SynthesisClinical transplantation2026
Subclinical and Borderline Rejection are Associated With Death-Censored Graft Loss After Kidney Transplantation: A Systematic Review and Meta-Analysis.
Synthesis in Clinical transplantation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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
2 citing papers in PubMed.
- Evaluation of a Pre-Transplant Serum FTIR Rejection-Risk Score Across Time Horizons and Rejection Phenotype-Defined Endpoints in Kidney Transplantation.Journal of personalized medicine · 2026Article
- Impact of antibody-mediated rejection detected on one-year protocol biopsies on long-term kidney allograft survival.Frontiers in medicine · 2026Article
Corrections and comments
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Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe prognostic significance of subclinical rejection (SCR) and borderline rejection (BLR) detected on surveillance kidney allograft biopsies remains uncertain.
methodsWe performed a systematic review and meta-analysis of studies enrolling adult kidney transplant (KT) recipients undergoing protocol biopsies. The primary outcome was death-censored graft loss (DCGL); the secondary outcome was subsequent rejection. Random-effects models, sensitivity analyses, and meta-regression were used.
resultsFifteen studies (5428 recipients) were included. SCR was associated with a higher risk of DCGL (RR 2.22; 95% CI 1.67-2.95) and subsequent rejection (RR 3.09; 95% CI 2.34-4.09), with low heterogeneity. Both T cell-mediated rejection (RR 1.82; 95% CI 1.28-2.61) and antibody-mediated rejection (ABMR) (RR 3.35; 95% CI 2.11-5.33) were associated with increased DCGL. BLR was associated with increased DCGL (RR 2.40; 95% CI 1.67-3.46) and subsequent rejection (RR 2.79; 95% CI 2.10-3.69). Findings were robust across sensitivity analyses, including contemporary Banff-era definitions.
conclusionsSCR and BLR are associated with inferior long-term graft outcomes. These findings underscore their prognostic significance and warrant prospective studies to determine optimal management strategies.
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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.