The Use of Decomposition Methods in Real-World Treatment Benefits Evaluation for Patients with Type 2 Diabetes Initiating Different Injectable Therapies: Findings from the INITIATOR Study.
Value Health · 2017
Last updated 2026-05-28In a real-world study of people with type 2 diabetes starting either insulin glargine or liraglutide, those on insulin glargine saw a larger drop in blood sugar control after one year (-1.39% vs. -0.74%). The bigger improvement with insulin glargine was mostly linked to differences in patients’ starting conditions, such as higher starting blood sugar or being treated by an endocrinologist. Persistence with treatment was also higher for insulin glargine (65% vs. 49%), mainly because of the treatment itself rather than patient characteristics.
AI summary of the abstract below.
| Journal | Value Health, 2017 |
|---|---|
| Citations | 9 |
| Relative citation ratio | 0.32 |
| NIH percentile | 19 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes |
Abstract
BACKGROUND: Determining characteristics of patients likely to benefit from a particular treatment could help physicians set personalized targets.
OBJECTIVES: To use decomposition methodology on real-world data to identify the relative contributions of treatment effects and patients' baseline characteristics.
METHODS: Decomposition analyses were performed on data from the Initiation of New Injectable Treatment Introduced after Antidiabetic Therapy with Oral-only Regimens (INITIATOR) study, a real-world study of patients with type 2 diabetes started on insulin glargine (GLA) or liraglutide (LIRA). These analyses investigated relative contributions of differences in baseline characteristics and treatment effects to observed differences in 1-year outcomes for reduction in glycated hemoglobin A (HbA) and treatment persistence.
RESULTS: The greater HbA reduction seen with GLA compared with LIRA (-1.39% vs. -0.74%) was primarily due to differences in baseline characteristics (HbA and endocrinologist as prescribing physician; P < 0.050). Patients with baseline HbA of 9.0% or more or evidence of diagnosis codes related to mental illness achieved greater HbA reductions with GLA, whereas patients with baseline polypharmacy (6-10 classes) or hypogylcemia achieved greater reductions with LIRA. Decomposition analyses also showed that the higher persistence seen with GLA (65% vs. 49%) was mainly caused by differences in treatment effects (P < 0.001). Patients 65 years and older, those with HbA of 9.0% or more, those taking three oral antidiabetes drugs, and those with polypharmacy of more than 10 classes had higher persistence with GLA; patients 18 to 39 years and those with HbA of 7.0% to less than 8.0% had higher persistence with LIRA.
CONCLUSIONS: Although decomposition does not demonstrate causal relationships, this method could be useful for examining the source of differences in outcomes between treatments in a real-world setting and could help physicians identify patients likely to respond to a particular treatment.
Verbatim abstract via PubMed 29241884 ↗