Evidence map›Paper›PMID 37840498›Full record

ArticleJournal of Alzheimer's disease : JAD2023

Genetic Insights into the Risk of Metabolic Syndrome and Its Components on Dementia: A Mendelian Randomization.

Qiang He, Wenjing Wang, Hao Li, Yang Xiong, Chuanyuan Tao, Lu Ma, Chao You

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% of its field
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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
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

7 authors at 2 institutions in 1 country.

Qiang HeDepartment of Neurosurgery, West China Hospital, Sichuan University, Wuhou District, Chengdu, Sichuan, China.
Wenjing WangDepartment of Pharmacy, Institute of Metabolic Diseases and Pharmacotherapy, West China Hospital, Sichuan University, Wuhou District, Chengdu, China.
Hao LiState Key Laboratory of Proteomics, National Center for Protein Sciences at Beijing, Beijing Institute of Radiation Medicine, Beijing, China.
Yang XiongDepartment of Urology, West China Hospital, Sichuan University, Chengdu, China.
Chuanyuan TaoDepartment of Neurosurgery, West China Hospital, Sichuan University, Wuhou District, Chengdu, Sichuan, China.
Lu MaDepartment of Neurosurgery, West China Hospital, Sichuan University, Wuhou District, Chengdu, Sichuan, China.
Chao YouDepartment of Neurosurgery, West China Hospital, Sichuan University, Wuhou District, Chengdu, Sichuan, China.
Sichuan University · CNBeijing Proteome Research Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of metabolic syndrome (MetS) on dementia is disputed.

objectiveWe conducted a Mendelian randomization to clarify whether the genetically predicted MetS and its components are casually associated with the risk of different dementia types.

methodsThe genetic predictors of MetS and its five components (waist circumference, hypertension, fasting blood glucose, triglycerides, and high-density lipoprotein cholesterol [HDL-C]) come from comprehensive public genome-wide association studies (GWAS). Different dementia types are collected from the GWAS in the European population. Inverse variance weighting is utilized as the main method, complemented by several sensitivity approaches to verify the robustness of the results.

resultsGenetically predicted MetS and its five components are not causally associated with the increasing risk of dementia (all p > 0.05). In addition, no significant association between MetS and its components and Alzheimer's disease, vascular dementia, frontotemporal dementia, dementia with Lewy bodies, and dementia due to Parkinson's disease (all p > 0.05), except the association between HDL-C and dementia with Lewy bodies. HDL-C may play a protective role in dementia with Lewy bodies (OR: 0.81, 95% CI: 0.72-0.92, p = 0.0010).

conclusionsFrom the perspective of genetic variants, our study provides novel evidence that MetS and its components are not associated with different dementia types.

Indexed as

Lewy Body DiseaseMetabolic SyndromeCholesterol, HDLGenome-Wide Association StudyHumansMendelian Randomization AnalysisRisk FactorsTriglyceridesCholesterol, HDLTriglyceridesAlzheimer’s diseasecausal associationcomponentsdementiaMendelian randomizationmetabolic syndrometypes

Identifiers

PMID37840498
PMCPMC10657705
OpenAlexW4387613942

What OpenQuestion holds

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LicenceCC BY-NC
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 OpenQuestion graph.