HbA1c change
Type 2 diabetes (adults); background therapy: basal insulin with or without non insulin drugs
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
Effects compared with Placebo
| Treatment | Bayesian MD (95% CrI) | 95% prediction interval | Frequentist 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
League table
| Row versus column | PLACEBO | INS_ASPART | SEMA_SC | LIRA_SC | LIXI_SC | DULA_SC | EXEN_SC | INS_LISPRO | STANDARD_CARE |
|---|---|---|---|---|---|---|---|---|---|
| PLACEBO | PLACEBO | 1.75 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)
Frequentist check (netmeta)
Inconsistency
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
Fewer than ten trial comparisons, too few to judge funnel plot asymmetry.
Baseline characteristics of the trials
| Trial | Baseline 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 | 8.4 | S2 | 12 | 3.06 | 59 | 30 |
| AWARD-9 S000446 | 8.4 | S2 | 13 | 0.33 | 60.4 | 28 |
| GETGOAL-L-ASIA S000488 | 8.53 | S2 | 13.9 | 100 | 58.35 | 24 |
| NCT00960661 S000609 | 8.25 | S2 | 11.5 median | 5 | 59.45 | 30 |
| PREVAIL S000693 | 6.57 | S2 | 3.65 median | 11.84 Asian subgroup rows | 57.66 | 8 |
| NCT01617434 S000926 | 8.25 | S2 | 12.1 | not reported | 58.4 | 26 |
| SUSTAIN™ 5 S001872 | 8.37 | S2 | 13.3 | 16.67 | 58.8 | 30 |
| SIMPLE S002252 | 12.05 | S2 | 10 | not reported | 47.41 | 26 |
Comparability of the trials
- 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
| Trial | time weeks | analysis set | definition | instrument | adjudicated | proportion method | intercurrent events (discontinuation) | intercurrent events (rescue) | blinding | funding | start year | Eligibility |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT00765817 | 30 | full_analysis | not stated | not stated | not stated | not stated | not stated | not stated | double_blind | industry | 2008 | adults 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-9 | 28 | modified_itt | not stated | not stated | not stated | not stated | not stated | not stated | double_blind | industry | 2014 | adults with T2D on basal insulin glargine with or without metformin |
| GETGOAL-L-ASIA | 24 | modified_itt | not stated | not stated | not stated | not stated | not stated | not stated | double_blind | industry | 2009 | age 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 |
| NCT00960661 | 30 | per_protocol | not stated | not stated | not stated | not stated | not stated | not stated | open_label | industry | 2009 | age 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 |
| PREVAIL | 20 | modified_itt | not stated | not stated | not stated | not stated | not stated | not stated | open_label | non_industry | 2014 | age 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 |
| NCT01617434 | 26 | full_analysis | not stated | not stated | not stated | not stated | not stated | not stated | double_blind | industry | 2012 | age 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™ 5 | 30 | full_analysis | not stated | not stated | not stated | not stated | not stated | not stated | double_blind | industry | 2014 | age 18 or older (20 in Japan); HbA1c 7.0 to 10.0 percent; stable basal insulin with or without metformin; eGFR 30 or more |
| SIMPLE | 26 | completers | not stated | not stated | not stated | not stated | not stated | not stated | open_label | industry | 2014 | age 18 or older; HbA1c 10 or higher; no prandial insulin, DPP-4 inhibitor or GLP-1 RA |
Trial data
| Trial | Arm | Treatment | Week | Data | Value | SE | Events / N | Flags | Source |
|---|---|---|---|---|---|---|---|---|---|
| NCT00765817 | A1 | EXEN_SC | 30 | arm, change | -1.740 | 0.089 | 137 | R0027069:Table 2 | |
| NCT00765817 | A2 | PLACEBO | 30 | arm, change | -1.040 | 0.092 | 122 | R0027069:Table 2 | |
| AWARD-9 | A1 | DULA_SC | 28 | arm, change | -1.440 | 0.090 | 150 | registry:outcomes | |
| AWARD-9 | A2 | PLACEBO | 28 | arm, change | -0.670 | 0.090 | 150 | registry:outcomes | |
| GETGOAL-L-ASIA | A1 | LIXI_SC | 24 | contrast, md | -0.880 | 0.119 | R0022626:Results | ||
| GETGOAL-L-ASIA | A2 | PLACEBO | 24 | contrast, md | R0022626:Results | ||||
| NCT00960661 | A1 | EXEN_SC | 30 | arm, change | -1.130 | 0.050 | 247 | R0016788:Table 2 | |
| NCT00960661 | A2 | INS_LISPRO | 30 | arm, change | -1.100 | 0.050 | 263 | R0016788:Table 2 | |
| PREVAIL | A1 | STANDARD_CARE | 20 | arm, final | 6.700 | 0.100 | 33 | R0010144:Table 2 | |
| PREVAIL | A2 | INS_LISPRO | 20 | arm, final | 6.600 | 0.090 | 35 | R0010144:Table 2 | |
| PREVAIL | A3 | EXEN_SC | 20 | arm, final | 6.600 | 0.100 | 34 | R0010144:Table 2 | |
| NCT01617434 | A1 | LIRA_SC | 26 | arm, change | -1.300 | 0.069 | 215 | registry:outcomes | |
| NCT01617434 | A2 | PLACEBO | 26 | arm, change | -0.110 | 0.074 | 217 | registry:outcomes | |
| SUSTAIN™ 5 | A1+A2 | SEMA_SC | 30 | arm, change | -1.649 | 0.065 | 263 | arms_combined | registry:outcomes |
| SUSTAIN™ 5 | A3 | PLACEBO | 30 | arm, change | -0.090 | 0.090 | 133 | registry:outcomes | |
| SIMPLE | A1 | INS_ASPART | 26 | arm, change | 3.400 | 0.332 | 44 | registry:outcomes | |
| SIMPLE | A2 | LIRA_SC | 26 | arm, change | 4.100 | 0.332 | 46 | registry:outcomes |
Rerun this analysis yourself
Remove treatments or trials and refit the frequentist and Bayesian models in your browser, with the same methods as the published analysis.