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Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity
by
Flannick, Jason
, Parker, Margaret M.
, Hinkle, Gregory
, Ticau, Simina
, Yee, Elaine
, Willis, Carissa
, Deaton, Aimee M.
, Noetzli, Leila
, Vaishnaw, Akshay K.
, Fitzgerald, Kevin
, Hoffing, Rachel A.
, Nioi, Paul
, Dubey, Aditi
, Holleman, Aaron M.
, Dornbos, Peter
, Plekan, Mollie E.
, Ward, Lucas D.
in
45/43
/ 631/154/555
/ 631/208/205
/ 692/699/2743/393
/ Abdomen
/ Activin
/ Activin Receptors, Type I - genetics
/ Body Mass Index
/ Cardiovascular disease
/ Cardiovascular diseases
/ Coronary artery disease
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ Gene deletion
/ Genes
/ Genetic diversity
/ Genetic variance
/ Health risks
/ Heart diseases
/ Hip
/ Humanities and Social Sciences
/ Humans
/ Inhibin-beta Subunits - genetics
/ multidisciplinary
/ Obesity
/ Obesity - genetics
/ Obesity, Abdominal - genetics
/ Phenotypes
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Therapeutic applications
/ Therapeutic targets
/ Waist-Hip Ratio
2022
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Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity
by
Flannick, Jason
, Parker, Margaret M.
, Hinkle, Gregory
, Ticau, Simina
, Yee, Elaine
, Willis, Carissa
, Deaton, Aimee M.
, Noetzli, Leila
, Vaishnaw, Akshay K.
, Fitzgerald, Kevin
, Hoffing, Rachel A.
, Nioi, Paul
, Dubey, Aditi
, Holleman, Aaron M.
, Dornbos, Peter
, Plekan, Mollie E.
, Ward, Lucas D.
in
45/43
/ 631/154/555
/ 631/208/205
/ 692/699/2743/393
/ Abdomen
/ Activin
/ Activin Receptors, Type I - genetics
/ Body Mass Index
/ Cardiovascular disease
/ Cardiovascular diseases
/ Coronary artery disease
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ Gene deletion
/ Genes
/ Genetic diversity
/ Genetic variance
/ Health risks
/ Heart diseases
/ Hip
/ Humanities and Social Sciences
/ Humans
/ Inhibin-beta Subunits - genetics
/ multidisciplinary
/ Obesity
/ Obesity - genetics
/ Obesity, Abdominal - genetics
/ Phenotypes
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Therapeutic applications
/ Therapeutic targets
/ Waist-Hip Ratio
2022
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Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity
by
Flannick, Jason
, Parker, Margaret M.
, Hinkle, Gregory
, Ticau, Simina
, Yee, Elaine
, Willis, Carissa
, Deaton, Aimee M.
, Noetzli, Leila
, Vaishnaw, Akshay K.
, Fitzgerald, Kevin
, Hoffing, Rachel A.
, Nioi, Paul
, Dubey, Aditi
, Holleman, Aaron M.
, Dornbos, Peter
, Plekan, Mollie E.
, Ward, Lucas D.
in
45/43
/ 631/154/555
/ 631/208/205
/ 692/699/2743/393
/ Abdomen
/ Activin
/ Activin Receptors, Type I - genetics
/ Body Mass Index
/ Cardiovascular disease
/ Cardiovascular diseases
/ Coronary artery disease
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ Gene deletion
/ Genes
/ Genetic diversity
/ Genetic variance
/ Health risks
/ Heart diseases
/ Hip
/ Humanities and Social Sciences
/ Humans
/ Inhibin-beta Subunits - genetics
/ multidisciplinary
/ Obesity
/ Obesity - genetics
/ Obesity, Abdominal - genetics
/ Phenotypes
/ Proteins
/ Science
/ Science (multidisciplinary)
/ Therapeutic applications
/ Therapeutic targets
/ Waist-Hip Ratio
2022
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Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity
Journal Article
Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity
2022
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Overview
Identifying genetic variants associated with lower waist-to-hip ratio can reveal new therapeutic targets for abdominal obesity. We use exome sequences from 362,679 individuals to identify genes associated with waist-to-hip ratio adjusted for BMI (WHRadjBMI), a surrogate for abdominal fat that is causally linked to type 2 diabetes and coronary heart disease. Predicted loss of function (pLOF) variants in
INHBE
associate with lower WHRadjBMI and this association replicates in data from AMP-T2D-GENES.
INHBE
encodes a secreted protein, the hepatokine activin E. In vitro characterization of the most common
INHBE
pLOF variant in our study, indicates an in-frame deletion resulting in a 90% reduction in secreted protein levels. We detect associations with lower WHRadjBMI for variants in
ACVR1C
, encoding an activin receptor, further highlighting the involvement of activins in regulating fat distribution. These findings highlight activin E as a potential therapeutic target for abdominal obesity, a phenotype linked to cardiometabolic disease.
Abdominal fat has been shown to increase cardiometabolic disease risk. In this study, the authors report that loss-of-function variants in the gene
INHBE
associate with lower BMI-adjusted waist-to-hip ratio, a surrogate measure of abdominal fat.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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