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Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome

BACKGROUND/OBJECTIVES: A major risk factor of type 2 diabetes mellitus (T2DM) is a positive family history of diabetes. First degree relatives (FDR) of patients with T2DM are more insulin resistant and are reported to have larger abdominal subcutaneous adipocytes than adults without a family history...

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Autores principales: Anthanont, Pimjai, Ramos, Paola, Jensen, Michael D, Hames, Kazanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818259/
https://www.ncbi.nlm.nih.gov/pubmed/28736442
http://dx.doi.org/10.1038/ijo.2017.171
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author Anthanont, Pimjai
Ramos, Paola
Jensen, Michael D
Hames, Kazanna C.
author_facet Anthanont, Pimjai
Ramos, Paola
Jensen, Michael D
Hames, Kazanna C.
author_sort Anthanont, Pimjai
collection PubMed
description BACKGROUND/OBJECTIVES: A major risk factor of type 2 diabetes mellitus (T2DM) is a positive family history of diabetes. First degree relatives (FDR) of patients with T2DM are more insulin resistant and are reported to have larger abdominal subcutaneous adipocytes than adults without a family history. Our objectives were to assess whether a family history of T2DM is associated with larger abdominal adipocytes independent of age, sex, and abdominal subcutaneous fat and to assess whether FDR of T2DM is also independently related to femoral adipocyte size, as well as visceral fat and fasting plasma triglyceride (TG) concentrations. METHODS: We extracted adipocyte size, body composition, plasma TG and demographic data of non-diabetic research participants of previous studies conducted in our laboratory. We ascertained the family history of T2DM from the electronic medical records. Multivariate regression analysis was used to assess whether FDR of T2DM are more likely to have other risk factors after adjusting for known covariates. RESULTS: Of 604 participants, 148 were a FDR of T2DM. Although abdominal and femoral adipocyte size was greater in FDR of T2DM than those without a family history (0.74 ± 0.33 vs 0.63 ± 0.33 µg lipid/cell, P < 0.001; 0.81 ± 0.29 vs 0.72 ± 0.33 µg lipid/cell, P=0.01, respectively), this was confounded by FDR of T2DM being older, having greater BMI’s and percent body fat. A family history of T2DM was a significant predictor of abdominal adipocyte size after adjustment for age and body fat distribution parameters in females (total R(2)=0.5, p < 0.0001), but not in males. A family history of T2DM was not independently predictive of femoral adipocyte size, visceral fat area or TG. CONCLUSIONS: FDR of T2DM females have larger abdominal, but not femoral, adipocytes, even after accounting for age and body fat distribution.
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spelling pubmed-58182592018-02-19 Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome Anthanont, Pimjai Ramos, Paola Jensen, Michael D Hames, Kazanna C. Int J Obes (Lond) Article BACKGROUND/OBJECTIVES: A major risk factor of type 2 diabetes mellitus (T2DM) is a positive family history of diabetes. First degree relatives (FDR) of patients with T2DM are more insulin resistant and are reported to have larger abdominal subcutaneous adipocytes than adults without a family history. Our objectives were to assess whether a family history of T2DM is associated with larger abdominal adipocytes independent of age, sex, and abdominal subcutaneous fat and to assess whether FDR of T2DM is also independently related to femoral adipocyte size, as well as visceral fat and fasting plasma triglyceride (TG) concentrations. METHODS: We extracted adipocyte size, body composition, plasma TG and demographic data of non-diabetic research participants of previous studies conducted in our laboratory. We ascertained the family history of T2DM from the electronic medical records. Multivariate regression analysis was used to assess whether FDR of T2DM are more likely to have other risk factors after adjusting for known covariates. RESULTS: Of 604 participants, 148 were a FDR of T2DM. Although abdominal and femoral adipocyte size was greater in FDR of T2DM than those without a family history (0.74 ± 0.33 vs 0.63 ± 0.33 µg lipid/cell, P < 0.001; 0.81 ± 0.29 vs 0.72 ± 0.33 µg lipid/cell, P=0.01, respectively), this was confounded by FDR of T2DM being older, having greater BMI’s and percent body fat. A family history of T2DM was a significant predictor of abdominal adipocyte size after adjustment for age and body fat distribution parameters in females (total R(2)=0.5, p < 0.0001), but not in males. A family history of T2DM was not independently predictive of femoral adipocyte size, visceral fat area or TG. CONCLUSIONS: FDR of T2DM females have larger abdominal, but not femoral, adipocytes, even after accounting for age and body fat distribution. 2017-07-24 2017-11 /pmc/articles/PMC5818259/ /pubmed/28736442 http://dx.doi.org/10.1038/ijo.2017.171 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Anthanont, Pimjai
Ramos, Paola
Jensen, Michael D
Hames, Kazanna C.
Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title_full Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title_fullStr Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title_full_unstemmed Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title_short Family History of Type 2 Diabetes, Abdominal Adipocyte Size and Markers of the Metabolic Syndrome
title_sort family history of type 2 diabetes, abdominal adipocyte size and markers of the metabolic syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818259/
https://www.ncbi.nlm.nih.gov/pubmed/28736442
http://dx.doi.org/10.1038/ijo.2017.171
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