Literature DB >> 24081739

Overfeeding over 24 hours does not activate brown adipose tissue in humans.

Mathias Schlögl1, Paolo Piaggi, Pradeep Thiyyagura, Eric M Reiman, Kewei Chen, Calvin Lutrin, Jonathan Krakoff, Marie S Thearle.   

Abstract

CONTEXT: Human brown adipose tissue (BAT) is activated with cold exposure, but it is unknown whether overfeeding activates BAT.
OBJECTIVE: We determined BAT activation with cold, fasting, and overfeeding and the relationship of BAT activation with future weight change. DESIGN, SETTING, PARTICIPANTS, AND
INTERVENTIONS: Sixteen healthy adults were evaluated during energy balance, fasting, and 24 hours of 200% overfeeding. All subjects had a fluorodeoxyglucose-positron emission tomography (PET) scan after exposure to 16°C to determine cold-induced BAT activity (CIBA). The first six subjects had a second PET scan after 36 hours of fasting to establish the lack of BAT activation at 22°C. The other subjects' second PET scan occurred after 24 hours of overfeeding at 22°C but only if they demonstrated CIBA. Twelve subjects returned at 6 months for reassessment of body composition. MAIN OUTCOME MEASURES: BAT was defined in cool scans as voxels with a standardized uptake value (SUV) of 2.0 or greater and Hounsfield units between -250 and -10. Body composition was assessed by dual-energy x-ray absorptiometry.
RESULTS: Although 75% of the subjects demonstrated visible CIBA, none had visual BAT activity after overfeeding. CIBA was greater than that observed in the same defined BAT voxels after fasting (n = 6; 2.9 ± 0.5 vs 1.2 ± 0.2; Δ = -1.7; 95% confidence interval -2.4, -1.0 SUV; P < .01). In the second cohort, CIBA was also higher than observed BAT voxel activity after 24 hours overfeeding (n = 8; 3.5 ± 0.7 vs 0.9 ± 0.2; Δ = -2.6; 95% confidence interval -3.2, -1.9 SUV; P < .01). Baseline CIBA negatively correlated with changes in fat mass after 6 months (r = -0.72, P = .009).
CONCLUSIONS: BAT may be important in weight regulation unrelated to the response to overeating.

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Year:  2013        PMID: 24081739      PMCID: PMC3849677          DOI: 10.1210/jc.2013-2387

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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