Adipose tissue in muscle: a novel depot similar in size to visceral adipose tissue
- PMID: 15817870
- PMCID: PMC1482784
- DOI: 10.1093/ajcn/81.4.903
Adipose tissue in muscle: a novel depot similar in size to visceral adipose tissue
Abstract
Background: The manner in which fat depot volumes and distributions, particularly the adipose tissue (AT) between the muscles, vary by race is unknown.
Objective: The objective was to quantify a previously unstudied and novel intermuscular AT (IMAT) depot and subcutaneous AT, visceral AT (VAT), and total-body skeletal muscle mass in healthy sedentary African American (AA), Asian, and white adults by whole-body magnetic resonance imaging. IMAT is the AT between muscles and within the boundary of the muscle fascia.
Design: Analyses were conducted on 227 women [AA (n = 79): body mass index (BMI; in kg/m(2)), 29.0 +/- 5.5; age, 45.7 +/- 16.9 y; Asian (n = 38): BMI, 21.7 +/- 2.9; age, 47.2 +/- 19.9 y; whites (n = 110): BMI, 24.9 +/- 5.4; age, 43.7 +/- 16.2 y]) and 111 men [AA (n = 39): BMI, 25.6 +/- 3.2; age, 45.5 +/- 18.8 y; Asian (n = 13): BMI, 24.9 +/- 2.5; age, 45.6 +/- 25.0 y; white (n = 59): BMI, 25.8 +/- 3.8; age 44.5 +/- 16.3 y].
Results: IMAT depots were not significantly different in size between race groups at low levels of adiposity; however, with increasing adiposity, AAs had a significantly greater increment in the proportion of total AT (TAT) than did the whites and Asians (58, 46, and 44 g IMAT/kg TAT, respectively; P = 0.001). VAT depots were not significantly different in size at low levels of adiposity but, with increasing adiposity, VAT accumulation was greater than IMAT accumulation in the Asians and whites; no significant differences were observed in AAs.
Conclusion: Race differences in AT distribution extend to IMAT, a depot that may influence race-ethnicity differences in dysglycemia.
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Comment in
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Racial differences in fat distribution: the importance of intermuscular fat.Am J Clin Nutr. 2005 Apr;81(4):731-2. doi: 10.1093/ajcn/81.4.731. Am J Clin Nutr. 2005. PMID: 15817844 No abstract available.
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