Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes

Abstract The frequent ACE insertion/deletion polymorphism (I/D) is, albeit inconsistently, associated with impaired glucose tolerance and insulin resistance. We recently observed an enhanced upregulation of ACE by elevated fat intake in GG-carriers of the I/D-surrogate rs4343 variant and therefore i...

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Autores principales: Rita Schüler, Martin A. Osterhoff, Turid Frahnow, Matthias Möhlig, Joachim Spranger, Darko Stefanovski, Richard N. Bergman, Li Xu, Anne-Cathrin Seltmann, Stefan Kabisch, Silke Hornemann, Michael Kruse, Andreas F. H. Pfeiffer
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:0913f2fc8a184fa1805fcb5bc6470a622021-12-02T12:32:38ZDietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes10.1038/s41598-017-08300-72045-2322https://doaj.org/article/0913f2fc8a184fa1805fcb5bc6470a622017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08300-7https://doaj.org/toc/2045-2322Abstract The frequent ACE insertion/deletion polymorphism (I/D) is, albeit inconsistently, associated with impaired glucose tolerance and insulin resistance. We recently observed an enhanced upregulation of ACE by elevated fat intake in GG-carriers of the I/D-surrogate rs4343 variant and therefore investigated its potential nutrigenetic role in glucose metabolism. In this nutritional intervention study 46 healthy and non-obese twin pairs consumed recommended low fat diets for 6 weeks before they received a 6-week high fat (HF) diet under isocaloric conditions. Intravenous glucose tolerance tests were performed before and after 1 and 6 weeks of HF diet. While glucose tolerance did not differ between genotypes at baseline it significantly declined in GG-carriers after 6 weeks HF diet (p = 0.001) with higher 2 h glucose and insulin concentrations compared to AA/AG-carriers (p = 0.003 and p = 0.042). Furthermore, the gene-diet interaction was confirmed in the cross-sectional Metabolic Syndrome Berlin Potsdam study (p = 0.012), with the GG-genotypes being significantly associated with prevalent type 2 diabetes for participants with high dietary fat intake ≥37% (GG vs. AA/AG, OR 2.36 [1.02–5.49], p = 0.045). In conclusion, the association between the rs4343 variant and glucose tolerance is modulated by dietary fat intake. The ACE rs4343 variant is a novel nutrient-sensitive type 2 diabetes risk marker potentially applicable for nutrigenetic dietary counseling.Rita SchülerMartin A. OsterhoffTurid FrahnowMatthias MöhligJoachim SprangerDarko StefanovskiRichard N. BergmanLi XuAnne-Cathrin SeltmannStefan KabischSilke HornemannMichael KruseAndreas F. H. PfeifferNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rita Schüler
Martin A. Osterhoff
Turid Frahnow
Matthias Möhlig
Joachim Spranger
Darko Stefanovski
Richard N. Bergman
Li Xu
Anne-Cathrin Seltmann
Stefan Kabisch
Silke Hornemann
Michael Kruse
Andreas F. H. Pfeiffer
Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
description Abstract The frequent ACE insertion/deletion polymorphism (I/D) is, albeit inconsistently, associated with impaired glucose tolerance and insulin resistance. We recently observed an enhanced upregulation of ACE by elevated fat intake in GG-carriers of the I/D-surrogate rs4343 variant and therefore investigated its potential nutrigenetic role in glucose metabolism. In this nutritional intervention study 46 healthy and non-obese twin pairs consumed recommended low fat diets for 6 weeks before they received a 6-week high fat (HF) diet under isocaloric conditions. Intravenous glucose tolerance tests were performed before and after 1 and 6 weeks of HF diet. While glucose tolerance did not differ between genotypes at baseline it significantly declined in GG-carriers after 6 weeks HF diet (p = 0.001) with higher 2 h glucose and insulin concentrations compared to AA/AG-carriers (p = 0.003 and p = 0.042). Furthermore, the gene-diet interaction was confirmed in the cross-sectional Metabolic Syndrome Berlin Potsdam study (p = 0.012), with the GG-genotypes being significantly associated with prevalent type 2 diabetes for participants with high dietary fat intake ≥37% (GG vs. AA/AG, OR 2.36 [1.02–5.49], p = 0.045). In conclusion, the association between the rs4343 variant and glucose tolerance is modulated by dietary fat intake. The ACE rs4343 variant is a novel nutrient-sensitive type 2 diabetes risk marker potentially applicable for nutrigenetic dietary counseling.
format article
author Rita Schüler
Martin A. Osterhoff
Turid Frahnow
Matthias Möhlig
Joachim Spranger
Darko Stefanovski
Richard N. Bergman
Li Xu
Anne-Cathrin Seltmann
Stefan Kabisch
Silke Hornemann
Michael Kruse
Andreas F. H. Pfeiffer
author_facet Rita Schüler
Martin A. Osterhoff
Turid Frahnow
Matthias Möhlig
Joachim Spranger
Darko Stefanovski
Richard N. Bergman
Li Xu
Anne-Cathrin Seltmann
Stefan Kabisch
Silke Hornemann
Michael Kruse
Andreas F. H. Pfeiffer
author_sort Rita Schüler
title Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
title_short Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
title_full Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
title_fullStr Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
title_full_unstemmed Dietary Fat Intake Modulates Effects of a Frequent ACE Gene Variant on Glucose Tolerance with association to Type 2 Diabetes
title_sort dietary fat intake modulates effects of a frequent ace gene variant on glucose tolerance with association to type 2 diabetes
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/0913f2fc8a184fa1805fcb5bc6470a62
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