Evidence map›Paper›PMID 39972065›Full record

ArticleScientific reports2025

The correlation between the atherogenic index of plasma and the severity of coronary artery disease in acute myocardial infarction patients under different glucose metabolic states.

Kaiqin Jin, Zijun Ma, Chuanglu Zhao, Xintao Zhou, Hao Xu, Dongfeng Li, Xinwen Min, Handong Yang, Wenwen Wu, Jixin Zhong and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 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

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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
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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

12 authors.

Kaiqin Jin *Sinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Zijun Ma *Sinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Chuanglu Zhao *Sinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Xintao ZhouSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Hao XuSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Dongfeng LiSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Xinwen MinSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Handong YangSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Wenwen WuSchool of Public Health, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Jixin ZhongDepartment of Rheumatology and Immunology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, 430030, Hubei, China.
Jishun ChenSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China. 364988870@qq.com.
Jun ChenSinopharm Dongfeng General Hospital (Hubei Clinical Research Center of Hypertension), Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, 442000, Hubei, China. chenjun0121@126.com.

Funding

National Natural Science Foundation of China 81400288, 81573244
6 · The paper itself

Abstract

The atherogenic index of plasma (AIP) is a recent biomarker linked to atherosclerosis that has been validated as a novel indicator for myocardial infarction (MI). However, the relationship between AIP and the severity of coronary artery disease (CAD) in MI patients is still ambiguous, particularly among individuals with different glucose metabolic conditions. A total of 741 participants who were immediately assessed with coronary angiography upon admission and diagnosed with acute MI were recruited. The severity of CAD was assessed based on the number of narrowed vessels. AIP tertiles were used to divide the patients into three groups (T1: AIP < 0.030; T2: 0.030 ≤ AIP ≤ 0.316; T3: AIP > 0.316). The American Diabetes Association's guidelines define three types of glucose metabolic state: diabetes mellitus (DM), prediabetes (Pre-DM), and normal glucose regulation (NGR). Logistic regression analysis was utilized to confirm an association between AIP and CAD severity in MI patients. ROC curves were employed to evaluate the diagnostic utility of AIP for CAD severity in MI patients. In MI patients, a statistically significant correlation was found between AIP and the severity of CAD, with logistic regression analysis revealing a strong association (OR: 2.055; 95% CI: 1.189-3.550; P = 0.009). Following adjustments for risk factors in the logistic regression model, AIP remained an independent predictor of multi-vessel CAD (OR: 2.902;95% CI: 1.555-5.521 ; P < 0.001). Moreover, compared with the T1 group, the odds ratios for multi-vessel CAD in the T2 and T3 groups were 2.039 (95% CI: 1.321-3.175; P = 0.001) and 2.087 (95% CI: 1.317-3.340; P = 0.001), respectively. The area under the curve for predicting CAD severity with AIP was 0.568 (95% CI: 0.520-0.616; p = 0.006). In addition, a significant association was observed between AIP and an increased risk of multi-vessel CAD in the Pre-DM group. In MI patients, AIP is closely associated with the risk of multi-vessel CAD and the prediction of the severity of CAD. In Pre-DM patients, AIP is clearly associated with the severity of CAD, whereas this association is absent in the NGR and DM groups.

Indexed as

AtherosclerosisBlood GlucoseCoronary Artery DiseaseMyocardial InfarctionAgedBiomarkersCoronary AngiographyFemaleHumansMaleMiddle AgedPrediabetic StateRisk FactorsROC CurveSeverity of Illness IndexBiomarkersBlood GlucoseAtherogenic index of plasmaCoronary artery diseaseGlucose metabolic statesMyocardial infarctionThe severity of coronary artery disease

Identifiers

PMID39972065
PMCPMC11839988

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