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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Glycemic Status, Stent Count, and In-Stent Restenosis: Exploratory Decomposition and Sex-Related Analyses in a Retrospective Cohort

  1. 1Department of Endocrinology and Metabolism, The Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China

Abstract

Background/Objectives: Fasting blood glucose (FBG) and stent count have been associated with in-stent restenosis (ISR), but their interrelationships remain unclear. We evaluated the FBG–ISR association and explored baseline stent count as a potential mediator. Methods: This single-center retrospective cohort comprised 510 patients with follow-up angiography after percutaneous coronary intervention (PCI). Analyses included multivariable regression, exploratory decomposition in 468 patients sampled before PCI, and intravascular imaging analyses in 284 patients. Results: ISR was observed in 56 patients (11.0%). The adjusted FBG–ISR odds ratio (OR) was 1.100 per mmol/L (95% confidence interval [CI] 1.001–1.208; p = 0.048); Firth and diabetes-adjusted CIs included 1. For FBG increasing from 5.07 to 7.59 mmol/L, the indirect component associated with baseline stent count was 0.48 percentage points (95% CI 0.06 to 1.05); the direct and total CIs included zero. Exploratory analyses suggested higher direct-effect estimates in men and positive indirect-effect estimates in women; between-sex indirect differences remained uncertain. Higher stent count was associated with underexpansion, which was associated with ISR (adjusted OR 4.47, 95% CI 1.85–10.78). Conclusions: Higher FBG showed a modest positive association with ISR, with uncertainty across sensitivity analyses. Exploratory analyses yielded a positive indirect estimate for stent count and linked underexpansion to ISR.

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BibTeX
@article{wang2026glycemic,
  title = {{Glycemic Status, Stent Count, and In-Stent Restenosis: Exploratory Decomposition and Sex-Related Analyses in a Retrospective Cohort}},
  author = {Yuan Wang and Yan Zhuang and Liao Zhang and Haiyan Song},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = nov,
  doi = {10.3390/jcm15218685},
  url = {https://www.mdpi.com/2077-0383/15/21/8685},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Glycemic Status, Stent Count, and In-Stent Restenosis: Exploratory Decomposition and Sex-Related Analyses in a Retrospective Cohort
AU  - Yuan Wang
AU  - Yan Zhuang
AU  - Liao Zhang
AU  - Haiyan Song
PY  - 2026
DA  - 2026/11/07
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15218685
UR  - https://www.mdpi.com/2077-0383/15/21/8685
AB  - Background/Objectives: Fasting blood glucose (FBG) and stent count have been associated with in-stent restenosis (ISR), but their interrelationships remain unclear. We evaluated the FBG–ISR association and explored baseline stent count as a potential mediator. Methods: This single-center retrospective cohort comprised 510 patients with follow-up angiography after percutaneous coronary intervention (PCI). Analyses included multivariable regression, exploratory decomposition in 468 patients sampled before PCI, and intravascular imaging analyses in 284 patients. Results: ISR was observed in 56 patients (11.0%). The adjusted FBG–ISR odds ratio (OR) was 1.100 per mmol/L (95% confidence interval [CI] 1.001–1.208; p = 0.048); Firth and diabetes-adjusted CIs included 1. For FBG increasing from 5.07 to 7.59 mmol/L, the indirect component associated with baseline stent count was 0.48 percentage points (95% CI 0.06 to 1.05); the direct and total CIs included zero. Exploratory analyses suggested higher direct-effect estimates in men and positive indirect-effect estimates in women; between-sex indirect differences remained uncertain. Higher stent count was associated with underexpansion, which was associated with ISR (adjusted OR 4.47, 95% CI 1.85–10.78). Conclusions: Higher FBG showed a modest positive association with ISR, with uncertainty across sensitivity analyses. Exploratory analyses yielded a positive indirect estimate for stent count and linked underexpansion to ISR.
SN  - 2077-0383
ER  -