Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Fig 1.

Study schema.

DPP-4: dipeptidyl peptidase-4, SKDB: Shizuoka Kokuho Database. Cohort entry was defined as the later of the date of registration with the health insurance provider or April 1, 2012. The index data were collected on the day that the participants were first prescribed a DPP-4 inhibitor or a biguanide. The follow-up period was defined as the interval between the index date and the end date of the study (September 30, 2021), the date of withdrawal from the health insurance system, or the date of occurrence of an outcome.

More »

Fig 1 Expand

Fig 2.

Flow diagram for the participants.

More »

Fig 2 Expand

Table 1.

Participant characteristics after propensity score matching.

More »

Table 1 Expand

Table 2.

Antidiabetic medication prescribed and the number of health care visits within the year following the index date and after propensity score matching.

More »

Table 2 Expand

Fig 3.

Cumulative incidences of cardiac and cerebrovascular events or mortality, and diabetic complications in the matched cohort.

DPP-4i: dipeptidyl peptidase-4 inhibitor. Cumulative incidences of (a) the composite outcome of cardiac or cerebrovascular outcomes or mortality and (a) diabetic complications, including diabetic retinopathy, nephropathy, neuropathy, and other conditions, in the propensity score-matched cohort.

More »

Fig 3 Expand

Table 3.

Comparison of the outcomes of participants who were prescribed biguanide or a DPP-4 inhibitor.

More »

Table 3 Expand

Fig 4.

Results of the subgroup analysis of the composite outcome.

HR: hazard ratio, CI: confidence interval.

More »

Fig 4 Expand

Fig 5.

Results of the subgroup analysis of diabetic complications.

HR: hazard ratio, CI: confidence interval.

More »

Fig 5 Expand