P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers
BackgroundNon-alcoholic fatty liver disease (NAFLD) affects approximately one in four of the global adult population, and ranges in severity from benign fatty liver infiltration, to hepatitis, cirrhosis, hepatocellular carcinoma, and death. NAFLD has important implications for clinical trial volunte...
Gespeichert in:
Veröffentlicht in: | Gut 2023-09, Vol.72 (Suppl 3), p.A66-A67 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | A67 |
---|---|
container_issue | Suppl 3 |
container_start_page | A66 |
container_title | Gut |
container_volume | 72 |
creator | York, Thomas Rikard, James McCann, Bronagh Taubel, Jorg |
description | BackgroundNon-alcoholic fatty liver disease (NAFLD) affects approximately one in four of the global adult population, and ranges in severity from benign fatty liver infiltration, to hepatitis, cirrhosis, hepatocellular carcinoma, and death. NAFLD has important implications for clinical trial volunteers as an occult co-morbid condition – there is evidence that NAFLD modulates drug metabolism, with studies1 suggesting that Grade 3–4 liver reactions are four times more common in healthy volunteers with probable NAFLD than without.This research sought to develop a non-invasive, low-cost tool, utilising supervised machine learning techniques, to predict NAFLD in a clinical trial population.MethodsThis is an ongoing, observational cross-sectional study with a total of 1500 clinical trial volunteers attending the unit for a single day of biomarker assessment, including bioimpedance vector analysis (visceral fat%, total body fat% and skeletal muscle%), anthropometric measurement (BMI, waist circumference), and laboratory bloods (including HBA1c, liver enzymes and WCC). A FibroScan is performed as a pragmatic gold standard ‘outcome’ for NAFLD.In this interim analysis of 570 volunteers, a logistic regression model was trained for ability to predict the outcome of the fibroscan from a data subset containing: Age, Sex, Ethnicity/Race, Height, Weight, BMI, Waist Circumference, Body Fat Percentage. The programming language R was used to build the model.The data was divided into a training set of 399 volunteers (70%) used to build the model, and 171 volunteers (30%) used to validate its predictive accuracy.ResultsDemographics of the included volunteers were assessed as representative of a typical early-phase population. An initial fitting of individual predictive variables into the model showed that Age, Weight, BMI, Waist Circumference and Body Fat Percentage were highly statistically significant.On fitting a full model, Age, Ethnicity/Race, and Waist Circumference were ultimately included. Weight, Height, and BMI were removed due to a high degree of collinearity, problematic to model performance.When validating the model against the volunteer test dataset, it achieved a 82.4% predictive accuracy in identifying FibroScan result.Abstract P82 Figure 1ConclusionThis preliminary model shows promising results as an early-stage clinical tool to accurately predict steatosis amongst trial volunteers.This is a group where the effective detection of concomitant, occult fatty live |
doi_str_mv | 10.1136/gutjnl-2023-BASL.97 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_2866446083</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2866446083</sourcerecordid><originalsourceid>FETCH-proquest_journals_28664460833</originalsourceid><addsrcrecordid>eNqNjjtOxDAQhi0EEuFxApqRqLPYSUicckEgCgok6FcWmWwcOXYYT1bajoYDcEVOgkEcgOqXvv-bhxAXSq6UKuur7cKjd3khizK_WT8_rtrmQGSqqnVeFlofikxK1eTXTdUei5MYRyml1q3KxOeTLr7eP9YerGckOwHhHIgheOABocMdujBP6BPqwYAPCYBx20CWhwn6QL_iTNjZV7ZpLnm9Yd6Dszsk6GxEEzEdgAGN42EPxncwG7Y_W5mscbALbkkPIMUzcdQbF_H8L0_F5f3dy-1DPlN4WzDyZgwL-VRtCl3XVVVLXZb_s74BQJhgfQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2866446083</pqid></control><display><type>article</type><title>P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers</title><source>PubMed Central</source><creator>York, Thomas ; Rikard, James ; McCann, Bronagh ; Taubel, Jorg</creator><creatorcontrib>York, Thomas ; Rikard, James ; McCann, Bronagh ; Taubel, Jorg</creatorcontrib><description>BackgroundNon-alcoholic fatty liver disease (NAFLD) affects approximately one in four of the global adult population, and ranges in severity from benign fatty liver infiltration, to hepatitis, cirrhosis, hepatocellular carcinoma, and death. NAFLD has important implications for clinical trial volunteers as an occult co-morbid condition – there is evidence that NAFLD modulates drug metabolism, with studies1 suggesting that Grade 3–4 liver reactions are four times more common in healthy volunteers with probable NAFLD than without.This research sought to develop a non-invasive, low-cost tool, utilising supervised machine learning techniques, to predict NAFLD in a clinical trial population.MethodsThis is an ongoing, observational cross-sectional study with a total of 1500 clinical trial volunteers attending the unit for a single day of biomarker assessment, including bioimpedance vector analysis (visceral fat%, total body fat% and skeletal muscle%), anthropometric measurement (BMI, waist circumference), and laboratory bloods (including HBA1c, liver enzymes and WCC). A FibroScan is performed as a pragmatic gold standard ‘outcome’ for NAFLD.In this interim analysis of 570 volunteers, a logistic regression model was trained for ability to predict the outcome of the fibroscan from a data subset containing: Age, Sex, Ethnicity/Race, Height, Weight, BMI, Waist Circumference, Body Fat Percentage. The programming language R was used to build the model.The data was divided into a training set of 399 volunteers (70%) used to build the model, and 171 volunteers (30%) used to validate its predictive accuracy.ResultsDemographics of the included volunteers were assessed as representative of a typical early-phase population. An initial fitting of individual predictive variables into the model showed that Age, Weight, BMI, Waist Circumference and Body Fat Percentage were highly statistically significant.On fitting a full model, Age, Ethnicity/Race, and Waist Circumference were ultimately included. Weight, Height, and BMI were removed due to a high degree of collinearity, problematic to model performance.When validating the model against the volunteer test dataset, it achieved a 82.4% predictive accuracy in identifying FibroScan result.Abstract P82 Figure 1ConclusionThis preliminary model shows promising results as an early-stage clinical tool to accurately predict steatosis amongst trial volunteers.This is a group where the effective detection of concomitant, occult fatty liver disease is difficult and has significant implications for adverse drug reactions in first-in-human studies. Recruitment is expected to conclude in 2023 and, along with utilisation of the wider dataset including laboratory assessments, this is expected to improve the model’s predictive power.ReferenceTakyar V, Nath A, Beri A, et al. How healthy are the “healthy volunteers”? Penetrance of NAFLD in the biomedical research volunteer pool. Hepatology 2017;66:825–33.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2023-BASL.97</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Age ; Body fat ; Body measurements ; Cirrhosis ; Clinical trials ; Drug metabolism ; Ethnicity ; Fatty liver ; Hepatitis ; Hepatocellular carcinoma ; Liver diseases ; Medical research ; Minority & ethnic groups ; Skeletal muscle ; Statistical analysis ; Steatosis ; Volunteers ; Weight</subject><ispartof>Gut, 2023-09, Vol.72 (Suppl 3), p.A66-A67</ispartof><rights>2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>York, Thomas</creatorcontrib><creatorcontrib>Rikard, James</creatorcontrib><creatorcontrib>McCann, Bronagh</creatorcontrib><creatorcontrib>Taubel, Jorg</creatorcontrib><title>P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers</title><title>Gut</title><description>BackgroundNon-alcoholic fatty liver disease (NAFLD) affects approximately one in four of the global adult population, and ranges in severity from benign fatty liver infiltration, to hepatitis, cirrhosis, hepatocellular carcinoma, and death. NAFLD has important implications for clinical trial volunteers as an occult co-morbid condition – there is evidence that NAFLD modulates drug metabolism, with studies1 suggesting that Grade 3–4 liver reactions are four times more common in healthy volunteers with probable NAFLD than without.This research sought to develop a non-invasive, low-cost tool, utilising supervised machine learning techniques, to predict NAFLD in a clinical trial population.MethodsThis is an ongoing, observational cross-sectional study with a total of 1500 clinical trial volunteers attending the unit for a single day of biomarker assessment, including bioimpedance vector analysis (visceral fat%, total body fat% and skeletal muscle%), anthropometric measurement (BMI, waist circumference), and laboratory bloods (including HBA1c, liver enzymes and WCC). A FibroScan is performed as a pragmatic gold standard ‘outcome’ for NAFLD.In this interim analysis of 570 volunteers, a logistic regression model was trained for ability to predict the outcome of the fibroscan from a data subset containing: Age, Sex, Ethnicity/Race, Height, Weight, BMI, Waist Circumference, Body Fat Percentage. The programming language R was used to build the model.The data was divided into a training set of 399 volunteers (70%) used to build the model, and 171 volunteers (30%) used to validate its predictive accuracy.ResultsDemographics of the included volunteers were assessed as representative of a typical early-phase population. An initial fitting of individual predictive variables into the model showed that Age, Weight, BMI, Waist Circumference and Body Fat Percentage were highly statistically significant.On fitting a full model, Age, Ethnicity/Race, and Waist Circumference were ultimately included. Weight, Height, and BMI were removed due to a high degree of collinearity, problematic to model performance.When validating the model against the volunteer test dataset, it achieved a 82.4% predictive accuracy in identifying FibroScan result.Abstract P82 Figure 1ConclusionThis preliminary model shows promising results as an early-stage clinical tool to accurately predict steatosis amongst trial volunteers.This is a group where the effective detection of concomitant, occult fatty liver disease is difficult and has significant implications for adverse drug reactions in first-in-human studies. Recruitment is expected to conclude in 2023 and, along with utilisation of the wider dataset including laboratory assessments, this is expected to improve the model’s predictive power.ReferenceTakyar V, Nath A, Beri A, et al. How healthy are the “healthy volunteers”? Penetrance of NAFLD in the biomedical research volunteer pool. Hepatology 2017;66:825–33.</description><subject>Age</subject><subject>Body fat</subject><subject>Body measurements</subject><subject>Cirrhosis</subject><subject>Clinical trials</subject><subject>Drug metabolism</subject><subject>Ethnicity</subject><subject>Fatty liver</subject><subject>Hepatitis</subject><subject>Hepatocellular carcinoma</subject><subject>Liver diseases</subject><subject>Medical research</subject><subject>Minority & ethnic groups</subject><subject>Skeletal muscle</subject><subject>Statistical analysis</subject><subject>Steatosis</subject><subject>Volunteers</subject><subject>Weight</subject><issn>0017-5749</issn><issn>1468-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqNjjtOxDAQhi0EEuFxApqRqLPYSUicckEgCgok6FcWmWwcOXYYT1bajoYDcEVOgkEcgOqXvv-bhxAXSq6UKuur7cKjd3khizK_WT8_rtrmQGSqqnVeFlofikxK1eTXTdUei5MYRyml1q3KxOeTLr7eP9YerGckOwHhHIgheOABocMdujBP6BPqwYAPCYBx20CWhwn6QL_iTNjZV7ZpLnm9Yd6Dszsk6GxEEzEdgAGN42EPxncwG7Y_W5mscbALbkkPIMUzcdQbF_H8L0_F5f3dy-1DPlN4WzDyZgwL-VRtCl3XVVVLXZb_s74BQJhgfQ</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>York, Thomas</creator><creator>Rikard, James</creator><creator>McCann, Bronagh</creator><creator>Taubel, Jorg</creator><general>BMJ Publishing Group LTD</general><scope>K9.</scope></search><sort><creationdate>20230901</creationdate><title>P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers</title><author>York, Thomas ; Rikard, James ; McCann, Bronagh ; Taubel, Jorg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_28664460833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Age</topic><topic>Body fat</topic><topic>Body measurements</topic><topic>Cirrhosis</topic><topic>Clinical trials</topic><topic>Drug metabolism</topic><topic>Ethnicity</topic><topic>Fatty liver</topic><topic>Hepatitis</topic><topic>Hepatocellular carcinoma</topic><topic>Liver diseases</topic><topic>Medical research</topic><topic>Minority & ethnic groups</topic><topic>Skeletal muscle</topic><topic>Statistical analysis</topic><topic>Steatosis</topic><topic>Volunteers</topic><topic>Weight</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>York, Thomas</creatorcontrib><creatorcontrib>Rikard, James</creatorcontrib><creatorcontrib>McCann, Bronagh</creatorcontrib><creatorcontrib>Taubel, Jorg</creatorcontrib><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>York, Thomas</au><au>Rikard, James</au><au>McCann, Bronagh</au><au>Taubel, Jorg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers</atitle><jtitle>Gut</jtitle><date>2023-09-01</date><risdate>2023</risdate><volume>72</volume><issue>Suppl 3</issue><spage>A66</spage><epage>A67</epage><pages>A66-A67</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><abstract>BackgroundNon-alcoholic fatty liver disease (NAFLD) affects approximately one in four of the global adult population, and ranges in severity from benign fatty liver infiltration, to hepatitis, cirrhosis, hepatocellular carcinoma, and death. NAFLD has important implications for clinical trial volunteers as an occult co-morbid condition – there is evidence that NAFLD modulates drug metabolism, with studies1 suggesting that Grade 3–4 liver reactions are four times more common in healthy volunteers with probable NAFLD than without.This research sought to develop a non-invasive, low-cost tool, utilising supervised machine learning techniques, to predict NAFLD in a clinical trial population.MethodsThis is an ongoing, observational cross-sectional study with a total of 1500 clinical trial volunteers attending the unit for a single day of biomarker assessment, including bioimpedance vector analysis (visceral fat%, total body fat% and skeletal muscle%), anthropometric measurement (BMI, waist circumference), and laboratory bloods (including HBA1c, liver enzymes and WCC). A FibroScan is performed as a pragmatic gold standard ‘outcome’ for NAFLD.In this interim analysis of 570 volunteers, a logistic regression model was trained for ability to predict the outcome of the fibroscan from a data subset containing: Age, Sex, Ethnicity/Race, Height, Weight, BMI, Waist Circumference, Body Fat Percentage. The programming language R was used to build the model.The data was divided into a training set of 399 volunteers (70%) used to build the model, and 171 volunteers (30%) used to validate its predictive accuracy.ResultsDemographics of the included volunteers were assessed as representative of a typical early-phase population. An initial fitting of individual predictive variables into the model showed that Age, Weight, BMI, Waist Circumference and Body Fat Percentage were highly statistically significant.On fitting a full model, Age, Ethnicity/Race, and Waist Circumference were ultimately included. Weight, Height, and BMI were removed due to a high degree of collinearity, problematic to model performance.When validating the model against the volunteer test dataset, it achieved a 82.4% predictive accuracy in identifying FibroScan result.Abstract P82 Figure 1ConclusionThis preliminary model shows promising results as an early-stage clinical tool to accurately predict steatosis amongst trial volunteers.This is a group where the effective detection of concomitant, occult fatty liver disease is difficult and has significant implications for adverse drug reactions in first-in-human studies. Recruitment is expected to conclude in 2023 and, along with utilisation of the wider dataset including laboratory assessments, this is expected to improve the model’s predictive power.ReferenceTakyar V, Nath A, Beri A, et al. How healthy are the “healthy volunteers”? Penetrance of NAFLD in the biomedical research volunteer pool. Hepatology 2017;66:825–33.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/gutjnl-2023-BASL.97</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0017-5749 |
ispartof | Gut, 2023-09, Vol.72 (Suppl 3), p.A66-A67 |
issn | 0017-5749 1468-3288 |
language | eng |
recordid | cdi_proquest_journals_2866446083 |
source | PubMed Central |
subjects | Age Body fat Body measurements Cirrhosis Clinical trials Drug metabolism Ethnicity Fatty liver Hepatitis Hepatocellular carcinoma Liver diseases Medical research Minority & ethnic groups Skeletal muscle Statistical analysis Steatosis Volunteers Weight |
title | P82 An interim report on the development of a novel algorithm for the prediction of fatty liver disease in healthy and patient trial volunteers |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T13%3A47%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=P82%E2%80%85An%20interim%20report%20on%20the%20development%20of%20a%20novel%20algorithm%20for%20the%20prediction%20of%20fatty%20liver%20disease%20in%20healthy%20and%20patient%20trial%20volunteers&rft.jtitle=Gut&rft.au=York,%20Thomas&rft.date=2023-09-01&rft.volume=72&rft.issue=Suppl%203&rft.spage=A66&rft.epage=A67&rft.pages=A66-A67&rft.issn=0017-5749&rft.eissn=1468-3288&rft_id=info:doi/10.1136/gutjnl-2023-BASL.97&rft_dat=%3Cproquest%3E2866446083%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2866446083&rft_id=info:pmid/&rfr_iscdi=true |