LivingGLP1
Network meta-analysis

HbA1c change

Type 2 diabetes (adults); background therapy: basal insulin with or without non insulin drugs

weeks 20 to 36 (target week 26)Not stated by the trialsDoses of a drug pooledMean difference
8
Randomized trials
9
Treatments
2,089
Participants
17
Trial arms

In plain language

Across 8 trials with 2,089 participants, 5 of 8 treatments had a clearly better result than placebo on HbA1c change, and for 3 the evidence could not tell them apart from placebo. The most favorable estimate was for Insulin aspart (prandial): mean difference -1.75 percentage points (95% credible interval -2.88 to -0.41).

Lower values favor the treatment. "Clearly" means the 95% credible interval excludes no difference. These are averages across trials; they do not say how any one person will respond. Not medical advice.

Network of trials

Each circle is a treatment; each line joins treatments that were randomized against each other in at least one trial.
DULA_SCEXEN_SCINS_ASPARTINS_LISPROLIRA_SCLIXI_SCPLACEBOSEMA_SCSTANDARD_CARE
Node area shows participants; line width shows trials comparing two treatments directly. Blue: GLP-1 receptor agonist containing treatments; grey: comparators. Hover over or tab to a node or line for details.

Effects compared with Placebo

Mean difference in percentage points. Lower values favor the treatment.
-3-2-10← favors treatmentfavors reference →Insulin aspart (prandial)Semaglutide injectionLiraglutide injectionLixisenatide injectionDulaglutide injectionExenatide injectionInsulin lispro (prandial)Standard care or no added treatm…
Versus Placebo. Blue: Bayesian random effects posterior median with 95% credible interval (thick) and 95% prediction interval (dashed). Amber diamond: frequentist estimate with 95% confidence interval. Hover over or tab to a row for its values.
Effects of each treatment versus Placebo
TreatmentBayesian MD (95% CrI)95% prediction intervalFrequentist MD (95% CI)Verdict
Insulin aspart (prandial)
INS_ASPART
-1.75 (-2.88 to -0.41)-3.02 to -0.30-1.89 (-2.83 to -0.95)Better
Semaglutide injection
SEMA_SC
-1.55 (-2.15 to -0.84)-2.43 to -0.59-1.56 (-1.78 to -1.34)Better
Liraglutide injection
LIRA_SC
-1.16 (-1.65 to -0.40)-1.96 to -0.12-1.19 (-1.39 to -0.99)Better
Lixisenatide injection
LIXI_SC
-0.88 (-1.51 to -0.20)-1.77 to 0.07-0.88 (-1.11 to -0.65)Better
Dulaglutide injection
DULA_SC
-0.76 (-1.42 to -0.02)-1.70 to 0.21-0.77 (-1.02 to -0.52)Better
Exenatide injection
EXEN_SC
-0.67 (-1.25 to 0.08)-1.50 to 0.32-0.70 (-0.95 to -0.45)Unclear
Insulin lispro (prandial)
INS_LISPRO
-0.65 (-1.36 to 0.29)-1.56 to 0.50-0.68 (-0.96 to -0.40)Unclear
Standard care or no added treatment
STANDARD_CARE
-0.55 (-1.34 to 0.48)-1.57 to 0.69-0.59 (-0.94 to -0.24)Unclear

Ranking

How likely each treatment is to be among the best. Rankings ignore the size of differences and their certainty, so read them with the effects above.

League table

Every treatment against every other: mean difference of the row treatment versus the column treatment, posterior median and 95% credible interval. Green: row clearly better; red: row clearly worse.
Every treatment in a row compared with every treatment in a column
Row versus columnPLACEBOINS_ASPARTSEMA_SCLIRA_SCLIXI_SCDULA_SCEXEN_SCINS_LISPROSTANDARD_CARE
PLACEBOPLACEBO1.75
0.41 to 2.88
1.55
0.84 to 2.15
1.16
0.40 to 1.65
0.88
0.20 to 1.51
0.76
0.02 to 1.42
0.67
-0.08 to 1.25
0.65
-0.29 to 1.36
0.55
-0.48 to 1.34
INS_ASPART-1.75
-2.88 to -0.41
INS_ASPART-0.21
-1.51 to 1.25
-0.60
-1.67 to 0.49
-0.88
-2.17 to 0.58
-1.00
-2.31 to 0.48
-1.10
-2.39 to 0.35
-1.12
-2.48 to 0.35
-1.21
-2.66 to 0.37
SEMA_SC-1.55
-2.15 to -0.84
0.21
-1.25 to 1.51
SEMA_SC-0.39
-1.40 to 0.42
-0.67
-1.55 to 0.30
-0.78
-1.74 to 0.20
-0.87
-1.87 to 0.02
-0.90
-2.00 to 0.06
-0.99
-2.20 to 0.06
LIRA_SC-1.16
-1.65 to -0.40
0.60
-0.49 to 1.67
0.39
-0.42 to 1.40
LIRA_SC-0.28
-1.08 to 0.77
-0.40
-1.25 to 0.65
-0.49
-1.33 to 0.45
-0.52
-1.47 to 0.53
-0.61
-1.69 to 0.46
LIXI_SC-0.88
-1.51 to -0.20
0.88
-0.58 to 2.17
0.67
-0.30 to 1.55
0.28
-0.77 to 1.08
LIXI_SC-0.12
-1.05 to 0.82
-0.21
-1.20 to 0.68
-0.24
-1.35 to 0.72
-0.32
-1.55 to 0.72
DULA_SC-0.76
-1.42 to -0.02
1.00
-0.48 to 2.31
0.78
-0.20 to 1.74
0.40
-0.65 to 1.25
0.12
-0.82 to 1.05
DULA_SC-0.09
-1.13 to 0.81
-0.11
-1.28 to 0.87
-0.21
-1.45 to 0.84
EXEN_SC-0.67
-1.25 to 0.08
1.10
-0.35 to 2.39
0.87
-0.02 to 1.87
0.49
-0.45 to 1.33
0.21
-0.68 to 1.20
0.09
-0.81 to 1.13
EXEN_SC-0.02
-0.53 to 0.42
-0.12
-0.81 to 0.52
INS_LISPRO-0.65
-1.36 to 0.29
1.12
-0.35 to 2.48
0.90
-0.06 to 2.00
0.52
-0.53 to 1.47
0.24
-0.72 to 1.35
0.11
-0.87 to 1.28
0.02
-0.42 to 0.53
INS_LISPRO-0.09
-0.78 to 0.55
STANDARD_CARE-0.55
-1.34 to 0.48
1.21
-0.37 to 2.66
0.99
-0.06 to 2.20
0.61
-0.46 to 1.69
0.32
-0.72 to 1.55
0.21
-0.84 to 1.45
0.12
-0.52 to 0.81
0.09
-0.55 to 0.78
STANDARD_CARE

Heterogeneity, fit and convergence

Bayesian random effects (primary)

Heterogeneity (tau)
0.150 (95% CrI 0.006 to 0.780)
Residual deviance
15.5 for 16 data points
DIC
30.9 (pD 15.4)
Largest R-hat
1.002
Smallest ESS
bulk 966, tail 1,232
Divergent transitions
0
Convergence
All criteria met
Priors
PR01 N(0, 5^2); PR03 N(0, 2.5^2); PR07 half normal(0, 0.5^2) on tau

Frequentist check (netmeta)

Method
inverse variance, REML, MD
Tau
0.000
I squared
0%
Q (total)
0.04 on 1 df, P = 0.844
Q (between designs)
0.04, P = 0.844

Inconsistency

Do trials comparing two treatments directly agree with the indirect evidence through other treatments?

No comparison here has both direct and indirect evidence, so inconsistency cannot be checked by node splitting; the between designs Q above is the global check.

Small study effects

A comparison adjusted funnel plot: each point is one trial comparison, centered on its own network estimate. Asymmetry can signal that small trials with unfavorable results are missing.

Fewer than ten trial comparisons, too few to judge funnel plot asymmetry.

Baseline characteristics of the trials

The baseline value of each effect modifier or prognostic factor that applies here, per trial: mean or percent over arms, weighted by the number randomized. A note under a value names a stand in (a median for a mean, 100 minus the male share, Asian subgroup rows, an all Asian site list); "not reported" means no source of the trial prints it.
Baseline effect modifiers and prognostic factors per trial
TrialBaseline HbA1c (percent)
effect modifier, prognostic factor; 8 of 8
Background glucose lowering therapy (stratum S0 to S4)
effect modifier, prognostic factor; 8 of 8
Diabetes duration (years)
effect modifier, prognostic factor; 8 of 8
Asian ancestry or region (percent Asian)
effect modifier, prognostic factor; 6 of 8
Age (years)
prognostic factor; 8 of 8
Treatment duration (weeks)
effect modifier; 8 of 8
NCT00765817
S000345
8.4S2123.065930
AWARD-9
S000446
8.4S2130.3360.428
GETGOAL-L-ASIA
S000488
8.53S213.910058.3524
NCT00960661
S000609
8.25S211.5
median
559.4530
PREVAIL
S000693
6.57S23.65
median
11.84
Asian subgroup rows
57.668
NCT01617434
S000926
8.25S212.1not reported58.426
SUSTAIN™ 5
S001872
8.37S213.316.6758.830
SIMPLE
S002252
12.05S210not reported47.4126

Comparability of the trials

Checked across designs (the set of treatments each trial compares) for eligibility, outcome definition and assessment, and the baseline factors above. Flags point to possible intransitivity; notes describe variation that is not tied to design.
  • FlagBaseline, Baseline HbA1c: design means range from 6.6 (EXEN_SC vs INS_LISPRO vs STANDARD_CARE) to 12.0 (INS_ASPART vs LIRA_SC) percent; threshold 0.5
  • FlagBaseline, Diabetes duration: design means range from 3.6 (EXEN_SC vs INS_LISPRO vs STANDARD_CARE) to 13.9 (LIXI_SC vs PLACEBO) years; threshold 3
  • FlagBaseline, Asian ancestry or region: not reported by 2 of 8 trials
  • FlagBaseline, Asian ancestry or region: design means range from 0.3 (DULA_SC vs PLACEBO) to 100.0 (LIXI_SC vs PLACEBO) percent Asian; threshold 30
  • FlagBaseline, Age: design means range from 47.4 (INS_ASPART vs LIRA_SC) to 60.4 (DULA_SC vs PLACEBO) years; threshold 10
  • NoteOutcome assessment, time point: selected time points span 20 to 30 weeks
  • NoteOutcome assessment, analysis set: mixed: completers 1, full_analysis 3, modified_itt 3, per_protocol 1
  • NoteRisk of bias, blinding: mixed: double_blind 5, open_label 3
  • NoteRisk of bias, funding: mixed: industry 7, non_industry 1
  • NoteData handling, input conversions: arms_combined 1
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT0076581730full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2008adults 18 or older; insulin glargine 20 U/d or more alone or with metformin or pioglitazone; HbA1c 7.1 to 10.5 percent; BMI 45 or less
AWARD-928modified_ittnot statednot statednot statednot statednot statednot stateddouble_blindindustry2014adults with T2D on basal insulin glargine with or without metformin
GETGOAL-L-ASIA24modified_ittnot statednot statednot statednot statednot statednot stateddouble_blindindustry2009age 25 to 81; type 2 diabetes at least 1 year; stable basal insulin at least 10 U/day with or without sulfonylurea; HbA1c 7 to 10 percent
NCT0096066130per_protocolnot statednot statednot statednot statednot statednot statedopen_labelindustry2009age 18 or older; T2D on insulin glargine and metformin with or without sulfonylurea; HbA1c 7.0 to 10.0; BMI 25.0 (23.0 in South Korea) to 45.0; HbA1c above 7.0 after optimization
PREVAIL20modified_ittnot statednot statednot statednot statednot statednot statedopen_labelnon_industry2014age 30 to 80; T2D 7 years or less; A1c 6.0 to 9.5 percent off drugs or 5.5 to 9.0 on up to 2 oral drugs
NCT0161743426full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2012age 18 to 80; HbA1c 7.0 to 10.0 percent; BMI 20 to 45; basal insulin analogue 20 U or more with or without metformin
SUSTAIN™ 530full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2014age 18 or older (20 in Japan); HbA1c 7.0 to 10.0 percent; stable basal insulin with or without metformin; eGFR 30 or more
SIMPLE26completersnot statednot statednot statednot statednot statednot statedopen_labelindustry2014age 18 or older; HbA1c 10 or higher; no prandial insulin, DPP-4 inhibitor or GLP-1 RA

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the mean difference on the analysis scale against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
NCT00765817A1EXEN_SC30arm, change-1.7400.089137R0027069:Table 2
NCT00765817A2PLACEBO30arm, change-1.0400.092122R0027069:Table 2
AWARD-9A1DULA_SC28arm, change-1.4400.090150registry:outcomes
AWARD-9A2PLACEBO28arm, change-0.6700.090150registry:outcomes
GETGOAL-L-ASIAA1LIXI_SC24contrast, md-0.8800.119R0022626:Results
GETGOAL-L-ASIAA2PLACEBO24contrast, mdR0022626:Results
NCT00960661A1EXEN_SC30arm, change-1.1300.050247R0016788:Table 2
NCT00960661A2INS_LISPRO30arm, change-1.1000.050263R0016788:Table 2
PREVAILA1STANDARD_CARE20arm, final6.7000.10033R0010144:Table 2
PREVAILA2INS_LISPRO20arm, final6.6000.09035R0010144:Table 2
PREVAILA3EXEN_SC20arm, final6.6000.10034R0010144:Table 2
NCT01617434A1LIRA_SC26arm, change-1.3000.069215registry:outcomes
NCT01617434A2PLACEBO26arm, change-0.1100.074217registry:outcomes
SUSTAIN™ 5A1+A2SEMA_SC30arm, change-1.6490.065263arms_combinedregistry:outcomes
SUSTAIN™ 5A3PLACEBO30arm, change-0.0900.090133registry:outcomes
SIMPLEA1INS_ASPART26arm, change3.4000.33244registry:outcomes
SIMPLEA2LIRA_SC26arm, change4.1000.33246registry:outcomes

Rerun this analysis yourself

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