Evidence map›Paper›PMID 42490696›Full record

ArticlePloS one2026

Lipid-modifying pharmacotherapy in diabetes mellitus: A protocol for a systematic review and network meta-analysis of randomised trials.

Xudong Zhao, Cheng Tang, Tianqi Yuan, Jiafan Chen, Cuijuan Shi, Xiaoyu Liu, Ruigeng Yang, Yushang Zhi, Wenrui Huang, Chunyan Zhu and 2 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xudong ZhaoDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.ORCID https://orcid.org/0009-0008-7450-7273
Cheng TangDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Tianqi YuanQihuang College of Beijing University of Chinese Medicine, Beijing, China.
Jiafan ChenDepartment of Cardiology, Guang' anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Cuijuan ShiDepartment of Endocrinology and Metabolism, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Xiaoyu LiuDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Ruigeng YangDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yushang ZhiGraduate School of Beijing University of Chinese Medicine, Beijing, China.
Wenrui HuangShenzhen Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, China.
Chunyan ZhuPeripheral Vascular Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yu ChenDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Shidong WangDepartment of Endocrinology and Nephrology II, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe global prevalence of diabetes mellitus (DM) has risen markedly, with patients facing a substantially higher risk of atherosclerotic cardiovascular disease (ASCVD) and related mortality. Although lipid-modifying agents, including statins, fibrates, cholesterol absorption inhibitors, proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i), bromodomain and extra-terminal motif inhibitors (BETi), and adenosine triphosphate-citrate lyase inhibitors (ACLi) continue to emerge, their comparative efficacy and safety in patients with DM remain uncertain. This study aims to address this gap through a comprehensive network meta-analysis (NMA) of randomized controlled trials (RCTs) evaluating cardiovascular outcomes, lipid-modifying efficacy, and safety among these therapies. METHODS AND ANALYSIS: A systematic search will be performed in PubMed, Web of Science, Scopus, the Cochrane Central Register of Controlled Trials (CENTRAL), Embase (via Ovid), International Clinical Trials Registry Platform (ICTRP) and ClinicalTrials.gov from inception, without language or regional restrictions. Eligible studies will include parallel-design RCTs comparing monotherapy or combination therapy. The primary outcome will be cardiovascular events (composite and individual), and secondary outcomes will include cardiac biomarkers, ASCVD risk scores, lipid parameters (TC, LDL-C, HDL-C, TG) and safety outcomes. Two reviewers will independently conduct study selection, data extraction, and quality assessment using the Cochrane Risk of Bias 2 (RoB 2.0) tool, with evidence certainty evaluated via the Confidence in Network Meta-Analysis (CINeMA) framework. Data will be standardized where appropriate, and analyses, including assessment of publication bias, will be conducted using Stata 18 and R. The protocol is registered with PROSPERO, and findings will be disseminated through peer-reviewed publication. Registration: PROSPERO CRD420251163974.

Indexed as

Diabetes MellitusHypolipidemic AgentsHumansNetwork Meta-Analysis as TopicRandomized Controlled Trials as TopicSystematic Reviews as TopicHypolipidemic Agents

Identifiers

PMID42490696
PMCPMC13395341

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.