Evidence map›Paper›PMID 29121669›Full record

ArticlePloS one2017

Application and interpretation of functional data analysis techniques to differential scanning calorimetry data from lupus patients.

Sarah K Kendrick, Qi Zheng, Nichola C Garbett, Guy N Brock

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Sarah K KendrickUniversity of Louisville, School of Public Health and Information Sciences, Department of Bioinformatics and Biostatistics, Louisville, KY, United States of America.ORCID http://orcid.org/0000-0001-7726-0386
Qi ZhengUniversity of Louisville, School of Public Health and Information Sciences, Department of Bioinformatics and Biostatistics, Louisville, KY, United States of America.
Nichola C GarbettUniversity of Louisville, James Graham Brown Cancer Center, Department of Medicine, Louisville, KY, United States of America.
Guy N BrockUniversity of Louisville, School of Public Health and Information Sciences, Department of Bioinformatics and Biostatistics, Louisville, KY, United States of America.
University of Louisville · US

Funding

The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
PROJ 12: STEM CELL-BASED VACCINE FOR CANCER PROPHYLAXISP20RR018733 · NCRR · UNIVERSITY OF LOUISVILLE · PI ZACHARIAS, WOLFGANG · 2003 to 2011
$18.9M
Molecular Targets COBREP20GM103482 · NIGMS · UNIVERSITY OF LOUISVILLE · PI MILLER, DONALD M. · 2012 to 2012
$2.0M
Plasma DSC for early detection of disease and therapeutic efficacy in melanomaR21CA187345 · NCI · UNIVERSITY OF LOUISVILLE · PI GARBETT, NICHOLA C. · 2014 to 2015
$359k
NCATS NIH HHS UL1 TR001070NCI NIH HHS R21 CA187345NCRR NIH HHS P20 RR018733NIGMS NIH HHS P20 GM103482
6 · The paper itself

Abstract

backgroundDSC is used to determine thermally-induced conformational changes of biomolecules within a blood plasma sample. Recent research has indicated that DSC curves (or thermograms) may have different characteristics based on disease status and, thus, may be useful as a monitoring and diagnostic tool for some diseases. Since thermograms are curves measured over a range of temperature values, they are considered functional data. In this paper we apply functional data analysis techniques to analyze differential scanning calorimetry (DSC) data from individuals from the Lupus Family Registry and Repository (LFRR). The aim was to assess the effect of lupus disease status as well as additional covariates on the thermogram profiles, and use FD analysis methods to create models for classifying lupus vs. control patients on the basis of the thermogram curves.

methodsThermograms were collected for 300 lupus patients and 300 controls without lupus who were matched with diseased individuals based on sex, race, and age. First, functional regression with a functional response (DSC) and categorical predictor (disease status) was used to determine how thermogram curve structure varied according to disease status and other covariates including sex, race, and year of birth. Next, functional logistic regression with disease status as the response and functional principal component analysis (FPCA) scores as the predictors was used to model the effect of thermogram structure on disease status prediction. The prediction accuracy for patients with Osteoarthritis and Rheumatoid Arthritis but without Lupus was also calculated to determine the ability of the classifier to differentiate between Lupus and other diseases. Data were divided 1000 times into separate 2/3 training and 1/3 test data for evaluation of predictions. Finally, derivatives of thermogram curves were included in the models to determine whether they aided in prediction of disease status.

resultsFunctional regression with thermogram as a functional response and disease status as predictor showed a clear separation in thermogram curve structure between cases and controls. The logistic regression model with FPCA scores as the predictors gave the most accurate results with a mean 79.22% correct classification rate with a mean sensitivity = 79.70%, and specificity = 81.48%. The model correctly classified OA and RA patients without Lupus as controls at a rate of 75.92% on average with a mean sensitivity = 79.70% and specificity = 77.6%. Regression models including FPCA scores for derivative curves did not perform as well, nor did regression models including covariates.

conclusionChanges in thermograms observed in the disease state likely reflect covalent modifications of plasma proteins or changes in large protein-protein interacting networks resulting in the stabilization of plasma proteins towards thermal denaturation. By relating functional principal components from thermograms to disease status, our Functional Principal Component Analysis model provides results that are more easily interpretable compared to prior studies. Further, the model could also potentially be coupled with other biomarkers to improve diagnostic classification for lupus.

Indexed as

Statistics as TopicCalorimetry, Differential ScanningCase-Control StudiesFemaleHumansLogistic ModelsLupus Erythematosus, SystemicMalePrincipal Component AnalysisRacial Groups

Identifiers

PMID29121669
PMCPMC5679774
OpenAlexW2767421114

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.