Evidence map›Paper›PMID 38371655›Full record

Observational studyGlobal heart2024

Heartache and Heartbreak: An Observational and Mendelian Randomization Study.

Dihui Cai, Mengming Xia, Xuhui Chen, Kunimasa Yagi, Liang Xu, Bingyu Wang, Yanyi Wang, Yujie Zhou, Jianhui Liu

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Global heart, 2024. 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
3.9field-weighted citation impact, top 7% 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. Identification ofDepression and anxiety · 2025
    Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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 at 1 institution in 2 countries.

Dihui CaiDepartment of Cardiology, Ningbo Medical Center of Lihuili Hospital, Ningbo, Zhejiang, China.
Mengming XiaDepartment of Pharmacy, Ningbo Medical Center of Lihuili Hospital, Ningbo, Zhejiang, China.
Xuhui ChenDepartment of Pharmacy, Ningbo Medical Center of Lihuili Hospital, Ningbo, Zhejiang, China.
Kunimasa YagiSchool of Medicine, Kanazawa Medical University, Kanazawa, Ishikawa, Japan.
Liang XuSchool of Laboratory Medicine and Life Sciences, Wenzhou Medial University, Wenzhou, Zhejiang, China.
Bingyu WangDepartment of Cardiology, Ningbo Medical Center of Lihuili Hospital, Ningbo, Zhejiang, China.
Yanyi WangHealth Science Center, Ningbo University, Ningbo, Zhejiang, China.
Yujie ZhouHealth Science Center, Ningbo University, Ningbo, Zhejiang, China.
Jianhui LiuDepartment of Cardiology, Ningbo Medical Center of Lihuili Hospital, Ningbo, Zhejiang, China.
Ningbo University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Depression has a significant effect on cardiovascular disease (CVD), but uncertainties persist regarding which modifiable risk factors mediate the causal effects. We aim to determine whether depression is causally linked to CVD and which modifiable risk factors play potential mediating roles. Methods: We used a two-sample Mendelian randomization (MR) approach and NHANES 2007-2018 data to estimate the effects of depression on various CVD cases and investigated 28 potential mediators of the association between depression and CVD. Results: The results of our MR analysis indicated that genetically determined depression was associated with increased risk of several CVD, including coronary heart disease (odds ratio (OR) = 1.14; 95% confidence interval (CI): 1.05,1.22), myocardial infarction (OR = 1.19; 95% CI, 1.09,1.31), atrial fibrillation (OR = 1.14; 95% CI, 1.06,1.22), and stroke (OR = 1.13; 95% CI, 1.05,1.22). However, there was no causal association between depression and heart failure. Four out of 28 cardiometabolic risk factors, including hyperlipidemia, hypertension, diabetes, and prescription opioid use, were identified as mediators of the association between depression and various CVDs. Observational association analyses from NHANES data yielded consistent results. Conclusion: Our findings demonstrated that depression has a causal detrimental effect on various CVDs. Four causal mediators (hyperlipidemia, hypertension, diabetes, and prescription opioid use) were screened to explain the causal effect. Implementing targeted management strategies for these risk factors may be warranted to mitigate the public health burden of CVD among individuals with depression.

Indexed as

Cardiovascular DiseasesDiabetes MellitusHyperlipidemiasHypertensionMyocardial InfarctionAnalgesics, OpioidHumansMendelian Randomization AnalysisNutrition SurveysPolymorphism, Single NucleotideAnalgesics, Opioidcardiovascular diseasesdepressionMendelian randomization

Identifiers

PMID38371655
PMCPMC10870952
OpenAlexW4391910923

What OpenQuestion 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 OpenQuestion graph.