Evidence map›Paper›PMID 37799151›Full record

ArticleFrontiers in public health2023

A machine learning approach to personalized predictors of dyslipidemia: a cohort study.

Guadalupe Gutiérrez-Esparza, Tomas Pulido, Mireya Martínez-García, Tania Ramírez-delReal, Lucero E Groves-Miralrio, Manlio F Márquez-Murillo, Luis M Amezcua-Guerra, Gilberto Vargas-Alarcón, Enrique Hernández-Lemus

Open access · goldAbstract read
In one paragraph

Article in Frontiers in public health, 2023. 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
2.1field-weighted citation impact, top 12% 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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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 3 institutions in 1 country.

Guadalupe Gutiérrez-Esparza *Researcher for Mexico CONAHCYT, National Council of Humanities Sciences, and Technologies, Mexico City, Mexico.
Tomas Pulido *Clinical Research, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Mireya Martínez-GarcíaDepartment of Immunology, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Tania Ramírez-delRealResearcher for Mexico CONAHCYT, National Council of Humanities Sciences, and Technologies, Mexico City, Mexico.
Lucero E Groves-MiralrioDepartment of Immunology, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Manlio F Márquez-MurilloDepartment of Electrocardiology, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Luis M Amezcua-GuerraDepartment of Immunology, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Gilberto Vargas-AlarcónDepartment of Molecular Biology and Endocrinology, National Institute of Cardiology "Ignacio Chávez", Mexico City, Mexico.
Enrique Hernández-LemusComputational Genomics Division, National Institute of Genomic Medicine, Mexico City, Mexico.
Instituto Nacional de Cardiología · MXConsejo Nacional de Humanidades, Ciencias y Tecnologías · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mexico ranks second in the global prevalence of obesity in the adult population, which increases the probability of developing dyslipidemia. Dyslipidemia is closely related to cardiovascular diseases, which are the leading cause of death in the country. Therefore, developing tools that facilitate the prediction of dyslipidemias is essential for prevention and early treatment. Methods: In this study, we utilized a dataset from a Mexico City cohort consisting of 2,621 participants, men and women aged between 20 and 50 years, with and without some type of dyslipidemia. Our primary objective was to identify potential factors associated with different types of dyslipidemia in both men and women. Machine learning algorithms were employed to achieve this goal. To facilitate feature selection, we applied the Variable Importance Measures (VIM) of Random Forest (RF), XGBoost, and Gradient Boosting Machine (GBM). Additionally, to address class imbalance, we employed Synthetic Minority Over-sampling Technique (SMOTE) for dataset resampling. The dataset encompassed anthropometric measurements, biochemical tests, dietary intake, family health history, and other health parameters, including smoking habits, alcohol consumption, quality of sleep, and physical activity. Results: Our results revealed that the VIM algorithm of RF yielded the most optimal subset of attributes, closely followed by GBM, achieving a balanced accuracy of up to 80%. The selection of the best subset of attributes was based on the comparative performance of classifiers, evaluated through balanced accuracy, sensitivity, and specificity metrics. Discussion: The top five features contributing to an increased risk of various types of dyslipidemia were identified through the machine learning technique. These features include body mass index, elevated uric acid levels, age, sleep disorders, and anxiety. The findings of this study shed light on significant factors that play a role in dyslipidemia development, aiding in the early identification, prevention, and treatment of this condition.

Indexed as

Cardiovascular DiseasesDyslipidemiasAdultAlgorithmsCohort StudiesFemaleHumansMachine LearningMaleMiddle AgedYoung Adultfeature selectionhypercholesterolemiahypertriglyceridemiahypoalphalipoproteinemiamachine learningMexico Citymixed hyperlipidemiasTlalpan 2020 cohort

Identifiers

PMID37799151
PMCPMC10548235
OpenAlexW4386930669

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.