Observational studyMedicine2026
Impact of metabolic syndrome and its components on the tumor aggressiveness of renal cell carcinoma.
Observational study in Medicine, 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.
- Obesity-driven metabolic reprogramming and immune dysfunction in renal cancer.Frontiers in immunology · 2026Review
- The impact of metabolic syndrome on survival outcomes in urothelial carcinoma: a retrospective cohort study.Frontiers in oncology · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This retrospective study aimed to assess the impact of metabolic syndrome (MS) and its components on tumor size, Fuhrman grade (FG), and tumor-node-metastasis stage in patients with renal cell carcinoma (RCC). Data from 151 patients who underwent surgery for RCC between January 2010 and April 2018 were retrospectively reviewed. The criteria included blood test results, presence of chronic ailments, and body mass index. Tumor size, FG, and TNM stage were compared. The criteria for defining MS and statistical methods were used for the comparative investigation. Of the 151 patients operated for RCC in our clinic, the prevalence of MS, diabetes mellitus, hypertension (HT), dyslipidemia, and obesity was 27.2%, 29.1%, 41.1%, 64.9%, and 27.2%, respectively. Tumor size was significantly larger, and FG and TNM stages were more advanced in patients with MS than in patients without MS (P = .046, P = .005, P = .030, respectively). The study revealed a statistically significant increase in tumor size associated with diabetes mellitus, HT, dyslipidemia (DysL), and obesity (P = .017, P = .007, P < .001, P = .005, respectively). The TNM stage was significantly higher in patients with HT, DysL, and obesity (P < .001, all of them). In patients undergoing surgery for RCC, MS, and its components showed a statistically significant correlation with tumor size. In addition, HT, DysL, and obesity were associated with a high TNM stage. These findings underscore the potential clinical relevance of addressing the metabolic factors in RCC management.
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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.