Evidence map›Paper›PMID 40636316›Full record

ArticleInternational journal of cardiology. Cardiovascular risk and prevention2025

Prognostic value of

Nga Thi Ngoc Pham, Lien Nguyen Thao Tran, Cang Huynh Trung, Hoang Minh Phan, Dung The Bui, Chau Minh Tran, Thuc Tri Nguyen, Phuong Minh Nguyen, An Viet Tran

Abstract read
In one paragraph

Article in International journal of cardiology. Cardiovascular risk and prevention, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

9 authors.

Nga Thi Ngoc PhamFaculty of Basic Science, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
Lien Nguyen Thao TranDepartment of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
Cang Huynh TrungDepartment of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
Hoang Minh PhanHo Chi Minh City Hospital of Rehabilitation and Occupational Disease, 131 Au Duong Lan, Ward 2, District 8, Ho Chi Minh City, 71100, Viet Nam.
Dung The BuiDepartment of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
Chau Minh TranDepartment of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
Thuc Tri NguyenCho Ray Hospital, 201B Nguyen Chi Thanh Street, Ward 12, District 5, Ho Chi Minh City, 71100, Viet Nam.
Phuong Minh NguyenFaculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.
An Viet TranDepartment of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho City, 90000, Viet Nam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Objectives: To determine the prognostic value of the Materials and methods: A cross-sectional descriptive study with longitudinal follow-up, conducted at the Interventional Cardiology Department of Can Tho Central General Hospital from October 2022 to June 2024. AMI patients underwent clinical examination, genetic sequencing, and cardiovascular event monitoring. Results: Among 150 patients (mean age 63.8 ± 10.3 years, 70.7 % male), genotype distribution showed TT as the most prevalent (55.3 %), TC (38.7 %), and CC (6.0 %). Diabetes mellitus was more prevalent in the TT genotype (28.9 %) versus TC (12.1 %) and CC (11.1 %). Severe coronary artery lesions were more common in TT genotype patients (65.7 % vs. 45.4 %; p < 0.05), with the T allele identified as a risk allele (OR = 2.22; 95 % CI: 1.29-3.81; p < 0.05). Multi-vessel coronary artery disease (CAD) was also more frequent in TT genotype patients (59.8 % vs. 49.2 %; p < 0.05). At the 9-month follow-up, event rates were: mortality 4.0 %, stroke 0.7 %, HF hospitalization 6.0 %, and MACE 10.7 %. Independent predictors for MACE initiation included age (HR = 1.05), diabetes (HR = 2.98), TT genotype (HR = 3.63), and T allele (HR = 3.39). Conclusion: AMI patients with the T allele of the

Indexed as

Acute myocardial infarction (AMI)ANRIL geners1333040 polymorphism

Identifiers

PMID40636316
PMCPMC12240131

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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.