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Predicting functional decline and survival in amyotrophic lateral sclerosis

Predicting functional decline and survival in amyotrophic lateral sclerosis
Predicting functional decline and survival in amyotrophic lateral sclerosis
Background: better predictors of amyotrophic lateral sclerosis disease course could enable smaller and more targeted clinical trials. Partially to address this aim, the Prize for Life foundation collected de-identified records from amyotrophic lateral sclerosis sufferers who participated in clinical trials of investigational drugs and made them available to researchers in the PRO-ACT database.

Methods: in this study, time series data from PRO-ACT subjects were fitted to exponential models. Binary classes for decline in the total score of amyotrophic lateral sclerosis functional rating scale revised (ALSFRS-R) (fast/slow progression) and survival (high/low death risk) were derived. Data was segregated into training and test sets via cross validation. Learning algorithms were applied to the demographic, clinical and laboratory parameters in the training set to predict ALSFRS-R decline and the derived fast/slow progression and high/low death risk categories. The performance of predictive models was assessed by cross-validation in the test set using Receiver Operator Curves and root mean squared errors.

Results: a model created using a boosting algorithm containing the decline in four parameters (weight, alkaline phosphatase, albumin and creatine kinase) post baseline, was able to predict functional decline class (fast or slow) with fair accuracy (AUC=0.82). However similar approaches to build a predictive model for decline class by baseline subject characteristics were not successful. In contrast, baseline values of total bilirubin, gamma glutamyltransferase, urine specific gravity and ALSFRS-R item score - climbing stairs were sufficient to predict survival class.

Conclusions: using combinations of small numbers of variables it was possible to predict classes of functional decline and survival across the 1-2 year timeframe available in PRO-ACT. These findings may have utility for design of future ALS clinical trials.
Holbrook, Joanna
69989b79-2710-4f12-946e-c6214e1b6513
Ong, Mei-Lyn
f5580640-95e1-4da7-9295-5c498dba6497
Tang, Pei Fang
ba27ef3c-75b4-4aea-bcd2-2bad46406fa7
Holbrook, Joanna
69989b79-2710-4f12-946e-c6214e1b6513
Ong, Mei-Lyn
f5580640-95e1-4da7-9295-5c498dba6497
Tang, Pei Fang
ba27ef3c-75b4-4aea-bcd2-2bad46406fa7

Holbrook, Joanna, Ong, Mei-Lyn and Tang, Pei Fang (2017) Predicting functional decline and survival in amyotrophic lateral sclerosis. PLoS ONE, 12 (4). (doi:10.1371/journal.pone.0174925).

Record type: Article

Abstract

Background: better predictors of amyotrophic lateral sclerosis disease course could enable smaller and more targeted clinical trials. Partially to address this aim, the Prize for Life foundation collected de-identified records from amyotrophic lateral sclerosis sufferers who participated in clinical trials of investigational drugs and made them available to researchers in the PRO-ACT database.

Methods: in this study, time series data from PRO-ACT subjects were fitted to exponential models. Binary classes for decline in the total score of amyotrophic lateral sclerosis functional rating scale revised (ALSFRS-R) (fast/slow progression) and survival (high/low death risk) were derived. Data was segregated into training and test sets via cross validation. Learning algorithms were applied to the demographic, clinical and laboratory parameters in the training set to predict ALSFRS-R decline and the derived fast/slow progression and high/low death risk categories. The performance of predictive models was assessed by cross-validation in the test set using Receiver Operator Curves and root mean squared errors.

Results: a model created using a boosting algorithm containing the decline in four parameters (weight, alkaline phosphatase, albumin and creatine kinase) post baseline, was able to predict functional decline class (fast or slow) with fair accuracy (AUC=0.82). However similar approaches to build a predictive model for decline class by baseline subject characteristics were not successful. In contrast, baseline values of total bilirubin, gamma glutamyltransferase, urine specific gravity and ALSFRS-R item score - climbing stairs were sufficient to predict survival class.

Conclusions: using combinations of small numbers of variables it was possible to predict classes of functional decline and survival across the 1-2 year timeframe available in PRO-ACT. These findings may have utility for design of future ALS clinical trials.

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journal.pone.0174925 - Version of Record
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More information

Accepted/In Press date: 18 March 2017
e-pub ahead of print date: 13 April 2017
Published date: 13 April 2017
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 407985
URI: http://eprints.soton.ac.uk/id/eprint/407985
PURE UUID: 02466deb-ccb5-43e2-aa3c-20557d534e38
ORCID for Joanna Holbrook: ORCID iD orcid.org/0000-0003-1791-6894

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Date deposited: 06 May 2017 01:03
Last modified: 15 Mar 2024 13:36

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Contributors

Author: Joanna Holbrook ORCID iD
Author: Mei-Lyn Ong
Author: Pei Fang Tang

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