Evidence map›Paper›PMID 30845215›Full record

ArticlePloS one2019

Association of cardiovascular events and lipoprotein particle size: Development of a risk score based on functional data analysis.

Charles M Rowland, Dov Shiffman, Michael Caulfield, Veronica Garcia, Olle Melander, Trevor Hastie

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
  2. Article
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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.

Charles M RowlandQuest Diagnostics, San Juan Capistrano, CA, United States of America.ORCID 0000-0002-0317-5717
Dov ShiffmanQuest Diagnostics, San Juan Capistrano, CA, United States of America.
Michael CaulfieldQuest Diagnostics, San Juan Capistrano, CA, United States of America.
Veronica GarciaQuest Diagnostics, San Juan Capistrano, CA, United States of America.
Olle MelanderDepartment of Clinical Sciences, Lund University, Malmö, Sweden.
Trevor HastieDepartment of Statistics, Stanford University, Stanford, CA, United States of America.

Funding

British Heart Foundation FS/12/82/29736Medical Research Council G9521010Medical Research Council MC_EX_MR/M009203/1Medical Research Council MC_PC_14089Medical Research Council MR/M009203/1
6 · The paper itself

Abstract

backgroundFunctional data is data represented by functions (curves or surfaces of a low-dimensional index). Functional data often arise when measurements are collected over time or across locations. In the field of medicine, plasma lipoprotein particles can be quantified according to particle diameter by ion mobility. GOAL: We wanted to evaluate the utility of functional analysis for assessing the association of plasma lipoprotein size distribution with cardiovascular disease after adjustment for established risk factors including standard lipids.

methodsWe developed a model to predict risk of cardiovascular disease among participants in a case-cohort study of the Malmö Prevention Project. We used a linear model with 311 coefficients, corresponding to measures of lipoprotein mass at each of 311 diameters, and assumed these coefficients varied smoothly along the diameter index. The smooth function was represented as an expansion of natural cubic splines where the smoothness parameter was chosen by assessment of a series of nested splines. Cox proportional hazards models of time to a first cardiovascular disease event were used to estimate the smooth coefficient function among a training set consisting of one half of the participants. The resulting model was used to calculate a functional risk score for the remaining half of the participants (test set) and its association with events was assessed in Cox models that adjusted for traditional cardiovascular risk factors.

resultsIn the test set, participants with a functional risk score in the highest quartile were found to be at increased risk of cardiovascular events compared with the lowest quartile (Hazard ratio = 1.34; 95% Confidence Interval: 1.05 to 1.70) after adjustment for established risk factors.

conclusionIn an independent test set of Malmö Prevention Project participants, the functional risk score was found to be associated with cardiovascular events after adjustment for traditional risk factors including standard lipids.

Indexed as

AgedCardiovascular DiseasesCase-Control StudiesFemaleHumansLipoproteinsMaleMiddle AgedParticle SizeProportional Hazards ModelsRisk FactorsLipoproteins

Identifiers

PMID30845215
PMCPMC6405139

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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.