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HIV infection does not prevent the metabolic benefits of diet‐induced weight loss in women with obesity
Author(s) -
Reeds Dominic N.,
Pietka Terri A.,
Yarasheski Kevin E.,
Cade W. Todd,
Patterson Bruce W.,
Okunade Adewole,
Abumrad Nada A.,
Klein Samuel
Publication year - 2017
Publication title -
obesity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.438
H-Index - 199
eISSN - 1930-739X
pISSN - 1930-7381
DOI - 10.1002/oby.21793
Subject(s) - adipose tissue , weight loss , medicine , endocrinology , insulin resistance , obesity , inflammation , insulin
Objective To test the hypothesis that HIV infection impairs the beneficial effects of weight loss on insulin sensitivity, adipose tissue inflammation, and endoplasmic reticulum (ER) stress. Methods A prospective clinical trial evaluated the effects of moderate diet‐induced weight loss on body composition, metabolic function, and adipose tissue biology in women with obesity who were HIV‐seronegative (HIV−) or HIV‐positive (HIV+). Body composition, multiorgan insulin sensitivity (assessed by using a two‐stage hyperinsulinemic‐euglycemic clamp procedure with stable isotopically labeled tracer infusions), and adipose tissue expression of markers of inflammation, autophagy, and ER stress were evaluated in 8 HIV− and 20 HIV+ women with obesity before and after diet‐induced weight loss of 6% to 8%. Results Although weight loss was not different between groups (∼7.5%), the decrease in fat‐free mass was greater in HIV+ than HIV− subjects (−4.4 ± 0.7% vs. −1.7 ± 1.0%, P < 0.05). Weight loss improved insulin sensitivity in adipose tissue (suppression of palmitate rate of appearance [Ra]), liver (suppression of glucose Ra), and muscle (glucose disposal) similarly in both groups. Weight loss did not affect adipose tissue expression of markers of inflammation or ER stress in either group. Conclusions Moderate diet‐induced weight loss improves multiorgan insulin sensitivity in HIV+ women to the same extent as women who are HIV−. However, weight loss causes a greater decline in fat‐free mass in HIV+ than HIV− women.