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J Appl Physiol 100: 609-614, 2006. First published October 13, 2005; doi:10.1152/japplphysiol.00797.2005
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Increased intramyocellular lipid accumulation in HIV-infected women with fat redistribution

Martin Torriani,1 Bijoy J. Thomas,1 Robert B. Barlow,1 Jamie Librizzi,2 Sara Dolan,2 and Steven Grinspoon2

1Division of Musculoskeletal Radiology and 2Program in Nutritional Metabolism, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts

Submitted 6 July 2005 ; accepted in final form 10 October 2005

The human immunodeficiency virus (HIV)-lipodystrophy syndrome is associated with fat redistribution and metabolic abnormalities, including insulin resistance. Increased intramyocellular lipid (IMCL) concentrations are thought to contribute to insulin resistance, being linked to metabolic and body composition variables. We examined 46 women: HIV infected with fat redistribution (n = 25), and age- and body mass index-matched HIV-negative controls (n = 21). IMCL was measured by 1H-magnetic resonance spectroscopy, and body composition was assessed with computed tomography, dual-energy X-ray absorptiometry (DEXA), and magnetic resonance imaging. Plasma lipid profile and markers of glucose homeostasis were obtained. IMCL was significantly increased in tibialis anterior [135.0 ± 11.5 vs. 85.1 ± 13.2 institutional units (IU); P = 0.007] and soleus [643.7 ± 61.0 vs. 443.6 ± 47.2 IU, P = 0.017] of HIV-infected subjects compared with controls. Among HIV-infected subjects, calf subcutaneous fat area (17.8 ± 2.3 vs. 35.0 ± 2.5 cm2, P < 0.0001) and extremity fat by DEXA (11.8 ± 1.1 vs. 15.6 ± 1.2 kg, P = 0.024) were reduced, whereas visceral abdominal fat (125.2 ± 11.3 vs. 74.4 ± 12.3 cm2, P = 0.004), triglycerides (131.1 ± 11.0 vs. 66.3 ± 12.3 mg/dl, P = 0.0003), and fasting insulin (10.8 ± 0.9 vs. 7.0 ± 0.9 µIU/ml, P = 0.004) were increased compared with control subjects. Triglycerides (r = 0.39, P = 0.05) and extremity fat as percentage of whole body fat by DEXA (r = –0.51, P = 0.01) correlated significantly with IMCL in the HIV but not the control group. Extremity fat (beta = –633.53, P = 0.03) remained significantly associated with IMCL among HIV-infected patients, controlling for visceral abdominal fat, abdominal subcutaneous fat, and antiretroviral medications in a regression model. These data demonstrate increased IMCL in HIV-infected women with a mixed lipodystrophy pattern, being most significantly associated with reduced extremity fat. Further studies are necessary to determine the relationship between extremity fat loss and increased IMCL in HIV-infected women.

magnetic resonance spectroscopy; insulin resistance; protease inhibitor; acquired immunodeficiency syndrome



Address for reprint requests and other correspondence: M. Torriani, Division of Musculoskeletal Radiology, Dept. of Radiology, Massachusetts General Hospital, 55 Fruit St., YAW 6048, Boston, MA 02114 (e-mail: mtorriani{at}partners.org)




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