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Efficacies of Stem Cell Therapies for Functional Improvement of the β Cell in Patients with Diabetes: A Systematic Review of Controlled Clinical Trials
International Journal of Stem Cells 2019;12:195-205
Published online July 30, 2019;  
© 2019 Korean Society for Stem Cell Research.

Gyudeok Hwang1, Hyunsuk Jeong2, Hae Kyung Yang3, Hun-Sung Kim4, Hanter Hong1, Na Jin Kim5, Il-Hoan Oh6, Hyeon Woo Yim2

1The Catholic University of Korea, Catholic Medical Center, Seoul, Korea
2Department of Preventive Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea
3Cell and Gene Therapy Products Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea
4Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
5Medical Library, The Catholic University of Korea, Seoul, Korea
6Catholic High-Performance Cell Therapy Center & Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seoul, Korea
Correspondence to: Hyeon Woo Yim
Department of Preventive Medicine, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea
Tel: +82-2-2258-7860, Fax: +82-2-532-3820, E-mail: y1693@catholic.ac.kr
Received September 4, 2018; Revised January 2, 2019; Accepted February 11, 2019.
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Background and Objectives

This study was performed to investigate whether stem cell therapy enhances β cell function by meta-analysis with proper consideration of variability of outcome measurements in controlled trial of type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM) patients.

Methods

A systematic search was performed from inception to January 2018 in PubMed, EMBASE, and Cochrane databases. β cell function was assessed by stimulated C-peptide, fasting C-peptide, normal glycosylated hemoglobin levels (HbA1C), and exogenous insulin dose patterns. The quality of the studies were assessed by both the Cochrane Collaboration’s Risk of Bias (ROB) for Randomized controlled trials and the Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I) for non-randomized controlled trials.

Results

From the selected final 15 articles, total of 16 trials were analyzed. There were 6 T1DM trials (total 153 cases) and 10 T2DM trials (total 457 cases). In T2DM patients, the changes in stimulated C-peptide, HbA1c, and exogenous insulin dose versus baseline showed a favorable pattern with a significant heterogeneity in stem cell therapy. In T1DM, there was no significant difference between control group and stem cell therapy group in three indicators except for HbA1c. Most of the studies were rated as having high risk of bias in the quality assessment.

Conclusions

The stem cell therapy for DM patients is not effective in T1DM but seems to be effective in improving the β cell function in T2DM. However the observed effect should be interpreted with caution due to the significant heterogeneity and high risk of bias within the studies. Further verification through a rigorously designed study is warranted.

Keywords : Diabetes mellitus, C-peptide, β cell, Stem cell
Introduction

Type 1 diabetes (T1DM) is a disease in which selective insulin-producing β-cell destruction occurs due to genetic or sporadic autoimmunity. Attempts have been made to stop destruction of β-cell function. C-peptide is reduced by approximately 0.1 to 0.2 ng/ml per year, even when intensive insulin therapy with 3 to 4 insulin injections per day is given (1). In Type 2 Diabetes (T2DM), gradual increase in insulin resistance and temporal insulin secretion increase occurs, eventually leading to β-cell dysfunction (2). Even intensive therapy using drugs such as metformin and sulfonylurea, including insulin, eventually leads to deterioration of β-cell function and glycemic control becomes difficult (3, 4). In T2DM, the β-cell function is initially reduced by about 10% in 10 years, and at some point, it decreases rapidly by about 10% in 2 years, eventually resulting in insulin-dependent diabetes (5).

Therefore, treatment with stem cells having functions of immune modulation and regeneration has been continuously tried to improve the β-cell function. There are many types of cell therapy trials for DM such as pancreatic islet cell transplantation, pancreatic ductal stem cells, MSC transplantation or hematopoietic stem cells (or bone marrow transplantation). C-peptide was significantly increased by immunosuppression and immune resetting with administration of hematopoietic stem cells after immune ablation conditioning in type 1 diabetes (6). However, bone marrow transplantation (BMT) can cause many side effects such as graft versus host disease (GVHD), gonad dysfunction, and endocrine dysfunction, as well as infection by immune suppression (7). Also, treatment-related mortality for immune ablation BMT may be present, although less than 1% (8), Thus BMT is a burden for diabetes patients who have no hematologic malignancy. In T2DM patients, C-peptide was significantly increased by locally injecting bone marrow mononuclear cells via pancreatic artery (9). In T1DM patients, autologous bone marrow stem cells were injected via spleen artery, and increased c-peptide levels were maintained for 3 years. Controlled trials also were conducted to compare the efficacy of stem cell therapies (10, 11).

C-peptide, glycated hemoglobin (HbA1c) and required exogenous insulin dose have been used to evaluate the efficacy of stem cell therapy in diabetic patients, and c-peptide is recommended as a surrogate marker for evaluating β-cell function in insulin-dependent diabetes mellitus (1214). C-peptide was measured by a fasting sample, a non-fasting random sample, and a formal stimulation test, and there are various kinds of stimulation tests like an intravenous glucagon stimulation (IVGS), a standardized mixed-meal tolerance test (MMTT), and oral glucose tolerance test (OGTT). In the study of stem cell therapy in diabetic patients, C-peptide measurements were measured in various ways.

Three meta-analyses of stem cell therapy in DM patients have been reported (1517). However, in an analysis of whether stem cell therapy improves β-cell function, comparative analysis of only controlled studies to avoid overestimation of stem cell therapy effectiveness was not performed. Diversity of c-peptide measurements as an index of β-cell functional improvement was not considered. And C-peptide, glycated hemoglobin (HbA1c) and the required exogenous insulin dose were not analyzed integrally in the evaluation of β-cell function improvement.

Therefore, this systematic review aims to investigate whether the injected stem cell therapy promotes β-cell function, we analyzed controlled trials that evaluated the effect of stem cell treatment on diabetic patients. Diversity of c-peptide measurement method was analyzed and the exogenous insulin dose and HBA1C concentration were considered integratively.

Materials and Methods

Search strategy and study selection

A systematic search was performed from inception to January 2018 in PubMed, EMBASE, and Cochrane databases to search stem cell therapy studies applied to DM patients. The search terms such as, ‘Diabetes Mellitus’, ‘Stem cell therapy’, and ‘Efficacies or Safety’ were used. Selection criteria for the relevant study were as follows. (1) Controlled trials. (2) Patients with DM. (3) Including any kind of stem cells. Stem cells derived from the fetal organs were also included without excluding (11, 18). (4) Including fasting or stimulated C-peptide data. (5) Without a restriction on language. Abstracts are included if they are in English. The text in Chinese is also included (19) with the help of Chinese expert. Exclusion criteria are as follows. (1) No full text. (2) No control groups without stem cell therapies. (3) Treatments for DM complications. (4) Islet cell or pancreas transplantations. (5) Traditional bone marrow stem cell transplantations. (6) Less than 4 participants. (7) No C-peptide data.

Data extraction

A total of 2,472 articles were searched initially except for duplication of data. Two independent investigators reviewed titles and abstracts and selected 104 potentially eligible studies. Then full text review was conducted. When opinions differ in the selection of articles, divergences were resolved by mutual consultation. Finally, 15 articles were selected (10, 11, 1830) (Fig. 1).

The extracted items in each document are country of patient enrollment, numbers of patients allocated to stem cell treatment and control groups, route of stem cell administration, MSC cell type, cell origin, injection dose, and follow-up period. The mean, standard deviation, and total sample size were extracted for both treatment and control groups at baseline and the each follow-up points of C-peptide, HbA1c, insulin requirements. In the case standard deviation cannot be obtained (30), the author of this document was contacted by e-mail, and if cannot get the response, data was only used for qualitative synthesis

In a single article, two totally different trials were presented with the respective control group (11), and T1DM and T2DM trials were separated and analyzed as independent trials. The number of patients randomized in each trial or the number of patients assigned at the start of the study were extracted. The term ‘end of study follow up point’ used in this paper refers to the end of trials or the last follow up point of each document.

Quality assessment

In the case of the randomized controlled trial (RCT), the quality assessment was conducted with Cochrane Collaboration’s tool for assessing risk of bias. In the case of non-randomized controlled trial (NRCT), the Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I) was used. Two investigators independently performed analysis and divergences were solved through consensus. In RCT, if the control group had the sham procedures such as bone marrow aspiration, catheterization, and saline injection, it was evaluated as a low risk of bias in the blindness domain. In case of selective reporting domain, the registered research protocol was found and compared, and when the protocol was not registered, it was evaluated as unclear. In a case, the registered study protocol was non-randomized 4 factorial design, but was RCT in the reported trial, the study was evaluated based on abstract and full text (19). The confounding elements for NRCTs were age, diabetic duration, and the severity of disease evaluated as a c-peptide baseline level, and if evaluated it was accessed as moderate risk of bias and if even adjustment was performed, it was accessed as low risk of bias. Only the overall risk of bias for each trial was presented as a table (Table 1).

Statistical analyses

Data analysis was conducted using Review Manager 5.3. C-peptide was converted to ‘ng/ml’ using the relation (12) of ‘1 nmol/l=1 pmol/ml=3 ng/ml’. We used % as the unit for HbA1c, and for insulin used internal unit (IU). For patients of T1DM, unit for daily required exogenous dose of insulin was IU/d/kg, daily dose divided by the body weight of patients, and for T2DM we used unit of IU/d. When data is presented only as a figure, the exact numerical values of the data are extracted from the images using the Web Plot Digitizer Version 3.9 (20, 23, 24, 26, 27). Value of area under the curve (AUC) was selected for the analysis of the stimulated C-peptide. Peak value (28) was used when there was no AUC value. In case standard deviation was not presented, it was calculated from interquartile range, range, standard error values. When there are multiple intervention groups (10, 2022) or multiple control groups (20), they are combined into one group before analysis. In this meta-analysis the random effect model was used, because the type, origin, cell number and the end of study follow up time of stem cell treatment vary in each trial and the possible heterogeneity is suspected. For fasting C-peptide meta-analysis, weighted mean differences were used. For stimulated C-peptide analysis, we used weighted mean differences when AUC was included in the meta-analysis, but the standard mean differences method was used when AUC and peak value were included in the meta-analysis. The I2 statistic was used to evaluate the degree of heterogeneity. We conducted subgroup and meta-regression analyses to explore methodological and clinical heterogeneity. Since the subgroup and meta-regression analyses required more than 10 studies, we analyzed after combining T1DM and T2DM studies. To investigate the clinical heterogeneity, we analyzed the differences according to DM type, cell origin, cell type, and route of administration. When it comes to explore the methodological heterogeneity, we analyzed only the differences in treatment effects according to the study design. For fasting C-peptide, stimulated C-peptide, HbA1c, and required exogenous insulin dose, changes from the baseline to the end of study follow-up points were meta-analyzed and mean differences were calculated.

Results

Characteristics of the included trials

From the selected final 15 articles, total of 16 trials were analyzed and six were T1DM and 10 were T2DM trials (Table 1). A total of 610 patients (153 T1DM, 457 T2DM) underwent stem cell therapy or conventional therapy. Stem cell therapy group was total of 332 patients, and control group without stem cell therapy was total of 278 patients. The smallest sample size was 12, the largest sample size was 118, and the median of the sample size was 28.5. Stem cells used were either autologous or allogeneic stem cells depending on their origin. Stem cells were administered by intravenous (IV) injection or by catheterization to target arteries such as pancreatic duodenal or pancreatic artery. 3 cases had the follow up period over 24 months, 9 cases of 12 months, and 4 cases under 6 months.

There were 13 RCTs and 3 non-RCTs.

Quality assessment

The RCT quality was assessed by Cochrane collaboration tool for assessing risk of bias and all 13 trials were high risk of bias (Table 1). There was a possibility of bias in terms of appropriateness of randomization, whether it was blinded in measurement of outcomes, or report of selective results (Supplementary Table S1).

No trial was assessed as low risk of bias in the quality assessment of NRCT with ROBINS-I. Two were moderate risk of bias, and one was serious risk of bias (Table 1). Trial with serious risk of bias did not referred to dietary and exercise behaviors as confounding variables, and the definition of intervention group was not clear (Supplementary Table S2).

Various C-peptide measurements methods used for each study were presented in Table 2. Fasting C-peptide was measured in 4 trials of T1DM and 8 trials of T2DM, and we could not extract standard deviation information in 1 out of 8 T2DM cases. Stimulated C-peptide was measured in 4 trials of T1DM and in 6 trials of T2DM, and we could not extract standard deviation information in 1 out of 6 T2DM cases. We contacted the authors to gain information of the standard deviation. However, it was not possible to obtain the data; we excluded those trials from the meta-analysis. 5 Types of stimulus methods were used to measure Stimulated C-peptide, oral glucose tolerance test (OGTT), mixed meal tolerance test (MMTT), IV glucagon stimulation (IVGS), Hyperglycemic clamp (CLAMP), and steamed bread post prandial (PP). Three methods used to measure the stimulated C-peptides include measuring the area under the curve (AUC), the value at specific time points, and the peak value.

Treatment effects of stem cell therapy (SCT) were different between T1DM and T2DM. In T1DM, there was no significant difference between the intervention group and the control group in fasting C-peptide and stimulated C-peptide at the time of follow-up (MD: 0.19, 95% CI: −0.01 to 0.39 p=0.07 and MD: −0.04, 95% CI: −0.26 to 0.19 p=0.75, respectively) with significant heterogeneity (I2= 71% and I2=51%, respectively). In T2DM, fasting C-peptide and stimulated C-peptide were significantly increased in the group receiving stem cell therapy compared to the control group (MD: 0.62, 95% CI: 0.41 to 0.83 p<0.001 and MD: 1.12, 95% CI: 0.49 to 1.75 p<0.001, respectively) with significant heterogeneity I2=56% and I2=64%, respectively) (Fig. 2).

The effect of SCT on T1DM and T2DM was different in the alterations from the baseline to the end of study follow-up points in C-peptide, HbA1c, and daily required exogenous insulin dose (Fig. 3). In T1DM, there was no significant difference between SCT group and control group in fasting C-peptide, stimulated C-peptide, and exogenous insulin requirements. HbA1C only showed favorable stem cell. On the other hand, T2DM showed a favorable SCT pattern in all of stimulated C-peptide, exogenous insulin requirement, and HbA1C, except fasting C-peptide changes.

Discussion

There are several limitations in the interpretation of β-cell function. Since maintaining the near normal glycemic control in diabetes treatment is the standard of care, HbA1c is usually kept at 7 or less, and thus evaluating the effect of stem cells on β-cell function by only HbA1C changes is limited (12). The required exogenous insulin dose also indirectly and imperfectly reflects the β-cell function and can be greatly influenced by patient compliance, exercise, and insulin sensitivity (12).

C-peptide is a surrogate marker that represents endogenous insulin secretion. Methods for assessing C-peptide responsiveness include the use of serum C-peptide levels in the fasting state and the stimulation method. There are many factors that affect insulin secretion in β-cells. The key regulator factor is blood glucose level, and other factors include β-cell function, β-cell secretory capacity, insulin resistance, insulin sensitivity, glucotoxicity, exogenous insulin therapy, exercise and nutrition, etc. (31). Especially fasting blood glucose (FBG) level can be greatly influenced by other factors rather than the therapeutic effect, so it is of limited value to evaluate the β-cell function using fasting C-peptide levels which is regulated by FBG. There was a report that a large dinner meal of previous day elevated the “fasting” glucose level in the next morning despite sufficient post-fasting measurements (32). Fasting C-peptide levels are used primarily to reflect insulin resistance in patients who do not have insulin therapy. Fasting C-peptide levels are low because β-cell stimulation is low in insulin therapy patients, and it should be considered integratively together with the glucose level (33). Stimulated C-peptide rather than fasting C-peptide is recommended to measure the therapeutic efficacy of β-cell function (1214).

When interpreted centering on stimulated C-peptide, there was no difference between stem cell therapy group and control group in T1DM patients, and in T2DM patients, favoring stem cell therapy is shown, thus the use of stem cells seems to improve β-cell function only in patients with T2DM (Fig. 2).

To determine whether locally injected stem cell treatment has enhanced β-cell function in diabetic patients, it is necessary to consider the exogenous insulin dose, HBA1C concentration, fasting C-peptide, and stimulated C-peptide change patterns simultaneously. In T2DM patients, there were significant favoring patterns for stem cell therapies in the changes of stimulated C-peptide, HbA1c, and exogenous insulin dose versus baseline, and fasting C-peptide also showed favoring pattern though it was not significant statistically (Fig. 3). Use of stem cells in patients with T2DM improved β-cell function.

Four major mechanisms for C-peptide responsiveness after stem cell therapy could be considered. First, injected stem cells could directly differentiate into pancreatic β cells. In vitro, it has been reported that embryonic stem cells (ESCs) differentiated into functional β-cells, and in rodents it has been reported that stem cells derived from hematopoietic organs differentiated into functional pancreatic endocrine cells (34). The second is the generation of new β-cells by recruiting progenitor cells with potency to differentiate into β-cells by the paracrine effect. It was reported when diabetic mouse was intravenously injected with enhanced green fluorescent protein (eGFP) labeled adult stem cells, its hyperglycemia normalized and β cell mass recovered fully, but there was no evidence of insulin secreting eGFP positive donor cells and only increased cell cycle activity of remaining (eGFP negative) β cells were shown (35). The third is to protect the remaining β-cells and facilitate repair and proliferation by reducing pro-inflammatory cytokines and increasing anti-inflammatory cytokines. After ‘Stem cell educator’ therapy in T1DM and T2DM patients which is to reinject lymphocytes after educating them into human cord blood-derived multipotent stem cells in vitro, number of regulatory T cells (Tregs) increased, the cytokine balance between T helper (Th) cells recovered, and C-peptide increased (36, 37). The fourth is to inhibit autoimmunity and hence prevent further destruction of residual β cells and slow or reverse the progression of DM. There was a report that by non-myeloablative autologous hematopoietic stem cell transplantation in patients with T1DM, anti-glutamic acid decarboxylase (GAD) antibody titers were significantly reduced compared to baseline, and HbA1c and exogenous insulin dose also showed favoring reactions (38).

In T1DM, there was no significant difference between control group and stem cell therapy group in changes of three indicators except for HbA1c (Fig. 3). Considering the T1DM pathologic mechanism of selective insulin-producing β-cell destruction by autoimmunity, stem cell therapy did not delay or reverse T1DM progression because it does not significantly reduce autoimmunity or restore the inflammatory cytokine balance of the population.

Previous meta-analyses have shown that stem cell therapy is effective in both T1DM and T2DM patients. (1517). However, there were several limitations with the previous meta-analysis. No trial with a control group was used in the analysis of C-peptide in patients with T1DM and included conventional BMT trials and analysis without distinction between fasting C-peptide and stimulated C-peptide.

As for the limitation of this study, first, the current meta-analysis showed high heterogeneity. The sub-group analysis did not explain the heterogeneity both clinical factors, including DM type, cell origin, cell type, and route of administration and methodological characteristic (study design) (Supplementary Table S3). None of the variables was related to influential factors in meta-regression analysis (Supplementary Table S4). There might be the variability in true effect sizes due to the factors that have not yet been identified. If the heterogeneity is substantially high, the observed direction and magnitude of effect should be interpreted with caution. However, in addition to the results of stimulated C-peptide, fasting C-peptide, HbA1c, and daily insulin requirement changes also showed moving toward improving diabetes together. It is suggestive of that observed directions of effect of stem cell therapy may improve β cell function in T2DM. Second, the quality of the included studies was low using both the Cochrane ROB and ROBINS-I. The RCTs were high risk of bias and NRCTs were evaluated as moderate or serious risk of bias. Further verification through a rigorously designed study is warranted.

Supplementary Information
Acknowledgments

This research was supported by a grant (18172MFDS-182) from the Ministry of Food & Drug Safety in 2018. The Ministry of Food & Drug Safety had no further role in areas of study design, collection, Ms. Songui Choi conducted Chinese translation into Korean of the reference written in Chinese.

Potential Conflict of Interest

The authors have no conflicting financial interest.

Author Contributions

GH, HH, and HJ participated in eligibility screening, and data extraction. HH and HJ conducted protocol preparation, data analysis and interpretation. GH attended writing the manuscript; HWY participated in the scientific concept, eligibility screen, data extraction, quality assessment data analysis, analysis and interpretation of data, protocol preparation, scientific guidance, and critical review of the manuscript. HY, HK, and IO participated in data verification and critical review of the manuscript. NK participated in the systematic data search as a medical librarian. All authors read and approved the final manuscript.

Supplementary Materials

Supplementary data including four table can be found with this article online at http://pdf.medrang.co.kr/paper/pdf/IJSC/IJSC-12-s18076.pdf.

Figures
Fig. 1. Flow diagram of studies included in this review.
Fig. 2. Forest plots of effect sizes at end of study follow-up points in C-peptide. (a) Fasting C-peptide of T1DM, (b) Stimulated C-peptide of T1DM, (c) Fasting C-peptide of T2DM, (d) Stimulated C-peptide of T2DM.
Fig. 3. The alterations from the baseline at the end of study follow-up points in C-peptide, HbA1c and daily required exogenous insulin dose. (a) T1DM, (b) T2DM.
TABLES

Characteristics of included trials

AuthorCountrySCT/Control (n)Cell originCell typeDelivery routeFollow-upC-peptideStudy designQuality assessment
T1DM
 Cai 2016China21/21Allo/AutoUC-MSC/BM-MNCPA/IV12 moF/StRCTHigh
 Carlsson 2015Sweden10/10AutoBM-MSCIV12 moF/StRCTHigh
 Ghodsi 2012(T1DM)Iran15/15AlloFL-HSCIV12 moFRCTHigh
 Giannopoulou 2013Germany7/10AutoUCBIV12 moStNRCTModerate
 Haller 2013USA10/5AutoUCBIV12 moStRCTHigh
 Hu 2013China15/14AlloWJ-MSCIV24 moFRCTHigh
T2DM
 Bhansali 2014India13/13AutoBM-MNCPDA/IV12 moStRCTHigh
 Bhansali 2017India10/10/10*AutoBM-MSC/BM-MNC*PDA12 moF/StRCTHigh
 Chen 2016China6/6AlloUC-MSCPA/IV6 moStRCTHigh
 Ghodsi 2012(T2DM)Iran13/13AlloFL-HSCIV12 moFRCTHigh
 Hu 2012China56/62AutoBM-MNCPA36 moF/StNRCTModerate
 Hu 2016China31/30AlloWJ-MSCIV36 moFRCTHigh
 Skyler 2015USA45/15AlloBM-MPCIV3 moFRCTHigh
 Sood 2017India21/7AutoBM-MNCPDA/SA/IV6 moF/StRCTHigh
 Ulyanova 2016Kazakhstan8/6AlloFP-SCIV3 moFNRCTSerious
 Wu 2014China41/41AutoBM-MNCPA12 moF/StRCTHigh

T1DM: type 1 diabetes mellitus, T2DM: type 2 diabetes mellitus, SCT: stem cell therapy, Allo: allogeneic, Auto: autologous, UC: umbilical cord, BM: bone marrow, FL: fetal liver, WJ: Wharton jelly, FP: fetal pancreas, MSC: mesenchymal stem cell, MNC: mononuclear cell, HSC: hematopoietic stem cell, UCB: umbilical cord blood, MPC: mesenchymal precursor cell, SC: stem cell, PA: Pancreatic artery, IV: Intravenous, PDA: Pancreatico-duodenal artery, SA: splenic artery, F: Fasting C-peptide, St: Stimulated C-peptide, RCT: Randomized Controlled Trial, NRCT: non-Randomized Controlled Trial.

2 intervention groups (BM-MSC was used for one intervention group and BM-MNC for the other) and 1 control group,
No standard deviation data of C-peptide,
Cochrane collaboration’s tool for assessing risk of bias for RCTs and ROBINS-I (Risk Of Bias In Non-randomised Studies - of Interventions) version 19 September 2016 for NRCTs were used for the quality assessment.

Mean differences of C-peptide compared to the control group

TrialsFasting C-peptide (95%CI)Stimulated C-peptide (95%CI)

Stimulation methodAUCPeakSpecific time point
T1DM
 Cai 20160.10 (0.06, 0.15)*3h OGTT0.10 (0.03, 0.17)*
 Carlsson 20150.09 (−0.29, 0.47)2h MMTT0.15 (−0.66, 0.95)0.44 (−0.63, 1.50)
 Ghodsi 2012 (T1DM)0.02 (−0.53, 0.57)
 Giannopoulou 20132h MMTT−0.29 (−0.63, 0.04)−0.30 (−0.73, 0.13)
 Haller 20132h MMTT−0.12 (−0.54, 0.30)−0.15 (−0.65, 0.35)
 Hu 20130.41 (0.23, 0.60)*
T2DM
 Bhansali 2014IVGS1.28 (0.68, 1.87)*1.30 (0.60, 2.00)*
 Bhansali 2017−0.43 (−1.28, 0.43)CLAMP0.06 (−1.05, 1.18)§
IVGS0.06 (−0.26, 0.38)
 Chen 20163h OGTT0.14 (0.06, 0.23)*
 Ghodsi 2012(T2DM)0.40 (−0.69, 1.49)
 Hu 2012−0.159 ( −, − )2h PP1.645 ( −, − )
 Hu 20160.71 (0.62, 0.80)*
 Skyler 2015−0.17 (−1.07, 0.74)
 Sood 20170.94 (0.54, 1.35)*IVGS1.02 (0.12, 1.92)*
 Ulyanova 20161.18 (0.18, 2.18)*
 Wu 20140.60 (0.42, 0.79)*3h OGTT0.90 (0.61, 1.18)*

The unit of all C-peptide values is ng/ml.

AUC: area under curve, CI: confidence interval, OGTT: Oral Glucose Tolerance Test, MMTT: Mixed meal tolerance test, IVGS: intravenous glucagon stimulation, CLAMP: hyperglycemic clamp, PP: post-prandial(steamed bread).

p<0.05,
6 min after glucagon stimulation,
2 hour after steamed bread,
last follow-up point is 6 month,
No standard deviation data of C-peptide.

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