Evidence map›Paper›PMID 41625765›Full record

Trial reportFrontiers in medicine2025

Colchicine reduces inflammatory cytokines and improves symptoms in HFpEF: an observational pilot study.

Meijing Shi, Xinyue Zhang, Lizhuo Li, Yu Wang, Qingzhen Zhao, Yuzhi Zhen, Yaomeng Huang, Chao Liu

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07654231 (Reducing Inflammation to Improve Vascular and Bone Outcomes With Low-dose Colchicine in CKD), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

NCT07654231 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Reducing Inflammation to Improve Vascular and Bone Outcomes With Low-dose Colchicine in CKD: A Pilot Randomized Open-Label Trial (RESOLVE-CKD Trial)

TypeinterventionalSponsorUniversity of Texas Southwestern Medical CenterRan2026 to 2027Enrolled60ConditionsChronic Kidney Disease Mineral and Bone Disorder, Hypertension, Diabetes, DyslipidemiaArmsLow-dose Colchicine at 0.5mg daily, Usual Care
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Meijing ShiSchool of Graduate, Hebei Medical University, Shijiazhuang, China.
Xinyue ZhangSchool of Graduate, Hebei Medical University, Shijiazhuang, China.
Lizhuo LiDepartment of Cardiology, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Yu WangDepartment of Cardiology, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Qingzhen ZhaoDepartment of Cardiology, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Yuzhi ZhenDepartment of Cardiology, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Yaomeng HuangLaboratory Center, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Chao LiuDepartment of Cardiology, The First Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The objective of this study was to investigate whether colchicine could safely and effectively reduce inflammatory marker levels and improve the prognosis in patients with heart failure with preserved ejection fraction (HFpEF). Methods: This study enrolled patients diagnosed with HFpEF. Venous blood samples were collected to assess the levels of inflammatory markers such as IL-6, IL-8, and TNF-α. If these markers were elevated, patients were treated with colchicine 0.5 mg once daily. Inflammatory markers were reassessed after 2 weeks of treatment in the outpatient department. The primary endpoint was the change in inflammatory factor levels before and after colchicine treatment. Secondary outcomes included assessments of anxiety (HAMA), depression (HAMD), and quality of life (KCCQ) after 1 month of colchicine treatment. The clinical trial was registered at Chinese Clinical Trail Registry (ChiCTR2500103522). Results: A total of 126 patients were included. The serum inflammatory markers most notably elevated in the HFpEF cohort were IL-8 and IL-6, with IL-8 showing the most significant increase. After 2 weeks of colchicine treatment, serum levels of inflammatory markers decreased significantly. IL-8 levels decreased by -28.65 (95% CI: -54.20 to -11.47, Conclusion: This study is the first to explore colchicine as an anti-inflammatory treatment for HFpEF. Our results indicate that colchicine can safely and effectively reduce inflammatory markers such as IL-8 and IL-6. After 1 month of treatment, significant improvements were observed in anxiety, depression, and quality of life. These findings support colchicine's potential as a therapeutic option for managing inflammation and improving outcomes in patients with HFpEF.

Indexed as

colchicineheart failure with preserved ejection fractioninflammatory cytokinesobservational pilot studysymptoms

Identifiers

PMID41625765
PMCPMC12857056

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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 OpenQuestion graph.