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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...

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Autores principales: Dahal, Chetana, Wawro, Nina, Meisinger, Christa, Breuninger, Taylor A., Thorand, Barbara, Rathmann, Wolfgang, Koenig, Wolfgang, Hauner, Hans, Peters, Annette, Linseisen, Jakob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604647/
https://www.ncbi.nlm.nih.gov/pubmed/36294895
http://dx.doi.org/10.3390/life12101460
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author Dahal, Chetana
Wawro, Nina
Meisinger, Christa
Breuninger, Taylor A.
Thorand, Barbara
Rathmann, Wolfgang
Koenig, Wolfgang
Hauner, Hans
Peters, Annette
Linseisen, Jakob
author_facet Dahal, Chetana
Wawro, Nina
Meisinger, Christa
Breuninger, Taylor A.
Thorand, Barbara
Rathmann, Wolfgang
Koenig, Wolfgang
Hauner, Hans
Peters, Annette
Linseisen, Jakob
author_sort Dahal, Chetana
collection PubMed
description 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.
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spelling pubmed-96046472022-10-27 Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study Dahal, Chetana Wawro, Nina Meisinger, Christa Breuninger, Taylor A. Thorand, Barbara Rathmann, Wolfgang Koenig, Wolfgang Hauner, Hans Peters, Annette Linseisen, Jakob Life (Basel) Article 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. MDPI 2022-09-20 /pmc/articles/PMC9604647/ /pubmed/36294895 http://dx.doi.org/10.3390/life12101460 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dahal, Chetana
Wawro, Nina
Meisinger, Christa
Breuninger, Taylor A.
Thorand, Barbara
Rathmann, Wolfgang
Koenig, Wolfgang
Hauner, Hans
Peters, Annette
Linseisen, Jakob
Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title_full Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title_fullStr Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title_full_unstemmed Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title_short Optimized Metabotype Definition Based on a Limited Number of Standard Clinical Parameters in the Population-Based KORA Study
title_sort optimized metabotype definition based on a limited number of standard clinical parameters in the population-based kora study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604647/
https://www.ncbi.nlm.nih.gov/pubmed/36294895
http://dx.doi.org/10.3390/life12101460
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