Observational studyMedicine2025
V-shaped relationship between platelet-to-lymphocyte ratio and mortality in patients with cardio-cerebrovascular disease: An observational study.
Observational study in Medicine, 2025. 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
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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
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
This study aimed to elucidate the association between platelet-to-lymphocyte ratio (PLR) and long-term mortality risk in patients with cardio-cerebrovascular diseases (CVD), providing insights for early intervention strategies. Nonlinear associations between the PLR and all-cause mortality were examined using spline smoothing plots analysis. The inflection point of PLR's effect on all-cause mortality was determined using threshold saturation and log-likelihood ratio tests. Subgroup analyses were performed to assess result stability. A competing risk model was employed to investigate the relationship between PLR and cardiovascular mortality. A total of 5024 adult patients with hypertension were included in this study. The average follow-up duration was 78 months. Spline smoothing plots analysis revealed a V-shaped relationship between PLR and all-cause mortality, with an inflection point at 64.48. When PLR was <64.48, the risk of all-cause mortality declined gradually (HR = 0.979, 95% CI: 0.968-0.990, P = .0003) with increasing PLR. Conversely, when PLR was ≥64.48, the risk of all-cause mortality gradually increased (HR = 1.002, 95% CI: 1.001-1.003, P < .0001) with increasing PLR. The competing risk model indicated a comparable association between PLR and cardiovascular mortality in patients with CVD. This study establishes a V-shaped PLR-mortality relationship in CVD patients with an inflection point at 64.48. This highlights the potential of PLR as a clinically actionable biomarker for precision risk management, offering a basis for early intervention strategies.
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