Evidence map›Paper›PMID 42681829›Full record

ArticleDiabetes, obesity & metabolism2026

Initiation of SGLT2 Inhibitors Versus DPP-4 Inhibitors in Metformin Users and Risk of Incident Depression: A Nationwide, Claims-Based Active-Comparator New-User Study.

Sangwoo Park, Seogsong Jeong, Hye Jun Kim, Dae Ho Lee, Soo Jung Choi, Sang Min Park

Abstract readComparative Study
In one paragraph

Article in Diabetes, obesity & metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sangwoo ParkDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul National University, Seoul, Republic of Korea.
Seogsong JeongDepartment of Biomedical Informatics, Korea University College of Medicine, Seoul, South Korea.
Hye Jun KimDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul National University, Seoul, Republic of Korea.
Dae Ho LeeDepartment of Internal Medicine, (Medical Corporation) Namchon Medical Foundation, Shihwa Medical Center, Siheung-si, Gyeonggi-do, Korea.ORCID https://orcid.org/0000-0002-8832-3052
Soo Jung ChoiDepartment of Family Medicine, Gachon University Gil Medical Center, Incheon, South Korea.
Sang Min ParkDepartment of Biomedical Sciences, Seoul National University Graduate School, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-7498-4829

Funding

Gachon University Gil Medical Center FRD2023-20 to Soo Jung ChoiNational Research Foundation of Korea RS-2024-00440371
6 · The paper itself

Abstract

aimsTo examine the association between initiation of sodium-glucose cotransporter-2 (SGLT2) inhibitors and risk of incident depression compared with dipeptidyl peptidase-4 (DPP-4) inhibitors among adults with newly diagnosed Type 2 diabetes receiving metformin. MATERIALS AND

methodsWe conducted a nationwide active-comparator new-user cohort study with a 90-day adherent-survivor landmark design, using the Korean National Health Insurance Service database linked with national health check-up and mortality data (2014-2022). Adults with newly diagnosed Type 2 diabetes receiving metformin who newly initiated SGLT2 inhibitors or DPP-4 inhibitors as add-on therapy were identified. This study was designed as a 90-day adherent-survivor landmark analysis. Propensity score matching was performed in a 1:1 ratio, yielding 10 013 matched pairs. The primary outcome was incident depression, defined as ≥ 2 outpatient or inpatient claims with ICD-10 codes F32-F33. The secondary outcome was suicide mortality. Cox proportional hazards models were used to estimate hazard ratios (HRs) under intention-to-treat and as-treated approaches.

resultsAmong 38 297 eligible participants, 300 depression events occurred among SGLT2 inhibitor users and 391 among DPP-4 inhibitor users in the matched cohort. Initiation of SGLT2 inhibitors was associated with a lower risk of depression compared with DPP-4 inhibitors (HR 0.85, 95% CI 0.73-0.99). Similar findings were observed in as-treated analyses (HR 0.80, 95% CI 0.65-0.98). Associations were generally consistent across clinically relevant subgroups and appeared more pronounced among older adults, females and individuals with greater comorbidity burden. Suicide mortality was infrequent in both groups.

conclusionsAmong 90-day adherent survivors with Type 2 diabetes receiving metformin, initiation of SGLT2 inhibitors as add-on therapy was associated with a lower risk of incident depression compared with DPP-4 inhibitors.

Indexed as

DepressionDiabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsHypoglycemic AgentsMetforminSodium-Glucose Transporter 2 InhibitorsAdultAgedCohort StudiesDrug Therapy, CombinationFemaleHumansIncidenceMaleMiddle AgedRepublic of KoreaDipeptidyl-Peptidase IV InhibitorsHypoglycemic AgentsMetforminSodium-Glucose Transporter 2 Inhibitorsantidiabetic drugcohort studyDPP‐IV inhibitorobservational studypharmaco‐epidemiologySGLT2 inhibitor

Identifiers

PMID42681829
PMCPMC13646365

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.