Evidence map›Paper›PMID 33121163›Full record

ArticleGenes2020

Genetic-Based Hypertension Subtype Identification Using Informative SNPs.

Yuanjing Ma, Hongmei Jiang, Sanjiv J Shah, Donna Arnett, Marguerite R Irvin, Yuan Luo

Abstract read
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Yuanjing MaDepartment of Statistics, Northwestern University, Evanston, IL 60208, USA.ORCID 0000-0003-3885-1604
Hongmei JiangDepartment of Statistics, Northwestern University, Evanston, IL 60208, USA.
Sanjiv J ShahFeinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Donna ArnettCollege of Medicine, University of Kentucky, Lexington, KY 40506, USA.
Marguerite R IrvinSchool of Public Health, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Yuan LuoFeinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

Funding

Study of Cardiac Mechanics in Systemic HypertensionR01HL107577 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHAH, SANJIV J · 2011 to 2019
$4.1M
Bayesian Generative Methods for Extracting and Modeling Relations in EHR NarrativesR21LM012618 · NLM · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LUO, YUAN · 2017 to 2018
$390k
NIH HHS R01HL107577NIH HHS R21LM012618
6 · The paper itself

Abstract

In this work, we proposed a process to select informative genetic variants for identifying clinically meaningful subtypes of hypertensive patients. We studied 575 African American (AA) and 612 Caucasian hypertensive participants enrolled in the Hypertension Genetic Epidemiology Network (HyperGEN) study and analyzed each race-based group separately. All study participants underwent GWAS (Genome-Wide Association Studies) and echocardiography. We applied a variety of statistical methods and filtering criteria, including generalized linear models, F statistics, burden tests, deleterious variant filtering, and others to select the most informative hypertension-related genetic variants. We performed an unsupervised learning algorithm non-negative matrix factorization (NMF) to identify hypertension subtypes with similar genetic characteristics. Kruskal-Wallis tests were used to demonstrate the clinical meaningfulness of genetic-based hypertension subtypes. Two subgroups were identified for both African American and Caucasian HyperGEN participants. In both AAs and Caucasians, indices of cardiac mechanics differed significantly by hypertension subtypes. African Americans tend to have more genetic variants compared to Caucasians; therefore, using genetic information to distinguish the disease subtypes for this group of people is relatively challenging, but we were able to identify two subtypes whose cardiac mechanics have statistically different distributions using the proposed process. The research gives a promising direction in using statistical methods to select genetic information and identify subgroups of diseases, which may inform the development and trial of novel targeted therapies.

Indexed as

AlgorithmsBlack or African AmericanBlood PressureGenome-Wide Association StudyHumansHypertensionMachine LearningPolymorphism, Single NucleotideWhite Peopleclustering algorithmhypertensionNMFsubtype identificationvariable selection

Identifiers

PMID33121163
PMCPMC7693873

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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.