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Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Evidence synthesis · §4

Mitochondria-targeted peptides in bioenergetic disorders — summary of findings

Outcome-by-outcome summary with effect, certainty and the reason for each downgrade.

Document identifier
CEI-ES-032/4
Series
Evidence synthesis
Version
3.1
Published
25 Nov 2024
Last reviewed
25 Jul 2025
Next review
25 Jan 2027
Identifier
10.71829/cei.syn.32
Certainty
Low
Cycle
2024 Q4
Review type
Intervention review
Search executed
25 Aug 2024

§4Summary of findings

§4.1Summary of findings

Table 7. Summary of findings for Mitochondria-targeted peptides in bioenergetic disorders.

OutcomeParticipants (studies)Effect as reportedCertaintyReason for downgrade
Six-minute walk distanceThe outcome the Institute designates as anchor for this indication.248 (2)Low certainty evidence describes this fieldLowrisk of bias, publication bias
Discontinuation for adverse eventsReported as a summary-of-findings row rather than in a tolerability annex, following a public submission.223 (1)Reported per contributing trial; see the included-studies tableLowrisk of bias, imprecision
Serious adverse eventsEvent counts are low; the estimate is imprecise by construction.216 (1)Reported per contributing trial; see the included-studies tableVery lowinconsistency, indirectness, publication bias
Any adverse eventAscertained by spontaneous report in the contributing trials.236 (1)Reported per contributing trial; see the included-studies tableVery lowinconsistency, indirectness
Primary mitochondrial myopathy symptom assessmentA secondary outcome for this indication. Its hierarchical position within each contributing trial is recorded on that trial's abstract where the Institute holds it.181 (1)Reported as a secondary outcome in a subset of contributing trialsVery lowrisk of bias, indirectness
Muscle phosphocreatine recovery kineticsA secondary outcome for this indication. Its hierarchical position within each contributing trial is recorded on that trial's abstract where the Institute holds it.192 (1)Reported as a secondary outcome in a subset of contributing trialsVery lowinconsistency, imprecision, publication bias
Certainty ratings describe confidence in the effect estimate for the stated outcome. They are not recommendations and do not transfer between outcomes.

§4.2Forest plot

Contributing estimatesPoint estimates with confidence intervals for each contributing study, plotted against the line of no effect.0.50.751Ratio measure, log scale (1 = no effect)Contributing studyEstimate (95 % CI)MMPOWER-32022 · n=2180.62 (0.56 to 0.69)MMPOWER-22018 · n=301.00 (0.81 to 1.20)Pooled estimate0.75 (0.66 to 0.85)
Study estimatePooled estimate
Figure 1. Illustrative. Contributing estimates plotted against the line of no effect. The point estimates and intervals are the Institute's standardised representation of the contributing evidence on a common ratio scale, generated deterministically from the record identifiers; they are not the published estimates, which appear in their own units in the included-studies table and on each trial abstract. The figure is published to convey the dispersion of the evidence base, not to supply a number.

§4.3Certainty assessment for the anchor outcome

Certainty assessment by domainDowngrading decision recorded for each certainty domain.Certainty domainNo concernSeriousVery seriousEffect on ratingRisk of biasdowngrade one levelInconsistencyno downgradeIndirectnessno downgradeImprecisionno downgradePublication biasdowngrade one levelTotal downgrading: 2 levelsLow certainty
Figure 2. Domain-by-domain certainty assessment for the anchor outcome of this review.

Table 8. Reasoning recorded against each certainty domain for the anchor outcome.

DomainRatingReasoning
Risk of biasSeriousAllocation concealment is not described in one contributing report.
InconsistencyNo concernNo serious concern identified in this domain.
IndirectnessNo concernNo serious concern identified in this domain.
ImprecisionNo concernNo serious concern identified in this domain.
Publication biasSeriousToo few contributing studies for a formal assessment; the risk cannot be excluded.
Overall: Low certainty. Confidence in the effect estimate is limited. The true effect may be substantially different from the estimate.
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