Association between skeletal muscle fat content and very‐low‐density lipoprotein‐apolipoprotein B‐100 transport in obesity: effect of weight loss. Issue 10 (29th May 2014)
- Record Type:
- Journal Article
- Title:
- Association between skeletal muscle fat content and very‐low‐density lipoprotein‐apolipoprotein B‐100 transport in obesity: effect of weight loss. Issue 10 (29th May 2014)
- Main Title:
- Association between skeletal muscle fat content and very‐low‐density lipoprotein‐apolipoprotein B‐100 transport in obesity: effect of weight loss
- Authors:
- Chan, D. C.
Gan, S. K.
Wong, A. T. Y.
Barrett, P. H. R.
Watts, G. F. - Abstract:
- <abstract abstract-type="main" id="dom12311-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="dom12311-sec-0001" sec-type="section"> <title>Aims</title> <p id="dom12311-para-0001">Ectopic deposition of fat in skeletal muscle is a feature of metabolic syndrome, but its specific association with very‐low‐density lipoprotein (VLDL)‐apolipoprotein (apo) B‐100 metabolism remains unclear.</p> </sec> <sec id="dom12311-sec-0002" sec-type="section"> <title>Methods</title> <p id="dom12311-para-0002">We examined the association between skeletal muscle fat content and VLDL‐apoB‐100 kinetics in 25 obese subjects, and the responses of these variables to weight loss. The fat contents of liver, abdomen and skeletal muscle were determined by magnetic resonance imaging, and VLDL‐apoB‐100 kinetics were assessed using stable isotope tracers.</p> </sec> <sec id="dom12311-sec-0003" sec-type="section"> <title>Results</title> <p id="dom12311-para-0003">In obese subjects who were insulin sensitive (homeostasis model assessment, HOMA, score ≤ 2.6, n = 12), skeletal muscle fat content was significantly associated with hepatic fat content (r = 0.636), energy intake (r = 0.694), plasma triglyceride (r = 0.644), apoB‐100 (r = 0.529), glucose (r = 0.622), VLDL‐apoB‐100 concentrations (r = 0.860), VLDL‐apoB‐100 fractional catabolic rate (FCR; r = −0.581) and VLDL‐apoB‐100 secretion rate (r = 0.607). These associations were not found in obese subjects who were insulin resistant (HOMA<abstract abstract-type="main" id="dom12311-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="dom12311-sec-0001" sec-type="section"> <title>Aims</title> <p id="dom12311-para-0001">Ectopic deposition of fat in skeletal muscle is a feature of metabolic syndrome, but its specific association with very‐low‐density lipoprotein (VLDL)‐apolipoprotein (apo) B‐100 metabolism remains unclear.</p> </sec> <sec id="dom12311-sec-0002" sec-type="section"> <title>Methods</title> <p id="dom12311-para-0002">We examined the association between skeletal muscle fat content and VLDL‐apoB‐100 kinetics in 25 obese subjects, and the responses of these variables to weight loss. The fat contents of liver, abdomen and skeletal muscle were determined by magnetic resonance imaging, and VLDL‐apoB‐100 kinetics were assessed using stable isotope tracers.</p> </sec> <sec id="dom12311-sec-0003" sec-type="section"> <title>Results</title> <p id="dom12311-para-0003">In obese subjects who were insulin sensitive (homeostasis model assessment, HOMA, score ≤ 2.6, n = 12), skeletal muscle fat content was significantly associated with hepatic fat content (r = 0.636), energy intake (r = 0.694), plasma triglyceride (r = 0.644), apoB‐100 (r = 0.529), glucose (r = 0.622), VLDL‐apoB‐100 concentrations (r = 0.860), VLDL‐apoB‐100 fractional catabolic rate (FCR; r = −0.581) and VLDL‐apoB‐100 secretion rate (r = 0.607). These associations were not found in obese subjects who were insulin resistant (HOMA score &gt;2.6, n = 13). Of these 25 subjects, 10 obese subjects underwent a 16‐week weight loss program. The low‐fat diet achieved significant reduction (p &lt; 0.05) in body weight, visceral and subcutaneous fat areas, liver and skeletal muscle fat, energy intake, triglyceride, insulin, HOMA score, VLDL‐apoB100 concentrations and VLDL‐apoB100 secretion rate. The percentage reduction of skeletal muscle fat with weight loss was significantly associated with the corresponding changes in VLDL‐apoB100 concentration (r = 0.770, p = 0.009) and VLDL‐apoB‐100 secretion (r = 0.682, p = 0.030).</p> </sec> <sec id="dom12311-sec-0004" sec-type="section"> <title>Conclusions</title> <p id="dom12311-para-0004">Skeletal muscle fat content is associated with VLDL‐apoB‐100 transport. Weight loss lowers skeletal muscle fat and VLDL‐apoB‐100 secretion.</p> </sec> </abstract> … (more)
- Is Part Of:
- Diabetes, obesity & metabolism. Volume 16:Issue 10(2014:Oct.)
- Journal:
- Diabetes, obesity & metabolism
- Issue:
- Volume 16:Issue 10(2014:Oct.)
- Issue Display:
- Volume 16, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 16
- Issue:
- 10
- Issue Sort Value:
- 2014-0016-0010-0000
- Page Start:
- 994
- Page End:
- 1000
- Publication Date:
- 2014-05-29
- Subjects:
- Diabetes -- Periodicals
Obesity -- Periodicals
Metabolism -- Disorders -- Periodicals
Clinical pharmacology -- Periodicals
616.462 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1462-8902&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1463-1326 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/dom.12311 ↗
- Languages:
- English
- ISSNs:
- 1462-8902
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.601970
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3087.xml