Optimized metabotype definition based on a limited number of standard clinical parameters in the population-based KORA study

  • The aim of metabotyping is to categorize individuals into metabolically similar groups. Earlier studies that explored metabotyping used numerous parameters, which made it less transferable to apply. Therefore, this study aimed to identify metabotypes based on a set of standard laboratory parameters that are regularly determined in clinical practice. K-means cluster analysis was used to group 3001 adults from the KORA F4 cohort into three clusters. We identified the clustering parameters through variable importance methods, without including any specific disease endpoint. Several unique combinations of selected parameters were used to create different metabotype models. Metabotype models were then described and evaluated, based on various metabolic parameters and on the incidence of cardiometabolic diseases. As a result, two optimal models were identified: a model composed of five parameters, which were fasting glucose, HDLc, non-HDLc, uric acid, and BMI (the metabolic disease model)The aim of metabotyping is to categorize individuals into metabolically similar groups. Earlier studies that explored metabotyping used numerous parameters, which made it less transferable to apply. Therefore, this study aimed to identify metabotypes based on a set of standard laboratory parameters that are regularly determined in clinical practice. K-means cluster analysis was used to group 3001 adults from the KORA F4 cohort into three clusters. We identified the clustering parameters through variable importance methods, without including any specific disease endpoint. Several unique combinations of selected parameters were used to create different metabotype models. Metabotype models were then described and evaluated, based on various metabolic parameters and on the incidence of cardiometabolic diseases. As a result, two optimal models were identified: a model composed of five parameters, which were fasting glucose, HDLc, non-HDLc, uric acid, and BMI (the metabolic disease model) for clustering; and a model that included four parameters, which were fasting glucose, HDLc, non-HDLc, and triglycerides (the cardiovascular disease model). These identified metabotypes are based on a few common parameters that are measured in everyday clinical practice. These metabotypes are cost-effective, and can be easily applied on a large scale in order to identify specific risk groups that can benefit most from measures to prevent cardiometabolic diseases, such as dietary recommendations and lifestyle interventions.show moreshow less

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Metadaten
Author:Chetana DahalORCiD, Nina WawroORCiD, Christa MeisingerGND, Taylor A. BreuningerORCiD, Barbara Thorand, Wolfgang Rathmann, Wolfgang Koenig, Hans Hauner, Annette Peters, Jakob LinseisenGND
URN:urn:nbn:de:bvb:384-opus4-984930
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/98493
ISSN:2075-1729OPAC
Parent Title (English):Life
Publisher:MDPI
Type:Article
Language:English
Date of first Publication:2022/09/20
Publishing Institution:Universität Augsburg
Release Date:2022/10/12
Tag:metabotype; cluster analysis; parameter selection; clinical marker; metabolic diseases; cardiovascular diseases
Volume:12
Issue:10
First Page:1460
DOI:https://doi.org/10.3390/life12101460
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Lehrstuhl für Epidemiologie
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):CC-BY 4.0: Creative Commons: Namensnennung (mit Print on Demand)