# Clinical efficacy and mechanistic study of fulvning granules in symptomatic atrial fibrillation: a randomized controlled trial with untargeted metabolomics analysis

**Authors:** Jinru Tao, Keke Liu, Tianyi Cheng, Mianmian Li, Chunrui Hu, Yulai Zhan, Qiuting Yu, Yinyifan Zhou, Xue Liu, Zilin Ma, Na Zhang, Bing Deng, Lin Shen, Nuo Tang, Qiong Wu

PMC · DOI: 10.3389/fphar.2026.1761563 · Frontiers in Pharmacology · 2026-02-24

## TL;DR

Fulvning Granules (FLN) effectively reduce symptoms of atrial fibrillation and improve quality of life, possibly by altering key metabolic pathways.

## Contribution

This study provides clinical evidence and mechanistic insights into FLN's efficacy for treating atrial fibrillation.

## Key findings

- FLN significantly improved AF control compared to placebo (78.57% vs. 54.39%).
- FLN reduced palpitation frequency and duration and improved psychological well-being.
- Metabolomics analysis revealed modulation of ketone, butanoate, and glycerophospholipid pathways by FLN.

## Abstract

Atrial fibrillation (AF) is the most prevalent sustained arrhythmia and a leading cause of morbidity and mortality worldwide. Although antiarrhythmic drugs and catheter ablation have improved AF management, their therapeutic efficacy remains suboptimal. Fulvning Granules (FLN), a regulated hospital preparation officially approved by the Shanghai Drug Administration, have shown promising clinical efficacy in local practice. However, robust high-level clinical evidence is required to validate their benefits and elucidate the underlying mechanisms.

A randomized, double-blind, placebo-controlled trial enrolled 136 symptomatic AF patients, who received either FLN or a placebo for 4 weeks in addition to standard guideline-directed medical therapy (GDMT). The primary endpoint was AF control effectiveness, assessed by 24-h Holter monitoring. Secondary endpoints included palpitation frequency and duration, echocardiographic evaluation of cardiac structure and function, N-terminal pro-B-type natriuretic peptide (NT-pro BNP)levels, Hamilton Anxiety (HAMA) and Depression (HAMD) Scales, and the 36-item Short-Form Health Survey (SF-36) from baseline to week 4. To further validate FLN’s efficacy and explore its mechanisms, serum-based metabolic pathway analysis was conducted to investigate the metabolic network associated with FLN treatment of AF.

FLN significantly improved AF control compared with placebo (78.57% vs. 54.39%; P = 0.001), with concomitant reductions in both the frequency and duration of palpitations. In addition, treatment with FLN markedly enhanced psychological well-being and health-related quality of life. Untargeted metabolomics analysis identified 23 bioactive compounds in FLN and revealed significant modulation of ketone, butanoate, and glycerophospholipid pathways (P < 0.05), primarily involving acylcarnitines, Lutein, and LysoPC (22:0).

FLN serves as a safe and effective adjuvant therapy for reducing AF episode frequency and ventricular rate in patients with symptomatic AF. Its mechanism may involve the modulation of cardiac energy metabolism.

ClinicalTrials.gov, identifier ChiCTR2000036835.

## Linked entities

- **Chemicals:** Lutein (PubChem CID 181579), LysoPC (22:0) (PubChem CID 24779479)
- **Diseases:** atrial fibrillation (MONDO:0004981)

## Full-text entities

- **Diseases:** palpitation (MESH:D006331), Depression (MESH:D003866), AF (MESH:D001281), arrhythmia (MESH:D001145), Anxiety (MESH:D001007)
- **Chemicals:** butanoate (-), Lutein (MESH:D014975), acylcarnitines (MESH:C116917), LysoPC (MESH:C006065), glycerophospholipid (MESH:D020404), ketone (MESH:D007659)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12971955/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12971955/full.md

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Source: https://tomesphere.com/paper/PMC12971955