Evidence map›Paper›PMID 39155699›Full record

ArticleJournal of diabetes2024

Influence of impaired glucose tolerance alone and combined with metabolic syndrome on long-term risk of cardiovascular events and mortality.

Fei Chen, Yifan He, Jinping Wang, Liping Yu, Qiuhong Gong, Yanyan Chen, Yali An, Siyao He, Guangwei Li, Bo Zhang

Abstract read
In one paragraph

Article in Journal of diabetes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  4. Review
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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

10 authors.

Fei ChenDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-1244-2194
Yifan HeDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, China.
Jinping WangDepartment of Cardiology, Da Qing First Hospital, Da Qing, China.
Liping YuDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, China.
Qiuhong GongEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID https://orcid.org/0000-0002-8781-1214
Yanyan ChenEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yali AnEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Siyao HeEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Guangwei LiDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-1061-7293
Bo ZhangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-3060-7850

Funding

National High Level Hospital Clinical Research Funding 2022-NHLHCRF-YS-01
6 · The paper itself

Abstract

backgroundThis study aimed to investigate the potential differences in the influence of impaired glucose tolerance (IGT) with and without metabolic syndrome (MetS) on cardiovascular (CV) events and mortality.

methodsParticipants having IGT with MetS (IGT_MetS), those having IGT without MetS (IGT_non_MetS), and those having normal glucose tolerance (NGT) without MetS (NGT_non_MetS) (N = 246, N = 294, and N = 471, respectively) were included in this study. Cox proportional hazards regression was used to examine the relationship among these three groups and CV events and mortality.

resultsOver the 30-year follow-up period, 57 (12.1%) participants having NGT_non_MetS, 55 (18.71%) with IGT_non_MetS, and 74 (30.08%) with IGT_MetS experienced CV mortality. After adjusting for risk factors, the hazard ratios for CV mortality were 2 (95% confidence interval [CI], 1.38-2.91) for the IGT_non_MetS group and 2.96 (95% CI, 2.09-4.19) for the IGT_MetS group, compared with the NGT_non_MetS group. Similar patterns were observed for CV events, with hazard ratios of 1.49 (95% CI, 1.19-1.88) for the IGT_non_MetS group and 1.97 (95% CI, 1.58-2.47) for the IGT_MetS group. Sensitivity analysis revealed that the hazard ratios of the IGT_non_MetS and IGT_MetS groups indicated a higher risk of all-cause mortality, myocardial infarction events or myocardial infarction mortality, and stroke events or stroke mortality compared with that of the NGT_non_MetS group.

conclusionIGT_non_MetS increased the risk of CV mortality and events. Furthermore, when it occurred in conjunction with MetS, it further increased the risk of CV mortality and events. This suggested that active intervention is required.

Indexed as

Cardiovascular DiseasesGlucose IntoleranceMetabolic SyndromeAdultAgedBlood GlucoseFemaleFollow-Up StudiesHumansMaleMiddle AgedProportional Hazards ModelsRisk FactorsBlood Glucosecardiovascular eventsimpaired glucose tolerancemetabolic syndromemortality

Identifiers

PMID39155699
PMCPMC11331028

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Registered trials

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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.