Evidence map›Paper›PMID 30898803›Full record

ArticleBMJ open2019

Familial aggregation of myocardial infarction and coaggregation of myocardial infarction and autoimmune disease: a nationwide population-based cross-sectional study in Taiwan.

Chun-Li Wang, Chang-Fu Kuo, Yung-Hsin Yeh, Mei-Yun Hsieh, Chi-Tai Kuo, Shang-Hung Chang

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Family studies in the age of big data.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  3. Systemic lupus erythematosus as a genetic disease.Clinical immunology (Orlando, Fla.) · 2022
    Article
  4. Review
  5. 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

6 authors at 3 institutions in 2 countries.

Chun-Li WangCardiovascular Department, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Chang-Fu KuoSchool of Medicine, Chang Gung University, Taoyuan, Taiwan.
Yung-Hsin YehCardiovascular Department, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Mei-Yun HsiehCenter for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Linkou, Taiwan.
Chi-Tai KuoCardiovascular Department, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Shang-Hung ChangCardiovascular Department, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Chang Gung University · TWUniversity of Nottingham · GBChang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study examined how a history of myocardial infarction (MI) in a person's first-degree relatives affects that person's risk of developing MI and autoimmune diseases.

designNationwide population-based cross-sectional study

settingAll healthcare facilities in Taiwan.

participantsA total of 24 361 345 individuals were enrolled.

methodsUsing data from the National Health Insurance Research Database in Taiwan, we conducted a nationwide cross-sectional study of data collected from all beneficiaries in the Taiwan National Health Insurance system in 2015, of whom 259 360 subjects had at least one first-degree relative affected by MI in 2015. We estimated the absolute risks and relative risks (RRs) of MI and autoimmune disease in those subjects, and the relative contribution of genetic and environmental factors to their MI susceptibility.

resultsThe absolute risks of MI for subjects with at least one affected first-degree relative and the general population were 0.87% and 0.56%, respectively, in 2015. Patients with affected first-degree relatives were significantly associated with a higher RR of MI (1.76, 95% CI: 1.68 to 1.85) compared with the general population. There was no association with a higher RR of autoimmune disease. The sibling, offspring and parental MI history conferred RRs (95% CI) for MI of 2.35 (1.96 to 2.83), 2.21 (2.05 to 2.39) and 1.60 (1.52 to 1.68), respectively. The contributions of heritability, shared environmental factors and non-shared environmental factors to MI susceptibility were 19.6%, 3.4% and 77.0%, respectively.

conclusionsIndividuals who have first-degree relatives with a history of MI have a higher risk of developing MI than the general population. Non-shared environmental factors contributed more significantly to MI susceptibility than did heritability and shared environmental factors. A family history of MI was not associated with an increased risk of autoimmune disease.

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultAgedAged, 80 and overAge DistributionAutoimmune DiseasesCross-Sectional StudiesEnvironmentFemaleHumansMaleMiddle AgedMyocardial InfarctionSex DistributionSocioeconomic Factorsautoimmune diseasefamilial aggregationfamily historymyocardial infarction

Identifiers

PMID30898803
PMCPMC6475449
OpenAlexW2924302461

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.