Cochrane · systematic review · CD006739

Dipeptidyl peptidase‐4 (DPP‐4) inhibitors for type 2 diabetes mellitus

Richter, B, Bandeira‐Echtler, E, Bergerhoff, K, et al. · Cochrane Database of Systematic Reviews · 2008 · Cochrane Library

Metabolic and Endocrine DisordersAMSTAR 2: not assessed
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
14
current version
GRADE rated
10
No studies
4
Included studies
NR
No studies 4 · 28.6%Ungraded 0 · 0%Very low 0 · 0%Low 0 · 0%Moderate 0 · 0%High 10 · 71.4%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Summary of findings: Sitagliptin

Population: type 2 diabetes mellitus
7 questions
OutcomeEffectEvidenceStatus / GRADE
Morbidity
no estimate extractedNRNo studies
Health‐related quality of life
no estimate extractedNRNo studies
Change in HbA1c from baseline to endpoint % (
no estimate extracted11 studies · 6907 participantsHigh
Change in HbA1c from baseline to endpoint ‐ Sitagliptin versus another single hypoglycaemic agent % (
no estimate extracted2 studies · 592 participantsHigh
Change in HbA1c from baseline to endpoint [%] ‐ Sitagliptin versus placebo % (
no estimate extracted3 studies · 1103 participantsHigh
Change in body weight from baseline to endpoint ‐ Sitagliptin versus placebo kg (
no estimate extracted3 studies · 1109 participantsHigh
Adverse events ‐ All‐cause infections (
RR 1.29 [1.09, 1.52]8 studies · 3589 participantsHigh

Summary of findings: Vildagliptin

Population: patients with type 2 diabetes mellitus
7 questions
OutcomeEffectEvidenceStatus / GRADE
Morbidity
no estimate extractedNRNo studies
Health‐related quality of life
no estimate extractedNRNo studies
Change in HbA1c from baseline to endpoint % (
no estimate extracted14 studies · 6308 participantsHigh
Change in HbA1c from baseline to endpoint ‐ Vildagliptin versus another single hypoglycaemic agent % (
no estimate extracted3 studies · 1764 participantsHigh
Change in HbA1c from baseline to endpoint ‐ Vildagliptin versus placebo % (
no estimate extracted6 studies · 1139 participantsHigh
Change in body weight from baseline to endpoint ‐ Vildagliptin versus placebo kg (
no estimate extracted3 studies · 484 participantsHigh
Adverse events ‐ All‐cause infections (
RR 1.04 [0.87, 1.24]10 studies · 3573 participantsHigh