LivingGLP1
Network meta-analysis

Systolic blood pressure change

Type 2 diabetes (adults)

weeks 64 to 130 (target week 104)Not stated by the trialsDoses of a drug pooledMean difference
3
Randomized trials
4
Treatments
8,384
Participants
6
Trial arms

In plain language

Across 3 trials with 8,384 participants, 0 of 3 treatments had a clearly better result than placebo on systolic blood pressure change, and for 3 the evidence could not tell them apart from placebo. The most favorable estimate was for Semaglutide tablet: mean difference -3.01 mmHg (95% credible interval -14.81 to 9.22).

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.
ALBI_SCPLACEBOSEMA_POSEMA_SC
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 mmHg. Lower values favor the treatment.
-20-10010← favors treatmentfavors reference →Semaglutide tabletSemaglutide injectionAlbiglutide injection
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
Semaglutide tablet
SEMA_PO
-3.01 (-14.81 to 9.22)-19.53 to 14.27-3.00 (-4.34 to -1.66)Unclear
Semaglutide injection
SEMA_SC
-1.88 (-13.38 to 10.03)-19.11 to 15.10-1.93 (-2.99 to -0.87)Unclear
Albiglutide injection
ALBI_SC
-0.31 (-12.40 to 11.97)-17.62 to 17.19-0.30 (-1.77 to 1.17)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 columnPLACEBOSEMA_POSEMA_SCALBI_SC
PLACEBOPLACEBO3.01
-9.22 to 14.81
1.88
-10.03 to 13.38
0.31
-11.97 to 12.40
SEMA_PO-3.01
-14.81 to 9.22
SEMA_PO-1.08
-17.69 to 15.79
-2.70
-18.83 to 14.62
SEMA_SC-1.88
-13.38 to 10.03
1.08
-15.79 to 17.69
SEMA_SC-1.54
-18.16 to 14.85
ALBI_SC-0.31
-12.40 to 11.97
2.70
-14.62 to 18.83
1.54
-14.85 to 18.16
ALBI_SC

Heterogeneity, fit and convergence

Bayesian random effects (primary)

Heterogeneity (tau)
3.825 (95% CrI 0.190 to 12.876)
Residual deviance
6.0 for 6 data points
DIC
12.0 (pD 6.0)
Largest R-hat
1.001
Smallest ESS
bulk 2,380, tail 2,750
Divergent transitions
0
Convergence
All criteria met
Priors
PR01 N(0, 60^2); PR03 N(0, 30^2); PR07 half normal(0, 6^2) on tau

Frequentist check (netmeta)

Method
inverse variance, REML, MD
Tau
0.000
Q (total)
0.00 on 0 df
Q (between designs)
0.00

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 BMI or body weight (kg/m2)
effect modifier, prognostic factor; 3 of 3
NCT02465515
S001074
32.3
PIONEER 6
S001381
32.3
SUSTAIN™ 6
S001933
32.8

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.
  • FlagOutcome assessment, analysis set: confounded with design: full_analysis 1, other 1, safety 1
  • FlagHeterogeneity, tau above threshold: tau 3.83 exceeds the outcome threshold 2; the flags of this network are candidate explanations
  • NoteOutcome assessment, time point: selected time points span 83 to 104.28 weeks
  • NoteData handling, input conversions: arms_combined 2
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT02465515104.28safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2015type 2 diabetes with established cardiovascular disease
PIONEER 683othernot statednot statednot statednot statednot statednot stateddouble_blindindustry2017T2D; age 50 or more with CVD or CKD, or 60 or more with CV risk factors
SUSTAIN™ 6104full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2013T2D HbA1c 7.0 or more; age 50 or more with CVD, CHF or CKD stage 3 or more, or age 60 or more with CV risk factor

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
NCT02465515A1PLACEBO104.28arm, change-0.9000.5531,133registry:outcomes
NCT02465515A2ALBI_SC104.28arm, change-1.2000.5061,198registry:outcomes
PIONEER 6A1SEMA_PO83arm, change-5.0000.4911,345registry:outcomes
PIONEER 6A2PLACEBO83arm, change-2.0000.4791,411registry:outcomes
SUSTAIN™ 6A1+A2SEMA_SC104arm, change-4.4030.3821,648arms_combinedregistry:outcomes
SUSTAIN™ 6A3+A4PLACEBO104arm, change-2.4750.3821,649arms_combinedregistry: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.

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