbA1c were the four independent predictors used to develop this score. Patients were allocated into one of three stages of diabetes severity. This study included recommendations on what type of surgery to perform: RYGB for mild disease and moderate disease, and SG for severe disease. In severe diabetes, the rate of remission is lower, so the least demanding technique is preferred. Unfortunately, biliopancreatic diversion with duodenal switch was not included in this score even though this procedure has been associated with higher remissions of associated comorbidities.
The general limitations of the scoring systems commented is that they were based on one or two procedure types, with RYGB as the leading procedure, and they are usually limited to a population with a defined race/ethnicity. That is why Duke Group developed a logistic regression model including a diverse racial/ethnicity and a large BPD/DS sample[30]. This model was based on a retrospective review of 602 patients who underwent RYGB, SG, LAGB or BPD/DS. The objective was to analyze the relation of remission to procedure type. DiaRem score was used to assess the perfor
Independent of the predictive model used, the procedure type is an independent risk factor for diabetes remission. Our results indicate BPD/DS as the procedure with a higher percentage of diabetes remission (Table 2). We believe that this procedure should be taken into account in future tools that include a recommendation of the procedure of choice.
Diarem | Diarem2 | IMS | ABCD | Duke diabetes remission | |
Procedure | Rygb | RYGB | RYGB or SG | RYGB or mini-gastric | RYGB, SG, AGB, BPD/DS |
Number of patients (n) | 690 | 307 | 659 | 63 | 602 |
Variables | Insulin use | Insulin use | Insulin use | Diabetes duration | Age |
Sex | |||||
Age | Age | Duration of diabetes | Age | Race | |
Insulin use | |||||
Hba1c | Hba1c | Hba1c | Baseline BMI | Hba1c | |
BMI | |||||
Type of antidiabetic drugs | Duration of diabetes | Number of diabetic medications | C-peptide level | Preop asthma, GERD, hypertension, hyperlipidemia, anticoagulation medication status | |
Type of antidiabetic drugs | |||||
Scale | 0-22 (5 groups) | 0-25 (High-Intermediate-Low remission) | 3 stages (Mild-Moderate-Severe) | 0-10 | Odds of remission according to preoperative variables and type of surgery |
Recommendation on procedure of choice | No | No | Yes | No | No |
Bariatric surgery is a safe and effective way to treat T2DM in those struggling with obesity. The effects can be seen fairly early prior to any substantial weight loss, thus highlighting the interplay of hormonal factors that leads to increased insulin sensitivity via activation of pancreatic β cells.
Several efforts have been made to prove the effectiveness of bariatric surgery in diabetes remission, including randomized clinical trials with 1, 3, 5 and even 10 years of follow-up. A variety of bariatric surgical procedures have demonstrated to be more effective than medical management for T2DM control, and BPD-DS and RYGB have shown some of the highest remission rates.
The literature available up to date still encounters certain limitations. For instance, in the STAMPEDE trial, patients had a relatively low BMI (mean 37 ± 3.5 kg/m2) with 37% of them having a BMI value < 35 kg/m2. This leaves aside the morbid and super obese population, but opens the discussion to lower the current indication guidelines to serve patients with T2DM and lower BMI.
In addition, remission was achieved in 23%-29% of patients submitted to surgery, but nothing is said about the remaining 70% who did not benefit from RYGB or SG. Could these patients benefit from another type of surgery such as biliopancreatic diversion with duodenal switch? Even the most recent information from a RCT by Mingrone et al[24] with the largest follow-up (10 years), exhibited maintained diabetes remission in only 37,5% of the patients when compared to conventional medical therapy.
BPD/DS is an under-utilized surgical procedure which has been associated with enhanced weight loss and resolution of comorbid disease[31], though postoperative complications are increased when compared to RYGB or SG[32]. Numerous studies, including our predictive model, have demonstrated that this procedure is related to increased weight loss and remission of diabetes and other comorbidities. Yet, its low implementation fails to show its benefits on a wide scale.
The discussion is no longer whether metabolic surgery achieves remission of diabetes or not, as this has broadly been demonstrated. Debate arises on which procedure is best for each individual patient. Predictive models are warranted to be improved once they succeed in including a large, diverse population, addressing duration of diabetes and insulin use, who are submitted to any of the surgical procedures available (AGB, SG, RYGB, distal bypass, BPD-DS etc.).
The following steps are yet to be determined. Large multicentric studies are awaited to test and improve the existing scores, in order to ultimately develop a calculator able to predict individualized surgical outcomes. Yet, there is still a feeling of uncertainty and apprehension surrounding the fate of patients who experience diabetes relapse or weight regain after metabolic surgery.
Manuscript source: Invited manuscript
Specialty type: Surgery
Country/Territory of origin: United States
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1. | Hales CM, Fryar CD, Carroll MD, Freedman DS, Ogden CL. Trends in Obesity and Severe Obesity Prevalence in US Youth and Adults by Sex and Age, 2007-2008 to 2015-2016. JAMA. 2018;319:1723-1725. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1143] [Cited by in F6Publishing: 1274] [Article Influence: 212.3] [Reference Citation Analysis (0)] |
2. | Flegal KM, Kruszon-Moran D, Carroll MD, Fryar CD, Ogden CL. Trends in Obesity Among Adults in the United States, 2005 to 2014. JAMA. 2016;315:2284-2291. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2216] [Cited by in F6Publishing: 2081] [Article Influence: 260.1] [Reference Citation Analysis (0)] |
3. | Ward ZJ, Bleich SN, Cradock AL, Barrett JL, Giles CM, Flax C, Long MW, Gortmaker SL. Projected U.S. State-Level Prevalence of Adult Obesity and Severe Obesity. N Engl J Med. 2019;381:2440-2450. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 756] [Cited by in F6Publishing: 1089] [Article Influence: 217.8] [Reference Citation Analysis (0)] |
4. | Al-Sulaiti H, Diboun I, Agha MV, Mohamed FFS, Atkin S, Dömling AS, Elrayess MA, Mazloum NA. Metabolic signature of obesity-associated insulin resistance and type 2 diabetes. J Transl Med. 2019;17:348. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 39] [Cited by in F6Publishing: 86] [Article Influence: 17.2] [Reference Citation Analysis (0)] |
5. | Chobot A, Górowska-Kowolik K, Sokołowska M, Jarosz-Chobot P. Obesity and diabetes-Not only a simple link between two epidemics. Diabetes Metab Res Rev. 2018;34:e3042. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 147] [Cited by in F6Publishing: 168] [Article Influence: 28.0] [Reference Citation Analysis (0)] |
6. | Leung MY, Carlsson NP, Colditz GA, Chang SH. The Burden of Obesity on Diabetes in the United States: Medical Expenditure Panel Survey, 2008 to 2012. Value Health. 2017;20:77-84. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 47] [Cited by in F6Publishing: 50] [Article Influence: 7.1] [Reference Citation Analysis (0)] |
7. | American Diabetes Association. Economic costs of diabetes in the U.S. in 2012. Diabetes Care. 2013;36:1033-1046. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1675] [Cited by in F6Publishing: 1695] [Article Influence: 154.1] [Reference Citation Analysis (0)] |
8. | Zhang P, Zhang X, Brown J, Vistisen D, Sicree R, Shaw J, Nichols G. Global healthcare expenditure on diabetes for 2010 and 2030. Diabetes Res Clin Pract. 2010;87:293-301. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 652] [Cited by in F6Publishing: 669] [Article Influence: 47.8] [Reference Citation Analysis (0)] |
9. | Wong K, Glovaci D, Malik S, Franklin SS, Wygant G, Iloeje U, Kan H, Wong ND. Comparison of demographic factors and cardiovascular risk factor control among U.S. adults with type 2 diabetes by insulin treatment classification. J Diabetes Complications. 2012;26:169-174. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 47] [Cited by in F6Publishing: 47] [Article Influence: 3.9] [Reference Citation Analysis (0)] |
10. | Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature. 2006;444:840-846. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 3146] [Cited by in F6Publishing: 3459] [Article Influence: 203.5] [Reference Citation Analysis (0)] |
11. | Courcoulas AP, Gallagher JW, Neiberg RH, Eagleton EB, DeLany JP, Lang W, Punchai S, Gourash W, Jakicic JM. Bariatric Surgery vs Lifestyle Intervention for Diabetes Treatment: 5-Year Outcomes From a Randomized Trial. J Clin Endocrinol Metab. 2020;105:866-876. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 58] [Cited by in F6Publishing: 87] [Article Influence: 21.8] [Reference Citation Analysis (0)] |
12. | Mingrone G, Panunzi S, De Gaetano A, Guidone C, Iaconelli A, Leccesi L, Nanni G, Pomp A, Castagneto M, Ghirlanda G, Rubino F. Bariatric surgery vs conventional medical therapy for type 2 diabetes. N Engl J Med. 2012;366:1577-1585. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1340] [Cited by in F6Publishing: 1233] [Article Influence: 102.8] [Reference Citation Analysis (0)] |
13. | Zhu J, Gupta R, Safwa M. The Mechanism of Metabolic Surgery: Gastric Center Hypothesis. Obes Surg. 2016;26:1639-1641. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 1.6] [Reference Citation Analysis (0)] |
14. | Steven S, Hollingsworth KG, Small PK, Woodcock SA, Pucci A, Aribasala B, Al-Mrabeh A, Batterham RL, Taylor R. Calorie restriction and not glucagon-like peptide-1 explains the acute improvement in glucose control after gastric bypass in Type 2 diabetes. Diabet Med. 2016;33:1723-1731. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 37] [Cited by in F6Publishing: 47] [Article Influence: 5.9] [Reference Citation Analysis (0)] |
15. | Jørgensen NB, Jacobsen SH, Dirksen C, Bojsen-Møller KN, Naver L, Hvolris L, Clausen TR, Wulff BS, Worm D, Lindqvist Hansen D, Madsbad S, Holst JJ. Acute and long-term effects of Roux-en-Y gastric bypass on glucose metabolism in subjects with Type 2 diabetes and normal glucose tolerance. Am J Physiol Endocrinol Metab. 2012;303:E122-E131. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 245] [Cited by in F6Publishing: 244] [Article Influence: 20.3] [Reference Citation Analysis (0)] |
16. | Falkén Y, Hellström PM, Holst JJ, Näslund E. Changes in glucose homeostasis after Roux-en-Y gastric bypass surgery for obesity at day three, two months, and one year after surgery: role of gut peptides. J Clin Endocrinol Metab. 2011;96:2227-2235. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 250] [Cited by in F6Publishing: 234] [Article Influence: 18.0] [Reference Citation Analysis (0)] |
17. | Holst JJ, Madsbad S, Bojsen-Møller KN, Svane MS, Jørgensen NB, Dirksen C, Martinussen C. Mechanisms in bariatric surgery: Gut hormones, diabetes resolution, and weight loss. Surg Obes Relat Dis. 2018;14:708-714. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 97] [Cited by in F6Publishing: 125] [Article Influence: 20.8] [Reference Citation Analysis (0)] |
18. | Martinussen C, Bojsen-Møller KN, Dirksen C, Jacobsen SH, Jørgensen NB, Kristiansen VB, Holst JJ, Madsbad S. Immediate enhancement of first-phase insulin secretion and unchanged glucose effectiveness in patients with type 2 diabetes after Roux-en-Y gastric bypass. Am J Physiol Endocrinol Metab. 2015;308:E535-E544. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 52] [Cited by in F6Publishing: 54] [Article Influence: 6.0] [Reference Citation Analysis (0)] |
19. | Makris MC, Alexandrou A, Papatsoutsos EG, Malietzis G, Tsilimigras DI, Guerron AD, Moris D. Ghrelin and Obesity: Identifying Gaps and Dispelling Myths. A Reappraisal. In Vivo. 2017;31:1047-1050. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 14] [Cited by in F6Publishing: 35] [Article Influence: 5.8] [Reference Citation Analysis (0)] |
20. | Batterham RL, Cummings DE. Mechanisms of Diabetes Improvement Following Bariatric/Metabolic Surgery. Diabetes Care. 2016;39:893-901. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 239] [Cited by in F6Publishing: 246] [Article Influence: 30.8] [Reference Citation Analysis (0)] |
21. | Cummings DE, Arterburn DE, Westbrook EO, Kuzma JN, Stewart SD, Chan CP, Bock SN, Landers JT, Kratz M, Foster-Schubert KE, Flum DR. Gastric bypass surgery vs intensive lifestyle and medical intervention for type 2 diabetes: the CROSSROADS randomised controlled trial. Diabetologia. 2016;59:945-953. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 206] [Cited by in F6Publishing: 204] [Article Influence: 25.5] [Reference Citation Analysis (0)] |
22. | Schauer PR, Bhatt DL, Kirwan JP, Wolski K, Aminian A, Brethauer SA, Navaneethan SD, Singh RP, Pothier CE, Nissen SE, Kashyap SR; STAMPEDE Investigators. Bariatric Surgery vs Intensive Medical Therapy for Diabetes - 5-Year Outcomes. N Engl J Med. 2017;376:641-651. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1626] [Cited by in F6Publishing: 1722] [Article Influence: 246.0] [Reference Citation Analysis (0)] |
23. | Hofsø D, Fatima F, Borgeraas H, Birkeland KI, Gulseth HL, Hertel JK, Johnson LK, Lindberg M, Nordstrand N, Cvancarova Småstuen M, Stefanovski D, Svanevik M, Gretland Valderhaug T, Sandbu R, Hjelmesæth J. Gastric bypass vs sleeve gastrectomy in patients with type 2 diabetes (Oseberg): a single-centre, triple-blind, randomised controlled trial. Lancet Diabetes Endocrinol. 2019;7:912-924. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 108] [Cited by in F6Publishing: 134] [Article Influence: 26.8] [Reference Citation Analysis (0)] |
24. | Mingrone G, Panunzi S, De Gaetano A, Guidone C, Iaconelli A, Capristo E, Chamseddine G, Bornstein SR, Rubino F. Metabolic surgery vs conventional medical therapy in patients with type 2 diabetes: 10-year follow-up of an open-label, single-centre, randomised controlled trial. Lancet. 2021;397:293-304. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 166] [Cited by in F6Publishing: 264] [Article Influence: 88.0] [Reference Citation Analysis (0)] |
25. | Shen SC, Wang W, Tam KW, Chen HA, Lin YK, Wang SY, Huang MT, Su YH. Validating Risk Prediction Models of Diabetes Remission After Sleeve Gastrectomy. Obes Surg. 2019;29:221-229. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 25] [Cited by in F6Publishing: 31] [Article Influence: 6.2] [Reference Citation Analysis (0)] |
26. | Still CD, Wood GC, Benotti P, Petrick AT, Gabrielsen J, Strodel WE, Ibele A, Seiler J, Irving BA, Celaya MP, Blackstone R, Gerhard GS, Argyropoulos G. Preoperative prediction of type 2 diabetes remission after Roux-en-Y gastric bypass surgery: a retrospective cohort study. Lancet Diabetes Endocrinol. 2014;2:38-45. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 233] [Cited by in F6Publishing: 238] [Article Influence: 23.8] [Reference Citation Analysis (0)] |
27. | Still CD, Benotti P, Mirshahi T, Cook A, Wood GC. DiaRem2: Incorporating duration of diabetes to improve prediction of diabetes remission after metabolic surgery. Surg Obes Relat Dis. 2019;15:717-724. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 2.0] [Reference Citation Analysis (0)] |
28. | Lee WJ, Hur KY, Lakadawala M, Kasama K, Wong SK, Chen SC, Lee YC, Ser KH. Predicting success of metabolic surgery: age, body mass index, C-peptide, and duration score. Surg Obes Relat Dis. 2013;9:379-384. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 155] [Cited by in F6Publishing: 183] [Article Influence: 15.3] [Reference Citation Analysis (0)] |
29. | Aminian A, Brethauer SA, Andalib A, Nowacki AS, Jimenez A, Corcelles R, Hanipah ZN, Punchai S, Bhatt DL, Kashyap SR, Burguera B, Lacy AM, Vidal J, Schauer PR. Individualized Metabolic Surgery Score: Procedure Selection Based on Diabetes Severity. Ann Surg. 2017;266:650-657. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 147] [Cited by in F6Publishing: 182] [Article Influence: 26.0] [Reference Citation Analysis (0)] |
30. | Guerron AD, Perez JE, Risoli T Jr, Lee HJ, Portenier D, Corsino L. Performance and improvement of the DiaRem score in diabetes remission prediction: a study with diverse procedure types. Surg Obes Relat Dis. 2020;16:1531-1542. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis (0)] |
31. | Dorman RB, Rasmus NF, al-Haddad BJ, Serrot FJ, Slusarek BM, Sampson BK, Buchwald H, Leslie DB, Ikramuddin S. Benefits and complications of the duodenal switch/biliopancreatic diversion compared to the Roux-en-Y gastric bypass. Surgery. 2012;152:758-65. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 61] [Cited by in F6Publishing: 61] [Article Influence: 5.1] [Reference Citation Analysis (0)] |
32. | Anderson B, Gill RS, de Gara CJ, Karmali S, Gagner M. Biliopancreatic diversion: the effectiveness of duodenal switch and its limitations. Gastroenterol Res Pract. 2013;2013:974762. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 3.2] [Reference Citation Analysis (0)] |