Dipeptidyl peptidase 4 (DPP-4) inhibitors are commonly prescribed second-line oral
glucose-lowering drugs in the treatment of type 2 diabetes, which have good safety
profiles compared with other antidiabetic drugs, such as low risk of hypoglycemia
and having neutral effects on cardiovascular outcomes. One recent pharmacovigilance
study using World Health Organization Vigibase found a consistent signal of reporting
of venous thromboembolism (VTE) associated with DPP-4 inhibitors (proportional reporting
ratio [PRR]: 2; 95% confidence interval [CI]: 1.7–2.3) especially at the gastrointestinal
levels (PRR: 13.4; 95% CI: 9.2–19·6).[1 ] Our study using Food and Drug Administration adverse-event reporting system database
found no association between DPP-4 inhibitors and VTE risk but with a moderate signal
of VTE at gastrointestinal levels.[2 ] However, spontaneous reporting databases have several limitations, such as reporting
bias, lack of denominator data, and confounding; this association requires further
investigation. Current evidence regarding the effect of DPP-4 inhibitors on VTE risk
is very limited, we thus performed a meta-analysis of large cardiovascular outcomes
trials (CVOTs) to evaluate the association between DPP-4 inhibitors and VTE risk among
the patients with type 2 diabetes.
We systematically searched Pubmed, Embase, and Cochrane Central Register of Controlled
Trials (CENTRAL) up to May 1, 2020 to identify the large randomized, double-blind,
placebo-controlled CVOTs. Two reviewers independently selected the trials according
to the following inclusion criteria: (1) CVOTs involving patients with type 2 diabetes;
(2) DPP-4 inhibitors versus placebo; (3) trials reported the events of VTE including
pulmonary embolism and gastrointestinal VTE. The events of VTE, pulmonary embolism,
or gastrointestinal VTE were defined based on the MedDRA[1 ] and were retrieved from the results of serious adverse events reported on Clinicaltrials.gov.
The risk of bias of included trials was judged as low, high, or unclear according
to the Cochrane risk of bias tool.[3 ] A pooled odds ratio (OR) with 95% CI was calculated using a fixed effects model
and an I
2 statistic was used to assess the possible between-study heterogeneity. Furthermore,
a meta-regression was performed to test the difference between the DPP-4 inhibitor
and a funnel plot as well as the Egger's test was performed to evaluate the publication
bias. We considered p -value < 0.05 as statistically significant. The meta-analysis was performed with STATA
(Version 14; Stata Corp., College Station, Texas, United States).
Finally, five CVOTs were included in this meta-analysis.[4 ]
[5 ]
[6 ]
[7 ]
[8 ] The basic characteristics of the included trials are summarized in [Table 1 ]. A total of 47,714 patients with type 2 diabetes and established or at high risk
of cardiovascular disease were randomly allocated to the DPP-4 inhibitor group (23,899
patients) and the placebo group (23,815 patients). The median duration of follow-up
ranged from 1.8 to 3 years. The mean age, baseline HbA1c%, and baseline body mass
index on included patients were 64.2 years, 7.8%, and 30.5 kg/m2 , respectively. The risk of bias of each trial was judged as low ([Table 1 ]). Results of individual trials as well as meta-analysis are presented in [Fig. 1 ]. For risk of VTE, 79 events in the DPP-4 inhibitor group and 70 events in the placebo
group were reported. Meta-analysis of the five trials did not find a significant association
between DPP-4 inhibitors and risk of VTE (OR: 1.12; 95% CI: 0.81–1.55). Furthermore,
there was no significant difference between DPP-4 inhibitors (p = 0.50). Similarly, no significant difference between DPP-4 inhibitors (31 events)
and placebo (27 events) was observed regarding the risk of pulmonary embolism (OR:
1.14; 95% CI: 0.68–1.90). For risk of gastrointestinal VTE, only two events were reported
in patients taking DPP-4 inhibitors and none were reported in the placebo group. There
was no significant association between DPP-4 inhibitors and placebo (OR: 2.98; 95%
CI: 0.31–28.70). No statistical heterogeneity was observed in the meta-analysis with
an I
2 ranged from 0 to 26.7%. There was no evidence of publication bias in the meta-analysis
based on funnel plot (figures not shown) and Egger's test (p > 0.05).
Table 1
Basic characteristics of included studies
Study
NCT
Name
No. of patients
Populations
Intervention
Age (y)
Baseline HbA1c (%)
Baseline BMI (kg/m2 )
Duration of diabetes (y)
Median follow-up (y)
Risk of bias[a ]
Scirica et al (2013)[4 ]
NCT01107886
SAVOR-TIMI 53
16,492
T2D patients with a history of or were at risk for CV events
Saxagliptin
65.1
8
31.2
10.3
2.1
Low
White et al (2013)[8 ]
NCT00968708
EXAMINE
5,380
T2D patients with either an acute myocardial infarction or unstable angina requiring
hospitalization within the previous 15–90 days
Alogliptin
61
8
28.7
7.2
1.5
Low
Green et al (2015)[6 ]
NCT00790205
TECOS
14,671
T2D patients with established CV disease
Sitagliptin
65.5
7.2
30.2
11.6
3
Low
Gantz et al (2017)[5 ]
NCT01703208
OMNEON
4,192
T2D patients with established CV disease
Omarigliptin
63.6
8
31.3
12
1.8
Low
Rosenstock et al (2019)[7 ]
NCT01897532
CARMELINA
6,979
T2D patients with high CV risk
Linagliptin
65.9
7.9
31.3
14.8
2.2
Low
Abbreviations: BMI, body mass index; CV, cardiovascular; T2D, type 2 diabetes.
a Risk of bias of each trial was judged as low, high, or unclear according to Cochrane
risk of bias tool.
Fig. 1 Meta-analysis of the association between DPP-4 inhibitors and risk of venous thromboembolism
and pulmonary embolism.
To our knowledge, this is the first meta-analysis of placebo-controlled CVOTs to assess
the risk of VTE associated with DPP-4 inhibitors among patients with type 2 diabetes.
Some evidence from spontaneous reporting databases indicated that DPP-4 inhibitors
were associated with an increased risk of VTE.[1 ]
[9 ] However, we found no significant difference in the risk of VTE between DPP-4 inhibitors
and placebo, which was also consistent with our previous study.[2 ] It has been proposed that DPP-4 inhibitors may have protective mechanisms against
thrombosis effects by inhibiting platelet aggregation through their inhibitory effect
on intracellular free calcium and tyrosine phosphorylation[10 ] and improving endothelium-dependent vasodilatation through increasing circulating
levels of GLP-1.[11 ] An increase in events of VTE at the gastrointestinal levels was observed in previous
studies,[1 ]
[2 ] while in this study only two events were reported in the DPP-4 inhibitor group,
which requires further investigation including their underlying mechanisms.
This study has several strengths including meta-analysis of available strong evidence
and only considering randomized placebo-controlled trials that balanced the background
therapy as well as other confounders. However, some limitations in this study should
be considered. First, the events of VTE were not the predefined outcomes in these
trials that the numbers of VTE are likely underestimated as only serious adverse events
of VTE were reported on the Clinicaltrials.gov. Second, given the low incidence of
VTE in this study, the study might be underpowered to detect that difference as significant.
For example, only two events of VTE were identified at the gastrointestinal levels.
Therefore, we cannot fully exclude the increased risk of VTE associated with DPP-4
inhibitors among the patients with type 2 diabetes. Third, due to lack of information
regarding the co-medication in individual patients from trials, we cannot evaluate
the potential drug–drug interaction in this study.
In conclusion, based on current available evidence from CVOTs, we did not find a significant
difference between DPP-4 inhibitors and risk of VTE. However, further meta-analyses
of individual data from all randomized controlled trials as well as well-designed
large prospective observational studies are warranted to confirm our findings.
