A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications
The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (...
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Published in | Nature communications Vol. 9; no. 1; pp. 1946 - 13 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
16.05.2018
Nature Publishing Group Nature Portfolio |
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Abstract | The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at
P
< 5 × 10
−8
, into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of “unexpected fat distribution given the BMI” and that a joint view of the genetics underlying related phenotypes can inform on important biology.
In GWAS, waist-to-hip ratio (WHR) is often adjusted for body mass index (BMI) to account for their correlation (WHRadjBMI). Here, Winkler et al. classify 159 genetic variants for BMI, WHR, or WHRadjBMI based on their effect directions for BMI and WHR to differentiate subtypes of adiposity genetics. |
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AbstractList | In GWAS, waist-to-hip ratio (WHR) is often adjusted for body mass index (BMI) to account for their correlation (WHRadjBMI). Here, Winkler et al. classify 159 genetic variants for BMI, WHR, or WHRadjBMI based on their effect directions for BMI and WHR to differentiate subtypes of adiposity genetics. The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10 −8 , into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of “unexpected fat distribution given the BMI” and that a joint view of the genetics underlying related phenotypes can inform on important biology. In GWAS, waist-to-hip ratio (WHR) is often adjusted for body mass index (BMI) to account for their correlation (WHRadjBMI). Here, Winkler et al. classify 159 genetic variants for BMI, WHR, or WHRadjBMI based on their effect directions for BMI and WHR to differentiate subtypes of adiposity genetics. The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10 −8 , into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of “unexpected fat distribution given the BMI” and that a joint view of the genetics underlying related phenotypes can inform on important biology. The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10-8, into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of "unexpected fat distribution given the BMI" and that a joint view of the genetics underlying related phenotypes can inform on important biology.The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10-8, into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of "unexpected fat distribution given the BMI" and that a joint view of the genetics underlying related phenotypes can inform on important biology. The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10−8, into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of “unexpected fat distribution given the BMI” and that a joint view of the genetics underlying related phenotypes can inform on important biology. The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here, we adopt a joint view of adiposity traits in ~322,154 subjects (GIANT consortium). We classify 159 signals associated with body mass index (BMI), waist-to-hip ratio (WHR), or WHR adjusted for BMI (WHRadjBMI) at P < 5 × 10 , into four classes based on the direction of their effects on BMI and WHR. Our classes help differentiate adiposity genetics with respect to anthropometry, fat depots, and metabolic health. Class-specific Mendelian randomization reveals that variants associated with both WHR-decrease and BMI increase are linked to metabolically rather favorable adiposity through beneficial hip fat. Class-specific enrichment analyses implicate digestive systems as a pathway in adiposity genetics. Our results demonstrate that WHRadjBMI variants capture relevant effects of "unexpected fat distribution given the BMI" and that a joint view of the genetics underlying related phenotypes can inform on important biology. |
ArticleNumber | 1946 |
Author | Kutalik, Zoltán Winkler, Thomas W Günther, Felix Höllerer, Simon Zimmermann, Martina Heid, Iris M Loos, Ruth JF |
Author_xml | – sequence: 1 givenname: Thomas W orcidid: 0000-0003-0292-5421 surname: Winkler fullname: Winkler, Thomas W email: thomas.winkler@ukr.de organization: Department of Genetic Epidemiology, University of Regensburg – sequence: 2 givenname: Felix surname: Günther fullname: Günther, Felix organization: Department of Genetic Epidemiology, University of Regensburg, Statistical Consulting Unit StaBLab, Department of Statistics, Ludwig-Maximilians-Universität Munich – sequence: 3 givenname: Simon surname: Höllerer fullname: Höllerer, Simon organization: Department of Genetic Epidemiology, University of Regensburg – sequence: 4 givenname: Martina orcidid: 0000-0002-6916-4404 surname: Zimmermann fullname: Zimmermann, Martina organization: Department of Genetic Epidemiology, University of Regensburg – sequence: 5 givenname: Ruth JF orcidid: 0000-0002-8532-5087 surname: Loos fullname: Loos, Ruth JF organization: The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, The Genetics of Obesity and Related Metabolic Traits Program, Icahn School of Medicine at Mount Sinai, The Mindich Child health and Development Institute, Icahn School of Medicine at Mount Sinai – sequence: 6 givenname: Zoltán surname: Kutalik fullname: Kutalik, Zoltán organization: Institute of Social and Preventive Medicine (IUMSP), Centre Hospitalier Universitaire Vaudois (CHUV), Swiss Institute of Bioinformatics – sequence: 7 givenname: Iris M surname: Heid fullname: Heid, Iris M email: iris.heid@ukr.de organization: Department of Genetic Epidemiology, University of Regensburg |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29769528$$D View this record in MEDLINE/PubMed |
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Snippet | The problem of the genetics of related phenotypes is often addressed by analyzing adjusted-model traits, but such traits warrant cautious interpretation. Here,... In GWAS, waist-to-hip ratio (WHR) is often adjusted for body mass index (BMI) to account for their correlation (WHRadjBMI). Here, Winkler et al. classify 159... |
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SubjectTerms | 38/43 631/208/205/2138 631/208/480 631/443/319/1642 Adipose tissue Adipose Tissue - metabolism Adiposity - genetics Anthropometry Body Mass Index Body size Consortia Energy Metabolism - genetics Genetic diversity Genetic variance Genetic Variation Genetics Genome-Wide Association Study - methods Hip Humanities and Social Sciences Humans Meta-Analysis as Topic Metabolism multidisciplinary Obesity - classification Obesity - genetics Obesity - metabolism Polymorphism, Single Nucleotide Science Science (multidisciplinary) Signal classification Waist-Hip Ratio |
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Title | A joint view on genetic variants for adiposity differentiates subtypes with distinct metabolic implications |
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