ArticleFrontiers in endocrinology2026
The association between SGLT2 inhibitor use and diabetic peripheral neuropathy in type 2 diabetes: a cross-sectional study.
Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: This study assessed the association between sodium-glucose cotransporter 2 (SGLT2) inhibitor use and the prevalence of diabetic peripheral neuropathy (DPN) in patients with type 2 diabetes mellitus (T2DM). Methods: We classified 2, 456 individuals with T2DM according to SGLT2 inhibitor treatment status. Propensity score matching (PSM) was implemented as the primary adjustment technique to achieve balance between groups on baseline demographics, laboratory values, comorbidities, and concurrent glucose-lowering agents. Additional propensity score weighting approaches were employed to examine the robustness of our findings, along with subgroup analyses and E-value calculations. Results: Among all participants, 399 (16.2%) had received SGLT2 inhibitors. Following PSM, each study arm comprised 398 patients. In the matched cohort, SGLT2 inhibitor use was associated with significantly increased odds of DPN (odds ratio 1.55; 95% confidence interval 1.17-2.05; p = 0.002). This association remained consistent across different propensity score methods, with odds ratios ranging from 1.55 to 1.7 (all p < 0.01). Subgroup analyses confirmed statistical significance, and E-value assessment supported the robustness of the observed effect. Conclusion: SGLT2 inhibitor use was associated with a higher prevalence of DPN. Further prospective studies are warranted to establish causality.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.