Evidence map›Paper›PMID 40820985›Full record

ArticleJournal of the American Heart Association2025

Microbiota γ-Butyrobetaine Is Associated With Increased Risk of Major Adverse Limb Events in People With Lower Extremity Arterial Disease Undergoing Endovascular Therapy.

Zheng-Wei Chen, Wei-Kai Wu, Jiun-Yang Chiang, Nai-Chen Cheng, Jen-Kuang Lee, Ming-Shiang Wu

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Zheng-Wei ChenDivision of Cardiology, Department of Internal Medicine National Taiwan University College of Medicine and Hospital Taipei Taiwan.ORCID 0000-0001-7728-6674
Wei-Kai WuDepartment of Medical Research National Taiwan University Hospital Taipei Taiwan.ORCID 0000-0002-9476-8998
Jiun-Yang ChiangDivision of Cardiology, Department of Internal Medicine National Taiwan University College of Medicine and Hospital Taipei Taiwan.ORCID 0000-0002-7405-0858
Nai-Chen ChengDivision of Plastic Surgery, Department of Surgery National Taiwan University College of Medicine and Hospital Taipei Taiwan.
Jen-Kuang LeeDivision of Cardiology, Department of Internal Medicine National Taiwan University College of Medicine and Hospital Taipei Taiwan.ORCID 0000-0003-3790-484X
Ming-Shiang WuDivision of Gastroenterology and Hepatology, Department of Internal Medicine National Taiwan University College of Medicine and Hospital Taipei Taiwan.ORCID 0000-0002-1940-6428

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeripheral artery disease (PAD), a significant contributor to both acute and chronic illnesses, indicates a grave prognosis, but it is often unrecognized and receives inadequate treatment. γ-Butyrobetaine, formed during gut microbial metabolism of L-carnitine, acts as a proatherogenic intermediate in the production of trimethylamine

methodsWe prospectively enrolled 395 patients with symptomatic PAD. Comprehensive medical histories, encompassing demographic and medication data, were collected, and serum biochemistry data, including TMAO and γ-butyrobetaine, were obtained. These patients, with a mean age of 72.2 years (61% men), were followed for an average of 1.5 years. They were categorized into 2 groups: 165 patients with intermittent claudication and 230 patients with critical limb-threatening ischemia. The primary outcome studied was major adverse limb events (MALE), which included lower-limb revascularization and amputation. MALE developed in 89 (22.5%) patients. Following adjustment for confounding factors in the multivariate Cox proportional hazards model, γ-butyrobetaine was significantly associated with MALE (hazard ratio, 1.93 [95% CI, 1.35-2.76]). By contrast, TMAO did not show a significant association with the risk of MALE.

conclusionsWhile both TMAO and γ-butyrobetaine were linked to increased major adverse cardiovascular events in patients with PAD, only γ-butyrobetaine was associated with an elevated risk of MALE.

Indexed as

BetaineEndovascular ProceduresGastrointestinal MicrobiomeIntermittent ClaudicationIschemiaLower ExtremityPeripheral Arterial DiseaseAgedAged, 80 and overAmputation, SurgicalBiomarkersCarnitineFemaleHumansMaleMethylaminesBetaineBiomarkersCarnitinegamma-butyrobetaineMethylaminestrimethyloxaminemajor adverse cardiovascular eventsmajor adverse limb eventsperipheral artery diseasetrimethylamine N‐oxideγ‐Butyrobetaine

Identifiers

PMID40820985
PMCPMC12748064

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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.