Abstract
Background
Remission of diabetes is seen in more than 60% of patients after bariatric surgery. There is extensive variability in the remission rates between different surgical procedures. We analyzed our database and aimed to develop an easy scoring system to predict the probability of diabetes remission after two surgical procedures i.e. Ileal Interposition coupled with Sleeve Gastrectomy (IISG) or Diverted Sleeve Gastrectomy (IIDSG).
Methods
In this retrospective study, we analyzed records pertaining to patients who underwent IISG (n = 46) and IIDSG (n = 29). The primary outcome measure was diabetes remission (A1c <6.5% and not requiring hypoglycemic drugs). We identified seven preoperative clinical variables (age, duration of diabetes, body mass index, micro and macrovascular complications, use of insulin and stimulated C-peptide) based on our previous reports to be included in the diabetes remission score (DRS). The DRS score (7 – 14) was compared between the patients with and without remission in both the surgery groups.
Results
Mean DRS in patients who underwent IISG was 9.2 ± 1.4. Twenty one (46%) had a remission in diabetes. DRS was significantly lower in patients with remission than patients without remission (8.1 ± 0.8 versus 10.2 ± 0.9, p < 0.0001). Mean DRS in patients who underwent IIDSG was 10.4 ± 1.3. Twenty one (72%) had a remission in diabetes. DRS was significantly lower in patients with remission than patients without remission (9.7 ± 0.8 versus 12.0 ± 0.5, p < 0.0001). Patients with a DRS ≥ 10 in IISG group and more than 12 in IIDSG group did not get into remission.
Conclusion
Preoperative DRS can be a useful tool to select the type of surgical procedure and to predict the postoperative diabetes remission.
Trial registration
Keywords: Type 2 Diabetes, Ileal interposition, Sleeve gastrectomy, Diabetes remission, Metabolic surgery
Background
Bariatric surgery in patients with type 2 diabetes is known to produce remission in a majority of cases. The improvement is not limited to diabetes alone and includes hypertension, dyslipidemia and obstructive sleep apnea as well. The magnitude and onset of this improvement outweighs the weight loss leading to the concept of ‘metabolic surgery’ rather than bariatric surgery [1]. The observed metabolic benefits lead to the extension of this concept to non obese patients also [2-5]. Bariatric surgical procedures are primarily divided into restrictive and malabsorptive types. The most common surgical procedures are sleeve gastrectomy (SG), gastric banding, Roux-en-Y-Gastric Bypass (RYGB) and Jejuno-Ileal Bypass (JIB). The observed remission in diabetes after these surgeries is reported to range between 45-95% [6].
The standard procedures have been modified to achieve maximum remission with minimal long term complications. The modified surgical techniques are Ileal Interposition (II), Diverted Sleeve Gastrectomy (DSG), Sleeve Gastrectomy with Duodeno-jejunal Bypass (SG + DJB), Mini-Gastric Bypass (MGB) and Single Anastomosis Duodeno-Ileal (SADI) procedure [6]. The results are often incomparable between procedures due to the differences involved in patients and the spectrum of diabetes. The proposed predictive factors for remission and other outcomes includes age, diabetes duration, insulin reserve& requirement, body mass index (BMI), ethnicity and number of preoperative medications required to manage blood glucose [7-12]. We observed a significant variability in the remission rates using IISG and IIDSG as reported previously [13-17]. A good predictive model is essential in helping the patients and clinicians to decide about the probability of remission based on preoperative criteria. We developed a novel scoring system known as Diabetes Remission Score (DRS) based on the previous database. Our intention is to develop a simple, effective and useful method to help the surgical teams in predicting the diabetes remission rates postoperatively.
Methods
The present study is a retrospective analysis of all the patients with poorly controlled type 2 diabetes mellitus (T2DM), who were subjected to the laparoscopic procedures of IISG or IIDSG at Kirloskar Hospital, Hyderabad, India. IISG was started in February 2008 and IIDSG was started in March 2010 and the study was duly approved by the hospital’s ethics committee (Institutional Review Board, Kirloskar Hospital, Hyderabad) and registered (NCT00834626). Informed consent was obtained from all patients participating in the study. Study participants were explained specifically about the benefits pertinent to nonobese subjects and the potential risks involved. The patient selection criteria and surgical techniques have been described in detail previously (13 – 17). Briefly, we included patients having T2DM of more than 1 year duration (>5 years duration for IIDSG), aged between 25 and 70 years, poor glycemic control with HbA1C > 7% on the optimum dosage of insulin ± oral hypoglycemic agents (OHA), stable weight, BMI ≥20 kg/m2 (>18.5 kg/m2 for IIDSG) and stimulated C-peptide level >1.5 ng/ml. The decision of mode of surgery (IISG or IIDSG) was taken by the surgical team in consultation with the endocrinologist and the patient’s preference. The study is a retrospective analysis of the patients profile precluding the possibility of random allocation into each group. We excluded patients with type 1 diabetes mellitus, undetectable fasting C-peptide, ketoacidosis in past 6 months, pregnancy and coexisting severe hepatic, pulmonary and psychiatric diseases.
Surgical technique
IISG
The surgical procedure involved the creation of a 170-cm segment of ileum, starting at 30 cm proximal to the ileo-cecal junction. This segment was interposed into the jejunum, which was divided between 20 and 50 cm from the ligament of Treitz. All three anastomoses were performed side by side with an endo-GIA stapler (Ethicon Endo-surgery, Cincinnati, OH, USA). A variable sleeve gastrectomy was performed after devascularization of the greater curvature from the antrum to the fundus area as shown in Figure 1. The lumen of the stomach was adjusted by a 32–60 French calibrator (Romsons International, New Delhi, India) that was placed along the lesser curvature. The size of the bougie is determined for each patient individually depending on the baseline body weight, BMI and the anticipated amount of weight loss. The size between 32 F to 38 F was used in majority of the patients. The endo-GIA stapler with 60-mm cartridges were used for resection. Nonobese patients were subjected to only fundectomy, leaving a good volume of residual stomach for normal food intake. The fundectomy was carried by removing the fundus and with the proximal limit of dissection 3 cm to cardia.
IIDSG
A variable sleeve gastrectomy was performed after devascularization of the greater curvature from the antrum to the fundus area as described above. The duodenum was transected using a 60-mm linear stapler with a blue cartridge. The role of surgical stapler is to provide tissue approximation and hemostasis without leading to necrosis and destruction. The tissue thickness varies in the stomach and it is important to select the most appropriate staple cartridge to accommodate the underlying tissue [18]. The staple cartridges are color coded as gray, white, blue, gold, green and black in the ascending order of closed staple height dimensions. The gastric pouch and proximal duodenum were then transposed through a window created at the root of the transverse mesocolon. A distal ileal segment of 170 cm was transected along with its mesentery pedicle, measured 30 cm proximal to the ileocecal valve. Continuity of small bowel is restored by ileo-ileal anastomosis and the proximal end of this transected ileal segment was anastomosed to the proximal duodenum as shown in Figure 2. A point in the jejunum 50 cm from the ligament of Treitz was measured and anastomosed to the distal part of the interposed ileum, side to side, using stapler.
Post operatively each participant was followed up at 1, 3, 6 ,9 and 12 months in the 1st year and every 6 months thereafter. They were subjected to clinical and biochemical assessment. HbA1C <6.5% (without requiring any medication for diabetes control) was defined as the criterion for remission in diabetes. Our study protocol was started in 2008 and the ADA defined diabetes remission into partial and complete in 2009 [19]. Hence, our definition is similar to that of partial remission given by the ADA.
Statistical analysis & scoring system
All outcome measures were evaluated prospectively from the third month onward at every visit. The seven variables to be included in the DRS have been derived from our previous reports. The details of the DRS components are given in Table 1. DRS was calculated in all the patients retrospectively and compared between IISG and IIDSG procedures. We used Graphpad Quickcalcs software (Graphpad Software Inc, La Jolla, CA, USA) for statistical calculations. The continuous variables were described in the form of mean ± standard deviation and comparison between the groups was done using unpaired student’s t test. All tests were two sided and a p value less than 0.05 were considered significant.
Table 1.
Parameter | Score | |
---|---|---|
1 | 2 | |
Age (yr) | 30 – 60 | < 30 or >60 |
Body Mass Index (kg/m 2 ) | ≥ 27 | < 27 |
Duration of T2DM (yr) | < 10 | ≥ 10 |
Microvascular complications | No | Yes |
Macrovascular complications | No | Yes |
Preoperative Insulin use | No | Yes |
Stimulated C-peptide (ng/mL) | ≥ 4 | < 4 |
Results
Forty six patients underwent IISG and 29 patients underwent IIDSG surgical procedures. The baseline demographic parameters are shown in Table 2 and the operation details in Table 3. Mean DRS in patients who underwent IISG (n = 46) was 9.2 ± 1.4 (Range: 7–13). Twenty one (46%) had a remission in diabetes. In the same group, patients with BMI ≥ 35 kg/m2, had a remission rate of 85%. Their mean DRS was 8.9 ± 1.7 versus mean DRS of 9.5 ± 1.1 in patients with BMI less than 35 (p = 0.07). DRS was significantly lower in patients with remission than patients without remission (8.1 ± 0.8 versus 10.2 ± 0.9, p < 0.0001). All the patients with DRS 7–8 achieved remission of diabetes, while only 35% patients with DRS 9 had diabetes remission. There was no remission in diabetes in patients with baseline DRS ≥ 10 in IISG group as shown in Table 4.
Table 2.
Parameter | Units | IISG group n = 46 | IIDSG group n = 29 |
---|---|---|---|
Age | years | 51.7 (13.3) | 57.6 (11.5) |
Sex | M:F | 29 : 17 | 20 : 9 |
BMI | Kg/m2 | 23.4 (4.5) | 25.6 (4.5) |
DM duration | Years | 9.9 (4.8) | 10.1 (5) |
Duration of insulin use | Years | 3.3 (2.9) | 3.6 (2.8) |
Daily Insulin dose | Units | 28.2 (10.6) | 75.5 (12) |
Daily Insulin dose | U/Kg | 0.45 (0.15) | 1.1 (0.1) |
Retinopathy | Number | 21 | 13 |
Acanthosis | Grade | 0.83 (0.9) | 1.1 (0.8) |
HbA1c | % | 8.1 (0.59) | 9 (0.78) |
HDL cholesterol | mg/dL | 40.2 (5.7) | 41 (5) |
LDL cholesterol | mg/dL | 92.7 (18.5) | 96 (18.9) |
Triglycerides | mg/dL | 106.7 (37.2) | 107 (44) |
Serum Iron | μg/dL | 104.5 (22.4) | 112.1 (18.7) |
Serum Ferritin | ng/mL | 44.7 (18.5) | 53.3 (12.2) |
Vitamin B12 | pg/mL | 423.3 (102.4) | 397.9 (92.9) |
Mean (S.D).
Table 3.
Parameter | Units | IISG group n = 46 | IIDSG group n = 29 |
---|---|---|---|
Operation time | Hours | 3.8 (0.9) | 5.8 (0.8) |
Hospital stay | Days | 4.2 (0.8) | 5.4 (1.2) |
Duration of follow up | Months | 30.2 (9.6) | 12.7 (5.3) |
Intraoperative complications | Number | Nil | 4* |
Postoperative complications | Number | Nausea - 12 | Nausea – 6 |
Long term complications | Number | Nil | B12 deficiency – 3 |
Data given as mean (S.D) * Explained in the results section.
Table 4.
IISG group (N = 46) | IIDSG group (N = 29) | ||||
---|---|---|---|---|---|
Obese | Non Obese | Obese | Non Obese | ||
Number of Patients | No | 32 | 14 | 21 | 8 |
Remission of DM | No (%) | 17 (53) | 4 (47) | 16 (55) | 5 (45) |
Baseline BMI | kg/m2 | 31.2(4.7) | 24.7(5.3) | 33.5(2.6) | 25.3(1.4) |
BMI at end point | kg/m2 | 27.1(4.8) | 23.5 (6.4) | 27.5(4.6) | 22.9 (5.1) |
Δ Body weight | kg | 9.7 (6.6) | 1.4(2.3) | 7.8(5.4) | 2.2 (1.7) |
DRS | Score | 8.1 (0.8) | 10.2 (0.9) | 9.7 (0.8) | 12 (0.5) |
BMI Body Mass Index, Δ Body weight Change in the weight from baseline, DRS Diabetes Remission Score.
Mean DRS in patients who underwent IIDSG (n = 29) was 10.4 ± 1.3 (Range: 8–14, significantly higher than II + SG group, p = 0.0004). Twenty one (72%) had a remission in diabetes. DRS was significantly lower in patients with remission than patients without remission (9.7 ± 0.8 versus 12.0 ± 0.5, p < 0.0001). All the patients with DRS 8–10 achieved remission, while 55% patients with DRS 11 had diabetes remission. There was no remission in diabetes in patients with baseline DRS ≥ 12.
Patients with DRS ≥ 10 in IISG group and DRS ≥ 12 in IIDSG group did not get into remission. DRS was not significantly different (p = 0.1468) in patients without remission in IISG (10.2 ± 0.9) versus patients with remission in IIDSG (9.7 ± 0.8). In patients with IIDSG, intraoperative complications were observed in 4 patients. One patient had a dusky duodenal stump leading to application of the drain. Another patient had a suture-passer tip breakage into the abdominal wall which was extricated by C arm. A 2 cm opening at the gastric antrum in another patient was closed in 3–0 PDS because of faulty stapling and the last patient had ileal perforation managed by exploratory laparotomy and closure. At 3 months postoperative follow up, none of these patients had any complications with regard to the intraoperative and immediate postoperative events.
Discussion
Our study focuses on the development of a novel score (DRS) preoperatively in predicting diabetes remission following IISG or IIDSG. DRS was derived from the variable factors predicting the remission in diabetes. Our previous studies on IISG have demonstrated duration of diabetes, BMI and stimulated C-peptide response as baseline parameters of response [14,15]. Previous studies of RYGB reported that old age, longer duration of diabetes, lower C-peptide level, and lower BMI reduce the likelihood of response to surgery [7,20,21]. In type 2 diabetes patients with duration of diabetes < 5 years, a resolution of the disease was obtained in 95%, whereas the rate of resolution was only 75% and 54% in those who had type 2 diabetes for 6–10 or >10 years [5]. Scopinaro et al. has shown that metabolic surgery is less effective in individuals with lower BMI [22,23]. Insulin resistance is a major contributing factor for diabetes in patients with high BMI, whereas beta cell dysfunction predominates in the normal weight individuals. Hence, the benefits of metabolic surgery are observed more in obese individuals when compared to nonobese patients. Our data also showed similar results in both the groups as shown in Table 4. IIDSG gives augmented stimulus to the enteroinsular hormonal axis leading to better resolution of diabetes. The baseline body weight and the amount of excess body weight lost determine the benefit rates in diabetes resolution. Previous reports suggest that diabetes remission is seen in 60% of patients with restrictive procedures and up to 80 – 90% in combined (restrictive and malabsorptive) procedures [6,23]. Advanced age is an important consideration for patient selection also, because of the augmented risks with surgery and weight loss [24,25].
DRS was significantly lower in patients with remission than patients without remission. This demonstrates that patients with lower baseline DRS have better remission rates and patients with DRS of 7–8 should only be subjected to IISG. Our data demonstrate that IIDSG may be taken up for patients with a DRS up to 11. Additionally DRS was not significantly different (p = 0.1468) in patients without remission in IISG (10.2 ± 0.9) versus patients with remission in IIDSG (9.7 ± 0.8). This indirectly suggests that IIDSG instead of IISG would have helped them in achieving remission.
IIDSG is more beneficial over the conventional IISG procedure due to the following points. The IIDSG excludes the duodenum, leading to attenuated release of Rubino’s factor (anti-incretin factor, which promotes insulin resistance) and Gastric Inhibitory Polypeptide (GIP) [26]. Disruption or attenuation of GIP action is associated with decreased glucagon release, diminished weight gain, resistance to diet-induced obesity, and improved insulin sensitivity in preclinical studies [27-30], whereas genetic variation within the human Gastric Inhibitory Polypeptide Receptor (GIPR) gene is linked to control of postprandial glucose and body weight [31,32]. Exclusion of duodenum also leads to abolition of hedonic (pleasure) value of food, resulting in lesser indulgence in feeding [33]. In comparison to IISG, the interposed ileal segment is shifted more proximally in IIDSG, leading to augmented glucagon like peptide (GLP-1) hormone secretion [16,17]. Our surgical technique has no risk of malabsorptive complications as the procedure does not involve removal of either intestinal digestive or absorptive surface. The previous published long term follow up studies using this technique also did not report any malabsorptive complications. Iron malabsorption is theoretically possible due to lack of gastric intrinsic factor after the surgery. However, we prescribed supplemental iron to all patients postoperatively preventing this complication.
The surgical technique used in this study is designed essentially for diabetes control and utilizes both the foregut and hindgut mechanisms [34]. The SG component restricts calorie intake and reduces ghrelin [35]; it also speeds up gastric transit of food, reaching the ileal segment faster. The GLP-1 response is defective in T2DM leading to diminished first phase of insulin secretion [36]. The ileal interposition helps in the rapid stimulation of ileal segment by ingested food leading to augmented GLP-1 secretion [13-15]. GLP-1 also influences glucose metabolism by inhibiting glucagon secretion, decreasing hepatic gluconeogenesis, delaying gastric emptying, promoting satiety, suppressing appetite, and stimulating glycogenesis [37-43].
We propose a baseline assessment of DRS as a possible predictor of remission in diabetes following IISG or IIDSG. The DRS may be divided into 3 grades as grade 1 (mild, DRS 7–8), grade 2 (moderate, 9–11) and grade 3 (severe, DRS 12–14). Higher scores indicate a diminished chance of achieving remission in a given patient. The advantages of DRS include an easy clinically relevant score, combining multiple factors affecting the diabetes and give an objective measure for comparison between the procedures. Our study has certain limitations. The study analysis and the development of DRS were based on retrospective observational analysis of the data. The DRS score was developed based on the data from sleeve gastrectomy and ileal interposition. Hence, DRS may not be useful for predicting remission of other bariatric or metabolic procedures. The status of obesity alone as a determinant of metabolic surgery is incorrect due to the identification of a phenotype called metabolically obese and normal weight individuals [44]. This also limits the wide application of this scoring system prior to the surgery. The study was inadequately powered to give a definite conclusion due to limited number of the patients and mixed population in each group. Moreover, our data from a single center may not represent the entire diabetes population of India.
Conclusion
Diabetes remission score is a useful tool for predicting the remission in patients with type 2 diabetes undergoing IISG or IIDSG. We propose to introduce DRS as a tool to select the type of surgical procedure and to predict the postoperative diabetes remission. Further multicenter studies of patients from various ethnicities are required to confirm our preliminary observations.
Acknowledgements
We thank all the patients for their participation in the study.
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
SU, KDM and NG enrolled all the patients into the surgical programme. SU proposed the concept and SKK did all the analytical aspects of the study. VN, VS, MS and KVSHK contributed to selection of patients, study design, and writing of the report. SU, NG, VS and VN did all the surgeries. KDM, SKK and KVSHK did the presurgery workup and postoperative follow up. SKK, KDM and SU wrote the report with help from all other authors. SU and KVSHK finally revised the manuscript and all the authors have accepted the final version of this manuscript.
Contributor Information
Surendra Ugale, Email: surenugale@gmail.com.
Neeraj Gupta, Email: whatneeraj@gmail.com.
Kirtikumar D Modi, Email: drkdmodi@yahoo.co.in.
Sunil K Kota, Email: hidocsunil@gmail.com.
Vasisht Satwalekar, Email: vrsatwalekar@yahoo.co.in.
Vishwas Naik, Email: vishwasgopalnaik@gmail.com.
Modukuri Swapna, Email: swapnamodukuri@yahoo.com.
KVS Hari Kumar, Email: hariendo@rediffmail.com.
References
- 1.Greenway SE, Greenway FL, 3rd, Klein S. Effects of Obesity Surgery on Non Insulin Dependent Diabetes Mellitus. Arch Surg. 2002;137:1109–1117. doi: 10.1001/archsurg.137.10.1109. [DOI] [PubMed] [Google Scholar]
- 2.De Paula AL, Macedo AL, Rassi N, Machado CA, Schraibman V, Silva LQ, Halpern A. Laparoscopic Treatment of Type 2 Diabetes Mellitus for Patients with a Body Mass Index less than 35. Surg Endosc. 2008;22:706–716. doi: 10.1007/s00464-007-9472-9. [DOI] [PubMed] [Google Scholar]
- 3.AL D p, Stival AR, Macedo A, Ribamar J, Mancini M, Halpern A, Vencio S. Prospective Randomized Controlled Trial Comparing 2 Versions of Laparoscopic Ileal Interposition Associated with Sleeve Gastrectomy for Patients with Type 2 Diabetes with BMI 21–34 kg/ m2. Surg Obes Relat Dis. 2010;6:296–305. doi: 10.1016/j.soard.2009.10.005. [DOI] [PubMed] [Google Scholar]
- 4.Tinoco A, El- Kadre L, Tinoco R, Savasi- Rocha P. Short-term and Mid-term Control of Type 2 Diabetes Mellitus by Laparoscopic Sleeve Gastrectomy with Ileal Interposition. World J Surg. 2011;35:2238–2244. doi: 10.1007/s00268-011-1188-2. [DOI] [PubMed] [Google Scholar]
- 5.Pories WJ, Swanson MS, MacDonald KG, Long SB, Morris PG, Brown BM, Barakat HA, deRamon RA, Israel G, Dolezal JM. Who would have thought it? An Operation Proves to be the Most Effective Therapy for Adult-Onset Diabetes Mellitus. Ann Surg. 1995;222:339–350. doi: 10.1097/00000658-199509000-00011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Buchwald H, Estok R, Fahrbach K, Banel D, Jensen MD, Pories WJ, Bantle JP, Sledge I. Weight and type 2 diabetes after bariatric surgery: systematic review and meta-analysis. Am J Med. 2009;122:248–256. doi: 10.1016/j.amjmed.2008.09.041. [DOI] [PubMed] [Google Scholar]
- 7.Dixon JB, Chuang LM, Chong K, Chen SC, Lambert GW, Straznicky NE, Lambert EA, Lee WJ. Predicting the glycemic response to gastric bypass surgery in patients with type 2 Diabetes. Diabetes Care. 2013;36:20–26. doi: 10.2337/dc12-0779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Schauer PR, Burguera B, Ikramuddin S, Cottam D, Gourash W, Hamad G, Eid GM, Mattar S, Ramanathan R, Barinas-Mitchel E, Rao RH, Kuller L, Kelley D. Effect of laparoscopic Roux-en Y gastric bypass on type 2 diabetes mellitus. Ann Surg. 2003;238:467–484. doi: 10.1097/01.sla.0000089851.41115.1b. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Dixon JB, O’Brien PE. Health outcomes of severely obese type 2 diabetic subjects 1 year after laparoscopic adjustable gastric banding. Diabetes Care. 2002;25:358–363. doi: 10.2337/diacare.25.2.358. [DOI] [PubMed] [Google Scholar]
- 10.Lee WJ, Hur KY, Lakadawala M, Kasama K, Wong SK, Lee YC. Gastrointestinal metabolic surgery for the treatment of diabetic patients: a multi-institutional international study. J Gastrointest Surg. 2012;16:45–51. doi: 10.1007/s11605-011-1740-2. [DOI] [PubMed] [Google Scholar]
- 11.Lee WJ, Chong K, Ser KH, Chen JC, Lee YC, Chen SC, Su YH, Tsai MH. C-peptide predicts the remission of type 2 diabetes after bariatric surgery. Obes Surg. 2012;22:293–298. doi: 10.1007/s11695-011-0565-0. [DOI] [PubMed] [Google Scholar]
- 12.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(1):38–45. doi: 10.1016/S2213-8587(13)70070-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hari Kumar KV, Ugale S, Gupta N, Naik V, Kumar P, Bhaskar P, Modi KD. Ileal Transposition with Sleeve Gastrectomy for Control of Type 2 Diabetes. Diabetes Technol Ther. 2009;11:1–5. doi: 10.1089/dia.2008.0040. [DOI] [PubMed] [Google Scholar]
- 14.Kumar Kota S, Ugale S, Gupta N, Naik V, Krishna Kota S, Hari Kumar KVS, Modi KD. Remission of type 2 diabetes mellitus by ileal interposition with sleeve gastrectomy. Int J Endocrinol Metab. 2011;9:374–381. doi: 10.5812/Kowsar.1726913X.2782. [DOI] [Google Scholar]
- 15.Kota SK, Ugale S, Gupta N, Naik V, Kumar KV, Modi KD. Ileal interposition with sleeve gastrectomy for treatment of type 2 diabetes mellitus. Indian J Endocr Metab. 2012;16:589–598. doi: 10.4103/2230-8210.98017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Kota SK, Ugale S, Gupta N, Modi KD. Laparoscopic ileal interposition with diverted sleeve gastrectomy for treatment of type 2 diabetes. Diabetes Metab Syndr. 2012;6:125–131. doi: 10.1016/j.dsx.2012.09.014. [DOI] [PubMed] [Google Scholar]
- 17.Kota SK, Ugale S, Gupta N, Krishna S, Modi KD. Ileal Interposition with diverted sleeve gastrectomy for treatment of type 2 diabetes. Indian J Endocr Metab. 2012;16:458–459. doi: 10.4103/2230-8210.104131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Elariny H, González H, Wang B. Tissue thickness of human stomach measured on excised gastric specimens from obese patients. Surg Technol Int. 2005;14:119–124. [PubMed] [Google Scholar]
- 19.Buse JB, Caprio S, Cefalu WT, Ceriello A, Del Prato S, Inzucchi SE, McLaughlin S, Phillips GL, 2nd, Robertson RP, Rubino F, Kahn R, Kirkman MS. How do we define cure of diabetes? Diabetes Care. 2009;32(11):2133–2135. doi: 10.2337/dc09-9036. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Broglio F, Arvat E, Benso A, Gottero C, Muccioli G, Papotti M, van der Lely AJ, Deghenghi R, Ghigo E. Ghrelin, a Natural GH Secretagogue Produced by the Stomach, Induces Hyperglycemia and Reduces Insulin Secretion in Humans. J Clin Endocrinol Metab. 2001;86:5083–5086. doi: 10.1210/jcem.86.10.8098. [DOI] [PubMed] [Google Scholar]
- 21.Lee WJ, Ser KH, Chong K, Lee YC, Chen SC, Tsou JJ, Chen JC, Chen CM. Laparoscopic sleeve gastrectomy for diabetes treatment in non morbidly obese patients: efficacy and change of insulin secretion. Surgery. 2010;147:664–669. doi: 10.1016/j.surg.2009.10.059. [DOI] [PubMed] [Google Scholar]
- 22.Scopinaro N, Adami GF, Papadia FS, Camerini G, Carlini F, Briatore L, D'Alessandro G, Parodi C, Weiss A, Andraghetti G, Catalano M, Cordera R. The effects of biliopancreatic diversion on type 2 diabetes mellitus in patients with mild obesity (BMI 30–35 kg/m2) and simple overweight (BMI 25–30 kg/m2): a prospective controlled study. Obes Surg. 2011;21:880–888. doi: 10.1007/s11695-011-0407-0. [DOI] [PubMed] [Google Scholar]
- 23.Scopinaro N, Adami GF, Papadia FS, Camerini G, Carlini F, Fried M, Briatore L, D'Alessandro G, Andraghetti G, Cordera R. Effects of biliopanceratic diversion on type 2 diabetes in patients with BMI 25 to 35. Ann Surg. 2011;253:699–703. doi: 10.1097/SLA.0b013e318203ae44. [DOI] [PubMed] [Google Scholar]
- 24.Oreopoulos A, Kalantar-Zadeh K, Sharma AM, Fonarow GC. The obesity paradox in the elderly: potential mechanisms and clinical implications. Clin Geriatr Med. 2009;25:643–659. doi: 10.1016/j.cger.2009.07.005. [DOI] [PubMed] [Google Scholar]
- 25.Ramanan B, Gupta PK, Gupta H, Fang X, Forse RA. Development and validation of a bariatric surgery mortality risk calculator. J Am Coll Surg. 2012;214:892–900. doi: 10.1016/j.jamcollsurg.2012.02.011. [DOI] [PubMed] [Google Scholar]
- 26.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. doi: 10.1097/01.sla.0000102989.54824.fc. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Meier JJ, Gallwitz B, Siepmann N, Holst JJ, Deacon CF, Schmidt WE, Nauck MA. Gastric inhibitory polypeptide (GIP) dose-dependently stimulates glucagon secretion in healthy human subjects at euglycaemia. Diabetologia. 2003;46:798–801. doi: 10.1007/s00125-003-1103-y. [DOI] [PubMed] [Google Scholar]
- 28.Kulkarni RN. GIP: no longer the neglected incretin twin? Sci Trans Med. 2010;2:49–47. doi: 10.1126/scitranslmed.3001027. [DOI] [PubMed] [Google Scholar]
- 29.Hall TC, Pellen MG, Sedman PC, Jain PK. Preoperative factors predicting remission of type 2 diabetes mellitus after Roux-en-Y gastric bypass surgery for obesity. Obes Surg. 2010;20:1245–1250. doi: 10.1007/s11695-010-0198-8. [DOI] [PubMed] [Google Scholar]
- 30.Irwin N, Flatt PR. Evidence for beneficial effects of compromised gastric inhibitory polypeptide action in obesity-related diabetes and possible therapeutic implications. Diabetologia. 2009;52:1724–1731. doi: 10.1007/s00125-009-1422-8. [DOI] [PubMed] [Google Scholar]
- 31.Saxena R, Hivert MF, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, Lyssenko V, Bouatia-Naji N, Dupuis J, Jackson AU, Kao WH, Li M, Glazer NL, Manning AK, Luan J, Stringham HM, Prokopenko I, Johnson T, Grarup N, Boesgaard TW, Lecoeur C, Shrader P, O'Connell J, Ingelsson E, Couper DJ, Rice K, Song K, Andreasen CH, Dina C, Köttgen A, Le Bacquer O, et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat Genet. 2010;42:142–148. doi: 10.1038/ng.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segrè AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpeläinen TO, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010;42:937–948. doi: 10.1038/ng.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Guyenet SJ, Schwartz MW. Clinical Review: Regulation of food intake, energy balance, and body fat mass: implications for the pathogenesis and treatment of obesity. J Clin Endocrinol Metab. 2012;97:745–755. doi: 10.1210/jc.2011-2525. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.De Paula AL, Macedo AL, Prudente A, Silva L, Schraibman V, Neto JG. Neuroendocrine Brake for the Treatment of Morbid Obesity: Preliminary Report. Einstei. 2005;3:110–114. [Google Scholar]
- 35.Pereferrer FS, Gonzàlez MH, Rovira AF, Blasco SB, Rivas AM, del Castillo DD. Influence of sleeve gastrectomy on several experimental models of obesity: metabolic and hormonal implications. Obes Surg. 2008;18(1):97–108. doi: 10.1007/s11695-007-9351-4. [DOI] [PubMed] [Google Scholar]
- 36.Nauck M, Stockmann F, Ebert R, Creutzfeldt W. Reduced Incretin Effect in Type 2 (noninsulin- dependent) Diabetes. Diabetologia. 1986;29:46–52. doi: 10.1007/BF02427280. [DOI] [PubMed] [Google Scholar]
- 37.Holst JJ. The Physiology of Glucagon-Like Peptide 1. Physiol Rev. 2007;87:1409–1439. doi: 10.1152/physrev.00034.2006. [DOI] [PubMed] [Google Scholar]
- 38.Kjems LL, Holst JJ, Volund A, Madsbad S. The Influence of GLP-1 on Glucose Stimulated Insulin Secretion: Effects on Beta-Cell Sensitivity in Type 2 and Nondiabetic Subjects. Diabetes. 2003;52:380–386. doi: 10.2337/diabetes.52.2.380. [DOI] [PubMed] [Google Scholar]
- 39.Drucker DJ. Enhancing Incretin Action for the Treatment of Type 2 Diabetes. Diabetes care. 2003;26:2929–2940. doi: 10.2337/diacare.26.10.2929. [DOI] [PubMed] [Google Scholar]
- 40.Irwin N, Gault VA, Green BD, Greer B, McCluskey JT, Harriott P, O'harte FP, Flatt PR. Effects of Short-Term Chemical Ablation of the GIP Receptor on Insulin Secretion, Islet Morphology and Glucose Homeostasis in Mice. Biol Chem. 2004;385:845–852. doi: 10.1515/BC.2004.110. [DOI] [PubMed] [Google Scholar]
- 41.Gault VA, Irwin N, Green BD, McCluskey JT, Greer B, Bailey CJ, Harriott P, O'harte FP, Flatt PR. Chemical Ablation of Gastric Inhibitory Polypeptide Receptor Action by Daily (Pro3) GIP Administration Improves Glucose Tolerance and Ameliorates Insulin Resistance and Abnormalities of Islet Structure in Obesity-Related Diabetes. Diabetes. 2005;54:2436–2446. doi: 10.2337/diabetes.54.8.2436. [DOI] [PubMed] [Google Scholar]
- 42.Ferrannini E, Cobelli C. The Kinetics of Insulin in Man. General Aspects. Diabetes Metab Rev. 1987;3:335–363. doi: 10.1002/dmr.5610030201. [DOI] [PubMed] [Google Scholar]
- 43.Vilsboll T, Holst JJ. Incretins, Insulin Secretion and Type 2 Diabetes Mellitus. Diabetologia. 2004;47:357–366. doi: 10.1007/s00125-004-1342-6. [DOI] [PubMed] [Google Scholar]
- 44.Aung K, Lorenzo C, Hinojosa MA, Haffner SM. Risk of developing diabetes and cardiovascular disease in metabolically unhealthy normal-weight and metabolically healthy obese individuals. J Clin Endocrinol Metab. 2014;99:462–468. doi: 10.1210/jc.2013-2832. [DOI] [PMC free article] [PubMed] [Google Scholar]