Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes

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Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes. / Ding, Cherlyn; Chan, Zhiling; Chooi, Yu Chung; Choo, John; Sadananthan, Suresh Anand; Michael, Navin; Velan, S Sendhil; Leow, Melvin K S; Magkos, Faidon.

I: Journal of Applied Physiology, Bind 125, Nr. 3, 2018, s. 909-915.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ding, C, Chan, Z, Chooi, YC, Choo, J, Sadananthan, SA, Michael, N, Velan, SS, Leow, MKS & Magkos, F 2018, 'Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes', Journal of Applied Physiology, bind 125, nr. 3, s. 909-915. https://doi.org/10.1152/japplphysiol.00250.2018

APA

Ding, C., Chan, Z., Chooi, Y. C., Choo, J., Sadananthan, S. A., Michael, N., Velan, S. S., Leow, M. K. S., & Magkos, F. (2018). Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes. Journal of Applied Physiology, 125(3), 909-915. https://doi.org/10.1152/japplphysiol.00250.2018

Vancouver

Ding C, Chan Z, Chooi YC, Choo J, Sadananthan SA, Michael N o.a. Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes. Journal of Applied Physiology. 2018;125(3):909-915. https://doi.org/10.1152/japplphysiol.00250.2018

Author

Ding, Cherlyn ; Chan, Zhiling ; Chooi, Yu Chung ; Choo, John ; Sadananthan, Suresh Anand ; Michael, Navin ; Velan, S Sendhil ; Leow, Melvin K S ; Magkos, Faidon. / Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes. I: Journal of Applied Physiology. 2018 ; Bind 125, Nr. 3. s. 909-915.

Bibtex

@article{749a8dda9e874dd18ea5a62647ec8879,
title = "Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes",
abstract = "Increased visceral adipose tissue (VAT) and intrahepatic triglyceride (IHTG) are important risk factors for the development of type 2 diabetes in subjects with obesity. The relative contribution of these ectopic fat depots to cardiometabolic risk differs between populations, depends on the degree of obesity and the level of cardiorespiratory fitness, and is difficult to dissect because VAT and IHTG typically covary. The aim of this study was to evaluate the effect of an isolated increase in VAT or IHTG on insulin sensitivity and insulin secretion in apparently healthy normal-weight Asian subjects. Total body fat (dual X-ray absorptiometry), VAT and IHTG (magnetic resonance), insulin sensitivity (4-h hyperinsulinemic-euglycemic clamp), beta cell responsivity and insulin secretion rate (3-h mixed meal with mathematical modeling), and cardiorespiratory fitness (maximal oxygen consumption [{\.V}O2max]) were evaluated in groups of lean subjects with low or high VAT (687 ± 94 vs. 1,279 ± 197 ml, matched for IHTG; n = 13 each) and low or high IHTG (1.7 ± 0.3 vs. 6.7 ± 2.0%, matched for VAT; n = 15 each). All groups were matched for age, sex, total body fat, and {\.V}O2max. High-VAT subjects had ~25% lower insulin sensitivity, ~20%–40% greater beta cell responsivity and insulin secretion rate, ~35% greater fasting triglyceride concentration, and ~40% lower adiponectin concentration than low-VAT subjects (all P < 0.05). No differences were observed between low-IHTG and high-IHTG subjects. Accumulation of excess fat in the intra-abdominal area is more strongly associated with metabolic dysfunction than accumulation of liver fat in lean Asians without diabetes.",
keywords = "Beta-cell function, Insulin secretion, Insulin sensitivity, Liver fat, Visceral fat",
author = "Cherlyn Ding and Zhiling Chan and Chooi, {Yu Chung} and John Choo and Sadananthan, {Suresh Anand} and Navin Michael and Velan, {S Sendhil} and Leow, {Melvin K S} and Faidon Magkos",
note = "(Ekstern)",
year = "2018",
doi = "10.1152/japplphysiol.00250.2018",
language = "English",
volume = "125",
pages = "909--915",
journal = "Journal of Applied Physiology",
issn = "8750-7587",
publisher = "American Physiological Society",
number = "3",

}

RIS

TY - JOUR

T1 - Visceral adipose tissue tracks more closely with metabolic dysfunction than intrahepatic triglyceride in lean Asians without diabetes

AU - Ding, Cherlyn

AU - Chan, Zhiling

AU - Chooi, Yu Chung

AU - Choo, John

AU - Sadananthan, Suresh Anand

AU - Michael, Navin

AU - Velan, S Sendhil

AU - Leow, Melvin K S

AU - Magkos, Faidon

N1 - (Ekstern)

PY - 2018

Y1 - 2018

N2 - Increased visceral adipose tissue (VAT) and intrahepatic triglyceride (IHTG) are important risk factors for the development of type 2 diabetes in subjects with obesity. The relative contribution of these ectopic fat depots to cardiometabolic risk differs between populations, depends on the degree of obesity and the level of cardiorespiratory fitness, and is difficult to dissect because VAT and IHTG typically covary. The aim of this study was to evaluate the effect of an isolated increase in VAT or IHTG on insulin sensitivity and insulin secretion in apparently healthy normal-weight Asian subjects. Total body fat (dual X-ray absorptiometry), VAT and IHTG (magnetic resonance), insulin sensitivity (4-h hyperinsulinemic-euglycemic clamp), beta cell responsivity and insulin secretion rate (3-h mixed meal with mathematical modeling), and cardiorespiratory fitness (maximal oxygen consumption [V̇O2max]) were evaluated in groups of lean subjects with low or high VAT (687 ± 94 vs. 1,279 ± 197 ml, matched for IHTG; n = 13 each) and low or high IHTG (1.7 ± 0.3 vs. 6.7 ± 2.0%, matched for VAT; n = 15 each). All groups were matched for age, sex, total body fat, and V̇O2max. High-VAT subjects had ~25% lower insulin sensitivity, ~20%–40% greater beta cell responsivity and insulin secretion rate, ~35% greater fasting triglyceride concentration, and ~40% lower adiponectin concentration than low-VAT subjects (all P < 0.05). No differences were observed between low-IHTG and high-IHTG subjects. Accumulation of excess fat in the intra-abdominal area is more strongly associated with metabolic dysfunction than accumulation of liver fat in lean Asians without diabetes.

AB - Increased visceral adipose tissue (VAT) and intrahepatic triglyceride (IHTG) are important risk factors for the development of type 2 diabetes in subjects with obesity. The relative contribution of these ectopic fat depots to cardiometabolic risk differs between populations, depends on the degree of obesity and the level of cardiorespiratory fitness, and is difficult to dissect because VAT and IHTG typically covary. The aim of this study was to evaluate the effect of an isolated increase in VAT or IHTG on insulin sensitivity and insulin secretion in apparently healthy normal-weight Asian subjects. Total body fat (dual X-ray absorptiometry), VAT and IHTG (magnetic resonance), insulin sensitivity (4-h hyperinsulinemic-euglycemic clamp), beta cell responsivity and insulin secretion rate (3-h mixed meal with mathematical modeling), and cardiorespiratory fitness (maximal oxygen consumption [V̇O2max]) were evaluated in groups of lean subjects with low or high VAT (687 ± 94 vs. 1,279 ± 197 ml, matched for IHTG; n = 13 each) and low or high IHTG (1.7 ± 0.3 vs. 6.7 ± 2.0%, matched for VAT; n = 15 each). All groups were matched for age, sex, total body fat, and V̇O2max. High-VAT subjects had ~25% lower insulin sensitivity, ~20%–40% greater beta cell responsivity and insulin secretion rate, ~35% greater fasting triglyceride concentration, and ~40% lower adiponectin concentration than low-VAT subjects (all P < 0.05). No differences were observed between low-IHTG and high-IHTG subjects. Accumulation of excess fat in the intra-abdominal area is more strongly associated with metabolic dysfunction than accumulation of liver fat in lean Asians without diabetes.

KW - Beta-cell function

KW - Insulin secretion

KW - Insulin sensitivity

KW - Liver fat

KW - Visceral fat

U2 - 10.1152/japplphysiol.00250.2018

DO - 10.1152/japplphysiol.00250.2018

M3 - Journal article

C2 - 29745794

VL - 125

SP - 909

EP - 915

JO - Journal of Applied Physiology

JF - Journal of Applied Physiology

SN - 8750-7587

IS - 3

ER -

ID: 203772898