Observational studyFrontiers in endocrinology2025
Assessment of urate-lowering therapies on lipid metabolism and kidney function in non-dialysis chronic kidney disease patients: 12 months multicenter cohort study.
Observational study in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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.
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Who cites it
2 citing papers in PubMed.
- Kidney-Vascular Metabolic Crosstalk: Altered Lipoproteins in CKD.Circulation research · 2026Review
- Association of uric acid-to-HDL cholesterol ratio and coronary atherosclerotic heart disease in patients with and without CKD.BMC cardiovascular disorders · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background and objectives: Urate lowering therapies (ULTs) are primarily used to manage hyperuricemia (HUA), which refers to an increase in serum uric acid (SUA) levels. SUA is an important marker for assessing kidney function in patients complicated with chronic kidney disease (CKD). Recent studies revealed a close relationship between SUA and lipid metabolism. We aim to investigate the impact of ULTs on kidney function and lipid profiles in CKD patients, and further explore the sex-specific ULTs effects on lipid profiles. Method: We conducted a multicenter, prospective observational cohort study, enrolled n=200 patients aged between 20 and 80 years old with stages 3/4 CKD. Patients were divided into two groups: the ULT group (n=94) who were receiving febuxostat or allopurinol, and the Non-ULT group (n=106) who were receiving their conventional CKD therapy, the study employed clinically indicated allocation. ULT initiation was based on physician judgment per guidelines persistent HUA with SUA ≥7 mg/dL in males and ≥6 mg/dL in females with CKD progression risk factors. Models adjusted for all collected confounders, renal function including estimated glomerular filtration rate (eGFR), serum creatinine (Scr), blood urea nitrogen (BUN), and SUA, and lipid profiles including high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c), triglyceride (TG), and total cholesterol (TC). Results remained consistent in sensitivity analyses stratifying by baseline characteristics. Subgroups were further analyzed based on sex, to evaluate sex-specific differences in lipid metabolism related to ULTs. All participants went through clinical assessment before and after treatment and were followed for 12 consecutive months. Results: LDL-c significantly decreased in the ULT group compared to the Non-ULT group after 12 months of observation (2.14 ± 0.32 vs. 2.42 ± 0.32 [95% CI: -0.36 to -0.18], Conclusion: In this cohort study of non-dialysis CKD patients, ULT use was associated with improved lipid profiles reduced LDL-c, TG, and TC; increased HDL-c, with greater HDL-c elevation and LDL-c reduction in males. ULTs exposure also correlated with attenuated CKD progression. These findings suggest potential interactions between SUA and lipid metabolism, highlighting ULTs' possible role in managing dyslipidemia and renal function decline in pre-dialysis CKD.
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