ArticleFrontiers in endocrinology2026
Association between hemoglobin glycation index and all-cause mortality in patients with non-ST-segment elevation myocardial infarction undergoing percutaneous coronary intervention.
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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The hemoglobin glycation index (HGI) has emerged as a potential marker for cardiovascular risk stratification. However, its prognostic value in patients with non-ST-segment elevation myocardial infarction (NSTEMI) undergoing percutaneous coronary intervention (PCI) remains unclear. This study investigated the association between HGI and all-cause mortality in this population. Methods: This single-center cohort study included 635 patients with NSTEMI who underwent PCI between January 2016 and July 2023. The primary endpoint was all-cause mortality. Kaplan-Meier analysis, Cox regression, restricted cubic spline (RCS) analysis, and subgroup analyses were performed. Results: Over a median follow-up of 60 months, higher HGI was associated with more favorable survival. In the fully adjusted model, a 1-unit increase in HGI was associated with a 43% lower risk of all-cause mortality (HR=0.57, 95% CI: 0.40-0.82, P=0.002). Patients in the highest HGI tertile also had a lower risk of mortality than those in the lowest HGI tertile (HR=0.26, 95% CI: 0.10-0.66, P=0.004). RCS analysis indicated a linear inverse association. Exploratory subgroup analyses suggested that the inverse association appeared more evident in men than in women. Conclusion: HGI was associated with all-cause mortality and may serve as a complementary marker for risk stratification in patients with NSTEMI undergoing PCI.
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.