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Clinical Research Papers:

Meta-analysis of bariatric surgery versus non-surgical treatment for type 2 diabetes mellitus

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Oncotarget. 2016; 7:87511-87522. https://doi.org/10.18632/oncotarget.11961

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Guo-zhong Wu, Bing Cai, Feng Yu, Zheng Fang, Xing-li Fu, Hai-sen Zhou, Wen Zhang and Zhi-qiang Tian _

Abstract

Guo-zhong Wu1,*, Bing Cai2,*, Feng Yu1,*, Zheng Fang1, Xing-li Fu3, Hai-sen Zhou4, Wen Zhang3 and Zhi-qiang Tian1,2

1 Department of General Surgery, The 101st Hospital of Chinese PLA, Wuxi, Jiangsu, China

2 Department of General Surgery, Wuxi People’s Hospital, Nanjing Medical University, Wuxi, Jiangsu, China

3 Health Science Center, Jiangsu University, Zhenjiang, Jiangsu, China

4 Nanjing Lishui People’s Hospital, Nanjing, Jiangsu, China

* These authors have contributed equally to this work

Correspondence to:

Zhi-qiang Tian, email:

Keywords: bariatric surgery, type 2 diabetes mellitus, non-surgical treatment, meta-analysis

Received: July 10, 2016 Accepted: September 07, 2016 Published: September 10, 2016

Abstract

Background: To compare short-term and long-term results of bariatric surgery vs non-surgical treatment for type 2 diabetes mellitus (T2DM).

Methods: A systematic search was conducted in the PubMed, Embase, and Cochrane Library databases for randomized controlled trials (RCTs). All statistical analysis was performed using Review Manager version 5.3. The dichotomous data was calculated using risk ratio (RR) and continuous data was using mean differences (MD) along with 95% confidence intervals (CI).

Results: A total of 8 RCTs with 619 T2DM patients were analyzed. Compared with non-surgical treatment group, bariatric surgery group was associated with higher rate T2DM remission (RR = 5.76, 95%CI:3.15-10.55, P < 0.00001), more reduction HbA1C (MD = 1.29, 95%CI: -1.70 to -0.87, P < 0.00001), more decrease fasting plasma glucose (MD = -36.38, 95%CI: -51.76 to -21.01, P < 0.00001), greater loss body weight (MD = -16.93, 95%CI: 19.78 to -14.08, P < 0.00001), more reduction body mass index (MD = -5.80, 95%CI: -6.95 to -4.64, P < 0.00001), more decrease triglyceride concentrations (MD = -51.27, 95%CI: -74.13 to -28.41, P < 0.0001), and higher increase density lipoprotein cholesterol (MD = 9.10, 95%CI: 7.99 to 10.21; P < 0.00001). But total and low density lipoprotein cholesterol were no significant changes.

Conclusion: Bariatric surgery for T2DM is efficacious and improves short- and long-term outcomes as compared with non-surgical treatment.


INTRODUCTION

Type 2 diabetes mellitus (T2DM) is a disease with high prevalence, associated with severe co-morbidities as well as being a huge burden on public health [1]. Strict glycemic control is known to decreases long-term morbidity and mortality [2]. The current standard therapy for T2DM is medical treatment which cornerstone is intensive lifestyle modification strategies [3]. However, only partially patients achieve adequate glycemic control and a reduction in cardiovascular risk [4-6].

Bariatric surgery has recently emerged as new therapeutic approach for patients with T2DM. Several observational studies [7-10] and randomized controlled trials(RCTs) [11-17] have shown T2DM remission after bariatric surgery [18]. But until recently, it is not fully understood the etiology of diabetes remission following bariatric surgery. Also, these trials have some limitations, such as a small sample size of the various types of surgery, uncertainty the durability of the metabolic benefits of surgery, long-term safety, quality of life, and effects on diabetes-related end-organ disease. These studies could inevitably increase the risk of bias being responsible for their conclusions, and more strong evidences are still needed to support the results of these studies.

The meta-analysis can test hypotheses about sources of differences and assess the magnitudes of biases when used to compare results from different studies. So, we performed a meta-analysis to obtain comprehensive estimates of the clinical benefit from all of the available data. This meta-analysis identified and screened the short-term and long-term results of bariatric surgery compared with non-surgical treatment for T2DM in RCT studies.

RESULTS

Search results

A total of 816 articles were identified in a combined search of the electronic databases covering studies published before June 15th 2016. 693 studies were in total excluded after title/abstract screening, then 55 studies were excluded following a further review full-text of the remaining 63 studies. In the end, 8 studies [12, 19-25] were included in this meta-analysis. Figure 1 demonstrated a flow chart of the selection process.

All of 8 studies were RCTs and conducted in Australia (1), China (1), Italy (1), and US (5). The majority of studies reported data from a single center and only one study [21] was multi-center study. Almost all studies did not report the numbers of participating surgeons and noted that patients were consecutively enrolled. 3 studies [21, 22, 24] had sample sizes greater than 100 patients. Two studies [20, 22] had 1-year follow-up, three studies [12, 21, 25] had 2-year follow-up, two studies [19, 24] had 3-year follow-up, and only one study [23] had 5-year follow-up. The characteristics of these 8 studies were described in Table 1.

A total of 619 T2DM patients were included in the meta-analysis: 341 in bariatric surgery group and 278 in non-surgery treatment group. Bariatric surgery techniques included Roux-en-Y gastric bypass, sleeve gastrectomy, laparoscopic adjustable gastric banding, and biliopancreatic diversion. Non-surgical treatment generally comprised alterations in dietary intake, physical activity, behavioral or lifestyle modification, and pharmacotherapy. Table 2 summarized the description of patients at baseline from these 8 studies.

Table 1: Basic characteristics of 8 studies included in this meta-analysis

Study

(Author, year)

Countrya

Design

Bariatric Surgery

Conventional Medical Treatment

T2DM variables,

IRB, IC, Reg

Follow-up

(year)

Courcoulas et al.,

2015 [19]

US

RCT, nonblinded

RYGB

LAGB

An intensive lifestyle weight loss intervention

FPG, HbA1C

IRB, IC, Reg.NCT01047735

3

Dixon et al.,

2008 [12]

US

RCT, nonblinded

LAGB

Conventional dietary and ifestyle change

FPG, HbA1C, insulin, HOMA IR

IRB, IC, Reg. ACTRN

012605000159651

2

Halperin et al.

2014 [20]

US

RCT, nonblinded

RYGB

An intensive diabetes medical and weight management

FPG, HbA1c

IRB, IC,

Reg. NCT01073020

1

Ikramuddin et al.,

2015 [21]

US

RCT, nonblinded,

Multi-center trial

RYGB

Lifestyle and medical management

FPG, HbA1C

IRB, IC

Reg.NCT00641251

2

Liang et al.,

2013 [22]

China

RCT, nonblinded

RYGB

Usual care plus Exenatide treatment

FPG, HbA1C, insulin, HOMA IR

IRB, IC

Reg.NCT01435980

1

Mingrone et al.,

2015 [23]

Italy

RCT, nonblinded

RYGB

BPD

Diet, exercise, lifestyle modification program

FPG, HbA1C

IRB, IC

Reg.NCT00888836

5

Schauer et al.,

2014 [24]

US

RCT, nonblinded

RYGB

LSG

Intensive medical therapy

FPG, HbA1C

IRB, IC

Reg. NCT00432809

3

Wentworth et al.,

2014

Australia

RCT, nonblinded

LAGB

multidisciplinary diabetes care

FPG, HbA1C,

HOMA IR

IRB, IC, ACTRN12609 000286246

2

a Country of first author’s affiliation. RCT, randomized controlled trial; RYGB, Roux-en-Y gastric bypass; LAGB, laparoscopic adjustable gastric banding; BPD, biliopancreatic diversion; LSG, laparoscopic sleeve gastrectomy; FPG, fasting plasma glucose; HbA1C, hemoglobin A1C; HOMA IR, insulin resistance by homeostatic model assessment; IRB, institutional review and/or ethics board approval obtained; IC, informed consent obtained; Reg., clinical trial registration number or governmental grant number;

Table 2: Description of patients at baseline from the 8 studies included in the meta-analysis

Study

(Author, year)

Group

No. of patients

Age

Mean(SD)

Female

(%)

Type 2 diabetes Duration (y)

BMI

Mean(SD)

Body weight(kg)

Mean(SD)

Courcoulas et al.,

2015

Bariatric surgery (RYGB+ LAGB) *

41

46.6(7.3)

81

6.8(4.5)

35.6(3.0)

101.1(14.0)

Control

20

48.9(4.7)

85

5.7(5.6)

35.7(3.3)

99.3(13.4)

Dixon et al.,

2008

Bariatric surgery (LAGB)

30

46.6(7.4)

50

<2

37(2.7)

105.6(13.8)

Control

30

47.1(8.7)

50

<2

37.2(2.5)

105.9(14.2)

Halperin et al.,

2014

Bariatric surgery (RYGB)

19

50.7(7.6)

68

10.6(6.6)

36.0(3.5)

104.6(15.5)

Control

19

52.6(4.3)

53

10.2(6.1)

36.5(3.4)

102.7(17.0)

Ikramuddin et al.,

2015

Bariatric surgery (RYGB)

60

49(9)

63

8.9(6.1)

34.9(3.0)

98.8(14.0)

Control

59

49(8)

57

9.1(5.7)

34.3(3.1)

97.9(17.0)

Liang et al.,

2013

Bariatric surgery (RYGB)

31

50.8(5.4)

29

7.4(1.7)

30.5(0.9)

82.0(3.5)

Control (control+control plus exenatide) *

70

51.4(6.2)

31

7.2(1.7)

30.3(1.7)

81.5(4.3)

Mingrone et al.,

2015

Bariatric surgery (RYGB+BPD) *

38

43.3(7.8)

55

6

45.0(6.5)

133.9(26.8)

Control

15

43.5(7.3)

50

6

45.1(7.8)

136.4(21.9)

Schauer et al.,

2014

Bariatric surgery (RYGB+LSG) *

97

47.9(8.2)

68

8.2(4.9)

36.6(3.7)

103.7(16.0)

Control

40

50.3(7.5)

68

8.8(5.4)

36.4(3.0)

104.5(14.2)

Wentworth et al.,

2014

Bariatric surgery (LAGB)

25

53(6)

76

2.2(1.7)

29(1)

81(10)

Control

26

53(7)

65

2.8(1.8)

29(1)

83(12)

RYGB, Roux-en-Y gastric bypass; LAGB, laparoscopic adjustable gastric banding; BPD, biliopancreatic diversion; LSG, laparoscopic sleeve gastrectomy; BMI, body mass index. *In three-arm studies, Courcoulas 2015, Mingrone 2015 and Schauer 2014 the two bariatric surgery groups were combined, and in Liang 2013 the two non-surgical groups were combined.

Flow diagram showing selection of relevant articles in this meta-analysis.

Figure 1: Flow diagram showing selection of relevant articles in this meta-analysis.

Quality assessment

The risk of bias for each study was performed with Cochrane Collaboration’s tool [26] (Figure 2A). All studies [12, 19-25] were adequate randomly generated the sequence. Six studies [12, 19-23] were unclear in clinic random allocation concealment. In all studies [12, 19-25], the participants and healthcare provider were not blinded. There were not the risk of incomplete outcome data and selective reporting in all studies [12, 19-25]. Therefore, there was a low risk of bias in this meta-analysis (Figure 2B).

Assessment of risk of bias in this meta-analysis.

Figure 2: Assessment of risk of bias in this meta-analysis. A. Summary of risk of bias for each study assessed by Cochrane Collaboration’s tool B. Risk of bias graph about each risk of bias item presented as percentages across all included studies.

Meta-analysis of short-term outcomes

With respect to short-term outcomes, four endpoints including glycemic control (HbA1c, fasting plasma glucose (FPG)), body weight (weight loss, body mass index(BMI)), plasma cholesterol (low density lipoprotein(LDL), high density lipoprotein(HDL), total cholesterol), and triglyceride concentration were taken into analysis. Risk ratio (RR) along with 95% confidence intervals (CI) was calculated for dichotomous data, and mean difference (MD) with 95% CI was calculated for continuous data.

Glycemic control

All of 8 studies [12, 19-25] reported the mean changes in glycated haemoglobin HbA1c level (%). Heterogeneity was high (P < 0.0001, I2 = 79%) and a random effect model was used. Bariatric surgery acquired more decrease of HbA1c compared with non-surgical treatment for T2DM (MD = -1.29, 95%CI: -1.70 to -0.87, P < 0.00001) (Figure 3A). Further subgroup analysis showed that HbA1c level reduction was not significantly different between the 1,2-year follow-up studies and the 3,5-year follow-up studies (difference of the mean difference 0.47%, P = 0.23). Statistical heterogeneity was moderate of the subgroup analyses (Figure 3A).

There were 7 studies [12, 19-21, 23-25] reported the mean changes in FPG level (mg/dL). Heterogeneity was high (P < 0.00001, I2 = 88%) and a random effect model was used. Bariatric surgery acquired more decrease of FPG compared with non-surgical treatment for T2DM (MD = -36.38, 95%CI: -51.76 to -21.01, P < 0.00001) (Figure 3B).

Mean changes in glycemic control after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Figure 3: Mean changes in glycemic control after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus. A. HbA1c levels (% points) B. fasting plasma glucose (mg/dL) (A conversion factor of 18 was used to convert values from mmol/L to mg/dL.).

Body weight

7 studies [19-25] reported the mean changes of BMI (kg/m2). The results of the heterogeneity were P < 0.00001/I2 = 92% and indicated high heterogeneity among the studies. So a random effect model was used. Bariatric surgery acquired more reduction of BMI compared with non-surgical treatment for T2DM (MD = -5.80, 95%CI: -6.95 to -4.64, P < 0.00001) (Figure 4A).

6 studies [12, 19, 21, 23-25] reported the mean changes of body weight loss (%). Heterogeneity was high (P = 0.003, I2 = 73%) and a random effect model was used. Bariatric surgery acquired greater weight loss compared with non-surgical treatment for T2DM (MD = -16.93, 95%CI: -19.78 to -14.08, P < 0.00001) (Figure 4B).

Mean changes in body weight after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Figure 4: Mean changes in body weight after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus. A. body mass index (kg/m2) B. percent weight loss (%).

Plasma cholesterol

There were 6 studies [19-21, 23, 25] reported the mean changes in LDL cholesterol concentration (mg/dL). Heterogeneity was high among the trials (P < 0.00001, I2 = 96%) and a random effect model was used. Change of LDL cholesterol was no significantly different between the two groups (MD = -13.69, 95%CI: -41.14 to 13.77, P = 0.33) (Figure 5A).

There were 7 studies [12, 19-23, 25] reported the mean changes of HDL cholesterol concentration (mg/dL). Heterogeneity was low (P = 0.22, I2 = 28%) and a fixed effect model was used. Bariatric surgery acquired higher increase of HDL cholesterol compared with non-surgical treatment for T2DM (MD = 9.07, 95%CI: 7.60 to 10.55, P < 0.00001) (Figure 5B).

There were 7 studies [12, 19-23, 25] reported the mean changes of total cholesterol concentration (mg/dL). Heterogeneity was high (P < 0.00001, I2 = 94%) and a random effect model was used. Changes of total cholesterol was no significantly different between the two groups (WMD = -8.24, 95%CI: -32.12 to 15.63, P = 0.50) (Figure 5C).

Mean changes in cholesterol concentrations (mg/dL) after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Figure 5: Mean changes in cholesterol concentrations (mg/dL) after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus. A. low density lipoprotein cholesterol B. high density lipoprotein cholesterol C. total cholesterol (A conversion factor of 38.67 was used to convert values from mmol/L to mg/dL).

Triglyceride concentration

7 studies [12, 19-23, 25] reported the mean changes of triglyceride concentration (mg/dL). Heterogeneity was high (P = 0.0008, I2 = 74%) and a random effect model was used. Bariatric surgery acquired more decrease of triglycerides compared with non-surgical treatment for T2DM (MD = -51.27, 95%CI: -74.13 to -28.41, P < 0.0001) (Figure 6).

Mean changes in triglyceride concentrations (mg/dL) after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Figure 6: Mean changes in triglyceride concentrations (mg/dL) after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus. (A conversion factor of 88.55 used to convert values from mmol/L to mg/dL).

Meta-analysis of long-term outcomes

With respect to long-term outcomes, three endpoints including T2DM remission, quality of life, and adverse events were taken into analysis.

Diabetes remission

T2DM remission rate was the primary end point. All of 8 studies [12, 19-25] reported the relative risk of T2DM remission. Bariatric surgery acquired higher diabetes remission compared with non-surgical treatment for T2DM (RR = 5.76; 95%CI: 3.15 to 10.55, P < 0.00001). Analysis indicated that there was moderate heterogeneity among the studies (P = 0.14, I2 = 36%) and a fixed effect model was used. Further subgroup analysis showed that T2DM remission was no significantly different between the 1,2-year follow-up studies and the 3,5-year follow-up studies (P = 0.53, I2 = 0%) (Figure 7).

Type 2 diabetes remission after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Figure 7: Type 2 diabetes remission after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus. Subgroup analysis was done for the 1,2-year follow-up studies versus 3,5-year follow-up studies.

Quality of life

There were 3 studies [20, 23, 24] reported quality of life which was assessed by the 36-Item Short Form Health Survey (SF-36). Schauer 2014 reported that five of eight mental and physical domains improved more among patients in the gastric-bypass group and two of eight domains in the sleeve-gastrectomy group, as compared with the medical-therapy group [24]. Halperin 2014 reported that SF-36 total scores were no significantly difference between bariatric surgery group and non-surgery group in at 1 year [20]. Mingrone 2015 reported that surgical patients scored significantly better than medically treated patients for all subdomains of quality of life and for the total score domains [23].

Adverse events

There were 6 studies [12, 19, 21, 23-25] reported the adverse events. There was no heterogeneity (P = 0.58, I2 = 0%) among the studies, so a random effect model was used. Our outcome was prone to a higher adverse events rate in bariatric surgery compared with non-surgical treatment for T2DM (RR = 2.08, 95%CI: 1.53 to 2.81, P < 0.00001) (Figure 8). However, early surgical complications were relatively benign. There were no perioperative deaths and no late surgical complications in bariatric surgical groups after 1-year follow-up. The only 5-year follow-up study reported that five major complications of diabetes (including one fatal myocardial infarction) arose in four (27%) patients in the medical group compared with only one complication in the bariatric surgery groups. [23]

Adverse events after bariatric surgery

Figure 8: Adverse events after bariatric surgery versus non-surgical treatment (control) for Type 2 diabetes mellitus.

Publication Bias

The publication bias in this meta-analysis was assessed by funnel plots to evaluate the reliability. However, the results of these tests are not reported, because this method is known to be unreliable when there are fewer than 10 studies in the meta-analysis [27] and because our qualitative analysis indicated a high likelihood of reporting bias.

DISCUSSION

Bariatric surgery is used at first to treat obesity that is often associated with T2DM. Some studies found that obesity patient could obtain T2DM remission after bariatric surgery. Further research indicated that mild to moderate obesity patients could also obtain T2DM remission after bariatric surgery. Therefore, this meta-analysis is to investigate the effective of bariatric surgery treatment for T2DM with or without obesity. It remains to be established whether bariatric surgery is an effective treatment for T2DM and how bariatric surgery compares with non-surgical treatment with respect to short-and long-term outcomes [18, 28]. And recent initial studies [19, 21, 23-25] have reported the feasibility, safety, and efficacy of bariatric surgery for T2DM. However, the studies are limited to a small number of patients. There is no convincing evidence on the efficacy of bariatric surgery for T2DM. Our goal of this meta-analysis was to evaluate the efficacy of bariatric surgery for T2DM compared with non-surgical treatment. We comprehensively identified all relevant RCTs and summarized the evidence on short- and long-term outcomes.

Diabetes remission is the most important question regarding the use of bariatric surgery for T2DM. Our analysis demonstrates that overall T2DM remission of bariatric surgery compared with non-surgical treatment were significantly different, 47.5 vs 6.8% (P < 0.001), respectively. And then, the efficacy of T2DM remission was quantified from the pooled risk ratios based on the 8 RCTs. Our pooled outcome provided convincing evidence that bariatric surgery led to higher T2DM remission than non-surgical treatment for up to 5-year follow-up.

With respect to short-term outcomes, bariatric surgery acquired more reduction HbA1c, FPG, BMI, weight, and triglyceride, more increase HDL cholesterol. However, changes of LDL and total cholesterol were no significantly different. Moreover, there were no perioperative deaths and no late surgical complications in bariatric surgical groups. This meta-analysis demonstrates that bariatric surgery for T2DM is more efficient than non-surgical treatment.

Three studies [19, 23, 24] in this meta-analysis proved that bariatric surgery compared with non-surgical treatment in glycemic control is not only marked improvement in short term, but also more durable over the long term. Schauer et al. reported a 31% rate of T2DM remission maintenance in bariatric surgery patients at 3-year follow-up vs 5.0 % in the medical therapy group [24]. Similarly, Courcoulas et al. reported a 34.1% rate of T2DM remission at 3-year follow-up vs none of intensive lifestyle weight loss intervention participants [19]. In addition, Mingrone et al. recently reported 50% of the surgical patients maintained diabetes remission at 5-year follow-up vs none of the medically treated patients [23].

The reduction of long-term diabetes-related complications is an important aspect regarding the use of bariatric surgery for the treatment of T2DM. A 5 year follow-up RCT shows that medically treated patients are greater incidence of diabetes-related complications including a fatal myocardial infarction and bariatric surgery could reduce risk of diabetes complications [23]. This finding is supported by a very long-term follow-up observational study showing that bariatric surgery is associated with fewer microvascular and macrovascular complications than usual care [29].

Our results are supported by two systematic reviews. A review and meta-analysis from 2013 [30] included three randomized controlled trials. It showed greater weight loss, glycemic control, and diabetes remission during 1 to 2 years of follow-up after bariatric surgery compared with non-surgical treatment. The other review and meta-analysis from 2014 [28] included 5 RCT studies and 11 observational studies and had similar results.

There are several limitations in this meta-analysis. Although the number of available RCTs was noteworthy, the evidence is insufficient to reach conclusions that bariatric surgery is the preferred treatment for T2DM than non-surgery treatment. Most of included studies were relatively small sample sizes and lack of long-term results. Only 3 studies had follow-up longer than 3 years [19, 23, 24]. Additionally, many of the studies were from single a single site, which may affect generalizability. A greater number of larger and even more definitive studies would have increased this study’s predictive strength.

Another limitation was the diversity of T2DM diagnosis and remission standards reported. Many studies determined T2DM outcomes idiosyncratically; the majority of studies did not define T2DM remission uniformly, some employing American Diabetes Association criteria, and others only biochemical marker of glycemic control. A uniform standard for reporting T2DM remission is needed to improve the scientific evidence base and support clinical decision making.

Another potential limitation was the intensity of patients treated by bariatric surgery may be inherently greater. Intensity of treatment in surgical therapy may improve weight loss and glucose outcomes. Caution is warranted when considering differences between surgical and non-surgical treatment when the intensity of treatment is not balanced in the two groups. Future studies should pay careful attention to this potential confounding factor.

In conclusion, our meta-analysis summarizes the best available evidence for short- and long-term results in directly comparative research studies of bariatric surgery vs non-surgical treatment in T2DM patients. This study demonstrates that bariatric surgery is associated with greater improvements in T2DM remission, HbA1c and fasting plasma glucose levels, weight loss, and hyperlipidemia than non-surgical treatment such as medications, diet, and behavioral changes for patients with T2DM. However, results are limited to a small number of studies and individuals and lack data about the durability of benefit. To fully characterize the efficacy of bariatric surgery for T2DM, the evidence calls for further research on larger, well design, and long-term outcomes studies.

materials and METHODS

Eligibility criteria

Studies were included for this meta-analysis if they met the following criteria: 1) study design: randomized controlled trials and each study to have at least 1-year follow-up; 2) investigated currently used laparoscopic or open bariatric surgery techniques (Roux-en-Y gastric bypass, adjustable gastric banding, sleeve gastrectomy, or biliopancreatic diversion); investigated as comparator non-surgical treatment for T2DM (diet, weight reducing drugs, behavioral therapy, or any combination thereof); 3) results: description of the details of T2DM remission, metabolic outcomes (glucose, lipids), weight loss, quality of life, and adverse events. The exclusion criteria included: 1) abstracts, letters, editorials and expert opinions, reviews without original data, case reports; 2) studies not reporting clinical outcomes of effectiveness or adverse events; and 3) studies with a sample size fewer than 10.

Information sources and search strategy

We performed a comprehensive search in PubMed, Embase and Cochrane Library databases to identify all relevant studies available from their inception to June 15th 2016. We also searched trial registries of ongoing trials.

The search strategy followed the identification and screening guidelines established by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The search terms included (“diabetes or diabetic*” or “diabetes mellitus”) and (“bariatric surgery” or “metabolic surgery” or “diabetes surgery” or “gastric banding” or “sleeve gastrectomy” or “gastric bypass” or “duodenal switch” or “biliopancreatic diversion”) and (randomized controlled trial). These terms were used in different Boolean combinations. Limits set to govern the searches stipulated journal articles on adult humans written in the English language. All eligible studies were retrieved, and the reference lists of the identified studies and reviews were evaluated or additional studies.

Data extraction

Two review authors (X.S. and X.F.) independently extracted data, and screened the quality and content of the included studies. Variable data of interest were extracted from included studies and entered into a dedicated database. The following data was extracted from each study: study characteristics (bariatric procedures, conventional treatments, study designs, bariatric surgery techniques, non-surgical treatments, and follow-up time), demographic and anthropometric measures (publication year, country, age, gender, BMI), T2DM remission, glycemic control (HbA1C and FPG), weight loss, lipids, quality of life, and adverse events. The other authors (Y.F. and Z.F.) checked for data accuracy and completeness. Discrepancies were resolved by consensus in all authors.

Risk of bias assessment

The quality of the inclusion of trials was assessed using the Cochrane risk of bias tool [26]. Two reviewers (G.W. and H.Z.) independently assessed risk of bias of the inclusion of studies. Disagreement was resolved by consensus.

Data synthesis and statistical analysis

All data were analyzed using Review Manager version 5.3 for Mac. RR along with 95% CI was calculated for dichotomous data, and MD along with 95% CI was calculated for continuous data. The mean change of the included studies from baseline to end of follow-up was calculated. Missing standard deviations were derived from other statistics, such as P values or confidence intervals if needed [31]. For example, P = 0.00001 was assumed when a P value was reported as P < 0.00001. When only a range was reported, a formula was used to estimate Standard deviation (SD): Estimate SD = Range/4 (15 < n < 70); Range/6 (n > 70), and median was approximately equal to mean [32]. Heterogeneity among combined study results was assessed by Cochran’s Q test and by the degree of inconsistency (I2). A random effect model was used if P < 0.05 and I2 > 50%. Otherwise, data were pooled by using the fixed effect model [27]. In the integration results, P < 0.05 indicated statistical significance. Publication bias in outcomes was assessed and treated using standard methodology. Publication bias was analyzed using a funnel plot.

CONFLICTS OF INTEREST

The authors have declared that no competing interests exist.

GRANT SUPPORT

This study was supported by Science and Technology Project Foundation of Nanjing (Grant no: 201303032); Medical Science and Technology Development Foundation of Jiangsu University (Grant no: JLY20140160).

Author Contributions

Z.T., G.W., and B.C. conducted and design of the study, acquisition of data, analysis and interpretation of data, discussed the idea of the meta-analysis, drafted the manuscript, submitted the paper. F.Y. and Z.F. completed the database searches and selected, screened, and reviewed the articles. W.Z., X.F., and H.Z. reviewed and extracted the data, and performed the data analyses. All authors reviewed the paper and approved the final manuscript. Z.T. had primary responsibility for final content.

REFERENCES

1. Zimmet P, Alberti KG and Shaw J. Global and societal implications of the diabetes epidemic. Nature. 2001; 414:782-787.

2. Varemo L and Nielsen J. Networking in metabolism and human disease. Oncotarget. 2015; 6:15708-15709. doi: 10.18632/oncotarget.4561.

3. Gregg EW, Chen H, Wagenknecht LE, Clark JM, Delahanty LM, Bantle J, Pownall HJ, Johnson KC, Safford MM, Kitabchi AE, Pi-Sunyer FX, Wing RR, Bertoni AG and Look ARG. Association of an intensive lifestyle intervention with remission of type 2 diabetes. JAMA. 2012; 308:2489-2496.

4. Look ARG, Wing RR, Bolin P, Brancati FL, Bray GA, Clark JM, Coday M, Crow RS, Curtis JM, Egan CM, Espeland MA, Evans M, Foreyt JP, Ghazarian S, Gregg EW, Harrison B, et al. Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. N Engl J Med. 2013; 369:145-154.

5. Ali MK, Bullard KM, Saaddine JB, Cowie CC, Imperatore G and Gregg EW. Achievement of goals in U.S. diabetes care, 1999-2010. N Engl J Med. 2013; 368:1613-1624.

6. Rahimi M, Vinciguerra M, Daghighi M, Ozcan B, Akbarkhanzadeh V, Sheedfar F, Amini M, Mazza T, Pazienza V, Motazacker MM, Mahmoudi M, De Rooij FW, Sijbrands E, Peppelenbosch MP and Rezaee F. Age-related obesity and type 2 diabetes dysregulate neuronal associated genes and proteins in humans. Oncotarget. 2015; 6:29818-29832. doi: 10.18632/oncotarget.4904.

7. Buchwald H, Estok R, Fahrbach K, Banel D, Jensen MD, Pories WJ, Bantle JP and Sledge I. Weight and type 2 diabetes after bariatric surgery: systematic review and meta-analysis. Am J Med. 2009; 122:248-256 e245.

8. Pories WJ, Swanson MS, MacDonald KG, Long SB, Morris PG, Brown BM, Barakat HA, deRamon RA, Israel G, Dolezal JM and et al. Who would have thought it? An operation proves to be the most effective therapy for adult-onset diabetes mellitus. Ann Surg. 1995; 222:339-350; discussion 350-332.

9. Rubino F, Schauer PR, Kaplan LM and Cummings DE. Metabolic surgery to treat type 2 diabetes: clinical outcomes and mechanisms of action. Annu Rev Med. 2010; 61:393-411.

10. 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 and Kelley D. Effect of laparoscopic Roux-en Y gastric bypass on type 2 diabetes mellitus. Ann Surg. 2003; 238:467-484; discussion 484-465.

11. Courcoulas AP, Goodpaster BH, Eagleton JK, Belle SH, Kalarchian MA, Lang W, Toledo FGS and Jakicic JM. Surgical vs medical treatments for type 2 diabetes mellitus: a randomized clinical trial. JAMA surgery. 2014; 149:707-715.

12. Dixon JB, O&apos;Brien PE, Playfair J, Chapman L, Schachter LM, Skinner S, Proietto J, Bailey M and Anderson M. Adjustable gastric banding and conventional therapy for type 2 diabetes: a randomized controlled trial. JAMA. 2008; 299:316-323.

13. Ikramuddin S, Korner J, Lee W-J, Connett JE, Inabnet WB, Billington CJ, Thomas AJ, Leslie DB, Chong K, Jeffery RW, Ahmed L, Vella A, Chuang L-M, Bessler M, Sarr MG, Swain JM, et al. Roux-en-Y gastric bypass vs intensive medical management for the control of type 2 diabetes, hypertension, and hyperlipidemia: the Diabetes Surgery Study randomized clinical trial. JAMA. 2013; 309:2240-2249.

14. Mingrone G, Panunzi S, De Gaetano A, Guidone C, Iaconelli A, Leccesi L, Nanni G, Pomp A, Castagneto M, Ghirlanda G and Rubino F. Bariatric surgery versus conventional medical therapy for type 2 diabetes. The New England journal of medicine. 2012; 366:1577-1585.

15. O&apos;Brien PE, Dixon JB, Laurie C, Skinner S, Proietto J, McNeil J, Strauss B, Marks S, Schachter L, Chapman L and Anderson M. Treatment of mild to moderate obesity with laparoscopic adjustable gastric banding or an intensive medical program: a randomized trial. Annals of internal medicine. 2006; 144:625-633.

16. Schauer PR, Kashyap SR, Wolski K, Brethauer SA, Kirwan JP, Pothier CE, Thomas S, Abood B, Nissen SE and Bhatt DL. Bariatric surgery versus intensive medical therapy in obese patients with diabetes. The New England journal of medicine. 2012; 366:1567-1576.

17. Kashyap SR, Bhatt DL, Wolski K, Watanabe RM, Abdul-Ghani M, Abood B, Pothier CE, Brethauer S, Nissen S, Gupta M, Kirwan JP and Schauer PR. Metabolic effects of bariatric surgery in patients with moderate obesity and type 2 diabetes: analysis of a randomized control trial comparing surgery with intensive medical treatment. Diabetes care. 2013; 36:2175-2182.

18. Cheng J, Gao J, Shuai X, Wang G and Tao K. The comprehensive summary of surgical versus non-surgical treatment for obesity: a systematic review and meta-analysis of randomized controlled trials. Oncotarget. 2016; 7:39216-39230. doi: 10.18632/oncotarget.9581.

19. Courcoulas AP, Belle SH, Neiberg RH, Pierson SK, Eagleton JK, Kalarchian MA, DeLany JP, Lang W and Jakicic JM. Three-Year Outcomes of Bariatric Surgery vs Lifestyle Intervention for Type 2 Diabetes Mellitus Treatment: A Randomized Clinical Trial. JAMA surgery. 2015; 150:931-940.

20. Halperin F, Ding S-A, Simonson DC, Panosian J, Goebel-Fabbri A, Wewalka M, Hamdy O, Abrahamson M, Clancy K, Foster K, Lautz D, Vernon A and Goldfine AB. Roux-en-Y gastric bypass surgery or lifestyle with intensive medical management in patients with type 2 diabetes: feasibility and 1-year results of a randomized clinical trial. JAMA surgery. 2014; 149:716-726.

21. Ikramuddin S, Billington CJ, Lee W-J, Bantle JP, Thomas AJ, Connett JE, Leslie DB, Inabnet WB, Jeffery RW, Chong K, Chuang L-M, Sarr MG, Jensen MD, Vella A, Ahmed L, Belani K, et al. Roux-en-Y gastric bypass for diabetes (the Diabetes Surgery Study): 2-year outcomes of a 5-year, randomised, controlled trial. Lancet Diabetes Endocrinol. 2015; 3:413-422.

22. Liang Z, Wu Q, Chen B, Yu P, Zhao H and Ouyang X. Effect of laparoscopic Roux-en-Y gastric bypass surgery on type 2 diabetes mellitus with hypertension: a randomized controlled trial. Diabetes research and clinical practice. 2013; 101:50-56.

23. Mingrone G, Panunzi S, De Gaetano A, Guidone C, Iaconelli A, Nanni G, Castagneto M, Bornstein S and Rubino F. Bariatric-metabolic surgery versus conventional medical treatment in obese patients with type 2 diabetes: 5 year follow-up of an open-label, single-centre, randomised controlled trial. Lancet. 2015; 386:964-973.

24. Schauer PR, Bhatt DL, Kirwan JP, Wolski K, Brethauer SA, Navaneethan SD, Aminian A, Pothier CE, Kim ESH, Nissen SE, Kashyap SR and Investigators S. Bariatric surgery versus intensive medical therapy for diabetes—3-year outcomes. The New England journal of medicine. 2014; 370:2002-2013.

25. Wentworth JM, Playfair J, Laurie C, Ritchie ME, Brown WA, Burton P, Shaw JE and O&apos;Brien PE. Multidisciplinary diabetes care with and without bariatric surgery in overweight people: a randomised controlled trial. Lancet Diabetes Endocrinol. 2014; 2:545-552.

26. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, Savovic J, Schulz KF, Weeks L, Sterne JA, Cochrane Bias Methods G and Cochrane Statistical Methods G. The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011; 343:d5928.

27. Higgins JPT GS. (2011). Cochrane Handbook for Systematic Reviews of Interventions Version.: The Cochrane Collaboration).

28. Ribaric G, Buchwald JN and McGlennon TW. Diabetes and weight in comparative studies of bariatric surgery vs conventional medical therapy: a systematic review and meta-analysis. Obes Surg. 2014; 24:437-455.

29. Sjostrom L, Peltonen M, Jacobson P, Ahlin S, Andersson-Assarsson J, Anveden A, Bouchard C, Carlsson B, Karason K, Lonroth H, Naslund I, Sjostrom E, Taube M, Wedel H, Svensson PA, Sjoholm K, et al. Association of bariatric surgery with long-term remission of type 2 diabetes and with microvascular and macrovascular complications. JAMA. 2014; 311:2297-2304.

30. Maggard-Gibbons M, Maglione M, Livhits M, Ewing B, Maher AR, Hu J, Li Z and Shekelle PG. Bariatric surgery for weight loss and glycemic control in nonmorbidly obese adults with diabetes: a systematic review. JAMA. 2013; 309:2250-2261.

31. Wiebe N, Vandermeer B, Platt RW, Klassen TP, Moher D and Barrowman NJ. A systematic review identifies a lack of standardization in methods for handling missing variance data. J Clin Epidemiol. 2006; 59:342-353.

32. Hozo SP, Djulbegovic B and Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005; 5:13.


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